Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 4848 |
|---|---|
| ensemblid | ENSG00000111596.14 |
| hgncid | 7878 |
| symbol | CNOT2 |
| name | CCR4-NOT transcription complex subunit 2 |
| refseq_nuc | NM_014515.7 |
| refseq_prot | NP_055330.1 |
| ensembl_nuc | ENST00000229195.8 |
| ensembl_prot | ENSP00000229195.3 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 70243433 |
| end | 70354993 |
| strand | + |
| ver | v1.2 |
| region | chr12:70243433-70354993 |
| region5000 | chr12:70238433-70359993 |
| regionname0 | CNOT2_chr12_70243433_70354993 |
| regionname5000 | CNOT2_chr12_70238433_70359993 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000 | 0/0 | 0 | 51 | 13 | 7 | 25 | 1 | 5 | 15 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001 | 1/1 | 540 | 229 | 79 | 53 | 65 | 9 | 21 | 51 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1623 | 129 | 50 | 33 | 29 | 5 | 11 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| c0002 | 0/1 | 1624 | 60 | 15 | 11 | 24 | 2 | 7 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| c0003 | 0/0 | 1622 | 51 | 13 | 7 | 25 | 1 | 5 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| c0004 | 0/0 | 1625 | 29 | 7 | 9 | 10 | 1 | 2 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| c0005 | 0/0 | 1626 | 6 | 3 | 0 | 2 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| c0006 | 0/0 | 1623 | 4 | 4 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| c0007 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1222 | 251 | 81 | 51 | 84 | 8 | 25 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| t0002 | 0/0 | 1222 | 11 | 7 | 1 | 3 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| t0003 | 0/0 | 1222 | 9 | 2 | 7 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| t0004 | 0/0 | 1222 | 3 | 0 | 0 | 3 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| t0005 | 0/0 | 1222 | 2 | 0 | 1 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| t0006 | 0/0 | 1222 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| t0007 | 0/0 | 1222 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| t0008 | 0/0 | 1222 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| t0009 | 0/0 | 1222 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0116 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0209 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0003 | 0/0 | 1622 | 51 | 13 | 7 | 25 | 1 | 5 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0001 | 1/0 | 1623 | 129 | 50 | 33 | 29 | 5 | 11 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0002 | 0/1 | 1624 | 60 | 15 | 11 | 24 | 2 | 7 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0004 | 0/0 | 1625 | 29 | 7 | 9 | 10 | 1 | 2 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0005 | 0/0 | 1626 | 6 | 3 | 0 | 2 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0006 | 0/0 | 1623 | 4 | 4 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0007 | 0/0 | 1623 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0003t0001 | 0/0 | 2843 | 49 | 11 | 7 | 25 | 1 | 5 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0000c0003t0002 | 0/0 | 2843 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0001t0001 | 1/0 | 2844 | 124 | 48 | 32 | 29 | 4 | 10 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0001t0005 | 0/0 | 2844 | 2 | 0 | 1 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0001t0006 | 0/0 | 2844 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0001t0007 | 0/0 | 2844 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0001t0008 | 0/0 | 2844 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0002t0001 | 0/1 | 2845 | 47 | 10 | 10 | 18 | 1 | 7 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0002t0002 | 0/0 | 2845 | 8 | 5 | 0 | 3 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0002t0003 | 0/0 | 2845 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0002t0004 | 0/0 | 2845 | 3 | 0 | 0 | 3 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0002t0009 | 0/0 | 2845 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0004t0001 | 0/0 | 2846 | 20 | 5 | 2 | 10 | 1 | 2 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0004t0002 | 0/0 | 2846 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0004t0003 | 0/0 | 2846 | 8 | 2 | 6 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0005t0001 | 0/0 | 2847 | 6 | 3 | 0 | 2 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0006t0001 | 0/0 | 2844 | 4 | 4 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| a0001c0007t0001 | 0/0 | 2844 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | copy fasta | chr12 | 70238433 | 70359993 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0000c0003t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0116 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0006g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0007g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0001t0008g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0001 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0209 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0003g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0002t0009g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0003g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0003g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0004t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0005t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0005t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0005t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0005t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0005t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0005t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0006t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0006t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0006t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0006t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| a0001c0007t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | GBR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00099 | hp2 | a0001 | c0001 | t0005 | g0155 | EUR | GBR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00280 | hp1 | a0001 | c0002 | t0009 | g0157 | EUR | FIN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00280 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | FIN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00323 | hp1 | a0001 | c0005 | t0001 | g0259 | EUR | FIN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00323 | hp2 | a0000 | c0003 | t0001 | g0158 | EUR | FIN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0096 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00438 | hp1 | a0000 | c0003 | t0001 | g0020 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0061 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00609 | hp1 | a0001 | c0004 | t0001 | g0258 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00609 | hp2 | a0000 | c0003 | t0001 | g0031 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00621 | hp1 | a0000 | c0003 | t0001 | g0040 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0228 | EAS | CHS | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0205 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG00741 | hp2 | a0000 | c0003 | t0001 | g0185 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01069 | hp2 | a0001 | c0004 | t0001 | g0272 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0203 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01081 | hp1 | a0001 | c0004 | t0001 | g0261 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01099 | hp1 | a0001 | c0004 | t0003 | g0253 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01099 | hp2 | a0000 | c0003 | t0001 | g0123 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0219 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01192 | hp1 | a0001 | c0004 | t0003 | g0243 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01192 | hp2 | a0001 | c0001 | t0005 | g0149 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01243 | hp2 | a0000 | c0003 | t0001 | g0036 | AMR | PUR | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01255 | hp1 | a0001 | c0004 | t0003 | g0257 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0207 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0208 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0117 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01496 | hp2 | a0001 | c0002 | t0003 | g0241 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01884 | hp2 | a0000 | c0003 | t0002 | g0229 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01891 | hp1 | a0001 | c0004 | t0001 | g0244 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01928 | hp1 | a0001 | c0004 | t0003 | g0270 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01934 | hp1 | a0001 | c0004 | t0003 | g0262 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01952 | hp1 | a0000 | c0003 | t0001 | g0074 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01952 | hp2 | a0001 | c0004 | t0003 | g0242 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01978 | hp2 | a0000 | c0003 | t0001 | g0130 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02015 | hp1 | a0000 | c0003 | t0001 | g0050 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02015 | hp2 | a0001 | c0004 | t0001 | g0079 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0088 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02040 | hp2 | a0000 | c0003 | t0001 | g0047 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02056 | hp2 | a0000 | c0003 | t0001 | g0216 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0080 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02080 | hp2 | a0000 | c0003 | t0001 | g0046 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02135 | hp1 | a0000 | c0003 | t0001 | g0122 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0082 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02145 | hp1 | a0001 | c0004 | t0001 | g0068 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0236 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02300 | hp1 | a0000 | c0003 | t0001 | g0124 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0173 | AMR | PEL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02451 | hp2 | a0000 | c0003 | t0001 | g0195 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02523 | hp1 | a0000 | c0003 | t0001 | g0043 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0093 | EAS | KHV | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02615 | hp1 | a0000 | c0003 | t0001 | g0179 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0071 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02622 | hp2 | a0001 | c0005 | t0001 | g0269 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02647 | hp2 | a0001 | c0005 | t0001 | g0250 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0223 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0076 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02698 | hp1 | a0000 | c0003 | t0001 | g0028 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02698 | hp2 | a0001 | c0001 | t0007 | g0152 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02735 | hp2 | a0000 | c0003 | t0001 | g0138 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02809 | hp1 | a0000 | c0003 | t0001 | g0189 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02818 | hp1 | a0000 | c0003 | t0001 | g0191 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0249 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0234 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02895 | hp1 | a0000 | c0003 | t0001 | g0011 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02970 | hp1 | a0001 | c0006 | t0001 | g0119 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0235 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0248 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02976 | hp2 | a0001 | c0006 | t0001 | g0018 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03041 | hp1 | a0001 | c0004 | t0001 | g0246 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0247 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03209 | hp1 | a0000 | c0003 | t0001 | g0192 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0005 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0073 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03490 | hp2 | a0001 | c0007 | t0001 | g0027 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0156 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03540 | hp1 | a0000 | c0003 | t0001 | g0194 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03579 | hp1 | a0000 | c0003 | t0001 | g0215 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03579 | hp2 | a0000 | c0003 | t0001 | g0190 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03669 | hp2 | a0000 | c0003 | t0001 | g0037 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | STU | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | STU | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03710 | hp1 | a0001 | c0004 | t0001 | g0251 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0077 | SAS | PJL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03927 | hp1 | a0000 | c0003 | t0001 | g0035 | SAS | BEB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0212 | SAS | BEB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0210 | SAS | BEB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | STU | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | STU | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG04204 | hp1 | a0001 | c0004 | t0001 | g0268 | SAS | STU | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | STU | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG04228 | hp1 | a0000 | c0003 | t0001 | g0015 | SAS | STU | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | STU | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0237 | AFR | YRI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18612 | hp1 | a0000 | c0003 | t0001 | g0038 | EAS | CHB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18612 | hp2 | a0001 | c0004 | t0001 | g0201 | EAS | CHB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18906 | hp1 | a0001 | c0005 | t0001 | g0252 | AFR | YRI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18906 | hp2 | a0000 | c0003 | t0001 | g0039 | AFR | YRI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18941 | hp1 | a0000 | c0003 | t0001 | g0057 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18941 | hp2 | a0001 | c0002 | t0004 | g0232 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18942 | hp1 | a0000 | c0003 | t0001 | g0055 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18942 | hp2 | a0001 | c0004 | t0001 | g0267 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18945 | hp1 | a0001 | c0002 | t0004 | g0238 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18954 | hp2 | a0001 | c0004 | t0001 | g0254 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18966 | hp1 | a0000 | c0003 | t0001 | g0033 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18970 | hp2 | a0001 | c0004 | t0001 | g0256 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18977 | hp1 | a0001 | c0005 | t0001 | g0264 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18977 | hp2 | a0001 | c0002 | t0004 | g0239 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18980 | hp1 | a0001 | c0004 | t0001 | g0266 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0265 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18987 | hp1 | a0001 | c0004 | t0001 | g0263 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18988 | hp1 | a0001 | c0002 | t0002 | g0233 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18988 | hp2 | a0001 | c0004 | t0001 | g0271 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18990 | hp1 | a0000 | c0003 | t0001 | g0078 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18990 | hp2 | a0000 | c0003 | t0001 | g0056 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18991 | hp1 | a0000 | c0003 | t0001 | g0042 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18991 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18997 | hp1 | a0001 | c0004 | t0001 | g0245 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18997 | hp2 | a0000 | c0003 | t0001 | g0058 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19003 | hp2 | a0000 | c0003 | t0001 | g0049 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19010 | hp1 | a0001 | c0005 | t0001 | g0202 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | LWK | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19043 | hp2 | a0001 | c0006 | t0001 | g0170 | AFR | LWK | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19057 | hp1 | a0000 | c0003 | t0001 | g0032 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19057 | hp2 | a0000 | c0003 | t0001 | g0064 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19058 | hp1 | a0000 | c0003 | t0001 | g0029 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19068 | hp2 | a0000 | c0003 | t0001 | g0059 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19078 | hp1 | a0000 | c0003 | t0001 | g0034 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19084 | hp2 | a0000 | c0003 | t0001 | g0002 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19087 | hp1 | a0000 | c0003 | t0001 | g0048 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | YRI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0069 | AFR | YRI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ASW | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20129 | hp2 | a0001 | c0004 | t0003 | g0255 | AFR | ASW | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | TSI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0222 | EUR | TSI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20805 | hp1 | a0001 | c0004 | t0001 | g0260 | EUR | TSI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | TSI | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0211 | SAS | GIH | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0086 | SAS | GIH | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01123 | hp1 | a0000 | c0003 | t0001 | g0121 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG01123 | hp2 | a0001 | c0004 | t0002 | g0227 | AMR | CLM | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02109 | hp1 | a0000 | c0003 | t0002 | g0230 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02109 | hp2 | a0000 | c0003 | t0001 | g0193 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02486 | hp2 | a0001 | c0001 | t0008 | g0196 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0231 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG02559 | hp2 | a0001 | c0006 | t0001 | g0150 | AFR | ACB | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG03471 | hp2 | a0001 | c0002 | t0001 | g0107 | AFR | MSL | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | USA | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | USA | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | USA | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA20300 | hp2 | a0001 | c0004 | t0003 | g0273 | AFR | USA | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | LWK | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | LWK | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0209 | REF | REF | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0116 | REF | REF | CNOT2_chr12_70238433_70359993 | CNOT2 | chr12 | 70238433 | 70359993 |
| 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 |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:70330452
|
G | A | 1 | a0001c0006 | 4 | HG02559.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
synonymous_variant | LOW | c.552G>A | p.Gln184Gln | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/16 | 695/2844 | 552/1623 | 184/540 | chr12 | 70330452 | ||
| chr12:70338700
|
G | A | 1 | a0001c0007 | 1 | HG03490.hp2 | synonymous_variant | LOW | c.1056G>A | p.Thr352Thr | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/16 | 1199/2844 | 1056/1623 | 352/540 | chr12 | 70338700 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:70243439
|
T | C | 1 | a0001c0001t0005 | 2 | HG00099.hp2 HG01192.hp2 |
5_prime_UTR_variant | MODIFIER | c.-137T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/16 | 34788 | chr12 | 70243439 | |||||
| chr12:70353913
|
T | TA | 5 | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(2): Show | 60 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*23dupA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 24 | INFO_REALIGN_3_PRIME | chr12 | 70353913 | ||||
| chr12:70353913
|
T | TAA | 3 | a0001c0004t0001a0001c0004t0002a0001c0004t0003 | 29 | HG00609.hp1 HG01069.hp2 HG01081.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*22_*23dupAA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 24 | INFO_REALIGN_3_PRIME | chr12 | 70353913 | ||||
| chr12:70353913
|
T | TAAA | 1 | a0001c0005t0001 | 6 | HG00323.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*21_*23dupAAA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 24 | INFO_REALIGN_3_PRIME | chr12 | 70353913 | ||||
| chr12:70353913
|
TA | T | 2 | a0000c0003t0001a0000c0003t0002 | 51 | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*23delA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 23 | INFO_REALIGN_3_PRIME | chr12 | 70353913 | ||||
| chr12:70353983
|
A | G | 1 | a0001c0002t0004 | 3 | NA18941.hp2 NA18945.hp1 NA18977.hp2 |
3_prime_UTR_variant | MODIFIER | c.*68A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 68 | chr12 | 70353983 | |||||
| chr12:70354053
|
C | T | 1 | a0001c0002t0009 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*138C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 138 | chr12 | 70354053 | |||||
| chr12:70354210
|
A | C | 1 | a0001c0001t0008 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*295A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 295 | chr12 | 70354210 | |||||
| chr12:70354449
|
G | A | 4 | a0000c0003t0002a0001c0002t0002a0001c0002t0004others(1): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*534G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 534 | chr12 | 70354449 | |||||
| chr12:70354471
|
T | C | 1 | a0001c0001t0006 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*556T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 556 | chr12 | 70354471 | |||||
| chr12:70354593
|
T | C | 4 | a0000c0003t0002a0001c0002t0002a0001c0002t0004others(1): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*678T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 678 | chr12 | 70354593 | |||||
| chr12:70354795
|
A | G | 1 | a0001c0001t0007 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*880A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 880 | chr12 | 70354795 | |||||
| chr12:70354820
|
A | G | 2 | a0001c0002t0003a0001c0004t0003 | 9 | HG01099.hp1 HG01192.hp1 HG01255.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*905A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 16/16 | 905 | chr12 | 70354820 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:70243503
|
G | A | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-96+23G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243503 | ||||||
| chr12:70243526
|
G | C | 9 | a0000c0003t0001g0011a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 9 | HG00639.hp1 HG01891.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-96+46G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243526 | ||||||
| chr12:70243549
|
C | T | 2 | a0001c0001t0001g0274a0001c0002t0001g0275 | 2 | NA18981.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.-96+69C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243549 | ||||||
| chr12:70243563
|
G | T | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-96+83G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243563 | ||||||
| chr12:70243681
|
G | A | 1 | a0000c0003t0001g0015 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-96+201G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243681 | ||||||
| chr12:70243736
|
C | G | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-96+256C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243736 | ||||||
| chr12:70243810
|
G | C | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-96+330G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243810 | ||||||
| chr12:70243839
|
C | A | 1 | a0001c0001t0001g0016 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-96+359C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243839 | ||||||
| chr12:70243920
|
C | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-96+440C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243920 | ||||||
| chr12:70243937
|
G | T | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-96+457G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70243937 | ||||||
| chr12:70244007
|
A | G | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-96+527A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70244007 | ||||||
| chr12:70244032
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-96+552T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70244032 | ||||||
| chr12:70244132
|
C | A | 1 | a0001c0006t0001g0018 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-96+652C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70244132 | ||||||
| chr12:70244355
|
A | T | 1 | a0000c0003t0001g0216 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-96+875A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70244355 | ||||||
| chr12:70244375
|
C | T | 9 | a0000c0003t0001g0011a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 9 | HG00639.hp1 HG01891.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-96+895C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70244375 | ||||||
| chr12:70244404
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-96+924T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70244404 | ||||||
| chr12:70244592
|
C | G | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-96+1112C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70244592 | ||||||
| chr12:70244603
|
G | A | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-96+1123G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70244603 | ||||||
| chr12:70244808
|
G | C | 1 | a0000c0003t0001g0020 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-96+1328G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70244808 | ||||||
| chr12:70245245
|
GA | G | 3 | a0000c0003t0001g0215a0001c0001t0001g0213a0001c0001t0001g0214 | 3 | HG03579.hp1 HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-96+1772delA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70245245 | |||||
| chr12:70245433
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-96+1953G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70245433 | ||||||
| chr12:70245452
|
A | T | 10 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0002t0001g0203others(7): Show | 10 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.-96+1972A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70245452 | ||||||
| chr12:70245520
|
T | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-96+2040T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70245520 | ||||||
| chr12:70245659
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-96+2179G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70245659 | ||||||
| chr12:70245662
|
A | C | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-96+2182A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70245662 | ||||||
| chr12:70246029
|
G | A | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-96+2549G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70246029 | ||||||
| chr12:70246074
|
A | C | 37 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(34): Show | 37 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.-96+2594A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70246074 | ||||||
| chr12:70246114
|
G | A | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-96+2634G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70246114 | ||||||
| chr12:70246235
|
A | G | 1 | a0001c0004t0003g0273 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-96+2755A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70246235 | ||||||
| chr12:70246358
|
C | G | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-96+2878C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70246358 | ||||||
| chr12:70246426
|
C | G | 1 | a0001c0002t0002g0240 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-96+2946C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70246426 | ||||||
| chr12:70246594
|
G | T | 15 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0001g0200others(12): Show | 15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-96+3114G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70246594 | ||||||
| chr12:70246815
|
C | T | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG03225.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-96+3335C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70246815 | ||||||
| chr12:70247078
|
G | T | 60 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(57): Show | 60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.-96+3598G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70247078 | ||||||
| chr12:70247369
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-96+3889A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70247369 | ||||||
| chr12:70247436
|
A | G | 60 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(57): Show | 60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.-96+3956A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70247436 | ||||||
| chr12:70247448
|
G | A | 1 | a0001c0002t0001g0061 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-96+3968G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70247448 | ||||||
| chr12:70247471
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-96+3991T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70247471 | ||||||
| chr12:70247500
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-96+4020G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70247500 | ||||||
| chr12:70247512
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-96+4032A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70247512 | ||||||
| chr12:70247585
|
T | C | 1 | a0001c0002t0003g0241 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-96+4105T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70247585 | ||||||
| chr12:70248328
|
A | T | 12 | a0000c0003t0001g0179a0000c0003t0001g0185a0001c0001t0001g0174others(9): Show | 12 | HG00741.hp2 HG01167.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.-96+4848A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70248328 | ||||||
| chr12:70248459
|
C | T | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-96+4979C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70248459 | ||||||
| chr12:70248538
|
T | A | 5 | a0000c0003t0001g0064a0001c0001t0001g0063a0001c0001t0001g0065others(2): Show | 5 | NA18954.hp1 NA18987.hp2 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.-96+5058T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70248538 | ||||||
| chr12:70248781
|
A | G | 14 | a0000c0003t0001g0020a0000c0003t0001g0048a0000c0003t0001g0049others(11): Show | 14 | HG00438.hp1 HG02015.hp1 NA18941.hp1 others(11): Show |
intron_variant | MODIFIER | c.-96+5301A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70248781 | ||||||
| chr12:70248790
|
G | C | 1 | a0001c0001t0001g0025 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-96+5310G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70248790 | ||||||
| chr12:70249206
|
T | A | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-96+5726T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70249206 | ||||||
| chr12:70249252
|
T | G | 6 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0071others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-96+5772T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70249252 | ||||||
| chr12:70249394
|
A | ATTAT | 60 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(57): Show | 60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.-96+5917_-96+5918i others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70249394 | |||||
| chr12:70249524
|
C | T | 1 | a0001c0002t0001g0173 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-96+6044C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70249524 | ||||||
| chr12:70249850
|
T | G | 1 | a0000c0003t0001g0074 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-96+6370T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70249850 | ||||||
| chr12:70250122
|
C | G | 1 | a0001c0002t0001g0212 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-96+6642C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70250122 | ||||||
| chr12:70250153
|
G | A | 1 | a0001c0002t0001g0173 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-96+6673G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70250153 | ||||||
| chr12:70250328
|
