| geneid | 4850 |
|---|---|
| ensemblid | ENSG00000080802.21 |
| hgncid | 7880 |
| symbol | CNOT4 |
| name | CCR4-NOT transcription complex subunit 4 |
| refseq_nuc | NM_001190850.2 |
| refseq_prot | NP_001177779.1 |
| ensembl_nuc | ENST00000541284.6 |
| ensembl_prot | ENSP00000445508.1 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 135361795 |
| end | 135510102 |
| strand | - |
| ver | v1.2 |
| region | chr7:135361795-135510102 |
| region5000 | chr7:135356795-135515102 |
| regionname0 | CNOT4_chr7_135361795_135510102 |
| regionname5000 | CNOT4_chr7_135356795_135515102 |
| 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 | 713 | 248 | 62 | 48 | 97 | 9 | 30 | 80 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0002 | 0/0 | 713 | 104 | 11 | 17 | 68 | 2 | 6 | 55 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0003 | 0/0 | 713 | 4 | 1 | 3 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0004 | 0/0 | 713 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0005 | 0/0 | 713 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0006 | 0/0 | 713 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0007 | 0/0 | 713 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2142 | 240 | 57 | 47 | 96 | 9 | 30 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| c0002 | 0/0 | 2142 | 103 | 11 | 17 | 68 | 2 | 5 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| c0003 | 1/0 | 2142 | 6 | 5 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| c0004 | 0/0 | 2142 | 4 | 1 | 3 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| c0005 | 0/0 | 2142 | 3 | 0 | 3 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| c0006 | 0/0 | 2142 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| c0007 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| c0008 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| c0009 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| c0010 | 0/0 | 2142 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| c0011 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| 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 | 1397 | 303 | 41 | 68 | 154 | 9 | 30 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| t0002 | 1/0 | 1397 | 41 | 30 | 4 | 0 | 3 | 3 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| t0003 | 0/0 | 1397 | 12 | 0 | 0 | 12 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| t0004 | 0/0 | 1397 | 2 | 0 | 0 | 0 | 0 | 2 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| t0005 | 0/0 | 1397 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| t0006 | 0/0 | 1397 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| t0007 | 0/0 | 1397 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| t0008 | 0/0 | 1397 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| 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 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0184 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0317 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2142 | 240 | 57 | 47 | 96 | 9 | 30 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0001c0003 | 1/0 | 2142 | 6 | 5 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0001c0008 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0001c0010 | 0/0 | 2142 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0002c0002 | 0/0 | 2142 | 103 | 11 | 17 | 68 | 2 | 5 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0002c0011 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0003c0004 | 0/0 | 2142 | 4 | 1 | 3 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0004c0005 | 0/0 | 2142 | 3 | 0 | 3 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0005c0006 | 0/0 | 2142 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0006c0007 | 0/0 | 2142 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0007c0009 | 0/0 | 2142 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3538 | 189 | 30 | 44 | 84 | 6 | 24 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0001c0001t0002 | 0/0 | 3538 | 34 | 25 | 3 | 0 | 3 | 3 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0001c0001t0003 | 0/0 | 3538 | 12 | 0 | 0 | 12 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0001c0001t0004 | 0/0 | 3538 | 2 | 0 | 0 | 0 | 0 | 2 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0001c0001t0005 | 0/0 | 3538 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0001c0001t0007 | 0/0 | 3538 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0001c0001t0008 | 0/0 | 3538 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0001c0003t0002 | 1/0 | 3538 | 6 | 5 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0001c0008t0001 | 0/0 | 3538 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0001c0010t0002 | 0/0 | 3538 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0002c0002t0001 | 0/0 | 3538 | 102 | 10 | 17 | 68 | 2 | 5 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0002c0002t0006 | 0/0 | 3538 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0002c0011t0001 | 0/0 | 3538 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0003c0004t0001 | 0/0 | 3538 | 4 | 1 | 3 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0004c0005t0001 | 0/0 | 3538 | 3 | 0 | 3 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0005c0006t0001 | 0/0 | 3538 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0006c0007t0001 | 0/0 | 3538 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| a0007c0009t0001 | 0/0 | 3538 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | copy fasta | chr7 | 135356795 | 135515102 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0317 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0003g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0003g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0003g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0003g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0004g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0004g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0005g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0007g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0001t0008g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0003t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0003t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0003t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0003t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0003t0002g0184 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0003t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0008t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0001c0010t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0002t0006g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0002c0011t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0003c0004t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0003c0004t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0003c0004t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0003c0004t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0004c0005t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0004c0005t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0004c0005t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0005c0006t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0006c0007t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| a0007c0009t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0190 | EUR | GBR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | GBR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0122 | EUR | FIN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0305 | EUR | FIN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0189 | EUR | FIN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00323 | hp2 | a0006 | c0007 | t0001 | g0311 | EUR | FIN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0351 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0340 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0362 | EAS | CHS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0020 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0333 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0103 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0116 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01106 | hp1 | a0004 | c0005 | t0001 | g0126 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01167 | hp1 | a0004 | c0005 | t0001 | g0128 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01167 | hp2 | a0003 | c0004 | t0001 | g0215 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01169 | hp1 | a0004 | c0005 | t0001 | g0127 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01175 | hp1 | a0003 | c0004 | t0001 | g0211 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01255 | hp1 | a0005 | c0006 | t0001 | g0224 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0344 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0101 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01257 | hp1 | a0003 | c0004 | t0001 | g0219 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0104 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0107 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01261 | hp1 | a0001 | c0010 | t0002 | g0326 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0051 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0050 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0319 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0056 | EUR | IBS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | IBS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | IBS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0043 | EUR | IBS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0233 | EUR | IBS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0288 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0099 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0105 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0096 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0060 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0106 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0102 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0098 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0300 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02055 | hp2 | a0003 | c0004 | t0001 | g0192 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02080 | hp1 | a0001 | c0008 | t0001 | g0325 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0354 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0019 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0294 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CDX | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | CDX | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0093 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02258 | hp1 | a0002 | c0002 | t0006 | g0002 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0097 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02280 | hp2 | a0001 | c0003 | t0002 | g0179 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0100 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02451 | hp2 | a0001 | c0003 | t0002 | g0182 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0348 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0337 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0138 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0291 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02886 | hp1 | a0001 | c0003 | t0002 | g0183 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0296 | AFR | ESN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ESN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02970 | hp2 | a0001 | c0003 | t0002 | g0181 | AFR | ESN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0301 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0302 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0046 | AFR | ESN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0346 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0048 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0347 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0049 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ESN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | ESN | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03669 | hp2 | a0002 | c0002 | t0001 | g0047 | SAS | PJL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0129 | SAS | STU | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | STU | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0086 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0330 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0329 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03927 | hp2 | a0002 | c0011 | t0001 | g0044 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0336 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | STU | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | STU | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0188 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | BEB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | STU | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | STU | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0323 | SAS | STU | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | CHB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CHB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | CHB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0358 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0353 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0352 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0055 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0186 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18980 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0359 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18992 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0360 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19000 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19004 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | LWK | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0303 | AFR | LWK | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19054 | hp1 | a0007 | c0009 | t0001 | g0024 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19075 | hp1 | a0001 | c0001 | t0003 | g0361 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0356 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19080 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0355 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0357 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19091 | hp1 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0292 | AFR | YRI | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA19240 | hp2 | a0001 | c0003 | t0002 | g0349 | AFR | YRI | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0293 | AFR | ASW | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA20129 | hp2 | a0001 | c0001 | t0008 | g0350 | AFR | ASW | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA20905 | hp1 | a0001 | c0001 | t0007 | g0225 | SAS | GIH | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | GIH | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0290 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0069 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | USA | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | USA | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | LWK | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0304 | AFR | LWK | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0317 | REF | REF | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0002 | g0184 | REF | REF | CNOT4_chr7_135356795_135515102 | CNOT4 | chr7 | 135356795 | 135515102 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:135362941
|
G | A | 1 | a0007 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.2086C>T | p.Pro696Ser | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 12/12 | 2392/3538 | 2086/2142 | 696/713 | chr7 | 135362941 | ||
| chr7:135364052
|
C | T | 3 | a0002a0004a0007 | 108 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(105): Show |
missense_variant | MODERATE | c.1642G>A | p.Val548Ile | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 11/12 | 1948/3538 | 1642/2142 | 548/713 | chr7 | 135364052 | ||
| chr7:135394272
|
C | T | 1 | a0006 | 1 | HG00323.hp2 | missense_variant | MODERATE | c.1273G>A | p.Val425Ile | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/12 | 1579/3538 | 1273/2142 | 425/713 | chr7 | 135394272 | ||
| chr7:135398201
|
G | C | 1 | a0003 | 4 | HG01167.hp2 HG01175.hp1 HG01257.hp1 others(1): Show |
missense_variant | MODERATE | c.847C>G | p.Leu283Val | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/12 | 1153/3538 | 847/2142 | 283/713 | chr7 | 135398201 | ||
| chr7:135410539
|
A | G | 1 | a0005 | 1 | HG01255.hp1 | missense_variant | MODERATE | c.797T>C | p.Val266Ala | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/12 | 1103/3538 | 797/2142 | 266/713 | chr7 | 135410539 | ||
| chr7:135438312
|
G | C | 1 | a0004 | 3 | HG01106.hp1 HG01167.hp1 HG01169.hp1 |
missense_variant | MODERATE | c.20C>G | p.Ala7Gly | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/12 | 326/3538 | 20/2142 | 7/713 | chr7 | 135438312 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:135362951
|
T | C | 10 | a0001c0001a0001c0008a0001c0010others(7): Show | 356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
synonymous_variant | LOW | c.2076A>G | p.Thr692Thr | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 12/12 | 2382/3538 | 2076/2142 | 692/713 | chr7 | 135362951 | ||
| chr7:135394093
|
C | T | 1 | a0001c0008 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.1452G>A | p.Ala484Ala | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/12 | 1758/3538 | 1452/2142 | 484/713 | chr7 | 135394093 | ||
| chr7:135413590
|
G | A | 1 | a0001c0010 | 1 | HG01261.hp1 | synonymous_variant | LOW | c.585C>T | p.Tyr195Tyr | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/12 | 891/3538 | 585/2142 | 195/713 | chr7 | 135413590 | ||
| chr7:135422168
|
T | C | 1 | a0002c0011 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.360A>G | p.Leu120Leu | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/12 | 666/3538 | 360/2142 | 120/713 | chr7 | 135422168 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:135361800
|
C | T | 14 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(11): Show | 320 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*1085G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 12/12 | 1085 | chr7 | 135361800 | |||||
| chr7:135362570
|
T | C | 1 | a0001c0001t0004 | 2 | HG03490.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*315A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 12/12 | 315 | chr7 | 135362570 | |||||
| chr7:135362703
|
T | G | 1 | a0001c0001t0007 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*182A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 12/12 | 182 | chr7 | 135362703 | |||||
| chr7:135509922
|
C | T | 1 | a0002c0002t0006 | 1 | HG02258.hp1 | 5_prime_UTR_variant | MODIFIER | c.-126G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/12 | 71591 | chr7 | 135509922 | |||||
| chr7:135509926
|
A | T | 1 | a0001c0001t0005 | 1 | HG02897.hp2 | 5_prime_UTR_variant | MODIFIER | c.-130T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/12 | 71595 | chr7 | 135509926 | |||||
| chr7:135509928
|
G | A | 1 | a0001c0001t0008 | 1 | NA20129.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-132C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/12 | chr7 | 135509928 | ||||||
| chr7:135510069
|
G | A | 1 | a0001c0001t0003 | 12 | HG00597.hp2 HG00673.hp2 HG02083.hp2 others(9): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-273C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/12 | chr7 | 135510069 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:135363212
|
G | A | 64 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(61): Show | 64 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.1841-26C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 11/11 | chr7 | 135363212 | ||||||
| chr7:135363217
|
T | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1841-31A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 11/11 | chr7 | 135363217 | ||||||
| chr7:135363281
|
G | C | 218 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(215): Show | 218 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.1841-95C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 11/11 | chr7 | 135363281 | ||||||
| chr7:135363494
|
G | A | 108 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0020others(105): Show | 108 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.1841-308C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 11/11 | chr7 | 135363494 | ||||||
| chr7:135363745
|
C | T | 320 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(317): Show | 320 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1840+109G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 11/11 | chr7 | 135363745 | ||||||
| chr7:135364612
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1628-546T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135364612 | ||||||
| chr7:135364677
|
T | C | 2 | a0002c0002t0001g0079a0002c0002t0001g0095 | 2 | HG02523.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1628-611A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135364677 | ||||||
| chr7:135364722
|
T | C | 1 | a0001c0001t0001g0260 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1628-656A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135364722 | ||||||
| chr7:135364935
|
T | C | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1628-869A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135364935 | ||||||
| chr7:135365202
|
C | G | 1 | a0001c0001t0001g0191 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1628-1136G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135365202 | ||||||
| chr7:135365325
|
GA | G | 61 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(58): Show | 61 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.1628-1260delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135365325 | ||||||
| chr7:135365423
|
A | AT | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.1628-1358dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135365423 | ||||||
| chr7:135365507
|
G | GATAA | 226 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(223): Show | 226 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.1628-1445_1628-144 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135365507 | ||||||
| chr7:135366078
|
C | T | 1 | a0002c0002t0006g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1628-2012G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366078 | ||||||
| chr7:135366127
|
G | A | 108 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0020others(105): Show | 108 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.1628-2061C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366127 | ||||||
| chr7:135366242
|
A | G | 56 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0022others(53): Show | 56 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.1628-2176T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366242 | ||||||
| chr7:135366285
|
T | C | 1 | a0002c0002t0001g0129 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1628-2219A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366285 | ||||||
| chr7:135366407
|
TA | T | 226 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(223): Show | 226 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.1628-2342delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366407 | ||||||
| chr7:135366502
|
G | A | 226 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(223): Show | 226 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.1628-2436C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366502 | ||||||
| chr7:135366569
|
A | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1628-2503T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366569 | ||||||
| chr7:135366701
|
G | A | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 95 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.1628-2635C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366701 | ||||||
| chr7:135366854
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1628-2788A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366854 | ||||||
| chr7:135366875
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1628-2809G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135366875 | ||||||
| chr7:135367002
|
A | G | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1628-2936T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367002 | ||||||
| chr7:135367147
|
C | T | 5 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0201others(2): Show | 5 | HG01243.hp2 HG02257.hp1 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.1628-3081G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367147 | ||||||
| chr7:135367150
|
T | G | 1 | a0001c0003t0002g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1628-3084A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367150 | ||||||
| chr7:135367215
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1628-3149A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367215 | ||||||
| chr7:135367227
|
C | T | 226 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(223): Show | 226 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(223): Show |
intron_variant | MODIFIER | c.1628-3161G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367227 | ||||||
| chr7:135367292
|
A | C | 108 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0020others(105): Show | 108 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.1628-3226T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367292 | ||||||
| chr7:135367448
|
G | C | 10 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0313others(7): Show | 10 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.1628-3382C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367448 | ||||||
| chr7:135367474
|
C | T | 102 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0020others(99): Show | 102 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1628-3408G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367474 | ||||||
| chr7:135367571
|
C | A | 1 | a0001c0001t0001g0276 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1628-3505G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367571 | ||||||
| chr7:135367596
|
C | T | 16 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(13): Show | 16 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1628-3530G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367596 | ||||||
| chr7:135367597
|
G | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1628-3531C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367597 | ||||||
| chr7:135367968
|
TA | T | 19 | a0001c0001t0001g0118a0001c0001t0001g0324a0001c0001t0001g0329others(16): Show | 19 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1628-3903delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135367968 | ||||||
| chr7:135368016
|
T | C | 320 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(317): Show | 320 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(317): Show |
intron_variant | MODIFIER | c.1628-3950A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368016 | ||||||
| chr7:135368148
|
C | T | 12 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(9): Show | 12 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1628-4082G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368148 | ||||||
| chr7:135368451
|
G | A | 3 | a0002c0002t0001g0025a0002c0002t0001g0026a0002c0002t0001g0027 | 3 | NA18986.hp2 NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1628-4385C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368451 | ||||||
| chr7:135368485
|
A | T | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1628-4419T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368485 | ||||||
| chr7:135368577
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1628-4511T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368577 | ||||||
| chr7:135368598
|
C | T | 1 | a0001c0001t0001g0337 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1628-4532G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368598 | ||||||
| chr7:135368655
|
C | T | 3 | a0004c0005t0001g0126a0004c0005t0001g0127a0004c0005t0001g0128 | 3 | HG01106.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1628-4589G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368655 | ||||||
| chr7:135368683
|
C | G | 1 | a0002c0002t0001g0069 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1628-4617G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368683 | ||||||
| chr7:135368710
|
A | G | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(121): Show | 124 | HG00099.hp2 HG00621.hp2 HG00642.hp1 others(121): Show |
intron_variant | MODIFIER | c.1628-4644T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368710 | ||||||
| chr7:135368744
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1628-4678A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368744 | ||||||
| chr7:135368886
|
C | T | 260 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(257): Show | 260 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(257): Show |
intron_variant | MODIFIER | c.1628-4820G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368886 | ||||||
| chr7:135368962
|
A | G | 9 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350others(6): Show | 9 | HG01243.hp2 HG02055.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1628-4896T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135368962 | ||||||
| chr7:135369017
|
G | GT | 19 | a0001c0001t0001g0118a0001c0001t0001g0324a0001c0001t0001g0329others(16): Show | 19 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1628-4952dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369017 | ||||||
| chr7:135369071
|
G | A | 1 | a0001c0001t0002g0137 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1628-5005C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369071 | ||||||
| chr7:135369134
|
G | A | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1628-5068C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369134 | ||||||
| chr7:135369280
|
C | T | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG01123.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1628-5214G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369280 | ||||||
| chr7:135369319
|
G | A | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1628-5253C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369319 | ||||||
| chr7:135369331
|
C | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1628-5265G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369331 | ||||||
| chr7:135369395
|
T | C | 43 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0306others(40): Show | 43 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1628-5329A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369395 | ||||||
| chr7:135369406
|
C | T | 25 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0306others(22): Show | 25 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.1628-5340G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369406 | ||||||
| chr7:135369435
|
C | G | 5 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0124others(2): Show | 5 | HG01081.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1628-5369G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369435 | ||||||
| chr7:135369542
|
C | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1628-5476G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369542 | ||||||
| chr7:135369619
|
G | A | 107 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(104): Show | 107 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.1628-5553C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369619 | ||||||
| chr7:135369686
|
C | T | 46 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0146others(43): Show | 46 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.1628-5620G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369686 | ||||||
| chr7:135369746
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1628-5680G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135369746 | ||||||
| chr7:135370011
|
A | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0334 | 3 | HG00733.hp2 HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1628-5945T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370011 | ||||||
| chr7:135370229
|
C | A | 6 | a0002c0002t0001g0300a0002c0002t0001g0301a0002c0002t0001g0302others(3): Show | 6 | HG02055.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1628-6163G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370229 | ||||||
| chr7:135370282
|
AAAC | A | 17 | a0001c0001t0001g0141a0001c0001t0001g0297a0001c0001t0001g0298others(14): Show | 17 | HG00597.hp2 HG02083.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.1628-6219_1628-621 others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370282 | ||||||
| chr7:135370295
|
A | C | 1 | a0002c0002t0001g0050 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1628-6229T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370295 | ||||||
| chr7:135370482
|
A | G | 1 | a0002c0002t0001g0067 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1628-6416T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370482 | ||||||
| chr7:135370531
|
T | C | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1628-6465A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370531 | ||||||
| chr7:135370637
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1628-6571T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370637 | ||||||
| chr7:135370650
|
T | C | 1 | a0001c0001t0001g0324 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1628-6584A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370650 | ||||||
| chr7:135370739
|
C | G | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-6673G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370739 | ||||||
| chr7:135370852
|
T | C | 65 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(62): Show | 65 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1628-6786A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370852 | ||||||
| chr7:135370876
|
A | G | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1628-6810T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370876 | ||||||
| chr7:135370956
|
A | C | 1 | a0001c0001t0001g0333 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1628-6890T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370956 | ||||||
| chr7:135370989
|
C | T | 212 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(209): Show | 212 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.1628-6923G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135370989 | ||||||
| chr7:135371000
|
G | A | 343 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 343 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(340): Show |
intron_variant | MODIFIER | c.1628-6934C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135371000 | ||||||
| chr7:135371363
|
A | C | 1 | a0001c0001t0001g0324 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1628-7297T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135371363 | ||||||
| chr7:135371589
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1628-7523A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135371589 | ||||||
| chr7:135371868
|
G | A | 356 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(353): Show | 356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.1628-7802C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135371868 | ||||||
| chr7:135371941
|
A | G | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1628-7875T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135371941 | ||||||
| chr7:135371985
|
G | A | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1628-7919C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135371985 | ||||||
| chr7:135372079
|
C | G | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-8013G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372079 | ||||||
| chr7:135372394
|
A | G | 107 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(104): Show | 107 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.1628-8328T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372394 | ||||||
| chr7:135372554
|
TG | T | 9 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0313others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1628-8489delC | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372554 | ||||||
| chr7:135372555
|
G | GT | 115 | a0001c0001t0001g0151a0001c0001t0001g0156a0001c0001t0001g0164others(112): Show | 115 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1628-8490dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372555 | ||||||
| chr7:135372555
|
GTT | G | 24 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(21): Show | 24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.1628-8491_1628-849 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372555 | ||||||
| chr7:135372562
|
T | G | 1 | a0001c0001t0001g0273 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1628-8496A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372562 | ||||||
| chr7:135372579
|
C | T | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-8513G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372579 | ||||||
| chr7:135372811
|
T | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1628-8745A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372811 | ||||||
| chr7:135372844
|
C | T | 2 | a0002c0002t0001g0029a0002c0002t0001g0043 | 2 | HG01081.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1628-8778G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372844 | ||||||
| chr7:135372845
|
G | A | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-8779C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135372845 | ||||||
| chr7:135373034
|
A | T | 1 | a0001c0001t0001g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1628-8968T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135373034 | ||||||
| chr7:135373137
|
A | G | 5 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0124others(2): Show | 5 | HG01081.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1628-9071T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135373137 | ||||||
| chr7:135373386
|
A | G | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-9320T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135373386 | ||||||
| chr7:135373464
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1628-9398C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135373464 | ||||||
| chr7:135373645
|
C | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1628-9579G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135373645 | ||||||
| chr7:135373743
|
A | AT | 105 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350others(102): Show | 105 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.1628-9678dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135373743 | ||||||
| chr7:135373802
|
G | A | 212 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(209): Show | 212 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.1628-9736C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135373802 | ||||||
| chr7:135373816
|
G | A | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1628-9750C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135373816 | ||||||
| chr7:135373858
|
G | C | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1628-9792C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135373858 | ||||||
| chr7:135374013
|
G | A | 1 | a0002c0002t0006g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1628-9947C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135374013 | ||||||
| chr7:135374173
|
C | T | 1 | a0001c0001t0001g0323 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1628-10107G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135374173 | ||||||
| chr7:135374390
|
T | G | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-10324A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135374390 | ||||||
| chr7:135374393
|
CTGA | C | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 194 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.1628-10330_1628-10 others(9): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135374393 | ||||||
| chr7:135374644
|
TA | T | 343 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 343 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(340): Show |
intron_variant | MODIFIER | c.1628-10579delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135374644 | ||||||
| chr7:135375000
|
T | A | 1 | a0001c0001t0002g0296 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1628-10934A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375000 | ||||||
| chr7:135375010
|
G | A | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-10944C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375010 | ||||||
| chr7:135375212
|
G | A | 1 | a0002c0002t0001g0066 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1628-11146C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375212 | ||||||
| chr7:135375368
|
T | A | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-11302A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375368 | ||||||
| chr7:135375476
|
T | TACAC | 18 | a0001c0001t0001g0324a0001c0001t0001g0329a0001c0001t0001g0330others(15): Show | 18 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1628-11414_1628-11 others(10): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375476 | ||||||
| chr7:135375483
|
A | G | 24 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(21): Show | 24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.1628-11417T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375483 | ||||||
| chr7:135375575
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1628-11509A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375575 | ||||||
| chr7:135375690
|
C | T | 6 | a0002c0002t0001g0300a0002c0002t0001g0301a0002c0002t0001g0302others(3): Show | 6 | HG02055.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1628-11624G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375690 | ||||||
| chr7:135375866
|
A | G | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-11800T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375866 | ||||||
| chr7:135375912
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1628-11846C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135375912 | ||||||
| chr7:135376027
|
A | G | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1628-11961T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135376027 | ||||||
| chr7:135376075
|
C | T | 1 | a0001c0001t0008g0350 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1628-12009G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135376075 | ||||||
| chr7:135376321
|
C | G | 1 | a0002c0002t0001g0069 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1628-12255G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135376321 | ||||||
| chr7:135376352
|
C | CT | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-12287dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135376352 | ||||||
| chr7:135376380
|
T | C | 1 | a0001c0001t0002g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1628-12314A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135376380 | ||||||
| chr7:135376577
|
C | T | 140 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 140 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(137): Show |
intron_variant | MODIFIER | c.1628-12511G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135376577 | ||||||
| chr7:135376684
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1628-12618A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135376684 | ||||||
| chr7:135376714
|
A | G | 24 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(21): Show | 24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.1628-12648T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135376714 | ||||||
| chr7:135376972
|
T | C | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-12906A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135376972 | ||||||
| chr7:135377003
|
T | C | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-12937A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377003 | ||||||
| chr7:135377161
|
T | A | 1 | a0001c0001t0001g0348 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1628-13095A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377161 | ||||||
| chr7:135377204
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1628-13138T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377204 | ||||||
| chr7:135377217
|
T | C | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1628-13151A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377217 | ||||||
| chr7:135377304
|
C | T | 18 | a0001c0001t0001g0324a0001c0001t0001g0329a0001c0001t0001g0330others(15): Show | 18 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1628-13238G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377304 | ||||||
| chr7:135377415
|
T | C | 2 | a0001c0001t0002g0189a0001c0001t0002g0190 | 2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.1628-13349A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377415 | ||||||
| chr7:135377646
|
A | G | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1628-13580T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377646 | ||||||
| chr7:135377795
|
T | C | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1628-13729A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377795 | ||||||
| chr7:135377804
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1628-13738T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377804 | ||||||
| chr7:135377878
|
G | A | 1 | a0001c0008t0001g0325 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1628-13812C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377878 | ||||||
| chr7:135377910
|
A | G | 344 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(341): Show | 344 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(341): Show |
intron_variant | MODIFIER | c.1628-13844T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377910 | ||||||
| chr7:135377977
|
T | C | 1 | a0001c0001t0001g0318 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1628-13911A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135377977 | ||||||
| chr7:135378075
|
G | C | 1 | a0001c0001t0003g0360 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1628-14009C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378075 | ||||||
| chr7:135378080
|
C | T | 12 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(9): Show | 12 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1628-14014G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378080 | ||||||
| chr7:135378251
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1628-14185G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378251 | ||||||
