| geneid | 57472 |
|---|---|
| ensemblid | ENSG00000113300.13 |
| hgncid | 14099 |
| symbol | CNOT6 |
| name | CCR4-NOT transcription complex subunit 6 |
| refseq_nuc | NM_001370472.1 |
| refseq_prot | NP_001357401.1 |
| ensembl_nuc | ENST00000261951.9 |
| ensembl_prot | ENSP00000261951.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 180494379 |
| end | 180578358 |
| strand | + |
| ver | v1.2 |
| region | chr5:180494379-180578358 |
| region5000 | chr5:180489379-180583358 |
| regionname0 | CNOT6_chr5_180494379_180578358 |
| regionname5000 | CNOT6_chr5_180489379_180583358 |
| 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 | 557 | 332 | 86 | 70 | 126 | 12 | 36 | 84 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0002 | 0/0 | 557 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| 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 | 1674 | 294 | 57 | 63 | 126 | 12 | 35 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| c0002 | 1/0 | 1674 | 35 | 26 | 7 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| c0003 | 0/0 | 1674 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| c0004 | 0/0 | 1674 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| c0005 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4554 | 66 | 6 | 15 | 34 | 3 | 8 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0002 | 0/0 | 4548 | 52 | 2 | 11 | 35 | 2 | 2 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0003 | 0/0 | 4558 | 17 | 1 | 8 | 4 | 1 | 3 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0004 | 1/0 | 4546 | 16 | 13 | 1 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0005 | 0/1 | 4550 | 15 | 11 | 0 | 2 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0006 | 0/0 | 4553 | 15 | 3 | 3 | 5 | 0 | 4 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0007 | 0/0 | 4549 | 13 | 0 | 1 | 12 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0008 | 0/0 | 4556 | 12 | 0 | 2 | 6 | 1 | 3 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0009 | 0/0 | 4560 | 10 | 1 | 0 | 5 | 0 | 4 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0010 | 0/0 | 4556 | 8 | 0 | 1 | 2 | 1 | 4 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0011 | 0/0 | 4554 | 6 | 6 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0012 | 0/0 | 4558 | 6 | 1 | 2 | 2 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0013 | 0/0 | 4552 | 6 | 4 | 2 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0014 | 0/0 | 4554 | 5 | 3 | 1 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0015 | 0/0 | 4553 | 5 | 4 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0016 | 0/0 | 4555 | 5 | 0 | 2 | 3 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0017 | 0/0 | 4552 | 5 | 5 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0018 | 0/0 | 4559 | 4 | 0 | 2 | 0 | 2 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0019 | 0/0 | 4550 | 4 | 0 | 0 | 4 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0020 | 0/0 | 4546 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0021 | 0/0 | 4548 | 3 | 0 | 0 | 0 | 0 | 3 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0022 | 0/0 | 4554 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0023 | 0/0 | 4562 | 3 | 2 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0024 | 0/0 | 4547 | 3 | 0 | 2 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0025 | 0/0 | 4558 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0026 | 0/0 | 4556 | 2 | 1 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0027 | 0/0 | 4558 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0028 | 0/0 | 4562 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0029 | 0/0 | 4556 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0030 | 0/0 | 4559 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0031 | 0/0 | 4557 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0032 | 0/0 | 4545 | 2 | 0 | 1 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0033 | 0/0 | 4552 | 2 | 1 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0034 | 0/0 | 4531 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0035 | 0/0 | 4562 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0036 | 0/0 | 4560 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0037 | 0/0 | 4556 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0038 | 0/0 | 4560 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0039 | 0/0 | 4550 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0040 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0041 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0042 | 0/0 | 4548 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0043 | 0/0 | 4558 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0044 | 0/0 | 4557 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0045 | 0/0 | 4566 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0046 | 0/0 | 4554 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0047 | 0/0 | 4554 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0048 | 0/0 | 4554 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0049 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0050 | 0/0 | 4548 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0051 | 0/0 | 4548 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0052 | 0/0 | 4548 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0053 | 0/0 | 4557 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0054 | 0/0 | 4553 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0055 | 0/0 | 4551 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0056 | 0/0 | 4556 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0057 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0058 | 0/0 | 4548 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0059 | 0/0 | 4554 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0060 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0061 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0062 | 0/0 | 4550 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0063 | 0/0 | 4548 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| t0064 | 0/0 | 4554 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| 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 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| 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 | 1674 | 294 | 57 | 63 | 126 | 12 | 35 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0002 | 1/0 | 1674 | 35 | 26 | 7 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0003 | 0/0 | 1674 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0005 | 0/0 | 1674 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0002c0004 | 0/0 | 1674 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6227 | 65 | 6 | 15 | 33 | 3 | 8 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0002 | 0/0 | 6221 | 44 | 1 | 5 | 35 | 2 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0003 | 0/0 | 6231 | 17 | 1 | 8 | 4 | 1 | 3 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0005 | 0/1 | 6223 | 5 | 1 | 0 | 2 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0006 | 0/0 | 6226 | 15 | 3 | 3 | 5 | 0 | 4 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0007 | 0/0 | 6222 | 13 | 0 | 1 | 12 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0008 | 0/0 | 6229 | 12 | 0 | 2 | 6 | 1 | 3 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0009 | 0/0 | 6233 | 10 | 1 | 0 | 5 | 0 | 4 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0010 | 0/0 | 6229 | 8 | 0 | 1 | 2 | 1 | 4 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0011 | 0/0 | 6227 | 6 | 6 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0012 | 0/0 | 6231 | 6 | 1 | 2 | 2 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0013 | 0/0 | 6225 | 6 | 4 | 2 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0014 | 0/0 | 6227 | 5 | 3 | 1 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0015 | 0/0 | 6226 | 5 | 4 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0016 | 0/0 | 6228 | 5 | 0 | 2 | 3 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0017 | 0/0 | 6225 | 5 | 5 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0018 | 0/0 | 6232 | 4 | 0 | 2 | 0 | 2 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0019 | 0/0 | 6223 | 4 | 0 | 0 | 4 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0021 | 0/0 | 6221 | 3 | 0 | 0 | 0 | 0 | 3 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0022 | 0/0 | 6227 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0023 | 0/0 | 6235 | 3 | 2 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0024 | 0/0 | 6220 | 3 | 0 | 2 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0025 | 0/0 | 6231 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0026 | 0/0 | 6229 | 2 | 1 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0027 | 0/0 | 6231 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0028 | 0/0 | 6235 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0029 | 0/0 | 6229 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0030 | 0/0 | 6232 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0031 | 0/0 | 6230 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0032 | 0/0 | 6218 | 2 | 0 | 1 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0033 | 0/0 | 6225 | 2 | 1 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0034 | 0/0 | 6204 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0035 | 0/0 | 6235 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0036 | 0/0 | 6233 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0037 | 0/0 | 6229 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0038 | 0/0 | 6233 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0039 | 0/0 | 6223 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0040 | 0/0 | 6223 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0041 | 0/0 | 6221 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0042 | 0/0 | 6221 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0043 | 0/0 | 6231 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0044 | 0/0 | 6230 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0045 | 0/0 | 6239 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0046 | 0/0 | 6227 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0047 | 0/0 | 6227 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0048 | 0/0 | 6227 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0049 | 0/0 | 6221 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0050 | 0/0 | 6221 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0051 | 0/0 | 6221 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0052 | 0/0 | 6221 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0053 | 0/0 | 6230 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0054 | 0/0 | 6226 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0055 | 0/0 | 6224 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0056 | 0/0 | 6229 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0057 | 0/0 | 6221 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0058 | 0/0 | 6221 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0059 | 0/0 | 6227 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0060 | 0/0 | 6223 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0061 | 0/0 | 6223 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0062 | 0/0 | 6223 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0063 | 0/0 | 6221 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0001t0064 | 0/0 | 6227 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0002t0002 | 0/0 | 6221 | 8 | 1 | 6 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0002t0004 | 1/0 | 6219 | 14 | 12 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0002t0005 | 0/0 | 6223 | 10 | 10 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0002t0020 | 0/0 | 6219 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0003t0022 | 0/0 | 6227 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0001c0005t0004 | 0/0 | 6219 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0002c0004t0001 | 0/0 | 6227 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| a0002c0004t0004 | 0/0 | 6219 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | copy fasta | chr5 | 180489379 | 180583358 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0005g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0010g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0010g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0010g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0010g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0010g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0010g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0010g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0010g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0011g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0011g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0011g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0011g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0011g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0011g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0012g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0012g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0012g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0012g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0012g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0012g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0013g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0013g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0013g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0013g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0013g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0013g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0014g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0014g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0014g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0014g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0014g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0015g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0015g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0015g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0015g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0015g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0016g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0016g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0016g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0016g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0016g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0017g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0017g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0017g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0017g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0017g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0018g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0018g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0018g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0018g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0019g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0019g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0019g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0019g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0021g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0021g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0021g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0022g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0023g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0023g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0023g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0024g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0024g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0024g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0025g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0025g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0026g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0026g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0027g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0027g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0028g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0028g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0029g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0029g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0030g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0030g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0031g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0031g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0032g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0032g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0033g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0033g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0034g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0035g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0036g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0037g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0038g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0039g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0040g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0041g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0042g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0043g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0044g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0045g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0046g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0047g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0048g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0049g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0050g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0051g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0052g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0053g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0054g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0055g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0056g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0057g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0058g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0059g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0060g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0061g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0062g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0063g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0064g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0235 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0020g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0020g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0020g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0003t0022g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0003t0022g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0005t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0002c0004t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0002c0004t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0018 | g0004 | EUR | GBR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0249 | EUR | GBR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0259 | EUR | FIN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00280 | hp2 | a0001 | c0001 | t0014 | g0167 | EUR | FIN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00408 | hp1 | a0001 | c0001 | t0006 | g0122 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00544 | hp2 | a0001 | c0001 | t0012 | g0112 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00609 | hp1 | a0001 | c0001 | t0058 | g0095 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00609 | hp2 | a0001 | c0001 | t0007 | g0141 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00639 | hp1 | a0001 | c0001 | t0050 | g0089 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00639 | hp2 | a0001 | c0001 | t0014 | g0174 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00642 | hp2 | a0001 | c0001 | t0013 | g0256 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00673 | hp2 | a0001 | c0001 | t0008 | g0276 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00733 | hp2 | a0001 | c0001 | t0031 | g0133 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00735 | hp1 | a0001 | c0001 | t0055 | g0153 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00735 | hp2 | a0001 | c0001 | t0008 | g0297 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00738 | hp1 | a0001 | c0001 | t0018 | g0007 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00738 | hp2 | a0001 | c0001 | t0010 | g0198 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00741 | hp2 | a0001 | c0001 | t0037 | g0171 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0034 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01074 | hp2 | a0001 | c0001 | t0031 | g0132 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0035 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01109 | hp1 | a0001 | c0001 | t0030 | g0131 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01109 | hp2 | a0001 | c0001 | t0030 | g0152 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01167 | hp1 | a0001 | c0002 | t0004 | g0049 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01167 | hp2 | a0001 | c0001 | t0027 | g0190 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01168 | hp1 | a0001 | c0001 | t0016 | g0116 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01168 | hp2 | a0001 | c0001 | t0024 | g0118 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01169 | hp1 | a0001 | c0001 | t0016 | g0120 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01169 | hp2 | a0001 | c0001 | t0027 | g0186 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01243 | hp1 | a0001 | c0001 | t0015 | g0127 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01243 | hp2 | a0001 | c0001 | t0033 | g0031 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0125 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0044 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01257 | hp1 | a0001 | c0001 | t0032 | g0128 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0045 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01261 | hp1 | a0001 | c0001 | t0026 | g0223 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01346 | hp2 | a0001 | c0001 | t0024 | g0151 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01358 | hp1 | a0001 | c0001 | t0018 | g0006 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0181 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01361 | hp2 | a0001 | c0001 | t0048 | g0311 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0046 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0197 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0207 | EUR | IBS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0313 | EUR | IBS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01516 | hp1 | a0001 | c0001 | t0008 | g0317 | EUR | IBS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01516 | hp2 | a0001 | c0001 | t0010 | g0208 | EUR | IBS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01884 | hp1 | a0001 | c0001 | t0026 | g0221 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0210 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01891 | hp2 | a0001 | c0002 | t0005 | g0022 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01975 | hp1 | a0001 | c0001 | t0042 | g0075 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01978 | hp1 | a0001 | c0001 | t0013 | g0271 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01978 | hp2 | a0001 | c0001 | t0008 | g0296 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01981 | hp1 | a0001 | c0001 | t0006 | g0136 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02004 | hp1 | a0001 | c0001 | t0051 | g0096 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0137 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02015 | hp1 | a0001 | c0001 | t0007 | g0129 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02027 | hp1 | a0001 | c0001 | t0009 | g0010 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02027 | hp2 | a0001 | c0001 | t0008 | g0303 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02055 | hp1 | a0001 | c0001 | t0015 | g0012 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02055 | hp2 | a0001 | c0003 | t0022 | g0222 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02071 | hp2 | a0001 | c0001 | t0039 | g0102 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02074 | hp1 | a0001 | c0001 | t0035 | g0017 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02083 | hp1 | a0001 | c0001 | t0036 | g0192 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02132 | hp1 | a0001 | c0001 | t0056 | g0266 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02132 | hp2 | a0001 | c0001 | t0059 | g0300 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02148 | hp1 | a0001 | c0001 | t0054 | g0145 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0170 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CDX | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | CDX | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | CDX | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | CDX | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02257 | hp1 | a0001 | c0001 | t0014 | g0175 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02257 | hp2 | a0001 | c0001 | t0061 | g0003 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02258 | hp1 | a0001 | c0001 | t0062 | g0030 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02258 | hp2 | a0001 | c0001 | t0064 | g0163 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02273 | hp1 | a0001 | c0001 | t0012 | g0321 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02273 | hp2 | a0001 | c0001 | t0012 | g0247 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02280 | hp1 | a0001 | c0001 | t0046 | g0011 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02280 | hp2 | a0001 | c0002 | t0004 | g0038 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02451 | hp1 | a0001 | c0002 | t0004 | g0058 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02451 | hp2 | a0001 | c0001 | t0040 | g0100 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02523 | hp2 | a0001 | c0001 | t0007 | g0143 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02572 | hp2 | a0001 | c0002 | t0005 | g0330 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0036 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02615 | hp2 | a0001 | c0001 | t0053 | g0117 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02622 | hp1 | a0001 | c0001 | t0017 | g0164 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02622 | hp2 | a0001 | c0002 | t0005 | g0025 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02630 | hp1 | a0001 | c0001 | t0045 | g0332 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0042 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02683 | hp1 | a0001 | c0001 | t0006 | g0124 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02683 | hp2 | a0001 | c0001 | t0010 | g0187 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0052 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02717 | hp1 | a0001 | c0002 | t0005 | g0028 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02717 | hp2 | a0001 | c0001 | t0013 | g0103 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02723 | hp1 | a0001 | c0002 | t0020 | g0054 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02735 | hp1 | a0001 | c0001 | t0021 | g0159 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02738 | hp1 | a0001 | c0001 | t0008 | g0298 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02738 | hp2 | a0001 | c0001 | t0021 | g0160 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02809 | hp1 | a0001 | c0002 | t0020 | g0055 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02809 | hp2 | a0001 | c0001 | t0060 | g0002 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02818 | hp1 | a0001 | c0001 | t0011 | g0216 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02818 | hp2 | a0001 | c0001 | t0013 | g0104 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02886 | hp1 | a0001 | c0001 | t0012 | g0279 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02886 | hp2 | a0001 | c0002 | t0005 | g0024 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02895 | hp1 | a0001 | c0002 | t0005 | g0021 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02895 | hp2 | a0001 | c0001 | t0017 | g0165 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02896 | hp1 | a0001 | c0001 | t0017 | g0166 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0156 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0053 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02922 | hp2 | a0001 | c0001 | t0025 | g0217 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02965 | hp1 | a0001 | c0001 | t0015 | g0115 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02965 | hp2 | a0001 | c0001 | t0011 | g0224 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02970 | hp1 | a0001 | c0002 | t0004 | g0051 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02970 | hp2 | a0001 | c0002 | t0004 | g0041 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02976 | hp1 | a0001 | c0001 | t0022 | g0225 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02976 | hp2 | a0001 | c0002 | t0005 | g0027 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0180 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03017 | hp2 | a0001 | c0001 | t0008 | g0295 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03098 | hp1 | a0001 | c0002 | t0004 | g0043 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03098 | hp2 | a0001 | c0001 | t0049 | g0333 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03130 | hp1 | a0001 | c0001 | t0017 | g0161 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03130 | hp2 | a0001 | c0001 | t0011 | g0214 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0039 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03139 | hp2 | a0001 | c0001 | t0015 | g0126 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03195 | hp1 | a0001 | c0001 | t0025 | g0219 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03195 | hp2 | a0001 | c0001 | t0014 | g0202 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0050 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0130 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03225 | hp1 | a0001 | c0001 | t0011 | g0213 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0201 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03453 | hp1 | a0001 | c0001 | t0011 | g0215 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03453 | hp2 | a0001 | c0005 | t0004 | g0019 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03486 | hp1 | a0001 | c0002 | t0020 | g0056 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03486 | hp2 | a0001 | c0001 | t0011 | g0212 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03491 | hp1 | a0001 | c0001 | t0043 | g0204 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03491 | hp2 | a0001 | c0001 | t0009 | g0173 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03540 | hp1 | a0001 | c0001 | t0041 | g0101 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03540 | hp2 | a0001 | c0002 | t0004 | g0057 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03579 | hp1 | a0001 | c0002 | t0005 | g0026 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0179 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03669 | hp2 | a0001 | c0001 | t0008 | g0228 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03704 | hp2 | a0001 | c0001 | t0009 | g0206 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03831 | hp1 | a0001 | c0001 | t0010 | g0182 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03831 | hp2 | a0001 | c0001 | t0021 | g0158 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0272 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03927 | hp1 | a0001 | c0001 | t0006 | g0324 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03942 | hp1 | a0001 | c0001 | t0009 | g0199 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03942 | hp2 | a0001 | c0001 | t0024 | g0157 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG04184 | hp1 | a0001 | c0001 | t0047 | g0242 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG04184 | hp2 | a0001 | c0001 | t0032 | g0154 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG04199 | hp1 | a0001 | c0001 | t0010 | g0209 | SAS | STU | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | STU | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG04204 | hp1 | a0001 | c0001 | t0009 | g0178 | SAS | STU | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | STU | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | STU | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG04228 | hp2 | a0001 | c0001 | t0006 | g0150 | SAS | STU | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18612 | hp1 | a0001 | c0001 | t0028 | g0327 | EAS | CHB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18612 | hp2 | a0001 | c0001 | t0023 | g0009 | EAS | CHB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | CHB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18747 | hp2 | a0001 | c0001 | t0016 | g0013 | EAS | CHB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18906 | hp1 | a0001 | c0001 | t0057 | g0059 | AFR | YRI | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18906 | hp2 | a0001 | c0001 | t0033 | g0033 | AFR | YRI | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18939 | hp2 | a0001 | c0001 | t0008 | g0288 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18941 | hp2 | a0001 | c0001 | t0052 | g0080 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18944 | hp1 | a0001 | c0001 | t0016 | g0331 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18944 | hp2 | a0001 | c0001 | t0008 | g0238 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18947 | hp1 | a0001 | c0001 | t0019 | g0286 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18950 | hp2 | a0001 | c0001 | t0007 | g0142 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18957 | hp2 | a0001 | c0001 | t0009 | g0014 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18961 | hp1 | a0001 | c0001 | t0009 | g0183 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18962 | hp2 | a0001 | c0001 | t0008 | g0262 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18963 | hp1 | a0001 | c0001 | t0007 | g0325 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18966 | hp1 | a0002 | c0004 | t0004 | g0252 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18966 | hp2 | a0001 | c0001 | t0007 | g0135 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18967 | hp2 | a0001 | c0001 | t0019 | g0292 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18968 | hp2 | a0001 | c0001 | t0016 | g0121 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18969 | hp1 | a0001 | c0001 | t0029 | g0234 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18969 | hp2 | a0002 | c0004 | t0001 | g0319 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18973 | hp1 | a0001 | c0001 | t0007 | g0149 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18977 | hp1 | a0001 | c0001 | t0009 | g0177 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18978 | hp1 | a0001 | c0001 | t0006 | g0146 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18980 | hp1 | a0001 | c0001 | t0010 | g0016 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18980 | hp2 | a0001 | c0001 | t0008 | g0285 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18982 | hp1 | a0001 | c0001 | t0029 | g0289 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18990 | hp1 | a0001 | c0001 | t0007 | g0140 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0147 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19004 | hp2 | a0001 | c0001 | t0034 | g0001 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19005 | hp2 | a0001 | c0001 | t0007 | g0155 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19012 | hp1 | a0001 | c0001 | t0007 | g0148 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19043 | hp1 | a0001 | c0001 | t0017 | g0162 | AFR | LWK | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0226 | AFR | LWK | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19054 | hp1 | a0001 | c0001 | t0007 | g0139 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19064 | hp1 | a0001 | c0001 | t0012 | g0264 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19064 | hp2 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19070 | hp2 | a0001 | c0001 | t0028 | g0233 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19077 | hp1 | a0001 | c0001 | t0005 | g0109 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19077 | hp2 | a0001 | c0001 | t0019 | g0257 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19080 | hp2 | a0001 | c0001 | t0007 | g0134 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19081 | hp1 | a0001 | c0001 | t0019 | g0258 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19081 | hp2 | a0001 | c0001 | t0006 | g0144 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19085 | hp1 | a0001 | c0001 | t0009 | g0015 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19090 | hp2 | a0001 | c0001 | t0010 | g0193 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19240 | hp1 | a0001 | c0001 | t0013 | g0107 | AFR | YRI | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19240 | hp2 | a0001 | c0002 | t0004 | g0040 | AFR | YRI | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0123 | AFR | ASW | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20129 | hp2 | a0001 | c0001 | t0015 | g0119 | AFR | ASW | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0085 | EUR | TSI | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20752 | hp2 | a0001 | c0001 | t0012 | g0255 | EUR | TSI | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20805 | hp1 | a0001 | c0001 | t0018 | g0005 | EUR | TSI | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0083 | EUR | TSI | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0323 | SAS | GIH | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20905 | hp2 | a0001 | c0001 | t0010 | g0194 | SAS | GIH | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0008 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0048 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02109 | hp1 | a0001 | c0001 | t0038 | g0218 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02109 | hp2 | a0001 | c0001 | t0023 | g0203 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02486 | hp1 | a0001 | c0002 | t0005 | g0023 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02486 | hp2 | a0001 | c0001 | t0044 | g0169 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03471 | hp1 | a0001 | c0002 | t0004 | g0037 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03471 | hp2 | a0001 | c0001 | t0063 | g0230 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG06807 | hp1 | a0001 | c0001 | t0013 | g0106 | AFR | USA | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG06807 | hp2 | a0001 | c0003 | t0022 | g0220 | AFR | USA | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20300 | hp1 | a0001 | c0002 | t0005 | g0047 | AFR | USA | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20300 | hp2 | a0001 | c0001 | t0014 | g0185 | AFR | USA | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | LWK | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA21309 | hp2 | a0001 | c0001 | t0023 | g0196 | AFR | LWK | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0081 | REF | REF | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0004 | g0235 | REF | REF | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180529302