A | G | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-96+6848A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70250328 | ||||||
| chr12:70250388
|
C | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | NA18966.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-96+6908C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70250388 | ||||||
| chr12:70250506
|
T | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-96+7026T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70250506 | ||||||
| chr12:70250600
|
A | C | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-96+7120A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70250600 | ||||||
| chr12:70250659
|
A | G | 2 | a0001c0006t0001g0018a0001c0006t0001g0170 | 2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-96+7179A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70250659 | ||||||
| chr12:70250763
|
G | A | 1 | a0000c0003t0001g0189 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-96+7283G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70250763 | ||||||
| chr12:70251012
|
G | T | 1 | a0001c0001t0001g0169 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-96+7532G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70251012 | ||||||
| chr12:70251463
|
G | A | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+7983G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70251463 | ||||||
| chr12:70251547
|
GA | G | 6 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0071others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-96+8075delA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70251547 | |||||
| chr12:70251548
|
A | G | 6 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0209others(3): Show | 6 | HG01256.hp1 HG01261.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.-96+8068A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70251548 | ||||||
| chr12:70251612
|
C | T | 7 | a0001c0001t0001g0062a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG00099.hp1 HG01074.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+8132C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70251612 | ||||||
| chr12:70251669
|
T | C | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-96+8189T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70251669 | ||||||
| chr12:70251752
|
A | T | 17 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0024others(14): Show | 17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-96+8272A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70251752 | ||||||
| chr12:70251765
|
A | G | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+8285A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70251765 | ||||||
| chr12:70252087
|
C | T | 70 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(67): Show | 70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.-96+8607C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70252087 | ||||||
| chr12:70252417
|
G | T | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-96+8937G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70252417 | ||||||
| chr12:70252512
|
A | T | 7 | a0000c0003t0001g0002a0000c0003t0001g0046a0000c0003t0001g0047others(4): Show | 7 | HG00408.hp2 HG02040.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+9032A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70252512 | ||||||
| chr12:70252555
|
G | A | 78 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(75): Show | 80 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.-96+9075G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70252555 | ||||||
| chr12:70252657
|
A | G | 3 | a0001c0001t0001g0004a0001c0001t0001g0161a0001c0001t0001g0162 | 4 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.-96+9177A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70252657 | ||||||
| chr12:70252673
|
C | G | 1 | a0001c0001t0001g0067 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-96+9193C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70252673 | ||||||
| chr12:70252675
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-96+9195G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70252675 | ||||||
| chr12:70252808
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-96+9328C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70252808 | ||||||
| chr12:70252871
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-96+9391C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70252871 | ||||||
| chr12:70253069
|
G | A | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+9589G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70253069 | ||||||
| chr12:70253168
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-96+9688G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70253168 | ||||||
| chr12:70253288
|
C | G | 1 | a0001c0002t0001g0211 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-96+9808C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70253288 | ||||||
| chr12:70253370
|
G | A | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-96+9890G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70253370 | ||||||
| chr12:70253464
|
A | C | 4 | a0001c0001t0001g0109a0001c0001t0001g0171a0001c0001t0001g0172others(1): Show | 4 | NA18966.hp2 NA18968.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.-96+9984A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70253464 | ||||||
| chr12:70253518
|
T | A | 78 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(75): Show | 80 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.-96+10038T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70253518 | ||||||
| chr12:70253702
|
A | C | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-96+10222A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70253702 | ||||||
| chr12:70253808
|
T | C | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-96+10328T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70253808 | ||||||
| chr12:70253815
|
A | C | 10 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0002t0001g0203others(7): Show | 10 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.-96+10335A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70253815 | ||||||
| chr12:70254020
|
C | T | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-96+10540C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70254020 | ||||||
| chr12:70254065
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-96+10585C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70254065 | ||||||
| chr12:70254213
|
G | A | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-96+10733G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70254213 | ||||||
| chr12:70254237
|
CA | C | 251 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(248): Show | 254 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.-96+10773delA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70254237 | |||||
| chr12:70254370
|
T | C | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-96+10890T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70254370 | ||||||
| chr12:70254467
|
A | G | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-96+10987A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70254467 | ||||||
| chr12:70254573
|
G | T | 2 | a0001c0001t0001g0106a0001c0002t0001g0107 | 2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-96+11093G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70254573 | ||||||
| chr12:70254896
|
G | T | 10 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0002t0001g0203others(7): Show | 10 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.-96+11416G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70254896 | ||||||
| chr12:70254923
|
G | A | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-96+11443G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70254923 | ||||||
| chr12:70254980
|
C | CA | 19 | a0000c0003t0001g0064a0000c0003t0001g0074a0000c0003t0001g0121others(16): Show | 19 | HG00558.hp1 HG01099.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.-96+11518dupA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70254980 | |||||
| chr12:70254980
|
CA | C | 78 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(75): Show | 78 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.-96+11518delA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70254980 | |||||
| chr12:70254980
|
CAAAAA | C | 74 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(71): Show | 76 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.-96+11514_-96+1151 others(9): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70254980 | |||||
| chr12:70254996
|
A | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0188others(1): Show | 4 | HG01891.hp2 HG02809.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-96+11516A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70254996 | ||||||
| chr12:70255044
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-96+11564G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70255044 | ||||||
| chr12:70255050
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-96+11570T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70255050 | ||||||
| chr12:70255073
|
A | C | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+11593A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70255073 | ||||||
| chr12:70255087
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-96+11607A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70255087 | ||||||
| chr12:70255136
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-96+11656C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70255136 | ||||||
| chr12:70255145
|
TTCTC | T | 17 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0024others(14): Show | 17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-96+11667_-96+1167 others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70255145 | |||||
| chr12:70255207
|
T | TA | 57 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(54): Show | 57 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.-96+11728dupA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70255207 | |||||
| chr12:70255409
|
C | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0118 | 2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-96+11929C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70255409 | ||||||
| chr12:70255464
|
T | C | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-96+11984T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70255464 | ||||||
| chr12:70255784
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-96+12304T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70255784 | ||||||
| chr12:70255850
|
A | G | 172 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(169): Show | 174 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.-96+12370A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70255850 | ||||||
| chr12:70256014
|
G | T | 1 | a0000c0003t0001g0043 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-96+12534G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256014 | ||||||
| chr12:70256028
|
C | T | 75 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(72): Show | 77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-96+12548C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256028 | ||||||
| chr12:70256125
|
C | G | 1 | a0000c0003t0001g0020 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-96+12645C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256125 | ||||||
| chr12:70256169
|
T | G | 17 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0024others(14): Show | 17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-96+12689T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256169 | ||||||
| chr12:70256172
|
A | T | 1 | a0001c0001t0001g0067 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-96+12692A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256172 | ||||||
| chr12:70256476
|
A | G | 17 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0024others(14): Show | 17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-96+12996A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256476 | ||||||
| chr12:70256582
|
T | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG01243.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.-96+13102T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256582 | ||||||
| chr12:70256582
|
T | TA | 98 | a0000c0003t0001g0011a0000c0003t0001g0029a0000c0003t0001g0064others(95): Show | 100 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.-96+13123dupA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70256582 | |||||
| chr12:70256582
|
T | TAA | 16 | a0000c0003t0001g0078a0000c0003t0002g0229a0000c0003t0002g0230others(13): Show | 16 | HG00621.hp2 HG01123.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.-96+13122_-96+1312 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70256582 | |||||
| chr12:70256582
|
T | TAAA | 30 | a0001c0001t0006g0005a0001c0002t0001g0200a0001c0002t0001g0248others(27): Show | 30 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.-96+13121_-96+1312 others(7): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70256582 | |||||
| chr12:70256626
|
A | G | 1 | a0001c0002t0009g0157 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-96+13146A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256626 | ||||||
| chr12:70256939
|
A | G | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-96+13459A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256939 | ||||||
| chr12:70256953
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-96+13473G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70256953 | ||||||
| chr12:70257026
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-96+13546A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257026 | ||||||
| chr12:70257033
|
AT | A | 12 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0023others(9): Show | 12 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.-96+13563delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257033 | |||||
| chr12:70257043
|
T | C | 1 | a0001c0002t0003g0241 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-96+13563T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257043 | ||||||
| chr12:70257162
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-96+13682G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257162 | ||||||
| chr12:70257243
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-96+13763A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257243 | ||||||
| chr12:70257285
|
A | G | 5 | a0001c0002t0001g0265a0001c0004t0001g0263a0001c0004t0001g0266others(2): Show | 5 | NA18977.hp1 NA18980.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.-96+13805A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257285 | ||||||
| chr12:70257309
|
G | A | 1 | a0001c0004t0003g0242 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-96+13829G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257309 | ||||||
| chr12:70257354
|
C | CT | 8 | a0000c0003t0001g0042a0001c0001t0001g0016a0001c0001t0001g0021others(5): Show | 8 | HG01106.hp2 HG01175.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.-96+13892dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257354 | |||||
| chr12:70257354
|
C | CTT | 7 | a0001c0001t0006g0005a0001c0002t0001g0248a0001c0004t0001g0246others(4): Show | 7 | HG01069.hp2 HG02647.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+13891_-96+1389 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257354 | |||||
| chr12:70257354
|
C | CTTT | 22 | a0001c0002t0001g0265a0001c0002t0003g0241a0001c0004t0001g0251others(19): Show | 22 | HG00323.hp1 HG00609.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.-96+13890_-96+1389 others(7): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257354 | |||||
| chr12:70257354
|
C | CTTTTTT | 6 | a0001c0002t0002g0233a0001c0002t0002g0234a0001c0002t0002g0235others(3): Show | 6 | HG02257.hp1 HG02886.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-96+13887_-96+1389 others(10): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257354 | |||||
| chr12:70257354
|
C | CTTTTTTT | 7 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(4): Show | 7 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+13886_-96+1389 others(11): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257354 | |||||
| chr12:70257354
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-96+13883_-96+1389 others(14): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257354 | |||||
| chr12:70257354
|
CT | C | 41 | a0000c0003t0001g0078a0001c0001t0001g0003a0001c0001t0001g0019others(38): Show | 43 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-96+13892delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257354 | |||||
| chr12:70257355
|
T | C | 10 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(7): Show | 10 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-96+13875T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257355 | ||||||
| chr12:70257360
|
TTTTTTTT others(6): Show |
T | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-96+13886_-96+1389 others(17): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257360 | |||||
| chr12:70257373
|
C | T | 62 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0016others(59): Show | 62 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.-96+13893C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257373 | ||||||
| chr12:70257391
|
C | T | 119 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(116): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.-96+13911C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257391 | ||||||
| chr12:70257417
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-96+13937G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257417 | ||||||
| chr12:70257461
|
C | T | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-96+13981C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257461 | ||||||
| chr12:70257536
|
AT | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG00639.hp1 HG03098.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-96+14067delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70257536 | |||||
| chr12:70257657
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0118 | 2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-96+14177G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257657 | ||||||
| chr12:70257687
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-96+14207T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257687 | ||||||
| chr12:70257696
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-96+14216C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257696 | ||||||
| chr12:70257737
|
A | G | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-96+14257A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257737 | ||||||
| chr12:70257881
|
A | G | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-96+14401A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70257881 | ||||||
| chr12:70258081
|
C | T | 1 | a0000c0003t0001g0215 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-96+14601C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70258081 | ||||||
| chr12:70258231
|
C | A | 1 | a0001c0002t0002g0240 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-96+14751C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70258231 | ||||||
| chr12:70258306
|
T | TA | 7 | a0001c0002t0002g0228a0001c0002t0002g0233a0001c0002t0002g0240others(4): Show | 7 | HG00621.hp2 HG01123.hp2 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.-96+14827dupA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70258306 | |||||
| chr12:70258315
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-96+14835A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70258315 | ||||||
| chr12:70258702
|
T | G | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-96+15222T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70258702 | ||||||
| chr12:70259028
|
C | T | 31 | a0000c0003t0001g0011a0000c0003t0001g0179a0000c0003t0001g0185others(28): Show | 31 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-96+15548C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259028 | ||||||
| chr12:70259033
|
A | G | 1 | a0001c0001t0001g0168 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-96+15553A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259033 | ||||||
| chr12:70259039
|
T | G | 38 | a0000c0003t0001g0078a0001c0001t0001g0003a0001c0001t0001g0019others(35): Show | 40 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.-96+15559T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259039 | ||||||
| chr12:70259056
|
C | T | 2 | a0000c0003t0001g0059a0001c0002t0001g0060 | 2 | NA18969.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.-96+15576C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259056 | ||||||
| chr12:70259123
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-96+15643A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259123 | ||||||
| chr12:70259132
|
C | T | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-96+15652C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259132 | ||||||
| chr12:70259315
|
A | AT | 119 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(116): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.-96+15844dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70259315 | |||||
| chr12:70259403
|
G | A | 1 | a0001c0004t0001g0251 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-96+15923G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259403 | ||||||
| chr12:70259786
|
C | T | 37 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(34): Show | 37 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.-96+16306C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259786 | ||||||
| chr12:70259799
|
C | T | 1 | a0001c0001t0001g0041 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-96+16319C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259799 | ||||||
| chr12:70259874
|
T | G | 1 | a0000c0003t0001g0138 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-96+16394T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259874 | ||||||
| chr12:70259925
|
G | C | 80 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(77): Show | 82 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.-96+16445G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70259925 | ||||||
| chr12:70260192
|
C | G | 1 | a0001c0001t0001g0204 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-96+16712C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70260192 | ||||||
| chr12:70260278
|
C | A | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-96+16798C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70260278 | ||||||
| chr12:70260402
|
G | T | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-96+16922G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70260402 | ||||||
| chr12:70260409
|
T | C | 17 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0024others(14): Show | 17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-96+16929T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70260409 | ||||||
| chr12:70260449
|
T | C | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-96+16969T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70260449 | ||||||
| chr12:70260471
|
G | A | 158 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(155): Show | 160 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.-96+16991G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70260471 | ||||||
| chr12:70260603
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-96+17123T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70260603 | ||||||
| chr12:70260613
|
AGTT | A | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-96+17139_-96+1714 others(7): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70260613 | |||||
| chr12:70260718
|
C | T | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-96+17238C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70260718 | ||||||
| chr12:70260853
|
A | AT | 33 | a0000c0003t0001g0020a0000c0003t0001g0048a0000c0003t0001g0049others(30): Show | 33 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(30): Show |
intron_variant | MODIFIER | c.-95-17265dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70260853 | |||||
| chr12:70260853
|
A | ATT | 44 | a0000c0003t0001g0058a0000c0003t0002g0229a0000c0003t0002g0230others(41): Show | 44 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.-95-17266_-95-1726 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70260853 | |||||
| chr12:70260853
|
A | ATTT | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02055.hp1 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-17267_-95-1726 others(7): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70260853 | |||||
| chr12:70260956
|
A | T | 189 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(186): Show | 191 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.-95-17176A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70260956 | ||||||
| chr12:70261008
|
T | G | 1 | a0001c0001t0001g0165 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-95-17124T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261008 | ||||||
| chr12:70261027
|
C | G | 1 | a0001c0002t0002g0240 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-95-17105C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261027 | ||||||
| chr12:70261129
|
TTGAGATG others(4): Show |
T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-95-17000_-95-1699 others(15): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70261129 | |||||
| chr12:70261281
|
T | A | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-95-16851T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261281 | ||||||
| chr12:70261305
|
C | CT | 79 | a0000c0003t0001g0002a0000c0003t0001g0020a0000c0003t0001g0028others(76): Show | 80 | HG00438.hp1 HG00609.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.-95-16800dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70261305 | |||||
| chr12:70261305
|
C | CTT | 17 | a0000c0003t0001g0015a0000c0003t0001g0037a0000c0003t0001g0038others(14): Show | 17 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.-95-16801_-95-1680 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70261305 | |||||
| chr12:70261305
|
C | CTTTT | 5 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0001g0113others(2): Show | 5 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.-95-16803_-95-1680 others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70261305 | |||||
| chr12:70261305
|
CT | C | 65 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0138others(62): Show | 67 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.-95-16800delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70261305 | |||||
| chr12:70261305
|
CTT | C | 8 | a0001c0001t0001g0218a0001c0001t0001g0220a0001c0001t0001g0221others(5): Show | 8 | HG00733.hp1 HG00738.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-16801_-95-1680 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70261305 | |||||
| chr12:70261305
|
CTTTTTT | C | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-95-16805_-95-1680 others(10): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70261305 | |||||
| chr12:70261338
|
G | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-16794G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261338 | ||||||
| chr12:70261415
|
C | T | 1 | a0001c0002t0001g0098 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-95-16717C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261415 | ||||||
| chr12:70261416
|
G | A | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-95-16716G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261416 | ||||||
| chr12:70261460
|
G | A | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-95-16672G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261460 | ||||||
| chr12:70261526
|
C | T | 2 | a0001c0001t0001g0140a0001c0002t0001g0139 | 2 | HG02055.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-95-16606C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261526 | ||||||
| chr12:70261656
|
T | G | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-16476T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261656 | ||||||
| chr12:70261834
|
A | AT | 9 | a0000c0003t0001g0078a0001c0001t0001g0095a0001c0001t0001g0118others(6): Show | 9 | HG00408.hp1 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-95-16282dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70261834 | |||||
| chr12:70261880
|
C | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-95-16252C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261880 | ||||||
| chr12:70261887
|
C | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG01106.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-95-16245C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261887 | ||||||
| chr12:70261928
|
C | G | 1 | a0001c0001t0001g0206 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-95-16204C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70261928 | ||||||
| chr12:70262057
|
C | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0165 | 2 | HG01074.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-95-16075C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262057 | ||||||
| chr12:70262263
|
T | C | 4 | a0001c0004t0001g0244a0001c0004t0001g0260a0001c0004t0001g0261others(1): Show | 4 | HG00323.hp1 HG01081.hp1 HG01891.hp1 others(1): Show |
intron_variant | MODIFIER | c.-95-15869T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262263 | ||||||
| chr12:70262334
|
C | T | 11 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0111others(8): Show | 11 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.-95-15798C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262334 | ||||||
| chr12:70262405
|
C | A | 1 | a0001c0001t0001g0112 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-95-15727C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262405 | ||||||
| chr12:70262571
|
G | A | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-95-15561G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262571 | ||||||
| chr12:70262588
|
A | G | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-95-15544A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262588 | ||||||
| chr12:70262592
|
T | C | 1 | a0001c0002t0001g0080 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-95-15540T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262592 | ||||||
| chr12:70262662
|
TA | T | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-95-15469delA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262662 | ||||||
| chr12:70262730
|
G | A | 1 | a0000c0003t0001g0037 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-95-15402G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262730 | ||||||
| chr12:70262760
|
A | G | 60 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(57): Show | 60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.-95-15372A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262760 | ||||||
| chr12:70262932
|
C | T | 75 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(72): Show | 77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-95-15200C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262932 | ||||||
| chr12:70262933
|
A | C | 75 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(72): Show | 77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-95-15199A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262933 | ||||||
| chr12:70262934
|
A | T | 75 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(72): Show | 77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-95-15198A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262934 | ||||||
| chr12:70262996
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-95-15136G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70262996 | ||||||
| chr12:70263075
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-95-15057C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70263075 | ||||||
| chr12:70263157
|
A | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-95-14975A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70263157 | ||||||
| chr12:70263158
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-95-14974C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70263158 | ||||||
| chr12:70263213
|
ACT | A | 17 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0024others(14): Show | 17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-95-14916_-95-1491 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70263213 | |||||
| chr12:70263478
|
G | A | 1 | a0001c0002t0002g0233 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-95-14654G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70263478 | ||||||
| chr12:70263740
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-95-14392A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70263740 | ||||||
| chr12:70264007
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0118 | 2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-95-14125A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70264007 | ||||||