| chr7:135378320
|
A | C | 6 | a0002c0002t0001g0300a0002c0002t0001g0301a0002c0002t0001g0302others(3): Show | 6 | HG02055.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1628-14254T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378320 | ||||||
| chr7:135378436
|
A | G | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-14370T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378436 | ||||||
| chr7:135378456
|
G | A | 24 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(21): Show | 24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.1628-14390C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378456 | ||||||
| chr7:135378482
|
C | T | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1628-14416G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378482 | ||||||
| chr7:135378518
|
G | GA | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1628-14453dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378518 | ||||||
| chr7:135378518
|
GA | G | 254 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(251): Show | 254 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(251): Show |
intron_variant | MODIFIER | c.1628-14453delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378518 | ||||||
| chr7:135378545
|
G | A | 1 | a0002c0002t0001g0088 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1628-14479C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378545 | ||||||
| chr7:135378595
|
T | C | 2 | a0001c0001t0001g0329a0001c0001t0001g0330 | 2 | HG03831.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1628-14529A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378595 | ||||||
| chr7:135378639
|
A | G | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 95 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.1628-14573T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378639 | ||||||
| chr7:135378714
|
G | A | 18 | a0001c0001t0001g0324a0001c0001t0001g0329a0001c0001t0001g0330others(15): Show | 18 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1628-14648C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378714 | ||||||
| chr7:135378788
|
C | T | 1 | a0001c0001t0002g0296 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1628-14722G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378788 | ||||||
| chr7:135378844
|
G | A | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1628-14778C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378844 | ||||||
| chr7:135378933
|
C | T | 18 | a0001c0001t0001g0324a0001c0001t0001g0329a0001c0001t0001g0330others(15): Show | 18 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1628-14867G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378933 | ||||||
| chr7:135378941
|
C | T | 1 | a0001c0001t0005g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1628-14875G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378941 | ||||||
| chr7:135378984
|
C | CA | 102 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 102 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.1628-14919dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378984 | ||||||
| chr7:135378984
|
C | CAA | 9 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0156others(6): Show | 9 | HG00738.hp1 HG01106.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1628-14920_1628-14 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378984 | ||||||
| chr7:135378984
|
C | CAAA | 13 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(10): Show | 13 | HG02083.hp2 NA18939.hp1 NA18941.hp1 others(10): Show |
intron_variant | MODIFIER | c.1628-14921_1628-14 others(9): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135378984 | ||||||
| chr7:135379047
|
A | G | 2 | a0001c0001t0001g0310a0006c0007t0001g0311 | 2 | HG00323.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.1627+14871T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379047 | ||||||
| chr7:135379055
|
A | T | 75 | a0001c0001t0001g0118a0001c0001t0001g0228a0001c0001t0001g0229others(72): Show | 75 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1627+14863T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379055 | ||||||
| chr7:135379185
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1627+14733G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379185 | ||||||
| chr7:135379218
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1627+14700G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379218 | ||||||
| chr7:135379564
|
C | A | 24 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(21): Show | 24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.1627+14354G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379564 | ||||||
| chr7:135379594
|
A | G | 18 | a0001c0001t0001g0324a0001c0001t0001g0329a0001c0001t0001g0330others(15): Show | 18 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1627+14324T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379594 | ||||||
| chr7:135379770
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+14148A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379770 | ||||||
| chr7:135379806
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1627+14112A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379806 | ||||||
| chr7:135379822
|
T | C | 1 | a0001c0001t0001g0114 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1627+14096A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379822 | ||||||
| chr7:135379866
|
C | T | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+14052G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379866 | ||||||
| chr7:135379931
|
T | C | 1 | a0001c0001t0002g0296 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1627+13987A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379931 | ||||||
| chr7:135379948
|
TA | T | 356 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(353): Show | 356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.1627+13969delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379948 | ||||||
| chr7:135379986
|
C | A | 356 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(353): Show | 356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.1627+13932G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135379986 | ||||||
| chr7:135380108
|
A | C | 1 | a0001c0001t0003g0351 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1627+13810T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380108 | ||||||
| chr7:135380130
|
A | C | 95 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(92): Show | 95 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.1627+13788T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380130 | ||||||
| chr7:135380131
|
A | C | 2 | a0002c0002t0001g0029a0002c0002t0001g0043 | 2 | HG01081.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1627+13787T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380131 | ||||||
| chr7:135380135
|
A | C | 1 | a0001c0001t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1627+13783T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380135 | ||||||
| chr7:135380209
|
C | T | 10 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(7): Show | 10 | HG01496.hp1 HG01891.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+13709G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380209 | ||||||
| chr7:135380211
|
G | C | 3 | a0001c0001t0001g0228a0001c0001t0004g0346a0001c0001t0004g0347 | 3 | HG03490.hp2 HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1627+13707C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380211 | ||||||
| chr7:135380420
|
A | G | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+13498T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380420 | ||||||
| chr7:135380513
|
T | A | 1 | a0001c0001t0001g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1627+13405A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380513 | ||||||
| chr7:135380621
|
G | A | 1 | a0002c0002t0006g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1627+13297C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380621 | ||||||
| chr7:135380637
|
A | C | 8 | a0002c0002t0001g0033a0002c0002t0001g0037a0002c0002t0001g0038others(5): Show | 8 | HG02165.hp2 NA18941.hp2 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.1627+13281T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380637 | ||||||
| chr7:135380708
|
T | A | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+13210A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380708 | ||||||
| chr7:135380729
|
C | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+13189G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380729 | ||||||
| chr7:135380756
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+13162A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380756 | ||||||
| chr7:135380791
|
C | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+13127G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380791 | ||||||
| chr7:135380795
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0175 | 2 | NA18984.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1627+13123G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380795 | ||||||
| chr7:135380859
|
T | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1627+13059A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135380859 | ||||||
| chr7:135381271
|
A | C | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+12647T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381271 | ||||||
| chr7:135381320
|
T | C | 1 | a0001c0001t0002g0290 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1627+12598A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381320 | ||||||
| chr7:135381372
|
C | G | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+12546G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381372 | ||||||
| chr7:135381485
|
C | T | 3 | a0001c0001t0003g0353a0001c0001t0003g0359a0001c0001t0003g0360 | 3 | NA18954.hp1 NA18990.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1627+12433G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381485 | ||||||
| chr7:135381533
|
T | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+12385A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381533 | ||||||
| chr7:135381627
|
G | A | 2 | a0001c0001t0002g0287a0001c0001t0002g0289 | 2 | HG01496.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1627+12291C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381627 | ||||||
| chr7:135381728
|
G | A | 1 | a0002c0002t0001g0089 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1627+12190C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381728 | ||||||
| chr7:135381733
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1627+12185C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381733 | ||||||
| chr7:135381771
|
C | T | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+12147G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381771 | ||||||
| chr7:135381933
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1627+11985A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135381933 | ||||||
| chr7:135382059
|
G | A | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+11859C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382059 | ||||||
| chr7:135382072
|
A | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1627+11846T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382072 | ||||||
| chr7:135382164
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1627+11754A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382164 | ||||||
| chr7:135382453
|
A | T | 356 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(353): Show | 356 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.1627+11465T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382453 | ||||||
| chr7:135382482
|
T | C | 209 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 209 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.1627+11436A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382482 | ||||||
| chr7:135382505
|
G | A | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1627+11413C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382505 | ||||||
| chr7:135382583
|
G | GA | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 107 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.1627+11334dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382583 | ||||||
| chr7:135382583
|
G | GAA | 103 | a0001c0001t0001g0014a0002c0002t0001g0018a0002c0002t0001g0019others(100): Show | 103 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.1627+11333_1627+11 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382583 | ||||||
| chr7:135382649
|
C | T | 1 | a0002c0002t0001g0045 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1627+11269G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382649 | ||||||
| chr7:135382704
|
C | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+11214G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382704 | ||||||
| chr7:135382880
|
G | A | 4 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0262others(1): Show | 4 | NA18948.hp2 NA18951.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+11038C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382880 | ||||||
| chr7:135382978
|
A | T | 1 | a0002c0002t0001g0083 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1627+10940T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135382978 | ||||||
| chr7:135383060
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1627+10858C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135383060 | ||||||
| chr7:135383362
|
C | A | 1 | a0001c0001t0001g0324 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1627+10556G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135383362 | ||||||
| chr7:135383384
|
C | CT | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.1627+10533dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135383384 | ||||||
| chr7:135383541
|
C | G | 1 | a0002c0002t0001g0187 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1627+10377G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135383541 | ||||||
| chr7:135383866
|
T | C | 1 | a0001c0001t0001g0274 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1627+10052A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135383866 | ||||||
| chr7:135383969
|
T | TG | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+9948_1627+994 others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135383969 | ||||||
| chr7:135384290
|
T | C | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+9628A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384290 | ||||||
| chr7:135384291
|
T | C | 335 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(332): Show | 335 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(332): Show |
intron_variant | MODIFIER | c.1627+9627A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384291 | ||||||
| chr7:135384292
|
T | C | 1 | a0001c0001t0001g0005 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1627+9626A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384292 | ||||||
| chr7:135384297
|
T | C | 1 | a0002c0002t0001g0035 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1627+9621A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384297 | ||||||
| chr7:135384316
|
G | A | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.1627+9602C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384316 | ||||||
| chr7:135384384
|
G | A | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+9534C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384384 | ||||||
| chr7:135384385
|
C | T | 1 | a0001c0001t0001g0312 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1627+9533G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384385 | ||||||
| chr7:135384434
|
G | A | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+9484C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384434 | ||||||
| chr7:135384476
|
G | A | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+9442C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384476 | ||||||
| chr7:135384498
|
G | T | 1 | a0001c0001t0001g0012 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1627+9420C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384498 | ||||||
| chr7:135384520
|
T | C | 43 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0306others(40): Show | 43 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.1627+9398A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384520 | ||||||
| chr7:135384559
|
A | G | 18 | a0001c0001t0001g0324a0001c0001t0001g0329a0001c0001t0001g0330others(15): Show | 18 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1627+9359T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384559 | ||||||
| chr7:135384648
|
C | G | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+9270G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384648 | ||||||
| chr7:135384807
|
A | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+9111T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384807 | ||||||
| chr7:135384952
|
A | C | 1 | a0001c0001t0001g0221 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1627+8966T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135384952 | ||||||
| chr7:135385024
|
GTTC | G | 65 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(62): Show | 65 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1627+8891_1627+889 others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135385024 | ||||||
| chr7:135385110
|
C | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+8808G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135385110 | ||||||
| chr7:135385197
|
T | C | 4 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(1): Show | 4 | HG00673.hp2 HG02083.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+8721A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135385197 | ||||||
| chr7:135385202
|
C | G | 1 | a0001c0001t0005g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1627+8716G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135385202 | ||||||
| chr7:135385364
|
C | T | 6 | a0002c0002t0001g0300a0002c0002t0001g0301a0002c0002t0001g0302others(3): Show | 6 | HG02055.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1627+8554G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135385364 | ||||||
| chr7:135385572
|
CTAAGAG | C | 40 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0033others(37): Show | 40 | HG00438.hp1 HG00673.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1627+8340_1627+834 others(10): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135385572 | ||||||
| chr7:135385856
|
T | C | 1 | a0001c0001t0002g0116 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1627+8062A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135385856 | ||||||
| chr7:135386100
|
G | GT | 17 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(14): Show | 17 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.1627+7817dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386100 | ||||||
| chr7:135386126
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1627+7792G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386126 | ||||||
| chr7:135386153
|
C | CT | 18 | a0001c0001t0001g0147a0001c0001t0001g0197a0001c0001t0001g0250others(15): Show | 18 | HG00673.hp1 HG01261.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.1627+7764dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386153 | ||||||
| chr7:135386153
|
CT | C | 22 | a0001c0001t0001g0141a0001c0001t0001g0204a0001c0001t0001g0258others(19): Show | 22 | HG00323.hp2 HG00597.hp2 HG02015.hp1 others(19): Show |
intron_variant | MODIFIER | c.1627+7764delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386153 | ||||||
| chr7:135386153
|
CTT | C | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+7763_1627+776 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386153 | ||||||
| chr7:135386169
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+7749A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386169 | ||||||
| chr7:135386184
|
G | T | 1 | a0002c0002t0001g0050 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1627+7734C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386184 | ||||||
| chr7:135386406
|
TAAC | T | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1627+7509_1627+751 others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386406 | ||||||
| chr7:135386568
|
C | T | 1 | a0001c0010t0002g0326 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1627+7350G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386568 | ||||||
| chr7:135386604
|
A | G | 13 | a0001c0001t0001g0197a0001c0001t0002g0287a0001c0001t0002g0288others(10): Show | 13 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1627+7314T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386604 | ||||||
| chr7:135386629
|
A | G | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+7289T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386629 | ||||||
| chr7:135386846
|
C | T | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(3): Show | 6 | HG01123.hp2 NA18968.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.1627+7072G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386846 | ||||||
| chr7:135386904
|
C | T | 1 | a0001c0001t0002g0290 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1627+7014G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135386904 | ||||||
| chr7:135387070
|
A | G | 1 | a0002c0002t0001g0019 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1627+6848T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387070 | ||||||
| chr7:135387136
|
A | G | 338 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(335): Show | 338 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(335): Show |
intron_variant | MODIFIER | c.1627+6782T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387136 | ||||||
| chr7:135387389
|
T | C | 102 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0020others(99): Show | 102 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.1627+6529A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387389 | ||||||
| chr7:135387467
|
T | G | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+6451A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387467 | ||||||
| chr7:135387521
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+6397A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387521 | ||||||
| chr7:135387554
|
C | CT | 65 | a0001c0001t0001g0118a0001c0001t0001g0228a0001c0001t0001g0229others(62): Show | 65 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1627+6363dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387554 | ||||||
| chr7:135387554
|
C | CTT | 9 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0313others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1627+6362_1627+636 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387554 | ||||||
| chr7:135387697
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1627+6221G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387697 | ||||||
| chr7:135387800
|
C | T | 16 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(13): Show | 16 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.1627+6118G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387800 | ||||||
| chr7:135387805
|
T | C | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1627+6113A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387805 | ||||||
| chr7:135387955
|
A | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+5963T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135387955 | ||||||
| chr7:135388010
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+5908A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135388010 | ||||||
| chr7:135388109
|
G | A | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1627+5809C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135388109 | ||||||
| chr7:135388184
|
C | T | 1 | a0001c0001t0001g0337 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1627+5734G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135388184 | ||||||
| chr7:135388295
|
T | C | 93 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(90): Show | 93 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.1627+5623A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135388295 | ||||||
| chr7:135388342
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1627+5576A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135388342 | ||||||
| chr7:135388395
|
C | T | 4 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | NA18941.hp1 NA18953.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+5523G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135388395 | ||||||
| chr7:135389157
|
C | CA | 25 | a0001c0001t0001g0244a0001c0001t0001g0247a0001c0001t0001g0258others(22): Show | 25 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.1627+4760dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389157 | ||||||
| chr7:135389157
|
C | CAA | 8 | a0001c0001t0001g0306a0001c0001t0001g0308a0001c0001t0001g0309others(5): Show | 8 | HG01081.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1627+4759_1627+476 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389157 | ||||||
| chr7:135389157
|
CA | C | 140 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 140 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(137): Show |
intron_variant | MODIFIER | c.1627+4760delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389157 | ||||||
| chr7:135389157
|
CAA | C | 9 | a0001c0001t0001g0227a0001c0001t0001g0264a0001c0001t0001g0337others(6): Show | 9 | HG01256.hp1 HG02145.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1627+4759_1627+476 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389157 | ||||||
| chr7:135389215
|
C | CT | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+4702_1627+470 others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389215 | ||||||
| chr7:135389227
|
TC | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+4690delG | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389227 | ||||||
| chr7:135389338
|
C | A | 7 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0210others(4): Show | 7 | HG01099.hp1 HG01255.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1627+4580G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389338 | ||||||
| chr7:135389342
|
A | C | 1 | a0001c0001t0008g0350 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1627+4576T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389342 | ||||||
| chr7:135389381
|
C | CT | 42 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(39): Show | 42 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1627+4536dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389381 | ||||||
| chr7:135389497
|
AGGTCAGA others(21): Show |
A | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+4393_1627+442 others(32): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389497 | ||||||
| chr7:135389554
|
T | C | 2 | a0001c0001t0003g0359a0001c0001t0003g0360 | 2 | NA18990.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1627+4364A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389554 | ||||||
| chr7:135389628
|
C | T | 2 | a0002c0002t0001g0029a0002c0002t0001g0043 | 2 | HG01081.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1627+4290G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389628 | ||||||
| chr7:135389814
|
A | T | 24 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(21): Show | 24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.1627+4104T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389814 | ||||||
| chr7:135389868
|
G | GA | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1627+4049dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135389868 | ||||||
| chr7:135390048
|
C | T | 6 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(3): Show | 6 | HG01515.hp2 HG01517.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1627+3870G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390048 | ||||||
| chr7:135390081
|
C | G | 18 | a0001c0001t0001g0324a0001c0001t0001g0329a0001c0001t0001g0330others(15): Show | 18 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1627+3837G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390081 | ||||||
| chr7:135390163
|
A | AC | 42 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(39): Show | 42 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.1627+3754dupG | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390163 | ||||||
| chr7:135390173
|
C | T | 1 | a0002c0002t0001g0073 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1627+3745G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390173 | ||||||
| chr7:135390304
|
A | C | 1 | a0001c0001t0001g0191 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1627+3614T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390304 | ||||||
| chr7:135390438
|
CAAT | C | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1627+3477_1627+347 others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390438 | ||||||
| chr7:135390450
|
A | T | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+3468T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390450 | ||||||
| chr7:135390471
|
T | A | 1 | a0001c0001t0001g0310 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1627+3447A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390471 | ||||||
| chr7:135390485
|
A | G | 2 | a0002c0002t0001g0074a0002c0002t0001g0076 | 2 | NA18995.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1627+3433T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390485 | ||||||
| chr7:135390606
|
C | A | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+3312G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390606 | ||||||
| chr7:135390769
|
T | A | 1 | a0002c0002t0006g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1627+3149A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390769 | ||||||
| chr7:135390985
|
G | A | 4 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316others(1): Show | 4 | HG01123.hp1 HG03654.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1627+2933C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135390985 | ||||||
| chr7:135391052
|
G | A | 1 | a0002c0002t0006g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1627+2866C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391052 | ||||||
| chr7:135391069
|
A | C | 1 | a0001c0001t0001g0144 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1627+2849T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391069 | ||||||
| chr7:135391078
|
C | G | 1 | a0002c0002t0001g0071 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1627+2840G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391078 | ||||||
| chr7:135391081
|
C | T | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+2837G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391081 | ||||||
| chr7:135391155
|
G | T | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+2763C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391155 | ||||||
| chr7:135391518
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1627+2400G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391518 | ||||||
| chr7:135391579
|
G | T | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+2339C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391579 | ||||||
| chr7:135391899
|
C | G | 4 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(1): Show | 4 | HG00673.hp2 HG02083.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+2019G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391899 | ||||||
| chr7:135391907
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1627+2011G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391907 | ||||||
| chr7:135391923
|
A | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+1995T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135391923 | ||||||
| chr7:135392056
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1627+1862A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392056 | ||||||
| chr7:135392240
|
C | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1627+1678G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392240 | ||||||
| chr7:135392268
|
T | C | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1627+1650A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392268 | ||||||
| chr7:135392456
|
T | C | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+1462A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392456 | ||||||
| chr7:135392592
|
T | A | 1 | a0002c0002t0001g0071 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1627+1326A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392592 | ||||||
| chr7:135392621
|
C | T | 4 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(1): Show | 4 | HG00673.hp2 HG02083.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627+1297G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392621 | ||||||
| chr7:135392700
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1627+1218G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392700 | ||||||
| chr7:135392814
|
G | A | 5 | a0002c0002t0001g0054a0002c0002t0001g0080a0002c0002t0001g0082others(2): Show | 5 | HG02129.hp1 NA18946.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1627+1104C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392814 | ||||||
| chr7:135392834
|
T | C | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627+1084A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392834 | ||||||
| chr7:135392901
|
T | C | 344 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(341): Show | 344 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(341): Show |
intron_variant | MODIFIER | c.1627+1017A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392901 | ||||||
| chr7:135392931
|
CAAT | C | 14 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(11): Show | 14 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.1627+984_1627+986d others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392931 | ||||||
| chr7:135392940
|
T | C | 1 | a0001c0001t0001g0332 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1627+978A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135392940 | ||||||
| chr7:135393155
|
A | C | 1 | a0001c0001t0002g0295 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1627+763T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135393155 | ||||||
| chr7:135393282
|
A | G | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1627+636T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135393282 | ||||||
| chr7:135393537
|
AT | A | 43 | a0001c0001t0001g0318a0002c0002t0001g0020a0002c0002t0001g0021others(40): Show | 43 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.1627+380delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135393537 | ||||||
| chr7:135393538
|
T | A | 23 | a0001c0001t0001g0141a0001c0001t0001g0297a0001c0001t0001g0298others(20): Show | 23 | HG00597.hp2 HG01891.hp2 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.1627+380A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135393538 | ||||||
| chr7:135393617
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1627+301C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 10/11 | chr7 | 135393617 | ||||||
| chr7:135394485
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1130-70G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 9/11 | chr7 | 135394485 | ||||||
| chr7:135394552
|
A | C | 1 | a0001c0001t0002g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1130-137T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 9/11 | chr7 | 135394552 | ||||||
| chr7:135394576
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1130-161C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 9/11 | chr7 | 135394576 | ||||||
| chr7:135394827
|
G | GA | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1130-413dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 9/11 | chr7 | 135394827 | ||||||
| chr7:135394957
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1130-542T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 9/11 | chr7 | 135394957 | ||||||
| chr7:135395001
|
A | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1130-586T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 9/11 | chr7 | 135395001 | ||||||
| chr7:135395255
|
G | A | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.1129+379C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 9/11 | chr7 | 135395255 | ||||||
| chr7:135395571
|
T | G | 1 | a0001c0001t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1129+63A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 9/11 | chr7 | 135395571 | ||||||
| chr7:135395980
|
T | G | 1 | a0001c0001t0001g0115 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.880-97A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135395980 | ||||||
| chr7:135396064
|
T | C | 65 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(62): Show | 65 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.880-181A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396064 | ||||||
| chr7:135396095
|
A | G | 1 | a0001c0001t0001g0160 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.880-212T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396095 | ||||||
| chr7:135396107
|
C | CT | 27 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0236others(24): Show | 27 | HG00280.hp1 HG00438.hp2 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.880-225dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | ||||||
| chr7:135396107
|
C | CTT | 9 | a0001c0001t0001g0342a0001c0001t0002g0120a0001c0001t0002g0131others(6): Show | 9 | HG01361.hp1 HG01496.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.880-226_880-225dup others(2): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | ||||||
| chr7:135396107
|
C | CTTT | 13 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0332others(10): Show | 13 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.880-227_880-225dup others(3): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | ||||||
| chr7:135396107
|
C | T | 1 | a0001c0001t0001g0274 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.880-224G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | ||||||
| chr7:135396107
|
CT | C | 20 | a0001c0001t0001g0141a0001c0001t0001g0297a0001c0001t0001g0299others(17): Show | 20 | HG00597.hp2 HG00639.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.880-225delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | ||||||
| chr7:135396107
|
CTT | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0318a0001c0001t0002g0296others(3): Show | 6 | HG00323.hp2 HG02055.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-226_880-225del others(2): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | ||||||
| chr7:135396107
|
CTTT | C | 8 | a0001c0001t0001g0307a0001c0001t0001g0308a0001c0001t0001g0309others(5): Show | 8 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-227_880-225del others(3): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | ||||||
| chr7:135396107
|
CTTTTTTT | C | 6 | a0001c0001t0001g0156a0001c0001t0001g0167a0001c0001t0001g0176others(3): Show | 6 | HG01099.hp1 HG02080.hp1 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-231_880-225del others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | ||||||
| chr7:135396107
|
CTTTTTTT others(1): Show |
C | 86 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 86 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.880-232_880-225del others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | ||||||
| chr7:135396107
|
CTTTTTTT others(5): Show |
C | 1 | a0002c0002t0001g0037 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.880-236_880-225del others(12): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | ||||||
| chr7:135396107
|
CTTTTTTT others(6): Show |
C | 101 | a0001c0001t0001g0322a0002c0002t0001g0018a0002c0002t0001g0019others(98): Show | 101 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.880-237_880-225del others(13): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396107 | ||||||
| chr7:135396108
|
T | C | 4 | a0001c0001t0003g0353a0001c0001t0003g0357a0001c0001t0003g0359others(1): Show | 4 | NA18954.hp1 NA18990.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-225A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396108 | ||||||
| chr7:135396109
|
T | C | 10 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(7): Show | 10 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-226A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396109 | ||||||
| chr7:135396187
|
G | A | 4 | a0002c0002t0001g0051a0002c0002t0001g0300a0002c0002t0001g0302others(1): Show | 4 | HG01346.hp1 HG02055.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-304C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396187 | ||||||
| chr7:135396265
|
G | A | 27 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0306others(24): Show | 27 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(24): Show |
intron_variant | MODIFIER | c.880-382C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396265 | ||||||
| chr7:135396307
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.880-424G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396307 | ||||||
| chr7:135396321
|
A | G | 330 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(327): Show | 330 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(327): Show |
intron_variant | MODIFIER | c.880-438T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396321 | ||||||
| chr7:135396415
|
C | A | 1 | a0001c0001t0001g0251 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.880-532G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396415 | ||||||
| chr7:135396447
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.880-564A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396447 | ||||||
| chr7:135396590
|
G | C | 1 | a0002c0002t0001g0302 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.880-707C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396590 | ||||||
| chr7:135396615
|
G | T | 1 | a0001c0010t0002g0326 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.880-732C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396615 | ||||||
| chr7:135396714
|
CTGATA | C | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.880-836_880-832del others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135396714 | ||||||
| chr7:135397276
|
G | T | 337 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(334): Show | 337 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(334): Show |
intron_variant | MODIFIER | c.879+893C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397276 | ||||||
| chr7:135397317
|
A | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.879+852T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397317 | ||||||
| chr7:135397607
|
C | CA | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 96 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.879+561dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397607 | ||||||
| chr7:135397635
|
T | C | 344 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(341): Show | 344 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(341): Show |
intron_variant | MODIFIER | c.879+534A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397635 | ||||||
| chr7:135397666
|
G | A | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.879+503C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397666 | ||||||
| chr7:135397694
|
A | G | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.879+475T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397694 | ||||||
| chr7:135397735
|
C | G | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.879+434G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397735 | ||||||
| chr7:135397736
|
T | C | 1 | a0002c0002t0001g0031 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.879+433A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397736 | ||||||
| chr7:135397821
|
G | A | 1 | a0001c0001t0001g0284 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.879+348C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397821 | ||||||
| chr7:135397848
|
C | G | 12 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(9): Show | 12 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.879+321G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397848 | ||||||
| chr7:135397850
|
A | G | 2 | a0001c0001t0003g0351a0001c0001t0003g0361 | 2 | HG00597.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.879+319T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397850 | ||||||
| chr7:135397922
|
A | C | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+247T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397922 | ||||||
| chr7:135397999
|
T | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 96 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.879+170A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 8/11 | chr7 | 135397999 | ||||||
| chr7:135398300
|
G | GA | 110 | a0001c0001t0001g0164a0001c0001t0001g0306a0001c0001t0001g0307others(107): Show | 110 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.822-75dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135398300 | ||||||
| chr7:135398473
|
C | T | 23 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(20): Show | 23 | HG00099.hp2 HG00621.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.822-247G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135398473 | ||||||
| chr7:135398727
|
C | T | 1 | a0002c0002t0001g0029 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.822-501G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135398727 | ||||||
| chr7:135398802
|
T | G | 1 | a0001c0001t0001g0207 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.822-576A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135398802 | ||||||
| chr7:135399139
|
ATAAC | A | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.822-917_822-914del others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135399139 | ||||||
| chr7:135399479
|
C | G | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.822-1253G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135399479 | ||||||
| chr7:135399764
|
G | C | 1 | a0001c0001t0001g0330 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.822-1538C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135399764 | ||||||
| chr7:135399849
|
C | T | 18 | a0001c0001t0001g0324a0001c0001t0001g0329a0001c0001t0001g0330others(15): Show | 18 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.822-1623G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135399849 | ||||||
| chr7:135399924
|
A | G | 1 | a0001c0001t0003g0359 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.822-1698T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135399924 | ||||||
| chr7:135399972
|
GTTTAAAC others(8): Show |
G | 1 | a0002c0002t0001g0052 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.822-1761_822-1747d others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135399972 | ||||||
| chr7:135400071
|
T | C | 1 | a0001c0010t0002g0326 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.822-1845A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400071 | ||||||
| chr7:135400229
|
GC | G | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.822-2004delG | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400229 | ||||||