|
C | T | 1 | a0002 | 2 | NA18966.hp1 NA18969.hp2 |
missense_variant | MODERATE | c.26C>T | p.Pro9Leu | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/12 | 413/6219 | 26/1674 | 9/557 | chr5 | 180529302 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180567099
|
G | A | 1 | a0001c0003 | 2 | HG02055.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.729G>A | p.Thr243Thr | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 8/12 | 1116/6219 | 729/1674 | 243/557 | chr5 | 180567099 | ||
| chr5:180569111
|
C | T | 3 | a0001c0001a0001c0003a0002c0004 | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
splice_region_variant&synonymous_variant | LOW | c.1029C>T | p.Ser343Ser | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/12 | 1416/6219 | 1029/1674 | 343/557 | chr5 | 180569111 | ||
| chr5:180571372
|
G | A | 1 | a0001c0005 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.1401G>A | p.Lys467Lys | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/12 | 1788/6219 | 1401/1674 | 467/557 | chr5 | 180571372 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180494391
|
C | T | 1 | a0001c0001t0064 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-375C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/12 | 34886 | chr5 | 180494391 | |||||
| chr5:180494461
|
TGGCGGCG others(16): Show |
T | 1 | a0001c0001t0034 | 1 | NA19004.hp2 | 5_prime_UTR_variant | MODIFIER | c.-300_-278delGCGGCG others(17): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/12 | 34789 | INFO_REALIGN_3_PRIME | chr5 | 180494461 | ||||
| chr5:180494503
|
C | T | 3 | a0001c0001t0033a0001c0001t0062a0001c0001t0063 | 4 | HG01243.hp2 HG02258.hp1 HG03471.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-263C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/12 | 34774 | chr5 | 180494503 | |||||
| chr5:180494513
|
A | C | 2 | a0001c0001t0017a0001c0001t0064 | 6 | HG02258.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-253A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/12 | 34764 | chr5 | 180494513 | |||||
| chr5:180494563
|
G | A | 1 | a0001c0002t0020 | 3 | HG02723.hp1 HG02809.hp1 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-203G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/12 | 34714 | chr5 | 180494563 | |||||
| chr5:180494726
|
A | C | 2 | a0001c0001t0060a0001c0001t0061 | 2 | HG02257.hp2 HG02809.hp2 |
5_prime_UTR_variant | MODIFIER | c.-40A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/12 | 34551 | chr5 | 180494726 | |||||
| chr5:180574338
|
A | G | 1 | a0001c0001t0059 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*138A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 138 | chr5 | 180574338 | |||||
| chr5:180574389
|
G | A | 1 | a0001c0001t0018 | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*189G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 189 | chr5 | 180574389 | |||||
| chr5:180574659
|
A | G | 1 | a0001c0001t0058 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*459A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 459 | chr5 | 180574659 | |||||
| chr5:180574737
|
A | T | 1 | a0001c0001t0018 | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*537A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 537 | chr5 | 180574737 | |||||
| chr5:180574867
|
G | C | 2 | a0001c0001t0035a0001c0001t0036 | 2 | HG02074.hp1 HG02083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*667G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 667 | chr5 | 180574867 | |||||
| chr5:180574872
|
C | T | 1 | a0001c0001t0057 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*672C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 672 | chr5 | 180574872 | |||||
| chr5:180574938
|
T | C | 1 | a0001c0001t0037 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*738T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 738 | chr5 | 180574938 | |||||
| chr5:180574980
|
C | G | 1 | a0001c0001t0056 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*780C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 780 | chr5 | 180574980 | |||||
| chr5:180575181
|
A | G | 1 | a0001c0002t0020 | 3 | HG02723.hp1 HG02809.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*981A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 981 | chr5 | 180575181 | |||||
| chr5:180575433
|
G | A | 8 | a0001c0001t0011a0001c0001t0021a0001c0001t0022others(5): Show | 18 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1233G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 1233 | chr5 | 180575433 | |||||
| chr5:180575452
|
T | TTTG | 1 | a0001c0001t0018 | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1273_*1275dupGTT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 1276 | INFO_REALIGN_3_PRIME | chr5 | 180575452 | ||||
| chr5:180575820
|
T | G | 1 | a0001c0001t0018 | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1620T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 1620 | chr5 | 180575820 | |||||
| chr5:180575849
|
A | C | 11 | a0001c0001t0006a0001c0001t0007a0001c0001t0015others(8): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1649A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 1649 | chr5 | 180575849 | |||||
| chr5:180575883
|
G | A | 3 | a0001c0001t0040a0001c0001t0041a0001c0001t0060 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1683G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 1683 | chr5 | 180575883 | |||||
| chr5:180575892
|
GT | G | 15 | a0001c0001t0006a0001c0001t0007a0001c0001t0015others(12): Show | 57 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1704delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 1704 | INFO_REALIGN_3_PRIME | chr5 | 180575892 | ||||
| chr5:180575938
|
G | A | 1 | a0001c0001t0042 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1738G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 1738 | chr5 | 180575938 | |||||
| chr5:180576085
|
C | T | 11 | a0001c0001t0006a0001c0001t0007a0001c0001t0015others(8): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1885C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 1885 | chr5 | 180576085 | |||||
| chr5:180576146
|
GT | G | 4 | a0001c0001t0018a0001c0001t0040a0001c0001t0041others(1): Show | 7 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1955delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 1955 | INFO_REALIGN_3_PRIME | chr5 | 180576146 | ||||
| chr5:180576664
|
A | G | 1 | a0001c0001t0052 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2464A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2464 | chr5 | 180576664 | |||||
| chr5:180576827
|
A | G | 1 | a0001c0001t0051 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2627A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2627 | chr5 | 180576827 | |||||
| chr5:180576995
|
A | G | 1 | a0001c0001t0011 | 6 | HG02818.hp1 HG02965.hp2 HG03130.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2795A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2795 | chr5 | 180576995 | |||||
| chr5:180577054
|
A | G | 1 | a0001c0001t0050 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2854A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2854 | chr5 | 180577054 | |||||
| chr5:180577154
|
T | A | 11 | a0001c0001t0003a0001c0001t0009a0001c0001t0010others(8): Show | 50 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*2954T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2954 | chr5 | 180577154 | |||||
| chr5:180577163
|
A | ATG | 12 | a0001c0001t0002a0001c0001t0021a0001c0001t0024others(9): Show | 66 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*2995_*2996dupGT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | ||||
| chr5:180577163
|
A | ATGTG | 8 | a0001c0001t0005a0001c0001t0007a0001c0001t0019others(5): Show | 36 | HG00609.hp2 HG01255.hp2 HG01891.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2993_*2996dupGTGT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | ||||
| chr5:180577163
|
A | ATGTGTG | 6 | a0001c0001t0013a0001c0001t0017a0001c0001t0033others(3): Show | 16 | HG00642.hp2 HG00735.hp1 HG01243.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2991_*2996dupGTGT others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | ||||
| chr5:180577163
|
A | ATGTGTGT others(1): Show |
11 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(8): Show | 93 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*2989_*2996dupGTGT others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | ||||
| chr5:180577163
|
A | ATGTGTGT others(3): Show |
6 | a0001c0001t0008a0001c0001t0010a0001c0001t0016others(3): Show | 29 | HG00673.hp2 HG00735.hp2 HG00738.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2987_*2996dupGTGT others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | ||||
| chr5:180577163
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0053 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2973_*2974insCGTG others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2974 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | ||||
| chr5:180577163
|
A | ATGTGTGT others(5): Show |
5 | a0001c0001t0003a0001c0001t0012a0001c0001t0027others(2): Show | 28 | HG00544.hp2 HG00733.hp2 HG01071.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2985_*2996dupGTGT others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | ||||
| chr5:180577163
|
A | ATGTGTGT others(7): Show |
3 | a0001c0001t0009a0001c0001t0030a0001c0001t0036 | 13 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2983_*2996dupGTGT others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | ||||
| chr5:180577163
|
A | ATGTGTGT others(9): Show |
3 | a0001c0001t0023a0001c0001t0028a0001c0001t0035 | 6 | HG02074.hp1 HG02109.hp2 NA18612.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2981_*2996dupGTGT others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | ||||
| chr5:180577163
|
A | ATGTGTGT others(13): Show |
1 | a0001c0001t0045 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2977_*2996dupGTGT others(16): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | ||||
| chr5:180577163
|
A | ATTGTGTG others(4): Show |
1 | a0001c0001t0044 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2964_*2965insTGTG others(7): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2965 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | ||||
| chr5:180577166
|
T | TGTGTGTG others(1): Show |
1 | a0001c0001t0015 | 5 | HG01243.hp1 HG02055.hp1 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2973_*2974insCGTG others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2974 | INFO_REALIGN_3_PRIME | chr5 | 180577166 | ||||
| chr5:180577173
|
G | GTGTGTGT others(5): Show |
1 | a0001c0001t0018 | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2984_*2985insTTGT others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2985 | INFO_REALIGN_3_PRIME | chr5 | 180577173 | ||||
| chr5:180577191
|
G | GTGTGTGT others(7): Show |
1 | a0001c0001t0038 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2996_*2997insGTGT others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577191 | ||||
| chr5:180577191
|
G | GTGTGTGT others(5): Show |
1 | a0001c0001t0025 | 2 | HG02922.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2996_*2997insGTGT others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577191 | ||||
| chr5:180577191
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0026 | 2 | HG01261.hp1 HG01884.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2996_*2997insGTGT others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577191 | ||||
| chr5:180577191
|
G | GTGTGTGT others(1): Show |
3 | a0001c0001t0011a0001c0001t0022a0001c0003t0022 | 9 | HG02055.hp2 HG02818.hp1 HG02965.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2996_*2997insGTTT others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577191 | ||||
| chr5:180577197
|
T | G | 1 | a0001c0001t0054 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2997T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | chr5 | 180577197 | |||||
| chr5:180577322
|
C | T | 1 | a0001c0001t0018 | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3122C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3122 | chr5 | 180577322 | |||||
| chr5:180577347
|
A | G | 1 | a0001c0001t0018 | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3147A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3147 | chr5 | 180577347 | |||||
| chr5:180577499
|
C | G | 1 | a0001c0001t0048 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3299C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3299 | chr5 | 180577499 | |||||
| chr5:180577544
|
G | A | 1 | a0001c0001t0046 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3344G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3344 | chr5 | 180577544 | |||||
| chr5:180577671
|
A | G | 1 | a0001c0001t0027 | 2 | HG01167.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3471A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3471 | chr5 | 180577671 | |||||
| chr5:180577740
|
C | T | 3 | a0001c0001t0017a0001c0001t0033a0001c0001t0064 | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3540C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3540 | chr5 | 180577740 | |||||
| chr5:180577742
|
A | C | 1 | a0001c0001t0043 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3542A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3542 | chr5 | 180577742 | |||||
| chr5:180577831
|
G | A | 1 | a0001c0001t0047 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3631G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3631 | chr5 | 180577831 | |||||
| chr5:180577936
|
C | T | 1 | a0001c0001t0019 | 4 | NA18947.hp1 NA18967.hp2 NA19077.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3736C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3736 | chr5 | 180577936 | |||||
| chr5:180578180
|
C | T | 1 | a0001c0001t0029 | 2 | NA18969.hp1 NA18982.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3980C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3980 | chr5 | 180578180 | |||||
| chr5:180578263
|
T | C | 9 | a0001c0001t0011a0001c0001t0021a0001c0001t0022others(6): Show | 19 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4063T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 4063 | chr5 | 180578263 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180494779
|
C | T | 1 | a0001c0001t0049g0333 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3+16C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180494779 | ||||||
| chr5:180494791
|
C | T | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+28C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180494791 | ||||||
| chr5:180494803
|
C | T | 1 | a0001c0001t0016g0331 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-3+40C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180494803 | ||||||
| chr5:180494907
|
T | C | 7 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(4): Show | 7 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+144T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180494907 | ||||||
| chr5:180494915
|
C | T | 1 | a0001c0002t0005g0330 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-3+152C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180494915 | ||||||
| chr5:180494935
|
G | A | 229 | a0001c0001t0001g0070a0001c0001t0001g0105a0001c0001t0001g0168others(226): Show | 229 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.-3+172G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180494935 | ||||||
| chr5:180494942
|
G | GCCCCGGG others(6): Show |
2 | a0001c0001t0001g0328a0001c0001t0001g0329 | 2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-3+190_-3+202dupCG others(11): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180494942 | |||||
| chr5:180494957
|
C | G | 1 | a0001c0001t0005g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-3+194C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180494957 | ||||||
| chr5:180494978
|
G | C | 2 | a0001c0001t0001g0227a0001c0001t0008g0228 | 2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-3+215G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180494978 | ||||||
| chr5:180495032
|
C | A | 1 | a0001c0001t0006g0008 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-3+269C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495032 | ||||||
| chr5:180495143
|
G | T | 1 | a0001c0001t0028g0327 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-3+380G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495143 | ||||||
| chr5:180495158
|
G | A | 2 | a0001c0001t0009g0010a0001c0001t0023g0009 | 2 | HG02027.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.-3+395G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495158 | ||||||
| chr5:180495180
|
T | C | 2 | a0001c0001t0060g0002a0001c0001t0061g0003 | 2 | HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-3+417T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495180 | ||||||
| chr5:180495218
|
C | T | 14 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(11): Show | 14 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3+455C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495218 | ||||||
| chr5:180495256
|
C | A | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-3+493C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495256 | ||||||
| chr5:180495284
|
T | G | 1 | a0001c0001t0015g0012 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-3+521T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495284 | ||||||
| chr5:180495313
|
A | G | 1 | a0001c0001t0003g0211 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-3+550A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495313 | ||||||
| chr5:180495506
|
G | A | 1 | a0001c0001t0016g0013 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-3+743G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495506 | ||||||
| chr5:180495515
|
T | G | 3 | a0001c0001t0009g0014a0001c0001t0009g0015a0001c0001t0010g0016 | 3 | NA18957.hp2 NA18980.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-3+752T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495515 | ||||||
| chr5:180495562
|
C | T | 1 | a0001c0001t0009g0210 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-3+799C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495562 | ||||||
| chr5:180495565
|
G | C | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+802G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495565 | ||||||
| chr5:180495883
|
T | G | 1 | a0001c0001t0035g0017 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-3+1120T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495883 | ||||||
| chr5:180495904
|
C | T | 58 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(55): Show | 58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+1141C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495904 | ||||||
| chr5:180496174
|
A | C | 3 | a0001c0001t0021g0158a0001c0001t0021g0159a0001c0001t0021g0160 | 3 | HG02735.hp1 HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-3+1411A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180496174 | ||||||
| chr5:180496261
|
A | C | 31 | a0001c0001t0003g0188a0001c0001t0003g0189a0001c0001t0003g0191others(28): Show | 31 | HG00738.hp2 HG01071.hp2 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.-3+1498A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180496261 | ||||||
| chr5:180496405
|
C | T | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+1642C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180496405 | ||||||
| chr5:180496416
|
G | A | 1 | a0001c0001t0002g0018 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-3+1653G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180496416 | ||||||
| chr5:180496549
|
A | T | 1 | a0001c0001t0001g0326 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-3+1786A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180496549 | ||||||
| chr5:180496576
|
C | T | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-3+1813C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180496576 | ||||||
| chr5:180496613
|
G | T | 1 | a0001c0001t0002g0114 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-3+1850G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180496613 | ||||||
| chr5:180496615
|
T | G | 1 | a0001c0001t0001g0229 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-3+1852T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180496615 | ||||||
| chr5:180497065
|
C | A | 6 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(3): Show | 6 | HG02258.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+2302C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497065 | ||||||
| chr5:180497325
|
C | CA | 159 | a0001c0001t0001g0070a0001c0001t0001g0168a0001c0001t0001g0227others(156): Show | 159 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.-3+2579dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180497325 | |||||
| chr5:180497325
|
C | CAAAA | 46 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(43): Show | 46 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.-3+2576_-3+2579dup others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180497325 | |||||
| chr5:180497354
|
G | T | 1 | a0001c0001t0003g0207 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-3+2591G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497354 | ||||||
| chr5:180497384
|
T | A | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+2621T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497384 | ||||||
| chr5:180497732
|
C | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+2969C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497732 | ||||||
| chr5:180497772
|
G | A | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-3+3009G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497772 | ||||||
| chr5:180497780
|
A | T | 1 | a0001c0001t0001g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-3+3017A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497780 | ||||||
| chr5:180497809
|
C | T | 1 | a0001c0001t0061g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-3+3046C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497809 | ||||||
| chr5:180497845
|
A | G | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-3+3082A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497845 | ||||||
| chr5:180497935
|
C | T | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+3172C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497935 | ||||||
| chr5:180497992
|
G | A | 1 | a0001c0001t0014g0167 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-3+3229G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497992 | ||||||
| chr5:180498157
|
G | A | 1 | a0001c0005t0004g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-3+3394G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498157 | ||||||
| chr5:180498212
|
G | A | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+3449G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498212 | ||||||
| chr5:180498223
|
T | G | 233 | a0001c0001t0001g0070a0001c0001t0001g0105a0001c0001t0001g0168others(230): Show | 233 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.-3+3460T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498223 | ||||||
| chr5:180498283
|
A | G | 18 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(15): Show | 18 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-3+3520A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498283 | ||||||
| chr5:180498329
|
A | C | 1 | a0001c0001t0005g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-3+3566A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498329 | ||||||
| chr5:180498350
|
A | G | 232 | a0001c0001t0001g0070a0001c0001t0001g0105a0001c0001t0001g0168others(229): Show | 232 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.-3+3587A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498350 | ||||||
| chr5:180498571
|
A | G | 113 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(110): Show | 113 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.-3+3808A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498571 | ||||||
| chr5:180498759
|
C | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+3996C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498759 | ||||||
| chr5:180498834
|
A | G | 115 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(112): Show | 115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-3+4071A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498834 | ||||||
| chr5:180498878
|
C | T | 1 | a0001c0001t0055g0153 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-3+4115C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498878 | ||||||
| chr5:180498946
|
C | G | 3 | a0001c0001t0024g0151a0001c0001t0024g0157a0001c0001t0030g0152 | 3 | HG01109.hp2 HG01346.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-3+4183C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498946 | ||||||
| chr5:180499010
|
T | C | 233 | a0001c0001t0001g0070a0001c0001t0001g0105a0001c0001t0001g0168others(230): Show | 233 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.-3+4247T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499010 | ||||||
| chr5:180499070
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-3+4307C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499070 | ||||||
| chr5:180499107
|
T | TTGGATAT others(6): Show |
1 | a0001c0001t0001g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-3+4346_-3+4358dup others(13): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180499107 | |||||
| chr5:180499141
|
A | G | 1 | a0001c0001t0009g0206 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-3+4378A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499141 | ||||||
| chr5:180499175
|
A | G | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-3+4412A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499175 | ||||||
| chr5:180499274
|
G | A | 1 | a0001c0005t0004g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-3+4511G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499274 | ||||||
| chr5:180499288
|
T | C | 58 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(55): Show | 58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+4525T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499288 | ||||||
| chr5:180499403
|
G | T | 1 | a0001c0001t0039g0102 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-3+4640G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499403 | ||||||
| chr5:180499429
|
G | C | 58 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(55): Show | 58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+4666G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499429 | ||||||
| chr5:180499479
|
G | A | 6 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(3): Show | 6 | HG02818.hp1 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+4716G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499479 | ||||||
| chr5:180499657
|
C | G | 1 | a0002c0004t0001g0319 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-3+4894C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499657 | ||||||
| chr5:180499693
|
G | A | 1 | a0001c0001t0016g0013 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-3+4930G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499693 | ||||||
| chr5:180499789
|
A | G | 1 | a0001c0001t0005g0113 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-3+5026A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499789 | ||||||
| chr5:180499839
|
T | C | 51 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(48): Show | 51 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.-3+5076T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499839 | ||||||
| chr5:180499908
|
G | A | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+5145G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499908 | ||||||
| chr5:180499943
|
T | C | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+5180T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499943 | ||||||
| chr5:180499957
|
C | T | 1 | a0001c0001t0006g0156 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-3+5194C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499957 | ||||||
| chr5:180500060
|
G | A | 58 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(55): Show | 58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+5297G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500060 | ||||||
| chr5:180500106
|
T | C | 1 | a0001c0001t0002g0020 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-3+5343T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500106 | ||||||
| chr5:180500106
|
TC | T | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+5349delC | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180500106 | |||||
| chr5:180500146
|
T | C | 9 | a0001c0002t0005g0021a0001c0002t0005g0022a0001c0002t0005g0023others(6): Show | 9 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3+5383T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500146 | ||||||
| chr5:180500233
|
C | G | 1 | a0001c0001t0003g0207 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-3+5470C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500233 | ||||||
| chr5:180500303
|
G | C | 51 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(48): Show | 51 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.-3+5540G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500303 | ||||||
| chr5:180500337
|
C | A | 2 | a0001c0001t0049g0333a0001c0005t0004g0019 | 2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-3+5574C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500337 | ||||||
| chr5:180500439
|
TTC | T | 49 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(46): Show | 49 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.-3+5678_-3+5679del others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180500439 | |||||
| chr5:180500441
|
C | CT | 209 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(206): Show | 209 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.-3+5692dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180500441 | |||||
| chr5:180500442
|
T | C | 49 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(46): Show | 49 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.-3+5679T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500442 | ||||||
| chr5:180500444
|
T | TC | 62 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(59): Show | 62 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3+5681_-3+5682ins others(1): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500444 | ||||||
| chr5:180500501
|
T | C | 333 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.-3+5738T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500501 | ||||||
| chr5:180500530
|
C | T | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-3+5767C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500530 | ||||||
| chr5:180500673
|
A | G | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+5910A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500673 | ||||||
| chr5:180500727
|
A | G | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-3+5964A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500727 | ||||||
| chr5:180500743
|
G | C | 171 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(168): Show | 171 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.-3+5980G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500743 | ||||||
| chr5:180500838
|
A | G | 55 | a0001c0001t0001g0070a0001c0001t0002g0018a0001c0001t0002g0020others(52): Show | 55 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.-3+6075A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500838 | ||||||
| chr5:180500849
|
G | T | 69 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(66): Show | 69 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.-3+6086G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500849 | ||||||
| chr5:180501173
|
C | T | 1 | a0001c0001t0009g0183 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-3+6410C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180501173 | ||||||
| chr5:180501243
|
C | T | 1 | a0001c0001t0006g0156 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-3+6480C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180501243 | ||||||
| chr5:180501383
|
C | T | 115 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(112): Show | 115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-3+6620C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180501383 | ||||||
| chr5:180501391
|
C | T | 18 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0006g0138others(15): Show | 18 | HG00609.hp2 HG01981.hp1 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.-3+6628C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180501391 | ||||||
| chr5:180501530
|
A | G | 1 | a0001c0001t0025g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-3+6767A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180501530 | ||||||
| chr5:180501760
|
A | G | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-3+6997A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180501760 | ||||||
| chr5:180501809
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-3+7046C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180501809 | ||||||
| chr5:180501920
|
G | A | 1 | a0001c0001t0005g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-3+7157G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180501920 | ||||||
| chr5:180501939
|
T | C | 2 | a0001c0002t0002g0034a0001c0002t0002g0035 | 2 | HG01069.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-3+7176T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180501939 | ||||||
| chr5:180502078
|
A | G | 2 | a0001c0001t0031g0132a0001c0001t0031g0133 | 2 | HG00733.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.-3+7315A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502078 | ||||||
| chr5:180502105
|
G | A | 17 | a0001c0001t0001g0070a0001c0001t0002g0018a0001c0001t0002g0029others(14): Show | 17 | HG00423.hp1 HG00621.hp1 NA18939.hp1 others(14): Show |
intron_variant | MODIFIER | c.-3+7342G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502105 | ||||||
| chr5:180502114
|
T | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+7351T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502114 | ||||||
| chr5:180502139
|
G | A | 59 | a0001c0001t0001g0070a0001c0001t0001g0105a0001c0001t0002g0018others(56): Show | 59 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.-3+7376G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502139 | ||||||
| chr5:180502192
|
C | T | 14 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(11): Show | 14 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3+7429C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502192 | ||||||
| chr5:180502204
|
C | G | 3 | a0001c0001t0030g0131a0001c0001t0031g0132a0001c0001t0031g0133 | 3 | HG00733.hp2 HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.-3+7441C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502204 | ||||||
| chr5:180502206
|
A | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+7443A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502206 | ||||||
| chr5:180502258
|
C | T | 1 | a0001c0001t0002g0099 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-3+7495C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502258 | ||||||
| chr5:180502308
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-3+7545C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502308 | ||||||
| chr5:180502343
|
C | T | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+7580C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502343 | ||||||
| chr5:180502364
|
TAGA | T | 8 | a0001c0001t0001g0105a0001c0001t0013g0103a0001c0001t0013g0104others(5): Show | 8 | HG01884.hp2 HG02717.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+7611_-3+7613del others(3): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180502364 | |||||
| chr5:180502386
|
A | C | 1 | a0001c0001t0003g0205 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-3+7623A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502386 | ||||||
| chr5:180502496
|
T | C | 1 | a0001c0002t0004g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-3+7733T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502496 | ||||||
| chr5:180502553
|
ATAG | A | 19 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(16): Show | 19 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-3+7794_-3+7796del others(3): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180502553 | |||||
| chr5:180502560
|
C | G | 1 | a0001c0001t0005g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-3+7797C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502560 | ||||||
| chr5:180502677
|
T | TTAGC | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+7917_-3+7918ins others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180502677 | |||||
| chr5:180502700
|
A | AT | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-3+7938dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180502700 | |||||
| chr5:180502768
|
C | G | 1 | a0001c0001t0008g0317 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-3+8005C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502768 | ||||||
| chr5:180502772
|
CAG | C | 6 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(3): Show | 6 | HG02258.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+8013_-3+8014del others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180502772 | |||||
| chr5:180502825
|
G | A | 51 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(48): Show | 51 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.-3+8062G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502825 | ||||||
| chr5:180502896
|
A | G | 1 | a0001c0002t0004g0058 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-3+8133A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502896 | ||||||
| chr5:180502919
|
C | G | 19 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(16): Show | 19 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-3+8156C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502919 | ||||||
| chr5:180503098
|
A | G | 1 | a0001c0001t0043g0204 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-3+8335A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503098 | ||||||
| chr5:180503106
|
C | G | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-3+8343C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503106 | ||||||
| chr5:180503262
|
C | CT | 55 | a0001c0001t0001g0168a0001c0001t0001g0318a0001c0001t0002g0073others(52): Show | 55 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.-3+8516dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180503262 | |||||
| chr5:180503407
|
G | T | 58 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(55): Show | 58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+8644G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503407 | ||||||
| chr5:180503427
|
C | G | 1 | a0001c0001t0003g0211 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-3+8664C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503427 | ||||||