| chr12:70264096
|
A | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-14036A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70264096 | ||||||
| chr12:70264369
|
C | T | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-95-13763C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70264369 | ||||||
| chr12:70264583
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-95-13549C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70264583 | ||||||
| chr12:70264682
|
C | T | 1 | a0000c0003t0001g0058 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-95-13450C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70264682 | ||||||
| chr12:70264802
|
G | A | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-95-13330G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70264802 | ||||||
| chr12:70264857
|
C | A | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-95-13275C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70264857 | ||||||
| chr12:70265048
|
G | A | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-95-13084G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265048 | ||||||
| chr12:70265055
|
A | T | 3 | a0000c0003t0001g0048a0000c0003t0001g0049a0000c0003t0001g0057 | 3 | NA18941.hp1 NA19003.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-95-13077A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265055 | ||||||
| chr12:70265189
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-95-12943A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265189 | ||||||
| chr12:70265271
|
G | GTCTCTTC others(8): Show |
4 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(1): Show | 4 | HG03098.hp1 HG03540.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-95-12860_-95-1285 others(19): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265271 | |||||
| chr12:70265271
|
G | GTCTCTTC others(18): Show |
1 | a0001c0001t0001g0007 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-95-12860_-95-1285 others(29): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265271 | |||||
| chr12:70265273
|
T | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG00639.hp1 HG03098.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-95-12859T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265273 | ||||||
| chr12:70265273
|
T | TTCTTC | 65 | a0000c0003t0001g0002a0000c0003t0001g0020a0000c0003t0001g0038others(62): Show | 66 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.-95-12809_-95-1280 others(9): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | |||||
| chr12:70265273
|
T | TTCTTCTC others(3): Show |
49 | a0000c0003t0001g0050a0000c0003t0001g0078a0000c0003t0002g0229others(46): Show | 51 | HG00280.hp2 HG00733.hp1 HG01069.hp1 others(48): Show |
intron_variant | MODIFIER | c.-95-12814_-95-1280 others(14): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | |||||
| chr12:70265273
|
T | TTCTTCTC others(8): Show |
1 | a0000c0003t0001g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-95-12846_-95-1284 others(19): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | |||||
| chr12:70265273
|
T | TTCTTCTC others(13): Show |
5 | a0000c0003t0001g0189a0000c0003t0001g0191a0000c0003t0001g0192others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-95-12846_-95-1284 others(24): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | |||||
| chr12:70265273
|
T | TTCTTCTC others(8): Show |
28 | a0000c0003t0001g0011a0000c0003t0001g0064a0001c0001t0001g0012others(25): Show | 28 | HG00438.hp2 HG00558.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.-95-12819_-95-1280 others(19): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | |||||
| chr12:70265273
|
T | TTCTTCTC others(13): Show |
4 | a0001c0001t0001g0062a0001c0001t0001g0141a0001c0001t0001g0168others(1): Show | 4 | HG01256.hp1 HG01433.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.-95-12824_-95-1280 others(24): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | |||||
| chr12:70265273
|
T | TTCTTCTC others(18): Show |
1 | a0001c0001t0001g0167 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-95-12829_-95-1280 others(29): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | |||||
| chr12:70265273
|
T | TTCTTCTC others(33): Show |
1 | a0001c0001t0001g0204 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-95-12844_-95-1280 others(44): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | |||||
| chr12:70265273
|
TTCTTC | T | 21 | a0000c0003t0001g0015a0000c0003t0001g0028a0000c0003t0001g0035others(18): Show | 21 | HG01099.hp2 HG01109.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-95-12809_-95-1280 others(9): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | |||||
| chr12:70265273
|
TTCTTCTC others(3): Show |
T | 11 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0113others(8): Show | 11 | HG02055.hp1 HG02056.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-95-12814_-95-1280 others(14): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | |||||
| chr12:70265273
|
TTCTTCTC others(8): Show |
T | 1 | a0001c0001t0001g0112 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-95-12819_-95-1280 others(19): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | |||||
| chr12:70265273
|
TTCTTCTC others(18): Show |
T | 1 | a0001c0002t0001g0096 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-95-12829_-95-1280 others(29): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265273 | |||||
| chr12:70265277
|
T | TCTCTTCT others(13): Show |
1 | a0000c0003t0001g0190 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-95-12846_-95-1284 others(24): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265277 | |||||
| chr12:70265297
|
T | C | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-95-12835T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265297 | ||||||
| chr12:70265321
|
T | G | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-95-12811T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265321 | ||||||
| chr12:70265321
|
T | TTCTCG | 4 | a0001c0004t0001g0247a0001c0004t0001g0263a0001c0004t0003g0242others(1): Show | 4 | HG01952.hp2 HG03195.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.-95-12807_-95-1280 others(9): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265321 | |||||
| chr12:70265321
|
T | TTCTCTTC others(3): Show |
17 | a0001c0001t0006g0005a0001c0002t0001g0248a0001c0002t0001g0265others(14): Show | 17 | HG00323.hp1 HG01099.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.-95-12805_-95-1280 others(14): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265321 | |||||
| chr12:70265321
|
T | TTCTCTTC others(8): Show |
9 | a0001c0004t0001g0245a0001c0004t0001g0249a0001c0004t0001g0258others(6): Show | 9 | HG00609.hp1 HG01069.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.-95-12805_-95-1280 others(19): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265321 | |||||
| chr12:70265321
|
T | TTCTCTTC others(13): Show |
4 | a0001c0004t0001g0246a0001c0004t0001g0251a0001c0004t0001g0261others(1): Show | 4 | HG01081.hp1 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-95-12805_-95-1280 others(24): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265321 | |||||
| chr12:70265323
|
C | CTCTT | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-12799_-95-1279 others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70265323 | |||||
| chr12:70265384
|
G | A | 272 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(269): Show | 275 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.-95-12748G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265384 | ||||||
| chr12:70265421
|
A | G | 3 | a0001c0002t0001g0061a0001c0002t0001g0084a0001c0002t0001g0093 | 3 | HG00438.hp2 HG02523.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-95-12711A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265421 | ||||||
| chr12:70265908
|
T | G | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-95-12224T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265908 | ||||||
| chr12:70265964
|
T | A | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-95-12168T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70265964 | ||||||
| chr12:70266003
|
C | CT | 119 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(116): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.-95-12114dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70266003 | |||||
| chr12:70266003
|
CT | C | 40 | a0000c0003t0001g0064a0001c0001t0001g0063a0001c0001t0001g0065others(37): Show | 40 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-95-12114delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70266003 | |||||
| chr12:70266023
|
G | T | 6 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0071others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-95-12109G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70266023 | ||||||
| chr12:70266099
|
G | GTAT | 9 | a0000c0003t0001g0020a0000c0003t0001g0189a0000c0003t0001g0190others(6): Show | 9 | HG00438.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-95-12013_-95-1201 others(7): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70266099 | |||||
| chr12:70266180
|
C | G | 1 | a0000c0003t0001g0124 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-95-11952C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70266180 | ||||||
| chr12:70266277
|
C | T | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-11855C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70266277 | ||||||
| chr12:70266359
|
G | C | 1 | a0001c0006t0001g0119 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-95-11773G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70266359 | ||||||
| chr12:70266512
|
T | C | 31 | a0000c0003t0001g0011a0000c0003t0001g0179a0000c0003t0001g0185others(28): Show | 31 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-95-11620T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70266512 | ||||||
| chr12:70266763
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-95-11369C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70266763 | ||||||
| chr12:70266794
|
GTA | G | 19 | a0000c0003t0001g0064a0000c0003t0001g0074a0000c0003t0001g0121others(16): Show | 19 | HG00558.hp1 HG01099.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.-95-11334_-95-1133 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70266794 | |||||
| chr12:70266830
|
G | A | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-11302G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70266830 | ||||||
| chr12:70266839
|
C | CT | 26 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(23): Show | 26 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.-95-11285dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70266839 | |||||
| chr12:70266963
|
A | T | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-95-11169A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70266963 | ||||||
| chr12:70266978
|
CAT | C | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-95-11153_-95-1115 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70266978 | ||||||
| chr12:70267065
|
T | C | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-11067T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70267065 | ||||||
| chr12:70267085
|
A | G | 1 | a0000c0003t0001g0189 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-95-11047A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70267085 | ||||||
| chr12:70267269
|
C | G | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG01167.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-95-10863C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70267269 | ||||||
| chr12:70267470
|
C | T | 5 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0192others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-95-10662C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70267470 | ||||||
| chr12:70267564
|
A | G | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-10568A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70267564 | ||||||
| chr12:70268038
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-95-10094A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70268038 | ||||||
| chr12:70268100
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-95-10032G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70268100 | ||||||
| chr12:70268594
|
C | T | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-95-9538C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70268594 | ||||||
| chr12:70268627
|
AT | A | 33 | a0000c0003t0001g0032a0001c0002t0001g0248a0001c0002t0001g0265others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-95-9492delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70268627 | |||||
| chr12:70268628
|
T | A | 3 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0004t0001g0245 | 3 | HG03486.hp1 HG06807.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.-95-9504T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70268628 | ||||||
| chr12:70268629
|
T | A | 32 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(29): Show | 32 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-95-9503T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70268629 | ||||||
| chr12:70268646
|
T | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-95-9486T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70268646 | ||||||
| chr12:70268875
|
T | C | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG01261.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-95-9257T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70268875 | ||||||
| chr12:70269025
|
G | A | 6 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0071others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-95-9107G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70269025 | ||||||
| chr12:70269217
|
C | T | 5 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0192others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-95-8915C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70269217 | ||||||
| chr12:70269275
|
CT | C | 18 | a0001c0001t0001g0016a0001c0001t0001g0067a0001c0001t0001g0099others(15): Show | 18 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.-95-8846delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70269275 | |||||
| chr12:70269290
|
CT | C | 26 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0017others(23): Show | 26 | HG00621.hp2 HG01109.hp1 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.-95-8829delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70269290 | |||||
| chr12:70269488
|
A | G | 10 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0002t0001g0203others(7): Show | 10 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.-95-8644A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70269488 | ||||||
| chr12:70269545
|
A | C | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-95-8587A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70269545 | ||||||
| chr12:70269862
|
C | T | 5 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0192others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-95-8270C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70269862 | ||||||
| chr12:70269870
|
T | C | 70 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(67): Show | 70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.-95-8262T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70269870 | ||||||
| chr12:70269995
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-95-8137C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70269995 | ||||||
| chr12:70270040
|
A | G | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-8092A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70270040 | ||||||
| chr12:70270410
|
T | C | 2 | a0000c0003t0001g0011a0001c0001t0001g0012 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-95-7722T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70270410 | ||||||
| chr12:70270576
|
A | G | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-95-7556A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70270576 | ||||||
| chr12:70270878
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-95-7254A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70270878 | ||||||
| chr12:70271085
|
T | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-95-7047T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271085 | ||||||
| chr12:70271203
|
A | G | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-95-6929A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271203 | ||||||
| chr12:70271264
|
C | A | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-95-6868C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271264 | ||||||
| chr12:70271341
|
G | A | 1 | a0000c0003t0001g0215 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-95-6791G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271341 | ||||||
| chr12:70271375
|
C | CT | 35 | a0001c0001t0001g0017a0001c0001t0001g0111a0001c0001t0001g0112others(32): Show | 35 | HG01069.hp2 HG01099.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-95-6735dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70271375 | |||||
| chr12:70271375
|
C | CTT | 7 | a0001c0001t0001g0021a0001c0001t0001g0110a0001c0001t0006g0005others(4): Show | 7 | HG00609.hp1 HG01081.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-95-6736_-95-6735d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70271375 | |||||
| chr12:70271375
|
CT | C | 183 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(180): Show | 186 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.-95-6735delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70271375 | |||||
| chr12:70271375
|
CTT | C | 9 | a0001c0001t0001g0014a0001c0001t0001g0183a0001c0001t0001g0213others(6): Show | 9 | HG01167.hp1 HG01891.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-95-6736_-95-6735d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70271375 | |||||
| chr12:70271375
|
CTTT | C | 17 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0024others(14): Show | 17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-95-6737_-95-6735d others(5): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70271375 | |||||
| chr12:70271405
|
G | C | 9 | a0000c0003t0001g0011a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 9 | HG00639.hp1 HG01891.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-95-6727G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271405 | ||||||
| chr12:70271420
|
C | T | 6 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0071others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-95-6712C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271420 | ||||||
| chr12:70271437
|
A | G | 70 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(67): Show | 70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.-95-6695A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271437 | ||||||
| chr12:70271443
|
A | G | 43 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(40): Show | 43 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.-95-6689A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271443 | ||||||
| chr12:70271509
|
G | A | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-95-6623G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271509 | ||||||
| chr12:70271517
|
G | A | 1 | a0001c0001t0001g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-95-6615G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271517 | ||||||
| chr12:70271852
|
C | T | 11 | a0001c0002t0002g0228a0001c0002t0002g0233a0001c0002t0002g0234others(8): Show | 11 | HG00621.hp2 HG01123.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-95-6280C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70271852 | ||||||
| chr12:70271918
|
C | CA | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-6208dupA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70271918 | |||||
| chr12:70272215
|
G | C | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-95-5917G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70272215 | ||||||
| chr12:70272246
|
G | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-5886G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70272246 | ||||||
| chr12:70272429
|
A | G | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-5703A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70272429 | ||||||
| chr12:70272509
|
G | C | 1 | a0001c0001t0001g0065 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-95-5623G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70272509 | ||||||
| chr12:70272565
|
A | T | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-95-5567A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70272565 | ||||||
| chr12:70272579
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0118 | 2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-95-5553G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70272579 | ||||||
| chr12:70273301
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-95-4831A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70273301 | ||||||
| chr12:70273313
|
C | CT | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-4809dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr12 | 70273313 | |||||
| chr12:70273472
|
T | C | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-95-4660T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70273472 | ||||||
| chr12:70273777
|
A | T | 1 | a0001c0006t0001g0119 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-95-4355A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70273777 | ||||||
| chr12:70273851
|
A | G | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-95-4281A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70273851 | ||||||
| chr12:70273957
|
T | A | 1 | a0001c0001t0001g0115 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-95-4175T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70273957 | ||||||
| chr12:70274167
|
A | T | 1 | a0001c0001t0001g0169 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-95-3965A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70274167 | ||||||
| chr12:70274274
|
A | G | 75 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(72): Show | 77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-95-3858A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70274274 | ||||||
| chr12:70274470
|
A | G | 10 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0002t0001g0203others(7): Show | 10 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.-95-3662A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70274470 | ||||||
| chr12:70274690
|
A | G | 3 | a0001c0002t0004g0232a0001c0002t0004g0238a0001c0002t0004g0239 | 3 | NA18941.hp2 NA18945.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.-95-3442A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70274690 | ||||||
| chr12:70274777
|
C | T | 98 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(95): Show | 100 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.-95-3355C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70274777 | ||||||
| chr12:70274929
|
G | A | 11 | a0001c0002t0002g0228a0001c0002t0002g0233a0001c0002t0002g0234others(8): Show | 11 | HG00621.hp2 HG01123.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-95-3203G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70274929 | ||||||
| chr12:70275155
|
T | G | 2 | a0000c0003t0001g0011a0001c0001t0001g0012 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-95-2977T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70275155 | ||||||
| chr12:70275184
|
T | C | 4 | a0000c0003t0001g0190a0000c0003t0001g0192a0000c0003t0001g0193others(1): Show | 4 | HG02109.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-95-2948T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70275184 | ||||||
| chr12:70275196
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-95-2936C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70275196 | ||||||
| chr12:70275341
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-95-2791G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70275341 | ||||||
| chr12:70275484
|
G | A | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG01099.hp1 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-2648G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70275484 | ||||||
| chr12:70275671
|
G | A | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-2461G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70275671 | ||||||
| chr12:70275768
|
G | C | 42 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(39): Show | 42 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.-95-2364G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70275768 | ||||||
| chr12:70276089
|
A | G | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-95-2043A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276089 | ||||||
| chr12:70276153
|
G | T | 274 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(271): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.-95-1979G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276153 | ||||||
| chr12:70276261
|
A | G | 17 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0024others(14): Show | 17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-95-1871A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276261 | ||||||
| chr12:70276298
|
T | A | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.-95-1834T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276298 | ||||||
| chr12:70276412
|
G | C | 75 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(72): Show | 77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-95-1720G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276412 | ||||||
| chr12:70276413
|
C | T | 2 | a0001c0002t0001g0203a0001c0002t0001g0205 | 2 | HG00733.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.-95-1719C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276413 | ||||||
| chr12:70276447
|
A | G | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-1685A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276447 | ||||||
| chr12:70276566
|
C | T | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-95-1566C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276566 | ||||||
| chr12:70276567
|
G | T | 1 | a0001c0001t0005g0155 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-95-1565G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276567 | ||||||
| chr12:70276806
|
G | C | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.-95-1326G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276806 | ||||||
| chr12:70276821
|
G | A | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-1311G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276821 | ||||||
| chr12:70276877
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-95-1255T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70276877 | ||||||
| chr12:70277366
|
A | G | 1 | a0000c0003t0001g0189 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-95-766A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277366 | ||||||
| chr12:70277447
|
T | G | 43 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(40): Show | 43 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.-95-685T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277447 | ||||||
| chr12:70277489
|
A | G | 1 | a0001c0004t0001g0272 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-95-643A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277489 | ||||||
| chr12:70277580
|
A | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-95-552A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277580 | ||||||
| chr12:70277643
|
G | T | 31 | a0000c0003t0001g0011a0000c0003t0001g0179a0000c0003t0001g0185others(28): Show | 31 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-95-489G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277643 | ||||||
| chr12:70277677
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-95-455G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277677 | ||||||
| chr12:70277680
|
G | A | 8 | a0001c0002t0001g0248a0001c0004t0001g0246a0001c0004t0001g0247others(5): Show | 8 | HG01069.hp2 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-452G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277680 | ||||||
| chr12:70277689
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-95-443A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277689 | ||||||
| chr12:70277864
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-95-268T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277864 | ||||||
| chr12:70277916
|
A | G | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.-95-216A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277916 | ||||||
| chr12:70277981
|
C | T | 1 | a0001c0002t0002g0234 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-95-151C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277981 | ||||||
| chr12:70277988
|
G | A | 20 | a0000c0003t0001g0179a0000c0003t0001g0185a0001c0001t0001g0017others(17): Show | 20 | HG00741.hp2 HG01109.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.-95-144G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277988 | ||||||
| chr12:70277995
|
T | C | 1 | a0001c0002t0002g0235 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-95-137T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70277995 | ||||||
| chr12:70278015
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-95-117G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70278015 | ||||||
| chr12:70278032
|
T | C | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-95-100T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 1/15 | chr12 | 70278032 | ||||||
| chr12:70278369
|
T | A | 70 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(67): Show | 70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.48+95T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70278369 | ||||||
| chr12:70278537
|
A | G | 42 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(39): Show | 42 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.48+263A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70278537 | ||||||
| chr12:70278677
|
A | G | 10 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0002t0001g0203others(7): Show | 10 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.48+403A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70278677 | ||||||
| chr12:70278770
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.48+496C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70278770 | ||||||
| chr12:70278820
|
T | C | 70 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(67): Show | 70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.48+546T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70278820 | ||||||
| chr12:70278992
|
G | A | 8 | a0001c0002t0001g0248a0001c0004t0001g0246a0001c0004t0001g0247others(5): Show | 8 | HG01069.hp2 HG02622.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+718G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70278992 | ||||||
| chr12:70279007
|
T | C | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+733T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70279007 | ||||||
| chr12:70279068
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.48+794T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70279068 | ||||||
| chr12:70279136
|
T | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+862T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70279136 | ||||||
| chr12:70279548
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.48+1274T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70279548 | ||||||
| chr12:70279705
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.48+1431A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70279705 | ||||||
| chr12:70279723
|
T | C | 31 | a0000c0003t0001g0011a0000c0003t0001g0179a0000c0003t0001g0185others(28): Show | 31 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.48+1449T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70279723 | ||||||
| chr12:70279799
|
A | G | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.48+1525A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70279799 | ||||||
| chr12:70279844
|
G | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+1570G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70279844 | ||||||
| chr12:70279857
|
CTTTCTAC others(20): Show |
C | 5 | a0001c0001t0001g0115a0001c0001t0001g0140a0001c0001t0001g0148others(2): Show | 5 | HG02055.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+1585_48+1611del others(27): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70279857 | |||||
| chr12:70279887
|
A | C | 119 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(116): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.48+1613A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70279887 | ||||||
| chr12:70280003
|
A | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | NA18966.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.48+1729A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280003 | ||||||