| chr7:135400305
|
T | G | 4 | a0001c0001t0001g0331a0001c0001t0001g0332a0001c0001t0001g0333others(1): Show | 4 | HG00735.hp1 HG00741.hp2 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.822-2079A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400305 | ||||||
| chr7:135400339
|
G | C | 1 | a0001c0001t0001g0319 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.822-2113C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400339 | ||||||
| chr7:135400358
|
C | T | 1 | a0002c0002t0006g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.822-2132G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400358 | ||||||
| chr7:135400407
|
C | T | 24 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(21): Show | 24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.822-2181G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400407 | ||||||
| chr7:135400423
|
G | A | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.822-2197C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400423 | ||||||
| chr7:135400464
|
C | T | 13 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(10): Show | 13 | HG01106.hp1 HG01167.hp1 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.822-2238G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400464 | ||||||
| chr7:135400642
|
A | G | 1 | a0002c0002t0001g0089 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.822-2416T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400642 | ||||||
| chr7:135400773
|
A | G | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.822-2547T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400773 | ||||||
| chr7:135400777
|
T | C | 15 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(12): Show | 15 | HG01069.hp1 HG01261.hp2 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.822-2551A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135400777 | ||||||
| chr7:135401086
|
A | T | 1 | a0001c0001t0001g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.822-2860T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135401086 | ||||||
| chr7:135401087
|
A | T | 1 | a0001c0001t0001g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.822-2861T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135401087 | ||||||
| chr7:135401088
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.822-2862T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135401088 | ||||||
| chr7:135401275
|
C | T | 1 | a0001c0001t0002g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.822-3049G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135401275 | ||||||
| chr7:135401546
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.822-3320A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135401546 | ||||||
| chr7:135401586
|
T | A | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.822-3360A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135401586 | ||||||
| chr7:135401921
|
G | T | 2 | a0001c0001t0001g0230a0001c0001t0001g0246 | 2 | HG00438.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.822-3695C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135401921 | ||||||
| chr7:135401937
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.822-3711A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135401937 | ||||||
| chr7:135402044
|
T | TCTCA | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.822-3819_822-3818i others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402044 | ||||||
| chr7:135402064
|
T | A | 1 | a0002c0002t0001g0030 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.822-3838A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402064 | ||||||
| chr7:135402083
|
T | G | 9 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0313others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.822-3857A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402083 | ||||||
| chr7:135402112
|
C | CT | 104 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 104 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.822-3887dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402112 | ||||||
| chr7:135402112
|
C | CTT | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.822-3888_822-3887d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402112 | ||||||
| chr7:135402144
|
C | T | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.822-3918G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402144 | ||||||
| chr7:135402185
|
C | T | 2 | a0001c0001t0001g0336a0001c0001t0001g0337 | 2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.822-3959G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402185 | ||||||
| chr7:135402188
|
C | A | 1 | a0001c0001t0001g0275 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.822-3962G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402188 | ||||||
| chr7:135402251
|
G | A | 1 | a0002c0002t0001g0093 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.822-4025C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402251 | ||||||
| chr7:135402283
|
T | C | 102 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0020others(99): Show | 102 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.822-4057A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402283 | ||||||
| chr7:135402299
|
G | A | 12 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(9): Show | 12 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.822-4073C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402299 | ||||||
| chr7:135402343
|
C | G | 1 | a0002c0002t0001g0086 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.822-4117G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402343 | ||||||
| chr7:135402389
|
G | A | 4 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(1): Show | 4 | HG00280.hp1 HG01361.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.822-4163C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402389 | ||||||
| chr7:135402433
|
A | C | 2 | a0001c0001t0001g0158a0001c0001t0001g0175 | 2 | NA18984.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.822-4207T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402433 | ||||||
| chr7:135402455
|
A | G | 1 | a0002c0002t0001g0088 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.822-4229T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402455 | ||||||
| chr7:135402472
|
T | A | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.822-4246A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402472 | ||||||
| chr7:135402645
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.822-4419G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402645 | ||||||
| chr7:135402744
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.822-4518A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402744 | ||||||
| chr7:135402842
|
C | T | 1 | a0001c0001t0001g0343 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.822-4616G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402842 | ||||||
| chr7:135402866
|
C | T | 13 | a0002c0002t0001g0025a0002c0002t0001g0026a0002c0002t0001g0027others(10): Show | 13 | NA18947.hp2 NA18948.hp1 NA18951.hp1 others(10): Show |
intron_variant | MODIFIER | c.822-4640G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135402866 | ||||||
| chr7:135403127
|
C | T | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.822-4901G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403127 | ||||||
| chr7:135403263
|
G | A | 1 | a0002c0002t0001g0064 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.822-5037C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403263 | ||||||
| chr7:135403489
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.822-5263G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403489 | ||||||
| chr7:135403508
|
G | A | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.822-5282C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403508 | ||||||
| chr7:135403554
|
G | A | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.822-5328C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403554 | ||||||
| chr7:135403556
|
A | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 141 | HG00099.hp2 HG00597.hp2 HG00621.hp2 others(138): Show |
intron_variant | MODIFIER | c.822-5330T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403556 | ||||||
| chr7:135403557
|
C | T | 1 | a0001c0001t0001g0348 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.822-5331G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403557 | ||||||
| chr7:135403862
|
T | C | 1 | a0002c0002t0001g0058 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.822-5636A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403862 | ||||||
| chr7:135403912
|
T | C | 1 | a0002c0002t0001g0068 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.822-5686A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403912 | ||||||
| chr7:135403969
|
A | G | 12 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0120others(9): Show | 12 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(9): Show |
intron_variant | MODIFIER | c.822-5743T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135403969 | ||||||
| chr7:135404013
|
C | T | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.822-5787G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135404013 | ||||||
| chr7:135404237
|
T | C | 24 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(21): Show | 24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.822-6011A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135404237 | ||||||
| chr7:135404284
|
CACTTA | C | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.822-6063_822-6059d others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135404284 | ||||||
| chr7:135404323
|
T | C | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.822-6097A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135404323 | ||||||
| chr7:135404375
|
T | G | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.821+6140A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135404375 | ||||||
| chr7:135404667
|
T | C | 2 | a0001c0001t0002g0124a0001c0001t0002g0125 | 2 | HG03225.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.821+5848A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135404667 | ||||||
| chr7:135404910
|
A | G | 42 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(39): Show | 42 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.821+5605T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135404910 | ||||||
| chr7:135404959
|
T | C | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.821+5556A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135404959 | ||||||
| chr7:135405179
|
C | T | 1 | a0001c0001t0001g0333 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.821+5336G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405179 | ||||||
| chr7:135405218
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.821+5297C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405218 | ||||||
| chr7:135405287
|
G | A | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.821+5228C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405287 | ||||||
| chr7:135405430
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.821+5085A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405430 | ||||||
| chr7:135405477
|
T | A | 1 | a0002c0002t0001g0052 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.821+5038A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405477 | ||||||
| chr7:135405561
|
A | T | 1 | a0002c0002t0001g0052 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.821+4954T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405561 | ||||||
| chr7:135405634
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.821+4881A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405634 | ||||||
| chr7:135405710
|
T | G | 5 | a0002c0002t0001g0300a0002c0002t0001g0301a0002c0002t0001g0302others(2): Show | 5 | HG02055.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.821+4805A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405710 | ||||||
| chr7:135405721
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.821+4794A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405721 | ||||||
| chr7:135405793
|
T | C | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.821+4722A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405793 | ||||||
| chr7:135405863
|
G | C | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.821+4652C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405863 | ||||||
| chr7:135405884
|
C | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.821+4631G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405884 | ||||||
| chr7:135405921
|
C | T | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.821+4594G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135405921 | ||||||
| chr7:135406299
|
C | T | 1 | a0002c0002t0001g0072 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.821+4216G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406299 | ||||||
| chr7:135406334
|
A | G | 1 | a0001c0001t0002g0296 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.821+4181T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406334 | ||||||
| chr7:135406403
|
T | C | 29 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(26): Show | 29 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.821+4112A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406403 | ||||||
| chr7:135406506
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.821+4009C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406506 | ||||||
| chr7:135406544
|
T | C | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.821+3971A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406544 | ||||||
| chr7:135406565
|
G | T | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.821+3950C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406565 | ||||||
| chr7:135406576
|
G | A | 107 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(104): Show | 107 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.821+3939C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406576 | ||||||
| chr7:135406820
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.821+3695A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406820 | ||||||
| chr7:135406932
|
T | C | 2 | a0002c0002t0001g0042a0002c0002t0001g0057 | 2 | HG00609.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.821+3583A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406932 | ||||||
| chr7:135406999
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.821+3516A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135406999 | ||||||
| chr7:135407157
|
C | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.821+3358G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407157 | ||||||
| chr7:135407439
|
T | G | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.821+3076A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407439 | ||||||
| chr7:135407500
|
G | A | 24 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(21): Show | 24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.821+3015C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407500 | ||||||
| chr7:135407689
|
G | GT | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.821+2825dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407689 | ||||||
| chr7:135407699
|
G | GT | 360 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(357): Show | 360 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.821+2815dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407699 | ||||||
| chr7:135407768
|
C | T | 1 | a0001c0001t0001g0336 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.821+2747G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407768 | ||||||
| chr7:135407769
|
G | A | 75 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0228others(72): Show | 75 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.821+2746C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407769 | ||||||
| chr7:135407806
|
A | G | 19 | a0001c0001t0001g0324a0001c0001t0001g0329a0001c0001t0001g0330others(16): Show | 19 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.821+2709T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407806 | ||||||
| chr7:135407807
|
T | A | 1 | a0001c0001t0001g0012 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.821+2708A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407807 | ||||||
| chr7:135407888
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.821+2627G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407888 | ||||||
| chr7:135407990
|
A | G | 1 | a0001c0001t0001g0281 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.821+2525T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135407990 | ||||||
| chr7:135408404
|
G | A | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.821+2111C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135408404 | ||||||
| chr7:135408629
|
C | G | 6 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(3): Show | 6 | HG01515.hp2 HG01517.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.821+1886G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135408629 | ||||||
| chr7:135408673
|
T | C | 1 | a0002c0002t0001g0098 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.821+1842A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135408673 | ||||||
| chr7:135408695
|
C | T | 266 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(263): Show | 266 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.821+1820G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135408695 | ||||||
| chr7:135408736
|
G | C | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.821+1779C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135408736 | ||||||
| chr7:135408795
|
C | A | 114 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(111): Show | 114 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.821+1720G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135408795 | ||||||
| chr7:135408984
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.821+1531A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135408984 | ||||||
| chr7:135409116
|
A | G | 5 | a0002c0002t0001g0300a0002c0002t0001g0301a0002c0002t0001g0302others(2): Show | 5 | HG02055.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.821+1399T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135409116 | ||||||
| chr7:135409207
|
C | T | 1 | a0002c0002t0006g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.821+1308G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135409207 | ||||||
| chr7:135409253
|
C | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.821+1262G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135409253 | ||||||
| chr7:135409452
|
C | A | 24 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(21): Show | 24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.821+1063G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135409452 | ||||||
| chr7:135409550
|
A | G | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.821+965T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135409550 | ||||||
| chr7:135409896
|
A | C | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.821+619T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135409896 | ||||||
| chr7:135409898
|
A | G | 1 | a0001c0001t0002g0296 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.821+617T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135409898 | ||||||
| chr7:135409901
|
T | A | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.821+614A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135409901 | ||||||
| chr7:135409910
|
G | C | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.821+605C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135409910 | ||||||
| chr7:135410013
|
A | G | 43 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(40): Show | 43 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.821+502T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135410013 | ||||||
| chr7:135410055
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.821+460C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135410055 | ||||||
| chr7:135410262
|
G | T | 1 | a0002c0002t0001g0071 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.821+253C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135410262 | ||||||
| chr7:135410271
|
T | C | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.821+244A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135410271 | ||||||
| chr7:135410384
|
A | G | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.821+131T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135410384 | ||||||
| chr7:135410430
|
A | C | 24 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(21): Show | 24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.821+85T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135410430 | ||||||
| chr7:135410510
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0166 | 2 | HG00642.hp2 HG01074.hp2 |
splice_region_variant&intron_variant | LOW | c.821+5G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 7/11 | chr7 | 135410510 | ||||||
| chr7:135410750
|
AATAAT | A | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.688-107_688-103del others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135410750 | ||||||
| chr7:135410761
|
T | A | 2 | a0001c0003t0002g0181a0001c0003t0002g0349 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.688-113A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135410761 | ||||||
| chr7:135410762
|
A | T | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.688-114T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135410762 | ||||||
| chr7:135411052
|
T | A | 1 | a0001c0001t0001g0298 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.688-404A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135411052 | ||||||
| chr7:135411062
|
T | C | 74 | a0001c0001t0001g0147a0001c0001t0001g0228a0001c0001t0001g0229others(71): Show | 74 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.688-414A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135411062 | ||||||
| chr7:135411249
|
T | A | 16 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0120others(13): Show | 16 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(13): Show |
intron_variant | MODIFIER | c.688-601A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135411249 | ||||||
| chr7:135411408
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.688-760T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135411408 | ||||||
| chr7:135411901
|
G | A | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.688-1253C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135411901 | ||||||
| chr7:135412115
|
A | G | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.687+1373T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135412115 | ||||||
| chr7:135412169
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.687+1319C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135412169 | ||||||
| chr7:135412185
|
G | A | 9 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0313others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.687+1303C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135412185 | ||||||
| chr7:135412328
|
A | C | 2 | a0001c0001t0001g0340a0001c0001t0001g0341 | 2 | HG00642.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.687+1160T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135412328 | ||||||
| chr7:135413015
|
A | G | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.687+473T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135413015 | ||||||
| chr7:135413031
|
A | G | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.687+457T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135413031 | ||||||
| chr7:135413387
|
T | C | 3 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0049 | 3 | HG03491.hp1 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.687+101A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 6/11 | chr7 | 135413387 | ||||||
| chr7:135413639
|
A | C | 5 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0124others(2): Show | 5 | HG01081.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.562-26T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135413639 | ||||||
| chr7:135413696
|
A | C | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.562-83T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135413696 | ||||||
| chr7:135413922
|
A | G | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.562-309T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135413922 | ||||||
| chr7:135413930
|
G | A | 19 | a0001c0001t0001g0324a0001c0001t0001g0329a0001c0001t0001g0330others(16): Show | 19 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.562-317C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135413930 | ||||||
| chr7:135413960
|
C | T | 24 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(21): Show | 24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.562-347G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135413960 | ||||||
| chr7:135414007
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.561+324G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135414007 | ||||||
| chr7:135414097
|
G | T | 9 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0313others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.561+234C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135414097 | ||||||
| chr7:135414187
|
C | G | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.561+144G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135414187 | ||||||
| chr7:135414295
|
TA | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0193a0001c0001t0001g0195others(5): Show | 8 | HG01069.hp2 HG01256.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.561+35delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135414295 | ||||||
| chr7:135414311
|
A | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0205 | 2 | NA19066.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.561+20T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135414311 | ||||||
| chr7:135414320
|
G | A | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.561+11C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 5/11 | chr7 | 135414320 | ||||||
| chr7:135414670
|
C | T | 19 | a0001c0001t0001g0324a0001c0001t0001g0329a0001c0001t0001g0330others(16): Show | 19 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.460-238G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 4/11 | chr7 | 135414670 | ||||||
| chr7:135414818
|
C | G | 1 | a0001c0001t0001g0336 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.459+358G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 4/11 | chr7 | 135414818 | ||||||
| chr7:135414900
|
C | T | 266 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(263): Show | 266 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.459+276G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 4/11 | chr7 | 135414900 | ||||||
| chr7:135415015
|
A | G | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG01081.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.459+161T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 4/11 | chr7 | 135415015 | ||||||
| chr7:135415152
|
G | A | 23 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(20): Show | 23 | HG00099.hp2 HG00621.hp2 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.459+24C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 4/11 | chr7 | 135415152 | ||||||
| chr7:135415440
|
A | G | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.373-178T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135415440 | ||||||
| chr7:135415454
|
A | G | 1 | a0002c0002t0001g0092 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.373-192T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135415454 | ||||||
| chr7:135415631
|
C | T | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-369G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135415631 | ||||||
| chr7:135415633
|
A | G | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.373-371T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135415633 | ||||||
| chr7:135415639
|
C | T | 73 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(70): Show | 73 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.373-377G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135415639 | ||||||
| chr7:135415671
|
TAA | T | 4 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0162others(1): Show | 4 | HG00738.hp1 HG01106.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.373-411_373-410del others(2): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135415671 | ||||||
| chr7:135415727
|
C | T | 266 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(263): Show | 266 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.373-465G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135415727 | ||||||
| chr7:135415881
|
T | C | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.373-619A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135415881 | ||||||
| chr7:135415987
|
A | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.373-725T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135415987 | ||||||
| chr7:135416081
|
C | T | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-819G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416081 | ||||||
| chr7:135416091
|
T | C | 1 | a0001c0001t0001g0008 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.373-829A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416091 | ||||||
| chr7:135416174
|
A | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.373-912T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416174 | ||||||
| chr7:135416208
|
C | T | 24 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(21): Show | 24 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(21): Show |
intron_variant | MODIFIER | c.373-946G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416208 | ||||||
| chr7:135416297
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.373-1035T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416297 | ||||||
| chr7:135416305
|
T | A | 2 | a0001c0001t0002g0288a0001c0001t0002g0292 | 2 | HG01891.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.373-1043A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416305 | ||||||
| chr7:135416353
|
T | C | 1 | a0001c0001t0001g0305 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.373-1091A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416353 | ||||||
| chr7:135416459
|
C | T | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-1197G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416459 | ||||||
| chr7:135416557
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.373-1295C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416557 | ||||||
| chr7:135416882
|
A | G | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.373-1620T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416882 | ||||||
| chr7:135416911
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.373-1649A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135416911 | ||||||
| chr7:135417043
|
T | C | 4 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(1): Show | 4 | HG00280.hp1 HG01361.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.373-1781A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135417043 | ||||||
| chr7:135417076
|
C | A | 1 | a0002c0002t0001g0092 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.373-1814G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135417076 | ||||||
| chr7:135417123
|
ATAGGTGC others(3): Show |
A | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.373-1871_373-1862d others(12): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135417123 | ||||||
| chr7:135417426
|
G | A | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.373-2164C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135417426 | ||||||
| chr7:135417623
|
G | C | 1 | a0002c0002t0001g0100 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.373-2361C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135417623 | ||||||
| chr7:135417726
|
C | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.373-2464G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135417726 | ||||||
| chr7:135417727
|
G | A | 2 | a0002c0002t0001g0301a0002c0002t0001g0304 | 2 | HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.373-2465C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135417727 | ||||||
| chr7:135418047
|
A | G | 1 | a0002c0002t0001g0078 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.373-2785T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418047 | ||||||
| chr7:135418173
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.373-2911G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418173 | ||||||
| chr7:135418248
|
T | C | 103 | a0001c0001t0001g0272a0002c0002t0001g0018a0002c0002t0001g0019others(100): Show | 103 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.373-2986A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418248 | ||||||
| chr7:135418332
|
A | G | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-3070T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418332 | ||||||
| chr7:135418355
|
A | G | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-3093T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418355 | ||||||
| chr7:135418359
|
C | T | 1 | a0002c0002t0001g0051 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.373-3097G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418359 | ||||||
| chr7:135418362
|
T | A | 1 | a0001c0010t0002g0326 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.373-3100A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418362 | ||||||
| chr7:135418459
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.373-3197A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418459 | ||||||
| chr7:135418547
|
A | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.373-3285T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418547 | ||||||
| chr7:135418628
|
A | G | 10 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.373-3366T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418628 | ||||||
| chr7:135418700
|
C | T | 269 | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0141others(266): Show | 269 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.373-3438G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418700 | ||||||
| chr7:135418770
|
T | A | 3 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0049 | 3 | HG03491.hp1 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.372+3386A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418770 | ||||||
| chr7:135418911
|
T | G | 142 | a0001c0001t0001g0155a0001c0001t0001g0166a0001c0001t0001g0169others(139): Show | 142 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.372+3245A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418911 | ||||||
| chr7:135418987
|
G | A | 4 | a0001c0001t0001g0197a0001c0001t0001g0216a0001c0001t0001g0223others(1): Show | 4 | HG02615.hp1 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.372+3169C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135418987 | ||||||
| chr7:135419029
|
G | C | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+3127C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419029 | ||||||
| chr7:135419103
|
A | AAAT | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.372+3052_372+3053i others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419103 | ||||||
| chr7:135419142
|
CT | C | 12 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(9): Show | 12 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.372+3013delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419142 | ||||||
| chr7:135419255
|
CCTATT | C | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.372+2896_372+2900d others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419255 | ||||||
| chr7:135419379
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.372+2777G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419379 | ||||||
| chr7:135419620
|
A | G | 1 | a0001c0001t0001g0277 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.372+2536T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419620 | ||||||
| chr7:135419685
|
T | C | 3 | a0002c0002t0001g0025a0002c0002t0001g0026a0002c0002t0001g0027 | 3 | NA18986.hp2 NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.372+2471A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419685 | ||||||
| chr7:135419888
|
C | A | 5 | a0001c0003t0002g0179a0001c0003t0002g0181a0001c0003t0002g0182others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+2268G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419888 | ||||||
| chr7:135419888
|
C | CA | 18 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(15): Show | 18 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.372+2267dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419888 | ||||||
| chr7:135419888
|
CA | C | 6 | a0001c0001t0001g0141a0001c0001t0001g0204a0001c0001t0001g0327others(3): Show | 6 | HG01167.hp2 HG03041.hp2 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.372+2267delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419888 | ||||||
| chr7:135419920
|
G | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.372+2236C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419920 | ||||||
| chr7:135419922
|
G | A | 1 | a0002c0002t0001g0052 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.372+2234C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419922 | ||||||
| chr7:135419942
|
C | A | 102 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0020others(99): Show | 102 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.372+2214G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135419942 | ||||||
| chr7:135420041
|
C | CA | 318 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(315): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.372+2114dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420041 | ||||||
| chr7:135420041
|
C | CAAACA | 39 | a0001c0001t0001g0141a0001c0001t0001g0324a0001c0001t0001g0327others(36): Show | 39 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.372+2114_372+2115i others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420041 | ||||||
| chr7:135420041
|
C | CAAACAAA others(2): Show |
4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.372+2114_372+2115i others(11): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420041 | ||||||
| chr7:135420046
|
A | AAC | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.372+2109_372+2110i others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420046 | ||||||
| chr7:135420047
|
C | A | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.372+2109G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420047 | ||||||
| chr7:135420074
|
C | CA | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.372+2081dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420074 | ||||||
| chr7:135420346
|
G | A | 1 | a0002c0002t0001g0064 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.372+1810C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420346 | ||||||
| chr7:135420394
|
T | C | 5 | a0002c0002t0001g0042a0002c0002t0001g0057a0002c0002t0001g0059others(2): Show | 5 | HG00609.hp2 HG02071.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.372+1762A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420394 | ||||||
| chr7:135420445
|
T | C | 3 | a0004c0005t0001g0126a0004c0005t0001g0127a0004c0005t0001g0128 | 3 | HG01106.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.372+1711A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420445 | ||||||
| chr7:135420539
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.372+1617A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420539 | ||||||
| chr7:135420577
|
C | CA | 37 | a0001c0001t0001g0012a0001c0001t0001g0118a0001c0001t0001g0145others(34): Show | 37 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.372+1578dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420577 | ||||||
| chr7:135420577
|
C | CAA | 95 | a0001c0001t0001g0299a0001c0001t0002g0131a0001c0001t0002g0132others(92): Show | 95 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.372+1577_372+1578d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420577 | ||||||
| chr7:135420577
|
C | CAAA | 7 | a0002c0002t0001g0025a0002c0002t0001g0026a0002c0002t0001g0027others(4): Show | 7 | HG02559.hp1 NA18978.hp2 NA18986.hp2 others(4): Show |
intron_variant | MODIFIER | c.372+1576_372+1578d others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420577 | ||||||
| chr7:135420577
|
CA | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0115a0001c0001t0001g0161others(9): Show | 12 | HG00621.hp2 HG01099.hp1 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.372+1578delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420577 | ||||||
| chr7:135420621
|
T | TAGTA | 5 | a0002c0002t0001g0300a0002c0002t0001g0301a0002c0002t0001g0302others(2): Show | 5 | HG02055.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+1531_372+1534d others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420621 | ||||||
| chr7:135420784
|
C | T | 73 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(70): Show | 73 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.372+1372G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135420784 | ||||||
| chr7:135421094
|
G | A | 11 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.372+1062C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421094 | ||||||
| chr7:135421199
|
A | G | 102 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0020others(99): Show | 102 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.372+957T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421199 | ||||||
| chr7:135421418
|
A | AT | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.372+737dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421418 | ||||||
| chr7:135421566
|
T | A | 1 | a0001c0001t0001g0210 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.372+590A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421566 | ||||||
| chr7:135421575
|
A | T | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.372+581T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421575 | ||||||
| chr7:135421577
|
G | A | 4 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(1): Show | 4 | HG01515.hp2 HG01517.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.372+579C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421577 | ||||||
| chr7:135421579
|
T | G | 1 | a0001c0001t0002g0180 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.372+577A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421579 | ||||||
| chr7:135421688
|
G | T | 25 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(22): Show | 25 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.372+468C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421688 | ||||||
| chr7:135421707
|
T | A | 5 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0001g0161others(2): Show | 5 | HG00642.hp2 HG01074.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.372+449A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421707 | ||||||
| chr7:135421733
|
C | G | 1 | a0001c0001t0001g0336 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.372+423G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421733 | ||||||
| chr7:135421808
|
C | T | 11 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.372+348G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421808 | ||||||
| chr7:135421899
|
T | C | 2 | a0002c0002t0001g0018a0002c0002t0001g0070 | 2 | NA18991.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.372+257A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421899 | ||||||
| chr7:135421982
|
G | A | 6 | a0002c0002t0001g0088a0002c0002t0001g0092a0002c0002t0001g0185others(3): Show | 6 | NA18975.hp1 NA19005.hp2 NA19054.hp1 others(3): Show |
intron_variant | MODIFIER | c.372+174C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135421982 | ||||||
| chr7:135422106
|
G | A | 1 | a0001c0001t0001g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.372+50C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135422106 | ||||||
| chr7:135422116
|
C | CAG | 11 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.372+39_372+40insCT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 3/11 | chr7 | 135422116 | ||||||
| chr7:135422379
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.175-26C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135422379 | ||||||
| chr7:135422396
|
T | G | 1 | a0001c0001t0003g0353 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.175-43A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135422396 | ||||||
| chr7:135422473
|
A | G | 2 | a0001c0001t0001g0327a0001c0001t0001g0328 | 2 | NA18953.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.175-120T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135422473 | ||||||
| chr7:135422567
|
C | A | 1 | a0002c0002t0001g0077 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.175-214G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135422567 | ||||||
| chr7:135422590
|
A | G | 11 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.175-237T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135422590 | ||||||
| chr7:135422873
|
G | C | 2 | a0002c0002t0001g0018a0002c0002t0001g0070 | 2 | NA18991.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.175-520C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135422873 | ||||||
| chr7:135422980
|
A | T | 1 | a0001c0001t0001g0318 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.175-627T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135422980 | ||||||
| chr7:135423000
|
C | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.175-647G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135423000 | ||||||
| chr7:135423339
|
A | C | 1 | a0002c0002t0001g0033 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.175-986T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135423339 | ||||||
| chr7:135423461
|
A | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-1108T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135423461 | ||||||
| chr7:135423471
|
T | TA | 15 | a0001c0001t0001g0283a0001c0001t0002g0287a0001c0001t0002g0288others(12): Show | 15 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.175-1119dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135423471 | ||||||
| chr7:135423471
|
TA | T | 10 | a0001c0001t0001g0324a0001c0001t0001g0348a0001c0001t0002g0130others(7): Show | 10 | HG01515.hp1 HG02145.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.175-1119delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135423471 | ||||||
| chr7:135423777
|
T | A | 1 | a0001c0001t0001g0348 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-1424A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135423777 | ||||||
| chr7:135424038
|
AAAACACA others(5): Show |
A | 1 | a0001c0001t0002g0294 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.175-1697_175-1686d others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424038 | ||||||
| chr7:135424039
|
AAACACAC others(4): Show |