| chr5:180503511
|
T | C | 115 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(112): Show | 115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-3+8748T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503511 | ||||||
| chr5:180503512
|
G | A | 1 | a0001c0001t0007g0134 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-3+8749G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503512 | ||||||
| chr5:180503516
|
C | T | 1 | a0001c0001t0001g0316 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-3+8753C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503516 | ||||||
| chr5:180503540
|
T | C | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+8777T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503540 | ||||||
| chr5:180503601
|
C | CT | 14 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(11): Show | 14 | HG00621.hp2 HG00741.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3+8862dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180503601 | |||||
| chr5:180503601
|
C | CTTT | 35 | a0001c0001t0006g0122a0001c0001t0006g0123a0001c0001t0006g0124others(32): Show | 35 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.-3+8860_-3+8862dup others(3): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180503601 | |||||
| chr5:180503601
|
C | CTTTT | 8 | a0001c0001t0006g0008a0001c0001t0006g0130a0001c0001t0006g0146others(5): Show | 8 | HG01123.hp1 HG02015.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+8859_-3+8862dup others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180503601 | |||||
| chr5:180503601
|
CT | C | 69 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0239others(66): Show | 69 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-3+8862delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180503601 | |||||
| chr5:180503601
|
CTT | C | 83 | a0001c0001t0001g0070a0001c0001t0001g0105a0001c0001t0001g0168others(80): Show | 83 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.-3+8861_-3+8862del others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180503601 | |||||
| chr5:180503601
|
CTTT | C | 6 | a0001c0001t0002g0074a0001c0001t0002g0098a0001c0001t0027g0186others(3): Show | 6 | HG01169.hp2 HG02071.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+8860_-3+8862del others(3): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180503601 | |||||
| chr5:180503698
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-3+8935C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503698 | ||||||
| chr5:180503709
|
G | A | 1 | a0001c0001t0061g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-3+8946G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503709 | ||||||
| chr5:180504010
|
G | A | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+9247G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180504010 | ||||||
| chr5:180504046
|
A | C | 9 | a0001c0002t0005g0021a0001c0002t0005g0022a0001c0002t0005g0023others(6): Show | 9 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3+9283A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180504046 | ||||||
| chr5:180504194
|
A | C | 5 | a0001c0001t0001g0299a0001c0001t0001g0301a0001c0001t0001g0302others(2): Show | 5 | HG00597.hp2 HG02015.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3+9431A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180504194 | ||||||
| chr5:180504403
|
G | A | 4 | a0001c0001t0024g0118a0001c0001t0024g0151a0001c0001t0024g0157others(1): Show | 4 | HG01109.hp2 HG01168.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+9640G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180504403 | ||||||
| chr5:180504491
|
C | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+9728C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180504491 | ||||||
| chr5:180504502
|
CG | C | 58 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(55): Show | 58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+9744delG | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180504502 | |||||
| chr5:180504672
|
A | G | 5 | a0001c0001t0008g0295a0001c0001t0008g0296a0001c0001t0008g0297others(2): Show | 5 | HG00735.hp2 HG01516.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3+9909A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180504672 | ||||||
| chr5:180504902
|
C | T | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+10139C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180504902 | ||||||
| chr5:180504955
|
A | AT | 8 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0312others(5): Show | 8 | HG01346.hp1 HG01515.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+10214dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180504955 | |||||
| chr5:180504955
|
A | ATTT | 11 | a0001c0001t0003g0207a0001c0001t0009g0210a0001c0001t0010g0208others(8): Show | 11 | HG00738.hp1 HG01515.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3+10212_-3+10214d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180504955 | |||||
| chr5:180504955
|
A | ATTTT | 38 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(35): Show | 38 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.-3+10211_-3+10214d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180504955 | |||||
| chr5:180504955
|
A | ATTTTT | 12 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0006g0146others(9): Show | 12 | HG01168.hp2 HG02027.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+10210_-3+10214d others(7): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180504955 | |||||
| chr5:180504955
|
A | ATTTTTT | 40 | a0001c0001t0003g0181a0001c0001t0006g0122a0001c0001t0006g0123others(37): Show | 40 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.-3+10209_-3+10214d others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180504955 | |||||
| chr5:180504955
|
A | ATTTTTTT | 8 | a0001c0001t0006g0008a0001c0001t0006g0130a0001c0001t0006g0150others(5): Show | 8 | HG01123.hp1 HG01257.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+10208_-3+10214d others(9): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180504955 | |||||
| chr5:180504955
|
AT | A | 102 | a0001c0001t0001g0070a0001c0001t0001g0241a0001c0001t0001g0243others(99): Show | 102 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-3+10214delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180504955 | |||||
| chr5:180504955
|
ATT | A | 15 | a0001c0001t0002g0020a0001c0001t0002g0074a0001c0001t0040g0100others(12): Show | 15 | HG01069.hp1 HG01891.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.-3+10213_-3+10214d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180504955 | |||||
| chr5:180505117
|
C | T | 1 | a0001c0001t0061g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-3+10354C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505117 | ||||||
| chr5:180505126
|
T | A | 1 | a0001c0001t0002g0074 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-3+10363T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505126 | ||||||
| chr5:180505162
|
G | A | 2 | a0001c0001t0015g0115a0001c0001t0015g0119 | 2 | HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-3+10399G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505162 | ||||||
| chr5:180505251
|
A | AT | 16 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0240others(13): Show | 16 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.-3+10510dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505251 | |||||
| chr5:180505251
|
A | ATT | 44 | a0001c0001t0001g0315a0001c0001t0006g0008a0001c0001t0006g0122others(41): Show | 44 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.-3+10509_-3+10510d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505251 | |||||
| chr5:180505251
|
A | ATTT | 6 | a0001c0001t0007g0149a0001c0001t0015g0012a0001c0001t0015g0126others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3+10508_-3+10510d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505251 | |||||
| chr5:180505251
|
AT | A | 111 | a0001c0001t0001g0105a0001c0001t0002g0018a0001c0001t0002g0020others(108): Show | 111 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.-3+10510delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505251 | |||||
| chr5:180505251
|
ATT | A | 57 | a0001c0001t0001g0168a0001c0001t0002g0060a0001c0001t0002g0074others(54): Show | 57 | HG00280.hp2 HG00639.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.-3+10509_-3+10510d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505251 | |||||
| chr5:180505281
|
A | G | 52 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(49): Show | 52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-3+10518A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505281 | ||||||
| chr5:180505294
|
C | T | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+10531C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505294 | ||||||
| chr5:180505301
|
T | G | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+10538T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505301 | ||||||
| chr5:180505305
|
G | A | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+10542G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505305 | ||||||
| chr5:180505307
|
C | G | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+10544C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505307 | ||||||
| chr5:180505318
|
C | T | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+10555C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505318 | ||||||
| chr5:180505324
|
C | T | 2 | a0001c0001t0029g0234a0001c0001t0029g0289 | 2 | NA18969.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-3+10561C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505324 | ||||||
| chr5:180505325
|
G | A | 1 | a0001c0001t0002g0061 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-3+10562G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505325 | ||||||
| chr5:180505328
|
T | C | 1 | a0001c0001t0028g0233 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-3+10565T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505328 | ||||||
| chr5:180505382
|
A | C | 4 | a0001c0002t0004g0036a0001c0002t0004g0049a0001c0002t0004g0050others(1): Show | 4 | HG01167.hp1 HG02615.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+10619A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505382 | ||||||
| chr5:180505422
|
A | AT | 6 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(3): Show | 6 | HG02258.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+10667dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505422 | |||||
| chr5:180505477
|
C | G | 58 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(55): Show | 58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+10714C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505477 | ||||||
| chr5:180505547
|
A | AT | 36 | a0001c0001t0001g0302a0001c0001t0001g0315a0001c0001t0001g0329others(33): Show | 36 | HG00733.hp1 HG01243.hp2 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.-3+10802dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505547 | |||||
| chr5:180505547
|
A | ATT | 99 | a0001c0001t0001g0168a0001c0001t0002g0018a0001c0001t0002g0020others(96): Show | 99 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.-3+10801_-3+10802d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505547 | |||||
| chr5:180505547
|
AT | A | 6 | a0001c0001t0001g0246a0001c0001t0001g0248a0001c0001t0012g0247others(3): Show | 6 | HG00099.hp1 HG01358.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+10802delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505547 | |||||
| chr5:180505601
|
G | A | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-3+10838G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505601 | ||||||
| chr5:180505612
|
ATC | A | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-3+10852_-3+10853d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505612 | |||||
| chr5:180505633
|
C | T | 1 | a0001c0001t0026g0223 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-3+10870C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505633 | ||||||
| chr5:180505687
|
A | C | 4 | a0001c0001t0021g0158a0001c0001t0021g0159a0001c0001t0021g0160others(1): Show | 4 | HG02071.hp2 HG02735.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+10924A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505687 | ||||||
| chr5:180505843
|
C | T | 1 | a0001c0001t0017g0161 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-3+11080C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505843 | ||||||
| chr5:180505943
|
A | G | 2 | a0001c0001t0002g0231a0001c0002t0004g0058 | 2 | HG02165.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-3+11180A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505943 | ||||||
| chr5:180505975
|
A | G | 1 | a0001c0001t0012g0112 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-3+11212A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505975 | ||||||
| chr5:180506000
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-3+11237G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180506000 | ||||||
| chr5:180506207
|
G | C | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+11444G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180506207 | ||||||
| chr5:180506359
|
A | G | 2 | a0001c0001t0040g0100a0001c0001t0041g0101 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-3+11596A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180506359 | ||||||
| chr5:180506650
|
T | G | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+11887T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180506650 | ||||||
| chr5:180506758
|
A | G | 3 | a0001c0002t0005g0026a0001c0002t0005g0027a0001c0002t0005g0028 | 3 | HG02717.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-3+11995A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180506758 | ||||||
| chr5:180506920
|
G | C | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+12157G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180506920 | ||||||
| chr5:180507151
|
A | G | 58 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(55): Show | 58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+12388A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180507151 | ||||||
| chr5:180507325
|
TGTG | T | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-3+12567_-3+12569d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180507325 | |||||
| chr5:180507399
|
A | G | 1 | a0001c0001t0057g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-3+12636A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180507399 | ||||||
| chr5:180507463
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-3+12700G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180507463 | ||||||
| chr5:180507559
|
G | A | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+12796G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180507559 | ||||||
| chr5:180507580
|
G | C | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+12817G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180507580 | ||||||
| chr5:180507615
|
AG | A | 58 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(55): Show | 58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+12853delG | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180507615 | ||||||
| chr5:180507735
|
A | C | 1 | a0001c0001t0009g0183 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-3+12972A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180507735 | ||||||
| chr5:180507778
|
C | T | 48 | a0001c0001t0001g0070a0001c0001t0002g0018a0001c0001t0002g0020others(45): Show | 48 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.-3+13015C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180507778 | ||||||
| chr5:180507818
|
A | AAGGTGAA others(244): Show |
49 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(46): Show | 49 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.-3+13058_-3+13308d others(253): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180507818 | |||||
| chr5:180507818
|
A | AAGGTGAA others(495): Show |
1 | a0001c0001t0007g0129 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-3+13308_-3+13309i others(504): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180507818 | |||||
| chr5:180507994
|
C | G | 58 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(55): Show | 58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+13231C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180507994 | ||||||
| chr5:180508192
|
T | G | 58 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(55): Show | 58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+13429T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508192 | ||||||
| chr5:180508293
|
G | A | 7 | a0001c0002t0002g0042a0001c0002t0004g0037a0001c0002t0004g0038others(4): Show | 7 | HG02280.hp2 HG02630.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+13530G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508293 | ||||||
| chr5:180508312
|
A | AATTTGTT others(11): Show |
1 | a0001c0001t0061g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-3+13551_-3+13568d others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180508312 | |||||
| chr5:180508419
|
C | G | 10 | a0001c0001t0006g0144a0001c0001t0006g0146a0001c0001t0007g0134others(7): Show | 10 | HG00609.hp2 HG02055.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3+13656C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508419 | ||||||
| chr5:180508477
|
A | G | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-3+13714A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508477 | ||||||
| chr5:180508512
|
G | T | 1 | a0001c0001t0001g0248 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-3+13749G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508512 | ||||||
| chr5:180508531
|
C | T | 3 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0009g0178 | 3 | HG03017.hp1 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-3+13768C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508531 | ||||||
| chr5:180508543
|
C | T | 8 | a0001c0001t0001g0287a0001c0001t0001g0305a0001c0001t0001g0307others(5): Show | 8 | HG00741.hp1 HG01074.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+13780C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508543 | ||||||
| chr5:180508601
|
C | T | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-3+13838C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508601 | ||||||
| chr5:180508710
|
T | A | 1 | a0001c0001t0019g0292 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-3+13947T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508710 | ||||||
| chr5:180508712
|
T | A | 1 | a0001c0001t0019g0292 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-3+13949T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508712 | ||||||
| chr5:180508718
|
G | T | 1 | a0001c0001t0019g0292 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-3+13955G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508718 | ||||||
| chr5:180508720
|
T | G | 1 | a0001c0001t0019g0292 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-3+13957T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508720 | ||||||
| chr5:180508722
|
A | G | 1 | a0001c0001t0019g0292 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-3+13959A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508722 | ||||||
| chr5:180508723
|
A | T | 1 | a0001c0001t0019g0292 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-3+13960A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508723 | ||||||
| chr5:180508725
|
C | T | 1 | a0001c0001t0019g0292 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-3+13962C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508725 | ||||||
| chr5:180508726
|
A | T | 1 | a0001c0001t0019g0292 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-3+13963A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508726 | ||||||
| chr5:180508763
|
C | T | 1 | a0001c0001t0003g0180 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-3+14000C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508763 | ||||||
| chr5:180508814
|
TA | T | 5 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(2): Show | 5 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+14053delA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180508814 | |||||
| chr5:180508815
|
A | T | 1 | a0001c0001t0019g0292 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-3+14052A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508815 | ||||||
| chr5:180508816
|
A | T | 5 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(2): Show | 5 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+14053A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508816 | ||||||
| chr5:180508818
|
T | A | 5 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(2): Show | 5 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+14055T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508818 | ||||||
| chr5:180508818
|
T | TTTA | 101 | a0001c0001t0001g0070a0001c0001t0002g0018a0001c0001t0002g0029others(98): Show | 101 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.-3+14070_-3+14072d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180508818 | |||||
| chr5:180508830
|
A | ATT | 9 | a0001c0001t0007g0134a0001c0001t0014g0174a0001c0001t0014g0175others(6): Show | 9 | HG00639.hp2 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3+14068_-3+14069d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180508830 | |||||
| chr5:180508833
|
A | ATT | 98 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(95): Show | 98 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.-3+14078_-3+14079d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180508833 | |||||
| chr5:180508833
|
A | ATTT | 16 | a0001c0001t0001g0105a0001c0001t0002g0020a0001c0001t0013g0103others(13): Show | 16 | HG01884.hp2 HG01891.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.-3+14077_-3+14079d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180508833 | |||||
| chr5:180508833
|
A | T | 14 | a0001c0001t0001g0248a0001c0001t0007g0134a0001c0001t0014g0174others(11): Show | 14 | HG00099.hp1 HG00639.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.-3+14070A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508833 | ||||||
| chr5:180508885
|
T | C | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+14122T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508885 | ||||||
| chr5:180508916
|
G | A | 58 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(55): Show | 58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+14153G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508916 | ||||||
| chr5:180508954
|
C | G | 51 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(48): Show | 51 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.-3+14191C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508954 | ||||||
| chr5:180509168
|
G | T | 3 | a0001c0001t0022g0225a0001c0003t0022g0220a0001c0003t0022g0222 | 3 | HG02055.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-3+14405G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180509168 | ||||||
| chr5:180509315
|
T | C | 53 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(50): Show | 53 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.-3+14552T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180509315 | ||||||
| chr5:180509424
|
C | T | 1 | a0001c0001t0024g0118 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-3+14661C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180509424 | ||||||
| chr5:180509695
|
G | A | 3 | a0001c0001t0003g0170a0001c0001t0003g0181a0001c0001t0003g0184 | 3 | HG01358.hp2 HG01993.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-3+14932G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180509695 | ||||||
| chr5:180509737
|
G | A | 8 | a0001c0002t0002g0034a0001c0002t0002g0035a0001c0002t0002g0044others(5): Show | 8 | HG01069.hp1 HG01106.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+14974G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180509737 | ||||||
| chr5:180509803
|
A | G | 1 | a0001c0002t0004g0058 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-3+15040A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180509803 | ||||||
| chr5:180509825
|
GGT | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+15065_-3+15066d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180509825 | |||||
| chr5:180509828
|
G | GT | 17 | a0001c0001t0001g0318a0001c0001t0001g0328a0001c0001t0002g0073others(14): Show | 17 | HG01106.hp2 HG01123.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.-3+15083dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180509828 | |||||
| chr5:180509828
|
GT | G | 54 | a0001c0001t0001g0251a0001c0001t0002g0076a0001c0001t0002g0077others(51): Show | 54 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.-3+15083delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180509828 | |||||
| chr5:180509846
|
T | C | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-3+15083T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180509846 | ||||||
| chr5:180509876
|
A | G | 1 | a0001c0001t0061g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-3+15113A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180509876 | ||||||
| chr5:180509911
|
C | G | 2 | a0001c0001t0002g0076a0001c0001t0002g0077 | 2 | HG01952.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-3+15148C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180509911 | ||||||
| chr5:180510091
|
G | A | 1 | a0001c0001t0049g0333 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3+15328G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510091 | ||||||
| chr5:180510123
|
C | T | 6 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(3): Show | 6 | HG02258.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+15360C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510123 | ||||||
| chr5:180510134
|
C | CT | 25 | a0001c0001t0001g0227a0001c0001t0001g0236a0001c0001t0001g0240others(22): Show | 25 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.-3+15406dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
C | CTT | 14 | a0001c0001t0001g0243a0001c0001t0001g0280a0001c0001t0001g0293others(11): Show | 14 | HG01256.hp2 HG01258.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.-3+15405_-3+15406d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
C | CTTT | 13 | a0001c0001t0001g0304a0001c0001t0002g0020a0001c0001t0002g0062others(10): Show | 13 | HG01069.hp1 HG01123.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.-3+15404_-3+15406d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
C | CTTTT | 31 | a0001c0001t0001g0070a0001c0001t0001g0294a0001c0001t0001g0313others(28): Show | 31 | HG00423.hp1 HG00642.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.-3+15403_-3+15406d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
C | CTTTTT | 21 | a0001c0001t0001g0244a0001c0001t0002g0018a0001c0001t0002g0029others(18): Show | 21 | HG00597.hp1 HG00639.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.-3+15402_-3+15406d others(7): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
C | CTTTTTT | 9 | a0001c0001t0002g0060a0001c0001t0002g0061a0001c0001t0002g0069others(6): Show | 9 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3+15401_-3+15406d others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
C | CTTTTTTT others(1): Show |
8 | a0001c0001t0001g0245a0001c0001t0001g0281a0001c0001t0001g0282others(5): Show | 8 | HG01069.hp2 HG01071.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+15399_-3+15406d others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0002g0077a0001c0001t0008g0285a0001c0001t0058g0095 | 3 | HG00609.hp1 HG02723.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.-3+15396_-3+15406d others(13): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-3+15394_-3+15406d others(15): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
CT | C | 8 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(5): Show | 8 | HG01884.hp1 HG02965.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3+15406delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
CTTTTT | C | 9 | a0001c0001t0003g0195a0001c0001t0003g0201a0001c0001t0009g0010others(6): Show | 9 | HG00099.hp1 HG00738.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3+15402_-3+15406d others(7): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
CTTTTTT | C | 33 | a0001c0001t0003g0170a0001c0001t0003g0188a0001c0001t0003g0189others(30): Show | 33 | HG00738.hp2 HG01071.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.-3+15401_-3+15406d others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
CTTTTTTT | C | 49 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0172others(46): Show | 49 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.-3+15400_-3+15406d others(9): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
CTTTTTTT others(1): Show |
C | 10 | a0001c0001t0006g0156a0001c0001t0014g0167a0001c0001t0014g0174others(7): Show | 10 | HG00280.hp2 HG00639.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3+15399_-3+15406d others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
CTTTTTTT others(3): Show |
C | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG02258.hp2 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+15397_-3+15406d others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
CTTTTTTT others(4): Show |
C | 8 | a0001c0002t0005g0021a0001c0002t0005g0022a0001c0002t0005g0023others(5): Show | 8 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+15396_-3+15406d others(13): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0049g0333 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3+15395_-3+15406d others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
CTTTTTTT others(6): Show |
C | 7 | a0001c0001t0001g0253a0001c0001t0001g0254a0001c0001t0001g0316others(4): Show | 7 | HG00544.hp1 HG00544.hp2 HG00621.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+15394_-3+15406d others(15): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0021g0158 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-3+15393_-3+15406d others(16): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
CTTTTTTT others(8): Show |
C | 5 | a0001c0001t0001g0105a0001c0001t0001g0250a0001c0001t0013g0104others(2): Show | 5 | HG01884.hp2 HG02818.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+15392_-3+15406d others(17): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0001g0251a0001c0001t0013g0103 | 2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-3+15391_-3+15406d others(18): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
CTTTTTTT others(10): Show |
C | 2 | a0002c0004t0001g0319a0002c0004t0004g0252 | 2 | NA18966.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-3+15390_-3+15406d others(19): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510134
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0057g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-3+15389_-3+15406d others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | |||||
| chr5:180510179
|
T | C | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+15416T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510179 | ||||||
| chr5:180510231
|
G | C | 115 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(112): Show | 115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-3+15468G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510231 | ||||||
| chr5:180510474
|
A | G | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+15711A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510474 | ||||||
| chr5:180510560
|
G | A | 6 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(3): Show | 6 | HG02818.hp1 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+15797G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510560 | ||||||
| chr5:180510661
|
C | T | 58 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(55): Show | 58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+15898C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510661 | ||||||
| chr5:180510665
|
A | G | 1 | a0001c0001t0016g0331 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-3+15902A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510665 | ||||||
| chr5:180510749
|
G | C | 2 | a0001c0001t0025g0217a0001c0001t0038g0218 | 2 | HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-3+15986G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510749 | ||||||
| chr5:180510854
|
G | C | 1 | a0001c0001t0023g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-3+16091G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510854 | ||||||
| chr5:180511094
|
C | T | 4 | a0001c0001t0014g0167a0001c0001t0014g0174a0001c0001t0014g0175others(1): Show | 4 | HG00280.hp2 HG00639.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+16331C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511094 | ||||||
| chr5:180511121
|
G | A | 2 | a0001c0001t0010g0187a0001c0001t0010g0194 | 2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-3+16358G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511121 | ||||||
| chr5:180511186
|
A | T | 162 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(159): Show | 162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.-3+16423A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511186 | ||||||
| chr5:180511298
|
T | C | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+16535T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511298 | ||||||
| chr5:180511317
|
A | C | 1 | a0001c0001t0017g0166 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-3+16554A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511317 | ||||||
| chr5:180511382
|
C | T | 58 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(55): Show | 58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+16619C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511382 | ||||||
| chr5:180511670
|
T | C | 1 | a0001c0001t0016g0331 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-3+16907T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511670 | ||||||
| chr5:180511732
|
C | T | 1 | a0001c0001t0006g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-3+16969C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511732 | ||||||
| chr5:180511808
|
G | A | 50 | a0001c0001t0001g0070a0001c0001t0002g0018a0001c0001t0002g0020others(47): Show | 50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.-3+17045G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511808 | ||||||
| chr5:180511856
|
A | G | 3 | a0001c0002t0005g0026a0001c0002t0005g0027a0001c0002t0005g0028 | 3 | HG02717.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-3+17093A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511856 | ||||||
| chr5:180511869
|
A | T | 3 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0009g0178 | 3 | HG03017.hp1 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-3+17106A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511869 | ||||||
| chr5:180511876
|
C | T | 1 | a0001c0001t0007g0140 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-3+17113C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511876 | ||||||
| chr5:180511884
|
G | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(159): Show | 162 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.-3+17121G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511884 | ||||||
| chr5:180511899
|
G | A | 51 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(48): Show | 51 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.-3+17136G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511899 | ||||||
| chr5:180512191
|
G | A | 1 | a0001c0001t0017g0162 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-2-17084G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180512191 | ||||||
| chr5:180512349
|
G | C | 1 | a0001c0001t0018g0004 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-2-16926G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180512349 | ||||||
| chr5:180512394
|
G | A | 9 | a0001c0002t0005g0021a0001c0002t0005g0022a0001c0002t0005g0023others(6): Show | 9 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-16881G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180512394 | ||||||
| chr5:180512658
|
G | A | 6 | a0001c0001t0003g0170a0001c0001t0003g0179a0001c0001t0003g0180others(3): Show | 6 | HG01358.hp2 HG01993.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-16617G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180512658 | ||||||
| chr5:180512744
|
G | T | 1 | a0001c0001t0032g0128 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-2-16531G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180512744 | ||||||
| chr5:180512789
|
G | A | 9 | a0001c0002t0005g0021a0001c0002t0005g0022a0001c0002t0005g0023others(6): Show | 9 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-16486G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180512789 | ||||||
| chr5:180512926
|
T | A | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-2-16349T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180512926 | ||||||
| chr5:180512958
|
C | T | 2 | a0001c0001t0001g0312a0001c0003t0022g0222 | 2 | HG02055.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-2-16317C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180512958 | ||||||
| chr5:180512991
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2-16284G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180512991 | ||||||
| chr5:180513035
|
A | G | 2 | a0001c0001t0001g0244a0001c0001t0001g0313 | 2 | HG01515.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-2-16240A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180513035 | ||||||
| chr5:180513036
|
C | A | 1 | a0001c0005t0004g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-2-16239C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180513036 | ||||||
| chr5:180513044
|
C | T | 58 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(55): Show | 58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-2-16231C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180513044 | ||||||
| chr5:180513091
|
A | G | 298 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(295): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-2-16184A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180513091 | ||||||
| chr5:180513221
|
T | A | 1 | a0001c0001t0013g0256 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-2-16054T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180513221 | ||||||
| chr5:180513228
|
C | T | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-2-16047C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180513228 | ||||||
| chr5:180513410
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0001g0273 | 2 | NA19075.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-2-15865G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180513410 | ||||||
| chr5:180513520
|
C | G | 1 | a0001c0001t0002g0087 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-2-15755C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180513520 | ||||||
| chr5:180513673
|
TTTTATTT others(5): Show |
T | 58 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(55): Show | 58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-2-15586_-2-15575d others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180513673 | |||||
| chr5:180513699
|
T | TTATTTAT others(9): Show |
4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-15575_-2-15574i others(18): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180513699 | |||||