| chr12:70280102
|
G | A | 3 | a0000c0003t0001g0215a0001c0001t0001g0213a0001c0001t0001g0214 | 3 | HG03579.hp1 HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.48+1828G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280102 | ||||||
| chr12:70280348
|
G | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.48+2074G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280348 | ||||||
| chr12:70280377
|
T | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0118others(2): Show | 5 | HG01109.hp1 HG02486.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+2103T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280377 | ||||||
| chr12:70280753
|
T | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+2479T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280753 | ||||||
| chr12:70280803
|
T | C | 2 | a0001c0001t0001g0125a0001c0001t0001g0126 | 2 | NA18961.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.48+2529T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280803 | ||||||
| chr12:70280808
|
T | C | 3 | a0001c0002t0002g0235a0001c0002t0002g0236a0001c0002t0002g0237 | 3 | HG02257.hp1 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.48+2534T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280808 | ||||||
| chr12:70280820
|
C | A | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+2546C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280820 | ||||||
| chr12:70280875
|
C | T | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+2601C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280875 | ||||||
| chr12:70280915
|
C | T | 9 | a0000c0003t0001g0011a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 9 | HG00639.hp1 HG01891.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.48+2641C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70280915 | ||||||
| chr12:70281084
|
C | CT | 17 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0106others(14): Show | 17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.48+2825dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70281084 | |||||
| chr12:70281084
|
CT | C | 50 | a0000c0003t0001g0039a0000c0003t0001g0189a0000c0003t0001g0190others(47): Show | 50 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(47): Show |
intron_variant | MODIFIER | c.48+2825delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70281084 | |||||
| chr12:70281100
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.48+2826C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281100 | ||||||
| chr12:70281137
|
G | T | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.48+2863G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281137 | ||||||
| chr12:70281157
|
T | C | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.48+2883T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281157 | ||||||
| chr12:70281194
|
C | T | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+2920C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281194 | ||||||
| chr12:70281260
|
T | A | 17 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0024others(14): Show | 17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.48+2986T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281260 | ||||||
| chr12:70281318
|
C | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+3044C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281318 | ||||||
| chr12:70281319
|
G | A | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.48+3045G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281319 | ||||||
| chr12:70281453
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.48+3179C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281453 | ||||||
| chr12:70281685
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.48+3411C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281685 | ||||||
| chr12:70281816
|
T | TTAAATTT others(18): Show |
22 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0112others(19): Show | 22 | HG00621.hp2 HG00733.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.48+3575_48+3599dup others(25): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70281816 | |||||
| chr12:70281816
|
T | TTAAATTT others(43): Show |
13 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(10): Show | 13 | HG01256.hp1 HG01261.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.48+3550_48+3599dup others(50): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70281816 | |||||
| chr12:70281922
|
A | G | 5 | a0001c0001t0001g0115a0001c0001t0001g0140a0001c0001t0001g0148others(2): Show | 5 | HG02055.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+3648A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281922 | ||||||
| chr12:70281932
|
T | G | 1 | a0001c0001t0001g0154 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.48+3658T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70281932 | ||||||
| chr12:70282102
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0118 | 2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.48+3828C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70282102 | ||||||
| chr12:70282243
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+3969C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70282243 | ||||||
| chr12:70282250
|
G | A | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+3976G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70282250 | ||||||
| chr12:70282332
|
G | A | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.48+4058G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70282332 | ||||||
| chr12:70282400
|
A | G | 1 | a0001c0002t0001g0093 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.48+4126A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70282400 | ||||||
| chr12:70282884
|
C | CT | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.48+4612dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70282884 | |||||
| chr12:70283106
|
A | G | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.48+4832A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283106 | ||||||
| chr12:70283111
|
T | C | 3 | a0001c0006t0001g0018a0001c0006t0001g0119a0001c0006t0001g0170 | 3 | HG02970.hp1 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.48+4837T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283111 | ||||||
| chr12:70283333
|
A | C | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.48+5059A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283333 | ||||||
| chr12:70283365
|
C | T | 1 | a0001c0001t0001g0007 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.48+5091C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283365 | ||||||
| chr12:70283366
|
G | A | 3 | a0001c0001t0001g0024a0001c0001t0001g0165a0001c0001t0001g0188 | 3 | HG01074.hp2 HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+5092G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283366 | ||||||
| chr12:70283420
|
A | AGG | 10 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0002t0001g0203others(7): Show | 10 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.48+5146_48+5147ins others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283420 | ||||||
| chr12:70283467
|
T | TGATA | 52 | a0000c0003t0001g0031a0000c0003t0001g0033a0000c0003t0001g0179others(49): Show | 52 | HG00558.hp1 HG00609.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.48+5232_48+5235dup others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283467 | |||||
| chr12:70283467
|
T | TGATAGAT others(1): Show |
114 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0028others(111): Show | 114 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.48+5228_48+5235dup others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283467 | |||||
| chr12:70283467
|
T | TGATAGAT others(5): Show |
36 | a0000c0003t0001g0020a0000c0003t0001g0037a0000c0003t0001g0039others(33): Show | 38 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.48+5224_48+5235dup others(12): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283467 | |||||
| chr12:70283467
|
T | TGATAGAT others(9): Show |
5 | a0001c0001t0001g0041a0001c0001t0001g0053a0001c0001t0001g0075others(2): Show | 5 | HG03225.hp2 HG03710.hp1 HG04115.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+5220_48+5235dup others(16): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283467 | |||||
| chr12:70283467
|
TGATA | T | 33 | a0000c0003t0001g0059a0000c0003t0001g0064a0000c0003t0001g0074others(30): Show | 33 | HG00609.hp1 HG00621.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.48+5232_48+5235del others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283467 | |||||
| chr12:70283467
|
TGATAGAT others(1): Show |
T | 5 | a0000c0003t0001g0011a0001c0001t0001g0012a0001c0001t0001g0204others(2): Show | 5 | HG00733.hp2 HG01070.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.48+5228_48+5235del others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283467 | |||||
| chr12:70283561
|
A | G | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+5287A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283561 | ||||||
| chr12:70283570
|
A | T | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.48+5296A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283570 | ||||||
| chr12:70283611
|
A | G | 1 | a0000c0003t0001g0038 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.48+5337A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283611 | ||||||
| chr12:70283647
|
T | TA | 78 | a0000c0003t0001g0011a0000c0003t0001g0034a0000c0003t0001g0078others(75): Show | 80 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.48+5393dupA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283647 | |||||
| chr12:70283647
|
TA | T | 20 | a0000c0003t0001g0043a0000c0003t0001g0055a0000c0003t0002g0229others(17): Show | 20 | HG01123.hp2 HG01884.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.48+5393delA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283647 | |||||
| chr12:70283653
|
A | C | 5 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0192others(2): Show | 5 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+5379A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283653 | ||||||
| chr12:70283658
|
A | AG | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+5384_48+5385ins others(1): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283658 | ||||||
| chr12:70283686
|
A | G | 111 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(108): Show | 113 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.48+5412A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283686 | ||||||
| chr12:70283707
|
C | T | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+5433C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283707 | ||||||
| chr12:70283846
|
T | C | 1 | a0001c0006t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.48+5572T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283846 | ||||||
| chr12:70283853
|
A | G | 6 | a0001c0001t0001g0004a0001c0001t0001g0142a0001c0001t0001g0145others(3): Show | 7 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+5579A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283853 | ||||||
| chr12:70283902
|
C | T | 2 | a0001c0002t0001g0001a0001c0002t0001g0090 | 4 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+5628C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70283902 | ||||||
| chr12:70283930
|
A | AT | 28 | a0000c0003t0001g0020a0000c0003t0001g0034a0000c0003t0001g0042others(25): Show | 28 | HG00438.hp1 HG01109.hp1 HG02015.hp1 others(25): Show |
intron_variant | MODIFIER | c.48+5679dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283930 | |||||
| chr12:70283930
|
A | ATT | 12 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.48+5678_48+5679dup others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283930 | |||||
| chr12:70283930
|
A | ATTT | 29 | a0000c0003t0001g0193a0001c0002t0001g0248a0001c0002t0001g0265others(26): Show | 29 | HG00323.hp1 HG00609.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.48+5677_48+5679dup others(3): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283930 | |||||
| chr12:70283930
|
A | ATTTT | 5 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0004t0001g0245others(2): Show | 5 | HG01069.hp2 HG03486.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.48+5676_48+5679dup others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70283930 | |||||
| chr12:70284030
|
C | T | 1 | a0001c0007t0001g0027 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.48+5756C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70284030 | ||||||
| chr12:70284314
|
C | T | 35 | a0001c0001t0001g0024a0001c0001t0001g0188a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+6040C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70284314 | ||||||
| chr12:70284575
|
CCT | C | 3 | a0001c0001t0001g0103a0001c0001t0001g0217a0001c0002t0001g0061 | 3 | HG00438.hp2 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.48+6302_48+6303del others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70284575 | ||||||
| chr12:70284575
|
CCTT | C | 66 | a0000c0003t0001g0011a0000c0003t0001g0078a0001c0001t0001g0003others(63): Show | 68 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.48+6302_48+6304del others(3): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70284575 | ||||||
| chr12:70284576
|
C | CTT | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.48+6320_48+6321dup others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70284576 | |||||
| chr12:70284576
|
CT | C | 43 | a0000c0003t0001g0055a0000c0003t0001g0064a0001c0001t0001g0016others(40): Show | 43 | HG00323.hp1 HG00609.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.48+6321delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70284576 | |||||
| chr12:70284576
|
CTT | C | 9 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(6): Show | 9 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.48+6320_48+6321del others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70284576 | |||||
| chr12:70284642
|
T | C | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+6368T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70284642 | ||||||
| chr12:70284694
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.48+6420C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70284694 | ||||||
| chr12:70284916
|
T | C | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.48+6642T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70284916 | ||||||
| chr12:70284994
|
G | A | 1 | a0001c0004t0001g0251 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.48+6720G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70284994 | ||||||
| chr12:70285191
|
A | G | 1 | a0001c0001t0001g0110 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.48+6917A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285191 | ||||||
| chr12:70285216
|
G | GT | 7 | a0001c0001t0001g0017a0001c0001t0001g0075a0001c0001t0001g0118others(4): Show | 7 | HG01109.hp1 HG02896.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+6954dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70285216 | |||||
| chr12:70285216
|
G | T | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.48+6942G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285216 | ||||||
| chr12:70285221
|
T | TG | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+6947_48+6948ins others(1): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285221 | ||||||
| chr12:70285222
|
T | G | 7 | a0001c0001t0001g0062a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | HG00099.hp1 HG01074.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+6948T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285222 | ||||||
| chr12:70285272
|
T | C | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+6998T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285272 | ||||||
| chr12:70285289
|
A | G | 2 | a0001c0002t0001g0203a0001c0002t0001g0205 | 2 | HG00733.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.48+7015A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285289 | ||||||
| chr12:70285331
|
T | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.48+7057T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285331 | ||||||
| chr12:70285384
|
AT | A | 61 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0016others(58): Show | 61 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.48+7123delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70285384 | |||||
| chr12:70285384
|
ATT | A | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+7122_48+7123del others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70285384 | |||||
| chr12:70285407
|
G | A | 1 | a0001c0005t0001g0269 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.48+7133G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285407 | ||||||
| chr12:70285492
|
A | G | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+7218A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285492 | ||||||
| chr12:70285496
|
G | A | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+7222G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285496 | ||||||
| chr12:70285498
|
G | A | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.48+7224G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285498 | ||||||
| chr12:70285638
|
A | G | 1 | a0001c0001t0001g0177 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.48+7364A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285638 | ||||||
| chr12:70285692
|
CAA | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.48+7420_48+7421del others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70285692 | |||||
| chr12:70285810
|
G | A | 215 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(212): Show | 217 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.48+7536G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70285810 | ||||||
| chr12:70286084
|
G | A | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+7810G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286084 | ||||||
| chr12:70286106
|
T | TCATATTT others(304): Show |
30 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(27): Show | 30 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.48+7841_48+7842ins others(311): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70286106 | |||||
| chr12:70286106
|
T | TCATATTT others(305): Show |
3 | a0001c0004t0001g0245a0001c0004t0003g0270a0001c0005t0001g0264 | 3 | HG01928.hp1 NA18977.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.48+7841_48+7842ins others(312): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70286106 | |||||
| chr12:70286106
|
T | TCATATTT others(320): Show |
1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.48+7841_48+7842ins others(327): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70286106 | |||||
| chr12:70286106
|
T | TCATATTT others(324): Show |
1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.48+7841_48+7842ins others(331): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70286106 | |||||
| chr12:70286155
|
C | A | 70 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(67): Show | 70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.48+7881C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286155 | ||||||
| chr12:70286212
|
C | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+7938C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286212 | ||||||
| chr12:70286239
|
G | T | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+7965G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286239 | ||||||
| chr12:70286280
|
A | G | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+8006A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286280 | ||||||
| chr12:70286359
|
A | ATTC | 158 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(155): Show | 160 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.48+8089_48+8091dup others(3): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70286359 | |||||
| chr12:70286439
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.48+8165G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286439 | ||||||
| chr12:70286613
|
A | G | 60 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(57): Show | 60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.48+8339A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286613 | ||||||
| chr12:70286759
|
C | G | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.48+8485C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286759 | ||||||
| chr12:70286822
|
C | T | 10 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.48+8548C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286822 | ||||||
| chr12:70286950
|
T | A | 78 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(75): Show | 80 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.48+8676T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286950 | ||||||
| chr12:70286969
|
T | C | 1 | a0000c0003t0001g0015 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.48+8695T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70286969 | ||||||
| chr12:70287153
|
A | AT | 15 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0001g0200others(12): Show | 15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.48+8887dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70287153 | |||||
| chr12:70287213
|
AT | A | 148 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(145): Show | 150 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.48+8946delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70287213 | |||||
| chr12:70287302
|
C | T | 1 | a0001c0001t0001g0066 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.48+9028C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70287302 | ||||||
| chr12:70287481
|
G | T | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+9207G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70287481 | ||||||
| chr12:70287509
|
T | G | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+9235T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70287509 | ||||||
| chr12:70287725
|
G | A | 1 | a0001c0004t0003g0270 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.48+9451G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70287725 | ||||||
| chr12:70287824
|
T | C | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.48+9550T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70287824 | ||||||
| chr12:70288034
|
C | T | 43 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(40): Show | 43 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.48+9760C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70288034 | ||||||
| chr12:70288056
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.48+9782T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70288056 | ||||||
| chr12:70288136
|
C | CT | 78 | a0000c0003t0001g0078a0000c0003t0001g0179a0000c0003t0001g0185others(75): Show | 80 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.48+9886dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70288136 | |||||
| chr12:70288136
|
C | CTT | 9 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0100others(6): Show | 9 | HG00438.hp2 HG02486.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.48+9885_48+9886dup others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70288136 | |||||
| chr12:70288136
|
CT | C | 59 | a0000c0003t0001g0015a0000c0003t0001g0020a0000c0003t0001g0028others(56): Show | 59 | HG00438.hp1 HG00621.hp2 HG00733.hp2 others(56): Show |
intron_variant | MODIFIER | c.48+9886delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70288136 | |||||
| chr12:70288136
|
CTTTTTT | C | 33 | a0000c0003t0001g0193a0001c0001t0001g0021a0001c0001t0006g0005others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.48+9881_48+9886del others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70288136 | |||||
| chr12:70288136
|
CTTTTTTT | C | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02451.hp2 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+9880_48+9886del others(7): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70288136 | |||||
| chr12:70288136
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0017a0001c0001t0001g0118 | 2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.48+9877_48+9886del others(10): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70288136 | |||||
| chr12:70288136
|
CTTTTTTT others(8): Show |
C | 6 | a0000c0003t0001g0074a0000c0003t0001g0121a0000c0003t0001g0122others(3): Show | 6 | HG01099.hp2 HG01123.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.48+9872_48+9886del others(15): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70288136 | |||||
| chr12:70288149
|
T | C | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.48+9875T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70288149 | ||||||
| chr12:70288399
|
G | A | 78 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(75): Show | 80 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.48+10125G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70288399 | ||||||
| chr12:70288652
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.48+10378C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70288652 | ||||||
| chr12:70289965
|
T | C | 42 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(39): Show | 42 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.48+11691T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70289965 | ||||||
| chr12:70290009
|
T | G | 1 | a0001c0002t0001g0061 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.48+11735T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70290009 | ||||||
| chr12:70290226
|
C | CT | 11 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(8): Show | 11 | HG02109.hp2 HG02145.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.48+11962dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70290226 | |||||
| chr12:70290282
|
A | C | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+12008A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70290282 | ||||||
| chr12:70290485
|
A | T | 10 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0002t0001g0203others(7): Show | 10 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.48+12211A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70290485 | ||||||
| chr12:70290577
|
A | C | 191 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(188): Show | 193 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.48+12303A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70290577 | ||||||
| chr12:70290640
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+12366C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70290640 | ||||||
| chr12:70290657
|
C | CTT | 223 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(220): Show | 225 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.48+12383_48+12384i others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70290657 | ||||||
| chr12:70290713
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.48+12439A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70290713 | ||||||
| chr12:70290875
|
C | G | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+12601C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70290875 | ||||||
| chr12:70291201
|
C | T | 219 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(216): Show | 221 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.48+12927C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291201 | ||||||
| chr12:70291378
|
G | A | 1 | a0000c0003t0001g0078 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.48+13104G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291378 | ||||||
| chr12:70291484
|
G | A | 2 | a0000c0003t0001g0191a0000c0003t0001g0194 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.48+13210G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291484 | ||||||
| chr12:70291492
|
A | G | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.48+13218A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291492 | ||||||
| chr12:70291547
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.48+13273C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291547 | ||||||
| chr12:70291708
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.48+13434C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291708 | ||||||
| chr12:70291733
|
C | T | 4 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(1): Show | 4 | HG02486.hp1 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.48+13459C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291733 | ||||||
| chr12:70291797
|
C | T | 1 | a0001c0001t0005g0155 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.48+13523C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291797 | ||||||
| chr12:70291863
|
G | A | 3 | a0000c0003t0001g0192a0000c0003t0001g0193a0000c0003t0001g0195 | 3 | HG02109.hp2 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.48+13589G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291863 | ||||||
| chr12:70291869
|
G | A | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.48+13595G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291869 | ||||||
| chr12:70291945
|
A | G | 3 | a0000c0003t0001g0215a0001c0001t0001g0213a0001c0001t0001g0214 | 3 | HG03579.hp1 HG06807.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.48+13671A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291945 | ||||||
| chr12:70291989
|
A | T | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.48+13715A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291989 | ||||||
| chr12:70291990
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+13716C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70291990 | ||||||
| chr12:70292283
|
C | A | 215 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(212): Show | 217 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.48+14009C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70292283 | ||||||
| chr12:70292370
|
C | A | 3 | a0001c0001t0001g0224a0001c0001t0001g0226a0001c0002t0001g0219 | 3 | HG01167.hp2 HG01169.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.48+14096C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70292370 | ||||||
| chr12:70292379
|
T | C | 1 | a0001c0004t0001g0201 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.48+14105T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70292379 | ||||||
| chr12:70292399
|
G | A | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.48+14125G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70292399 | ||||||
| chr12:70292449
|
G | A | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.48+14175G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70292449 | ||||||
| chr12:70292455
|
T | G | 1 | a0001c0004t0001g0258 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.48+14181T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70292455 | ||||||
| chr12:70292557
|
G | A | 1 | a0000c0003t0001g0056 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.48+14283G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70292557 | ||||||
| chr12:70292764
|
A | G | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+14490A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70292764 | ||||||
| chr12:70292780
|
T | C | 2 | a0001c0002t0001g0265a0001c0004t0001g0271 | 2 | NA18986.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.48+14506T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70292780 | ||||||
| chr12:70293051
|
A | T | 15 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0001g0200others(12): Show | 15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.48+14777A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293051 | ||||||
| chr12:70293094
|
T | C | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.48+14820T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293094 | ||||||
| chr12:70293124
|
G | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.48+14850G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293124 | ||||||
| chr12:70293130
|
A | C | 9 | a0000c0003t0001g0011a0001c0001t0001g0006a0001c0001t0001g0007others(6): Show | 9 | HG00639.hp1 HG01891.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.48+14856A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293130 | ||||||
| chr12:70293161
|
C | CT | 54 | a0000c0003t0001g0002a0000c0003t0001g0040a0000c0003t0001g0042others(51): Show | 54 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.48+14903dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70293161 | |||||
| chr12:70293161
|
CT | C | 27 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(24): Show | 27 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.48+14903delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70293161 | |||||
| chr12:70293236
|
A | C | 223 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(220): Show | 225 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.48+14962A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293236 | ||||||
| chr12:70293361
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.48+15087G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293361 | ||||||
| chr12:70293373
|