A | 1 | a0001c0001t0001g0266 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.175-1697_175-1687d others(13): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424039 | ||||||
| chr7:135424039
|
AAACACAC others(8): Show |
A | 2 | a0002c0002t0001g0030a0002c0002t0001g0047 | 2 | HG03669.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.175-1701_175-1687d others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424039 | ||||||
| chr7:135424040
|
A | AAC | 14 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0144others(11): Show | 14 | HG00642.hp2 HG00741.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.175-1689_175-1688d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | ||||||
| chr7:135424040
|
A | AACAC | 4 | a0001c0001t0001g0006a0001c0001t0001g0173a0001c0001t0001g0191others(1): Show | 4 | HG00733.hp1 HG02451.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-1691_175-1688d others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | ||||||
| chr7:135424040
|
AAC | A | 29 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0113others(26): Show | 29 | HG00099.hp1 HG00099.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.175-1689_175-1688d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | ||||||
| chr7:135424040
|
AACAC | A | 16 | a0001c0001t0001g0142a0001c0001t0001g0150a0001c0001t0001g0153others(13): Show | 16 | HG00323.hp1 HG00673.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.175-1691_175-1688d others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | ||||||
| chr7:135424040
|
AACACAC | A | 13 | a0001c0001t0001g0166a0001c0001t0001g0196a0001c0001t0001g0198others(10): Show | 13 | HG00280.hp1 HG00733.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.175-1693_175-1688d others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | ||||||
| chr7:135424040
|
AACACACA others(1): Show |
A | 30 | a0001c0001t0001g0146a0001c0001t0001g0206a0001c0001t0001g0207others(27): Show | 30 | HG00642.hp1 HG00735.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.175-1695_175-1688d others(10): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | ||||||
| chr7:135424040
|
AACACACA others(3): Show |
A | 29 | a0001c0001t0001g0118a0001c0001t0001g0158a0001c0001t0001g0175others(26): Show | 29 | HG00323.hp2 HG00639.hp1 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.175-1697_175-1688d others(12): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | ||||||
| chr7:135424040
|
AACACACA others(5): Show |
A | 26 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0228others(23): Show | 26 | HG00597.hp2 HG01081.hp2 HG02083.hp2 others(23): Show |
intron_variant | MODIFIER | c.175-1699_175-1688d others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | ||||||
| chr7:135424040
|
AACACACA others(7): Show |
A | 55 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0232others(52): Show | 55 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.175-1701_175-1688d others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | ||||||
| chr7:135424040
|
AACACACA others(9): Show |
A | 31 | a0001c0001t0001g0231a0001c0001t0001g0327a0001c0001t0001g0328others(28): Show | 31 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.175-1703_175-1688d others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | ||||||
| chr7:135424040
|
AACACACA others(11): Show |
A | 76 | a0001c0001t0001g0247a0002c0002t0001g0019a0002c0002t0001g0020others(73): Show | 76 | HG00438.hp1 HG00673.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.175-1705_175-1688d others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | ||||||
| chr7:135424040
|
AACACACA others(13): Show |
A | 7 | a0001c0001t0001g0145a0001c0001t0002g0130a0001c0001t0002g0131others(4): Show | 7 | HG01243.hp2 HG02486.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.175-1707_175-1688d others(22): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | ||||||
| chr7:135424040
|
AACACACA others(17): Show |
A | 1 | a0001c0001t0002g0138 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.175-1711_175-1688d others(26): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424040 | ||||||
| chr7:135424056
|
C | G | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(2): Show | 5 | HG02258.hp2 HG02622.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-1703G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424056 | ||||||
| chr7:135424058
|
C | G | 6 | a0002c0002t0001g0300a0002c0002t0001g0301a0002c0002t0001g0302others(3): Show | 6 | HG02055.hp1 HG02258.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-1705G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424058 | ||||||
| chr7:135424183
|
A | G | 11 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(8): Show | 11 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.175-1830T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424183 | ||||||
| chr7:135424480
|
T | C | 1 | a0001c0001t0001g0250 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.175-2127A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424480 | ||||||
| chr7:135424814
|
C | A | 1 | a0001c0001t0001g0246 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.175-2461G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424814 | ||||||
| chr7:135424814
|
C | T | 1 | a0002c0002t0001g0057 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.175-2461G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424814 | ||||||
| chr7:135424817
|
A | AC | 17 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(14): Show | 17 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.175-2465_175-2464i others(3): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424817 | ||||||
| chr7:135424818
|
A | C | 13 | a0001c0001t0001g0206a0001c0001t0001g0221a0001c0001t0002g0287others(10): Show | 13 | HG01099.hp1 HG01261.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.175-2465T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424818 | ||||||
| chr7:135424823
|
A | C | 25 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(22): Show | 25 | HG00597.hp2 HG02055.hp1 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.175-2470T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424823 | ||||||
| chr7:135424870
|
C | A | 1 | a0002c0002t0001g0057 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.175-2517G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424870 | ||||||
| chr7:135424971
|
A | G | 1 | a0002c0002t0001g0060 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.175-2618T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135424971 | ||||||
| chr7:135425074
|
T | C | 1 | a0002c0002t0001g0046 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.175-2721A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135425074 | ||||||
| chr7:135425121
|
A | C | 1 | a0001c0001t0001g0113 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.175-2768T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135425121 | ||||||
| chr7:135425194
|
A | C | 11 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.175-2841T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135425194 | ||||||
| chr7:135425195
|
G | A | 11 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.175-2842C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135425195 | ||||||
| chr7:135425664
|
A | G | 3 | a0001c0001t0001g0343a0001c0001t0001g0344a0001c0001t0001g0345 | 3 | HG01256.hp1 HG01258.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.175-3311T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135425664 | ||||||
| chr7:135425815
|
A | T | 11 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.175-3462T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135425815 | ||||||
| chr7:135425837
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0175 | 2 | NA18984.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.175-3484G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135425837 | ||||||
| chr7:135425865
|
C | G | 1 | a0001c0001t0001g0229 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.175-3512G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135425865 | ||||||
| chr7:135426023
|
C | A | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.175-3670G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426023 | ||||||
| chr7:135426030
|
G | T | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.175-3677C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426030 | ||||||
| chr7:135426315
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.175-3962A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426315 | ||||||
| chr7:135426323
|
C | G | 1 | a0001c0001t0001g0238 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.175-3970G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426323 | ||||||
| chr7:135426330
|
C | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.175-3977G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426330 | ||||||
| chr7:135426460
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.175-4107C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426460 | ||||||
| chr7:135426519
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.175-4166G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426519 | ||||||
| chr7:135426520
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.175-4167C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426520 | ||||||
| chr7:135426602
|
CA | C | 223 | a0001c0001t0001g0118a0001c0001t0001g0145a0001c0001t0001g0146others(220): Show | 223 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.175-4250delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426602 | ||||||
| chr7:135426615
|
A | G | 1 | a0002c0002t0001g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.175-4262T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426615 | ||||||
| chr7:135426618
|
AG | A | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.175-4266delC | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426618 | ||||||
| chr7:135426619
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-4266C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426619 | ||||||
| chr7:135426629
|
A | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-4276T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426629 | ||||||
| chr7:135426837
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.175-4484G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426837 | ||||||
| chr7:135426880
|
G | A | 1 | a0001c0001t0001g0348 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-4527C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426880 | ||||||
| chr7:135426923
|
CA | C | 15 | a0001c0001t0001g0005a0001c0001t0001g0141a0001c0001t0001g0327others(12): Show | 15 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.175-4571delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135426923 | ||||||
| chr7:135427105
|
T | G | 2 | a0001c0001t0001g0147a0001c0001t0008g0350 | 2 | HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.175-4752A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427105 | ||||||
| chr7:135427110
|
C | G | 2 | a0001c0001t0002g0189a0001c0001t0002g0190 | 2 | HG00099.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.175-4757G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427110 | ||||||
| chr7:135427265
|
C | G | 5 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0001g0161others(2): Show | 5 | HG00642.hp2 HG01074.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.175-4912G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427265 | ||||||
| chr7:135427326
|
CT | C | 102 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0020others(99): Show | 102 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.175-4974delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427326 | ||||||
| chr7:135427391
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.175-5038G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427391 | ||||||
| chr7:135427540
|
T | C | 1 | a0001c0001t0001g0348 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175-5187A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427540 | ||||||
| chr7:135427757
|
T | TA | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.175-5405dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427757 | ||||||
| chr7:135427762
|
AT | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-5410delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427762 | ||||||
| chr7:135427763
|
T | A | 1 | a0001c0001t0003g0359 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.175-5410A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427763 | ||||||
| chr7:135427993
|
G | A | 102 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0020others(99): Show | 102 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.175-5640C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135427993 | ||||||
| chr7:135428255
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.175-5902T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135428255 | ||||||
| chr7:135428345
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.175-5992T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135428345 | ||||||
| chr7:135428446
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-6093A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135428446 | ||||||
| chr7:135428898
|
A | G | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.175-6545T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135428898 | ||||||
| chr7:135429175
|
T | C | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG03098.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.175-6822A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135429175 | ||||||
| chr7:135429425
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.175-7072A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135429425 | ||||||
| chr7:135429527
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.175-7174A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135429527 | ||||||
| chr7:135429817
|
T | C | 1 | a0002c0002t0006g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.175-7464A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135429817 | ||||||
| chr7:135429845
|
C | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-7492G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135429845 | ||||||
| chr7:135429879
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-7526A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135429879 | ||||||
| chr7:135429993
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.175-7640G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135429993 | ||||||
| chr7:135430313
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.174+7845C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135430313 | ||||||
| chr7:135430329
|
A | G | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.174+7829T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135430329 | ||||||
| chr7:135430343
|
A | T | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.174+7815T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135430343 | ||||||
| chr7:135430389
|
G | A | 266 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(263): Show | 266 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.174+7769C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135430389 | ||||||
| chr7:135430623
|
C | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0312 | 2 | HG01496.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.174+7535G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135430623 | ||||||
| chr7:135430752
|
C | T | 1 | a0002c0002t0001g0072 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.174+7406G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135430752 | ||||||
| chr7:135431008
|
A | G | 3 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0180 | 3 | HG01081.hp2 HG02723.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.174+7150T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431008 | ||||||
| chr7:135431020
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+7138A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431020 | ||||||
| chr7:135431072
|
C | A | 1 | a0001c0001t0001g0220 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.174+7086G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431072 | ||||||
| chr7:135431086
|
G | A | 4 | a0002c0002t0001g0045a0002c0002t0001g0089a0002c0002t0001g0090others(1): Show | 4 | HG00673.hp1 NA18747.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+7072C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431086 | ||||||
| chr7:135431131
|
G | A | 7 | a0001c0001t0001g0338a0001c0001t0001g0339a0001c0001t0001g0340others(4): Show | 7 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+7027C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431131 | ||||||
| chr7:135431236
|
T | C | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.174+6922A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431236 | ||||||
| chr7:135431245
|
C | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+6913G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431245 | ||||||
| chr7:135431461
|
G | A | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+6697C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431461 | ||||||
| chr7:135431480
|
A | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+6678T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431480 | ||||||
| chr7:135431486
|
G | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+6672C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431486 | ||||||
| chr7:135431647
|
G | A | 4 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0049others(1): Show | 4 | HG03491.hp1 HG03492.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.174+6511C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431647 | ||||||
| chr7:135431651
|
G | A | 1 | a0002c0002t0001g0058 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.174+6507C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431651 | ||||||
| chr7:135431737
|
C | T | 1 | a0001c0001t0001g0324 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.174+6421G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431737 | ||||||
| chr7:135431743
|
C | CA | 10 | a0001c0001t0001g0235a0001c0001t0001g0245a0001c0001t0001g0248others(7): Show | 10 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(7): Show |
intron_variant | MODIFIER | c.174+6414dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431743 | ||||||
| chr7:135431759
|
C | CA | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.174+6398dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431759 | ||||||
| chr7:135431805
|
C | CA | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.174+6352dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431805 | ||||||
| chr7:135431809
|
C | A | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.174+6349G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431809 | ||||||
| chr7:135431979
|
T | C | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.174+6179A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135431979 | ||||||
| chr7:135432111
|
CAAT | C | 9 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0313others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.174+6044_174+6046d others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135432111 | ||||||
| chr7:135432178
|
C | T | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.174+5980G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135432178 | ||||||
| chr7:135432223
|
G | T | 1 | a0001c0001t0001g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.174+5935C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135432223 | ||||||
| chr7:135432304
|
A | T | 19 | a0001c0001t0001g0118a0002c0002t0001g0036a0002c0002t0001g0087others(16): Show | 19 | HG00438.hp1 HG01071.hp1 HG01255.hp2 others(16): Show |
intron_variant | MODIFIER | c.174+5854T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135432304 | ||||||
| chr7:135432471
|
T | C | 1 | a0001c0001t0001g0298 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.174+5687A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135432471 | ||||||
| chr7:135432732
|
G | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+5426C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135432732 | ||||||
| chr7:135432812
|
C | T | 3 | a0002c0002t0001g0034a0002c0002t0001g0055a0002c0002t0001g0081 | 3 | NA18957.hp2 NA18971.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.174+5346G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135432812 | ||||||
| chr7:135432894
|
G | A | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+5264C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135432894 | ||||||
| chr7:135432916
|
G | A | 1 | a0001c0001t0008g0350 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.174+5242C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135432916 | ||||||
| chr7:135433038
|
T | C | 1 | a0001c0001t0001g0251 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.174+5120A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433038 | ||||||
| chr7:135433082
|
T | G | 8 | a0001c0001t0001g0240a0001c0001t0002g0120a0001c0001t0002g0121others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+5076A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433082 | ||||||
| chr7:135433350
|
C | CT | 14 | a0001c0001t0001g0012a0001c0001t0001g0167a0001c0001t0001g0203others(11): Show | 14 | HG00280.hp2 HG02257.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.174+4807dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433350 | ||||||
| chr7:135433350
|
CT | C | 19 | a0001c0001t0001g0170a0001c0001t0001g0236a0001c0001t0001g0306others(16): Show | 19 | HG02258.hp1 HG02258.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.174+4807delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433350 | ||||||
| chr7:135433350
|
CTT | C | 13 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0003g0351others(10): Show | 13 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(10): Show |
intron_variant | MODIFIER | c.174+4806_174+4807d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433350 | ||||||
| chr7:135433371
|
T | C | 5 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0159others(2): Show | 5 | HG00738.hp1 HG01106.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.174+4787A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433371 | ||||||
| chr7:135433546
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+4612A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433546 | ||||||
| chr7:135433715
|
T | A | 1 | a0001c0001t0001g0333 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.174+4443A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433715 | ||||||
| chr7:135433855
|
C | A | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.174+4303G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433855 | ||||||
| chr7:135433943
|
C | G | 1 | a0001c0001t0001g0241 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.174+4215G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433943 | ||||||
| chr7:135433946
|
T | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0166 | 2 | HG00642.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.174+4212A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135433946 | ||||||
| chr7:135434070
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.174+4088G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135434070 | ||||||
| chr7:135434186
|
C | G | 1 | a0001c0001t0001g0348 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.174+3972G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135434186 | ||||||
| chr7:135434195
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+3963A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135434195 | ||||||
| chr7:135434314
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.174+3844C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135434314 | ||||||
| chr7:135434632
|
G | T | 1 | a0001c0001t0001g0348 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.174+3526C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135434632 | ||||||
| chr7:135434669
|
A | G | 268 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(265): Show | 268 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.174+3489T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135434669 | ||||||
| chr7:135434900
|
ACT | A | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+3256_174+3257d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135434900 | ||||||
| chr7:135434920
|
T | C | 4 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0154others(1): Show | 4 | NA18980.hp1 NA18994.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+3238A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135434920 | ||||||
| chr7:135434951
|
A | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+3207T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135434951 | ||||||
| chr7:135435005
|
C | A | 1 | a0001c0001t0001g0017 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.174+3153G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435005 | ||||||
| chr7:135435025
|
C | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+3133G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435025 | ||||||
| chr7:135435026
|
A | G | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+3132T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435026 | ||||||
| chr7:135435061
|
T | C | 17 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(14): Show | 17 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.174+3097A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435061 | ||||||
| chr7:135435083
|
C | T | 267 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(264): Show | 267 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.174+3075G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435083 | ||||||
| chr7:135435084
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.174+3074C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435084 | ||||||
| chr7:135435115
|
C | T | 8 | a0002c0002t0001g0096a0002c0002t0001g0098a0002c0002t0001g0099others(5): Show | 8 | HG01257.hp2 HG01258.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.174+3043G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435115 | ||||||
| chr7:135435448
|
A | G | 268 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(265): Show | 268 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(265): Show |
intron_variant | MODIFIER | c.174+2710T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435448 | ||||||
| chr7:135435562
|
C | T | 13 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(10): Show | 13 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(10): Show |
intron_variant | MODIFIER | c.174+2596G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435562 | ||||||
| chr7:135435711
|
A | C | 1 | a0001c0001t0001g0297 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.174+2447T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435711 | ||||||
| chr7:135435922
|
C | T | 1 | a0001c0001t0002g0296 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.174+2236G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435922 | ||||||
| chr7:135435969
|
AC | A | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.174+2188delG | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135435969 | ||||||
| chr7:135436009
|
T | G | 18 | a0001c0001t0002g0116a0001c0001t0002g0117a0001c0001t0002g0119others(15): Show | 18 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(15): Show |
intron_variant | MODIFIER | c.174+2149A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436009 | ||||||
| chr7:135436017
|
C | CT | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+2140dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436017 | ||||||
| chr7:135436057
|
T | C | 1 | a0002c0002t0006g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.174+2101A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436057 | ||||||
| chr7:135436082
|
A | G | 1 | a0002c0002t0001g0108 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.174+2076T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436082 | ||||||
| chr7:135436154
|
C | CT | 360 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(357): Show | 360 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.174+2003dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436154 | ||||||
| chr7:135436154
|
C | T | 1 | a0001c0001t0003g0357 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.174+2004G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436154 | ||||||
| chr7:135436393
|
A | G | 1 | a0001c0001t0001g0273 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.174+1765T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436393 | ||||||
| chr7:135436413
|
G | C | 1 | a0001c0001t0003g0357 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.174+1745C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436413 | ||||||
| chr7:135436486
|
TG | T | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.174+1671delC | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436486 | ||||||
| chr7:135436507
|
A | G | 1 | a0002c0002t0001g0070 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.174+1651T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436507 | ||||||
| chr7:135436520
|
C | CA | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.174+1637dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436520 | ||||||
| chr7:135436632
|
AT | A | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+1525delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436632 | ||||||
| chr7:135436785
|
GATAA | G | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.174+1369_174+1372d others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436785 | ||||||
| chr7:135436875
|
T | C | 2 | a0002c0002t0001g0020a0002c0002t0001g0051 | 2 | HG00735.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.174+1283A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135436875 | ||||||
| chr7:135437082
|
A | G | 1 | a0001c0001t0002g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.174+1076T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437082 | ||||||
| chr7:135437178
|
GCTTTT | G | 63 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(60): Show | 63 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.174+975_174+979del others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437178 | ||||||
| chr7:135437213
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.174+945C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437213 | ||||||
| chr7:135437221
|
G | C | 1 | a0002c0002t0001g0304 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.174+937C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437221 | ||||||
| chr7:135437222
|
C | T | 1 | a0002c0002t0001g0304 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.174+936G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437222 | ||||||
| chr7:135437291
|
G | C | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.174+867C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437291 | ||||||
| chr7:135437372
|
G | C | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.174+786C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437372 | ||||||
| chr7:135437410
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.174+748G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437410 | ||||||
| chr7:135437495
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.174+663C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437495 | ||||||
| chr7:135437694
|
T | G | 2 | a0001c0001t0001g0310a0006c0007t0001g0311 | 2 | HG00323.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.174+464A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437694 | ||||||
| chr7:135437881
|
T | C | 3 | a0002c0002t0001g0028a0002c0002t0001g0031a0002c0002t0001g0032 | 3 | NA18948.hp1 NA19007.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.174+277A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437881 | ||||||
| chr7:135437963
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+195A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135437963 | ||||||
| chr7:135438062
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.174+96A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135438062 | ||||||
| chr7:135438098
|
T | C | 2 | a0002c0002t0001g0104a0002c0002t0001g0107 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.174+60A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 2/11 | chr7 | 135438098 | ||||||
| chr7:135438654
|
C | T | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133 | 3 | HG02896.hp1 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-92-231G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135438654 | ||||||
| chr7:135438792
|
C | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-369G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135438792 | ||||||
| chr7:135438897
|
C | T | 4 | a0002c0002t0001g0080a0002c0002t0001g0082a0002c0002t0001g0084others(1): Show | 4 | NA18946.hp1 NA18968.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-474G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135438897 | ||||||
| chr7:135439170
|
C | A | 2 | a0001c0001t0002g0287a0001c0001t0002g0289 | 2 | HG01496.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-92-747G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135439170 | ||||||
| chr7:135439333
|
G | T | 5 | a0001c0003t0002g0179a0001c0003t0002g0181a0001c0003t0002g0182others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-910C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135439333 | ||||||
| chr7:135439449
|
A | G | 1 | a0001c0001t0001g0306 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-92-1026T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135439449 | ||||||
| chr7:135439498
|
C | A | 19 | a0001c0001t0001g0229a0001c0001t0001g0235a0001c0001t0001g0242others(16): Show | 19 | HG00609.hp1 HG02129.hp2 NA18946.hp2 others(16): Show |
intron_variant | MODIFIER | c.-92-1075G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135439498 | ||||||
| chr7:135439585
|
C | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-1162G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135439585 | ||||||
| chr7:135439591
|
C | A | 2 | a0001c0001t0001g0158a0001c0001t0001g0175 | 2 | NA18984.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-92-1168G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135439591 | ||||||
| chr7:135439730
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-1307A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135439730 | ||||||
| chr7:135440010
|
A | T | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-1587T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440010 | ||||||
| chr7:135440157
|
T | C | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-1734A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440157 | ||||||
| chr7:135440221
|
T | TA | 54 | a0001c0001t0001g0240a0001c0010t0002g0326a0002c0002t0001g0018others(51): Show | 54 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.-92-1799dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440221 | ||||||
| chr7:135440221
|
TA | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0141a0001c0001t0001g0160others(13): Show | 16 | HG00639.hp1 HG01069.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.-92-1799delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440221 | ||||||
| chr7:135440288
|
T | C | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-92-1865A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440288 | ||||||
| chr7:135440329
|
C | CT | 19 | a0001c0001t0001g0141a0001c0001t0001g0228a0001c0001t0001g0297others(16): Show | 19 | HG00597.hp2 HG02083.hp2 HG02622.hp2 others(16): Show |
intron_variant | MODIFIER | c.-92-1907dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440329 | ||||||
| chr7:135440329
|
CT | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-1907delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440329 | ||||||
| chr7:135440331
|
T | G | 1 | a0001c0001t0001g0230 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-92-1908A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440331 | ||||||
| chr7:135440414
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-92-1991G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440414 | ||||||
| chr7:135440780
|
G | A | 73 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(70): Show | 73 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-92-2357C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440780 | ||||||
| chr7:135440875
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-2452A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135440875 | ||||||
| chr7:135441118
|
G | A | 1 | a0001c0003t0002g0181 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-92-2695C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441118 | ||||||
| chr7:135441140
|
C | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-2717G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441140 | ||||||
| chr7:135441230
|
A | AT | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.-92-2808dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441230 | ||||||
| chr7:135441334
|
T | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-92-2911A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441334 | ||||||
| chr7:135441406
|
TA | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0256a0001c0001t0001g0283others(7): Show | 10 | HG01069.hp1 HG01257.hp2 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.-92-2984delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441406 | ||||||
| chr7:135441460
|
T | C | 1 | a0001c0001t0007g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-92-3037A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441460 | ||||||
| chr7:135441550
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-3127G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441550 | ||||||
| chr7:135441775
|
T | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-92-3352A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441775 | ||||||
| chr7:135441914
|
T | C | 6 | a0002c0002t0001g0019a0002c0002t0001g0050a0002c0002t0001g0056others(3): Show | 6 | HG01358.hp1 HG01515.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-3491A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441914 | ||||||
| chr7:135441937
|
G | C | 1 | a0002c0002t0001g0058 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-92-3514C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441937 | ||||||
| chr7:135441964
|
A | G | 1 | a0001c0001t0001g0005 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-3541T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441964 | ||||||
| chr7:135441965
|
G | T | 1 | a0001c0001t0001g0005 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-3542C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135441965 | ||||||
| chr7:135442005
|
G | A | 1 | a0002c0002t0001g0081 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-92-3582C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442005 | ||||||
| chr7:135442052
|
C | T | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.-92-3629G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442052 | ||||||
| chr7:135442139
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-92-3716A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442139 | ||||||
| chr7:135442294
|
T | C | 2 | a0002c0002t0001g0048a0002c0002t0001g0049 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-92-3871A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442294 | ||||||
| chr7:135442450
|
T | A | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-4027A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442450 | ||||||
| chr7:135442456
|
G | A | 1 | a0001c0001t0008g0350 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-92-4033C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442456 | ||||||
| chr7:135442509
|
G | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-4086C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442509 | ||||||
| chr7:135442595
|
C | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-4172G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442595 | ||||||
| chr7:135442662
|
C | T | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-4239G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442662 | ||||||
| chr7:135442901
|
T | A | 1 | a0001c0001t0001g0297 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-92-4478A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135442901 | ||||||
| chr7:135443009
|
T | C | 1 | a0001c0001t0001g0337 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-92-4586A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443009 | ||||||
| chr7:135443036
|
G | T | 1 | a0001c0001t0001g0173 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-92-4613C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443036 | ||||||
| chr7:135443127
|
G | T | 1 | a0002c0002t0001g0020 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-92-4704C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443127 | ||||||
| chr7:135443188
|
CA | C | 156 | a0001c0001t0001g0015a0001c0001t0001g0118a0001c0001t0001g0297others(153): Show | 156 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.-92-4766delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443188 | ||||||
| chr7:135443190
|
A | C | 2 | a0001c0001t0001g0324a0002c0002t0006g0002 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-92-4767T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443190 | ||||||
| chr7:135443244
|
A | G | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-92-4821T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443244 | ||||||
| chr7:135443354
|
C | CA | 29 | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0147others(26): Show | 29 | HG01071.hp1 HG01256.hp2 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-92-4932dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443354 | ||||||
| chr7:135443356
|
A | C | 33 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(30): Show | 33 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.-92-4933T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443356 | ||||||
| chr7:135443358
|
A | C | 19 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(16): Show | 19 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.-92-4935T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443358 | ||||||
| chr7:135443376
|
C | T | 2 | a0002c0002t0001g0036a0002c0002t0001g0087 | 2 | NA19003.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-92-4953G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443376 | ||||||
| chr7:135443701
|
C | T | 1 | a0001c0001t0002g0288 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-92-5278G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443701 | ||||||
| chr7:135443742
|
C | A | 15 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(12): Show | 15 | HG00597.hp2 HG02083.hp2 HG02965.hp1 others(12): Show |
intron_variant | MODIFIER | c.-92-5319G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443742 | ||||||
| chr7:135443906
|
T | G | 1 | a0001c0001t0001g0310 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-92-5483A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443906 | ||||||
| chr7:135443940
|
G | T | 1 | a0001c0001t0001g0005 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-5517C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443940 | ||||||
| chr7:135443961
|
C | A | 1 | a0001c0001t0001g0317 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-92-5538G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135443961 | ||||||
| chr7:135444016
|
T | A | 1 | a0001c0001t0001g0005 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-5593A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444016 | ||||||
| chr7:135444041
|
G | T | 73 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(70): Show | 73 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-92-5618C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444041 | ||||||
| chr7:135444057
|
C | G | 1 | a0001c0001t0001g0170 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-92-5634G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444057 | ||||||
| chr7:135444061
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-92-5638C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444061 | ||||||
| chr7:135444144
|
A | AAAT | 17 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(14): Show | 17 | HG00597.hp2 HG02083.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.-92-5724_-92-5722d others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444144 | ||||||
| chr7:135444144
|
A | T | 1 | a0001c0001t0001g0164 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-92-5721T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444144 | ||||||
| chr7:135444144
|
AAAT | A | 37 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0239others(34): Show | 37 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.-92-5724_-92-5722d others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444144 | ||||||
| chr7:135444144
|
AAATAATA others(2): Show |
A | 60 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(57): Show | 60 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.-92-5730_-92-5722d others(11): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444144 | ||||||
| chr7:135444144
|
AAATAATA others(8): Show |
A | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-92-5736_-92-5722d others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444144 | ||||||
| chr7:135444179
|
G | A | 1 | a0002c0002t0001g0129 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-92-5756C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444179 | ||||||
| chr7:135444291
|
G | A | 9 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0313others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-92-5868C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444291 | ||||||
| chr7:135444305
|
A | G | 1 | a0002c0002t0001g0093 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-92-5882T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444305 | ||||||
| chr7:135444367
|
A | G | 5 | a0001c0001t0001g0235a0001c0001t0001g0245a0001c0001t0001g0248others(2): Show | 5 | NA18946.hp2 NA18962.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-5944T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444367 | ||||||
| chr7:135444502
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-6079C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444502 | ||||||
| chr7:135444520
|
C | T | 4 | a0001c0001t0001g0147a0001c0001t0003g0354a0001c0001t0003g0355others(1): Show | 4 | HG02083.hp2 HG03209.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.-92-6097G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444520 | ||||||
| chr7:135444695
|
G | A | 19 | a0001c0001t0001g0147a0001c0001t0001g0329a0001c0001t0001g0330others(16): Show | 19 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.-92-6272C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444695 | ||||||
| chr7:135444738
|
G | C | 1 | a0001c0001t0001g0005 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-6315C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444738 | ||||||
| chr7:135444826
|