| chr5:180513699
|
T | TTTTA | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-15560_-2-15557d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180513699 | |||||
| chr5:180513896
|
G | A | 2 | a0001c0001t0002g0076a0001c0001t0002g0077 | 2 | HG01952.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-2-15379G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180513896 | ||||||
| chr5:180514070
|
C | G | 1 | a0001c0001t0006g0156 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-2-15205C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514070 | ||||||
| chr5:180514165
|
C | T | 1 | a0001c0001t0023g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-2-15110C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514165 | ||||||
| chr5:180514180
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-2-15095T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514180 | ||||||
| chr5:180514190
|
G | A | 115 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(112): Show | 115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-2-15085G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514190 | ||||||
| chr5:180514195
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-2-15080G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514195 | ||||||
| chr5:180514242
|
T | C | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-2-15033T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514242 | ||||||
| chr5:180514274
|
C | A | 58 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(55): Show | 58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-2-15001C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514274 | ||||||
| chr5:180514284
|
T | G | 4 | a0001c0001t0019g0257a0001c0001t0019g0258a0001c0001t0019g0286others(1): Show | 4 | NA18947.hp1 NA18967.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-14991T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514284 | ||||||
| chr5:180514295
|
G | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0227a0001c0001t0001g0229others(97): Show | 100 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.-2-14980G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514295 | ||||||
| chr5:180514401
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-2-14874G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514401 | ||||||
| chr5:180514409
|
G | A | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-14866G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514409 | ||||||
| chr5:180514643
|
G | A | 1 | a0001c0001t0008g0285 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-2-14632G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514643 | ||||||
| chr5:180514646
|
T | C | 115 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(112): Show | 115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-2-14629T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514646 | ||||||
| chr5:180514728
|
G | A | 1 | a0001c0001t0008g0296 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-2-14547G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514728 | ||||||
| chr5:180514872
|
G | GA | 4 | a0001c0001t0033g0031a0001c0001t0033g0033a0001c0001t0062g0030others(1): Show | 4 | HG01243.hp2 HG02258.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-14396dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180514872 | |||||
| chr5:180515256
|
CA | C | 54 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(51): Show | 54 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.-2-14008delA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180515256 | |||||
| chr5:180515395
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0227a0001c0001t0001g0229others(97): Show | 100 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.-2-13880C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180515395 | ||||||
| chr5:180515452
|
ATAGT | A | 103 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(100): Show | 103 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.-2-13819_-2-13816d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180515452 | |||||
| chr5:180515464
|
G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0227a0001c0001t0001g0229others(98): Show | 101 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.-2-13811G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180515464 | ||||||
| chr5:180515660
|
A | G | 2 | a0001c0001t0025g0217a0001c0001t0038g0218 | 2 | HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-2-13615A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180515660 | ||||||
| chr5:180515687
|
G | A | 1 | a0001c0001t0049g0333 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-2-13588G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180515687 | ||||||
| chr5:180515714
|
C | T | 3 | a0001c0001t0006g0144a0001c0001t0006g0146a0001c0001t0007g0134 | 3 | NA18978.hp1 NA19080.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-2-13561C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180515714 | ||||||
| chr5:180515762
|
T | G | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-13513T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180515762 | ||||||
| chr5:180515904
|
A | T | 333 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.-2-13371A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180515904 | ||||||
| chr5:180515914
|
A | T | 1 | a0001c0001t0009g0183 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-2-13361A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180515914 | ||||||
| chr5:180516182
|
A | AT | 54 | a0001c0001t0001g0070a0001c0001t0001g0306a0001c0001t0001g0322others(51): Show | 54 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.-2-13076dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180516182 | |||||
| chr5:180516182
|
AT | A | 106 | a0001c0001t0001g0168a0001c0001t0001g0237a0001c0001t0001g0239others(103): Show | 106 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.-2-13076delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180516182 | |||||
| chr5:180516182
|
ATT | A | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-13077_-2-13076d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180516182 | |||||
| chr5:180516205
|
G | A | 2 | a0002c0004t0001g0319a0002c0004t0004g0252 | 2 | NA18966.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-2-13070G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516205 | ||||||
| chr5:180516292
|
T | C | 3 | a0001c0001t0001g0260a0001c0001t0012g0255a0001c0001t0012g0321 | 3 | HG02273.hp1 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-2-12983T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516292 | ||||||
| chr5:180516310
|
G | A | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-2-12965G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516310 | ||||||
| chr5:180516329
|
G | A | 3 | a0001c0001t0001g0001a0001c0001t0034g0001a0001c0001t0045g0332 | 3 | HG02630.hp1 NA19004.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-2-12946G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516329 | ||||||
| chr5:180516380
|
A | C | 1 | a0001c0001t0002g0029 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-2-12895A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516380 | ||||||
| chr5:180516423
|
G | A | 119 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(116): Show | 119 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.-2-12852G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516423 | ||||||
| chr5:180516502
|
G | T | 1 | a0001c0001t0016g0331 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-2-12773G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516502 | ||||||
| chr5:180516584
|
A | T | 115 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(112): Show | 115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-2-12691A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516584 | ||||||
| chr5:180516587
|
C | T | 1 | a0001c0002t0004g0058 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-2-12688C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516587 | ||||||
| chr5:180516634
|
A | T | 58 | a0001c0001t0001g0070a0001c0001t0001g0105a0001c0001t0002g0018others(55): Show | 58 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.-2-12641A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516634 | ||||||
| chr5:180516709
|
T | C | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-12566T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516709 | ||||||
| chr5:180516774
|
C | A | 1 | a0001c0001t0002g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-2-12501C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516774 | ||||||
| chr5:180516790
|
T | C | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-12485T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516790 | ||||||
| chr5:180516816
|
C | T | 1 | a0001c0003t0022g0222 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-2-12459C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516816 | ||||||
| chr5:180516955
|
A | G | 36 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0006g0138others(33): Show | 36 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.-2-12320A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516955 | ||||||
| chr5:180516978
|
C | T | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-12297C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516978 | ||||||
| chr5:180517005
|
A | AG | 8 | a0001c0001t0001g0261a0001c0001t0001g0307a0001c0001t0003g0184others(5): Show | 8 | HG00741.hp1 HG00741.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-12265dupG | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180517005 | |||||
| chr5:180517082
|
T | C | 3 | a0001c0001t0022g0225a0001c0003t0022g0220a0001c0003t0022g0222 | 3 | HG02055.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-2-12193T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517082 | ||||||
| chr5:180517276
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-2-11999G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517276 | ||||||
| chr5:180517310
|
G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0227a0001c0001t0001g0229others(98): Show | 101 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.-2-11965G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517310 | ||||||
| chr5:180517363
|
A | G | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-11912A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517363 | ||||||
| chr5:180517684
|
C | G | 6 | a0001c0001t0005g0113a0001c0001t0005g0272a0001c0001t0019g0257others(3): Show | 6 | HG03834.hp2 NA18947.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-11591C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517684 | ||||||
| chr5:180517782
|
TC | T | 61 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(58): Show | 61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.-2-11491delC | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180517782 | |||||
| chr5:180517821
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-2-11454C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517821 | ||||||
| chr5:180517841
|
C | T | 2 | a0001c0001t0013g0106a0001c0001t0013g0107 | 2 | HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2-11434C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517841 | ||||||
| chr5:180517879
|
A | T | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-2-11396A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517879 | ||||||
| chr5:180517892
|
G | C | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-2-11383G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517892 | ||||||
| chr5:180517939
|
C | T | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-11336C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517939 | ||||||
| chr5:180517965
|
G | A | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-11310G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517965 | ||||||
| chr5:180518008
|
CCCTCTCT others(3): Show |
C | 112 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(109): Show | 112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-2-11265_-2-11256d others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180518008 | |||||
| chr5:180518042
|
C | T | 1 | a0001c0001t0028g0327 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-2-11233C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518042 | ||||||
| chr5:180518094
|
T | C | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-11181T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518094 | ||||||
| chr5:180518251
|
T | C | 1 | a0001c0001t0006g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-2-11024T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518251 | ||||||
| chr5:180518259
|
C | T | 1 | a0001c0001t0002g0091 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-2-11016C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518259 | ||||||
| chr5:180518334
|
G | A | 115 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(112): Show | 115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-2-10941G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518334 | ||||||
| chr5:180518336
|
C | G | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-10939C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518336 | ||||||
| chr5:180518504
|
T | G | 14 | a0001c0001t0003g0188a0001c0001t0003g0189a0001c0001t0003g0200others(11): Show | 14 | HG00738.hp2 HG01071.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-10771T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518504 | ||||||
| chr5:180518589
|
G | A | 1 | a0001c0001t0063g0230 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-2-10686G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518589 | ||||||
| chr5:180518801
|
C | T | 2 | a0001c0001t0003g0170a0001c0001t0003g0184 | 2 | HG01993.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-2-10474C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518801 | ||||||
| chr5:180518827
|
C | T | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-2-10448C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518827 | ||||||
| chr5:180518865
|
C | CT | 6 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(3): Show | 6 | HG02818.hp1 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-10408dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180518865 | |||||
| chr5:180518933
|
G | A | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-10342G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518933 | ||||||
| chr5:180519059
|
A | G | 61 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(58): Show | 61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.-2-10216A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519059 | ||||||
| chr5:180519077
|
A | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-10198A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519077 | ||||||
| chr5:180519108
|
G | A | 5 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(2): Show | 5 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-10167G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519108 | ||||||
| chr5:180519289
|
G | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-9986G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519289 | ||||||
| chr5:180519311
|
T | C | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-9964T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519311 | ||||||
| chr5:180519496
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-2-9779G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519496 | ||||||
| chr5:180519505
|
T | C | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-9770T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519505 | ||||||
| chr5:180519560
|
T | C | 3 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0001t0008g0238 | 3 | NA18944.hp2 NA18959.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-2-9715T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519560 | ||||||
| chr5:180519762
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-2-9513G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519762 | ||||||
| chr5:180519766
|
C | CT | 60 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(57): Show | 60 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.-2-9497dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180519766 | |||||
| chr5:180519766
|
CT | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0227a0001c0001t0001g0229others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.-2-9497delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180519766 | |||||
| chr5:180519806
|
A | G | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-9469A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519806 | ||||||
| chr5:180519833
|
C | CTT | 52 | a0001c0001t0001g0070a0001c0001t0001g0280a0001c0001t0002g0018others(49): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.-2-9428_-2-9427dup others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180519833 | |||||
| chr5:180519833
|
CT | C | 105 | a0001c0001t0001g0168a0001c0001t0001g0237a0001c0001t0002g0176others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-2-9427delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180519833 | |||||
| chr5:180519833
|
CTT | C | 10 | a0001c0001t0015g0126a0001c0001t0015g0127a0001c0001t0017g0161others(7): Show | 10 | HG01243.hp1 HG01243.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-9428_-2-9427del others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180519833 | |||||
| chr5:180519941
|
C | T | 1 | a0001c0001t0009g0183 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-2-9334C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519941 | ||||||
| chr5:180519974
|
T | C | 1 | a0001c0001t0023g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-2-9301T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519974 | ||||||
| chr5:180520061
|
T | G | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-9214T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180520061 | ||||||
| chr5:180520073
|
A | G | 1 | a0001c0002t0004g0058 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-2-9202A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180520073 | ||||||
| chr5:180520151
|
T | G | 3 | a0001c0001t0025g0217a0001c0001t0026g0223a0001c0001t0038g0218 | 3 | HG01261.hp1 HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-2-9124T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180520151 | ||||||
| chr5:180520185
|
A | G | 2 | a0001c0001t0001g0245a0001c0001t0001g0284 | 2 | NA18941.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-2-9090A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180520185 | ||||||
| chr5:180520251
|
AAAGAGTT others(7): Show |
A | 52 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(49): Show | 52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-2-9012_-2-8999del others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180520251 | |||||
| chr5:180520469
|
C | A | 1 | a0001c0001t0009g0014 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-2-8806C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180520469 | ||||||
| chr5:180520851
|
T | A | 332 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(329): Show | 332 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(329): Show |
intron_variant | MODIFIER | c.-2-8424T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180520851 | ||||||
| chr5:180520873
|
C | T | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-8402C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180520873 | ||||||
| chr5:180521008
|
A | G | 1 | a0001c0001t0057g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-2-8267A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180521008 | ||||||
| chr5:180521067
|
G | A | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-8208G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180521067 | ||||||
| chr5:180521547
|
A | C | 1 | a0001c0001t0005g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-2-7728A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180521547 | ||||||
| chr5:180521558
|
T | A | 2 | a0001c0001t0005g0226a0001c0002t0002g0048 | 2 | HG01123.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-2-7717T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180521558 | ||||||
| chr5:180521748
|
G | A | 115 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(112): Show | 115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-2-7527G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180521748 | ||||||
| chr5:180521754
|
A | G | 1 | a0001c0001t0019g0258 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-2-7521A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180521754 | ||||||
| chr5:180521874
|
C | G | 1 | a0001c0001t0001g0251 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2-7401C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180521874 | ||||||
| chr5:180522029
|
A | G | 6 | a0001c0001t0003g0191a0001c0001t0003g0195a0001c0001t0003g0290others(3): Show | 6 | HG02027.hp1 NA18612.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-7246A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522029 | ||||||
| chr5:180522041
|
T | G | 1 | a0001c0002t0004g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-2-7234T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522041 | ||||||
| chr5:180522090
|
G | T | 1 | a0001c0001t0003g0207 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-2-7185G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522090 | ||||||
| chr5:180522109
|
TTATCTGT others(13): Show |
T | 1 | a0002c0004t0004g0252 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-2-7156_-2-7137del others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180522109 | |||||
| chr5:180522156
|
C | T | 1 | a0001c0001t0025g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-2-7119C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522156 | ||||||
| chr5:180522256
|
T | C | 1 | a0001c0001t0021g0159 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-2-7019T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522256 | ||||||
| chr5:180522297
|
T | G | 78 | a0001c0001t0001g0001a0001c0001t0001g0227a0001c0001t0001g0229others(75): Show | 78 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.-2-6978T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522297 | ||||||
| chr5:180522304
|
G | T | 1 | a0001c0001t0006g0156 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-2-6971G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522304 | ||||||
| chr5:180522316
|
T | C | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-6959T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522316 | ||||||
| chr5:180522366
|
G | A | 4 | a0001c0001t0001g0299a0001c0001t0001g0301a0001c0001t0008g0303others(1): Show | 4 | HG00597.hp2 HG02027.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-6909G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522366 | ||||||
| chr5:180522532
|
TGTTA | T | 3 | a0001c0001t0030g0131a0001c0001t0031g0132a0001c0001t0031g0133 | 3 | HG00733.hp2 HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.-2-6739_-2-6736del others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180522532 | |||||
| chr5:180522797
|
C | T | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-2-6478C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522797 | ||||||
| chr5:180522804
|
G | C | 1 | a0001c0001t0001g0246 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-2-6471G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522804 | ||||||
| chr5:180522831
|
C | T | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-6444C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522831 | ||||||
| chr5:180522907
|
C | T | 1 | a0001c0001t0025g0219 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-2-6368C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522907 | ||||||
| chr5:180522923
|
G | A | 2 | a0001c0001t0040g0100a0001c0001t0041g0101 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-6352G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522923 | ||||||
| chr5:180523023
|
A | G | 51 | a0001c0001t0001g0070a0001c0001t0002g0018a0001c0001t0002g0020others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.-2-6252A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180523023 | ||||||
| chr5:180523066
|
G | A | 1 | a0001c0005t0004g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-2-6209G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180523066 | ||||||
| chr5:180523220
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-2-6055G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180523220 | ||||||
| chr5:180523301
|
T | C | 3 | a0001c0001t0025g0217a0001c0001t0026g0223a0001c0001t0038g0218 | 3 | HG01261.hp1 HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-2-5974T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180523301 | ||||||
| chr5:180523448
|
C | G | 2 | a0001c0001t0006g0138a0001c0001t0006g0147 | 2 | NA18995.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-2-5827C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180523448 | ||||||
| chr5:180523452
|
A | AT | 55 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(52): Show | 55 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.-2-5820dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180523452 | |||||
| chr5:180523726
|
C | T | 1 | a0001c0001t0006g0156 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-2-5549C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180523726 | ||||||
| chr5:180523776
|
G | T | 3 | a0001c0001t0009g0014a0001c0001t0009g0015a0001c0001t0010g0016 | 3 | NA18957.hp2 NA18980.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-2-5499G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180523776 | ||||||
| chr5:180523873
|
G | A | 3 | a0001c0002t0005g0026a0001c0002t0005g0027a0001c0002t0005g0028 | 3 | HG02717.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-2-5402G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180523873 | ||||||
| chr5:180524180
|
C | A | 4 | a0001c0001t0002g0062a0001c0001t0002g0065a0001c0001t0002g0066others(1): Show | 4 | NA18955.hp2 NA18960.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-5095C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524180 | ||||||
| chr5:180524183
|
T | C | 1 | a0001c0001t0041g0101 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-2-5092T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524183 | ||||||
| chr5:180524250
|
T | A | 1 | a0001c0001t0041g0101 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-2-5025T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524250 | ||||||
| chr5:180524273
|
G | A | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-5002G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524273 | ||||||
| chr5:180524366
|
C | G | 1 | a0001c0001t0030g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-2-4909C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524366 | ||||||
| chr5:180524405
|
T | G | 2 | a0001c0001t0006g0138a0001c0001t0006g0147 | 2 | NA18995.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-2-4870T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524405 | ||||||
| chr5:180524574
|
C | T | 115 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(112): Show | 115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-2-4701C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524574 | ||||||
| chr5:180524789
|
A | G | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-2-4486A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524789 | ||||||
| chr5:180524801
|
C | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-4474C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524801 | ||||||
| chr5:180524994
|
G | A | 1 | a0001c0001t0002g0114 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-2-4281G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524994 | ||||||
| chr5:180525057
|
GTGTT | G | 59 | a0001c0001t0001g0070a0001c0001t0001g0105a0001c0001t0002g0018others(56): Show | 59 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.-2-4213_-2-4210del others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180525057 | |||||
| chr5:180525080
|
AT | A | 5 | a0001c0001t0001g0105a0001c0001t0013g0103a0001c0001t0013g0104others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-4188delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180525080 | |||||
| chr5:180525114
|
A | C | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-4161A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525114 | ||||||
| chr5:180525275
|
G | A | 1 | a0001c0001t0024g0157 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-2-4000G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525275 | ||||||
| chr5:180525431
|
C | T | 1 | a0001c0001t0061g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-2-3844C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525431 | ||||||
| chr5:180525437
|
G | T | 1 | a0001c0001t0006g0144 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-2-3838G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525437 | ||||||
| chr5:180525442
|
G | A | 5 | a0001c0001t0001g0105a0001c0001t0013g0103a0001c0001t0013g0104others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-3833G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525442 | ||||||
| chr5:180525538
|
C | CA | 11 | a0001c0001t0001g0250a0001c0001t0001g0306a0001c0001t0002g0032others(8): Show | 11 | HG01069.hp2 HG01167.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2-3720dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180525538 | |||||
| chr5:180525538
|
CA | C | 12 | a0001c0001t0001g0168a0001c0001t0002g0064a0001c0001t0002g0074others(9): Show | 12 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-3720delA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180525538 | |||||
| chr5:180525543
|
A | C | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-3732A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525543 | ||||||
| chr5:180525634
|
G | A | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-3641G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525634 | ||||||
| chr5:180525727
|
A | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-3548A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525727 | ||||||
| chr5:180525811
|
G | A | 1 | a0001c0001t0003g0290 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-2-3464G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525811 | ||||||
| chr5:180525822
|
C | T | 1 | a0001c0001t0010g0193 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-2-3453C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525822 | ||||||
| chr5:180525828
|
C | T | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-2-3447C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525828 | ||||||
| chr5:180525881
|
C | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-3394C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525881 | ||||||
| chr5:180525920
|
T | TA | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-3355_-2-3354ins others(1): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525920 | ||||||
| chr5:180525921
|
T | A | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-3354T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525921 | ||||||
| chr5:180525921
|
T | TA | 7 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(4): Show | 7 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-3345dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180525921 | |||||
| chr5:180526047
|
C | T | 2 | a0001c0001t0007g0148a0001c0001t0007g0149 | 2 | NA18973.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-2-3228C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180526047 | ||||||
| chr5:180526048
|
C | G | 298 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(295): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.-2-3227C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180526048 | ||||||
| chr5:180526053
|
A | G | 1 | a0001c0001t0003g0205 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-2-3222A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180526053 | ||||||
| chr5:180526078
|
C | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0284 | 2 | NA18941.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-2-3197C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180526078 | ||||||
| chr5:180526226
|
TGA | T | 61 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(58): Show | 61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.-2-3044_-2-3043del others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180526226 | |||||
| chr5:180526275
|
T | C | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-3000T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180526275 | ||||||
| chr5:180526402
|
G | A | 1 | a0001c0001t0007g0129 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-2-2873G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180526402 | ||||||
| chr5:180526617
|
C | A | 1 | a0001c0001t0009g0199 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-2-2658C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180526617 | ||||||
| chr5:180526646
|
T | G | 61 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(58): Show | 61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.-2-2629T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180526646 | ||||||
| chr5:180526883
|
CT | C | 118 | a0001c0001t0001g0168a0001c0001t0001g0239a0001c0001t0002g0176others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-2-2375delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180526883 | |||||
| chr5:180526982
|
C | T | 2 | a0001c0001t0013g0106a0001c0001t0013g0107 | 2 | HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2-2293C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180526982 | ||||||
| chr5:180527092
|
C | G | 1 | a0001c0001t0001g0251 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2-2183C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527092 | ||||||
| chr5:180527232
|
C | A | 1 | a0001c0001t0001g0305 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-2-2043C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527232 | ||||||
| chr5:180527284
|
T | G | 20 | a0001c0001t0001g0245a0001c0001t0001g0267a0001c0001t0001g0268others(17): Show | 20 | HG00423.hp2 HG00642.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2-1991T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527284 | ||||||
| chr5:180527352
|
A | G | 2 | a0001c0001t0001g0168a0001c0001t0002g0176 | 2 | NA18955.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-2-1923A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527352 | ||||||
| chr5:180527394
|
G | A | 61 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(58): Show | 61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.-2-1881G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527394 | ||||||
| chr5:180527406
|
G | A | 18 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(15): Show | 18 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-2-1869G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527406 | ||||||
| chr5:180527615
|
A | C | 18 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(15): Show | 18 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-2-1660A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527615 | ||||||
| chr5:180527687
|
G | A | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1588G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527687 | ||||||
| chr5:180527840
|
C | T | 1 | a0001c0002t0005g0330 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-2-1435C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527840 | ||||||
| chr5:180527896
|
C | G | 1 | a0001c0001t0039g0102 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-2-1379C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527896 | ||||||
| chr5:180527936
|
G | A | 1 | a0001c0001t0007g0143 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-2-1339G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527936 | ||||||
| chr5:180527937
|
T | C | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-2-1338T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527937 | ||||||
| chr5:180527994
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-2-1281C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527994 | ||||||
| chr5:180528073
|
C | T | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-2-1202C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180528073 | ||||||
| chr5:180528089
|
A | AT | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-2-1186_-2-1185ins others(1): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180528089 | ||||||
| chr5:180528144
|
A | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1131A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180528144 | ||||||
| chr5:180528303
|
A | AT | 3 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0009g0178 | 3 | HG03017.hp1 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-2-970dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180528303 | |||||
| chr5:180528398
|
C | T | 1 | a0001c0001t0006g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-2-877C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180528398 | ||||||
| chr5:180528644
|
C | T | 1 | a0001c0001t0007g0139 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-2-631C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180528644 | ||||||
| chr5:180528798
|
T | G | 1 | a0001c0001t0024g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-2-477T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180528798 | ||||||
| chr5:180528876
|
T | G | 53 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(50): Show | 53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.-2-399T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180528876 | ||||||
| chr5:180528933
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-2-342G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180528933 | ||||||
| chr5:180529037
|
C | T | 2 | a0001c0001t0001g0251a0001c0001t0045g0332 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-2-238C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180529037 | ||||||
| chr5:180529042
|
G | C | 115 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(112): Show | 115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-2-233G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180529042 | ||||||
| chr5:180529082
|
G | A | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-193G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180529082 | ||||||
| chr5:180529144
|
G | GC | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-129dupC | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180529144 | |||||
| chr5:180529197
|
C | CA | 24 | a0001c0001t0001g0281a0001c0001t0006g0136a0001c0001t0006g0324others(21): Show | 24 | HG01884.hp1 HG01981.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.-2-62dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180529197 | |||||
| chr5:180529197
|
C | CAAA | 53 | a0001c0001t0002g0176a0001c0001t0003g0170a0001c0001t0003g0172others(50): Show | 53 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.-2-64_-2-62dupAAA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180529197 | |||||
| chr5:180529622
|
C | A | 52 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(49): Show | 52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.112+234C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180529622 | ||||||
| chr5:180529629
|
C | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+241C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180529629 | ||||||
| chr5:180529948
|
T | C | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+560T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180529948 | ||||||
| chr5:180529952
|
A | G | 2 | a0001c0001t0003g0172a0001c0001t0037g0171 | 2 | HG00741.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.112+564A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180529952 | ||||||
| chr5:180530182
|
G | T | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+794G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180530182 | ||||||
| chr5:180530283
|
G | A | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+895G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180530283 | ||||||
| chr5:180530400
|
T | A | 1 | a0002c0004t0001g0319 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.112+1012T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180530400 | ||||||
| chr5:180530492
|
G | A | 3 | a0001c0001t0001g0260a0001c0001t0012g0255a0001c0001t0012g0321 | 3 | HG02273.hp1 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.112+1104G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180530492 | ||||||
| chr5:180530561
|
C | CT | 42 | a0001c0001t0002g0061a0001c0001t0003g0188a0001c0001t0003g0189others(39): Show | 42 | HG00621.hp1 HG00738.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.112+1191dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180530561 | |||||
| chr5:180530561
|
CT | C | 12 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0263others(9): Show | 12 | HG00099.hp1 HG01069.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.112+1191delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180530561 | |||||
| chr5:180530716
|
C | T | 298 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(295): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.112+1328C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180530716 | ||||||
| chr5:180530721
|
G | T | 1 | a0001c0001t0039g0102 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.112+1333G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180530721 | ||||||
| chr5:180530781
|
G | A | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.112+1393G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180530781 | ||||||
| chr5:180530865
|
A | T | 1 | a0001c0001t0001g0307 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.112+1477A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180530865 | ||||||
| chr5:180530874
|
G | A | 1 | a0001c0001t0003g0195 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.112+1486G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180530874 | ||||||
| chr5:180531044
|
C | T | 5 | a0001c0001t0003g0205a0001c0001t0018g0004a0001c0001t0018g0005others(2): Show | 5 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+1656C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531044 | ||||||
| chr5:180531107
|
GGGCAGAG others(87): Show |
G | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.112+1747_112+1840d others(96): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180531107 | |||||
| chr5:180531143
|
T | C | 65 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(62): Show | 65 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.112+1755T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531143 | ||||||
| chr5:180531190
|
G | GGGCGGCT others(33): Show |
5 | a0001c0001t0001g0105a0001c0001t0013g0103a0001c0001t0013g0104others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.112+1841_112+1842i others(42): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180531190 | |||||
| chr5:180531230
|
G | T | 6 | a0001c0001t0001g0105a0001c0001t0005g0226a0001c0001t0013g0103others(3): Show | 6 | HG01884.hp2 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.112+1842G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531230 | ||||||
| chr5:180531234
|
G | A | 61 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(58): Show | 61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.112+1846G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531234 | ||||||
| chr5:180531241
|
G | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(157): Show | 160 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.112+1853G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531241 | ||||||
| chr5:180531273
|
T | C | 115 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(112): Show | 115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.112+1885T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531273 | ||||||
| chr5:180531274
|
G | A | 61 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(58): Show | 61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.112+1886G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531274 | ||||||
| chr5:180531283
|
G | A | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.112+1895G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531283 | ||||||
| chr5:180531287
|
C | T | 115 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(112): Show | 115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.112+1899C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531287 | ||||||
| chr5:180531305
|
C | CG | 12 | a0001c0001t0002g0093a0001c0001t0002g0098a0001c0001t0003g0184others(9): Show | 12 | HG00438.hp2 HG01361.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.112+1921dupG | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180531305 | |||||
| chr5:180531305
|
C | T | 1 | a0001c0001t0002g0066 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.112+1917C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531305 | ||||||
| chr5:180531318
|
G | A | 53 | a0001c0001t0001g0070a0001c0001t0002g0018a0001c0001t0002g0020others(50): Show | 53 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.112+1930G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531318 | ||||||
| chr5:180531429
|
C | T | 1 | a0001c0001t0001g0320 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.112+2041C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531429 | ||||||
| chr5:180531430
|
G | A | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.112+2042G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531430 | ||||||
| chr5:180531470
|
G | A | 18 | a0001c0001t0001g0070a0001c0001t0002g0018a0001c0001t0002g0029others(15): Show | 18 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.112+2082G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531470 | ||||||
| chr5:180531470
|
G | T | 1 | a0001c0001t0049g0333 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.112+2082G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531470 | ||||||
| chr5:180531520
|
GGCTCCTC others(32): Show |
G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+2142_112+2180d others(41): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180531520 | |||||
| chr5:180531532
|
C | T | 111 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(108): Show | 111 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.112+2144C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531532 | ||||||
| chr5:180531539
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.112+2151G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531539 | ||||||
| chr5:180531577
|
C | CG | 11 | a0001c0001t0001g0307a0001c0001t0002g0079a0001c0001t0002g0098others(8): Show | 11 | HG00544.hp2 HG00735.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.112+2193dupG | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180531577 | |||||
| chr5:180531586
|
G | A | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.112+2198G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531586 | ||||||
| chr5:180531732
|
C | T | 2 | a0001c0001t0062g0030a0001c0001t0063g0230 | 2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.112+2344C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531732 | ||||||
| chr5:180531744
|
A | T | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.112+2356A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531744 | ||||||
| chr5:180531768
|
G | T | 2 | a0001c0001t0040g0100a0001c0001t0041g0101 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.112+2380G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531768 | ||||||
| chr5:180531803
|
C | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+2415C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531803 | ||||||
| chr5:180531803
|
C | T | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.112+2415C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531803 | ||||||
| chr5:180531827
|
T | C | 4 | a0001c0001t0021g0158a0001c0001t0021g0159a0001c0001t0021g0160others(1): Show | 4 | HG02071.hp2 HG02735.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+2439T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531827 | ||||||
| chr5:180531948
|
C | T | 1 | a0001c0001t0015g0119 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.112+2560C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531948 | ||||||
| chr5:180531984
|
G | A | 61 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(58): Show | 61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.112+2596G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531984 | ||||||
| chr5:180531992
|
G | A | 59 | a0001c0001t0001g0070a0001c0001t0001g0105a0001c0001t0002g0018others(56): Show | 59 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.112+2604G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531992 | ||||||
| chr5:180532021
|
A | G | 2 | a0001c0001t0003g0197a0001c0001t0023g0196 | 2 | HG01433.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.112+2633A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532021 | ||||||
| chr5:180532063
|
G | A | 20 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(17): Show | 20 | HG00280.hp2 HG00639.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.112+2675G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532063 | ||||||
| chr5:180532149
|
A | C | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+2761A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532149 | ||||||
| chr5:180532220
|
G | A | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.112+2832G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532220 | ||||||
| chr5:180532327
|
C | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+2939C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532327 | ||||||
| chr5:180532486
|
T | C | 2 | a0001c0001t0001g0241a0001c0001t0001g0273 | 2 | NA19075.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.112+3098T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532486 | ||||||
| chr5:180532519
|
G | C | 61 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(58): Show | 61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.112+3131G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532519 | ||||||
| chr5:180532602
|
G | T | 1 | a0001c0001t0017g0166 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.112+3214G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532602 | ||||||
| chr5:180532708
|
A | C | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+3320A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532708 | ||||||
| chr5:180532834
|
T | C | 2 | a0001c0001t0002g0020a0001c0001t0042g0075 | 2 | HG01975.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.112+3446T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532834 | ||||||
| chr5:180532979
|
A | G | 52 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(49): Show | 52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.112+3591A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532979 | ||||||
| chr5:180533034
|
T | C | 2 | a0001c0001t0040g0100a0001c0001t0041g0101 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.112+3646T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533034 | ||||||
| chr5:180533227
|
T | C | 20 | a0001c0001t0001g0245a0001c0001t0001g0267a0001c0001t0001g0268others(17): Show | 20 | HG00423.hp2 HG00642.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.112+3839T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533227 | ||||||
| chr5:180533311
|
C | CAT | 28 | a0001c0001t0001g0229a0001c0001t0001g0239a0001c0001t0001g0241others(25): Show | 28 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.112+3923_112+3924i others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533311 | ||||||
| chr5:180533311
|
C | CATAT | 3 | a0001c0001t0001g0253a0001c0001t0001g0261a0001c0001t0001g0273 | 3 | HG00544.hp1 HG03927.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.112+3923_112+3924i others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533311 | ||||||
| chr5:180533311
|
C | CATATAT | 3 | a0001c0001t0001g0318a0001c0001t0005g0113a0002c0004t0004g0252 | 3 | HG02572.hp1 NA18960.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.112+3923_112+3924i others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533311 | ||||||
| chr5:180533311
|
C | CATATATA others(3): Show |
1 | a0001c0001t0001g0316 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.112+3923_112+3924i others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533311 | ||||||
| chr5:180533311
|
C | CATATATA others(13): Show |
1 | a0001c0001t0001g0227 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.112+3923_112+3924i others(22): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533311 | ||||||
| chr5:180533311
|
CCT | C | 3 | a0001c0001t0001g0244a0001c0001t0001g0263a0001c0001t0001g0278 | 3 | HG00558.hp1 HG02559.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.112+3924_112+3925d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533311 | ||||||
| chr5:180533312
|
C | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0227a0001c0001t0001g0229others(93): Show | 96 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.112+3924C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533312 | ||||||
| chr5:180533312
|
C | CTA | 3 | a0001c0001t0002g0066a0001c0001t0057g0059a0001c0005t0004g0019 | 3 | HG03453.hp2 NA18906.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.112+3954_112+3955d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATA | 11 | a0001c0001t0002g0231a0001c0001t0005g0226a0001c0002t0002g0044others(8): Show | 11 | HG01256.hp2 HG01258.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.112+3952_112+3955d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATA | 6 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0002t0002g0034others(3): Show | 6 | HG01069.hp1 HG01106.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.112+3950_112+3955d others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATAT others(3): Show |
8 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0087others(5): Show | 8 | HG00438.hp1 HG03704.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.112+3946_112+3955d others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATAT others(5): Show |
9 | a0001c0001t0002g0020a0001c0001t0002g0032a0001c0001t0002g0083others(6): Show | 9 | HG00438.hp2 HG00639.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.112+3944_112+3955d others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATAT others(7): Show |
2 | a0001c0001t0002g0018a0001c0001t0002g0082 | 2 | HG00642.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.112+3942_112+3955d others(16): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATAT others(9): Show |
3 | a0001c0001t0001g0105a0001c0001t0002g0074a0001c0001t0013g0104 | 3 | HG01884.hp2 HG02818.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.112+3940_112+3955d others(18): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATAT others(11): Show |
3 | a0001c0001t0013g0103a0001c0001t0013g0106a0001c0001t0013g0107 | 3 | HG02717.hp2 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.112+3938_112+3955d others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATAT others(13): Show |
1 | a0001c0001t0005g0081 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.112+3936_112+3955d others(22): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATAT others(15): Show |
1 | a0001c0001t0002g0092 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.112+3934_112+3955d others(24): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATAT others(17): Show |
2 | a0001c0001t0002g0071a0001c0001t0002g0072 | 2 | NA18939.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.112+3932_112+3955d others(26): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATAT others(19): Show |
3 | a0001c0001t0002g0061a0001c0001t0002g0065a0001c0001t0002g0088 | 3 | HG00621.hp1 HG02165.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.112+3930_112+3955d others(28): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATAT others(21): Show |
3 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0058g0095 | 3 | HG00609.hp1 NA18947.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.112+3928_112+3955d others(30): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATAT others(23): Show |
1 | a0001c0001t0002g0064 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.112+3926_112+3955d others(32): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATAT others(25): Show |
3 | a0001c0001t0002g0029a0001c0001t0002g0060a0001c0001t0002g0108 | 3 | NA18955.hp2 NA19012.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.112+3955_112+3956i others(34): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATAT others(27): Show |
3 | a0001c0001t0002g0067a0001c0001t0002g0098a0001c0001t0002g0232 | 3 | HG00597.hp1 HG02071.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.112+3955_112+3956i others(36): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATAT others(29): Show |
1 | a0001c0001t0001g0070 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.112+3955_112+3956i others(38): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATAT others(31): Show |
1 | a0001c0001t0002g0063 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.112+3955_112+3956i others(40): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATAT others(33): Show |
1 | a0001c0001t0002g0073 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.112+3955_112+3956i others(42): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATGT others(21): Show |
1 | a0001c0001t0002g0076 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.112+3929_112+3930i others(30): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
C | CTATATGT others(43): Show |
1 | a0001c0001t0002g0077 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.112+3929_112+3930i others(52): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
CTA | C | 5 | a0001c0001t0017g0166a0001c0001t0025g0219a0001c0001t0026g0223others(2): Show | 5 | HG01261.hp1 HG02257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+3954_112+3955d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
CTATA | C | 13 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(10): Show | 13 | HG01243.hp2 HG01884.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.112+3952_112+3955d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
CTATATA | C | 14 | a0001c0001t0002g0097a0001c0001t0002g0111a0001c0001t0011g0212others(11): Show | 14 | HG01256.hp1 HG01361.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.112+3950_112+3955d others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
CTATATAT others(9): Show |
C | 52 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(49): Show | 52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.112+3940_112+3955d others(18): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533312
|
CTATATAT others(11): Show |
C | 7 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(4): Show | 7 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+3938_112+3955d others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | |||||
| chr5:180533331
|
TATATATA | T | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.112+3944_112+3950d others(9): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533331 | ||||||
| chr5:180533339
|
T | C | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.112+3951T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533339 | ||||||
| chr5:180533341
|
T | C | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.112+3953T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533341 | ||||||
| chr5:180533651
|
G | A | 4 | a0001c0001t0021g0158a0001c0001t0021g0159a0001c0001t0021g0160others(1): Show | 4 | HG02071.hp2 HG02735.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+4263G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533651 | ||||||
| chr5:180533756
|
T | C | 52 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(49): Show | 52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.112+4368T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533756 | ||||||
| chr5:180533771
|
A | G | 1 | a0001c0002t0002g0052 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.112+4383A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533771 | ||||||
| chr5:180533901
|
TC | T | 7 | a0001c0001t0002g0088a0001c0001t0002g0090a0001c0001t0002g0092others(4): Show | 7 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+4515delC | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533901 | |||||
| chr5:180533932
|
G | A | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+4544G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533932 | ||||||
| chr5:180534082
|
G | A | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.112+4694G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534082 | ||||||
| chr5:180534243
|
A | C | 2 | a0001c0001t0003g0201a0001c0001t0003g0205 | 2 | HG02559.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.112+4855A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534243 | ||||||
| chr5:180534383
|
T | G | 1 | a0001c0001t0026g0221 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.112+4995T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534383 | ||||||
| chr5:180534464
|
G | A | 2 | a0001c0002t0004g0037a0001c0002t0004g0051 | 2 | HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.112+5076G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534464 | ||||||
| chr5:180534502
|
A | G | 53 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(50): Show | 53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.112+5114A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534502 | ||||||
| chr5:180534507
|
C | T | 52 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(49): Show | 52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.112+5119C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534507 | ||||||
| chr5:180534589
|
C | A | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+5201C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534589 | ||||||
| chr5:180534612
|
GGGGGTCC others(189): Show |
G | 3 | a0001c0001t0001g0246a0001c0001t0001g0275a0001c0001t0001g0315 | 3 | NA18978.hp2 NA19005.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.112+5271_112+5466d others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180534612 | |||||
| chr5:180534612
|
GGGGGTCC others(238): Show |
G | 9 | a0001c0002t0005g0021a0001c0002t0005g0022a0001c0002t0005g0023others(6): Show | 9 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.112+5438_112+5682d others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180534612 | |||||
| chr5:180534612
|
GGGGGTCC others(287): Show |
G | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.112+5271_112+5564d others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180534612 | |||||
| chr5:180534619
|
C | T | 1 | a0001c0001t0022g0225 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.112+5231C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534619 | ||||||
| chr5:180534659
|
G | C | 60 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(57): Show | 60 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.112+5271G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534659 | ||||||
| chr5:180534659
|
GCTGGGGT others(42): Show |
G | 53 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(50): Show | 53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.112+5467_112+5515d others(51): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180534659 | |||||
| chr5:180534667
|
C | T | 60 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(57): Show | 60 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.112+5279C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534667 | ||||||
| chr5:180534702
|
G | A | 1 | a0001c0001t0002g0088 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.112+5314G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534702 | ||||||
| chr5:180534708
|
C | G | 9 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(6): Show | 9 | HG00099.hp1 HG00738.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.112+5320C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534708 | ||||||
| chr5:180534748
|
G | A | 5 | a0001c0001t0010g0182a0001c0001t0014g0167a0001c0001t0014g0174others(2): Show | 5 | HG00280.hp2 HG00639.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+5360G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534748 | ||||||
| chr5:180534757
|
C | G | 60 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(57): Show | 60 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.112+5369C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534757 | ||||||
| chr5:180534757
|
CCTGGGGT others(140): Show |
C | 1 | a0001c0001t0018g0006 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.112+5516_112+5662d others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180534757 | |||||
| chr5:180534806
|
CCTGGGGT others(91): Show |
C | 3 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0007 | 3 | HG00099.hp1 HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.112+5516_112+5613d others(100): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180534806 | |||||
| chr5:180534814
|
C | T | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.112+5426C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534814 | ||||||
| chr5:180534826
|
CGGAATCC others(238): Show |
C | 60 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(57): Show | 60 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.112+5472_112+5716d others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180534826 | |||||
| chr5:180534848
|
C | T | 1 | a0001c0001t0006g0137 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.112+5460C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534848 | ||||||
| chr5:180534865
|
G | A | 2 | a0001c0001t0001g0240a0001c0001t0008g0238 | 2 | NA18944.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.112+5477G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534865 | ||||||
| chr5:180534882
|
C | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(152): Show | 155 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.112+5494C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534882 | ||||||
| chr5:180534914
|
G | A | 2 | a0001c0001t0001g0244a0001c0001t0001g0313 | 2 | HG01515.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.112+5526G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534914 | ||||||
| chr5:180534953
|
C | G | 3 | a0001c0001t0002g0087a0001c0001t0002g0099a0001c0001t0002g0114 | 3 | HG00438.hp1 HG02135.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.112+5565C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534953 | ||||||
| chr5:180535002
|
C | G | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.112+5614C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535002 | ||||||
| chr5:180535022
|
CGGAATCC others(42): Show |
C | 53 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(50): Show | 53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.112+5668_112+5716d others(51): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535022 | |||||
| chr5:180535071
|
T | C | 5 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(2): Show | 5 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+5683T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535071 | ||||||
| chr5:180535111
|
A | C | 10 | a0001c0002t0004g0036a0001c0002t0004g0041a0001c0002t0004g0049others(7): Show | 10 | HG01167.hp1 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.112+5723A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535111 | ||||||
| chr5:180535141
|
A | G | 1 | a0001c0001t0040g0100 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.112+5753A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535141 | ||||||
| chr5:180535180
|
G | C | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+5792G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535180 | ||||||
| chr5:180535206
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.112+5818C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535206 | ||||||
| chr5:180535237
|
C | T | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+5849C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535237 | ||||||
| chr5:180535314
|
G | A | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.112+5926G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535314 | ||||||
| chr5:180535319
|
C | A | 61 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(58): Show | 61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.112+5931C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535319 | ||||||
| chr5:180535366
|
A | G | 1 | a0001c0001t0057g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.112+5978A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535366 | ||||||
| chr5:180535521
|
G | A | 1 | a0001c0001t0053g0117 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.112+6133G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535521 | ||||||
| chr5:180535707
|
T | C | 2 | a0001c0002t0004g0057a0001c0002t0004g0058 | 2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.112+6319T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535707 | ||||||
| chr5:180535811
|
G | A | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+6423G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535811 | ||||||
| chr5:180535915
|
G | A | 1 | a0001c0001t0009g0178 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.112+6527G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535915 | ||||||
| chr5:180535951
|
A | G | 1 | a0001c0001t0002g0084 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.112+6563A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535951 | ||||||
| chr5:180535959
|
T | C | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+6571T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535959 | ||||||
| chr5:180535988
|
G | GT | 45 | a0001c0001t0002g0018a0001c0001t0002g0020a0001c0001t0002g0029others(42): Show | 45 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.112+6629dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535988 | |||||
| chr5:180535988
|
G | GTT | 15 | a0001c0001t0001g0070a0001c0001t0002g0062a0001c0001t0002g0066others(12): Show | 15 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(12): Show |
intron_variant | MODIFIER | c.112+6628_112+6629d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535988 | |||||
| chr5:180535988
|
GT | G | 21 | a0001c0001t0008g0303a0001c0001t0026g0221a0001c0001t0062g0030others(18): Show | 21 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.112+6629delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535988 | |||||
| chr5:180535988
|
GTT | G | 25 | a0001c0001t0001g0227a0001c0001t0001g0241a0001c0001t0001g0244others(22): Show | 25 | HG00544.hp2 HG00621.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.112+6628_112+6629d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535988 | |||||
| chr5:180535988
|
GTTT | G | 72 | a0001c0001t0001g0001a0001c0001t0001g0229a0001c0001t0001g0236others(69): Show | 72 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.112+6627_112+6629d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535988 | |||||
| chr5:180535988
|
GTTTTT | G | 13 | a0001c0001t0002g0176a0001c0001t0003g0170a0001c0001t0003g0172others(10): Show | 13 | HG00733.hp2 HG01243.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.112+6625_112+6629d others(7): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535988 | |||||
| chr5:180535988
|
GTTTTTT | G | 70 | a0001c0001t0001g0168a0001c0001t0003g0179a0001c0001t0003g0180others(67): Show | 70 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.112+6624_112+6629d others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535988 | |||||
| chr5:180535988
|
GTTTTTTT | G | 28 | a0001c0001t0003g0188a0001c0001t0003g0197a0001c0001t0003g0200others(25): Show | 28 | HG00738.hp2 HG01071.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.112+6623_112+6629d others(9): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535988 | |||||
| chr5:180535988
|
GTTTTTTT others(11): Show |
G | 1 | a0001c0001t0060g0002 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.112+6612_112+6629d others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535988 | |||||
| chr5:180535992
|
T | G | 1 | a0001c0001t0001g0251 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.112+6604T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535992 | ||||||
| chr5:180536017
|
T | G | 49 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(46): Show | 49 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.112+6629T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536017 | ||||||
| chr5:180536027
|
A | G | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+6639A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536027 | ||||||
| chr5:180536029
|
T | C | 1 | a0001c0001t0003g0191 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.112+6641T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536029 | ||||||
| chr5:180536034
|
T | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(305): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.112+6646T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536034 | ||||||
| chr5:180536127
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.112+6739C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536127 | ||||||
| chr5:180536171
|
AT | A | 298 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(295): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.112+6792delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180536171 | |||||
| chr5:180536190
|
G | A | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+6802G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536190 | ||||||
| chr5:180536239
|
T | G | 4 | a0001c0001t0007g0135a0001c0001t0007g0141a0001c0001t0007g0142others(1): Show | 4 | HG00609.hp2 HG02523.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+6851T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536239 | ||||||
| chr5:180536240
|
C | T | 4 | a0001c0001t0024g0118a0001c0001t0024g0151a0001c0001t0024g0157others(1): Show | 4 | HG01109.hp2 HG01168.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+6852C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536240 | ||||||
| chr5:180536244
|
C | T | 1 | a0001c0001t0002g0060 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.112+6856C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536244 | ||||||
| chr5:180536316
|
T | G | 53 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(50): Show | 53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.112+6928T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536316 | ||||||
| chr5:180536353
|
C | A | 1 | a0001c0001t0061g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.112+6965C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536353 | ||||||
| chr5:180536572
|
A | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+7184A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536572 | ||||||
| chr5:180536636
|
G | A | 1 | a0001c0001t0003g0195 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.112+7248G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536636 | ||||||
| chr5:180536636
|
G | T | 1 | a0001c0001t0015g0127 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.112+7248G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536636 | ||||||
| chr5:180537039
|
C | A | 1 | a0001c0001t0057g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.112+7651C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180537039 | ||||||
| chr5:180537047
|
C | T | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.112+7659C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180537047 | ||||||
| chr5:180537137
|
T | C | 1 | a0001c0001t0026g0223 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.112+7749T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180537137 | ||||||
| chr5:180537526
|
C | T | 7 | a0001c0001t0002g0088a0001c0001t0002g0090a0001c0001t0002g0092others(4): Show | 7 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+8138C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180537526 | ||||||
| chr5:180537527
|
G | A | 1 | a0001c0002t0005g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.112+8139G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180537527 | ||||||
| chr5:180537800
|
C | G | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.112+8412C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180537800 | ||||||
| chr5:180537804
|
C | CT | 209 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(206): Show | 209 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.112+8430dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180537804 | |||||
| chr5:180537804
|
C | CTT | 20 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(17): Show | 20 | HG01243.hp2 HG01261.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.112+8429_112+8430d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180537804 | |||||
| chr5:180537804
|
CT | C | 54 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(51): Show | 54 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.112+8430delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180537804 | |||||
| chr5:180537910
|
T | G | 1 | a0001c0005t0004g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.112+8522T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180537910 | ||||||
| chr5:180537926
|
T | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+8538T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180537926 | ||||||
| chr5:180538034
|
C | CT | 7 | a0001c0001t0018g0004a0001c0001t0018g0006a0001c0001t0018g0007others(4): Show | 7 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+8668dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538034 | |||||
| chr5:180538034
|
CT | C | 274 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(271): Show | 274 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.112+8668delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538034 | |||||
| chr5:180538034
|
CTT | C | 17 | a0001c0001t0001g0237a0001c0001t0002g0079a0001c0001t0002g0097others(14): Show | 17 | HG00733.hp2 HG01243.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.112+8667_112+8668d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538034 | |||||
| chr5:180538106
|
T | C | 52 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(49): Show | 52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.112+8718T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538106 | ||||||
| chr5:180538149
|
C | T | 1 | a0001c0001t0002g0062 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.112+8761C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538149 | ||||||
| chr5:180538300
|