G | C | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.48+15099G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293373 | ||||||
| chr12:70293552
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.48+15278C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293552 | ||||||
| chr12:70293579
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.48+15305A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293579 | ||||||
| chr12:70293634
|
A | G | 2 | a0001c0001t0001g0003a0001c0002t0001g0003 | 2 | NA18970.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.48+15360A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293634 | ||||||
| chr12:70293794
|
G | A | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.48+15520G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293794 | ||||||
| chr12:70293811
|
G | A | 2 | a0000c0003t0001g0055a0001c0001t0001g0054 | 2 | NA18942.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.48+15537G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293811 | ||||||
| chr12:70293850
|
A | G | 60 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(57): Show | 60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.48+15576A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70293850 | ||||||
| chr12:70293914
|
C | CT | 7 | a0000c0003t0001g0130a0000c0003t0001g0194a0001c0001t0001g0006others(4): Show | 7 | HG00738.hp1 HG01109.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.48+15666dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70293914 | |||||
| chr12:70293914
|
C | CTTT | 8 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0002t0001g0203others(5): Show | 8 | HG01070.hp1 HG01256.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.48+15664_48+15666d others(5): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70293914 | |||||
| chr12:70293914
|
CT | C | 120 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(117): Show | 122 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.48+15666delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70293914 | |||||
| chr12:70293914
|
CTT | C | 52 | a0000c0003t0001g0034a0000c0003t0001g0059a0000c0003t0002g0229others(49): Show | 52 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.48+15665_48+15666d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70293914 | |||||
| chr12:70294150
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0118 | 2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.48+15876G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70294150 | ||||||
| chr12:70294608
|
A | G | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-16287A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70294608 | ||||||
| chr12:70294667
|
A | G | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-16228A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70294667 | ||||||
| chr12:70294834
|
T | A | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-16061T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70294834 | ||||||
| chr12:70294932
|
A | G | 25 | a0001c0002t0001g0265a0001c0002t0003g0241a0001c0004t0001g0244others(22): Show | 25 | HG00323.hp1 HG00609.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.49-15963A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70294932 | ||||||
| chr12:70294941
|
C | T | 1 | a0001c0002t0009g0157 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.49-15954C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70294941 | ||||||
| chr12:70295033
|
C | T | 222 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(219): Show | 224 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.49-15862C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70295033 | ||||||
| chr12:70295075
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.49-15820A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70295075 | ||||||
| chr12:70295219
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.49-15676C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70295219 | ||||||
| chr12:70295333
|
AG | A | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-15561delG | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70295333 | ||||||
| chr12:70295340
|
C | T | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-15555C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70295340 | ||||||
| chr12:70295357
|
T | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-15538T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70295357 | ||||||
| chr12:70295378
|
A | G | 1 | a0000c0003t0001g0031 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.49-15517A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70295378 | ||||||
| chr12:70295689
|
C | G | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-15206C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70295689 | ||||||
| chr12:70295736
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.49-15159G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70295736 | ||||||
| chr12:70296305
|
G | A | 43 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(40): Show | 43 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-14590G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70296305 | ||||||
| chr12:70296308
|
T | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-14587T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70296308 | ||||||
| chr12:70296313
|
A | G | 3 | a0001c0002t0001g0081a0001c0002t0001g0087a0001c0002t0001g0088 | 3 | HG02040.hp1 NA18945.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.49-14582A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70296313 | ||||||
| chr12:70296408
|
G | A | 70 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(67): Show | 70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.49-14487G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70296408 | ||||||
| chr12:70296616
|
A | G | 10 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-14279A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70296616 | ||||||
| chr12:70296654
|
G | GT | 8 | a0000c0003t0001g0058a0000c0003t0001g0215a0001c0001t0001g0009others(5): Show | 8 | HG02486.hp2 HG03098.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-14228dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70296654 | |||||
| chr12:70296654
|
GT | G | 15 | a0000c0003t0001g0048a0001c0001t0001g0016a0001c0001t0001g0021others(12): Show | 15 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.49-14228delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70296654 | |||||
| chr12:70296654
|
GTT | G | 55 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(52): Show | 55 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.49-14229_49-14228d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70296654 | |||||
| chr12:70296757
|
G | GCC | 15 | a0001c0002t0001g0265a0001c0002t0003g0241a0001c0004t0001g0254others(12): Show | 15 | HG00609.hp1 HG01099.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.49-14129_49-14128d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70296757 | |||||
| chr12:70296757
|
GC | G | 71 | a0000c0003t0001g0078a0001c0001t0001g0003a0001c0001t0001g0016others(68): Show | 73 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.49-14128delC | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70296757 | |||||
| chr12:70296822
|
C | T | 158 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(155): Show | 160 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.49-14073C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70296822 | ||||||
| chr12:70296831
|
A | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-14064A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70296831 | ||||||
| chr12:70296879
|
A | G | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.49-14016A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70296879 | ||||||
| chr12:70297134
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.49-13761G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70297134 | ||||||
| chr12:70297167
|
G | A | 43 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(40): Show | 43 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-13728G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70297167 | ||||||
| chr12:70297172
|
T | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG01261.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.49-13723T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70297172 | ||||||
| chr12:70297201
|
G | A | 1 | a0001c0004t0001g0251 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.49-13694G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70297201 | ||||||
| chr12:70297525
|
C | T | 70 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(67): Show | 70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.49-13370C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70297525 | ||||||
| chr12:70297543
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.49-13352A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70297543 | ||||||
| chr12:70297546
|
A | G | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-13349A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70297546 | ||||||
| chr12:70297685
|
T | C | 4 | a0000c0003t0001g0046a0000c0003t0001g0047a0001c0001t0001g0044others(1): Show | 4 | HG00408.hp2 HG02040.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-13210T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70297685 | ||||||
| chr12:70297893
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.49-13002C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70297893 | ||||||
| chr12:70298071
|
C | A | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-12824C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298071 | ||||||
| chr12:70298123
|
G | A | 1 | a0001c0004t0001g0254 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.49-12772G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298123 | ||||||
| chr12:70298257
|
T | C | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-12638T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298257 | ||||||
| chr12:70298264
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.49-12631C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298264 | ||||||
| chr12:70298288
|
A | G | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-12607A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298288 | ||||||
| chr12:70298326
|
C | T | 1 | a0001c0006t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.49-12569C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298326 | ||||||
| chr12:70298361
|
T | C | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-12534T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298361 | ||||||
| chr12:70298409
|
C | T | 215 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(212): Show | 217 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.49-12486C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298409 | ||||||
| chr12:70298465
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.49-12430A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298465 | ||||||
| chr12:70298552
|
A | G | 1 | a0001c0004t0001g0201 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.49-12343A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298552 | ||||||
| chr12:70298626
|
G | A | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-12269G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70298626 | ||||||
| chr12:70298695
|
A | AT | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-12196dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70298695 | |||||
| chr12:70299009
|
T | C | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.49-11886T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299009 | ||||||
| chr12:70299040
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.49-11855C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299040 | ||||||
| chr12:70299135
|
C | T | 17 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0024others(14): Show | 17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.49-11760C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299135 | ||||||
| chr12:70299136
|
G | A | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-11759G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299136 | ||||||
| chr12:70299140
|
C | T | 148 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(145): Show | 150 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.49-11755C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299140 | ||||||
| chr12:70299146
|
G | C | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-11749G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299146 | ||||||
| chr12:70299148
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.49-11747G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299148 | ||||||
| chr12:70299213
|
A | ATT | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-11673_49-11672d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70299213 | |||||
| chr12:70299336
|
T | G | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-11559T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299336 | ||||||
| chr12:70299362
|
GTCCCTCC others(7): Show |
G | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.49-11532_49-11519d others(16): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299362 | ||||||
| chr12:70299374
|
T | C | 1 | a0001c0002t0001g0098 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.49-11521T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299374 | ||||||
| chr12:70299374
|
T | TC | 8 | a0000c0003t0001g0035a0000c0003t0001g0042a0000c0003t0001g0123others(5): Show | 8 | HG00741.hp2 HG01099.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.49-11515dupC | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70299374 | |||||
| chr12:70299380
|
C | A | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.49-11515C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299380 | ||||||
| chr12:70299381
|
AC | A | 10 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0002t0001g0203others(7): Show | 10 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-11508delC | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70299381 | |||||
| chr12:70299386
|
C | A | 1 | a0000c0003t0001g0043 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.49-11509C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299386 | ||||||
| chr12:70299491
|
G | T | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49-11404G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299491 | ||||||
| chr12:70299738
|
C | G | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-11157C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299738 | ||||||
| chr12:70299839
|
A | G | 2 | a0001c0001t0001g0106a0001c0002t0001g0107 | 2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.49-11056A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299839 | ||||||
| chr12:70299840
|
G | A | 2 | a0001c0001t0001g0106a0001c0002t0001g0107 | 2 | HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.49-11055G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299840 | ||||||
| chr12:70299923
|
T | G | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-10972T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70299923 | ||||||
| chr12:70300021
|
T | G | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-10874T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300021 | ||||||
| chr12:70300045
|
G | A | 10 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-10850G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300045 | ||||||
| chr12:70300065
|
T | G | 1 | a0000c0003t0001g0124 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.49-10830T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300065 | ||||||
| chr12:70300181
|
C | T | 6 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0071others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-10714C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300181 | ||||||
| chr12:70300190
|
G | A | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-10705G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300190 | ||||||
| chr12:70300247
|
G | T | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49-10648G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300247 | ||||||
| chr12:70300256
|
G | A | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.49-10639G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300256 | ||||||
| chr12:70300301
|
A | G | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-10594A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300301 | ||||||
| chr12:70300327
|
T | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.49-10568T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300327 | ||||||
| chr12:70300412
|
T | G | 5 | a0001c0002t0001g0061a0001c0002t0001g0082a0001c0002t0001g0084others(2): Show | 5 | HG00438.hp2 HG02015.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.49-10483T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300412 | ||||||
| chr12:70300501
|
G | A | 14 | a0001c0002t0001g0265a0001c0002t0003g0241a0001c0004t0001g0263others(11): Show | 14 | HG01099.hp1 HG01192.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.49-10394G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300501 | ||||||
| chr12:70300555
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.49-10340C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300555 | ||||||
| chr12:70300617
|
C | T | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-10278C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300617 | ||||||
| chr12:70300623
|
C | G | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-10272C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300623 | ||||||
| chr12:70300652
|
G | A | 1 | a0001c0002t0001g0108 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.49-10243G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300652 | ||||||
| chr12:70300685
|
A | T | 1 | a0001c0001t0001g0112 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.49-10210A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300685 | ||||||
| chr12:70300724
|
AACTTTAA others(3): Show |
A | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.49-10169_49-10160d others(12): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70300724 | |||||
| chr12:70300779
|
G | T | 1 | a0000c0003t0001g0179 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.49-10116G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300779 | ||||||
| chr12:70300827
|
C | T | 2 | a0001c0002t0001g0076a0001c0002t0001g0086 | 2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.49-10068C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300827 | ||||||
| chr12:70300834
|
G | A | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.49-10061G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300834 | ||||||
| chr12:70300846
|
G | C | 1 | a0001c0001t0001g0166 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.49-10049G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300846 | ||||||
| chr12:70300847
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.49-10048T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300847 | ||||||
| chr12:70300856
|
G | T | 1 | a0001c0001t0001g0166 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.49-10039G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300856 | ||||||
| chr12:70300880
|
T | A | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.49-10015T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300880 | ||||||
| chr12:70300919
|
T | C | 1 | a0001c0004t0001g0272 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.49-9976T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70300919 | ||||||
| chr12:70301067
|
T | A | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-9828T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301067 | ||||||
| chr12:70301096
|
A | C | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | NA18994.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.49-9799A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301096 | ||||||
| chr12:70301097
|
T | C | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | NA18994.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.49-9798T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301097 | ||||||
| chr12:70301182
|
T | C | 10 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0002t0001g0203others(7): Show | 10 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-9713T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301182 | ||||||
| chr12:70301269
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.49-9626T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301269 | ||||||
| chr12:70301378
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.49-9517A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301378 | ||||||
| chr12:70301407
|
T | G | 1 | a0001c0004t0001g0263 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.49-9488T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301407 | ||||||
| chr12:70301464
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.49-9431A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301464 | ||||||
| chr12:70301484
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG01261.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.49-9411C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301484 | ||||||
| chr12:70301485
|
GT | G | 213 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(210): Show | 215 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.49-9402delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70301485 | |||||
| chr12:70301486
|
T | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG01261.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.49-9409T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301486 | ||||||
| chr12:70301522
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49-9373G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301522 | ||||||
| chr12:70301534
|
T | G | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-9361T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301534 | ||||||
| chr12:70301535
|
C | T | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-9360C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301535 | ||||||
| chr12:70301536
|
T | G | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-9359T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301536 | ||||||
| chr12:70301559
|
C | G | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-9336C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301559 | ||||||
| chr12:70301636
|
G | A | 1 | a0001c0004t0001g0258 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.49-9259G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301636 | ||||||
| chr12:70301696
|
C | G | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-9199C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301696 | ||||||
| chr12:70301770
|
T | G | 11 | a0001c0001t0001g0016a0001c0001t0001g0165a0001c0001t0001g0218others(8): Show | 11 | HG00733.hp1 HG00738.hp2 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.49-9125T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301770 | ||||||
| chr12:70301773
|
T | C | 1 | a0001c0002t0002g0240 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.49-9122T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301773 | ||||||
| chr12:70301784
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.49-9111C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301784 | ||||||
| chr12:70301797
|
A | G | 119 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(116): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.49-9098A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301797 | ||||||
| chr12:70301807
|
C | T | 1 | a0000c0003t0001g0158 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.49-9088C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301807 | ||||||
| chr12:70301878
|
T | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-9017T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301878 | ||||||
| chr12:70301884
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.49-9011C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301884 | ||||||
| chr12:70301961
|
T | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.49-8934T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70301961 | ||||||
| chr12:70302199
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.49-8696T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302199 | ||||||
| chr12:70302209
|
A | G | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-8686A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302209 | ||||||
| chr12:70302232
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.49-8663T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302232 | ||||||
| chr12:70302283
|
C | T | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.49-8612C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302283 | ||||||
| chr12:70302430
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0118 | 2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.49-8465G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302430 | ||||||
| chr12:70302485
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.49-8410T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302485 | ||||||
| chr12:70302521
|
A | T | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-8374A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302521 | ||||||
| chr12:70302543
|
T | C | 2 | a0001c0002t0001g0076a0001c0002t0001g0086 | 2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.49-8352T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302543 | ||||||
| chr12:70302570
|
G | C | 3 | a0001c0002t0001g0061a0001c0002t0001g0084a0001c0002t0001g0093 | 3 | HG00438.hp2 HG02523.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.49-8325G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302570 | ||||||
| chr12:70302709
|
A | C | 1 | a0001c0001t0001g0022 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.49-8186A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302709 | ||||||
| chr12:70302734
|
A | C | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-8161A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302734 | ||||||
| chr12:70302871
|
A | C | 1 | a0001c0001t0001g0186 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.49-8024A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302871 | ||||||
| chr12:70302959
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.49-7936A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302959 | ||||||
| chr12:70302992
|
A | T | 1 | a0001c0001t0001g0166 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.49-7903A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70302992 | ||||||
| chr12:70303010
|
T | C | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.49-7885T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303010 | ||||||
| chr12:70303029
|
G | A | 6 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0071others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-7866G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303029 | ||||||
| chr12:70303175
|
G | T | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.49-7720G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303175 | ||||||
| chr12:70303215
|
C | T | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-7680C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303215 | ||||||
| chr12:70303271
|
G | A | 1 | a0000c0003t0001g0191 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.49-7624G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303271 | ||||||
| chr12:70303274
|
G | T | 1 | a0001c0001t0001g0014 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.49-7621G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303274 | ||||||
| chr12:70303283
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.49-7612C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303283 | ||||||
| chr12:70303392
|
G | C | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.49-7503G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303392 | ||||||
| chr12:70303395
|
A | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-7500A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303395 | ||||||
| chr12:70303425
|
G | C | 1 | a0001c0001t0001g0218 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.49-7470G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303425 | ||||||
| chr12:70303482
|
G | T | 1 | a0001c0001t0001g0178 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.49-7413G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303482 | ||||||
| chr12:70303538
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.49-7357A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303538 | ||||||
| chr12:70303574
|
G | T | 75 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(72): Show | 77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.49-7321G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303574 | ||||||
| chr12:70303576
|
C | T | 76 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(73): Show | 78 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.49-7319C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303576 | ||||||
| chr12:70303638
|
A | C | 1 | a0001c0001t0001g0052 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.49-7257A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303638 | ||||||
| chr12:70303661
|
A | C | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.49-7234A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303661 | ||||||
| chr12:70303699
|
C | A | 18 | a0000c0003t0001g0036a0000c0003t0002g0229a0000c0003t0002g0230others(15): Show | 18 | HG00621.hp2 HG01123.hp2 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.49-7196C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303699 | ||||||
| chr12:70303739
|
A | G | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.49-7156A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303739 | ||||||
| chr12:70303754
|
A | C | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.49-7141A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303754 | ||||||
| chr12:70303803
|
C | G | 5 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(2): Show | 5 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.49-7092C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303803 | ||||||
| chr12:70303837
|
G | A | 37 | a0001c0001t0001g0021a0001c0001t0001g0183a0001c0001t0001g0184others(34): Show | 37 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.49-7058G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303837 | ||||||
| chr12:70303938
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.49-6957C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303938 | ||||||
| chr12:70303958
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.49-6937G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303958 | ||||||
| chr12:70303967
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.49-6928C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70303967 | ||||||
| chr12:70304023
|
C | T | 15 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0001g0200others(12): Show | 15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.49-6872C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304023 | ||||||
| chr12:70304025
|
C | T | 1 | a0001c0002t0002g0240 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.49-6870C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304025 | ||||||
| chr12:70304032
|
G | A | 17 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0024others(14): Show | 17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.49-6863G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304032 | ||||||
| chr12:70304047
|
G | T | 1 | a0001c0001t0001g0169 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.49-6848G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304047 | ||||||
| chr12:70304096
|
C | G | 3 | a0001c0002t0004g0232a0001c0002t0004g0238a0001c0002t0004g0239 | 3 | NA18941.hp2 NA18945.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.49-6799C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304096 | ||||||
| chr12:70304102
|
G | A | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.49-6793G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304102 | ||||||
| chr12:70304134
|
T | C | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.49-6761T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304134 | ||||||
| chr12:70304136
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.49-6759C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304136 | ||||||
| chr12:70304202
|
C | G | 1 | a0001c0001t0001g0166 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.49-6693C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304202 | ||||||
| chr12:70304218
|
G | C | 60 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(57): Show | 60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.49-6677G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304218 | ||||||
| chr12:70304219
|
G | GTCCAGCT others(66): Show |