A | T | 1 | a0001c0001t0001g0005 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-6403T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444826 | ||||||
| chr7:135444838
|
T | C | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-6415A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444838 | ||||||
| chr7:135444983
|
C | CT | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.-92-6561dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135444983 | ||||||
| chr7:135445213
|
A | G | 64 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(61): Show | 64 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.-92-6790T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445213 | ||||||
| chr7:135445583
|
T | G | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-7160A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445583 | ||||||
| chr7:135445591
|
T | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-7168A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445591 | ||||||
| chr7:135445607
|
T | C | 3 | a0001c0001t0001g0150a0001c0001t0001g0153a0001c0001t0001g0156 | 3 | NA18939.hp2 NA18940.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.-92-7184A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445607 | ||||||
| chr7:135445668
|
G | A | 19 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(16): Show | 19 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.-92-7245C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445668 | ||||||
| chr7:135445700
|
T | A | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-92-7277A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445700 | ||||||
| chr7:135445754
|
T | C | 1 | a0001c0001t0001g0284 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-92-7331A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445754 | ||||||
| chr7:135445782
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-7359C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445782 | ||||||
| chr7:135445883
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-7460A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445883 | ||||||
| chr7:135445945
|
T | C | 2 | a0001c0001t0004g0346a0001c0001t0004g0347 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-92-7522A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135445945 | ||||||
| chr7:135446050
|
T | G | 1 | a0001c0001t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-92-7627A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446050 | ||||||
| chr7:135446085
|
T | C | 1 | a0001c0001t0001g0282 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-92-7662A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446085 | ||||||
| chr7:135446107
|
C | G | 1 | a0001c0001t0001g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-92-7684G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446107 | ||||||
| chr7:135446234
|
T | C | 60 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(57): Show | 60 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.-92-7811A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446234 | ||||||
| chr7:135446271
|
G | A | 3 | a0001c0001t0001g0228a0001c0001t0004g0346a0001c0001t0004g0347 | 3 | HG03490.hp2 HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-92-7848C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446271 | ||||||
| chr7:135446288
|
T | A | 4 | a0001c0001t0001g0236a0001c0001t0001g0243a0001c0001t0001g0262others(1): Show | 4 | NA18948.hp2 NA18951.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-7865A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446288 | ||||||
| chr7:135446336
|
C | G | 6 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0272others(3): Show | 6 | HG02071.hp2 HG03834.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.-92-7913G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446336 | ||||||
| chr7:135446406
|
A | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-7983T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446406 | ||||||
| chr7:135446475
|
C | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-8052G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446475 | ||||||
| chr7:135446601
|
G | C | 266 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(263): Show | 266 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.-92-8178C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446601 | ||||||
| chr7:135446609
|
A | C | 3 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140 | 3 | HG02572.hp2 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-92-8186T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446609 | ||||||
| chr7:135446905
|
AACTATAT others(303): Show |
A | 73 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(70): Show | 73 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-92-8792_-92-8483d others(2): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446905 | ||||||
| chr7:135446950
|
T | A | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-8527A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135446950 | ||||||
| chr7:135447001
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-92-8578C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447001 | ||||||
| chr7:135447013
|
C | T | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-8590G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447013 | ||||||
| chr7:135447097
|
C | T | 8 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(5): Show | 8 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(5): Show |
intron_variant | MODIFIER | c.-92-8674G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447097 | ||||||
| chr7:135447130
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-8707A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447130 | ||||||
| chr7:135447147
|
A | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-8724T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447147 | ||||||
| chr7:135447246
|
A | T | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-8823T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447246 | ||||||
| chr7:135447266
|
A | T | 5 | a0001c0003t0002g0179a0001c0003t0002g0181a0001c0003t0002g0182others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-8843T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447266 | ||||||
| chr7:135447343
|
T | C | 1 | a0001c0001t0002g0290 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-92-8920A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447343 | ||||||
| chr7:135447504
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-9081A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447504 | ||||||
| chr7:135447770
|
A | G | 1 | a0001c0001t0001g0323 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-92-9347T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447770 | ||||||
| chr7:135447903
|
GT | G | 4 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0162others(1): Show | 4 | HG00738.hp1 HG01106.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-92-9481delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135447903 | ||||||
| chr7:135448086
|
G | A | 1 | a0002c0002t0001g0087 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-92-9663C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448086 | ||||||
| chr7:135448209
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0003g0357 | 2 | NA18941.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-92-9786G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448209 | ||||||
| chr7:135448341
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-9918C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448341 | ||||||
| chr7:135448543
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-10120C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448543 | ||||||
| chr7:135448546
|
A | G | 1 | a0001c0001t0001g0005 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-10123T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448546 | ||||||
| chr7:135448547
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-10124C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448547 | ||||||
| chr7:135448558
|
A | G | 1 | a0001c0001t0001g0005 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-10135T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448558 | ||||||
| chr7:135448559
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-92-10136C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448559 | ||||||
| chr7:135448559
|
G | GGGAGGGA others(9): Show |
6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-10137_-92-1013 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448559 | ||||||
| chr7:135448583
|
C | A | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-92-10160G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448583 | ||||||
| chr7:135448722
|
T | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-92-10299A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448722 | ||||||
| chr7:135448772
|
A | G | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-10349T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448772 | ||||||
| chr7:135448792
|
G | A | 2 | a0002c0002t0001g0110a0002c0002t0001g0111 | 2 | NA18956.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-92-10369C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448792 | ||||||
| chr7:135448883
|
T | G | 1 | a0001c0001t0001g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-92-10460A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135448883 | ||||||
| chr7:135449056
|
C | T | 1 | a0001c0001t0008g0350 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-92-10633G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135449056 | ||||||
| chr7:135449083
|
A | T | 7 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(4): Show | 7 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(4): Show |
intron_variant | MODIFIER | c.-92-10660T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135449083 | ||||||
| chr7:135449098
|
C | T | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-10675G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135449098 | ||||||
| chr7:135449551
|
G | A | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-11128C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135449551 | ||||||
| chr7:135449828
|
G | T | 7 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(4): Show | 7 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(4): Show |
intron_variant | MODIFIER | c.-92-11405C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135449828 | ||||||
| chr7:135449828
|
GT | G | 205 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0228others(202): Show | 205 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(202): Show |
intron_variant | MODIFIER | c.-92-11406delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135449828 | ||||||
| chr7:135450032
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-92-11609A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135450032 | ||||||
| chr7:135450054
|
A | C | 63 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(60): Show | 63 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-92-11631T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135450054 | ||||||
| chr7:135450511
|
G | A | 3 | a0001c0001t0001g0343a0001c0001t0001g0344a0001c0001t0001g0345 | 3 | HG01256.hp1 HG01258.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-92-12088C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135450511 | ||||||
| chr7:135450579
|
C | A | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-12156G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135450579 | ||||||
| chr7:135450641
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-92-12218C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135450641 | ||||||
| chr7:135450783
|
A | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-12360T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135450783 | ||||||
| chr7:135450914
|
G | A | 5 | a0002c0002t0001g0054a0002c0002t0001g0080a0002c0002t0001g0082others(2): Show | 5 | HG02129.hp1 NA18946.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.-92-12491C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135450914 | ||||||
| chr7:135451033
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-92-12610G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451033 | ||||||
| chr7:135451063
|
T | C | 1 | a0001c0001t0001g0331 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-92-12640A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451063 | ||||||
| chr7:135451085
|
A | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-12662T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451085 | ||||||
| chr7:135451175
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-12752C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451175 | ||||||
| chr7:135451238
|
C | G | 1 | a0001c0001t0001g0159 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-92-12815G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451238 | ||||||
| chr7:135451392
|
C | G | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-92-12969G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451392 | ||||||
| chr7:135451750
|
C | T | 17 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(14): Show | 17 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-92-13327G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451750 | ||||||
| chr7:135451767
|
G | C | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-92-13344C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451767 | ||||||
| chr7:135451814
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-13391C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451814 | ||||||
| chr7:135451890
|
T | C | 1 | a0002c0002t0001g0098 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-92-13467A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451890 | ||||||
| chr7:135451975
|
T | C | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-13552A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135451975 | ||||||
| chr7:135452065
|
T | A | 1 | a0001c0001t0002g0294 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-92-13642A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452065 | ||||||
| chr7:135452132
|
C | T | 64 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(61): Show | 64 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.-92-13709G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452132 | ||||||
| chr7:135452241
|
A | C | 1 | a0001c0001t0001g0331 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-92-13818T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452241 | ||||||
| chr7:135452280
|
T | TAAGAAAA others(314): Show |
1 | a0001c0001t0001g0141 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-92-13858_-92-1385 others(325): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452280 | ||||||
| chr7:135452280
|
T | TAAGAAAA others(314): Show |
12 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0003g0351others(9): Show | 12 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(9): Show |
intron_variant | MODIFIER | c.-92-13858_-92-1385 others(325): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452280 | ||||||
| chr7:135452280
|
T | TAAGAAAA others(315): Show |
1 | a0001c0001t0003g0352 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-92-13858_-92-1385 others(326): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452280 | ||||||
| chr7:135452448
|
T | A | 1 | a0002c0002t0006g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-92-14025A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452448 | ||||||
| chr7:135452616
|
G | A | 1 | a0002c0002t0001g0073 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-92-14193C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452616 | ||||||
| chr7:135452805
|
T | C | 1 | a0002c0002t0001g0029 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-92-14382A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452805 | ||||||
| chr7:135452879
|
T | C | 1 | a0001c0001t0002g0296 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-92-14456A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452879 | ||||||
| chr7:135452954
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-92-14531A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452954 | ||||||
| chr7:135452981
|
C | T | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-14558G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452981 | ||||||
| chr7:135452983
|
T | C | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-14560A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452983 | ||||||
| chr7:135452987
|
T | C | 1 | a0002c0002t0001g0067 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-92-14564A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135452987 | ||||||
| chr7:135453045
|
G | A | 2 | a0001c0001t0001g0336a0001c0001t0001g0337 | 2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-92-14622C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453045 | ||||||
| chr7:135453173
|
T | A | 1 | a0001c0001t0001g0313 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-92-14750A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453173 | ||||||
| chr7:135453583
|
G | A | 127 | a0001c0001t0001g0118a0001c0001t0001g0324a0001c0001t0002g0116others(124): Show | 127 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.-92-15160C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453583 | ||||||
| chr7:135453623
|
G | T | 1 | a0002c0002t0001g0066 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-92-15200C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453623 | ||||||
| chr7:135453767
|
CAT | C | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-92-15346_-92-1534 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453767 | ||||||
| chr7:135453801
|
AATAT | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-92-15382_-92-1537 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453801 | ||||||
| chr7:135453809
|
TAA | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-15388_-92-1538 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453809 | ||||||
| chr7:135453814
|
A | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-15391T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453814 | ||||||
| chr7:135453824
|
T | TTATATAT others(5): Show |
1 | a0001c0001t0001g0342 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-92-15402_-92-1540 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453824 | ||||||
| chr7:135453826
|
T | A | 1 | a0001c0001t0001g0342 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-92-15403A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | ||||||
| chr7:135453826
|
T | TTA | 38 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0160others(35): Show | 38 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.-92-15405_-92-1540 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | ||||||
| chr7:135453826
|
T | TTATATAT others(3): Show |
29 | a0001c0001t0001g0145a0001c0001t0001g0330a0001c0001t0001g0331others(26): Show | 29 | HG00438.hp1 HG00621.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.-92-15413_-92-1540 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | ||||||
| chr7:135453826
|
T | TTATATAT others(5): Show |
41 | a0001c0001t0001g0335a0001c0001t0001g0338a0001c0001t0001g0339others(38): Show | 41 | HG00597.hp1 HG00609.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.-92-15415_-92-1540 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | ||||||
| chr7:135453826
|
T | TTATATAT others(7): Show |
16 | a0001c0001t0001g0329a0001c0001t0001g0336a0001c0001t0001g0337others(13): Show | 16 | HG00642.hp1 HG00735.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.-92-15417_-92-1540 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | ||||||
| chr7:135453826
|
T | TTATATAT others(9): Show |
12 | a0001c0001t0001g0343a0001c0001t0001g0344a0001c0001t0001g0345others(9): Show | 12 | HG01256.hp1 HG01258.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.-92-15419_-92-1540 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | ||||||
| chr7:135453826
|
T | TTATATAT others(11): Show |
2 | a0002c0002t0001g0055a0002c0002t0001g0082 | 2 | NA18946.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.-92-15421_-92-1540 others(22): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | ||||||
| chr7:135453826
|
T | TTATATAT others(13): Show |
1 | a0002c0002t0001g0080 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-92-15423_-92-1540 others(24): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | ||||||
| chr7:135453826
|
T | TTATATAT others(15): Show |
2 | a0004c0005t0001g0127a0004c0005t0001g0128 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-92-15404_-92-1540 others(26): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | ||||||
| chr7:135453826
|
T | TTATATAT others(17): Show |
1 | a0004c0005t0001g0126 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-92-15404_-92-1540 others(28): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | ||||||
| chr7:135453826
|
TTA | T | 70 | a0001c0001t0001g0204a0001c0001t0001g0228a0001c0001t0001g0229others(67): Show | 70 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-92-15405_-92-1540 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | ||||||
| chr7:135453826
|
TTATATA | T | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-15409_-92-1540 others(10): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453826 | ||||||
| chr7:135453847
|
T | TATATATA others(3): Show |
1 | a0002c0002t0001g0108 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-92-15425_-92-1542 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453847 | ||||||
| chr7:135453847
|
T | TATATATA others(4): Show |
1 | a0002c0002t0001g0041 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-92-15425_-92-1542 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453847 | ||||||
| chr7:135453847
|
T | TATATATA others(5): Show |
8 | a0002c0002t0001g0031a0002c0002t0001g0072a0002c0002t0001g0073others(5): Show | 8 | NA18947.hp2 NA18948.hp1 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.-92-15425_-92-1542 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453847 | ||||||
| chr7:135453847
|
T | TATATATA others(7): Show |
2 | a0002c0002t0001g0028a0002c0002t0001g0032 | 2 | NA19007.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.-92-15425_-92-1542 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453847 | ||||||
| chr7:135453847
|
T | TATATATA others(9): Show |
3 | a0002c0002t0001g0025a0002c0002t0001g0026a0002c0002t0001g0027 | 3 | NA18986.hp2 NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-92-15425_-92-1542 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453847 | ||||||
| chr7:135453848
|
T | A | 125 | a0001c0001t0001g0118a0001c0001t0002g0116a0001c0001t0002g0117others(122): Show | 125 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.-92-15425A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453848 | ||||||
| chr7:135453955
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-92-15532A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453955 | ||||||
| chr7:135453987
|
T | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-92-15564A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453987 | ||||||
| chr7:135453989
|
C | CAT | 17 | a0001c0001t0001g0266a0001c0001t0001g0329a0001c0001t0001g0331others(14): Show | 17 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-92-15568_-92-1556 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453989 | ||||||
| chr7:135453989
|
C | CATAT | 3 | a0001c0001t0001g0330a0001c0001t0001g0348a0001c0010t0002g0326 | 3 | HG01261.hp1 HG02572.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-92-15570_-92-1556 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453989 | ||||||
| chr7:135453989
|
C | CATATAT | 15 | a0001c0001t0002g0116a0001c0001t0002g0121a0001c0001t0002g0123others(12): Show | 15 | HG00099.hp1 HG00323.hp1 HG01081.hp2 others(12): Show |
intron_variant | MODIFIER | c.-92-15572_-92-1556 others(10): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453989 | ||||||
| chr7:135453989
|
C | CATATATA others(1): Show |
4 | a0001c0001t0002g0117a0001c0001t0002g0120a0001c0001t0002g0122others(1): Show | 4 | HG00280.hp1 HG01361.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-15574_-92-1556 others(12): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453989 | ||||||
| chr7:135453989
|
CAT | C | 21 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0243others(18): Show | 21 | HG02083.hp2 HG02258.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.-92-15568_-92-1556 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135453989 | ||||||
| chr7:135454115
|
A | G | 5 | a0001c0001t0001g0155a0001c0001t0001g0160a0001c0001t0001g0161others(2): Show | 5 | HG00642.hp2 HG01074.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-92-15692T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135454115 | ||||||
| chr7:135454263
|
C | T | 248 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(245): Show | 248 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(245): Show |
intron_variant | MODIFIER | c.-92-15840G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135454263 | ||||||
| chr7:135454385
|
A | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-15962T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135454385 | ||||||
| chr7:135454514
|
A | AT | 4 | a0001c0001t0001g0272a0001c0001t0001g0282a0001c0001t0001g0284others(1): Show | 4 | HG02071.hp2 NA18612.hp2 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-16092dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135454514 | ||||||
| chr7:135454516
|
T | TA | 243 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(240): Show | 243 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.-92-16094dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135454516 | ||||||
| chr7:135454611
|
T | C | 1 | a0001c0001t0001g0208 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-92-16188A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135454611 | ||||||
| chr7:135454662
|
GTAAA | G | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-16243_-92-1624 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135454662 | ||||||
| chr7:135454684
|
G | A | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | HG02818.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-92-16261C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135454684 | ||||||
| chr7:135454976
|
T | C | 3 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137 | 3 | HG02486.hp1 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-92-16553A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135454976 | ||||||
| chr7:135455081
|
C | T | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-92-16658G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135455081 | ||||||
| chr7:135455215
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-92-16792T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135455215 | ||||||
| chr7:135455298
|
C | T | 1 | a0002c0002t0001g0063 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-92-16875G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135455298 | ||||||
| chr7:135455299
|
G | A | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-92-16876C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135455299 | ||||||
| chr7:135455485
|
T | C | 1 | a0001c0003t0002g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-92-17062A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135455485 | ||||||
| chr7:135455663
|
C | T | 5 | a0001c0001t0001g0235a0001c0001t0001g0245a0001c0001t0001g0248others(2): Show | 5 | NA18946.hp2 NA18962.hp2 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-17240G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135455663 | ||||||
| chr7:135455721
|
A | G | 1 | a0002c0002t0001g0045 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-92-17298T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135455721 | ||||||
| chr7:135455751
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-17328C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135455751 | ||||||
| chr7:135456200
|
T | G | 2 | a0001c0001t0001g0319a0001c0001t0001g0320 | 2 | HG01361.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.-92-17777A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135456200 | ||||||
| chr7:135456263
|
TCTACCAT others(3023): Show |
T | 2 | a0001c0001t0001g0251a0001c0001t0001g0319 | 2 | HG01361.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.-92-20870_-92-1784 others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135456263 | ||||||
| chr7:135456321
|
T | C | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-17898A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135456321 | ||||||
| chr7:135456372
|
C | T | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-17949G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135456372 | ||||||
| chr7:135456607
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-18184A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135456607 | ||||||
| chr7:135456816
|
A | C | 1 | a0003c0004t0001g0215 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-92-18393T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135456816 | ||||||
| chr7:135456868
|
G | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-18445C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135456868 | ||||||
| chr7:135457003
|
C | T | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-18580G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457003 | ||||||
| chr7:135457018
|
C | A | 1 | a0002c0002t0001g0301 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-92-18595G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457018 | ||||||
| chr7:135457372
|
T | C | 225 | a0001c0001t0001g0118a0001c0001t0001g0145a0001c0001t0001g0146others(222): Show | 225 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.-92-18949A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457372 | ||||||
| chr7:135457424
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-92-19001T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457424 | ||||||
| chr7:135457513
|
T | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-19090A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457513 | ||||||
| chr7:135457537
|
T | C | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-19114A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457537 | ||||||
| chr7:135457595
|
T | C | 61 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(58): Show | 61 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.-92-19172A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457595 | ||||||
| chr7:135457612
|
G | A | 1 | a0002c0002t0001g0093 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-92-19189C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457612 | ||||||
| chr7:135457654
|
T | C | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-19231A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457654 | ||||||
| chr7:135457711
|
C | T | 263 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(260): Show | 263 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.-92-19288G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457711 | ||||||
| chr7:135457779
|
A | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-19356T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457779 | ||||||
| chr7:135457980
|
T | C | 2 | a0001c0001t0001g0155a0001c0001t0001g0166 | 2 | HG00642.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.-92-19557A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135457980 | ||||||
| chr7:135458018
|
C | T | 4 | a0002c0002t0001g0108a0002c0002t0001g0109a0002c0002t0001g0110others(1): Show | 4 | HG00438.hp1 NA18956.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-19595G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135458018 | ||||||
| chr7:135458151
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-92-19728A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135458151 | ||||||
| chr7:135458235
|
T | C | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(3): Show | 6 | HG01123.hp2 NA18968.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-19812A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135458235 | ||||||
| chr7:135458391
|
T | C | 33 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0235others(30): Show | 33 | HG00438.hp2 HG00609.hp1 HG01934.hp2 others(30): Show |
intron_variant | MODIFIER | c.-92-19968A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135458391 | ||||||
| chr7:135458540
|
G | A | 3 | a0004c0005t0001g0126a0004c0005t0001g0127a0004c0005t0001g0128 | 3 | HG01106.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.-92-20117C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135458540 | ||||||
| chr7:135458546
|
C | T | 1 | a0001c0001t0001g0193 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-92-20123G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135458546 | ||||||
| chr7:135458673
|
T | C | 3 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0049 | 3 | HG03491.hp1 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-92-20250A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135458673 | ||||||
| chr7:135458762
|
T | C | 1 | a0001c0001t0008g0350 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-92-20339A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135458762 | ||||||
| chr7:135458921
|
C | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-20498G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135458921 | ||||||
| chr7:135459103
|
A | C | 1 | a0001c0001t0007g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-92-20680T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135459103 | ||||||
| chr7:135459223
|
G | A | 263 | a0001c0001t0001g0006a0001c0001t0001g0118a0001c0001t0001g0141others(260): Show | 263 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.-92-20800C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135459223 | ||||||
| chr7:135459270
|
CAGAT | C | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-20851_-92-2084 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135459270 | ||||||
| chr7:135459680
|
T | C | 2 | a0001c0001t0002g0116a0001c0001t0002g0117 | 2 | HG01081.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-92-21257A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135459680 | ||||||
| chr7:135459766
|
G | A | 5 | a0001c0003t0002g0179a0001c0003t0002g0181a0001c0003t0002g0182others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-21343C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135459766 | ||||||
| chr7:135459799
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0166 | 2 | HG00642.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.-92-21376C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135459799 | ||||||
| chr7:135459886
|
C | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-21463G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135459886 | ||||||
| chr7:135459914
|
T | C | 266 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(263): Show | 266 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.-92-21491A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135459914 | ||||||
| chr7:135460067
|
A | G | 1 | a0001c0001t0005g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-92-21644T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460067 | ||||||
| chr7:135460093
|
G | T | 2 | a0001c0001t0001g0324a0002c0002t0006g0002 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-92-21670C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460093 | ||||||
| chr7:135460208
|
C | T | 1 | a0002c0002t0001g0070 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-92-21785G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460208 | ||||||
| chr7:135460209
|
G | A | 1 | a0001c0001t0002g0130 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-92-21786C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460209 | ||||||
| chr7:135460437
|
A | C | 17 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(14): Show | 17 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-92-22014T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460437 | ||||||
| chr7:135460590
|
A | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-22167T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460590 | ||||||
| chr7:135460633
|
A | G | 1 | a0002c0002t0006g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-92-22210T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460633 | ||||||
| chr7:135460636
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-92-22213A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460636 | ||||||
| chr7:135460789
|
T | C | 1 | a0001c0001t0003g0360 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-92-22366A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460789 | ||||||
| chr7:135460825
|
T | C | 6 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0001t0001g0168others(3): Show | 6 | NA18944.hp2 NA18967.hp1 NA19006.hp2 others(3): Show |
intron_variant | MODIFIER | c.-92-22402A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460825 | ||||||
| chr7:135460828
|
C | G | 7 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(4): Show | 7 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(4): Show |
intron_variant | MODIFIER | c.-92-22405G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135460828 | ||||||
| chr7:135461006
|
G | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-92-22583C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135461006 | ||||||
| chr7:135461007
|
C | G | 1 | a0001c0001t0001g0318 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-92-22584G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135461007 | ||||||
| chr7:135461176
|
C | T | 17 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(14): Show | 17 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-92-22753G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135461176 | ||||||
| chr7:135461182
|
T | C | 1 | a0002c0002t0001g0051 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-92-22759A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135461182 | ||||||
| chr7:135461555
|
G | C | 5 | a0001c0003t0002g0179a0001c0003t0002g0181a0001c0003t0002g0182others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-23132C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135461555 | ||||||
| chr7:135461849
|
T | A | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-92-23426A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135461849 | ||||||
| chr7:135462006
|
T | G | 1 | a0001c0008t0001g0325 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-92-23583A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462006 | ||||||
| chr7:135462064
|
T | TA | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-23642dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462064 | ||||||
| chr7:135462114
|
T | TG | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-23692dupC | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462114 | ||||||
| chr7:135462145
|
A | G | 1 | a0002c0002t0001g0035 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-92-23722T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462145 | ||||||
| chr7:135462362
|
C | T | 1 | a0002c0011t0001g0044 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-92-23939G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462362 | ||||||
| chr7:135462365
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-92-23942C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462365 | ||||||
| chr7:135462465
|
A | C | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-24042T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462465 | ||||||
| chr7:135462478
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-92-24055C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462478 | ||||||
| chr7:135462515
|
C | T | 2 | a0002c0002t0001g0050a0002c0002t0001g0060 | 2 | HG01358.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-92-24092G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462515 | ||||||
| chr7:135462517
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-92-24094G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462517 | ||||||
| chr7:135462545
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-92-24122C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462545 | ||||||
| chr7:135462677
|
A | C | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-24254T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462677 | ||||||
| chr7:135462766
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-92-24343T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462766 | ||||||
| chr7:135462796
|
A | G | 1 | a0001c0001t0001g0348 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-92-24373T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462796 | ||||||
| chr7:135462874
|
T | C | 13 | a0002c0002t0001g0025a0002c0002t0001g0026a0002c0002t0001g0027others(10): Show | 13 | NA18947.hp2 NA18948.hp1 NA18951.hp1 others(10): Show |
intron_variant | MODIFIER | c.-92-24451A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135462874 | ||||||
| chr7:135463009
|
G | A | 3 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140 | 3 | HG02572.hp2 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-92-24586C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463009 | ||||||
| chr7:135463144
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-24721A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463144 | ||||||
| chr7:135463266
|
G | T | 1 | a0002c0002t0001g0304 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-92-24843C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463266 | ||||||
| chr7:135463304
|
G | A | 1 | a0002c0002t0001g0035 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-92-24881C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463304 | ||||||
| chr7:135463309
|
G | A | 16 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(13): Show | 16 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-92-24886C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463309 | ||||||
| chr7:135463438
|
T | C | 9 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0313others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-92-25015A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463438 | ||||||
| chr7:135463498
|
A | AT | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.-92-25076dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463498 | ||||||
| chr7:135463544
|
C | CA | 17 | a0001c0001t0001g0144a0001c0001t0001g0155a0001c0001t0001g0170others(14): Show | 17 | HG00438.hp1 HG00642.hp2 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.-92-25122dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463544 | ||||||
| chr7:135463544
|
CA | C | 149 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0146others(146): Show | 149 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.-92-25122delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463544 | ||||||
| chr7:135463575
|
C | CA | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.-92-25153dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463575 | ||||||
| chr7:135463594
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-25171C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463594 | ||||||
| chr7:135463622
|
G | A | 63 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(60): Show | 63 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-92-25199C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463622 | ||||||
| chr7:135463664
|
A | C | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | NA18948.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.-92-25241T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135463664 | ||||||
| chr7:135464024
|
C | CAAAA | 25 | a0001c0001t0001g0146a0001c0001t0001g0251a0001c0001t0001g0264others(22): Show | 25 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.-92-25605_-92-2560 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464024 | ||||||
| chr7:135464024
|
C | CAAAAA | 91 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(88): Show | 91 | HG00280.hp2 HG00438.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.-92-25606_-92-2560 others(9): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464024 | ||||||
| chr7:135464024
|
C | CAAAAAA | 123 | a0001c0001t0001g0239a0001c0001t0001g0260a0001c0001t0001g0306others(120): Show | 123 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(120): Show |
intron_variant | MODIFIER | c.-92-25607_-92-2560 others(10): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464024 | ||||||
| chr7:135464024
|
C | CAAAAAAA | 10 | a0001c0001t0001g0147a0001c0001t0001g0297a0001c0001t0001g0298others(7): Show | 10 | HG01099.hp2 HG02602.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-92-25608_-92-2560 others(11): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464024 | ||||||
| chr7:135464024
|
C | CAAAAAAA others(1): Show |
15 | a0001c0001t0001g0299a0001c0001t0001g0329a0001c0001t0001g0330others(12): Show | 15 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.-92-25609_-92-2560 others(12): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464024 | ||||||
| chr7:135464024
|
CA | C | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(3): Show | 6 | HG01123.hp2 NA18968.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-25602delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464024 | ||||||
| chr7:135464047
|
G | A | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-92-25624C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464047 | ||||||
| chr7:135464121
|
GCAGTATG others(9): Show |
G | 1 | a0001c0001t0001g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-92-25714_-92-2569 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464121 | ||||||
| chr7:135464465
|
T | C | 10 | a0002c0002t0001g0045a0002c0002t0001g0088a0002c0002t0001g0089others(7): Show | 10 | HG00673.hp1 NA18747.hp1 NA18969.hp1 others(7): Show |
intron_variant | MODIFIER | c.-92-26042A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464465 | ||||||
| chr7:135464482
|
A | G | 2 | a0001c0001t0001g0324a0002c0002t0006g0002 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-92-26059T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464482 | ||||||
| chr7:135464596
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-26173G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464596 | ||||||
| chr7:135464635
|
A | T | 1 | a0001c0001t0002g0122 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-92-26212T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464635 | ||||||
| chr7:135464696
|
T | C | 1 | a0002c0002t0001g0071 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-92-26273A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464696 | ||||||
| chr7:135464764
|
A | T | 1 | a0001c0001t0005g0001 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-92-26341T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464764 | ||||||
| chr7:135464816
|
A | G | 1 | a0001c0001t0001g0308 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-92-26393T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135464816 | ||||||
| chr7:135465010
|