G | A | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+8912G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538300 | ||||||
| chr5:180538355
|
T | TA | 61 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(58): Show | 61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.112+8973dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538355 | |||||
| chr5:180538414
|
G | A | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.112+9026G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538414 | ||||||
| chr5:180538466
|
A | G | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+9078A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538466 | ||||||
| chr5:180538545
|
G | A | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.112+9157G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538545 | ||||||
| chr5:180538585
|
G | A | 1 | a0001c0001t0026g0221 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.112+9197G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538585 | ||||||
| chr5:180538637
|
A | G | 52 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(49): Show | 52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.112+9249A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538637 | ||||||
| chr5:180538685
|
G | GGTATATA others(3): Show |
3 | a0001c0001t0001g0284a0001c0001t0012g0321a0001c0001t0061g0003 | 3 | HG02257.hp2 HG02273.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.112+9298_112+9307d others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538685 | |||||
| chr5:180538685
|
GGTATATA others(3): Show |
G | 2 | a0001c0001t0003g0172a0001c0001t0003g0290 | 2 | HG01934.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.112+9298_112+9307d others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538685 | ||||||
| chr5:180538685
|
GGTATATA others(5): Show |
G | 59 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(56): Show | 59 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.112+9298_112+9309d others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538685 | ||||||
| chr5:180538686
|
G | GTA | 5 | a0001c0001t0001g0105a0001c0001t0005g0226a0001c0001t0013g0103others(2): Show | 5 | HG01884.hp2 HG02717.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+9327_112+9328d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | |||||
| chr5:180538686
|
G | GTATA | 3 | a0001c0001t0013g0104a0001c0001t0062g0030a0001c0001t0063g0230 | 3 | HG02258.hp1 HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.112+9325_112+9328d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | |||||
| chr5:180538686
|
G | GTATATAT others(1): Show |
3 | a0001c0002t0005g0022a0001c0002t0005g0027a0001c0002t0005g0028 | 3 | HG01891.hp2 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.112+9321_112+9328d others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | |||||
| chr5:180538686
|
G | GTATATAT others(3): Show |
2 | a0001c0001t0002g0114a0001c0002t0005g0023 | 2 | HG02135.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.112+9319_112+9328d others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | |||||
| chr5:180538686
|
G | GTATATAT others(5): Show |
2 | a0001c0002t0005g0021a0001c0002t0005g0026 | 2 | HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.112+9317_112+9328d others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | |||||
| chr5:180538686
|
G | GTATATAT others(7): Show |
19 | a0001c0001t0002g0018a0001c0001t0002g0062a0001c0001t0002g0063others(16): Show | 19 | HG00597.hp1 HG00639.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.112+9315_112+9328d others(16): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | |||||
| chr5:180538686
|
G | GTATATAT others(9): Show |
13 | a0001c0001t0001g0070a0001c0001t0002g0020a0001c0001t0002g0029others(10): Show | 13 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(10): Show |
intron_variant | MODIFIER | c.112+9313_112+9328d others(18): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | |||||
| chr5:180538686
|
G | GTATATAT others(11): Show |
8 | a0001c0001t0002g0073a0001c0001t0002g0077a0001c0001t0002g0087others(5): Show | 8 | HG02165.hp1 HG02165.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.112+9311_112+9328d others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | |||||
| chr5:180538686
|
G | GTATATAT others(13): Show |
4 | a0001c0001t0002g0084a0001c0001t0002g0090a0001c0001t0002g0094others(1): Show | 4 | HG02004.hp1 NA18968.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+9309_112+9328d others(22): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | |||||
| chr5:180538686
|
G | GTATATAT others(15): Show |
1 | a0001c0001t0002g0076 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.112+9307_112+9328d others(24): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | |||||
| chr5:180538686
|
G | GTATATAT others(17): Show |
2 | a0001c0001t0002g0078a0001c0001t0002g0086 | 2 | HG03704.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.112+9305_112+9328d others(26): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | |||||
| chr5:180538686
|
G | GTATATAT others(19): Show |
5 | a0001c0001t0002g0068a0001c0001t0002g0093a0001c0001t0002g0099others(2): Show | 5 | HG00438.hp1 HG00438.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+9303_112+9328d others(28): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | |||||
| chr5:180538686
|
G | GTATATAT others(23): Show |
1 | a0001c0001t0058g0095 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.112+9299_112+9328d others(32): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | |||||
| chr5:180538686
|
G | GTATATAT others(29): Show |
1 | a0001c0001t0002g0066 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.112+9328_112+9329i others(38): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | |||||
| chr5:180538686
|
GTA | G | 20 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0046g0011others(17): Show | 20 | HG01069.hp1 HG01106.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.112+9327_112+9328d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | |||||
| chr5:180538686
|
GTATATAT others(3): Show |
G | 1 | a0001c0001t0021g0158 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.112+9319_112+9328d others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | |||||
| chr5:180538686
|
GTATATAT others(5): Show |
G | 54 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(51): Show | 54 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.112+9317_112+9328d others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | |||||
| chr5:180538686
|
GTATATAT others(11): Show |
G | 14 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(11): Show | 14 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.112+9311_112+9328d others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | |||||
| chr5:180538688
|
A | ATATATAT others(1): Show |
20 | a0001c0001t0001g0260a0001c0001t0001g0263a0001c0001t0001g0267others(17): Show | 20 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.112+9307_112+9308i others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538688 | |||||
| chr5:180538690
|
A | ATATATG | 76 | a0001c0001t0001g0001a0001c0001t0001g0227a0001c0001t0001g0229others(73): Show | 76 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.112+9307_112+9308i others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538690 | |||||
| chr5:180538713
|
T | TATATATA others(9): Show |
1 | a0001c0001t0060g0002 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.112+9328_112+9329i others(18): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538713 | |||||
| chr5:180538717
|
C | T | 1 | a0001c0001t0061g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.112+9329C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538717 | ||||||
| chr5:180538909
|
C | T | 1 | a0001c0001t0061g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.112+9521C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538909 | ||||||
| chr5:180539019
|
CA | C | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+9637delA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539019 | |||||
| chr5:180539067
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.112+9679C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539067 | ||||||
| chr5:180539121
|
G | A | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.112+9733G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539121 | ||||||
| chr5:180539173
|
C | CA | 6 | a0001c0001t0001g0301a0001c0001t0001g0315a0001c0001t0008g0303others(3): Show | 6 | HG00597.hp2 HG02027.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.112+9803dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539173 | |||||
| chr5:180539173
|
C | CAA | 56 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(53): Show | 56 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.112+9802_112+9803d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539173 | |||||
| chr5:180539173
|
C | CAAA | 47 | a0001c0001t0003g0172a0001c0001t0006g0123a0001c0001t0006g0124others(44): Show | 47 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.112+9801_112+9803d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539173 | |||||
| chr5:180539173
|
C | CAAAA | 11 | a0001c0001t0006g0122a0001c0001t0006g0146a0001c0001t0016g0121others(8): Show | 11 | HG00408.hp1 HG01243.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.112+9800_112+9803d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539173 | |||||
| chr5:180539221
|
C | T | 1 | a0001c0001t0005g0081 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.112+9833C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539221 | ||||||
| chr5:180539243
|
G | A | 1 | a0001c0001t0006g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.112+9855G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539243 | ||||||
| chr5:180539272
|
C | T | 1 | a0001c0002t0004g0040 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.112+9884C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539272 | ||||||
| chr5:180539295
|
C | A | 3 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0007 | 3 | HG00099.hp1 HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.112+9907C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539295 | ||||||
| chr5:180539295
|
C | CA | 61 | a0001c0001t0001g0301a0001c0001t0002g0066a0001c0001t0006g0008others(58): Show | 61 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.112+9916dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539295 | |||||
| chr5:180539298
|
A | AC | 52 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(49): Show | 52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.112+9910_112+9911i others(3): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539298 | ||||||
| chr5:180539322
|
T | C | 53 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(50): Show | 53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.112+9934T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539322 | ||||||
| chr5:180539413
|
G | C | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+10025G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539413 | ||||||
| chr5:180539548
|
GTTCTTTT others(6): Show |
G | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.112+10163_112+1017 others(17): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539548 | |||||
| chr5:180539548
|
GTTCTTTT others(7): Show |
G | 3 | a0001c0001t0011g0224a0001c0001t0025g0217a0001c0001t0038g0218 | 3 | HG02109.hp1 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.112+10163_112+1017 others(18): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539548 | |||||
| chr5:180539548
|
GTTCTTTT others(8): Show |
G | 2 | a0001c0001t0011g0212a0001c0001t0011g0216 | 2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.112+10163_112+1017 others(19): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539548 | |||||
| chr5:180539548
|
GTTCTTTT others(21): Show |
G | 2 | a0001c0001t0001g0168a0001c0001t0002g0176 | 2 | NA18955.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.112+10163_112+1019 others(32): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539548 | |||||
| chr5:180539548
|
GTTCTTTT others(22): Show |
G | 1 | a0001c0001t0011g0215 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.112+10163_112+1019 others(33): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539548 | |||||
| chr5:180539551
|
C | T | 1 | a0001c0001t0026g0223 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.112+10163C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539551 | ||||||
| chr5:180539551
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0002t0002g0048a0001c0002t0020g0055 | 2 | HG01123.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.112+10209_112+1021 others(15): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0002t0002g0034a0001c0002t0002g0035a0001c0002t0020g0054 | 3 | HG01069.hp1 HG01106.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.112+10208_112+1021 others(16): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0002t0002g0044a0001c0002t0002g0045 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.112+10207_112+1021 others(17): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0021g0158a0001c0001t0039g0102 | 2 | HG02071.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.112+10206_112+1021 others(18): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0021g0159a0001c0001t0025g0219 | 2 | HG02735.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.112+10204_112+1021 others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.112+10201_112+1021 others(23): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0035g0017 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.112+10200_112+1021 others(24): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0036g0192 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.112+10199_112+1021 others(25): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(15): Show |
C | 3 | a0001c0001t0010g0193a0001c0001t0013g0256a0001c0001t0014g0202 | 3 | HG00642.hp2 HG03195.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.112+10198_112+1021 others(26): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(16): Show |
C | 15 | a0001c0001t0005g0113a0001c0001t0009g0010a0001c0001t0009g0015others(12): Show | 15 | HG00280.hp2 HG00639.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.112+10197_112+1021 others(27): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(17): Show |
C | 17 | a0001c0001t0001g0265a0001c0001t0003g0170a0001c0001t0003g0181others(14): Show | 17 | HG00741.hp2 HG01257.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.112+10196_112+1021 others(28): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(18): Show |
C | 34 | a0001c0001t0001g0248a0001c0001t0001g0269a0001c0001t0001g0281others(31): Show | 34 | HG00438.hp1 HG00738.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.112+10195_112+1021 others(29): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(19): Show |
C | 69 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(66): Show | 69 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.112+10194_112+1021 others(30): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(20): Show |
C | 84 | a0001c0001t0001g0227a0001c0001t0001g0229a0001c0001t0001g0236others(81): Show | 84 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.112+10193_112+1021 others(31): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(21): Show |
C | 17 | a0001c0001t0002g0108a0001c0001t0006g0008a0001c0001t0006g0122others(14): Show | 17 | HG00408.hp1 HG01109.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.112+10192_112+1021 others(32): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(22): Show |
C | 35 | a0001c0001t0006g0124a0001c0001t0006g0130a0001c0001t0006g0136others(32): Show | 35 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.112+10191_112+1021 others(33): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(23): Show |
C | 3 | a0001c0001t0006g0323a0001c0001t0032g0128a0001c0002t0002g0046 | 3 | HG01257.hp1 HG01433.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.112+10190_112+1021 others(34): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(24): Show |
C | 9 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002others(6): Show | 9 | HG01167.hp1 HG02451.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.112+10189_112+1021 others(35): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(26): Show |
C | 1 | a0001c0002t0004g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.112+10187_112+1021 others(37): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(29): Show |
C | 1 | a0001c0001t0049g0333 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.112+10184_112+1021 others(40): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(30): Show |
C | 3 | a0001c0001t0022g0225a0001c0003t0022g0220a0001c0003t0022g0222 | 3 | HG02055.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.112+10183_112+1021 others(41): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(31): Show |
C | 1 | a0001c0001t0002g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.112+10182_112+1021 others(42): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(33): Show |
C | 9 | a0001c0002t0005g0021a0001c0002t0005g0022a0001c0002t0005g0023others(6): Show | 9 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.112+10180_112+1021 others(44): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539551
|
CTTTTTTT others(37): Show |
C | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+10176_112+1021 others(48): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | |||||
| chr5:180539564
|
T | G | 2 | a0001c0001t0011g0213a0001c0001t0011g0214 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.112+10176T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539564 | ||||||
| chr5:180539565
|
T | G | 3 | a0001c0001t0011g0224a0001c0001t0025g0217a0001c0001t0038g0218 | 3 | HG02109.hp1 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.112+10177T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539565 | ||||||
| chr5:180539566
|
T | G | 2 | a0001c0001t0011g0212a0001c0001t0011g0216 | 2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.112+10178T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539566 | ||||||
| chr5:180539580
|
T | G | 1 | a0001c0001t0011g0215 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.112+10192T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539580 | ||||||
| chr5:180539663
|
T | C | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.113-10268T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539663 | ||||||
| chr5:180539673
|
T | C | 20 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(17): Show | 20 | HG00280.hp2 HG00639.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.113-10258T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539673 | ||||||
| chr5:180539694
|
A | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-10237A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539694 | ||||||
| chr5:180539714
|
C | T | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.113-10217C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539714 | ||||||
| chr5:180539750
|
C | T | 2 | a0001c0001t0009g0210a0001c0001t0010g0209 | 2 | HG01891.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.113-10181C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539750 | ||||||
| chr5:180539791
|
G | T | 3 | a0001c0001t0008g0262a0001c0001t0029g0234a0001c0001t0029g0289 | 3 | NA18962.hp2 NA18969.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.113-10140G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539791 | ||||||
| chr5:180539825
|
A | G | 49 | a0001c0001t0001g0070a0001c0001t0002g0018a0001c0001t0002g0020others(46): Show | 49 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.113-10106A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539825 | ||||||
| chr5:180539831
|
C | T | 1 | a0001c0001t0002g0086 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.113-10100C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539831 | ||||||
| chr5:180539833
|
C | T | 1 | a0001c0005t0004g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.113-10098C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539833 | ||||||
| chr5:180539836
|
G | A | 1 | a0001c0001t0009g0199 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.113-10095G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539836 | ||||||
| chr5:180539836
|
G | C | 1 | a0001c0001t0014g0202 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.113-10095G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539836 | ||||||
| chr5:180539841
|
G | A | 2 | a0001c0001t0045g0332a0001c0001t0049g0333 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.113-10090G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539841 | ||||||
| chr5:180539955
|
T | C | 1 | a0001c0005t0004g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.113-9976T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539955 | ||||||
| chr5:180540171
|
A | C | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-9760A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180540171 | ||||||
| chr5:180540386
|
A | G | 2 | a0001c0002t0004g0039a0001c0002t0004g0040 | 2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.113-9545A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180540386 | ||||||
| chr5:180540423
|
C | G | 160 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(157): Show | 160 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.113-9508C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180540423 | ||||||
| chr5:180540473
|
C | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-9458C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180540473 | ||||||
| chr5:180540509
|
A | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0227a0001c0001t0001g0229others(97): Show | 100 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.113-9422A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180540509 | ||||||
| chr5:180540738
|
C | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-9193C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180540738 | ||||||
| chr5:180540803
|
C | A | 115 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(112): Show | 115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.113-9128C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180540803 | ||||||
| chr5:180541076
|
A | G | 3 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0054g0145 | 3 | HG01981.hp1 HG02004.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.113-8855A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541076 | ||||||
| chr5:180541142
|
AT | A | 6 | a0001c0001t0001g0312a0001c0001t0002g0072a0001c0001t0009g0177others(3): Show | 6 | HG00738.hp1 HG01169.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-8775delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180541142 | |||||
| chr5:180541285
|
C | T | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.113-8646C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541285 | ||||||
| chr5:180541348
|
A | G | 1 | a0001c0001t0009g0183 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.113-8583A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541348 | ||||||
| chr5:180541381
|
C | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-8550C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541381 | ||||||
| chr5:180541440
|
A | ATTTT | 31 | a0001c0001t0001g0168a0001c0001t0003g0172a0001c0001t0003g0179others(28): Show | 31 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.113-8491_113-8490i others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541440 | ||||||
| chr5:180541440
|
A | ATTTTT | 19 | a0001c0001t0002g0176a0001c0001t0003g0170a0001c0001t0003g0195others(16): Show | 19 | HG00408.hp1 HG00735.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.113-8491_113-8490i others(7): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541440 | ||||||
| chr5:180541440
|
A | ATTTTTT | 29 | a0001c0001t0003g0181a0001c0001t0003g0188a0001c0001t0003g0189others(26): Show | 29 | HG00280.hp2 HG00609.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.113-8491_113-8490i others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541440 | ||||||
| chr5:180541440
|
A | ATTTTTTT | 16 | a0001c0001t0006g0008a0001c0001t0006g0146a0001c0001t0006g0147others(13): Show | 16 | HG00738.hp2 HG01123.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.113-8491_113-8490i others(9): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541440 | ||||||
| chr5:180541440
|
A | ATTTTTTT others(1): Show |
6 | a0001c0001t0006g0323a0001c0001t0017g0162a0001c0001t0017g0165others(3): Show | 6 | HG01109.hp1 HG02258.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-8491_113-8490i others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541440 | ||||||
| chr5:180541440
|
A | ATTTTTTT others(3): Show |
5 | a0001c0001t0006g0150a0001c0001t0006g0324a0001c0001t0031g0133others(2): Show | 5 | HG00733.hp2 HG01243.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-8491_113-8490i others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541440 | ||||||
| chr5:180541440
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0024g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.113-8491_113-8490i others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541440 | ||||||
| chr5:180541441
|
A | AT | 74 | a0001c0001t0001g0227a0001c0001t0001g0229a0001c0001t0001g0240others(71): Show | 74 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.113-8462dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180541441 | |||||
| chr5:180541441
|
A | ATT | 25 | a0001c0001t0001g0070a0001c0001t0002g0029a0001c0001t0002g0061others(22): Show | 25 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(22): Show |
intron_variant | MODIFIER | c.113-8463_113-8462d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180541441 | |||||
| chr5:180541441
|
A | T | 113 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(110): Show | 113 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.113-8490A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541441 | ||||||
| chr5:180541613
|
T | C | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-8318T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541613 | ||||||
| chr5:180541614
|
G | A | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-8317G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541614 | ||||||
| chr5:180541635
|
G | A | 2 | a0001c0001t0001g0282a0001c0001t0001g0306 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.113-8296G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541635 | ||||||
| chr5:180541674
|
G | C | 8 | a0001c0002t0002g0034a0001c0002t0002g0035a0001c0002t0002g0044others(5): Show | 8 | HG01069.hp1 HG01106.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.113-8257G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541674 | ||||||
| chr5:180541758
|
AT | A | 6 | a0001c0001t0001g0241a0001c0001t0001g0273a0001c0001t0002g0084others(3): Show | 6 | HG01256.hp2 HG02896.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-8159delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180541758 | |||||
| chr5:180541847
|
G | T | 1 | a0001c0001t0017g0161 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.113-8084G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541847 | ||||||
| chr5:180541858
|
A | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-8073A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541858 | ||||||
| chr5:180541899
|
C | A | 61 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(58): Show | 61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.113-8032C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541899 | ||||||
| chr5:180541914
|
G | A | 2 | a0001c0001t0009g0210a0001c0001t0010g0209 | 2 | HG01891.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.113-8017G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541914 | ||||||
| chr5:180541986
|
C | G | 61 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(58): Show | 61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.113-7945C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541986 | ||||||
| chr5:180542167
|
C | T | 1 | a0001c0001t0013g0103 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.113-7764C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542167 | ||||||
| chr5:180542179
|
T | C | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.113-7752T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542179 | ||||||
| chr5:180542208
|
TAGGTTTT others(4): Show |
T | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.113-7709_113-7699d others(13): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180542208 | |||||
| chr5:180542261
|
C | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-7670C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542261 | ||||||
| chr5:180542293
|
C | T | 1 | a0001c0001t0013g0103 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.113-7638C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542293 | ||||||
| chr5:180542355
|
C | T | 52 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(49): Show | 52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.113-7576C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542355 | ||||||
| chr5:180542390
|
G | A | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.113-7541G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542390 | ||||||
| chr5:180542394
|
A | AGC | 3 | a0001c0001t0002g0062a0001c0001t0002g0065a0001c0001t0002g0108 | 3 | NA18955.hp2 NA18960.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.113-7536_113-7535d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180542394 | |||||
| chr5:180542560
|
C | T | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.113-7371C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542560 | ||||||
| chr5:180542596
|
C | A | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-7335C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542596 | ||||||
| chr5:180542654
|
G | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-7277G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542654 | ||||||
| chr5:180542751
|
T | A | 1 | a0001c0001t0047g0242 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.113-7180T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542751 | ||||||
| chr5:180542823
|
T | A | 4 | a0001c0001t0014g0167a0001c0001t0014g0174a0001c0001t0014g0175others(1): Show | 4 | HG00280.hp2 HG00639.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-7108T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542823 | ||||||
| chr5:180542882
|
G | C | 3 | a0001c0001t0030g0131a0001c0001t0031g0132a0001c0001t0031g0133 | 3 | HG00733.hp2 HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.113-7049G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542882 | ||||||
| chr5:180543120
|
A | G | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-6811A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543120 | ||||||
| chr5:180543121
|
C | T | 53 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(50): Show | 53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.113-6810C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543121 | ||||||
| chr5:180543141
|
C | T | 2 | a0001c0001t0002g0020a0001c0001t0042g0075 | 2 | HG01975.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.113-6790C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543141 | ||||||
| chr5:180543186
|
G | A | 1 | a0001c0001t0013g0256 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.113-6745G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543186 | ||||||
| chr5:180543335
|
AG | A | 53 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(50): Show | 53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.113-6594delG | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180543335 | |||||
| chr5:180543351
|
A | G | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-6580A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543351 | ||||||
| chr5:180543527
|
T | C | 53 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(50): Show | 53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.113-6404T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543527 | ||||||
| chr5:180543536
|
G | A | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-6395G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543536 | ||||||
| chr5:180543596
|
A | G | 1 | a0001c0001t0028g0327 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.113-6335A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543596 | ||||||
| chr5:180543645
|
T | C | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-6286T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543645 | ||||||
| chr5:180543681
|
A | G | 1 | a0001c0001t0006g0136 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.113-6250A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543681 | ||||||
| chr5:180543741
|
T | G | 1 | a0001c0001t0002g0082 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.113-6190T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543741 | ||||||
| chr5:180543765
|
C | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0227a0001c0001t0001g0229others(97): Show | 100 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.113-6166C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543765 | ||||||
| chr5:180543828
|
T | G | 1 | a0001c0001t0023g0203 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.113-6103T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543828 | ||||||
| chr5:180543936
|
A | C | 1 | a0001c0001t0001g0313 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.113-5995A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543936 | ||||||
| chr5:180543951
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.113-5980C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543951 | ||||||
| chr5:180544036
|
C | T | 1 | a0001c0001t0009g0173 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.113-5895C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544036 | ||||||
| chr5:180544052
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.113-5879C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544052 | ||||||
| chr5:180544136
|
T | C | 1 | a0001c0001t0017g0164 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.113-5795T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544136 | ||||||
| chr5:180544235
|
A | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-5696A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544235 | ||||||
| chr5:180544305
|
G | A | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-5626G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544305 | ||||||
| chr5:180544339
|
A | C | 1 | a0001c0001t0006g0123 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.113-5592A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544339 | ||||||
| chr5:180544409
|
A | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-5522A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544409 | ||||||
| chr5:180544463
|
C | T | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-5468C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544463 | ||||||
| chr5:180544486
|
C | A | 61 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(58): Show | 61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.113-5445C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544486 | ||||||
| chr5:180544532
|
C | T | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-5399C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544532 | ||||||
| chr5:180544559
|
T | C | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-5372T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544559 | ||||||
| chr5:180544604
|
T | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-5327T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544604 | ||||||
| chr5:180544831
|
C | T | 53 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(50): Show | 53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.113-5100C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544831 | ||||||
| chr5:180545067
|
C | T | 1 | a0001c0001t0003g0211 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.113-4864C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180545067 | ||||||
| chr5:180545124
|
CT | C | 52 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(49): Show | 52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.113-4805delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180545124 | |||||
| chr5:180545459
|
C | T | 53 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(50): Show | 53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.113-4472C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180545459 | ||||||
| chr5:180545499
|
T | C | 114 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(111): Show | 114 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.113-4432T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180545499 | ||||||
| chr5:180545571
|
G | C | 1 | a0001c0001t0010g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.113-4360G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180545571 | ||||||
| chr5:180545732
|
A | T | 1 | a0001c0001t0001g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.113-4199A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180545732 | ||||||
| chr5:180545734
|
A | T | 1 | a0001c0001t0001g0322 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.113-4197A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180545734 | ||||||
| chr5:180545781
|
A | G | 1 | a0001c0001t0001g0301 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.113-4150A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180545781 | ||||||
| chr5:180546031
|
C | CT | 53 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(50): Show | 53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.113-3891dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180546031 | |||||
| chr5:180546053
|
G | T | 6 | a0001c0001t0003g0170a0001c0001t0003g0179a0001c0001t0003g0180others(3): Show | 6 | HG01358.hp2 HG01993.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-3878G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180546053 | ||||||
| chr5:180546105
|
A | G | 1 | a0001c0001t0014g0202 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.113-3826A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180546105 | ||||||
| chr5:180546642
|
T | A | 61 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(58): Show | 61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.113-3289T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180546642 | ||||||
| chr5:180546663
|
C | T | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-3268C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180546663 | ||||||
| chr5:180546770
|
A | G | 2 | a0002c0004t0001g0319a0002c0004t0004g0252 | 2 | NA18966.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.113-3161A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180546770 | ||||||
| chr5:180546865
|
G | C | 3 | a0001c0001t0006g0150a0001c0001t0006g0323a0001c0001t0006g0324 | 3 | HG03927.hp1 HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.113-3066G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180546865 | ||||||
| chr5:180547071
|
C | A | 1 | a0001c0001t0005g0272 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.113-2860C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547071 | ||||||
| chr5:180547097
|