6 | a0000c0003t0001g0074a0000c0003t0001g0121a0000c0003t0001g0122others(3): Show | 6 | HG01099.hp2 HG01123.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-6670_49-6598dup others(73): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70304219 | |||||
| chr12:70304398
|
G | T | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0002t0001g0107 | 3 | HG01081.hp2 HG02615.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.49-6497G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304398 | ||||||
| chr12:70304440
|
G | A | 6 | a0001c0001t0001g0120a0001c0001t0001g0125a0001c0001t0001g0126others(3): Show | 6 | HG02056.hp1 NA18961.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-6455G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304440 | ||||||
| chr12:70304627
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0118 | 2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.49-6268C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304627 | ||||||
| chr12:70304680
|
A | G | 38 | a0000c0003t0001g0078a0001c0001t0001g0003a0001c0001t0001g0019others(35): Show | 40 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.49-6215A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304680 | ||||||
| chr12:70304681
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.49-6214A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304681 | ||||||
| chr12:70304777
|
G | A | 17 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0024others(14): Show | 17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.49-6118G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304777 | ||||||
| chr12:70304829
|
G | A | 15 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0001g0200others(12): Show | 15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.49-6066G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304829 | ||||||
| chr12:70304879
|
A | G | 199 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(196): Show | 201 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.49-6016A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304879 | ||||||
| chr12:70304950
|
C | T | 1 | a0001c0002t0001g0108 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.49-5945C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304950 | ||||||
| chr12:70304956
|
C | T | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-5939C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304956 | ||||||
| chr12:70304980
|
G | A | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.49-5915G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70304980 | ||||||
| chr12:70305011
|
C | T | 1 | a0001c0005t0001g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.49-5884C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305011 | ||||||
| chr12:70305067
|
G | A | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-5828G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305067 | ||||||
| chr12:70305146
|
C | T | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-5749C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305146 | ||||||
| chr12:70305192
|
C | T | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG03225.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.49-5703C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305192 | ||||||
| chr12:70305222
|
C | G | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.49-5673C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305222 | ||||||
| chr12:70305298
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG01167.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.49-5597C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305298 | ||||||
| chr12:70305388
|
C | G | 1 | a0001c0004t0001g0256 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.49-5507C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305388 | ||||||
| chr12:70305402
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.49-5493C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305402 | ||||||
| chr12:70305403
|
G | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-5492G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305403 | ||||||
| chr12:70305408
|
G | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.49-5487G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305408 | ||||||
| chr12:70305482
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.49-5413G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305482 | ||||||
| chr12:70305490
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.49-5405G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305490 | ||||||
| chr12:70305685
|
G | A | 2 | a0000c0003t0001g0191a0000c0003t0001g0194 | 2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.49-5210G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305685 | ||||||
| chr12:70305771
|
G | A | 17 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0024others(14): Show | 17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.49-5124G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305771 | ||||||
| chr12:70305873
|
G | GT | 158 | a0000c0003t0001g0011a0000c0003t0001g0032a0000c0003t0001g0042others(155): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.49-5001dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70305873 | |||||
| chr12:70305873
|
G | GTT | 42 | a0000c0003t0001g0015a0000c0003t0001g0020a0000c0003t0001g0028others(39): Show | 42 | HG00438.hp1 HG00609.hp2 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.49-5002_49-5001dup others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70305873 | |||||
| chr12:70305873
|
G | GTTT | 18 | a0000c0003t0001g0002a0000c0003t0001g0034a0000c0003t0001g0040others(15): Show | 18 | HG00408.hp2 HG00621.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.49-5003_49-5001dup others(3): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70305873 | |||||
| chr12:70305873
|
G | GTTTT | 10 | a0001c0001t0001g0016a0001c0001t0001g0198a0001c0001t0001g0218others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-5004_49-5001dup others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70305873 | |||||
| chr12:70305873
|
GT | G | 29 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0004t0001g0244others(26): Show | 29 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.49-5001delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70305873 | |||||
| chr12:70305878
|
T | G | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49-5017T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305878 | ||||||
| chr12:70305954
|
T | G | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-4941T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70305954 | ||||||
| chr12:70306055
|
G | A | 10 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0002t0001g0203others(7): Show | 10 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-4840G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306055 | ||||||
| chr12:70306126
|
T | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-4769T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306126 | ||||||
| chr12:70306160
|
T | A | 18 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0021others(15): Show | 18 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.49-4735T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306160 | ||||||
| chr12:70306203
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.49-4692A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306203 | ||||||
| chr12:70306258
|
C | A | 1 | a0000c0003t0002g0229 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.49-4637C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306258 | ||||||
| chr12:70306467
|
T | G | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49-4428T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306467 | ||||||
| chr12:70306508
|
G | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.49-4387G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306508 | ||||||
| chr12:70306515
|
T | TGTCTTGA others(6): Show |
1 | a0001c0001t0001g0111 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.49-4377_49-4365dup others(13): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70306515 | |||||
| chr12:70306566
|
T | A | 1 | a0001c0001t0001g0053 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.49-4329T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306566 | ||||||
| chr12:70306584
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.49-4311A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306584 | ||||||
| chr12:70306598
|
TA | T | 60 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(57): Show | 60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.49-4288delA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70306598 | |||||
| chr12:70306634
|
G | A | 6 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0071others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-4261G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306634 | ||||||
| chr12:70306756
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.49-4139G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306756 | ||||||
| chr12:70306891
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.49-4004T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306891 | ||||||
| chr12:70306950
|
C | T | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG01261.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-3945C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306950 | ||||||
| chr12:70306967
|
T | C | 43 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(40): Show | 43 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-3928T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70306967 | ||||||
| chr12:70307061
|
C | T | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-3834C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307061 | ||||||
| chr12:70307062
|
G | A | 1 | a0000c0003t0001g0055 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.49-3833G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307062 | ||||||
| chr12:70307126
|
A | T | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.49-3769A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307126 | ||||||
| chr12:70307224
|
C | G | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.49-3671C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307224 | ||||||
| chr12:70307234
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.49-3661C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307234 | ||||||
| chr12:70307307
|
G | A | 38 | a0000c0003t0001g0078a0001c0001t0001g0003a0001c0001t0001g0019others(35): Show | 40 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.49-3588G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307307 | ||||||
| chr12:70307452
|
G | A | 199 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(196): Show | 201 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.49-3443G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307452 | ||||||
| chr12:70307557
|
C | T | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | NA18994.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.49-3338C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307557 | ||||||
| chr12:70307578
|
A | ACCAAATT others(347): Show |
1 | a0001c0001t0001g0218 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.49-3302_49-3301ins others(354): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70307578 | |||||
| chr12:70307681
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.49-3214C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307681 | ||||||
| chr12:70307873
|
A | G | 15 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0001g0200others(12): Show | 15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.49-3022A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307873 | ||||||
| chr12:70307899
|
T | TA | 11 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0111others(8): Show | 11 | HG01069.hp2 HG01109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.49-2982dupA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70307899 | |||||
| chr12:70307899
|
TA | T | 75 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0138others(72): Show | 77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.49-2982delA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70307899 | |||||
| chr12:70307932
|
T | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.49-2963T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307932 | ||||||
| chr12:70307990
|
C | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0118 | 2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.49-2905C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70307990 | ||||||
| chr12:70308002
|
C | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-2893C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308002 | ||||||
| chr12:70308032
|
A | G | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.49-2863A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308032 | ||||||
| chr12:70308047
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.49-2848A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308047 | ||||||
| chr12:70308365
|
T | C | 199 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(196): Show | 201 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
intron_variant | MODIFIER | c.49-2530T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308365 | ||||||
| chr12:70308555
|
T | TTC | 6 | a0000c0003t0001g0215a0001c0001t0001g0146a0001c0001t0001g0147others(3): Show | 6 | HG01192.hp2 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-2311_49-2310dup others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308555 | |||||
| chr12:70308555
|
T | TTCTTTC | 28 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(25): Show | 28 | HG00609.hp1 HG01069.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.49-2337_49-2336ins others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308555 | |||||
| chr12:70308555
|
T | TTCTTTCT others(3): Show |
1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49-2337_49-2336ins others(10): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308555 | |||||
| chr12:70308555
|
TTC | T | 30 | a0001c0001t0001g0016a0001c0001t0001g0169a0001c0001t0001g0204others(27): Show | 30 | HG00733.hp1 HG00733.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.49-2311_49-2310del others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308555 | |||||
| chr12:70308558
|
T | G | 1 | a0001c0001t0005g0155 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.49-2337T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308558 | ||||||
| chr12:70308559
|
C | T | 4 | a0001c0004t0001g0244a0001c0004t0001g0245a0001c0004t0001g0256others(1): Show | 4 | HG00323.hp1 HG01891.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-2336C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308559 | ||||||
| chr12:70308582
|
T | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0180 | 3 | HG02647.hp1 HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.49-2313T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308582 | ||||||
| chr12:70308582
|
TCTCA | T | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG03225.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.49-2311_49-2308del others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308582 | |||||
| chr12:70308584
|
T | A | 39 | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0023others(36): Show | 39 | HG00609.hp1 HG00733.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.49-2311T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308584 | ||||||
| chr12:70308584
|
T | TCA | 7 | a0000c0003t0001g0123a0001c0001t0001g0110a0001c0001t0001g0111others(4): Show | 7 | HG01099.hp2 HG02145.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.49-2288_49-2287dup others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308584 | |||||
| chr12:70308584
|
T | TCACA | 78 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(75): Show | 80 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.49-2290_49-2287dup others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308584 | |||||
| chr12:70308584
|
T | TCACACA | 30 | a0000c0003t0001g0011a0000c0003t0001g0028a0000c0003t0001g0036others(27): Show | 30 | HG00408.hp1 HG00558.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.49-2292_49-2287dup others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308584 | |||||
| chr12:70308584
|
T | TCTCA | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG01261.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-2310_49-2309ins others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308584 | |||||
| chr12:70308584
|
T | TCTCTCTC others(3): Show |
10 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(7): Show | 10 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-2310_49-2309ins others(10): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308584 | |||||
| chr12:70308584
|
T | TCTCTCTC others(7): Show |
3 | a0001c0002t0001g0200a0001c0002t0004g0232a0001c0002t0004g0238 | 3 | HG02055.hp1 NA18941.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.49-2310_49-2309ins others(14): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308584 | |||||
| chr12:70308584
|
T | TCTCTCTC others(9): Show |
1 | a0001c0002t0004g0239 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.49-2310_49-2309ins others(16): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308584 | |||||
| chr12:70308584
|
T | TCTCTCTC others(21): Show |
1 | a0001c0001t0001g0024 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.49-2310_49-2309ins others(28): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308584 | |||||
| chr12:70308584
|
T | TCTCTCTC others(19): Show |
1 | a0001c0001t0001g0188 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.49-2310_49-2309ins others(26): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70308584 | |||||
| chr12:70308586
|
A | T | 5 | a0000c0003t0001g0215a0001c0001t0001g0021a0001c0001t0001g0213others(2): Show | 5 | HG03486.hp1 HG03579.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.49-2309A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308586 | ||||||
| chr12:70308867
|
A | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.49-2028A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70308867 | ||||||
| chr12:70309020
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.49-1875C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70309020 | ||||||
| chr12:70309224
|
A | G | 6 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0071others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.49-1671A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70309224 | ||||||
| chr12:70309278
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.49-1617T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70309278 | ||||||
| chr12:70309300
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.49-1595G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70309300 | ||||||
| chr12:70309607
|
A | C | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.49-1288A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70309607 | ||||||
| chr12:70309623
|
C | T | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.49-1272C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70309623 | ||||||
| chr12:70309893
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.49-1002G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70309893 | ||||||
| chr12:70309917
|
A | G | 70 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(67): Show | 70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.49-978A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70309917 | ||||||
| chr12:70309958
|
A | G | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49-937A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70309958 | ||||||
| chr12:70310025
|
G | A | 43 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(40): Show | 43 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.49-870G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70310025 | ||||||
| chr12:70310061
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.49-834A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70310061 | ||||||
| chr12:70310185
|
T | C | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.49-710T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70310185 | ||||||
| chr12:70310228
|
A | C | 15 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0001g0200others(12): Show | 15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.49-667A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70310228 | ||||||
| chr12:70310468
|
G | A | 17 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0024others(14): Show | 17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.49-427G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70310468 | ||||||
| chr12:70310589
|
CTATG | C | 4 | a0001c0006t0001g0018a0001c0006t0001g0119a0001c0006t0001g0150others(1): Show | 4 | HG02559.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.49-301_49-298delTA others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr12 | 70310589 | |||||
| chr12:70310722
|
C | T | 3 | a0000c0003t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066 | 3 | NA18954.hp1 NA19057.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.49-173C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70310722 | ||||||
| chr12:70310761
|
G | T | 1 | a0001c0002t0002g0240 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.49-134G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 2/15 | chr12 | 70310761 | ||||||
| chr12:70311382
|
A | G | 1 | a0001c0002t0001g0093 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.171+365A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70311382 | ||||||
| chr12:70311383
|
C | T | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG03225.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.171+366C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70311383 | ||||||
| chr12:70311567
|
T | A | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+550T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70311567 | ||||||
| chr12:70311751
|
T | C | 1 | a0000c0003t0001g0034 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.171+734T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70311751 | ||||||
| chr12:70311831
|
A | G | 1 | a0001c0004t0001g0251 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.171+814A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70311831 | ||||||
| chr12:70312061
|
A | C | 1 | a0001c0006t0001g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.171+1044A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70312061 | ||||||
| chr12:70312189
|
T | C | 1 | a0001c0002t0001g0087 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.171+1172T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70312189 | ||||||
| chr12:70312212
|
A | C | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.171+1195A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70312212 | ||||||
| chr12:70312249
|
T | A | 1 | a0001c0002t0001g0107 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.171+1232T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70312249 | ||||||
| chr12:70312585
|
C | T | 215 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(212): Show | 217 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.171+1568C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70312585 | ||||||
| chr12:70312755
|
A | G | 119 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(116): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.171+1738A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70312755 | ||||||
| chr12:70312884
|
G | A | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.171+1867G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70312884 | ||||||
| chr12:70312925
|
A | G | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.171+1908A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70312925 | ||||||
| chr12:70313076
|
A | T | 2 | a0000c0003t0001g0028a0001c0001t0001g0041 | 2 | HG02698.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.171+2059A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70313076 | ||||||
| chr12:70313174
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.171+2157A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70313174 | ||||||
| chr12:70313236
|
C | T | 15 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0001g0200others(12): Show | 15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.171+2219C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70313236 | ||||||
| chr12:70313374
|
AATTAAAT others(3): Show |
A | 1 | a0001c0004t0001g0251 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.171+2360_171+2369d others(12): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 70313374 | |||||
| chr12:70313489
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.171+2472A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70313489 | ||||||
| chr12:70313566
|
G | C | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.171+2549G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70313566 | ||||||
| chr12:70313582
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.171+2565C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70313582 | ||||||
| chr12:70313803
|
G | A | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.171+2786G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70313803 | ||||||
| chr12:70313819
|
C | T | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+2802C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70313819 | ||||||
| chr12:70313925
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.171+2908C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70313925 | ||||||
| chr12:70314023
|
T | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.171+3006T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314023 | ||||||
| chr12:70314072
|
T | C | 2 | a0001c0002t0001g0070a0001c0002t0001g0071 | 2 | HG02257.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.171+3055T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314072 | ||||||
| chr12:70314076
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.171+3059G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314076 | ||||||
| chr12:70314081
|
G | C | 2 | a0001c0002t0001g0203a0001c0002t0001g0205 | 2 | HG00733.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.171+3064G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314081 | ||||||
| chr12:70314251
|
T | C | 1 | a0000c0003t0001g0050 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.171+3234T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314251 | ||||||
| chr12:70314349
|
C | G | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG01261.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.171+3332C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314349 | ||||||
| chr12:70314439
|
C | T | 1 | a0001c0002t0001g0084 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.171+3422C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314439 | ||||||
| chr12:70314443
|
A | G | 4 | a0000c0003t0001g0074a0000c0003t0001g0123a0000c0003t0001g0124others(1): Show | 4 | HG01099.hp2 HG01952.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+3426A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314443 | ||||||
| chr12:70314794
|
A | G | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.171+3777A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314794 | ||||||
| chr12:70314829
|
C | G | 1 | a0001c0001t0007g0152 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.171+3812C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314829 | ||||||
| chr12:70314837
|
C | CTTGT | 20 | a0000c0003t0001g0015a0000c0003t0001g0033a0000c0003t0001g0064others(17): Show | 20 | HG01099.hp2 HG01123.hp1 HG01952.hp1 others(17): Show |
intron_variant | MODIFIER | c.171+3847_171+3850d others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 70314837 | |||||
| chr12:70314837
|
CTTGT | C | 58 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(55): Show | 58 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(55): Show |
intron_variant | MODIFIER | c.171+3847_171+3850d others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 70314837 | |||||
| chr12:70314902
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.171+3885T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314902 | ||||||
| chr12:70314925
|
A | G | 43 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(40): Show | 43 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.171+3908A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314925 | ||||||
| chr12:70314949
|
C | T | 1 | a0000c0003t0001g0043 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.171+3932C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70314949 | ||||||
| chr12:70315127
|
G | A | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.171+4110G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70315127 | ||||||
| chr12:70315153
|
C | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.171+4136C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70315153 | ||||||
| chr12:70315910
|
GTAT | G | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.172-3383_172-3381d others(5): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 70315910 | |||||
| chr12:70315912
|
A | G | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.172-3386A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70315912 | ||||||
| chr12:70316246
|
T | C | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.172-3052T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316246 | ||||||
| chr12:70316264
|
A | G | 1 | a0000c0003t0001g0215 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.172-3034A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316264 | ||||||
| chr12:70316568
|
C | G | 25 | a0001c0002t0001g0265a0001c0002t0003g0241a0001c0004t0001g0244others(22): Show | 25 | HG00323.hp1 HG00609.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.172-2730C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316568 | ||||||
| chr12:70316665
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.172-2633C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316665 | ||||||
| chr12:70316687
|
G | T | 1 | a0001c0001t0001g0143 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.172-2611G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316687 | ||||||
| chr12:70316756
|
G | A | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-2542G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316756 | ||||||
| chr12:70316794
|
T | A | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.172-2504T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316794 | ||||||
| chr12:70316845
|
C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0184 | 2 | HG01167.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.172-2453C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316845 | ||||||
| chr12:70316901
|
G | A | 78 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(75): Show | 80 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.172-2397G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316901 | ||||||
| chr12:70316905
|
G | A | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.172-2393G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316905 | ||||||
| chr12:70316926
|
A | G | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.172-2372A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316926 | ||||||
| chr12:70316975
|
A | G | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-2323A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70316975 | ||||||
| chr12:70317021
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.172-2277G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70317021 | ||||||
| chr12:70317465
|
A | C | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.172-1833A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70317465 | ||||||
| chr12:70317513
|
G | A | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.172-1785G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70317513 | ||||||
| chr12:70317575
|
A | T | 70 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(67): Show | 70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.172-1723A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70317575 | ||||||
| chr12:70317611
|
A | AT | 21 | a0000c0003t0001g0035a0000c0003t0001g0036a0000c0003t0001g0121others(18): Show | 21 | HG00408.hp1 HG01123.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.172-1662dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 70317611 | |||||
| chr12:70317611
|
A | ATT | 5 | a0001c0001t0008g0196a0001c0002t0001g0073a0001c0004t0001g0068others(2): Show | 5 | HG02145.hp1 HG02486.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.172-1663_172-1662d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 70317611 | |||||
| chr12:70317611
|
AT | A | 56 | a0000c0003t0001g0011a0000c0003t0001g0028a0000c0003t0001g0038others(53): Show | 57 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.172-1662delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 70317611 | |||||