C | T | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-92-26587G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135465010 | ||||||
| chr7:135465192
|
G | T | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-92-26769C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135465192 | ||||||
| chr7:135465714
|
CAT | C | 6 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0001t0001g0168others(3): Show | 6 | NA18944.hp2 NA18967.hp1 NA19006.hp2 others(3): Show |
intron_variant | MODIFIER | c.-92-27293_-92-2729 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135465714 | ||||||
| chr7:135465731
|
C | CA | 27 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(24): Show | 27 | HG00099.hp2 HG00621.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.-92-27309dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135465731 | ||||||
| chr7:135465875
|
C | G | 1 | a0001c0001t0001g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-92-27452G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135465875 | ||||||
| chr7:135466036
|
G | A | 1 | a0001c0001t0001g0332 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-92-27613C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135466036 | ||||||
| chr7:135466111
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-27688C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135466111 | ||||||
| chr7:135466118
|
T | TTG | 265 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(262): Show | 265 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.-92-27697_-92-2769 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135466118 | ||||||
| chr7:135466125
|
T | C | 1 | a0002c0002t0006g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-92-27702A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135466125 | ||||||
| chr7:135466391
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-27968G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135466391 | ||||||
| chr7:135466455
|
G | A | 1 | a0002c0002t0001g0082 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-92-28032C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135466455 | ||||||
| chr7:135466475
|
C | CA | 17 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0216others(14): Show | 17 | HG01891.hp2 HG02145.hp2 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.-92-28053dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135466475 | ||||||
| chr7:135466475
|
CA | C | 17 | a0001c0001t0001g0008a0001c0001t0001g0158a0001c0001t0001g0235others(14): Show | 17 | HG01169.hp2 HG01256.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.-92-28053delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135466475 | ||||||
| chr7:135466834
|
A | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-28411T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135466834 | ||||||
| chr7:135467134
|
A | G | 3 | a0001c0001t0003g0354a0001c0001t0003g0355a0001c0001t0003g0356 | 3 | HG02083.hp2 NA19080.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-92-28711T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135467134 | ||||||
| chr7:135467298
|
C | T | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-92-28875G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135467298 | ||||||
| chr7:135467523
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-92-29100G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135467523 | ||||||
| chr7:135467949
|
C | G | 1 | a0003c0004t0001g0215 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-92-29526G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135467949 | ||||||
| chr7:135467998
|
G | A | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-92-29575C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135467998 | ||||||
| chr7:135468035
|
G | A | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-29612C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468035 | ||||||
| chr7:135468138
|
C | G | 17 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(14): Show | 17 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-92-29715G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468138 | ||||||
| chr7:135468202
|
C | T | 2 | a0001c0001t0001g0348a0001c0003t0002g0179 | 2 | HG02280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-92-29779G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468202 | ||||||
| chr7:135468209
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-92-29786G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468209 | ||||||
| chr7:135468239
|
T | A | 1 | a0001c0001t0001g0324 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-92-29816A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468239 | ||||||
| chr7:135468338
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-92-29915T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468338 | ||||||
| chr7:135468367
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-92-29944A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468367 | ||||||
| chr7:135468443
|
G | A | 106 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(103): Show | 106 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(103): Show |
intron_variant | MODIFIER | c.-92-30020C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468443 | ||||||
| chr7:135468502
|
A | G | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-30079T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468502 | ||||||
| chr7:135468684
|
C | CA | 201 | a0001c0001t0001g0118a0001c0001t0001g0145a0001c0001t0001g0146others(198): Show | 201 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.-92-30262dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468684 | ||||||
| chr7:135468684
|
C | CAA | 35 | a0001c0001t0001g0239a0001c0001t0001g0286a0001c0001t0001g0297others(32): Show | 35 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.-92-30263_-92-3026 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468684 | ||||||
| chr7:135468684
|
CA | C | 7 | a0001c0001t0001g0004a0001c0001t0001g0151a0001c0001t0001g0154others(4): Show | 7 | HG01069.hp1 HG01934.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-92-30262delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135468684 | ||||||
| chr7:135469021
|
G | A | 63 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(60): Show | 63 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-92-30598C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469021 | ||||||
| chr7:135469079
|
G | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-30656C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469079 | ||||||
| chr7:135469102
|
T | A | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-30679A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469102 | ||||||
| chr7:135469158
|
C | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-30735G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469158 | ||||||
| chr7:135469168
|
T | C | 21 | a0001c0001t0001g0011a0001c0001t0001g0141a0001c0001t0001g0306others(18): Show | 21 | HG00597.hp2 HG01981.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.-92-30745A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469168 | ||||||
| chr7:135469194
|
A | G | 3 | a0002c0002t0001g0185a0002c0002t0001g0186a0002c0002t0001g0187 | 3 | NA18975.hp1 NA19084.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-92-30771T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469194 | ||||||
| chr7:135469767
|
A | G | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-31344T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469767 | ||||||
| chr7:135469818
|
TTTTG | T | 19 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(16): Show | 19 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-92-31399_-92-3139 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469818 | ||||||
| chr7:135469882
|
C | A | 5 | a0001c0003t0002g0179a0001c0003t0002g0181a0001c0003t0002g0182others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-31459G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469882 | ||||||
| chr7:135469882
|
C | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-31459G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469882 | ||||||
| chr7:135469934
|
G | C | 1 | a0001c0001t0001g0012 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-92-31511C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469934 | ||||||
| chr7:135469947
|
G | A | 5 | a0001c0001t0001g0331a0001c0001t0001g0332a0001c0001t0001g0333others(2): Show | 5 | HG00733.hp2 HG00735.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.-92-31524C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469947 | ||||||
| chr7:135469977
|
A | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-92-31554T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135469977 | ||||||
| chr7:135470100
|
G | C | 1 | a0001c0001t0001g0280 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-92-31677C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470100 | ||||||
| chr7:135470116
|
C | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-92-31693G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470116 | ||||||
| chr7:135470139
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-92-31716C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470139 | ||||||
| chr7:135470272
|
G | A | 1 | a0001c0001t0001g0276 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-92-31849C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470272 | ||||||
| chr7:135470295
|
T | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-31872A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470295 | ||||||
| chr7:135470332
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-92-31909C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470332 | ||||||
| chr7:135470398
|
T | TG | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-31976dupC | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470398 | ||||||
| chr7:135470456
|
T | C | 3 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0165 | 3 | HG01943.hp2 HG03490.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-92-32033A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470456 | ||||||
| chr7:135470547
|
G | A | 3 | a0002c0002t0001g0047a0002c0002t0001g0048a0002c0002t0001g0049 | 3 | HG03491.hp1 HG03492.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.-92-32124C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470547 | ||||||
| chr7:135470571
|
TA | T | 269 | a0001c0001t0001g0008a0001c0001t0001g0118a0001c0001t0001g0141others(266): Show | 269 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.-92-32149delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470571 | ||||||
| chr7:135470618
|
T | C | 38 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(35): Show | 38 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.-92-32195A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470618 | ||||||
| chr7:135470619
|
G | A | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-32196C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470619 | ||||||
| chr7:135470706
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-92-32283C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470706 | ||||||
| chr7:135470767
|
A | G | 16 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(13): Show | 16 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-92-32344T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470767 | ||||||
| chr7:135470839
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-92-32416C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135470839 | ||||||
| chr7:135471003
|
C | G | 1 | a0001c0001t0001g0318 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-92-32580G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135471003 | ||||||
| chr7:135471034
|
C | T | 2 | a0001c0001t0001g0227a0001c0001t0001g0320 | 2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-92-32611G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135471034 | ||||||
| chr7:135471250
|
C | A | 1 | a0001c0001t0001g0305 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-92-32827G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135471250 | ||||||
| chr7:135471325
|
G | A | 1 | a0001c0001t0001g0324 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-92-32902C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135471325 | ||||||
| chr7:135471381
|
C | A | 124 | a0001c0001t0001g0118a0001c0001t0002g0116a0001c0001t0002g0117others(121): Show | 124 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-92-32958G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135471381 | ||||||
| chr7:135471488
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-92-33065A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135471488 | ||||||
| chr7:135471576
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-92-33153A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135471576 | ||||||
| chr7:135471754
|
G | T | 1 | a0001c0010t0002g0326 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-92-33331C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135471754 | ||||||
| chr7:135471788
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-33365G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135471788 | ||||||
| chr7:135472044
|
G | C | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-33621C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472044 | ||||||
| chr7:135472116
|
T | C | 1 | a0001c0001t0001g0331 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-92-33693A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472116 | ||||||
| chr7:135472246
|
G | C | 1 | a0002c0002t0001g0060 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-92-33823C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472246 | ||||||
| chr7:135472257
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0016 | 3 | NA18954.hp2 NA19075.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.-92-33834G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472257 | ||||||
| chr7:135472338
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-33915C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472338 | ||||||
| chr7:135472375
|
G | T | 1 | a0002c0002t0006g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-92-33952C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472375 | ||||||
| chr7:135472409
|
G | A | 1 | a0001c0001t0001g0318 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-92-33986C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472409 | ||||||
| chr7:135472420
|
C | T | 266 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(263): Show | 266 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.-92-33997G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472420 | ||||||
| chr7:135472453
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-92-34030C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472453 | ||||||
| chr7:135472456
|
G | A | 2 | a0001c0001t0001g0227a0001c0001t0001g0320 | 2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-92-34033C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472456 | ||||||
| chr7:135472476
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0014 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-92-34063_-92-3405 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472476 | ||||||
| chr7:135472476
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0206 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-92-34065_-92-3405 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472476 | ||||||
| chr7:135472476
|
CAAAA | C | 6 | a0001c0001t0005g0001a0002c0002t0001g0033a0002c0002t0001g0054others(3): Show | 6 | HG01934.hp1 HG02004.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-34057_-92-3405 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472476 | ||||||
| chr7:135472476
|
CAAAAA | C | 7 | a0002c0002t0001g0052a0002c0002t0001g0065a0002c0002t0001g0068others(4): Show | 7 | HG01257.hp2 HG01258.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.-92-34058_-92-3405 others(9): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472476 | ||||||
| chr7:135472476
|
CAAAAAAA | C | 7 | a0001c0001t0001g0313a0001c0001t0002g0189a0001c0001t0002g0190others(4): Show | 7 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(4): Show |
intron_variant | MODIFIER | c.-92-34060_-92-3405 others(11): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472476 | ||||||
| chr7:135472476
|
CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0001g0115a0002c0002t0001g0025a0002c0002t0001g0026others(1): Show | 4 | HG00621.hp2 NA18986.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-34063_-92-3405 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472476 | ||||||
| chr7:135472476
|
CAAAAAAA others(11): Show |
C | 1 | a0001c0001t0001g0004 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-92-34071_-92-3405 others(22): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472476 | ||||||
| chr7:135472476
|
CAAAAAAA others(12): Show |
C | 1 | a0002c0002t0001g0096 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-92-34072_-92-3405 others(23): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472476 | ||||||
| chr7:135472498
|
AAAAAAAA others(17): Show |
A | 1 | a0001c0001t0003g0357 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-92-34099_-92-3407 others(28): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472498 | ||||||
| chr7:135472501
|
AAAAAAAA others(36): Show |
A | 1 | a0001c0008t0001g0325 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-92-34121_-92-3407 others(47): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472501 | ||||||
| chr7:135472502
|
AAAAAAAA others(17): Show |
A | 1 | a0001c0001t0001g0141 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-92-34103_-92-3408 others(28): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472502 | ||||||
| chr7:135472502
|
AAAAAAAA others(29): Show |
A | 1 | a0001c0003t0002g0183 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-92-34115_-92-3408 others(40): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472502 | ||||||
| chr7:135472503
|
AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0001g0316 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-92-34093_-92-3408 others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472503 | ||||||
| chr7:135472503
|
AAAAAAAA others(14): Show |
A | 1 | a0001c0001t0003g0353 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-92-34101_-92-3408 others(25): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472503 | ||||||
| chr7:135472503
|
AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0001g0200 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-92-34103_-92-3408 others(27): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472503 | ||||||
| chr7:135472503
|
AAAAAAAA others(22): Show |
A | 1 | a0001c0001t0001g0279 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-92-34109_-92-3408 others(33): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472503 | ||||||
| chr7:135472503
|
AAAAAAAA others(26): Show |
A | 1 | a0001c0001t0001g0285 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-92-34113_-92-3408 others(37): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472503 | ||||||
| chr7:135472503
|
AAAAAAAA others(30): Show |
A | 1 | a0001c0003t0002g0182 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-92-34117_-92-3408 others(41): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472503 | ||||||
| chr7:135472504
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0317 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-92-34095_-92-3408 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472504 | ||||||
| chr7:135472504
|
AAAAAAAA others(9): Show |
A | 3 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133 | 3 | HG02896.hp1 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-92-34097_-92-3408 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472504 | ||||||
| chr7:135472504
|
AAAAAAAA others(11): Show |
A | 1 | a0002c0002t0006g0002 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-92-34099_-92-3408 others(22): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472504 | ||||||
| chr7:135472504
|
AAAAAAAA others(13): Show |
A | 1 | a0001c0001t0003g0359 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-92-34101_-92-3408 others(24): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472504 | ||||||
| chr7:135472504
|
AAAAAAAA others(23): Show |
A | 1 | a0001c0001t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-92-34111_-92-3408 others(34): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472504 | ||||||
| chr7:135472504
|
AAAAAAAA others(25): Show |
A | 4 | a0001c0001t0001g0260a0001c0001t0001g0272a0001c0001t0001g0282others(1): Show | 4 | NA18612.hp2 NA18940.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-34113_-92-3408 others(36): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472504 | ||||||
| chr7:135472504
|
AAAAAAAA others(27): Show |
A | 1 | a0001c0003t0002g0179 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-92-34115_-92-3408 others(38): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472504 | ||||||
| chr7:135472504
|
AAAAAAAA others(29): Show |
A | 4 | a0001c0001t0001g0118a0001c0001t0001g0342a0001c0003t0002g0181others(1): Show | 4 | HG01255.hp2 HG02523.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-92-34117_-92-3408 others(40): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472504 | ||||||
| chr7:135472505
|
AAAAAAAA others(6): Show |
A | 3 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0333 | 3 | HG00741.hp2 HG01123.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-92-34095_-92-3408 others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472505 | ||||||
| chr7:135472505
|
AAAAAAAA others(10): Show |
A | 2 | a0001c0001t0001g0332a0001c0001t0001g0335 | 2 | HG00735.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.-92-34099_-92-3408 others(21): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472505 | ||||||
| chr7:135472505
|
AAAAAAAA others(18): Show |
A | 1 | a0001c0001t0001g0324 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-92-34107_-92-3408 others(29): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472505 | ||||||
| chr7:135472505
|
AAAAAAAA others(20): Show |
A | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | HG02622.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.-92-34109_-92-3408 others(31): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472505 | ||||||
| chr7:135472505
|
AAAAAAAA others(22): Show |
A | 2 | a0001c0001t0001g0283a0001c0001t0001g0299 | 2 | HG02723.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-92-34111_-92-3408 others(33): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472505 | ||||||
| chr7:135472505
|
AAAAAAAA others(24): Show |
A | 2 | a0001c0001t0001g0238a0001c0001t0002g0135 | 2 | HG01175.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-92-34113_-92-3408 others(35): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472505 | ||||||
| chr7:135472506
|
A | AATATATA others(5): Show |
1 | a0001c0001t0001g0155 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-92-34084_-92-3408 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472506 | ||||||
| chr7:135472506
|
A | T | 2 | a0001c0001t0001g0312a0001c0001t0001g0322 | 2 | HG01496.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-92-34083T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472506 | ||||||
| chr7:135472506
|
AAAAAAAA others(3): Show |
A | 2 | a0002c0002t0001g0062a0002c0002t0001g0100 | 2 | HG02293.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.-92-34093_-92-3408 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472506 | ||||||
| chr7:135472506
|
AAAAAAAA others(5): Show |
A | 3 | a0001c0001t0001g0328a0001c0001t0001g0337a0001c0001t0002g0122 | 3 | HG00280.hp1 HG02602.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.-92-34095_-92-3408 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472506 | ||||||
| chr7:135472506
|
AAAAAAAA others(13): Show |
A | 2 | a0001c0001t0001g0348a0001c0001t0003g0360 | 2 | HG02572.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-92-34103_-92-3408 others(24): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472506 | ||||||
| chr7:135472506
|
AAAAAAAA others(15): Show |
A | 1 | a0001c0001t0001g0202 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-92-34105_-92-3408 others(26): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472506 | ||||||
| chr7:135472506
|
AAAAAAAA others(21): Show |
A | 7 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(4): Show | 7 | NA18944.hp1 NA18992.hp1 NA18995.hp2 others(4): Show |
intron_variant | MODIFIER | c.-92-34111_-92-3408 others(32): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472506 | ||||||
| chr7:135472506
|
AAAAAAAA others(25): Show |
A | 20 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233others(17): Show | 20 | HG00280.hp2 HG01515.hp2 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.-92-34115_-92-3408 others(36): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472506 | ||||||
| chr7:135472506
|
AAAAAAAA others(29): Show |
A | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-92-34119_-92-3408 others(40): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472506 | ||||||
| chr7:135472507
|
AAAAAAAA others(4): Show |
A | 5 | a0002c0002t0001g0029a0002c0002t0001g0034a0002c0002t0001g0066others(2): Show | 5 | HG01081.hp1 HG02040.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-92-34095_-92-3408 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472507 | ||||||
| chr7:135472507
|
AAAAAAAA others(6): Show |
A | 4 | a0001c0001t0001g0343a0001c0001t0002g0121a0001c0001t0002g0123others(1): Show | 4 | HG01433.hp2 HG03654.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.-92-34097_-92-3408 others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472507 | ||||||
| chr7:135472507
|
AAAAAAAA others(10): Show |
A | 2 | a0001c0001t0001g0331a0002c0002t0001g0055 | 2 | HG01169.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-92-34101_-92-3408 others(21): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472507 | ||||||
| chr7:135472507
|
AAAAAAAA others(12): Show |
A | 1 | a0001c0001t0001g0334 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-92-34103_-92-3408 others(23): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472507 | ||||||
| chr7:135472507
|
AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0001g0308 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-92-34107_-92-3408 others(27): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472507 | ||||||
| chr7:135472507
|
AAAAAAAA others(18): Show |
A | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-92-34109_-92-3408 others(29): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472507 | ||||||
| chr7:135472507
|
AAAAAAAA others(20): Show |
A | 1 | a0001c0001t0001g0276 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-92-34111_-92-3408 others(31): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472507 | ||||||
| chr7:135472507
|
AAAAAAAA others(22): Show |
A | 1 | a0001c0001t0001g0319 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-92-34113_-92-3408 others(33): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472507 | ||||||
| chr7:135472507
|
AAAAAAAA others(24): Show |
A | 7 | a0001c0001t0001g0228a0001c0001t0001g0236a0001c0001t0001g0237others(4): Show | 7 | HG00639.hp2 HG00738.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.-92-34115_-92-3408 others(35): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472507 | ||||||
| chr7:135472508
|
A | AATATATA others(3): Show |
2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-92-34086_-92-3408 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | ||||||
| chr7:135472508
|
A | AATATATA others(9): Show |
1 | a0001c0001t0001g0152 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-92-34086_-92-3408 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | ||||||
| chr7:135472508
|
A | ATATATAT | 3 | a0001c0001t0001g0216a0001c0001t0001g0223a0002c0002t0001g0078 | 3 | HG02896.hp2 HG02897.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-92-34086_-92-3408 others(11): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | ||||||
| chr7:135472508
|
A | ATATATAT others(8): Show |
1 | a0002c0002t0001g0030 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-92-34086_-92-3408 others(19): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | ||||||
| chr7:135472508
|
A | T | 12 | a0001c0001t0001g0155a0001c0001t0001g0178a0001c0001t0001g0201others(9): Show | 12 | HG00323.hp2 HG00642.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.-92-34085T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | ||||||
| chr7:135472508
|
AAAAAAAA others(3): Show |
A | 7 | a0001c0001t0001g0160a0001c0001t0002g0120a0002c0002t0001g0064others(4): Show | 7 | HG00621.hp1 HG01361.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.-92-34095_-92-3408 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | ||||||
| chr7:135472508
|
AAAAAAAA others(5): Show |
A | 6 | a0001c0001t0001g0144a0001c0001t0001g0327a0001c0001t0001g0344others(3): Show | 6 | HG01256.hp1 HG01258.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-92-34097_-92-3408 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | ||||||
| chr7:135472508
|
AAAAAAAA others(7): Show |
A | 2 | a0001c0001t0001g0336a0001c0001t0001g0340 | 2 | HG00642.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-92-34099_-92-3408 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | ||||||
| chr7:135472508
|
AAAAAAAA others(9): Show |
A | 5 | a0001c0001t0001g0148a0001c0001t0001g0338a0001c0001t0001g0339others(2): Show | 5 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-92-34101_-92-3408 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | ||||||
| chr7:135472508
|
AAAAAAAA others(15): Show |
A | 1 | a0001c0001t0001g0309 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-92-34107_-92-3408 others(26): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | ||||||
| chr7:135472508
|
AAAAAAAA others(23): Show |
A | 2 | a0001c0001t0001g0265a0001c0001t0001g0321 | 2 | HG01891.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.-92-34115_-92-3408 others(34): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | ||||||
| chr7:135472508
|
AAAAAAAA others(25): Show |
A | 13 | a0001c0001t0001g0221a0001c0001t0001g0229a0001c0001t0001g0235others(10): Show | 13 | HG02129.hp2 HG02615.hp2 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.-92-34117_-92-3408 others(36): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | ||||||
| chr7:135472508
|
AAAAAAAA others(27): Show |
A | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-92-34119_-92-3408 others(38): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472508 | ||||||
| chr7:135472509
|
AAAAAAAT others(2): Show |
A | 7 | a0001c0001t0001g0196a0001c0001t0001g0199a0001c0001t0003g0358others(4): Show | 7 | HG00673.hp1 HG01516.hp2 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.-92-34095_-92-3408 others(13): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472509 | ||||||
| chr7:135472509
|
AAAAAAAT others(4): Show |
A | 6 | a0001c0001t0002g0117a0001c0001t0002g0130a0002c0002t0001g0067others(3): Show | 6 | HG02486.hp2 HG02723.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-34097_-92-3408 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472509 | ||||||
| chr7:135472509
|
AAAAAAAT others(6): Show |
A | 2 | a0001c0001t0002g0116a0002c0002t0001g0022 | 2 | HG01081.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.-92-34099_-92-3408 others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472509 | ||||||
| chr7:135472509
|
AAAAAAAT others(8): Show |
A | 1 | a0001c0001t0002g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-92-34101_-92-3408 others(19): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472509 | ||||||
| chr7:135472509
|
AAAAAAAT others(14): Show |
A | 1 | a0001c0001t0001g0159 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-92-34107_-92-3408 others(25): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472509 | ||||||
| chr7:135472509
|
AAAAAAAT others(16): Show |
A | 2 | a0001c0001t0001g0306a0002c0002t0001g0101 | 2 | HG01256.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-92-34109_-92-3408 others(27): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472509 | ||||||
| chr7:135472509
|
AAAAAAAT others(22): Show |
A | 2 | a0001c0001t0001g0270a0002c0002t0001g0304 | 2 | HG03942.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-92-34115_-92-3408 others(33): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472509 | ||||||
| chr7:135472509
|
AAAAAAAT others(24): Show |
A | 7 | a0001c0001t0001g0244a0001c0001t0001g0246a0001c0001t0001g0258others(4): Show | 7 | HG00438.hp2 HG02572.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.-92-34117_-92-3408 others(35): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472509 | ||||||
| chr7:135472510
|
A | ATAT | 3 | a0001c0001t0001g0205a0001c0001t0007g0225a0002c0002t0001g0105 | 3 | HG01943.hp1 NA19074.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-92-34088_-92-3408 others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | ||||||
| chr7:135472510
|
A | ATATAT | 3 | a0001c0001t0001g0176a0002c0002t0001g0077a0002c0002t0001g0112 | 3 | NA18989.hp1 NA19004.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.-92-34088_-92-3408 others(9): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | ||||||
| chr7:135472510
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0166 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-92-34088_-92-3408 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | ||||||
| chr7:135472510
|
A | ATATATAT others(6): Show |
1 | a0002c0002t0001g0072 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-92-34088_-92-3408 others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | ||||||
| chr7:135472510
|
A | ATATATAT others(10): Show |
1 | a0002c0002t0001g0082 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-92-34088_-92-3408 others(21): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | ||||||
| chr7:135472510
|
A | T | 27 | a0001c0001t0001g0115a0001c0001t0001g0152a0001c0001t0001g0155others(24): Show | 27 | HG00323.hp2 HG00621.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-92-34087T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | ||||||
| chr7:135472510
|
AAAAAATA others(3): Show |
A | 6 | a0001c0001t0001g0161a0001c0001t0002g0188a0001c0001t0002g0287others(3): Show | 6 | HG01496.hp1 HG02647.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-34097_-92-3408 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | ||||||
| chr7:135472510
|
AAAAAATA others(5): Show |
A | 1 | a0002c0002t0001g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-92-34099_-92-3408 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | ||||||
| chr7:135472510
|
AAAAAATA others(7): Show |
A | 1 | a0001c0001t0001g0330 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-92-34101_-92-3408 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | ||||||
| chr7:135472510
|
AAAAAATA others(11): Show |
A | 1 | a0001c0001t0003g0361 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-92-34105_-92-3408 others(22): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | ||||||
| chr7:135472510
|
AAAAAATA others(15): Show |
A | 1 | a0001c0001t0001g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-92-34109_-92-3408 others(26): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | ||||||
| chr7:135472510
|
AAAAAATA others(23): Show |
A | 3 | a0001c0001t0001g0230a0001c0001t0001g0242a0001c0001t0001g0247 | 3 | HG00609.hp1 HG01934.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-92-34117_-92-3408 others(34): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | ||||||
| chr7:135472510
|
AAAAAATA others(25): Show |
A | 1 | a0001c0001t0008g0350 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-92-34119_-92-3408 others(36): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | ||||||
| chr7:135472510
|
AAAAAATA others(27): Show |
A | 1 | a0001c0001t0002g0124 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-92-34121_-92-3408 others(38): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472510 | ||||||
| chr7:135472511
|
AAAAATAT others(4): Show |
A | 5 | a0001c0001t0002g0295a0002c0002t0001g0036a0002c0002t0001g0088others(2): Show | 5 | HG01167.hp1 HG01169.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-92-34099_-92-3408 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472511 | ||||||
| chr7:135472511
|
AAAAATAT others(8): Show |
A | 1 | a0001c0001t0001g0195 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-92-34103_-92-3408 others(19): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472511 | ||||||
| chr7:135472511
|
AAAAATAT others(10): Show |
A | 2 | a0002c0002t0001g0051a0003c0004t0001g0211 | 2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-92-34105_-92-3408 others(21): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472511 | ||||||
| chr7:135472512
|
A | ATATAT | 3 | a0001c0001t0001g0197a0001c0001t0001g0208a0003c0004t0001g0215 | 3 | HG01167.hp2 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-92-34090_-92-3408 others(9): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472512 | ||||||
| chr7:135472512
|
A | T | 56 | a0001c0001t0001g0115a0001c0001t0001g0152a0001c0001t0001g0155others(53): Show | 56 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.-92-34089T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472512 | ||||||
| chr7:135472512
|
AAAATATA others(3): Show |
A | 2 | a0002c0002t0001g0056a0004c0005t0001g0126 | 2 | HG01106.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-92-34099_-92-3409 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472512 | ||||||
| chr7:135472512
|
AAAATATA others(9): Show |
A | 1 | a0001c0001t0003g0351 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-92-34105_-92-3409 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472512 | ||||||
| chr7:135472512
|
AAAATATA others(25): Show |
A | 1 | a0001c0001t0001g0114 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-92-34121_-92-3409 others(36): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472512 | ||||||
| chr7:135472513
|
AAATATAT others(22): Show |
A | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-92-34119_-92-3409 others(33): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472513 | ||||||
| chr7:135472514
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0213 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(28): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | ||||||
| chr7:135472514
|
A | AAAAAAAT others(4): Show |
1 | a0001c0001t0001g0169 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | ||||||
| chr7:135472514
|
A | AAAAAATA others(3): Show |
2 | a0001c0001t0001g0005a0001c0001t0001g0174 | 2 | NA18945.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.-92-34092_-92-3409 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | ||||||
| chr7:135472514
|
A | AAAAAATA others(5): Show |
1 | a0001c0001t0001g0003 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | ||||||
| chr7:135472514
|
A | AAAAAATA others(7): Show |
1 | a0001c0001t0001g0017 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | ||||||
| chr7:135472514
|
A | AAAAAATA others(11): Show |
1 | a0001c0001t0001g0193 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(22): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | ||||||
| chr7:135472514
|
A | AAAAATAT others(6): Show |
1 | a0001c0001t0001g0016 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | ||||||
| chr7:135472514
|
A | AAAAATAT others(8): Show |
1 | a0001c0001t0001g0012 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(19): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | ||||||
| chr7:135472514
|
A | AAAATATA others(3): Show |
1 | a0001c0001t0001g0320 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | ||||||
| chr7:135472514
|
A | AAAATATA others(5): Show |
1 | a0001c0001t0001g0170 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | ||||||
| chr7:135472514
|
A | AAAATATA others(13): Show |
1 | a0005c0006t0001g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(24): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | ||||||
| chr7:135472514
|
A | AATATATA others(5): Show |
1 | a0002c0002t0001g0032 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-92-34103_-92-3409 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | ||||||
| chr7:135472514
|
A | ATATATAT | 3 | a0001c0001t0001g0150a0001c0001t0001g0204a0003c0004t0001g0192 | 3 | HG02055.hp2 HG03041.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.-92-34092_-92-3409 others(11): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | ||||||
| chr7:135472514
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0156 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | ||||||
| chr7:135472514
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0177 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-92-34092_-92-3409 others(19): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | ||||||
| chr7:135472514
|
A | T | 79 | a0001c0001t0001g0004a0001c0001t0001g0115a0001c0001t0001g0142others(76): Show | 79 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.-92-34091T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | ||||||
| chr7:135472514
|
AATATATA others(5): Show |
A | 2 | a0001c0001t0002g0119a0001c0001t0002g0290 | 2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-92-34103_-92-3409 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472514 | ||||||
| chr7:135472515
|
ATATATAT others(18): Show |
A | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-92-34117_-92-3409 others(29): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472515 | ||||||
| chr7:135472520
|
T | A | 1 | a0002c0002t0001g0020 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-92-34097A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472520 | ||||||
| chr7:135472542
|
T | A | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-92-34119A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472542 | ||||||
| chr7:135472544
|
T | A | 1 | a0001c0001t0001g0013 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-92-34121A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472544 | ||||||
| chr7:135472558
|
T | C | 1 | a0001c0001t0002g0291 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-92-34135A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472558 | ||||||
| chr7:135472674
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-34251A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472674 | ||||||
| chr7:135472680
|
T | TATGC | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-34261_-92-3425 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472680 | ||||||
| chr7:135472683
|
G | A | 1 | a0001c0001t0001g0297 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-92-34260C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472683 | ||||||
| chr7:135472712
|
C | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-92-34289G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472712 | ||||||
| chr7:135472884
|
C | A | 1 | a0001c0001t0001g0324 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-92-34461G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135472884 | ||||||
| chr7:135473232
|
T | C | 4 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0162others(1): Show | 4 | HG00738.hp1 HG01106.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-92-34809A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473232 | ||||||
| chr7:135473287
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-92-34864C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473287 | ||||||
| chr7:135473312
|
T | C | 1 | a0002c0002t0001g0086 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-92-34889A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473312 | ||||||
| chr7:135473373
|
A | C | 9 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0313others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-92-34950T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473373 | ||||||
| chr7:135473425
|
T | C | 1 | a0001c0001t0001g0146 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-92-35002A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473425 | ||||||
| chr7:135473526
|
C | T | 1 | a0001c0001t0002g0139 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-92-35103G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473526 | ||||||
| chr7:135473591
|
A | G | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-35168T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473591 | ||||||
| chr7:135473615
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-92-35192A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473615 | ||||||
| chr7:135473685
|
C | T | 2 | a0001c0001t0001g0273a0001c0001t0001g0278 | 2 | NA18944.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.-92-35262G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473685 | ||||||
| chr7:135473728
|
T | C | 1 | a0001c0001t0001g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-92-35305A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473728 | ||||||
| chr7:135473833
|
A | T | 2 | a0001c0001t0003g0352a0001c0001t0003g0358 | 2 | NA18939.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.-92-35410T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473833 | ||||||
| chr7:135473852
|
T | G | 1 | a0002c0002t0001g0051 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-92-35429A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473852 | ||||||
| chr7:135473982
|
G | GT | 31 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0142others(28): Show | 31 | HG00323.hp2 HG00621.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-92-35560dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473982 | ||||||
| chr7:135473982
|
GT | G | 59 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(56): Show | 59 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-92-35560delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135473982 | ||||||
| chr7:135474038
|
G | GGTGCAAT others(1): Show |
18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-35623_-92-3561 others(12): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474038 | ||||||
| chr7:135474276
|
A | AT | 66 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0012others(63): Show | 66 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.-93+35612dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474276 | ||||||
| chr7:135474276
|
A | ATT | 24 | a0001c0001t0001g0253a0001c0001t0001g0270a0001c0001t0001g0331others(21): Show | 24 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.-93+35611_-93+3561 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474276 | ||||||
| chr7:135474276
|
A | ATTT | 6 | a0001c0001t0001g0329a0001c0001t0001g0333a0001c0001t0001g0334others(3): Show | 6 | HG00733.hp2 HG00735.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+35610_-93+3561 others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474276 | ||||||
| chr7:135474276
|
AT | A | 48 | a0001c0001t0001g0003a0001c0001t0001g0141a0001c0001t0001g0148others(45): Show | 48 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.-93+35612delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474276 | ||||||
| chr7:135474276
|
ATTTTTTT others(3): Show |