G | C | 1 | a0001c0001t0006g0156 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.113-2834G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547097 | ||||||
| chr5:180547221
|
G | GTACAT | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-2708_113-2707i others(7): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180547221 | |||||
| chr5:180547245
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0227a0001c0001t0001g0229others(97): Show | 100 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.113-2686C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547245 | ||||||
| chr5:180547388
|
C | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-2543C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547388 | ||||||
| chr5:180547390
|
G | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-2541G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547390 | ||||||
| chr5:180547393
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.113-2538G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547393 | ||||||
| chr5:180547402
|
C | A | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-2529C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547402 | ||||||
| chr5:180547479
|
C | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0227a0001c0001t0001g0229others(96): Show | 99 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.113-2452C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547479 | ||||||
| chr5:180547609
|
C | T | 1 | a0001c0001t0047g0242 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.113-2322C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547609 | ||||||
| chr5:180547671
|
G | A | 118 | a0001c0001t0001g0168a0001c0001t0002g0176a0001c0001t0003g0170others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-2260G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547671 | ||||||
| chr5:180547692
|
T | C | 1 | a0001c0001t0001g0309 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.113-2239T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547692 | ||||||
| chr5:180547696
|
T | A | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.113-2235T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547696 | ||||||
| chr5:180547799
|
G | A | 1 | a0001c0001t0055g0153 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.113-2132G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547799 | ||||||
| chr5:180547817
|
G | T | 119 | a0001c0001t0001g0168a0001c0001t0001g0293a0001c0001t0002g0176others(116): Show | 119 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.113-2114G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547817 | ||||||
| chr5:180547890
|
T | C | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.113-2041T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547890 | ||||||
| chr5:180547975
|
C | G | 1 | a0001c0001t0061g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.113-1956C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547975 | ||||||
| chr5:180548104
|
T | C | 318 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(315): Show | 318 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.113-1827T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180548104 | ||||||
| chr5:180548149
|
A | AAG | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.113-1782_113-1781i others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180548149 | ||||||
| chr5:180548178
|
A | G | 1 | a0001c0001t0001g0326 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.113-1753A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180548178 | ||||||
| chr5:180548236
|
C | T | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.113-1695C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180548236 | ||||||
| chr5:180548385
|
C | T | 53 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(50): Show | 53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.113-1546C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180548385 | ||||||
| chr5:180548619
|
T | C | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.113-1312T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180548619 | ||||||
| chr5:180548673
|
G | C | 1 | a0001c0002t0004g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.113-1258G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180548673 | ||||||
| chr5:180548792
|
C | T | 15 | a0001c0002t0002g0034a0001c0002t0002g0035a0001c0002t0002g0042others(12): Show | 15 | HG01069.hp1 HG01106.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.113-1139C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180548792 | ||||||
| chr5:180548828
|
T | A | 2 | a0001c0001t0001g0168a0001c0001t0002g0176 | 2 | NA18955.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.113-1103T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180548828 | ||||||
| chr5:180549012
|
T | C | 3 | a0001c0001t0001g0246a0001c0001t0001g0275a0001c0001t0001g0315 | 3 | NA18978.hp2 NA19005.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.113-919T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549012 | ||||||
| chr5:180549038
|
AAAGGTCT others(21): Show |
A | 1 | a0001c0001t0049g0333 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.113-892_113-865del others(28): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549038 | ||||||
| chr5:180549067
|
C | T | 1 | a0001c0001t0049g0333 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.113-864C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549067 | ||||||
| chr5:180549201
|
G | C | 1 | a0001c0001t0037g0171 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.113-730G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549201 | ||||||
| chr5:180549334
|
T | G | 1 | a0001c0002t0004g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.113-597T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549334 | ||||||
| chr5:180549375
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.113-556C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549375 | ||||||
| chr5:180549376
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.113-555A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549376 | ||||||
| chr5:180549387
|
T | C | 1 | a0001c0002t0005g0028 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.113-544T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549387 | ||||||
| chr5:180549389
|
C | T | 4 | a0001c0002t0004g0036a0001c0002t0004g0041a0001c0002t0004g0049others(1): Show | 4 | HG01167.hp1 HG02615.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-542C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549389 | ||||||
| chr5:180549396
|
C | T | 2 | a0001c0001t0006g0323a0001c0001t0006g0324 | 2 | HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.113-535C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549396 | ||||||
| chr5:180549472
|
A | G | 5 | a0001c0001t0002g0018a0001c0001t0002g0029a0001c0001t0002g0061others(2): Show | 5 | HG00621.hp1 NA18973.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-459A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549472 | ||||||
| chr5:180549476
|
C | G | 1 | a0001c0001t0017g0166 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.113-455C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549476 | ||||||
| chr5:180549600
|
GATCACGC others(4): Show |
G | 1 | a0001c0001t0001g0239 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.113-330_113-320del others(11): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549600 | ||||||
| chr5:180549628
|
A | G | 2 | a0001c0001t0002g0076a0001c0001t0002g0077 | 2 | HG01952.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.113-303A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549628 | ||||||
| chr5:180549636
|
G | A | 3 | a0001c0001t0025g0217a0001c0001t0026g0223a0001c0001t0038g0218 | 3 | HG01261.hp1 HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.113-295G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549636 | ||||||
| chr5:180549646
|
T | C | 3 | a0001c0001t0016g0116a0001c0001t0016g0120a0001c0001t0050g0089 | 3 | HG00639.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.113-285T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549646 | ||||||
| chr5:180549819
|
T | A | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.113-112T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549819 | ||||||
| chr5:180549905
|
C | T | 1 | a0001c0001t0002g0068 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.113-26C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549905 | ||||||
| chr5:180550388
|
G | T | 116 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.299+271G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180550388 | ||||||
| chr5:180550608
|
T | C | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.299+491T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180550608 | ||||||
| chr5:180550868
|
G | A | 1 | a0001c0001t0006g0138 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.299+751G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180550868 | ||||||
| chr5:180551115
|
G | A | 1 | a0001c0001t0001g0308 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.299+998G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551115 | ||||||
| chr5:180551181
|
C | CA | 9 | a0001c0001t0001g0301a0001c0001t0001g0315a0001c0001t0002g0110others(6): Show | 9 | HG00099.hp1 HG00597.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.299+1079dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 180551181 | |||||
| chr5:180551198
|
C | T | 1 | a0001c0001t0007g0125 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.299+1081C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551198 | ||||||
| chr5:180551286
|
G | A | 6 | a0001c0001t0001g0269a0001c0001t0001g0282a0001c0001t0001g0283others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.299+1169G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551286 | ||||||
| chr5:180551351
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0168a0001c0001t0001g0227others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.299+1234T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551351 | ||||||
| chr5:180551425
|
T | G | 1 | a0001c0001t0032g0128 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.299+1308T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551425 | ||||||
| chr5:180551580
|
T | A | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.299+1463T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551580 | ||||||
| chr5:180551663
|
C | G | 3 | a0001c0001t0003g0191a0001c0001t0009g0010a0001c0001t0023g0009 | 3 | HG02027.hp1 NA18612.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.299+1546C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551663 | ||||||
| chr5:180551716
|
A | C | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.299+1599A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551716 | ||||||
| chr5:180551761
|
A | G | 2 | a0001c0001t0001g0326a0001c0001t0011g0216 | 2 | HG02818.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.300-1625A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551761 | ||||||
| chr5:180551794
|
A | T | 49 | a0001c0001t0001g0245a0001c0001t0001g0284a0001c0001t0006g0008others(46): Show | 49 | HG00408.hp1 HG00609.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.300-1592A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551794 | ||||||
| chr5:180551796
|
G | T | 49 | a0001c0001t0001g0245a0001c0001t0001g0284a0001c0001t0006g0008others(46): Show | 49 | HG00408.hp1 HG00609.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.300-1590G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551796 | ||||||
| chr5:180551891
|
C | T | 12 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002others(9): Show | 12 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.300-1495C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551891 | ||||||
| chr5:180551926
|
A | G | 9 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(6): Show | 9 | HG02451.hp2 HG02809.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.300-1460A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551926 | ||||||
| chr5:180552067
|
C | T | 1 | a0001c0001t0049g0333 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.300-1319C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552067 | ||||||
| chr5:180552075
|
G | A | 1 | a0001c0002t0004g0053 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.300-1311G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552075 | ||||||
| chr5:180552120
|
C | T | 3 | a0001c0001t0021g0158a0001c0001t0021g0159a0001c0001t0021g0160 | 3 | HG02735.hp1 HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.300-1266C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552120 | ||||||
| chr5:180552348
|
G | C | 105 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(102): Show | 105 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.300-1038G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552348 | ||||||
| chr5:180552377
|
A | C | 1 | a0001c0001t0002g0108 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.300-1009A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552377 | ||||||
| chr5:180552382
|
A | G | 3 | a0001c0001t0011g0212a0001c0001t0011g0215a0001c0001t0011g0216 | 3 | HG02818.hp1 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.300-1004A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552382 | ||||||
| chr5:180552391
|
GCA | G | 52 | a0001c0001t0001g0070a0001c0001t0002g0018a0001c0001t0002g0020others(49): Show | 52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.300-991_300-990del others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 180552391 | |||||
| chr5:180552399
|
T | C | 1 | a0001c0001t0001g0312 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.300-987T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552399 | ||||||
| chr5:180552407
|
C | T | 112 | a0001c0001t0001g0301a0001c0001t0003g0170a0001c0001t0003g0172others(109): Show | 112 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.300-979C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552407 | ||||||
| chr5:180552424
|
A | G | 5 | a0001c0001t0001g0304a0001c0001t0002g0074a0001c0001t0002g0091others(2): Show | 5 | HG02083.hp2 NA18942.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.300-962A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552424 | ||||||
| chr5:180552426
|
A | G | 5 | a0001c0001t0001g0304a0001c0001t0002g0074a0001c0001t0002g0091others(2): Show | 5 | HG02083.hp2 NA18942.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.300-960A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552426 | ||||||
| chr5:180552427
|
G | A | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.300-959G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552427 | ||||||
| chr5:180552430
|
T | A | 5 | a0001c0001t0001g0304a0001c0001t0002g0074a0001c0001t0002g0091others(2): Show | 5 | HG02083.hp2 NA18942.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.300-956T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552430 | ||||||
| chr5:180552434
|
G | T | 1 | a0001c0001t0061g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.300-952G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552434 | ||||||
| chr5:180552437
|
C | T | 9 | a0001c0001t0002g0018a0001c0001t0002g0029a0001c0001t0002g0061others(6): Show | 9 | HG00621.hp1 HG02486.hp2 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.300-949C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552437 | ||||||
| chr5:180552438
|
G | A | 4 | a0001c0001t0019g0257a0001c0001t0019g0258a0001c0001t0019g0286others(1): Show | 4 | NA18947.hp1 NA18967.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.300-948G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552438 | ||||||
| chr5:180552443
|
C | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(287): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.300-943C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552443 | ||||||
| chr5:180552458
|
G | A | 56 | a0001c0001t0001g0105a0001c0001t0002g0085a0001c0001t0006g0008others(53): Show | 56 | HG00408.hp1 HG00609.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.300-928G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552458 | ||||||
| chr5:180552502
|
T | A | 1 | a0001c0001t0009g0206 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.300-884T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552502 | ||||||
| chr5:180552504
|
G | A | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.300-882G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552504 | ||||||
| chr5:180552514
|
C | T | 1 | a0001c0001t0009g0206 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.300-872C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552514 | ||||||
| chr5:180552515
|
A | G | 113 | a0001c0001t0001g0001a0001c0001t0001g0168a0001c0001t0001g0227others(110): Show | 113 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.300-871A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552515 | ||||||
| chr5:180552519
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.300-867A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552519 | ||||||
| chr5:180552577
|
C | T | 3 | a0001c0001t0003g0170a0001c0001t0003g0181a0001c0001t0003g0184 | 3 | HG01358.hp2 HG01993.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.300-809C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552577 | ||||||
| chr5:180552580
|
A | G | 51 | a0001c0001t0001g0070a0001c0001t0002g0018a0001c0001t0002g0020others(48): Show | 51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.300-806A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552580 | ||||||
| chr5:180552601
|
G | A | 2 | a0001c0001t0010g0187a0001c0001t0010g0194 | 2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.300-785G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552601 | ||||||
| chr5:180552611
|
A | T | 4 | a0001c0001t0002g0088a0001c0001t0002g0090a0001c0001t0002g0093others(1): Show | 4 | HG00438.hp2 HG02165.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.300-775A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552611 | ||||||
| chr5:180552625
|
A | G | 1 | a0001c0001t0039g0102 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.300-761A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552625 | ||||||
| chr5:180552627
|
T | C | 125 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(122): Show | 125 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.300-759T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552627 | ||||||
| chr5:180552628
|
G | A | 1 | a0001c0001t0039g0102 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.300-758G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552628 | ||||||
| chr5:180552645
|
C | CA | 116 | a0001c0001t0001g0001a0001c0001t0001g0275a0001c0001t0001g0294others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.300-726dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 180552645 | |||||
| chr5:180552836
|
CTGT | C | 51 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(48): Show | 51 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.300-548_300-546del others(3): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 180552836 | |||||
| chr5:180552887
|
T | C | 2 | a0001c0001t0035g0017a0001c0001t0036g0192 | 2 | HG02074.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.300-499T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552887 | ||||||
| chr5:180552970
|
A | ATCATTTC others(325): Show |
2 | a0001c0002t0004g0037a0001c0002t0004g0051 | 2 | HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.300-400_300-399ins others(332): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 180552970 | |||||
| chr5:180552970
|
A | ATCATTTC others(338): Show |
1 | a0001c0002t0004g0038 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.300-400_300-399ins others(345): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 180552970 | |||||
| chr5:180552970
|
A | ATCATTTC others(346): Show |
1 | a0001c0002t0004g0043 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.300-400_300-399ins others(353): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 180552970 | |||||
| chr5:180552970
|
A | ATCATTTC others(361): Show |
1 | a0001c0002t0002g0042 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.300-400_300-399ins others(368): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 180552970 | |||||
| chr5:180553066
|
C | T | 10 | a0001c0002t0004g0036a0001c0002t0004g0041a0001c0002t0004g0049others(7): Show | 10 | HG01167.hp1 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.300-320C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180553066 | ||||||
| chr5:180553118
|
G | A | 3 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0007 | 3 | HG00099.hp1 HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.300-268G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180553118 | ||||||
| chr5:180553171
|
A | G | 1 | a0001c0001t0010g0208 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.300-215A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180553171 | ||||||
| chr5:180553211
|
T | C | 1 | a0001c0001t0057g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.300-175T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180553211 | ||||||
| chr5:180553215
|
A | C | 110 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(107): Show | 110 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.300-171A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180553215 | ||||||
| chr5:180553251
|
G | A | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.300-135G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180553251 | ||||||
| chr5:180553302
|
T | A | 110 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(107): Show | 110 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.300-84T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180553302 | ||||||
| chr5:180553378
|
A | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.300-8A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180553378 | ||||||
| chr5:180553527
|
A | G | 117 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(114): Show | 117 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.385+56A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180553527 | ||||||
| chr5:180553661
|
CT | C | 7 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(4): Show | 7 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.385+199delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180553661 | |||||
| chr5:180553676
|
GGA | G | 4 | a0001c0001t0019g0257a0001c0001t0019g0258a0001c0001t0019g0286others(1): Show | 4 | NA18947.hp1 NA18967.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+206_385+207del others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180553676 | ||||||
| chr5:180553711
|
A | G | 117 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(114): Show | 117 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.385+240A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180553711 | ||||||
| chr5:180553844
|
A | G | 3 | a0001c0001t0001g0246a0001c0001t0001g0275a0001c0001t0001g0315 | 3 | NA18978.hp2 NA19005.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.385+373A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180553844 | ||||||
| chr5:180553847
|
T | C | 5 | a0001c0001t0001g0299a0001c0001t0001g0301a0001c0001t0001g0302others(2): Show | 5 | HG00597.hp2 HG02015.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+376T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180553847 | ||||||
| chr5:180553941
|
G | A | 1 | a0001c0001t0009g0173 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.385+470G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180553941 | ||||||
| chr5:180554054
|
C | G | 1 | a0001c0001t0001g0227 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.385+583C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554054 | ||||||
| chr5:180554124
|
T | G | 3 | a0001c0002t0005g0026a0001c0002t0005g0027a0001c0002t0005g0028 | 3 | HG02717.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.385+653T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554124 | ||||||
| chr5:180554168
|
A | G | 2 | a0001c0001t0016g0116a0001c0001t0016g0120 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.385+697A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554168 | ||||||
| chr5:180554330
|
C | T | 117 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(114): Show | 117 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.385+859C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554330 | ||||||
| chr5:180554417
|
TA | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.385+962delA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180554417 | |||||
| chr5:180554417
|
TAAAAA | T | 15 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(12): Show | 15 | HG01261.hp1 HG01884.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.385+958_385+962del others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180554417 | |||||
| chr5:180554487
|
T | C | 1 | a0001c0001t0001g0318 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.385+1016T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554487 | ||||||
| chr5:180554517
|
G | GT | 59 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(56): Show | 59 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.385+1054dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180554517 | |||||
| chr5:180554517
|
G | GTT | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.385+1053_385+1054d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180554517 | |||||
| chr5:180554517
|
G | GTTT | 49 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(46): Show | 49 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.385+1052_385+1054d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180554517 | |||||
| chr5:180554557
|
C | T | 52 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(49): Show | 52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.385+1086C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554557 | ||||||
| chr5:180554603
|
T | TG | 294 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(291): Show | 294 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.385+1132_385+1133i others(3): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554603 | ||||||
| chr5:180554604
|
T | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+1133T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554604 | ||||||
| chr5:180554632
|
A | G | 1 | a0001c0001t0006g0124 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.385+1161A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554632 | ||||||
| chr5:180554938
|
A | G | 1 | a0001c0001t0002g0077 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.385+1467A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554938 | ||||||
| chr5:180554950
|
G | A | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.385+1479G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554950 | ||||||
| chr5:180555010
|
C | CT | 6 | a0001c0001t0002g0073a0001c0001t0007g0143a0001c0001t0009g0173others(3): Show | 6 | HG01243.hp1 HG02280.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.385+1553dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180555010 | |||||
| chr5:180555111
|
A | C | 118 | a0001c0001t0001g0287a0001c0001t0001g0305a0001c0001t0001g0307others(115): Show | 118 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.385+1640A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180555111 | ||||||
| chr5:180555151
|
T | C | 308 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(305): Show | 308 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(305): Show |
intron_variant | MODIFIER | c.385+1680T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180555151 | ||||||
| chr5:180555278
|
G | A | 307 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(304): Show | 307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.385+1807G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180555278 | ||||||
| chr5:180555281
|
A | G | 111 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(108): Show | 111 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.385+1810A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180555281 | ||||||
| chr5:180555423
|
G | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+1952G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180555423 | ||||||
| chr5:180555459
|
A | C | 118 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(115): Show | 118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.385+1988A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180555459 | ||||||
| chr5:180555935
|
G | A | 2 | a0001c0001t0003g0211a0001c0001t0009g0177 | 2 | NA18977.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.385+2464G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180555935 | ||||||
| chr5:180556221
|
C | T | 113 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(110): Show | 113 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.385+2750C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556221 | ||||||
| chr5:180556367
|
A | G | 1 | a0001c0001t0061g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.385+2896A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556367 | ||||||
| chr5:180556600
|
T | C | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.385+3129T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556600 | ||||||
| chr5:180556602
|
T | C | 110 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(107): Show | 110 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.385+3131T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556602 | ||||||
| chr5:180556618
|
G | T | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.385+3147G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556618 | ||||||
| chr5:180556661
|
A | G | 1 | a0001c0001t0049g0333 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.385+3190A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556661 | ||||||
| chr5:180556748
|
C | T | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.385+3277C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556748 | ||||||
| chr5:180556776
|
C | T | 1 | a0001c0002t0004g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.385+3305C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556776 | ||||||
| chr5:180556779
|
C | T | 1 | a0001c0001t0002g0066 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.385+3308C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556779 | ||||||
| chr5:180556895
|
G | A | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.385+3424G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556895 | ||||||
| chr5:180556942
|
C | T | 2 | a0001c0001t0002g0076a0001c0001t0002g0077 | 2 | HG01952.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.385+3471C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556942 | ||||||
| chr5:180556943
|
G | A | 1 | a0001c0001t0002g0071 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.385+3472G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556943 | ||||||
| chr5:180556955
|
C | CA | 12 | a0001c0001t0005g0113a0001c0001t0005g0272a0001c0001t0018g0004others(9): Show | 12 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.385+3499dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180556955 | |||||
| chr5:180557108
|
G | A | 1 | a0001c0001t0011g0215 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.385+3637G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557108 | ||||||
| chr5:180557360
|
A | ACCAGCAG others(6): Show |
116 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.385+3889_385+3890i others(15): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557360 | ||||||
| chr5:180557361
|
A | G | 116 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.385+3890A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557361 | ||||||
| chr5:180557485
|
A | G | 52 | a0001c0001t0002g0073a0001c0001t0006g0008a0001c0001t0006g0122others(49): Show | 52 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.385+4014A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557485 | ||||||
| chr5:180557612
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.385+4141G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557612 | ||||||
| chr5:180557625
|
A | C | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.385+4154A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557625 | ||||||
| chr5:180557678
|
G | T | 1 | a0001c0002t0005g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.385+4207G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557678 | ||||||
| chr5:180557748
|
G | C | 101 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(98): Show | 101 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.385+4277G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557748 | ||||||
| chr5:180557848
|
A | G | 51 | a0001c0001t0001g0320a0001c0001t0003g0170a0001c0001t0003g0172others(48): Show | 51 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.385+4377A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557848 | ||||||
| chr5:180557874
|
T | C | 6 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(3): Show | 6 | HG02818.hp1 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.385+4403T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557874 | ||||||
| chr5:180557905
|
TTTTG | T | 46 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(43): Show | 46 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.385+4436_385+4439d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180557905 | |||||
| chr5:180557921
|
C | T | 1 | a0001c0001t0007g0142 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.385+4450C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557921 | ||||||
| chr5:180557952
|
A | T | 2 | a0001c0001t0016g0116a0001c0001t0016g0120 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.385+4481A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557952 | ||||||
| chr5:180558155
|
G | A | 1 | a0001c0001t0048g0311 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.385+4684G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558155 | ||||||
| chr5:180558276
|
T | C | 1 | a0001c0005t0004g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.385+4805T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558276 | ||||||
| chr5:180558277
|
G | A | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.385+4806G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558277 | ||||||
| chr5:180558333
|
T | C | 121 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(118): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.385+4862T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558333 | ||||||
| chr5:180558451
|
G | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+4980G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558451 | ||||||
| chr5:180558465
|
C | T | 1 | a0001c0002t0005g0024 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.385+4994C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558465 | ||||||
| chr5:180558496
|
C | T | 10 | a0001c0002t0004g0036a0001c0002t0004g0041a0001c0002t0004g0049others(7): Show | 10 | HG01167.hp1 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.385+5025C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558496 | ||||||
| chr5:180558510
|
T | TAA | 50 | a0001c0001t0003g0170a0001c0001t0006g0008a0001c0001t0006g0122others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.385+5049_385+5050d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180558510 | |||||
| chr5:180558510
|
T | TAAA | 48 | a0001c0001t0003g0172a0001c0001t0003g0179a0001c0001t0003g0180others(45): Show | 48 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.385+5048_385+5050d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180558510 | |||||
| chr5:180558521
|
A | AAC | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.385+5050_385+5051i others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558521 | ||||||
| chr5:180558522
|
C | A | 116 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.385+5051C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558522 | ||||||
| chr5:180558549
|
A | G | 1 | a0001c0001t0044g0169 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.385+5078A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558549 | ||||||
| chr5:180558588
|
C | T | 1 | a0001c0001t0002g0088 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.385+5117C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558588 | ||||||
| chr5:180558620
|
G | GCT | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.385+5150_385+5151d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180558620 | |||||
| chr5:180558622
|
T | TC | 62 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(59): Show | 62 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.385+5151_385+5152i others(3): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558622 | ||||||
| chr5:180558623
|
T | C | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+5152T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558623 | ||||||
| chr5:180558804
|
TTTATTTG others(4): Show |
T | 109 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(106): Show | 109 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.385+5336_385+5346d others(13): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180558804 | |||||
| chr5:180558831
|
C | T | 1 | a0001c0001t0046g0011 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.385+5360C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558831 | ||||||
| chr5:180558834
|
G | A | 1 | a0001c0001t0035g0017 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.385+5363G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558834 | ||||||
| chr5:180558863
|
C | T | 2 | a0001c0001t0062g0030a0001c0001t0063g0230 | 2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.385+5392C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558863 | ||||||
| chr5:180558909
|
G | T | 1 | a0001c0001t0002g0094 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.385+5438G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558909 | ||||||
| chr5:180558934
|
C | T | 51 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(48): Show | 51 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.385+5463C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558934 | ||||||
| chr5:180558962
|
T | C | 49 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(46): Show | 49 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.385+5491T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558962 | ||||||
| chr5:180559567
|
G | T | 4 | a0001c0002t0004g0036a0001c0002t0004g0041a0001c0002t0004g0049others(1): Show | 4 | HG01167.hp1 HG02615.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-4922G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180559567 | ||||||
| chr5:180559694
|
A | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-4795A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180559694 | ||||||
| chr5:180559950
|
A | AT | 59 | a0001c0001t0001g0070a0001c0001t0001g0237a0001c0001t0001g0248others(56): Show | 59 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.386-4523dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180559950 | |||||
| chr5:180559980
|
G | C | 2 | a0001c0002t0004g0037a0001c0002t0004g0051 | 2 | HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.386-4509G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180559980 | ||||||
| chr5:180560009
|
C | T | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.386-4480C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560009 | ||||||
| chr5:180560147