| chr12:70317611
|
ATT | A | 13 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(10): Show | 13 | HG00099.hp1 HG00639.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.172-1663_172-1662d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 70317611 | |||||
| chr12:70317611
|
ATTTTT | A | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.172-1666_172-1662d others(7): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr12 | 70317611 | |||||
| chr12:70317816
|
A | G | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.172-1482A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70317816 | ||||||
| chr12:70317867
|
G | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-1431G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70317867 | ||||||
| chr12:70317868
|
G | A | 2 | a0001c0002t0001g0082a0001c0004t0001g0079 | 2 | HG02015.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.172-1430G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70317868 | ||||||
| chr12:70317958
|
C | T | 1 | a0001c0001t0001g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.172-1340C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70317958 | ||||||
| chr12:70317959
|
C | T | 1 | a0001c0002t0001g0080 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.172-1339C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70317959 | ||||||
| chr12:70318084
|
G | C | 60 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(57): Show | 60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.172-1214G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70318084 | ||||||
| chr12:70318170
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.172-1128C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70318170 | ||||||
| chr12:70318219
|
A | G | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.172-1079A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70318219 | ||||||
| chr12:70318253
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.172-1045C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70318253 | ||||||
| chr12:70318516
|
C | T | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.172-782C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70318516 | ||||||
| chr12:70318641
|
A | G | 2 | a0001c0001t0005g0149a0001c0001t0005g0155 | 2 | HG00099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.172-657A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70318641 | ||||||
| chr12:70318860
|
T | A | 209 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(206): Show | 211 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.172-438T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70318860 | ||||||
| chr12:70318924
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.172-374A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70318924 | ||||||
| chr12:70319028
|
G | T | 60 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(57): Show | 60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.172-270G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70319028 | ||||||
| chr12:70319116
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.172-182C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70319116 | ||||||
| chr12:70319209
|
T | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0118 | 2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.172-89T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 3/15 | chr12 | 70319209 | ||||||
| chr12:70319438
|
C | G | 15 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0001g0200others(12): Show | 15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.238+74C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70319438 | ||||||
| chr12:70319519
|
A | G | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.238+155A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70319519 | ||||||
| chr12:70319720
|
C | CTG | 36 | a0000c0003t0001g0194a0001c0001t0001g0024a0001c0001t0006g0005others(33): Show | 36 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.238+374_238+375dup others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70319720 | |||||
| chr12:70319720
|
CTG | C | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.238+374_238+375del others(2): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70319720 | |||||
| chr12:70319743
|
T | C | 214 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(211): Show | 216 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.238+379T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70319743 | ||||||
| chr12:70319875
|
G | A | 158 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(155): Show | 160 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.238+511G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70319875 | ||||||
| chr12:70319964
|
G | A | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.238+600G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70319964 | ||||||
| chr12:70320036
|
T | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | HG01106.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.238+672T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70320036 | ||||||
| chr12:70320221
|
T | G | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.238+857T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70320221 | ||||||
| chr12:70320615
|
CT | C | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.238+1252delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70320615 | ||||||
| chr12:70320891
|
G | A | 60 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(57): Show | 60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.238+1527G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70320891 | ||||||
| chr12:70320925
|
A | G | 1 | a0000c0003t0001g0028 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.238+1561A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70320925 | ||||||
| chr12:70321193
|
T | C | 1 | a0001c0001t0001g0025 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.238+1829T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70321193 | ||||||
| chr12:70321230
|
A | T | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.238+1866A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70321230 | ||||||
| chr12:70321694
|
C | G | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+2330C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70321694 | ||||||
| chr12:70321710
|
C | A | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.238+2346C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70321710 | ||||||
| chr12:70321792
|
C | CAAGAAAG others(308): Show |
1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.238+2443_238+2444i others(317): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70321792 | |||||
| chr12:70321975
|
A | G | 15 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0001g0200others(12): Show | 15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.238+2611A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70321975 | ||||||
| chr12:70321986
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.238+2622C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70321986 | ||||||
| chr12:70321989
|
G | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0118 | 2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.238+2625G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70321989 | ||||||
| chr12:70322191
|
A | T | 12 | a0000c0003t0001g0179a0000c0003t0001g0185a0001c0001t0001g0174others(9): Show | 12 | HG00741.hp2 HG01167.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.238+2827A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322191 | ||||||
| chr12:70322222
|
A | C | 6 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0071others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+2858A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322222 | ||||||
| chr12:70322225
|
A | G | 2 | a0000c0003t0002g0229a0000c0003t0002g0230 | 2 | HG01884.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.238+2861A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322225 | ||||||
| chr12:70322522
|
A | G | 10 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+3158A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322522 | ||||||
| chr12:70322584
|
G | T | 1 | a0001c0002t0001g0108 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.238+3220G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322584 | ||||||
| chr12:70322678
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.238+3314C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322678 | ||||||
| chr12:70322699
|
G | A | 6 | a0000c0003t0001g0074a0000c0003t0001g0121a0000c0003t0001g0122others(3): Show | 6 | HG01099.hp2 HG01123.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.238+3335G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322699 | ||||||
| chr12:70322797
|
A | G | 2 | a0001c0001t0001g0017a0001c0001t0001g0118 | 2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.238+3433A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322797 | ||||||
| chr12:70322839
|
C | T | 1 | a0001c0006t0001g0119 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.238+3475C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322839 | ||||||
| chr12:70322976
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0006g0005 | 2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.238+3612C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70322976 | ||||||
| chr12:70323091
|
G | A | 3 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0231 | 3 | HG01884.hp2 HG02109.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.238+3727G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323091 | ||||||
| chr12:70323166
|
C | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.238+3802C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323166 | ||||||
| chr12:70323240
|
A | G | 1 | a0001c0004t0001g0268 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.238+3876A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323240 | ||||||
| chr12:70323280
|
G | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.238+3916G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323280 | ||||||
| chr12:70323287
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.238+3923C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323287 | ||||||
| chr12:70323451
|
T | C | 60 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(57): Show | 60 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.238+4087T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323451 | ||||||
| chr12:70323456
|
T | A | 1 | a0001c0001t0001g0102 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.238+4092T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323456 | ||||||
| chr12:70323809
|
C | A | 1 | a0001c0004t0001g0258 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.238+4445C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323809 | ||||||
| chr12:70323892
|
C | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.238+4528C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323892 | ||||||
| chr12:70323901
|
GAC | G | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG03225.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.238+4542_238+4543d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70323901 | |||||
| chr12:70323912
|
A | G | 1 | a0001c0004t0001g0254 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.238+4548A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70323912 | ||||||
| chr12:70324098
|
A | C | 10 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+4734A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324098 | ||||||
| chr12:70324265
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.238+4901A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324265 | ||||||
| chr12:70324305
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.238+4941A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324305 | ||||||
| chr12:70324344
|
G | GGA | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.238+4995_238+4996d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70324344 | |||||
| chr12:70324367
|
G | A | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+5003G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324367 | ||||||
| chr12:70324513
|
T | A | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG01261.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.239-4910T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324513 | ||||||
| chr12:70324657
|
C | T | 78 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(75): Show | 80 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.239-4766C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324657 | ||||||
| chr12:70324819
|
A | G | 25 | a0001c0002t0001g0265a0001c0002t0003g0241a0001c0004t0001g0244others(22): Show | 25 | HG00323.hp1 HG00609.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.239-4604A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324819 | ||||||
| chr12:70324825
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.239-4598C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324825 | ||||||
| chr12:70324914
|
T | C | 217 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(214): Show | 219 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.239-4509T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324914 | ||||||
| chr12:70324935
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.239-4488T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324935 | ||||||
| chr12:70324981
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.239-4442A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70324981 | ||||||
| chr12:70325014
|
C | T | 15 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0001g0200others(12): Show | 15 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.239-4409C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70325014 | ||||||
| chr12:70325175
|
GAGAAAGA | G | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.239-4237_239-4231d others(9): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70325175 | |||||
| chr12:70325215
|
G | A | 1 | a0001c0002t0001g0069 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.239-4208G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70325215 | ||||||
| chr12:70325565
|
T | C | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.239-3858T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70325565 | ||||||
| chr12:70325785
|
A | G | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.239-3638A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70325785 | ||||||
| chr12:70325876
|
T | G | 1 | a0001c0001t0001g0169 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.239-3547T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70325876 | ||||||
| chr12:70325974
|
G | A | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-3449G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70325974 | ||||||
| chr12:70326044
|
ATTC | A | 10 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0002t0001g0203others(7): Show | 10 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-3376_239-3374d others(5): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70326044 | |||||
| chr12:70326055
|
G | C | 1 | a0001c0002t0001g0071 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.239-3368G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70326055 | ||||||
| chr12:70326222
|
T | A | 10 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-3201T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70326222 | ||||||
| chr12:70326340
|
T | G | 2 | a0001c0002t0001g0001a0001c0002t0001g0090 | 4 | HG00280.hp2 HG01069.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-3083T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70326340 | ||||||
| chr12:70326404
|
GTT | G | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.239-3016_239-3015d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70326404 | |||||
| chr12:70326454
|
C | CT | 39 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0188others(36): Show | 39 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.239-2960dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70326454 | |||||
| chr12:70326454
|
C | CTT | 21 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(18): Show | 21 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.239-2961_239-2960d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70326454 | |||||
| chr12:70326752
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.239-2671A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70326752 | ||||||
| chr12:70327023
|
T | C | 204 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(201): Show | 206 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.239-2400T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327023 | ||||||
| chr12:70327182
|
T | A | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-2241T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327182 | ||||||
| chr12:70327245
|
A | G | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.239-2178A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327245 | ||||||
| chr12:70327270
|
GAA | G | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-2151_239-2150d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70327270 | |||||
| chr12:70327331
|
C | T | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.239-2092C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327331 | ||||||
| chr12:70327396
|
A | G | 75 | a0000c0003t0001g0064a0000c0003t0001g0189a0000c0003t0001g0190others(72): Show | 75 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.239-2027A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327396 | ||||||
| chr12:70327417
|
T | C | 6 | a0000c0003t0001g0050a0000c0003t0001g0055a0000c0003t0001g0056others(3): Show | 6 | HG02015.hp1 NA18942.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.239-2006T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327417 | ||||||
| chr12:70327824
|
T | TATC | 43 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(40): Show | 43 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.239-1597_239-1596i others(5): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr12 | 70327824 | |||||
| chr12:70327862
|
C | T | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.239-1561C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327862 | ||||||
| chr12:70327898
|
A | G | 1 | a0000c0003t0001g0195 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.239-1525A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327898 | ||||||
| chr12:70327959
|
T | C | 1 | a0001c0002t0001g0207 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.239-1464T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327959 | ||||||
| chr12:70327990
|
T | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.239-1433T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70327990 | ||||||
| chr12:70328109
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.239-1314A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70328109 | ||||||
| chr12:70328218
|
A | T | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.239-1205A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70328218 | ||||||
| chr12:70328359
|
T | A | 1 | a0001c0001t0001g0169 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.239-1064T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70328359 | ||||||
| chr12:70328368
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.239-1055C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70328368 | ||||||
| chr12:70328394
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.239-1029T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70328394 | ||||||
| chr12:70328626
|
A | C | 3 | a0000c0003t0001g0002a0000c0003t0001g0216a0001c0001t0001g0002 | 3 | HG02056.hp2 NA19084.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.239-797A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70328626 | ||||||
| chr12:70328742
|
T | C | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.239-681T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70328742 | ||||||
| chr12:70328956
|
A | T | 80 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(77): Show | 80 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.239-467A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70328956 | ||||||
| chr12:70329021
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.239-402C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 4/15 | chr12 | 70329021 | ||||||
| chr12:70329697
|
T | C | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.386+127T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 5/15 | chr12 | 70329697 | ||||||
| chr12:70329980
|
C | T | 10 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0002t0001g0203others(7): Show | 10 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.387-307C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 5/15 | chr12 | 70329980 | ||||||
| chr12:70329989
|
A | T | 70 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(67): Show | 70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.387-298A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 5/15 | chr12 | 70329989 | ||||||
| chr12:70330201
|
C | A | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.387-86C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 5/15 | chr12 | 70330201 | ||||||
| chr12:70330227
|
A | T | 70 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(67): Show | 70 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.387-60A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 5/15 | chr12 | 70330227 | ||||||
| chr12:70330273
|
G | A | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.387-14G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 5/15 | chr12 | 70330273 | ||||||
| chr12:70330477
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG00558.hp1 | splice_region_variant&intron_variant | LOW | c.569+8G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70330477 | ||||||
| chr12:70330500
|
G | A | 1 | a0001c0001t0001g0159 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.569+31G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70330500 | ||||||
| chr12:70330590
|
A | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.569+121A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70330590 | ||||||
| chr12:70330939
|
C | A | 1 | a0000c0003t0001g0042 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.569+470C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70330939 | ||||||
| chr12:70331021
|
T | G | 1 | a0001c0002t0001g0098 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.569+552T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70331021 | ||||||
| chr12:70331025
|
C | T | 1 | a0000c0003t0001g0190 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.569+556C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70331025 | ||||||
| chr12:70331028
|
A | G | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.569+559A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70331028 | ||||||
| chr12:70331030
|
A | G | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG01261.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.569+561A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70331030 | ||||||
| chr12:70331144
|
C | CA | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.569+676dupA | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr12 | 70331144 | |||||
| chr12:70331185
|
C | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.569+716C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70331185 | ||||||
| chr12:70331210
|
T | C | 1 | a0000c0003t0001g0138 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.569+741T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70331210 | ||||||
| chr12:70331341
|
C | T | 5 | a0001c0002t0001g0061a0001c0002t0001g0082a0001c0002t0001g0084others(2): Show | 5 | HG00438.hp2 HG02015.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.569+872C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70331341 | ||||||
| chr12:70331584
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.569+1115T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70331584 | ||||||
| chr12:70331890
|
T | C | 1 | a0001c0001t0001g0105 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.570-877T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70331890 | ||||||
| chr12:70332079
|
A | T | 42 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(39): Show | 42 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.570-688A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70332079 | ||||||
| chr12:70332293
|
G | A | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.570-474G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70332293 | ||||||
| chr12:70332340
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.570-427A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 6/15 | chr12 | 70332340 | ||||||
| chr12:70333050
|
G | A | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.649+204G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70333050 | ||||||
| chr12:70333092
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.649+246C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70333092 | ||||||
| chr12:70333094
|
G | A | 5 | a0001c0002t0001g0207a0001c0002t0001g0208a0001c0002t0001g0210others(2): Show | 5 | HG01256.hp1 HG01261.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.649+248G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70333094 | ||||||
| chr12:70333874
|
A | G | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.649+1028A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70333874 | ||||||
| chr12:70334108
|
A | G | 3 | a0001c0002t0004g0232a0001c0002t0004g0238a0001c0002t0004g0239 | 3 | NA18941.hp2 NA18945.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.649+1262A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334108 | ||||||
| chr12:70334123
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.649+1277A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334123 | ||||||
| chr12:70334144
|
T | C | 5 | a0001c0001t0001g0062a0001c0001t0001g0163a0001c0001t0001g0165others(2): Show | 5 | HG00099.hp1 HG01074.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.650-1294T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334144 | ||||||
| chr12:70334161
|
A | G | 10 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0002t0001g0203others(7): Show | 10 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.650-1277A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334161 | ||||||
| chr12:70334274
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.650-1164G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334274 | ||||||
| chr12:70334297
|
C | T | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.650-1141C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334297 | ||||||
| chr12:70334484
|
T | C | 119 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(116): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.650-954T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334484 | ||||||
| chr12:70334627
|
A | G | 35 | a0001c0001t0001g0021a0001c0001t0006g0005a0001c0002t0001g0248others(32): Show | 35 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.650-811A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334627 | ||||||
| chr12:70334647
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.650-791T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334647 | ||||||
| chr12:70334751
|
T | C | 3 | a0001c0001t0001g0004a0001c0001t0001g0161a0001c0001t0001g0162 | 4 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(1): Show |
intron_variant | MODIFIER | c.650-687T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334751 | ||||||
| chr12:70334899
|
C | A | 133 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(130): Show | 135 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.650-539C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334899 | ||||||
| chr12:70334903
|
C | T | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.650-535C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70334903 | ||||||
| chr12:70335040
|
A | G | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.650-398A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70335040 | ||||||
| chr12:70335061
|
A | G | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.650-377A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70335061 | ||||||
| chr12:70335105
|
G | A | 1 | a0001c0004t0001g0245 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.650-333G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70335105 | ||||||
| chr12:70335190
|
T | G | 1 | a0001c0006t0001g0150 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.650-248T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70335190 | ||||||
| chr12:70335269
|
A | G | 29 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0017others(26): Show | 29 | HG00621.hp2 HG01109.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.650-169A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70335269 | ||||||
| chr12:70335323
|
C | T | 1 | a0001c0004t0001g0267 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.650-115C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70335323 | ||||||
| chr12:70335346
|
G | A | 1 | a0001c0006t0001g0170 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.650-92G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 7/15 | chr12 | 70335346 | ||||||
| chr12:70335816
|
G | T | 6 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0071others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.775+253G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70335816 | ||||||
| chr12:70335985
|
A | G | 7 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0071others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.775+422A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70335985 | ||||||
| chr12:70335988
|
T | TCCA | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.775+427_775+429dup others(3): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr12 | 70335988 | |||||
| chr12:70336035
|
T | C | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.775+472T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336035 | ||||||
| chr12:70336036
|
G | A | 18 | a0000c0003t0001g0011a0001c0001t0001g0006a0001c0001t0001g0007others(15): Show | 18 | HG00099.hp1 HG00639.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.775+473G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336036 | ||||||
| chr12:70336063
|
T | A | 39 | a0000c0003t0001g0038a0000c0003t0001g0078a0001c0001t0001g0019others(36): Show | 41 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.775+500T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336063 | ||||||
| chr12:70336101
|
A | G | 3 | a0001c0002t0001g0200a0001c0005t0001g0250a0001c0005t0001g0252 | 3 | HG02055.hp1 HG02647.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.775+538A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336101 | ||||||
| chr12:70336345
|
A | T | 1 | a0001c0001t0005g0149 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.775+782A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336345 | ||||||
| chr12:70336349
|
G | A | 1 | a0001c0004t0003g0262 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.775+786G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336349 | ||||||
| chr12:70336421
|
G | A | 18 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0110others(15): Show | 18 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.775+858G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336421 | ||||||
| chr12:70336561
|
T | A | 1 | a0001c0001t0001g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.776-828T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336561 | ||||||
| chr12:70336659
|
C | A | 1 | a0001c0004t0001g0256 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.776-730C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336659 | ||||||
| chr12:70336668
|
T | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | NA18966.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.776-721T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336668 | ||||||
| chr12:70336759
|
G | A | 1 | a0001c0001t0001g0153 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.776-630G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336759 | ||||||
| chr12:70336940
|
A | C | 2 | a0000c0003t0001g0038a0001c0001t0001g0026 | 2 | NA18612.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.776-449A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70336940 | ||||||
| chr12:70337022
|
T | C | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.776-367T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70337022 | ||||||
| chr12:70337264
|
C | T | 1 | a0000c0003t0001g0043 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.776-125C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70337264 | ||||||
| chr12:70337343
|