A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+35603_-93+3561 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474276 | ||||||
| chr7:135474616
|
T | C | 2 | a0001c0001t0003g0351a0001c0001t0003g0361 | 2 | HG00597.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.-93+35273A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474616 | ||||||
| chr7:135474644
|
G | A | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+35245C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474644 | ||||||
| chr7:135474833
|
T | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-93+35056A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474833 | ||||||
| chr7:135474844
|
T | A | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-93+35045A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474844 | ||||||
| chr7:135474892
|
T | G | 72 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(69): Show | 72 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-93+34997A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135474892 | ||||||
| chr7:135475097
|
G | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+34792C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135475097 | ||||||
| chr7:135475419
|
G | A | 1 | a0001c0001t0007g0225 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-93+34470C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135475419 | ||||||
| chr7:135475521
|
C | T | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+34368G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135475521 | ||||||
| chr7:135475606
|
T | C | 1 | a0001c0001t0001g0335 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-93+34283A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135475606 | ||||||
| chr7:135475632
|
G | A | 1 | a0002c0002t0001g0073 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.-93+34257C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135475632 | ||||||
| chr7:135475746
|
C | A | 2 | a0002c0002t0001g0110a0002c0002t0001g0111 | 2 | NA18956.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-93+34143G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135475746 | ||||||
| chr7:135475930
|
T | C | 2 | a0001c0001t0001g0260a0001c0001t0001g0261 | 2 | HG03834.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-93+33959A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135475930 | ||||||
| chr7:135475955
|
A | G | 1 | a0002c0002t0001g0020 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-93+33934T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135475955 | ||||||
| chr7:135476231
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-93+33658C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135476231 | ||||||
| chr7:135476232
|
A | T | 1 | a0001c0001t0001g0203 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-93+33657T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135476232 | ||||||
| chr7:135476520
|
G | A | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-93+33369C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135476520 | ||||||
| chr7:135476697
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+33192A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135476697 | ||||||
| chr7:135477089
|
C | T | 1 | a0002c0002t0001g0083 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-93+32800G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477089 | ||||||
| chr7:135477139
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-93+32750G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477139 | ||||||
| chr7:135477217
|
C | G | 1 | a0001c0001t0002g0291 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-93+32672G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477217 | ||||||
| chr7:135477343
|
C | CA | 108 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(105): Show | 108 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.-93+32545dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477343 | ||||||
| chr7:135477524
|
ATCTTGTA others(6): Show |
A | 2 | a0001c0001t0001g0230a0001c0001t0001g0246 | 2 | HG00438.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.-93+32352_-93+3236 others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477524 | ||||||
| chr7:135477594
|
A | C | 1 | a0002c0002t0001g0076 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-93+32295T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477594 | ||||||
| chr7:135477614
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+32275G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477614 | ||||||
| chr7:135477631
|
T | A | 1 | a0001c0001t0001g0164 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-93+32258A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477631 | ||||||
| chr7:135477633
|
T | A | 1 | a0001c0001t0001g0164 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-93+32256A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477633 | ||||||
| chr7:135477637
|
C | G | 1 | a0001c0001t0001g0164 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-93+32252G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477637 | ||||||
| chr7:135477638
|
T | A | 1 | a0001c0001t0001g0164 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-93+32251A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477638 | ||||||
| chr7:135477641
|
A | T | 1 | a0001c0001t0001g0164 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-93+32248T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477641 | ||||||
| chr7:135477642
|
T | G | 1 | a0001c0001t0001g0164 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-93+32247A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477642 | ||||||
| chr7:135477644
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-93+32245G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477644 | ||||||
| chr7:135477875
|
T | A | 1 | a0001c0001t0002g0116 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-93+32014A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477875 | ||||||
| chr7:135477893
|
CCAATATA others(10): Show |
C | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-93+31979_-93+3199 others(21): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477893 | ||||||
| chr7:135477960
|
TTAATA | T | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+31924_-93+3192 others(9): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477960 | ||||||
| chr7:135477964
|
T | C | 1 | a0001c0001t0002g0296 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-93+31925A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135477964 | ||||||
| chr7:135478149
|
C | T | 263 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(260): Show | 263 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(260): Show |
intron_variant | MODIFIER | c.-93+31740G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478149 | ||||||
| chr7:135478179
|
C | T | 124 | a0001c0001t0001g0118a0001c0001t0002g0116a0001c0001t0002g0117others(121): Show | 124 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-93+31710G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478179 | ||||||
| chr7:135478187
|
A | G | 63 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(60): Show | 63 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-93+31702T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478187 | ||||||
| chr7:135478235
|
T | G | 1 | a0001c0001t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-93+31654A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478235 | ||||||
| chr7:135478314
|
A | G | 38 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(35): Show | 38 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.-93+31575T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478314 | ||||||
| chr7:135478506
|
C | T | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-93+31383G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478506 | ||||||
| chr7:135478544
|
A | G | 3 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0001t0002g0190 | 3 | HG00099.hp1 HG00323.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-93+31345T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478544 | ||||||
| chr7:135478773
|
A | C | 1 | a0001c0001t0001g0164 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-93+31116T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478773 | ||||||
| chr7:135478787
|
G | C | 17 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(14): Show | 17 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-93+31102C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478787 | ||||||
| chr7:135478811
|
C | T | 2 | a0001c0001t0001g0340a0001c0001t0001g0341 | 2 | HG00642.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.-93+31078G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478811 | ||||||
| chr7:135478817
|
A | G | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+31072T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135478817 | ||||||
| chr7:135479003
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+30886G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479003 | ||||||
| chr7:135479045
|
T | C | 2 | a0002c0002t0001g0019a0002c0002t0001g0056 | 2 | HG01515.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-93+30844A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479045 | ||||||
| chr7:135479089
|
C | T | 3 | a0002c0002t0001g0185a0002c0002t0001g0186a0002c0002t0001g0187 | 3 | NA18975.hp1 NA19084.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-93+30800G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479089 | ||||||
| chr7:135479121
|
C | T | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-93+30768G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479121 | ||||||
| chr7:135479198
|
A | AT | 33 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0142others(30): Show | 33 | HG00639.hp1 HG01069.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.-93+30690dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479198 | ||||||
| chr7:135479198
|
A | ATT | 66 | a0001c0001t0001g0141a0001c0001t0001g0228a0001c0001t0001g0229others(63): Show | 66 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.-93+30689_-93+3069 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479198 | ||||||
| chr7:135479198
|
A | ATTT | 17 | a0001c0001t0001g0241a0001c0001t0001g0244a0001c0001t0001g0246others(14): Show | 17 | HG00438.hp2 HG01123.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.-93+30688_-93+3069 others(7): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479198 | ||||||
| chr7:135479198
|
AT | A | 39 | a0001c0001t0001g0016a0001c0001t0001g0118a0001c0001t0001g0147others(36): Show | 39 | HG00642.hp1 HG00733.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.-93+30690delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479198 | ||||||
| chr7:135479198
|
ATT | A | 14 | a0001c0001t0001g0348a0001c0001t0002g0288a0001c0001t0002g0289others(11): Show | 14 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.-93+30689_-93+3069 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479198 | ||||||
| chr7:135479198
|
ATTTTTTT others(3): Show |
A | 1 | a0002c0002t0001g0050 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-93+30681_-93+3069 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479198 | ||||||
| chr7:135479198
|
ATTTTTTT others(7): Show |
A | 1 | a0001c0001t0001g0318 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-93+30677_-93+3069 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479198 | ||||||
| chr7:135479333
|
C | G | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG02735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-93+30556G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479333 | ||||||
| chr7:135479431
|
G | A | 3 | a0001c0001t0001g0229a0001c0001t0001g0249a0001c0001t0001g0252 | 3 | NA18957.hp1 NA18975.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.-93+30458C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479431 | ||||||
| chr7:135479451
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+30438G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479451 | ||||||
| chr7:135479501
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-93+30388C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479501 | ||||||
| chr7:135479556
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-93+30333C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479556 | ||||||
| chr7:135479575
|
A | AT | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+30313dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479575 | ||||||
| chr7:135479590
|
T | C | 1 | a0001c0001t0001g0348 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-93+30299A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479590 | ||||||
| chr7:135479672
|
A | G | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-93+30217T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479672 | ||||||
| chr7:135479753
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+30136G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479753 | ||||||
| chr7:135479918
|
T | C | 1 | a0001c0001t0001g0348 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-93+29971A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479918 | ||||||
| chr7:135479960
|
CTAAT | C | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+29925_-93+2992 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135479960 | ||||||
| chr7:135480202
|
C | T | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+29687G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135480202 | ||||||
| chr7:135480368
|
T | C | 1 | a0001c0001t0001g0012 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-93+29521A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135480368 | ||||||
| chr7:135480527
|
G | A | 38 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(35): Show | 38 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.-93+29362C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135480527 | ||||||
| chr7:135480672
|
C | A | 1 | a0002c0002t0001g0046 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-93+29217G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135480672 | ||||||
| chr7:135480739
|
C | T | 1 | a0002c0002t0001g0042 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-93+29150G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135480739 | ||||||
| chr7:135480888
|
C | CA | 21 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0178others(18): Show | 21 | HG01099.hp1 HG01243.hp2 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.-93+29000dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135480888 | ||||||
| chr7:135480888
|
C | CAA | 30 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(27): Show | 30 | HG00597.hp2 HG00733.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.-93+28999_-93+2900 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135480888 | ||||||
| chr7:135480906
|
T | A | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+28983A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135480906 | ||||||
| chr7:135480995
|
GA | G | 22 | a0001c0001t0001g0141a0001c0001t0001g0200a0001c0001t0001g0202others(19): Show | 22 | HG00597.hp2 HG01358.hp2 HG02083.hp2 others(19): Show |
intron_variant | MODIFIER | c.-93+28893delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135480995 | ||||||
| chr7:135481007
|
A | C | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+28882T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481007 | ||||||
| chr7:135481073
|
A | C | 1 | a0001c0001t0001g0005 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-93+28816T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481073 | ||||||
| chr7:135481076
|
A | G | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+28813T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481076 | ||||||
| chr7:135481211
|
A | G | 1 | a0006c0007t0001g0311 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-93+28678T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481211 | ||||||
| chr7:135481219
|
C | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+28670G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481219 | ||||||
| chr7:135481280
|
T | C | 1 | a0001c0001t0002g0296 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-93+28609A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481280 | ||||||
| chr7:135481321
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+28568A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481321 | ||||||
| chr7:135481773
|
C | T | 124 | a0001c0001t0001g0118a0001c0001t0002g0116a0001c0001t0002g0117others(121): Show | 124 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-93+28116G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481773 | ||||||
| chr7:135481910
|
A | T | 1 | a0001c0001t0001g0206 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-93+27979T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481910 | ||||||
| chr7:135481956
|
G | C | 63 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(60): Show | 63 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-93+27933C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135481956 | ||||||
| chr7:135482039
|
T | C | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+27850A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482039 | ||||||
| chr7:135482251
|
T | C | 190 | a0001c0001t0001g0118a0001c0001t0001g0147a0001c0001t0001g0228others(187): Show | 190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.-93+27638A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482251 | ||||||
| chr7:135482443
|
C | A | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-93+27446G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482443 | ||||||
| chr7:135482482
|
G | C | 1 | a0002c0002t0001g0046 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-93+27407C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482482 | ||||||
| chr7:135482543
|
C | A | 1 | a0005c0006t0001g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-93+27346G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482543 | ||||||
| chr7:135482612
|
T | C | 1 | a0001c0001t0001g0348 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-93+27277A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482612 | ||||||
| chr7:135482678
|
C | T | 1 | a0005c0006t0001g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-93+27211G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482678 | ||||||
| chr7:135482702
|
C | T | 2 | a0001c0001t0001g0327a0001c0001t0001g0328 | 2 | NA18953.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-93+27187G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482702 | ||||||
| chr7:135482986
|
C | CA | 24 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0273others(21): Show | 24 | HG00099.hp1 HG00323.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.-93+26902dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482986 | ||||||
| chr7:135482986
|
CA | C | 30 | a0001c0001t0001g0141a0001c0001t0001g0274a0001c0001t0001g0297others(27): Show | 30 | HG00280.hp1 HG00597.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.-93+26902delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482986 | ||||||
| chr7:135482986
|
CAA | C | 9 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0313others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-93+26901_-93+2690 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482986 | ||||||
| chr7:135482986
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0280 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-93+26893_-93+2690 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135482986 | ||||||
| chr7:135483152
|
T | C | 103 | a0001c0001t0001g0239a0002c0002t0001g0018a0002c0002t0001g0019others(100): Show | 103 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.-93+26737A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483152 | ||||||
| chr7:135483171
|
CA | C | 13 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(10): Show | 13 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(10): Show |
intron_variant | MODIFIER | c.-93+26717delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483171 | ||||||
| chr7:135483178
|
A | T | 1 | a0001c0001t0003g0361 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-93+26711T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483178 | ||||||
| chr7:135483180
|
T | A | 1 | a0001c0001t0003g0361 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-93+26709A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483180 | ||||||
| chr7:135483180
|
T | TA | 3 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0270 | 3 | HG03834.hp2 HG03942.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-93+26708_-93+2670 others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483180 | ||||||
| chr7:135483181
|
T | A | 30 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0146others(27): Show | 30 | HG00597.hp2 HG01243.hp2 HG02083.hp2 others(27): Show |
intron_variant | MODIFIER | c.-93+26708A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483181 | ||||||
| chr7:135483181
|
T | TA | 54 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(51): Show | 54 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-93+26707dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483181 | ||||||
| chr7:135483181
|
TA | T | 23 | a0001c0001t0001g0147a0001c0001t0001g0329a0001c0001t0001g0330others(20): Show | 23 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.-93+26707delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483181 | ||||||
| chr7:135483182
|
A | T | 1 | a0002c0002t0001g0020 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-93+26707T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483182 | ||||||
| chr7:135483199
|
C | T | 266 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(263): Show | 266 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.-93+26690G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483199 | ||||||
| chr7:135483251
|
T | C | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+26638A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483251 | ||||||
| chr7:135483252
|
T | C | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+26637A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483252 | ||||||
| chr7:135483337
|
C | CAA | 17 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(14): Show | 17 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-93+26550_-93+2655 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483337 | ||||||
| chr7:135483349
|
T | A | 2 | a0002c0002t0001g0050a0002c0002t0001g0060 | 2 | HG01358.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.-93+26540A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483349 | ||||||
| chr7:135483387
|
A | T | 1 | a0001c0001t0001g0222 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-93+26502T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483387 | ||||||
| chr7:135483592
|
G | C | 1 | a0001c0001t0001g0241 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-93+26297C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483592 | ||||||
| chr7:135483653
|
G | A | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+26236C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483653 | ||||||
| chr7:135483719
|
G | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+26170C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483719 | ||||||
| chr7:135483759
|
T | C | 1 | a0001c0001t0001g0324 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-93+26130A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483759 | ||||||
| chr7:135483893
|
A | G | 3 | a0002c0002t0001g0300a0002c0002t0001g0302a0002c0002t0001g0303 | 3 | HG02055.hp1 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-93+25996T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483893 | ||||||
| chr7:135483941
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-93+25948T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483941 | ||||||
| chr7:135483991
|
C | T | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0149others(3): Show | 6 | HG01123.hp2 NA18968.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+25898G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135483991 | ||||||
| chr7:135484503
|
T | A | 1 | a0001c0001t0001g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-93+25386A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135484503 | ||||||
| chr7:135484666
|
C | T | 124 | a0001c0001t0001g0118a0001c0001t0002g0116a0001c0001t0002g0117others(121): Show | 124 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.-93+25223G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135484666 | ||||||
| chr7:135484754
|
C | CA | 13 | a0001c0001t0001g0243a0001c0001t0001g0254a0001c0001t0001g0268others(10): Show | 13 | HG00735.hp1 HG02071.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.-93+25134dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135484754 | ||||||
| chr7:135484893
|
A | G | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+24996T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135484893 | ||||||
| chr7:135484942
|
C | T | 2 | a0002c0002t0001g0029a0002c0002t0001g0043 | 2 | HG01081.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-93+24947G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135484942 | ||||||
| chr7:135485134
|
A | G | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+24755T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485134 | ||||||
| chr7:135485139
|
C | T | 16 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(13): Show | 16 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.-93+24750G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485139 | ||||||
| chr7:135485175
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+24714G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485175 | ||||||
| chr7:135485198
|
G | A | 3 | a0001c0001t0002g0291a0001c0001t0002g0293a0001c0001t0002g0294 | 3 | HG02145.hp2 HG02809.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-93+24691C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485198 | ||||||
| chr7:135485225
|
G | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-93+24664C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485225 | ||||||
| chr7:135485361
|
C | T | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-93+24528G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485361 | ||||||
| chr7:135485368
|
C | T | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+24521G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485368 | ||||||
| chr7:135485454
|
T | TAAAAACA others(3): Show |
6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+24434_-93+2443 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485454 | ||||||
| chr7:135485681
|
A | AT | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.-93+24207dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485681 | ||||||
| chr7:135485700
|
A | G | 266 | a0001c0001t0001g0118a0001c0001t0001g0141a0001c0001t0001g0145others(263): Show | 266 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.-93+24189T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485700 | ||||||
| chr7:135485722
|
C | T | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+24167G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485722 | ||||||
| chr7:135485776
|
C | T | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-93+24113G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485776 | ||||||
| chr7:135485911
|
CA | C | 3 | a0002c0002t0001g0025a0002c0002t0001g0026a0002c0002t0001g0027 | 3 | NA18986.hp2 NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-93+23977delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135485911 | ||||||
| chr7:135486007
|
G | A | 17 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(14): Show | 17 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-93+23882C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486007 | ||||||
| chr7:135486055
|
G | T | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+23834C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486055 | ||||||
| chr7:135486100
|
A | T | 2 | a0001c0001t0001g0338a0001c0001t0001g0339 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-93+23789T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486100 | ||||||
| chr7:135486350
|
A | G | 107 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(104): Show | 107 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.-93+23539T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486350 | ||||||
| chr7:135486485
|
A | G | 3 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137 | 3 | HG02486.hp1 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-93+23404T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486485 | ||||||
| chr7:135486754
|
AACTCAGA others(4): Show |
A | 2 | a0002c0002t0001g0034a0002c0002t0001g0081 | 2 | NA18957.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.-93+23124_-93+2313 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486754 | ||||||
| chr7:135486829
|
A | G | 9 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0313others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-93+23060T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486829 | ||||||
| chr7:135486887
|
C | A | 1 | a0002c0002t0001g0088 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-93+23002G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486887 | ||||||
| chr7:135486902
|
T | G | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-93+22987A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486902 | ||||||
| chr7:135486963
|
C | T | 16 | a0001c0001t0001g0141a0001c0001t0001g0324a0001c0001t0001g0327others(13): Show | 16 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-93+22926G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135486963 | ||||||
| chr7:135487042
|
T | G | 3 | a0001c0001t0002g0188a0001c0001t0002g0189a0001c0001t0002g0190 | 3 | HG00099.hp1 HG00323.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-93+22847A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487042 | ||||||
| chr7:135487110
|
T | C | 4 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0154others(1): Show | 4 | NA18980.hp1 NA18994.hp2 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93+22779A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487110 | ||||||
| chr7:135487161
|
A | G | 16 | a0001c0001t0001g0141a0001c0001t0001g0324a0001c0001t0001g0327others(13): Show | 16 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-93+22728T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487161 | ||||||
| chr7:135487189
|
C | CT | 25 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(22): Show | 25 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(22): Show |
intron_variant | MODIFIER | c.-93+22699dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487189 | ||||||
| chr7:135487290
|
T | C | 1 | a0001c0001t0001g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-93+22599A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487290 | ||||||
| chr7:135487319
|
C | A | 1 | a0001c0001t0002g0295 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-93+22570G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487319 | ||||||
| chr7:135487384
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-93+22505G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487384 | ||||||
| chr7:135487468
|
A | G | 130 | a0001c0001t0001g0118a0001c0001t0001g0306a0001c0001t0001g0307others(127): Show | 130 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.-93+22421T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487468 | ||||||
| chr7:135487478
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-93+22411C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487478 | ||||||
| chr7:135487643
|
A | C | 1 | a0001c0001t0001g0221 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-93+22246T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487643 | ||||||
| chr7:135487698
|
A | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-93+22191T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487698 | ||||||
| chr7:135487744
|
C | T | 1 | a0003c0004t0001g0192 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-93+22145G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487744 | ||||||
| chr7:135487781
|
C | T | 5 | a0001c0001t0001g0158a0001c0001t0001g0169a0001c0001t0001g0170others(2): Show | 5 | NA18945.hp1 NA18963.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.-93+22108G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487781 | ||||||
| chr7:135487792
|
G | A | 1 | a0001c0001t0001g0348 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-93+22097C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487792 | ||||||
| chr7:135487981
|
C | A | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+21908G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135487981 | ||||||
| chr7:135488072
|
G | A | 289 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.-93+21817C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135488072 | ||||||
| chr7:135488296
|
G | A | 1 | a0001c0001t0002g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-93+21593C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135488296 | ||||||
| chr7:135488522
|
A | C | 1 | a0002c0002t0001g0047 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-93+21367T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135488522 | ||||||
| chr7:135488540
|
C | G | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+21349G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135488540 | ||||||
| chr7:135488549
|
G | A | 4 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | NA18941.hp1 NA18953.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+21340C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135488549 | ||||||
| chr7:135488763
|
C | T | 361 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(358): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.-93+21126G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135488763 | ||||||
| chr7:135488796
|
C | T | 34 | a0001c0001t0001g0141a0001c0001t0001g0324a0001c0001t0001g0327others(31): Show | 34 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.-93+21093G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135488796 | ||||||
| chr7:135488981
|
G | A | 101 | a0002c0002t0001g0018a0002c0002t0001g0019a0002c0002t0001g0020others(98): Show | 101 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.-93+20908C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135488981 | ||||||
| chr7:135489214
|
G | A | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+20675C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489214 | ||||||
| chr7:135489384
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-93+20505G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489384 | ||||||
| chr7:135489391
|
C | CT | 23 | a0001c0001t0001g0142a0001c0001t0001g0148a0001c0001t0001g0151others(20): Show | 23 | HG00438.hp2 HG00738.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.-93+20497dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489391 | ||||||
| chr7:135489391
|
CT | C | 119 | a0001c0001t0001g0214a0001c0001t0001g0243a0001c0001t0001g0262others(116): Show | 119 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(116): Show |
intron_variant | MODIFIER | c.-93+20497delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489391 | ||||||
| chr7:135489391
|
CTTTTTTT others(1): Show |
C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+20490_-93+2049 others(12): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489391 | ||||||
| chr7:135489391
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-93+20486_-93+2049 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489391 | ||||||
| chr7:135489427
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-93+20462C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489427 | ||||||
| chr7:135489685
|
T | C | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+20204A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489685 | ||||||
| chr7:135489693
|
G | A | 1 | a0001c0001t0002g0295 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-93+20196C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489693 | ||||||
| chr7:135489738
|
T | G | 1 | a0001c0001t0001g0161 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-93+20151A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489738 | ||||||
| chr7:135489747
|
T | C | 2 | a0001c0001t0003g0352a0001c0001t0003g0358 | 2 | NA18939.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.-93+20142A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489747 | ||||||
| chr7:135489939
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-93+19950A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135489939 | ||||||
| chr7:135490120
|
G | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+19769C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135490120 | ||||||
| chr7:135490144
|
T | C | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+19745A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135490144 | ||||||
| chr7:135490176
|
T | G | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+19713A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135490176 | ||||||
| chr7:135490238
|
C | T | 17 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(14): Show | 17 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-93+19651G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135490238 | ||||||
| chr7:135490298
|
C | T | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-93+19591G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135490298 | ||||||
| chr7:135490551
|
AAT | A | 17 | a0001c0001t0002g0287a0001c0001t0002g0288a0001c0001t0002g0289others(14): Show | 17 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-93+19336_-93+1933 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135490551 | ||||||
| chr7:135490578
|
A | G | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+19311T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135490578 | ||||||
| chr7:135491452
|
A | C | 2 | a0001c0001t0001g0145a0001c0001t0008g0350 | 2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-93+18437T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135491452 | ||||||
| chr7:135491723
|
G | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+18166C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135491723 | ||||||
| chr7:135491800
|
G | A | 1 | a0002c0002t0001g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-93+18089C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135491800 | ||||||
| chr7:135491940
|
T | C | 1 | a0001c0001t0001g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-93+17949A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135491940 | ||||||
| chr7:135492004
|
G | A | 1 | a0002c0002t0001g0092 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-93+17885C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492004 | ||||||
| chr7:135492204
|
T | C | 1 | a0001c0001t0001g0272 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-93+17685A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492204 | ||||||
| chr7:135492243
|
T | A | 1 | a0001c0001t0001g0011 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-93+17646A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492243 | ||||||
| chr7:135492271
|
T | G | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+17618A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492271 | ||||||
| chr7:135492468
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-93+17421G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492468 | ||||||
| chr7:135492491
|
C | G | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+17398G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492491 | ||||||
| chr7:135492504
|
G | A | 1 | a0002c0002t0001g0022 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-93+17385C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492504 | ||||||
| chr7:135492523
|
C | T | 2 | a0001c0001t0001g0193a0001c0001t0001g0195 | 2 | NA18942.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.-93+17366G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492523 | ||||||
| chr7:135492588
|
C | G | 1 | a0002c0002t0001g0096 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-93+17301G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492588 | ||||||
| chr7:135492632
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-93+17257A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492632 | ||||||
| chr7:135492947
|
A | G | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+16942T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135492947 | ||||||
| chr7:135493001
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-93+16888A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135493001 | ||||||
| chr7:135493011
|
C | G | 1 | a0001c0001t0001g0270 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-93+16878G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135493011 | ||||||
| chr7:135493195
|
T | G | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+16694A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135493195 | ||||||
| chr7:135493279
|
T | C | 237 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(234): Show | 237 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.-93+16610A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135493279 | ||||||
| chr7:135493312
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-93+16577G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135493312 | ||||||
| chr7:135493726
|
T | C | 1 | a0001c0001t0001g0319 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-93+16163A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135493726 | ||||||
| chr7:135493862
|
G | A | 1 | a0002c0002t0001g0301 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-93+16027C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135493862 | ||||||
| chr7:135494065
|
C | CA | 25 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0154others(22): Show | 25 | HG00597.hp2 HG00733.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.-93+15823dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494065 | ||||||
| chr7:135494065
|
CA | C | 120 | a0001c0001t0001g0118a0001c0001t0001g0336a0001c0001t0002g0116others(117): Show | 120 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.-93+15823delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494065 | ||||||
| chr7:135494083
|
C | T | 2 | a0001c0001t0004g0346a0001c0001t0004g0347 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-93+15806G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494083 | ||||||
| chr7:135494195
|
C | CGCAGTGG others(26): Show |
1 | a0002c0002t0001g0082 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-93+15661_-93+1569 others(37): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494195 | ||||||
| chr7:135494448
|
C | T | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+15441G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494448 | ||||||
| chr7:135494470
|
CA | C | 210 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(207): Show | 210 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.-93+15418delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494470 | ||||||
| chr7:135494470
|
CAA | C | 111 | a0001c0001t0001g0234a0001c0001t0001g0236a0001c0001t0001g0272others(108): Show | 111 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.-93+15417_-93+1541 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494470 | ||||||
| chr7:135494677
|
A | G | 1 | a0002c0002t0001g0077 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-93+15212T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494677 | ||||||
| chr7:135494717
|
G | C | 1 | a0001c0001t0002g0190 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-93+15172C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494717 | ||||||
| chr7:135494737
|
A | T | 72 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(69): Show | 72 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.-93+15152T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494737 | ||||||
| chr7:135494758
|
G | A | 1 | a0001c0001t0001g0273 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-93+15131C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494758 | ||||||
| chr7:135494890
|
T | C | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+14999A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135494890 | ||||||
| chr7:135495038
|
G | A | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+14851C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495038 | ||||||
| chr7:135495181
|
G | C | 16 | a0001c0001t0001g0141a0001c0001t0001g0324a0001c0001t0001g0327others(13): Show | 16 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-93+14708C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495181 | ||||||
| chr7:135495242
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-93+14647G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495242 | ||||||
| chr7:135495323
|
G | A | 1 | a0001c0001t0003g0352 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-93+14566C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495323 | ||||||
| chr7:135495347
|
A | C | 2 | a0002c0002t0001g0028a0002c0002t0001g0032 | 2 | NA19007.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.-93+14542T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495347 | ||||||
| chr7:135495488
|
G | A | 40 | a0002c0002t0001g0020a0002c0002t0001g0021a0002c0002t0001g0033others(37): Show | 40 | HG00438.hp1 HG00673.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.-93+14401C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495488 | ||||||
| chr7:135495492
|
G | A | 3 | a0002c0002t0001g0185a0002c0002t0001g0186a0002c0002t0001g0187 | 3 | NA18975.hp1 NA19084.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-93+14397C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495492 | ||||||
| chr7:135495504
|
C | CA | 32 | a0001c0001t0001g0012a0001c0001t0001g0118a0001c0001t0001g0155others(29): Show | 32 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.-93+14384dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495504 | ||||||
| chr7:135495504
|
CA | C | 189 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0223others(186): Show | 189 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(186): Show |
intron_variant | MODIFIER | c.-93+14384delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495504 | ||||||
| chr7:135495504
|
CAA | C | 8 | a0001c0001t0001g0281a0001c0001t0001g0306a0001c0001t0001g0307others(5): Show | 8 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93+14383_-93+1438 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495504 | ||||||
| chr7:135495662
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-93+14227G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495662 | ||||||
| chr7:135495669
|
CAAAAAAA others(5): Show |
C | 1 | a0002c0002t0001g0045 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-93+14208_-93+1421 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495669 | ||||||
| chr7:135495678
|
AAAAAAAA others(9): Show |
A | 1 | a0001c0001t0001g0196 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-93+14195_-93+1421 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495678 | ||||||