|
A | G | 3 | a0001c0001t0006g0136a0001c0001t0006g0137a0001c0001t0054g0145 | 3 | HG01981.hp1 HG02004.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.386-4342A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560147 | ||||||
| chr5:180560266
|
C | T | 9 | a0001c0002t0005g0021a0001c0002t0005g0022a0001c0002t0005g0023others(6): Show | 9 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.386-4223C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560266 | ||||||
| chr5:180560583
|
G | C | 1 | a0001c0001t0001g0320 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.386-3906G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560583 | ||||||
| chr5:180560631
|
G | A | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.386-3858G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560631 | ||||||
| chr5:180560768
|
C | A | 1 | a0001c0001t0010g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.386-3721C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560768 | ||||||
| chr5:180560818
|
C | T | 18 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(15): Show | 18 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.386-3671C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560818 | ||||||
| chr5:180560919
|
T | G | 58 | a0001c0001t0006g0122a0001c0001t0006g0123a0001c0001t0006g0124others(55): Show | 58 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.386-3570T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560919 | ||||||
| chr5:180560922
|
G | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0105a0001c0001t0001g0168others(132): Show | 135 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.386-3567G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560922 | ||||||
| chr5:180560937
|
T | G | 50 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(47): Show | 50 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.386-3552T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560937 | ||||||
| chr5:180560964
|
A | ATCAG | 306 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.386-3522_386-3521i others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180560964 | |||||
| chr5:180560964
|
A | G | 1 | a0001c0001t0002g0068 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.386-3525A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560964 | ||||||
| chr5:180561064
|
C | T | 1 | a0001c0001t0049g0333 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.386-3425C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561064 | ||||||
| chr5:180561240
|
C | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-3249C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561240 | ||||||
| chr5:180561276
|
T | G | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.386-3213T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561276 | ||||||
| chr5:180561277
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0168a0001c0001t0001g0227others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.386-3212A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561277 | ||||||
| chr5:180561283
|
C | T | 298 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(295): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.386-3206C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561283 | ||||||
| chr5:180561356
|
T | TTG | 107 | a0001c0001t0001g0001a0001c0001t0001g0229a0001c0001t0001g0236others(104): Show | 107 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.386-3097_386-3096d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | |||||
| chr5:180561356
|
T | TTGTG | 47 | a0001c0001t0001g0168a0001c0001t0001g0237a0001c0001t0001g0243others(44): Show | 47 | HG00280.hp2 HG00544.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.386-3099_386-3096d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | |||||
| chr5:180561356
|
T | TTGTGTG | 41 | a0001c0001t0001g0070a0001c0001t0001g0105a0001c0001t0001g0227others(38): Show | 41 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.386-3101_386-3096d others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | |||||
| chr5:180561356
|
T | TTGTGTGT others(1): Show |
16 | a0001c0001t0001g0253a0001c0001t0001g0265a0001c0001t0001g0301others(13): Show | 16 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.386-3103_386-3096d others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | |||||
| chr5:180561356
|
T | TTGTGTGT others(3): Show |
6 | a0001c0001t0002g0061a0001c0001t0002g0073a0001c0001t0002g0098others(3): Show | 6 | HG00609.hp1 HG00621.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.386-3105_386-3096d others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | |||||
| chr5:180561356
|
T | TTGTGTGT others(7): Show |
2 | a0001c0001t0002g0032a0001c0001t0005g0226 | 2 | HG02523.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.386-3109_386-3096d others(16): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | |||||
| chr5:180561356
|
T | TTGTGTGT others(9): Show |
3 | a0001c0001t0002g0079a0001c0001t0002g0110a0001c0001t0052g0080 | 3 | NA18941.hp2 NA18991.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.386-3111_386-3096d others(18): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | |||||
| chr5:180561356
|
T | TTGTGTGT others(11): Show |
1 | a0001c0001t0002g0084 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.386-3113_386-3096d others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | |||||
| chr5:180561356
|
TTG | T | 3 | a0001c0001t0001g0239a0001c0001t0036g0192a0001c0002t0004g0058 | 3 | HG02083.hp1 HG02155.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.386-3097_386-3096d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | |||||
| chr5:180561356
|
TTGTG | T | 3 | a0001c0001t0007g0148a0001c0001t0007g0149a0001c0001t0008g0262 | 3 | NA18962.hp2 NA18973.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.386-3099_386-3096d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | |||||
| chr5:180561356
|
TTGTGTG | T | 49 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(46): Show | 49 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.386-3101_386-3096d others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | |||||
| chr5:180561356
|
TTGTGTGT others(1): Show |
T | 12 | a0001c0001t0005g0081a0001c0001t0006g0156a0001c0001t0016g0116others(9): Show | 12 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.386-3103_386-3096d others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | |||||
| chr5:180561356
|
TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0061g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.386-3107_386-3096d others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | |||||
| chr5:180561695
|
C | T | 2 | a0001c0001t0010g0187a0001c0001t0010g0194 | 2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.386-2794C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561695 | ||||||
| chr5:180561711
|
G | A | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.386-2778G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561711 | ||||||
| chr5:180561770
|
T | C | 1 | a0001c0001t0007g0149 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.386-2719T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561770 | ||||||
| chr5:180561881
|
C | G | 1 | a0001c0001t0005g0226 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.386-2608C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561881 | ||||||
| chr5:180561943
|
G | C | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.386-2546G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561943 | ||||||
| chr5:180562165
|
G | A | 116 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.386-2324G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562165 | ||||||
| chr5:180562178
|
T | A | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.386-2311T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562178 | ||||||
| chr5:180562462
|
C | T | 1 | a0001c0001t0063g0230 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.386-2027C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562462 | ||||||
| chr5:180562469
|
G | A | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-2020G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562469 | ||||||
| chr5:180562512
|
G | A | 1 | a0001c0001t0061g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.386-1977G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562512 | ||||||
| chr5:180562516
|
G | A | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-1973G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562516 | ||||||
| chr5:180562542
|
C | T | 1 | a0001c0001t0057g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.386-1947C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562542 | ||||||
| chr5:180562555
|
G | A | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.386-1934G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562555 | ||||||
| chr5:180562556
|
C | T | 1 | a0001c0001t0045g0332 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.386-1933C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562556 | ||||||
| chr5:180562664
|
C | T | 13 | a0001c0001t0001g0229a0001c0001t0001g0248a0001c0001t0001g0253others(10): Show | 13 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.386-1825C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562664 | ||||||
| chr5:180562773
|
T | C | 18 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(15): Show | 18 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.386-1716T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562773 | ||||||
| chr5:180562871
|
T | C | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.386-1618T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562871 | ||||||
| chr5:180563048
|
A | G | 117 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(114): Show | 117 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.386-1441A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563048 | ||||||
| chr5:180563062
|
G | A | 1 | a0001c0002t0004g0057 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.386-1427G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563062 | ||||||
| chr5:180563107
|
G | A | 2 | a0001c0001t0025g0217a0001c0001t0038g0218 | 2 | HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.386-1382G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563107 | ||||||
| chr5:180563216
|
A | AT | 110 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(107): Show | 110 | HG00408.hp1 HG00609.hp2 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.386-1256dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180563216 | |||||
| chr5:180563217
|
T | A | 6 | a0001c0001t0001g0269a0001c0001t0001g0282a0001c0001t0001g0283others(3): Show | 6 | HG01069.hp2 HG01071.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-1272T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563217 | ||||||
| chr5:180563247
|
G | A | 1 | a0001c0001t0060g0002 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.386-1242G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563247 | ||||||
| chr5:180563380
|
G | GT | 6 | a0001c0001t0010g0182a0001c0001t0010g0193a0001c0001t0014g0202others(3): Show | 6 | HG02738.hp2 HG03195.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.386-1100dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180563380 | |||||
| chr5:180563400
|
GC | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(292): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.386-1088delC | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563400 | ||||||
| chr5:180563401
|
C | T | 3 | a0001c0001t0001g0241a0001c0001t0003g0197a0001c0001t0023g0196 | 3 | HG01433.hp2 NA19075.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.386-1088C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563401 | ||||||
| chr5:180563411
|
C | A | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-1078C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563411 | ||||||
| chr5:180563416
|
A | G | 117 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(114): Show | 117 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.386-1073A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563416 | ||||||
| chr5:180563433
|
G | A | 1 | a0001c0001t0002g0063 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.386-1056G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563433 | ||||||
| chr5:180563478
|
G | A | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-1011G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563478 | ||||||
| chr5:180563522
|
A | G | 117 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(114): Show | 117 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.386-967A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563522 | ||||||
| chr5:180563580
|
C | A | 1 | a0001c0001t0003g0179 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.386-909C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563580 | ||||||
| chr5:180563633
|
G | C | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.386-856G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563633 | ||||||
| chr5:180563846
|
T | C | 117 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(114): Show | 117 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.386-643T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563846 | ||||||
| chr5:180563882
|
C | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-607C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563882 | ||||||
| chr5:180563903
|
T | C | 1 | a0001c0001t0010g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.386-586T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563903 | ||||||
| chr5:180563925
|
G | A | 1 | a0001c0001t0061g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.386-564G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563925 | ||||||
| chr5:180563926
|
C | T | 1 | a0001c0001t0061g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.386-563C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563926 | ||||||
| chr5:180563933
|
A | AT | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.386-550dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180563933 | |||||
| chr5:180563980
|
C | T | 3 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0009g0178 | 3 | HG03017.hp1 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.386-509C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563980 | ||||||
| chr5:180564040
|
T | A | 1 | a0001c0001t0061g0003 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.386-449T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180564040 | ||||||
| chr5:180564099
|
C | T | 2 | a0001c0001t0040g0100a0001c0001t0041g0101 | 2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.386-390C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180564099 | ||||||
| chr5:180564162
|
G | A | 1 | a0001c0001t0010g0182 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.386-327G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180564162 | ||||||
| chr5:180564238
|
A | G | 1 | a0001c0001t0003g0201 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.386-251A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180564238 | ||||||
| chr5:180564276
|
C | A | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.386-213C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180564276 | ||||||
| chr5:180564366
|
AGTCTGAC others(8): Show |
A | 19 | a0001c0001t0003g0188a0001c0001t0003g0189a0001c0001t0003g0195others(16): Show | 19 | HG00738.hp2 HG01071.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.386-122_386-108del others(15): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180564366 | ||||||
| chr5:180564401
|
T | C | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-88T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180564401 | ||||||
| chr5:180564633
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.490+40G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 5/11 | chr5 | 180564633 | ||||||
| chr5:180564750
|
A | G | 1 | a0001c0002t0004g0039 | 1 | HG03139.hp1 | splice_region_variant&intron_variant | LOW | c.559+7A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180564750 | ||||||
| chr5:180564841
|
A | G | 117 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(114): Show | 117 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.559+98A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180564841 | ||||||
| chr5:180564886
|
C | A | 6 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(3): Show | 6 | HG02818.hp1 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.559+143C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180564886 | ||||||
| chr5:180564946
|
A | G | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.559+203A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180564946 | ||||||
| chr5:180564959
|
C | T | 116 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.559+216C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180564959 | ||||||
| chr5:180565218
|
T | G | 1 | a0001c0001t0001g0310 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.559+475T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565218 | ||||||
| chr5:180565566
|
C | T | 116 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.560-254C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565566 | ||||||
| chr5:180565571
|
C | T | 18 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(15): Show | 18 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.560-249C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565571 | ||||||
| chr5:180565582
|
C | T | 116 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.560-238C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565582 | ||||||
| chr5:180565609
|
G | A | 1 | a0001c0001t0021g0159 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.560-211G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565609 | ||||||
| chr5:180565629
|
T | G | 1 | a0001c0001t0006g0156 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.560-191T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565629 | ||||||
| chr5:180565633
|
C | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.560-187C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565633 | ||||||
| chr5:180565642
|
C | T | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.560-178C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565642 | ||||||
| chr5:180565645
|
G | C | 1 | a0001c0001t0001g0254 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.560-175G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565645 | ||||||
| chr5:180565708
|
T | A | 1 | a0001c0001t0017g0165 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.560-112T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565708 | ||||||
| chr5:180565795
|
A | G | 1 | a0001c0001t0032g0154 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.560-25A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565795 | ||||||
| chr5:180566024
|
G | A | 1 | a0001c0001t0003g0201 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.717+47G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | chr5 | 180566024 | ||||||
| chr5:180566123
|
C | T | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.717+146C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | chr5 | 180566123 | ||||||
| chr5:180566172
|
C | A | 1 | a0001c0001t0006g0130 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.717+195C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | chr5 | 180566172 | ||||||
| chr5:180566273
|
C | T | 1 | a0001c0001t0030g0152 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.717+296C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | chr5 | 180566273 | ||||||
| chr5:180566295
|
T | C | 1 | a0001c0001t0006g0150 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.717+318T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | chr5 | 180566295 | ||||||
| chr5:180566443
|
T | C | 1 | a0001c0001t0001g0326 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.717+466T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | chr5 | 180566443 | ||||||
| chr5:180566596
|
G | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.718-492G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | chr5 | 180566596 | ||||||
| chr5:180566640
|
C | CT | 24 | a0001c0001t0002g0018a0001c0001t0002g0065a0001c0001t0002g0067others(21): Show | 24 | HG00408.hp2 HG00642.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.718-421dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr5 | 180566640 | |||||
| chr5:180566640
|
CT | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0168a0001c0001t0001g0227others(93): Show | 96 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.718-421delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr5 | 180566640 | |||||
| chr5:180566640
|
CTT | C | 46 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0269others(43): Show | 46 | HG00738.hp2 HG00741.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.718-422_718-421del others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr5 | 180566640 | |||||
| chr5:180566640
|
CTTT | C | 14 | a0001c0001t0009g0014a0001c0001t0014g0167a0001c0001t0014g0174others(11): Show | 14 | HG00280.hp2 HG00639.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.718-423_718-421del others(3): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr5 | 180566640 | |||||
| chr5:180566640
|
CTTTT | C | 6 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(3): Show | 6 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-424_718-421del others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr5 | 180566640 | |||||
| chr5:180566640
|
CTTTTTTT others(3): Show |
C | 50 | a0001c0001t0001g0318a0001c0001t0006g0008a0001c0001t0006g0122others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.718-430_718-421del others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr5 | 180566640 | |||||
| chr5:180566719
|
G | C | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.718-369G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | chr5 | 180566719 | ||||||
| chr5:180566813
|
T | C | 298 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0105others(295): Show | 298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.718-275T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | chr5 | 180566813 | ||||||
| chr5:180567252
|
C | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+10C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 8/11 | chr5 | 180567252 | ||||||
| chr5:180567581
|
A | G | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.873-268A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 8/11 | chr5 | 180567581 | ||||||
| chr5:180567727
|
G | A | 1 | a0001c0001t0017g0161 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.873-122G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 8/11 | chr5 | 180567727 | ||||||
| chr5:180568091
|
A | G | 1 | a0001c0002t0005g0330 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1027+88A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568091 | ||||||
| chr5:180568230
|
C | CT | 100 | a0001c0001t0001g0001a0001c0001t0001g0168a0001c0001t0001g0227others(97): Show | 100 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1027+242dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr5 | 180568230 | |||||
| chr5:180568230
|
CT | C | 9 | a0001c0001t0005g0226a0001c0001t0011g0212a0001c0001t0013g0103others(6): Show | 9 | HG02451.hp2 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1027+242delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr5 | 180568230 | |||||
| chr5:180568230
|
CTT | C | 108 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(105): Show | 108 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.1027+241_1027+242d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr5 | 180568230 | |||||
| chr5:180568234
|
T | G | 1 | a0001c0001t0017g0165 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1027+231T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568234 | ||||||
| chr5:180568397
|
C | G | 14 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(11): Show | 14 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1027+394C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568397 | ||||||
| chr5:180568401
|
T | G | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1027+398T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568401 | ||||||
| chr5:180568493
|
A | G | 2 | a0001c0001t0029g0234a0001c0001t0029g0289 | 2 | NA18969.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1027+490A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568493 | ||||||
| chr5:180568546
|
C | T | 1 | a0001c0001t0049g0333 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1027+543C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568546 | ||||||
| chr5:180568633
|
A | G | 1 | a0001c0005t0004g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1028-477A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568633 | ||||||
| chr5:180568823
|
A | G | 1 | a0001c0001t0006g0156 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1028-287A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568823 | ||||||
| chr5:180568844
|
G | A | 116 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1028-266G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568844 | ||||||
| chr5:180568852
|
G | A | 3 | a0001c0001t0022g0225a0001c0003t0022g0220a0001c0003t0022g0222 | 3 | HG02055.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1028-258G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568852 | ||||||
| chr5:180568865
|
C | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1028-245C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568865 | ||||||
| chr5:180569009
|
T | G | 2 | a0001c0002t0002g0034a0001c0002t0002g0035 | 2 | HG01069.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1028-101T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180569009 | ||||||
| chr5:180569031
|
T | C | 1 | a0001c0001t0026g0221 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1028-79T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180569031 | ||||||
| chr5:180569381
|
A | G | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1258+41A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180569381 | ||||||
| chr5:180569513
|
C | T | 4 | a0001c0002t0004g0036a0001c0002t0004g0041a0001c0002t0004g0049others(1): Show | 4 | HG01167.hp1 HG02615.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1258+173C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180569513 | ||||||
| chr5:180569529
|
TGAG | T | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1258+193_1258+195d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr5 | 180569529 | |||||
| chr5:180569550
|
T | C | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1258+210T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180569550 | ||||||
| chr5:180569598
|
G | A | 9 | a0001c0001t0006g0144a0001c0001t0006g0146a0001c0001t0007g0134others(6): Show | 9 | HG00609.hp2 HG02523.hp2 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.1258+258G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180569598 | ||||||
| chr5:180569864
|
C | T | 3 | a0001c0001t0011g0212a0001c0001t0011g0215a0001c0001t0011g0216 | 3 | HG02818.hp1 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1258+524C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180569864 | ||||||
| chr5:180569875
|
G | A | 116 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1258+535G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180569875 | ||||||
| chr5:180569962
|
C | T | 2 | a0001c0001t0001g0274a0001c0001t0012g0279 | 2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1258+622C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180569962 | ||||||
| chr5:180570014
|
C | T | 1 | a0001c0001t0030g0152 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1258+674C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570014 | ||||||
| chr5:180570046
|
A | C | 50 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(47): Show | 50 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.1258+706A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570046 | ||||||
| chr5:180570086
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0168a0001c0001t0001g0227others(99): Show | 102 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1258+746C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570086 | ||||||
| chr5:180570099
|
C | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1258+759C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570099 | ||||||
| chr5:180570114
|
T | C | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1258+774T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570114 | ||||||
| chr5:180570156
|
G | C | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1258+816G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570156 | ||||||
| chr5:180570251
|
G | A | 4 | a0001c0001t0014g0167a0001c0001t0014g0174a0001c0001t0014g0175others(1): Show | 4 | HG00280.hp2 HG00639.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1258+911G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570251 | ||||||
| chr5:180570625
|
A | G | 57 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(54): Show | 57 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1259-605A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570625 | ||||||
| chr5:180570640
|
A | G | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1259-590A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570640 | ||||||
| chr5:180570701
|
A | G | 6 | a0001c0001t0011g0212a0001c0001t0011g0213a0001c0001t0011g0214others(3): Show | 6 | HG02818.hp1 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1259-529A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570701 | ||||||
| chr5:180570777
|
G | A | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1259-453G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570777 | ||||||
| chr5:180570783
|
C | T | 1 | a0001c0001t0057g0059 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1259-447C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570783 | ||||||
| chr5:180571454
|
C | T | 116 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1461+22C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180571454 | ||||||
| chr5:180571569
|
C | T | 1 | a0001c0001t0062g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1461+137C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180571569 | ||||||
| chr5:180571683
|
G | A | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1461+251G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180571683 | ||||||
| chr5:180571722
|
C | T | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1461+290C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180571722 | ||||||
| chr5:180571805
|
C | T | 50 | a0001c0001t0006g0008a0001c0001t0006g0122a0001c0001t0006g0123others(47): Show | 50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1461+373C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180571805 | ||||||
| chr5:180571968
|
AAAT | A | 116 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1461+540_1461+542d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180571968 | |||||
| chr5:180572060
|
A | C | 4 | a0001c0001t0014g0167a0001c0001t0014g0174a0001c0001t0014g0175others(1): Show | 4 | HG00280.hp2 HG00639.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1461+628A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180572060 | ||||||
| chr5:180572070
|
T | C | 1 | a0001c0001t0028g0233 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1461+638T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180572070 | ||||||
| chr5:180572251
|
G | A | 2 | a0001c0001t0006g0323a0001c0001t0006g0324 | 2 | HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1461+819G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180572251 | ||||||
| chr5:180572480
|
G | A | 2 | a0001c0001t0009g0014a0001c0001t0010g0016 | 2 | NA18957.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1461+1048G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180572480 | ||||||
| chr5:180572509
|
C | T | 2 | a0001c0001t0003g0197a0001c0001t0023g0196 | 2 | HG01433.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1461+1077C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180572509 | ||||||
| chr5:180572639
|
T | A | 8 | a0001c0001t0017g0161a0001c0001t0017g0162a0001c0001t0017g0164others(5): Show | 8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1461+1207T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180572639 | ||||||
| chr5:180572698
|
C | T | 4 | a0001c0001t0018g0004a0001c0001t0018g0005a0001c0001t0018g0006others(1): Show | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1461+1266C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180572698 | ||||||
| chr5:180572715
|
C | CT | 59 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(56): Show | 59 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.1462-1263dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180572715 | |||||
| chr5:180572824
|
G | A | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1462-1164G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180572824 | ||||||
| chr5:180572965
|
C | G | 1 | a0001c0001t0009g0183 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1462-1023C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180572965 | ||||||
| chr5:180573090
|
A | G | 116 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1462-898A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573090 | ||||||
| chr5:180573188
|
T | A | 12 | a0001c0001t0001g0229a0001c0001t0001g0248a0001c0001t0001g0253others(9): Show | 12 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.1462-800T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573188 | ||||||
| chr5:180573220
|
C | G | 116 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(113): Show | 116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1462-768C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573220 | ||||||
| chr5:180573552
|
A | AGT | 5 | a0001c0001t0062g0030a0001c0001t0063g0230a0001c0002t0005g0026others(2): Show | 5 | HG02258.hp1 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1462-387_1462-386d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573552 | |||||
| chr5:180573552
|
AGT | A | 9 | a0001c0002t0002g0034a0001c0002t0002g0035a0001c0002t0002g0042others(6): Show | 9 | HG01069.hp1 HG01106.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1462-387_1462-386d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573552 | |||||
| chr5:180573552
|
AGTGT | A | 9 | a0001c0002t0002g0044a0001c0002t0002g0045a0001c0002t0002g0052others(6): Show | 9 | HG01167.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1462-389_1462-386d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573552 | |||||
| chr5:180573552
|
AGTGTGTG others(1): Show |
A | 3 | a0001c0002t0004g0036a0001c0002t0004g0041a0001c0002t0004g0050 | 3 | HG02615.hp1 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1462-393_1462-386d others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573552 | |||||
| chr5:180573574
|
TGTGTGTG others(27): Show |
T | 3 | a0001c0001t0040g0100a0001c0001t0041g0101a0001c0001t0060g0002 | 3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1462-411_1462-378d others(36): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573574 | |||||
| chr5:180573582
|
TGTGTGTG others(15): Show |
T | 4 | a0001c0001t0019g0257a0001c0001t0019g0258a0001c0001t0019g0286others(1): Show | 4 | NA18947.hp1 NA18967.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.1462-403_1462-382d others(24): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573582 | |||||
| chr5:180573586
|
TGTGTGTG others(11): Show |
T | 2 | a0001c0001t0008g0297a0001c0001t0014g0202 | 2 | HG00735.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1462-399_1462-382d others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573586 | |||||
| chr5:180573590
|
TGTGTGTG others(7): Show |
T | 16 | a0001c0001t0001g0274a0001c0001t0007g0139a0001c0001t0010g0182others(13): Show | 16 | HG01261.hp1 HG02074.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.1462-395_1462-382d others(16): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573590 | |||||
| chr5:180573592
|
TGTGTGTG others(5): Show |
T | 44 | a0001c0001t0001g0070a0001c0001t0001g0237a0001c0001t0001g0263others(41): Show | 44 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.1462-393_1462-382d others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573592 | |||||
| chr5:180573594
|
TGTGTGTG others(3): Show |
T | 59 | a0001c0001t0001g0248a0001c0001t0001g0299a0001c0001t0001g0318others(56): Show | 59 | HG00408.hp2 HG00609.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1462-391_1462-382d others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573594 | |||||
| chr5:180573596
|
TGTGTGTC others(1): Show |
T | 52 | a0001c0001t0001g0105a0001c0001t0001g0168a0001c0001t0001g0229others(49): Show | 52 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1462-389_1462-382d others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573596 | |||||
| chr5:180573598
|
TGTGTCC | T | 66 | a0001c0001t0001g0001a0001c0001t0001g0241a0001c0001t0001g0249others(63): Show | 66 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1462-387_1462-382d others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573598 | |||||
| chr5:180573600
|
TGTCC | T | 27 | a0001c0001t0001g0236a0001c0001t0001g0245a0001c0001t0001g0246others(24): Show | 27 | HG00438.hp1 HG00438.hp2 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.1462-371_1462-368d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573600 | |||||
| chr5:180573601
|
G | C | 2 | a0001c0002t0002g0044a0001c0002t0002g0045 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1462-387G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573601 | ||||||
| chr5:180573602
|
T | C | 2 | a0001c0002t0002g0044a0001c0002t0002g0045 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1462-386T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573602 | ||||||
| chr5:180573602
|
TCC | T | 24 | a0001c0001t0001g0227a0001c0001t0001g0240a0001c0001t0001g0244others(21): Show | 24 | HG00544.hp2 HG01074.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1462-385_1462-384d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573602 | ||||||
| chr5:180573603
|
C | G | 11 | a0001c0001t0002g0062a0001c0001t0002g0108a0001c0001t0002g0176others(8): Show | 11 | HG00642.hp2 HG01361.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1462-385C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573603 | ||||||
| chr5:180573604
|
C | T | 11 | a0001c0001t0002g0062a0001c0001t0002g0108a0001c0001t0002g0176others(8): Show | 11 | HG00642.hp2 HG01361.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1462-384C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573604 | ||||||
| chr5:180573608
|
C | T | 50 | a0001c0001t0003g0170a0001c0001t0003g0172a0001c0001t0003g0179others(47): Show | 50 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.1462-380C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573608 | ||||||
| chr5:180573706
|
A | G | 1 | a0001c0001t0060g0002 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1462-282A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573706 | ||||||
| chr5:180573881
|
TTGTTC | T | 8 | a0001c0002t0002g0034a0001c0002t0002g0035a0001c0002t0002g0044others(5): Show | 8 | HG01069.hp1 HG01106.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.1462-96_1462-92del others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573881 |