| chr7:135495678
|
AAAAAAAA others(13): Show |
A | 2 | a0001c0001t0001g0199a0001c0001t0001g0216 | 2 | HG02015.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-93+14191_-93+1421 others(24): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495678 | ||||||
| chr7:135495678
|
AAAAAAAA others(25): Show |
A | 1 | a0003c0004t0001g0219 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-93+14179_-93+1421 others(36): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495678 | ||||||
| chr7:135495679
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0197 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-93+14195_-93+1420 others(19): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495679 | ||||||
| chr7:135495679
|
AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0001g0223 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-93+14187_-93+1420 others(27): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495679 | ||||||
| chr7:135495683
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0002g0188 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-93+14195_-93+1420 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495683 | ||||||
| chr7:135495683
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0240 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-93+14191_-93+1420 others(19): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495683 | ||||||
| chr7:135495683
|
AAAAAAAA others(12): Show |
A | 3 | a0001c0001t0003g0353a0002c0002t0001g0031a0002c0002t0001g0050 | 3 | HG01358.hp1 NA18948.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.-93+14187_-93+1420 others(23): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495683 | ||||||
| chr7:135495683
|
AAAAAAAA others(16): Show |
A | 2 | a0002c0002t0001g0021a0002c0002t0001g0093 | 2 | HG02257.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.-93+14183_-93+1420 others(27): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495683 | ||||||
| chr7:135495683
|
AAAAAAAA others(24): Show |
A | 1 | a0002c0002t0001g0022 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-93+14175_-93+1420 others(35): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495683 | ||||||
| chr7:135495684
|
AAAAAAAA others(7): Show |
A | 5 | a0001c0001t0001g0147a0001c0001t0001g0327a0001c0001t0001g0328others(2): Show | 5 | HG01081.hp2 HG03209.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.-93+14191_-93+1420 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495684 | ||||||
| chr7:135495684
|
AAAAAAAA others(11): Show |
A | 12 | a0001c0001t0001g0141a0001c0001t0003g0351a0001c0001t0003g0354others(9): Show | 12 | HG00597.hp2 HG02083.hp2 HG03490.hp2 others(9): Show |
intron_variant | MODIFIER | c.-93+14187_-93+1420 others(22): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495684 | ||||||
| chr7:135495684
|
AAAAAAAA others(15): Show |
A | 3 | a0002c0002t0001g0025a0002c0002t0001g0078a0002c0002t0001g0080 | 3 | NA18998.hp2 NA19079.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.-93+14183_-93+1420 others(26): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495684 | ||||||
| chr7:135495684
|
AAAAAAAA others(19): Show |
A | 1 | a0002c0002t0001g0074 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-93+14179_-93+1420 others(30): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495684 | ||||||
| chr7:135495684
|
AAAAAAAA others(23): Show |
A | 1 | a0002c0002t0001g0062 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-93+14175_-93+1420 others(34): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495684 | ||||||
| chr7:135495685
|
AAAAAAAA others(6): Show |
A | 1 | a0002c0002t0001g0072 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-93+14191_-93+1420 others(17): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495685 | ||||||
| chr7:135495685
|
AAAAAAAA others(10): Show |
A | 3 | a0001c0001t0001g0231a0001c0001t0003g0360a0001c0010t0002g0326 | 3 | HG01261.hp1 HG02683.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.-93+14187_-93+1420 others(21): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495685 | ||||||
| chr7:135495685
|
AAAAAAAA others(14): Show |
A | 6 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0273others(3): Show | 6 | HG00609.hp1 HG02109.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+14183_-93+1420 others(25): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495685 | ||||||
| chr7:135495685
|
AAAAAAAA others(18): Show |
A | 2 | a0001c0001t0001g0244a0001c0001t0001g0284 | 2 | NA18940.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-93+14179_-93+1420 others(29): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495685 | ||||||
| chr7:135495685
|
AAAAAAAA others(22): Show |
A | 1 | a0001c0001t0001g0255 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-93+14175_-93+1420 others(33): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495685 | ||||||
| chr7:135495685
|
AAAAAAAA others(46): Show |
A | 1 | a0001c0001t0001g0331 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-93+14151_-93+1420 others(57): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495685 | ||||||
| chr7:135495686
|
AAAAAAAA others(1): Show |
A | 14 | a0001c0001t0002g0122a0001c0001t0002g0189a0001c0001t0002g0190others(11): Show | 14 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+14195_-93+1420 others(12): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | ||||||
| chr7:135495686
|
AAAAAAAA others(5): Show |
A | 11 | a0001c0001t0002g0287a0002c0002t0001g0030a0002c0002t0001g0036others(8): Show | 11 | HG01496.hp1 HG03491.hp1 HG03669.hp2 others(8): Show |
intron_variant | MODIFIER | c.-93+14191_-93+1420 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | ||||||
| chr7:135495686
|
AAAAAAAA others(9): Show |
A | 2 | a0001c0001t0002g0288a0002c0002t0001g0051 | 2 | HG01346.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-93+14187_-93+1420 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | ||||||
| chr7:135495686
|
AAAAAAAA others(13): Show |
A | 5 | a0002c0002t0001g0028a0002c0002t0001g0032a0002c0002t0001g0034others(2): Show | 5 | NA18941.hp2 NA18947.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.-93+14183_-93+1420 others(24): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | ||||||
| chr7:135495686
|
AAAAAAAA others(17): Show |
A | 14 | a0001c0001t0001g0245a0002c0002t0001g0026a0002c0002t0001g0042others(11): Show | 14 | HG00609.hp2 HG01515.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+14179_-93+1420 others(28): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | ||||||
| chr7:135495686
|
AAAAAAAA others(21): Show |
A | 18 | a0001c0001t0001g0318a0001c0001t0002g0125a0002c0002t0001g0027others(15): Show | 18 | HG00597.hp1 HG00621.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+14175_-93+1420 others(32): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | ||||||
| chr7:135495686
|
AAAAAAAA others(25): Show |
A | 3 | a0001c0001t0002g0130a0002c0002t0001g0071a0002c0002t0001g0077 | 3 | HG02486.hp2 NA19004.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.-93+14171_-93+1420 others(36): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | ||||||
| chr7:135495686
|
AAAAAAAA others(29): Show |
A | 1 | a0002c0002t0001g0129 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-93+14167_-93+1420 others(40): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | ||||||
| chr7:135495686
|
AAAAAAAA others(33): Show |
A | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | HG02818.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93+14163_-93+1420 others(44): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | ||||||
| chr7:135495686
|
AAAAAAAA others(45): Show |
A | 17 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0332others(14): Show | 17 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.-93+14151_-93+1420 others(56): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495686 | ||||||
| chr7:135495687
|
AAAAAAAG | A | 11 | a0001c0001t0001g0198a0001c0001t0001g0239a0001c0001t0002g0117others(8): Show | 11 | HG00438.hp1 HG01071.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.-93+14195_-93+1420 others(11): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495687 | ||||||
| chr7:135495687
|
AAAAAAAG others(4): Show |
A | 7 | a0001c0001t0001g0241a0001c0001t0001g0297a0002c0002t0001g0049others(4): Show | 7 | HG02965.hp2 HG03492.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.-93+14191_-93+1420 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495687 | ||||||
| chr7:135495687
|
AAAAAAAG others(12): Show |
A | 6 | a0001c0001t0001g0175a0001c0001t0004g0347a0002c0002t0001g0040others(3): Show | 6 | HG02165.hp2 HG03492.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+14183_-93+1420 others(23): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495687 | ||||||
| chr7:135495687
|
AAAAAAAG others(16): Show |
A | 11 | a0001c0001t0001g0246a0001c0001t0001g0247a0001c0001t0001g0248others(8): Show | 11 | HG00280.hp2 HG00438.hp2 HG02071.hp1 others(8): Show |
intron_variant | MODIFIER | c.-93+14179_-93+1420 others(27): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495687 | ||||||
| chr7:135495687
|
AAAAAAAG others(20): Show |
A | 21 | a0001c0001t0001g0230a0001c0001t0001g0235a0001c0001t0001g0236others(18): Show | 21 | HG01106.hp1 HG01361.hp2 HG01934.hp2 others(18): Show |
intron_variant | MODIFIER | c.-93+14175_-93+1420 others(31): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495687 | ||||||
| chr7:135495687
|
AAAAAAAG others(24): Show |
A | 1 | a0001c0001t0001g0237 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-93+14171_-93+1420 others(35): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495687 | ||||||
| chr7:135495687
|
AAAAAAAG others(28): Show |
A | 1 | a0001c0001t0001g0271 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-93+14167_-93+1420 others(39): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495687 | ||||||
| chr7:135495687
|
AAAAAAAG others(36): Show |
A | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+14159_-93+1420 others(47): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495687 | ||||||
| chr7:135495688
|
A | G | 2 | a0001c0001t0001g0324a0002c0002t0006g0002 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-93+14201T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495688 | ||||||
| chr7:135495688
|
AAAAAAG | A | 6 | a0001c0001t0001g0007a0001c0001t0001g0151a0001c0001t0001g0165others(3): Show | 6 | HG01891.hp1 HG01943.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+14195_-93+1420 others(10): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495688 | ||||||
| chr7:135495688
|
AAAAAAGA others(3): Show |
A | 5 | a0001c0001t0001g0145a0001c0001t0001g0299a0002c0002t0001g0111others(2): Show | 5 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+14191_-93+1420 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495688 | ||||||
| chr7:135495688
|
AAAAAAGA others(7): Show |
A | 7 | a0001c0001t0001g0155a0001c0001t0001g0166a0001c0001t0001g0232others(4): Show | 7 | HG00642.hp2 HG01074.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.-93+14187_-93+1420 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495688 | ||||||
| chr7:135495688
|
AAAAAAGA others(11): Show |
A | 8 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0298others(5): Show | 8 | HG02145.hp2 HG02622.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.-93+14183_-93+1420 others(22): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495688 | ||||||
| chr7:135495688
|
AAAAAAGA others(15): Show |
A | 7 | a0001c0001t0001g0229a0001c0001t0001g0252a0001c0001t0001g0253others(4): Show | 7 | HG01993.hp1 HG06807.hp1 NA18944.hp1 others(4): Show |
intron_variant | MODIFIER | c.-93+14179_-93+1420 others(26): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495688 | ||||||
| chr7:135495688
|
AAAAAAGA others(19): Show |
A | 8 | a0001c0001t0001g0228a0001c0001t0001g0265a0001c0001t0001g0266others(5): Show | 8 | HG02071.hp2 HG02080.hp2 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.-93+14175_-93+1420 others(30): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495688 | ||||||
| chr7:135495688
|
AAAAAAGA others(23): Show |
A | 8 | a0001c0001t0001g0238a0001c0001t0001g0270a0001c0001t0001g0312others(5): Show | 8 | HG00323.hp2 HG00639.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93+14171_-93+1420 others(34): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495688 | ||||||
| chr7:135495689
|
A | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+14200T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495689 | ||||||
| chr7:135495689
|
AAAAAGAA others(10): Show |
A | 1 | a0001c0001t0001g0234 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-93+14183_-93+1419 others(21): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495689 | ||||||
| chr7:135495689
|
AAAAAGAA others(18): Show |
A | 2 | a0001c0001t0001g0159a0001c0001t0001g0310 | 2 | HG01074.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-93+14175_-93+1419 others(29): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495689 | ||||||
| chr7:135495689
|
AAAAAGAA others(22): Show |
A | 1 | a0001c0001t0001g0317 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-93+14171_-93+1419 others(33): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495689 | ||||||
| chr7:135495689
|
AAAAAGAA others(30): Show |
A | 1 | a0001c0001t0001g0272 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-93+14163_-93+1419 others(41): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495689 | ||||||
| chr7:135495690
|
A | G | 9 | a0001c0001t0001g0118a0001c0001t0002g0120a0001c0001t0002g0124others(6): Show | 9 | HG00735.hp2 HG01255.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.-93+14199T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495690 | ||||||
| chr7:135495690
|
AAAAG | A | 6 | a0001c0001t0001g0143a0001c0001t0001g0173a0001c0001t0001g0177others(3): Show | 6 | HG01123.hp2 HG01167.hp2 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+14195_-93+1419 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495690 | ||||||
| chr7:135495690
|
AAAAGAAA others(1): Show |
A | 13 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(10): Show | 13 | HG01069.hp1 HG01346.hp2 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.-93+14191_-93+1419 others(12): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495690 | ||||||
| chr7:135495690
|
AAAAGAAA others(5): Show |
A | 5 | a0001c0001t0001g0013a0001c0001t0001g0114a0001c0001t0001g0174others(2): Show | 5 | HG00673.hp2 HG01261.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+14187_-93+1419 others(16): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495690 | ||||||
| chr7:135495690
|
AAAAGAAA others(9): Show |
A | 4 | a0001c0001t0001g0014a0001c0001t0001g0200a0001c0001t0001g0201others(1): Show | 4 | HG00099.hp2 HG02293.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93+14183_-93+1419 others(20): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495690 | ||||||
| chr7:135495690
|
AAAAGAAA others(13): Show |
A | 1 | a0001c0001t0001g0158 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-93+14179_-93+1419 others(24): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495690 | ||||||
| chr7:135495690
|
AAAAGAAA others(17): Show |
A | 1 | a0001c0001t0001g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-93+14175_-93+1419 others(28): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495690 | ||||||
| chr7:135495691
|
AAAGAAAG | A | 7 | a0001c0001t0001g0017a0001c0001t0001g0113a0001c0001t0001g0115others(4): Show | 7 | HG00621.hp2 HG00733.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.-93+14191_-93+1419 others(11): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495691 | ||||||
| chr7:135495691
|
AAAGAAAG others(4): Show |
A | 8 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0169others(5): Show | 8 | HG02258.hp2 HG02717.hp1 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.-93+14187_-93+1419 others(15): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495691 | ||||||
| chr7:135495691
|
AAAGAAAG others(8): Show |
A | 1 | a0001c0001t0001g0202 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-93+14183_-93+1419 others(19): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495691 | ||||||
| chr7:135495691
|
AAAGAAAG others(12): Show |
A | 2 | a0001c0001t0001g0220a0001c0001t0001g0221 | 2 | HG02683.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-93+14179_-93+1419 others(23): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495691 | ||||||
| chr7:135495691
|
AAAGAAAG others(24): Show |
A | 2 | a0001c0001t0001g0162a0001c0001t0001g0163 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-93+14167_-93+1419 others(35): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495691 | ||||||
| chr7:135495692
|
AAGAAAGA others(3): Show |
A | 2 | a0001c0001t0001g0205a0005c0006t0001g0224 | 2 | HG01255.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.-93+14187_-93+1419 others(14): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495692 | ||||||
| chr7:135495692
|
AAGAAAGA others(23): Show |
A | 2 | a0001c0001t0001g0148a0001c0001t0001g0152 | 2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-93+14167_-93+1419 others(34): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495692 | ||||||
| chr7:135495698
|
G | A | 1 | a0001c0001t0001g0217 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-93+14191C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495698 | ||||||
| chr7:135495703
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-93+14186T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495703 | ||||||
| chr7:135495734
|
G | C | 2 | a0001c0001t0001g0327a0001c0001t0001g0328 | 2 | NA18953.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-93+14155C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495734 | ||||||
| chr7:135495735
|
A | G | 16 | a0002c0002t0001g0096a0002c0002t0001g0097a0002c0002t0001g0098others(13): Show | 16 | HG00438.hp1 HG01071.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.-93+14154T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495735 | ||||||
| chr7:135495738
|
G | C | 12 | a0001c0001t0001g0141a0001c0001t0003g0351a0001c0001t0003g0352others(9): Show | 12 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(9): Show |
intron_variant | MODIFIER | c.-93+14151C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495738 | ||||||
| chr7:135495739
|
A | G | 2 | a0002c0002t0001g0036a0002c0002t0001g0087 | 2 | NA19003.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-93+14150T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495739 | ||||||
| chr7:135495742
|
GAAAGAAA others(15): Show |
G | 1 | a0002c0002t0001g0019 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-93+14125_-93+1414 others(26): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495742 | ||||||
| chr7:135495746
|
GAAAGAAA others(7): Show |
G | 1 | a0001c0001t0001g0153 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-93+14129_-93+1414 others(18): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495746 | ||||||
| chr7:135495754
|
G | T | 1 | a0001c0001t0001g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-93+14135C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495754 | ||||||
| chr7:135495758
|
G | T | 1 | a0001c0001t0001g0321 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-93+14131C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495758 | ||||||
| chr7:135495762
|
G | T | 7 | a0001c0001t0001g0145a0001c0001t0001g0297a0001c0001t0001g0298others(4): Show | 7 | HG01243.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-93+14127C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495762 | ||||||
| chr7:135495763
|
A | T | 4 | a0001c0001t0001g0145a0001c0001t0001g0297a0001c0001t0001g0298others(1): Show | 4 | HG01243.hp2 HG02622.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+14126T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495763 | ||||||
| chr7:135495803
|
A | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG00738.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.-93+14086T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495803 | ||||||
| chr7:135495806
|
T | A | 1 | a0001c0001t0001g0229 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-93+14083A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135495806 | ||||||
| chr7:135496121
|
CTCACTCC others(32): Show |
C | 4 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(1): Show | 4 | HG00673.hp2 HG02083.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+13729_-93+1376 others(43): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135496121 | ||||||
| chr7:135496281
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0165 | 2 | HG01943.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-93+13608G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135496281 | ||||||
| chr7:135496289
|
C | T | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+13600G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135496289 | ||||||
| chr7:135496631
|
C | CCT | 23 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(20): Show | 23 | HG00597.hp2 HG00609.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.-93+13256_-93+1325 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135496631 | ||||||
| chr7:135496631
|
CCT | C | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+13256_-93+1325 others(6): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135496631 | ||||||
| chr7:135496631
|
CCTCT | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0165others(1): Show | 4 | HG01943.hp2 HG03490.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93+13254_-93+1325 others(8): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135496631 | ||||||
| chr7:135496633
|
T | G | 4 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316others(1): Show | 4 | HG01123.hp1 HG03654.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93+13256A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135496633 | ||||||
| chr7:135496707
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-93+13182T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135496707 | ||||||
| chr7:135496969
|
G | A | 4 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0162others(1): Show | 4 | HG00738.hp1 HG01106.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93+12920C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135496969 | ||||||
| chr7:135497084
|
G | T | 9 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0313others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-93+12805C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135497084 | ||||||
| chr7:135497144
|
A | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0167 | 2 | NA18967.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-93+12745T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135497144 | ||||||
| chr7:135497168
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(3): Show | 6 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-93+12721C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135497168 | ||||||
| chr7:135497586
|
C | G | 5 | a0002c0002t0001g0037a0002c0002t0001g0038a0002c0002t0001g0039others(2): Show | 5 | NA18941.hp2 NA18980.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.-93+12303G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135497586 | ||||||
| chr7:135497696
|
T | C | 13 | a0002c0002t0001g0025a0002c0002t0001g0026a0002c0002t0001g0027others(10): Show | 13 | NA18947.hp2 NA18948.hp1 NA18951.hp1 others(10): Show |
intron_variant | MODIFIER | c.-93+12193A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135497696 | ||||||
| chr7:135498162
|
A | ATACTAC | 17 | a0001c0001t0001g0320a0001c0001t0002g0287a0001c0001t0002g0288others(14): Show | 17 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.-93+11721_-93+1172 others(10): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135498162 | ||||||
| chr7:135498241
|
T | C | 9 | a0001c0001t0001g0273a0001c0001t0001g0274a0001c0001t0001g0275others(6): Show | 9 | NA18944.hp1 NA18945.hp2 NA18986.hp1 others(6): Show |
intron_variant | MODIFIER | c.-93+11648A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135498241 | ||||||
| chr7:135498599
|
AGTGCAAT | A | 3 | a0001c0001t0002g0138a0001c0001t0002g0139a0001c0001t0002g0140 | 3 | HG02572.hp2 HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-93+11283_-93+1128 others(11): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135498599 | ||||||
| chr7:135498851
|
A | G | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+11038T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135498851 | ||||||
| chr7:135499111
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-93+10778G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135499111 | ||||||
| chr7:135499246
|
G | T | 2 | a0001c0001t0001g0336a0001c0001t0001g0337 | 2 | HG02602.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-93+10643C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135499246 | ||||||
| chr7:135499333
|
T | C | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+10556A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135499333 | ||||||
| chr7:135499876
|
A | C | 2 | a0001c0001t0003g0351a0001c0001t0003g0361 | 2 | HG00597.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.-93+10013T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135499876 | ||||||
| chr7:135499976
|
C | T | 1 | a0002c0002t0001g0079 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-93+9913G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135499976 | ||||||
| chr7:135500206
|
A | T | 2 | a0002c0002t0001g0036a0002c0002t0001g0087 | 2 | NA19003.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-93+9683T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135500206 | ||||||
| chr7:135500471
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+9418A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135500471 | ||||||
| chr7:135500472
|
T | A | 29 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(26): Show | 29 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.-93+9417A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135500472 | ||||||
| chr7:135500574
|
A | G | 3 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299 | 3 | HG02622.hp2 HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-93+9315T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135500574 | ||||||
| chr7:135500765
|
T | C | 4 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(1): Show | 4 | HG02818.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-93+9124A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135500765 | ||||||
| chr7:135500912
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-93+8977A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135500912 | ||||||
| chr7:135500948
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-93+8941G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135500948 | ||||||
| chr7:135500983
|
C | CT | 69 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0147others(66): Show | 69 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.-93+8905dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135500983 | ||||||
| chr7:135500983
|
C | CTT | 59 | a0001c0001t0001g0228a0001c0001t0001g0230a0001c0001t0001g0231others(56): Show | 59 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-93+8904_-93+8905d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135500983 | ||||||
| chr7:135501009
|
A | C | 1 | a0001c0010t0002g0326 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-93+8880T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135501009 | ||||||
| chr7:135501028
|
G | C | 1 | a0001c0001t0003g0361 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-93+8861C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135501028 | ||||||
| chr7:135501069
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0008g0350 | 2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-93+8820G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135501069 | ||||||
| chr7:135501114
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-93+8775T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135501114 | ||||||
| chr7:135501183
|
C | G | 2 | a0001c0001t0001g0191a0001c0001t0007g0225 | 2 | HG00733.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-93+8706G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135501183 | ||||||
| chr7:135501618
|
A | C | 2 | a0001c0001t0001g0324a0002c0002t0006g0002 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-93+8271T>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135501618 | ||||||
| chr7:135501623
|
C | A | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+8266G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135501623 | ||||||
| chr7:135501942
|
T | C | 1 | a0001c0010t0002g0326 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-93+7947A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135501942 | ||||||
| chr7:135502040
|
C | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0008g0350 | 3 | HG01243.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-93+7849G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502040 | ||||||
| chr7:135502084
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-93+7805G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502084 | ||||||
| chr7:135502092
|
C | T | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+7797G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502092 | ||||||
| chr7:135502330
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-93+7559G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502330 | ||||||
| chr7:135502400
|
T | C | 1 | a0002c0002t0001g0304 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-93+7489A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502400 | ||||||
| chr7:135502566
|
A | G | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+7323T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502566 | ||||||
| chr7:135502571
|
T | C | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+7318A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502571 | ||||||
| chr7:135502581
|
G | A | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+7308C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502581 | ||||||
| chr7:135502583
|
A | G | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+7306T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502583 | ||||||
| chr7:135502589
|
C | T | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+7300G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502589 | ||||||
| chr7:135502590
|
A | G | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+7299T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502590 | ||||||
| chr7:135502631
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-93+7258T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502631 | ||||||
| chr7:135502681
|
T | C | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+7208A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502681 | ||||||
| chr7:135502689
|
G | A | 1 | a0002c0002t0001g0129 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-93+7200C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502689 | ||||||
| chr7:135502816
|
C | CA | 35 | a0001c0001t0001g0005a0001c0001t0001g0118a0001c0001t0001g0171others(32): Show | 35 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.-93+7072dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502816 | ||||||
| chr7:135502816
|
CA | C | 24 | a0001c0001t0001g0141a0001c0001t0001g0165a0001c0001t0001g0231others(21): Show | 24 | HG00597.hp2 HG01515.hp2 HG01517.hp1 others(21): Show |
intron_variant | MODIFIER | c.-93+7072delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502816 | ||||||
| chr7:135502994
|
A | G | 64 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(61): Show | 64 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.-93+6895T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135502994 | ||||||
| chr7:135503126
|
C | A | 1 | a0002c0002t0001g0023 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-93+6763G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135503126 | ||||||
| chr7:135503325
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-93+6564G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135503325 | ||||||
| chr7:135503333
|
T | C | 236 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(233): Show | 236 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.-93+6556A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135503333 | ||||||
| chr7:135503456
|
C | CA | 9 | a0001c0001t0001g0297a0001c0001t0001g0298a0001c0001t0001g0299others(6): Show | 9 | HG02486.hp2 HG02622.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-93+6432dupT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135503456 | ||||||
| chr7:135503456
|
C | CAA | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+6431_-93+6432d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135503456 | ||||||
| chr7:135503456
|
CA | C | 8 | a0001c0001t0001g0229a0001c0001t0002g0135a0001c0001t0002g0136others(5): Show | 8 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-93+6432delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135503456 | ||||||
| chr7:135503479
|
C | A | 20 | a0001c0001t0001g0141a0001c0001t0001g0306a0001c0001t0001g0307others(17): Show | 20 | HG00597.hp2 HG02083.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+6410G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135503479 | ||||||
| chr7:135503722
|
T | C | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+6167A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135503722 | ||||||
| chr7:135503839
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-93+6050A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135503839 | ||||||
| chr7:135504160
|
A | G | 3 | a0002c0002t0001g0025a0002c0002t0001g0026a0002c0002t0001g0027 | 3 | NA18986.hp2 NA18998.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-93+5729T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504160 | ||||||
| chr7:135504190
|
T | C | 5 | a0002c0002t0001g0300a0002c0002t0001g0301a0002c0002t0001g0302others(2): Show | 5 | HG02055.hp1 HG03041.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+5699A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504190 | ||||||
| chr7:135504254
|
T | C | 7 | a0001c0001t0002g0120a0001c0001t0002g0121a0001c0001t0002g0122others(4): Show | 7 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(4): Show |
intron_variant | MODIFIER | c.-93+5635A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504254 | ||||||
| chr7:135504263
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-93+5626A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504263 | ||||||
| chr7:135504295
|
A | AT | 8 | a0001c0001t0001g0151a0001c0001t0001g0164a0001c0001t0001g0228others(5): Show | 8 | HG02486.hp1 HG02717.hp2 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.-93+5593dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504295 | ||||||
| chr7:135504451
|
ACATCCGG others(327): Show |
A | 139 | a0001c0001t0001g0141a0001c0001t0001g0145a0001c0001t0001g0146others(136): Show | 139 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.-93+5104_-93+5437d others(2): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504451 | ||||||
| chr7:135504462
|
A | AT | 6 | a0001c0001t0001g0118a0001c0001t0002g0117a0001c0003t0002g0181others(3): Show | 6 | HG01106.hp1 HG01255.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+5426dupA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504462 | ||||||
| chr7:135504462
|
A | ATT | 8 | a0001c0001t0001g0004a0001c0001t0001g0176a0001c0001t0001g0177others(5): Show | 8 | HG00673.hp2 HG01069.hp1 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-93+5425_-93+5426d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504462 | ||||||
| chr7:135504462
|
AT | A | 84 | a0001c0001t0002g0131a0001c0001t0002g0132a0001c0001t0002g0133others(81): Show | 84 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.-93+5426delA | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504462 | ||||||
| chr7:135504462
|
ATT | A | 10 | a0002c0002t0001g0087a0002c0002t0001g0088a0002c0002t0001g0089others(7): Show | 10 | HG02257.hp2 NA18747.hp1 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.-93+5425_-93+5426d others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504462 | ||||||
| chr7:135504478
|
T | A | 1 | a0002c0002t0001g0095 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-93+5411A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504478 | ||||||
| chr7:135504484
|
T | A | 7 | a0001c0001t0001g0017a0001c0001t0001g0115a0001c0001t0001g0173others(4): Show | 7 | HG00099.hp2 HG00621.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.-93+5405A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504484 | ||||||
| chr7:135504484
|
T | TA | 13 | a0001c0001t0001g0016a0001c0001t0001g0164a0001c0001t0001g0165others(10): Show | 13 | HG00099.hp1 HG01074.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.-93+5404_-93+5405i others(3): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504484 | ||||||
| chr7:135504484
|
T | TTA | 56 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(53): Show | 56 | HG00280.hp1 HG00323.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.-93+5404_-93+5405i others(4): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504484 | ||||||
| chr7:135504484
|
T | TTTA | 21 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0150others(18): Show | 21 | HG00733.hp1 HG01358.hp2 HG01433.hp1 others(18): Show |
intron_variant | MODIFIER | c.-93+5404_-93+5405i others(5): Show |
CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504484 | ||||||
| chr7:135504496
|
A | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-93+5393T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504496 | ||||||
| chr7:135504549
|
G | C | 96 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(93): Show | 96 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.-93+5340C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504549 | ||||||
| chr7:135504569
|
C | G | 1 | a0001c0001t0001g0149 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-93+5320G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504569 | ||||||
| chr7:135504574
|
C | A | 12 | a0002c0002t0001g0096a0002c0002t0001g0097a0002c0002t0001g0098others(9): Show | 12 | HG01071.hp1 HG01256.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.-93+5315G>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504574 | ||||||
| chr7:135504612
|
A | G | 1 | a0002c0002t0001g0018 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-93+5277T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504612 | ||||||
| chr7:135504641
|
T | C | 4 | a0001c0001t0001g0176a0001c0001t0001g0177a0001c0001t0001g0178others(1): Show | 4 | HG00673.hp2 HG02083.hp1 NA19078.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+5248A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504641 | ||||||
| chr7:135504690
|
T | A | 1 | a0001c0001t0001g0227 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-93+5199A>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504690 | ||||||
| chr7:135504775
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-93+5114G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504775 | ||||||
| chr7:135504907
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-93+4982G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135504907 | ||||||
| chr7:135505061
|
A | G | 1 | a0001c0001t0001g0003 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-93+4828T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135505061 | ||||||
| chr7:135505114
|
G | A | 1 | a0001c0001t0001g0305 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-93+4775C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135505114 | ||||||
| chr7:135505176
|
C | T | 50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(47): Show | 50 | HG00642.hp2 HG00673.hp2 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.-93+4713G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135505176 | ||||||
| chr7:135505265
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(1): Show | 4 | HG02258.hp2 HG02622.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+4624C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135505265 | ||||||
| chr7:135505357
|
A | G | 2 | a0001c0001t0001g0324a0002c0002t0006g0002 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-93+4532T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135505357 | ||||||
| chr7:135505404
|
T | C | 8 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(5): Show | 8 | HG02258.hp1 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-93+4485A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135505404 | ||||||
| chr7:135505494
|
G | C | 9 | a0001c0001t0001g0310a0001c0001t0001g0312a0001c0001t0001g0313others(6): Show | 9 | HG00323.hp2 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-93+4395C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135505494 | ||||||
| chr7:135505516
|
C | T | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+4373G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135505516 | ||||||
| chr7:135506017
|
G | A | 1 | a0001c0001t0001g0319 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-93+3872C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506017 | ||||||
| chr7:135506210
|
T | C | 1 | a0001c0001t0001g0320 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-93+3679A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506210 | ||||||
| chr7:135506410
|
G | C | 99 | a0001c0001t0001g0321a0002c0002t0001g0018a0002c0002t0001g0019others(96): Show | 99 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.-93+3479C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506410 | ||||||
| chr7:135506624
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-93+3265G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506624 | ||||||
| chr7:135506716
|
C | T | 1 | a0001c0001t0001g0348 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-93+3173G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506716 | ||||||
| chr7:135506802
|
C | G | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG01243.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-93+3087G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506802 | ||||||
| chr7:135506830
|
A | G | 14 | a0001c0001t0001g0141a0001c0001t0001g0327a0001c0001t0001g0328others(11): Show | 14 | HG00597.hp2 HG02083.hp2 NA18939.hp1 others(11): Show |
intron_variant | MODIFIER | c.-93+3059T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506830 | ||||||
| chr7:135506877
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-93+3012C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506877 | ||||||
| chr7:135506957
|
A | G | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+2932T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506957 | ||||||
| chr7:135506993
|
C | T | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+2896G>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135506993 | ||||||
| chr7:135507022
|
T | C | 4 | a0002c0002t0001g0108a0002c0002t0001g0109a0002c0002t0001g0110others(1): Show | 4 | HG00438.hp1 NA18956.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.-93+2867A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135507022 | ||||||
| chr7:135507091
|
T | C | 1 | a0001c0001t0001g0323 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-93+2798A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135507091 | ||||||
| chr7:135507711
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0144 | 2 | HG01123.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.-93+2178T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135507711 | ||||||
| chr7:135507849
|
A | T | 1 | a0001c0001t0001g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-93+2040T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135507849 | ||||||
| chr7:135508281
|
G | T | 34 | a0001c0001t0001g0141a0001c0001t0001g0324a0001c0001t0001g0327others(31): Show | 34 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.-93+1608C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135508281 | ||||||
| chr7:135508543
|
G | T | 2 | a0001c0001t0001g0324a0002c0002t0006g0002 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-93+1346C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135508543 | ||||||
| chr7:135508683
|
G | A | 2 | a0001c0001t0001g0324a0002c0002t0006g0002 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-93+1206C>T | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135508683 | ||||||
| chr7:135508721
|
A | G | 6 | a0001c0001t0002g0135a0001c0001t0002g0136a0001c0001t0002g0137others(3): Show | 6 | HG02486.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.-93+1168T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135508721 | ||||||
| chr7:135508930
|
GA | G | 18 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(15): Show | 18 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+958delT | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135508930 | ||||||
| chr7:135509024
|
T | C | 1 | a0001c0001t0001g0348 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-93+865A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509024 | ||||||
| chr7:135509266
|
A | T | 5 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(2): Show | 5 | HG02486.hp2 HG02818.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-93+623T>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509266 | ||||||
| chr7:135509306
|
T | C | 1 | a0001c0008t0001g0325 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-93+583A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509306 | ||||||
| chr7:135509453
|
G | T | 123 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(120): Show | 123 | HG00280.hp1 HG00438.hp1 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.-93+436C>A | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509453 | ||||||
| chr7:135509518
|
G | C | 20 | a0001c0001t0001g0329a0001c0001t0001g0330a0001c0001t0001g0331others(17): Show | 20 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.-93+371C>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509518 | ||||||
| chr7:135509530
|
T | C | 1 | a0001c0010t0002g0326 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-93+359A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509530 | ||||||
| chr7:135509555
|
C | G | 3 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115 | 3 | HG00621.hp2 HG01433.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.-93+334G>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509555 | ||||||
| chr7:135509692
|
T | G | 34 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0329others(31): Show | 34 | HG00597.hp2 HG00642.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.-93+197A>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509692 | ||||||
| chr7:135509865
|
A | G | 110 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(107): Show | 110 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.-93+24T>C | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509865 | ||||||
| chr7:135509880
|
T | C | 1 | a0001c0003t0002g0349 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-93+9A>G | CNOT4 | ENSG00000080802.21 | transcript | ENST00000541284.6 | protein_coding | 1/11 | chr7 | 135509880 |