A | G | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.776-46A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70337343 | ||||||
| chr12:70337367
|
C | T | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.776-22C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 8/15 | chr12 | 70337367 | ||||||
| chr12:70337531
|
G | T | 1 | a0001c0005t0001g0269 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.900+18G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 9/15 | chr12 | 70337531 | ||||||
| chr12:70337960
|
G | A | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.900+447G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 9/15 | chr12 | 70337960 | ||||||
| chr12:70337967
|
A | G | 1 | a0001c0001t0001g0274 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.900+454A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 9/15 | chr12 | 70337967 | ||||||
| chr12:70338061
|
C | T | 14 | a0001c0002t0001g0265a0001c0002t0003g0241a0001c0004t0001g0263others(11): Show | 14 | HG01099.hp1 HG01192.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.901-382C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 9/15 | chr12 | 70338061 | ||||||
| chr12:70338171
|
AT | A | 79 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(76): Show | 81 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.901-261delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr12 | 70338171 | |||||
| chr12:70338965
|
T | G | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1178+143T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70338965 | ||||||
| chr12:70339014
|
A | ATG | 16 | a0000c0003t0001g0037a0000c0003t0001g0138a0000c0003t0001g0216others(13): Show | 16 | HG00733.hp2 HG01070.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.1178+227_1178+228d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339014 | |||||
| chr12:70339014
|
A | ATGTG | 20 | a0000c0003t0001g0002a0000c0003t0001g0124a0001c0001t0001g0002others(17): Show | 20 | HG01109.hp1 HG01256.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.1178+225_1178+228d others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339014 | |||||
| chr12:70339014
|
A | ATGTGTG | 12 | a0001c0001t0001g0019a0001c0001t0001g0099a0001c0001t0001g0100others(9): Show | 12 | HG01261.hp1 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1178+223_1178+228d others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339014 | |||||
| chr12:70339014
|
ATG | A | 15 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0021others(12): Show | 15 | HG01175.hp2 HG01192.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1178+227_1178+228d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339014 | |||||
| chr12:70339014
|
ATGTG | A | 64 | a0000c0003t0001g0011a0000c0003t0001g0179a0000c0003t0001g0185others(61): Show | 64 | HG00099.hp1 HG00323.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1178+225_1178+228d others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339014 | |||||
| chr12:70339014
|
ATGTGTG | A | 5 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0183others(2): Show | 5 | HG01069.hp2 HG01167.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1178+223_1178+228d others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339014 | |||||
| chr12:70339014
|
ATGTGTGT others(1): Show |
A | 12 | a0001c0001t0001g0105a0001c0001t0001g0217a0001c0001t0008g0196others(9): Show | 12 | HG01081.hp2 HG01192.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.1178+221_1178+228d others(10): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339014 | |||||
| chr12:70339014
|
ATGTGTGT others(3): Show |
A | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1178+219_1178+228d others(12): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339014 | |||||
| chr12:70339047
|
T | C | 1 | a0001c0004t0001g0079 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1178+225T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339047 | ||||||
| chr12:70339049
|
T | C | 6 | a0000c0003t0001g0033a0001c0002t0001g0061a0001c0002t0001g0082others(3): Show | 6 | HG00438.hp2 HG02015.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.1178+227T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339049 | ||||||
| chr12:70339066
|
A | ATGTGTG | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0024others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1178+250_1178+255d others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339066 | |||||
| chr12:70339066
|
A | ATGTGTGT others(1): Show |
8 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(5): Show | 8 | HG02055.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1178+248_1178+255d others(10): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339066 | |||||
| chr12:70339066
|
A | ATGTGTGT others(3): Show |
3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG03225.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1178+246_1178+255d others(12): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339066 | |||||
| chr12:70339066
|
A | ATGTGTGT others(5): Show |
2 | a0001c0001t0001g0017a0001c0001t0001g0118 | 2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1178+255_1178+256i others(14): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339066 | |||||
| chr12:70339076
|
G | A | 44 | a0000c0003t0001g0078a0001c0001t0001g0003a0001c0001t0001g0019others(41): Show | 46 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.1178+254G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339076 | ||||||
| chr12:70339076
|
G | GTGTA | 3 | a0000c0003t0001g0048a0000c0003t0001g0049a0000c0003t0001g0057 | 3 | NA18941.hp1 NA19003.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.1178+255_1178+256i others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339076 | |||||
| chr12:70339076
|
GTA | G | 3 | a0001c0001t0001g0021a0001c0001t0001g0186a0001c0006t0001g0150 | 3 | HG00558.hp1 HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1178+269_1178+270d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339076 | |||||
| chr12:70339078
|
A | G | 65 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(62): Show | 65 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(62): Show |
intron_variant | MODIFIER | c.1178+256A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339078 | ||||||
| chr12:70339080
|
A | G | 5 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(2): Show | 5 | HG02647.hp1 HG02809.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1178+258A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339080 | ||||||
| chr12:70339089
|
T | C | 17 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0197others(14): Show | 17 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1178+267T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339089 | ||||||
| chr12:70339089
|
T | TACAC | 9 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(6): Show | 9 | HG01261.hp1 HG02109.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1178+268_1178+269i others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339089 | |||||
| chr12:70339091
|
T | C | 83 | a0000c0003t0001g0048a0000c0003t0001g0049a0000c0003t0001g0057others(80): Show | 83 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.1178+269T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339091 | ||||||
| chr12:70339091
|
T | TAC | 66 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(63): Show | 68 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1178+290_1178+291d others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339091 | |||||
| chr12:70339091
|
T | TACAC | 4 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 4 | HG02486.hp1 HG02723.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1178+288_1178+291d others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339091 | |||||
| chr12:70339091
|
T | TACACAC | 6 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0071others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1178+286_1178+291d others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339091 | |||||
| chr12:70339091
|
T | TATAC | 38 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(35): Show | 38 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.1178+270_1178+271i others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339091 | |||||
| chr12:70339093
|
C | T | 3 | a0001c0001t0001g0142a0001c0001t0001g0145a0001c0002t0001g0156 | 3 | HG02717.hp2 HG03516.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1178+271C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339093 | ||||||
| chr12:70339113
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0198 | 2 | HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1178+291C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339113 | ||||||
| chr12:70339158
|
A | AGGAATTT others(185): Show |
1 | a0001c0001t0001g0199 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1178+345_1178+346i others(194): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70339158 | |||||
| chr12:70339190
|
C | T | 1 | a0000c0003t0001g0020 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1178+368C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339190 | ||||||
| chr12:70339283
|
C | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1178+461C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339283 | ||||||
| chr12:70339589
|
A | G | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1178+767A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339589 | ||||||
| chr12:70339882
|
A | G | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1178+1060A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70339882 | ||||||
| chr12:70340247
|
C | T | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1178+1425C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340247 | ||||||
| chr12:70340276
|
T | A | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1178+1454T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340276 | ||||||
| chr12:70340629
|
C | T | 1 | a0001c0002t0001g0084 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1179-1478C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340629 | ||||||
| chr12:70340763
|
G | T | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179-1344G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340763 | ||||||
| chr12:70340774
|
C | A | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179-1333C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340774 | ||||||
| chr12:70340778
|
C | G | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1179-1329C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340778 | ||||||
| chr12:70340813
|
C | G | 2 | a0001c0001t0001g0174a0001c0001t0001g0177 | 2 | HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1179-1294C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340813 | ||||||
| chr12:70340872
|
G | T | 75 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(72): Show | 77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1179-1235G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340872 | ||||||
| chr12:70340887
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1179-1220A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340887 | ||||||
| chr12:70340889
|
CT | C | 112 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(109): Show | 113 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1179-1195delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70340889 | |||||
| chr12:70340889
|
CTT | C | 100 | a0000c0003t0001g0011a0000c0003t0001g0034a0000c0003t0001g0078others(97): Show | 102 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.1179-1196_1179-119 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70340889 | |||||
| chr12:70340889
|
CTTT | C | 22 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(19): Show | 22 | HG01256.hp2 HG02109.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1179-1197_1179-119 others(7): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70340889 | |||||
| chr12:70340889
|
CTTTT | C | 26 | a0001c0002t0001g0265a0001c0002t0003g0241a0001c0004t0001g0244others(23): Show | 26 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.1179-1198_1179-119 others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr12 | 70340889 | |||||
| chr12:70340998
|
C | T | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179-1109C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340998 | ||||||
| chr12:70340999
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1179-1108G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70340999 | ||||||
| chr12:70341005
|
C | G | 27 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0017others(24): Show | 27 | HG00621.hp2 HG01109.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.1179-1102C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341005 | ||||||
| chr12:70341138
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1179-969G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341138 | ||||||
| chr12:70341172
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1179-935C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341172 | ||||||
| chr12:70341314
|
G | A | 72 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(69): Show | 72 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1179-793G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341314 | ||||||
| chr12:70341416
|
A | G | 2 | a0000c0003t0001g0011a0001c0001t0001g0012 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1179-691A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341416 | ||||||
| chr12:70341550
|
T | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1179-557T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341550 | ||||||
| chr12:70341717
|
T | C | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1179-390T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341717 | ||||||
| chr12:70341902
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1179-205T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341902 | ||||||
| chr12:70341953
|
G | A | 82 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(79): Show | 82 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.1179-154G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341953 | ||||||
| chr12:70341970
|
T | C | 1 | a0000c0003t0001g0194 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1179-137T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 11/15 | chr12 | 70341970 | ||||||
| chr12:70342333
|
A | G | 31 | a0000c0003t0001g0011a0000c0003t0001g0179a0000c0003t0001g0185others(28): Show | 31 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1290+26A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70342333 | ||||||
| chr12:70342418
|
A | T | 2 | a0000c0003t0001g0059a0001c0002t0001g0060 | 2 | NA18969.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1290+111A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70342418 | ||||||
| chr12:70342434
|
C | T | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1290+127C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70342434 | ||||||
| chr12:70342573
|
CTTATT | C | 2 | a0001c0001t0001g0274a0001c0002t0001g0275 | 2 | NA18981.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.1290+271_1290+275d others(7): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 70342573 | |||||
| chr12:70342797
|
G | A | 10 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0002t0001g0203others(7): Show | 10 | HG00733.hp2 HG01070.hp1 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1290+490G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70342797 | ||||||
| chr12:70342984
|
G | T | 1 | a0000c0003t0001g0179 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1290+677G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70342984 | ||||||
| chr12:70343166
|
A | G | 38 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(35): Show | 38 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.1290+859A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70343166 | ||||||
| chr12:70343332
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1291-796C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70343332 | ||||||
| chr12:70343333
|
G | A | 3 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0002t0001g0139 | 3 | HG02055.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1291-795G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70343333 | ||||||
| chr12:70343610
|
G | A | 3 | a0001c0001t0001g0017a0001c0001t0001g0118a0001c0001t0001g0217 | 3 | HG01109.hp1 HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1291-518G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70343610 | ||||||
| chr12:70343681
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1291-447C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70343681 | ||||||
| chr12:70343726
|
T | G | 215 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(212): Show | 217 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.1291-402T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70343726 | ||||||
| chr12:70343818
|
T | A | 73 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(70): Show | 73 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.1291-310T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70343818 | ||||||
| chr12:70343898
|
A | G | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1291-230A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70343898 | ||||||
| chr12:70343943
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1291-185T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70343943 | ||||||
| chr12:70344056
|
A | C | 1 | a0001c0002t0001g0070 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1291-72A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | chr12 | 70344056 | ||||||
| chr12:70344073
|
AT | A | 81 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(78): Show | 83 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1291-53delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr12 | 70344073 | |||||
| chr12:70344343
|
T | A | 1 | a0001c0002t0001g0087 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1391+115T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70344343 | ||||||
| chr12:70344659
|
T | C | 1 | a0001c0001t0005g0155 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1391+431T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70344659 | ||||||
| chr12:70344711
|
T | C | 1 | a0001c0001t0001g0184 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1391+483T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70344711 | ||||||
| chr12:70344742
|
A | G | 3 | a0001c0001t0001g0140a0001c0001t0001g0153a0001c0002t0001g0139 | 3 | HG02055.hp2 HG03209.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1391+514A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70344742 | ||||||
| chr12:70344839
|
T | G | 83 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(80): Show | 83 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.1391+611T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70344839 | ||||||
| chr12:70345058
|
C | G | 41 | a0000c0003t0001g0002a0000c0003t0001g0015a0000c0003t0001g0020others(38): Show | 41 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.1391+830C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70345058 | ||||||
| chr12:70345310
|
C | T | 37 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(34): Show | 37 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1392-870C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70345310 | ||||||
| chr12:70345575
|
A | C | 25 | a0001c0002t0001g0265a0001c0002t0003g0241a0001c0004t0001g0244others(22): Show | 25 | HG00323.hp1 HG00609.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.1392-605A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70345575 | ||||||
| chr12:70345617
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1392-563T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70345617 | ||||||
| chr12:70345715
|
G | C | 73 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(70): Show | 73 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(70): Show |
intron_variant | MODIFIER | c.1392-465G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70345715 | ||||||
| chr12:70345724
|
T | A | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1392-456T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70345724 | ||||||
| chr12:70345733
|
A | G | 4 | a0001c0001t0001g0115a0001c0001t0001g0140a0001c0001t0001g0153others(1): Show | 4 | HG02055.hp2 HG02922.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1392-447A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70345733 | ||||||
| chr12:70345771
|
C | A | 1 | a0000c0003t0001g0064 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1392-409C>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70345771 | ||||||
| chr12:70346049
|
G | A | 75 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(72): Show | 77 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.1392-131G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70346049 | ||||||
| chr12:70346096
|
C | T | 1 | a0000c0003t0001g0039 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1392-84C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70346096 | ||||||
| chr12:70346110
|
A | G | 10 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1392-70A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70346110 | ||||||
| chr12:70346122
|
A | G | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1392-58A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 14/15 | chr12 | 70346122 | ||||||
| chr12:70346414
|
G | A | 164 | a0000c0003t0001g0011a0000c0003t0001g0078a0000c0003t0001g0179others(161): Show | 166 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1536+90G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70346414 | ||||||
| chr12:70346475
|
T | C | 6 | a0001c0002t0001g0069a0001c0002t0001g0070a0001c0002t0001g0071others(3): Show | 6 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1536+151T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70346475 | ||||||
| chr12:70346492
|
A | G | 2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1536+168A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70346492 | ||||||
| chr12:70346496
|
A | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1536+172A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70346496 | ||||||
| chr12:70346840
|
T | C | 25 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0017others(22): Show | 25 | HG00621.hp2 HG01109.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.1536+516T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70346840 | ||||||
| chr12:70346896
|
C | G | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG01261.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1536+572C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70346896 | ||||||
| chr12:70346897
|
G | A | 3 | a0001c0001t0001g0224a0001c0001t0001g0226a0001c0002t0001g0219 | 3 | HG01167.hp2 HG01169.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1536+573G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70346897 | ||||||
| chr12:70346955
|
G | C | 72 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(69): Show | 72 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1536+631G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70346955 | ||||||
| chr12:70346979
|
T | TAGAGAAT others(20): Show |
36 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0006g0005others(33): Show | 36 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.1536+668_1536+694d others(29): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 70346979 | |||||
| chr12:70347059
|
ACAACTC | A | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1536+738_1536+743d others(8): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 70347059 | |||||
| chr12:70347216
|
G | A | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1536+892G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70347216 | ||||||
| chr12:70347353
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1536+1029C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70347353 | ||||||
| chr12:70347598
|
A | C | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1536+1274A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70347598 | ||||||
| chr12:70347814
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0118 | 2 | HG01109.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1536+1490G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70347814 | ||||||
| chr12:70347828
|
T | C | 37 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(34): Show | 37 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1536+1504T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70347828 | ||||||
| chr12:70347926
|
A | G | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1536+1602A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70347926 | ||||||
| chr12:70348121
|
T | G | 72 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(69): Show | 72 | HG00323.hp1 HG00609.hp1 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.1536+1797T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348121 | ||||||
| chr12:70348126
|
G | T | 10 | a0001c0001t0001g0017a0001c0001t0001g0110a0001c0001t0001g0111others(7): Show | 10 | HG01109.hp1 HG02145.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1536+1802G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348126 | ||||||
| chr12:70348161
|
G | A | 1 | a0001c0002t0001g0200 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1536+1837G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348161 | ||||||
| chr12:70348180
|
G | T | 37 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(34): Show | 37 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1536+1856G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348180 | ||||||
| chr12:70348274
|
A | G | 7 | a0001c0001t0001g0217a0001c0002t0001g0069a0001c0002t0001g0070others(4): Show | 7 | HG02145.hp1 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1536+1950A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348274 | ||||||
| chr12:70348320
|
A | G | 5 | a0001c0001t0001g0115a0001c0001t0001g0140a0001c0001t0001g0148others(2): Show | 5 | HG02055.hp2 HG02922.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1536+1996A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348320 | ||||||
| chr12:70348464
|
TAGGTGAT others(1470): Show |
T | 1 | a0001c0004t0001g0258 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1536+2145_1536+362 others(4): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 70348464 | |||||
| chr12:70348676
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1536+2352A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348676 | ||||||
| chr12:70348697
|
C | T | 27 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0001t0001g0017others(24): Show | 27 | HG00621.hp2 HG01109.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.1536+2373C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348697 | ||||||
| chr12:70348821
|
G | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1536+2497G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348821 | ||||||
| chr12:70348903
|
A | T | 1 | a0001c0001t0001g0183 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1536+2579A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348903 | ||||||
| chr12:70348965
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1536+2641T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70348965 | ||||||
| chr12:70349120
|
A | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1536+2796A>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70349120 | ||||||
| chr12:70349243
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1536+2919G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70349243 | ||||||
| chr12:70349385
|
C | T | 1 | a0001c0002t0001g0211 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1536+3061C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70349385 | ||||||
| chr12:70349405
|
C | G | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1536+3081C>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70349405 | ||||||
| chr12:70349587
|
G | C | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | NA18994.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1536+3263G>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70349587 | ||||||
| chr12:70349619
|
T | C | 4 | a0001c0006t0001g0018a0001c0006t0001g0119a0001c0006t0001g0150others(1): Show | 4 | HG02559.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536+3295T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70349619 | ||||||
| chr12:70349624
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1536+3300T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70349624 | ||||||
| chr12:70349829
|
GTC | G | 36 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(33): Show | 36 | HG00323.hp1 HG01069.hp2 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1536+3509_1536+351 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 70349829 | |||||
| chr12:70349830
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1536+3506T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70349830 | ||||||
| chr12:70349971
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1536+3647A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70349971 | ||||||
| chr12:70350004
|
T | C | 1 | a0001c0002t0002g0233 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1536+3680T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70350004 | ||||||
| chr12:70350057
|
C | T | 8 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(5): Show | 8 | HG02109.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1536+3733C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70350057 | ||||||
| chr12:70350059
|
T | C | 1 | a0000c0003t0001g0190 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1536+3735T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70350059 | ||||||
| chr12:70350768
|
T | C | 1 | a0001c0001t0001g0198 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1537-3061T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70350768 | ||||||
| chr12:70350889
|
AGT | A | 7 | a0000c0003t0001g0189a0000c0003t0001g0190a0000c0003t0001g0191others(4): Show | 7 | HG02109.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1537-2933_1537-293 others(6): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 70350889 | |||||
| chr12:70351143
|
A | G | 8 | a0000c0003t0001g0179a0000c0003t0001g0185a0001c0001t0001g0175others(5): Show | 8 | HG00741.hp2 HG01361.hp2 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.1537-2686A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351143 | ||||||
| chr12:70351314
|
C | T | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1537-2515C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351314 | ||||||
| chr12:70351320
|
C | T | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1537-2509C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351320 | ||||||
| chr12:70351388
|
A | G | 1 | a0001c0002t0001g0098 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1537-2441A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351388 | ||||||
| chr12:70351477
|
A | G | 3 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0199 | 3 | HG03225.hp2 HG03453.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1537-2352A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351477 | ||||||
| chr12:70351541
|
C | T | 1 | a0000c0003t0001g0038 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1537-2288C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351541 | ||||||
| chr12:70351680
|
T | C | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1537-2149T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351680 | ||||||
| chr12:70351693
|
A | G | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(3): Show | 6 | HG01261.hp1 HG02486.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1537-2136A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351693 | ||||||
| chr12:70351976
|
A | G | 1 | a0001c0001t0006g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1537-1853A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351976 | ||||||
| chr12:70351995
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1537-1834A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70351995 | ||||||
| chr12:70352222
|
G | T | 1 | a0001c0004t0001g0245 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1537-1607G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352222 | ||||||
| chr12:70352248
|
G | A | 1 | a0001c0001t0008g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1537-1581G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352248 | ||||||
| chr12:70352255
|
G | GT | 276 | a0000c0003t0001g0002a0000c0003t0001g0011a0000c0003t0001g0015others(273): Show | 279 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.1537-1574_1537-157 others(5): Show |
CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352255 | ||||||
| chr12:70352362
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1537-1467T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352362 | ||||||
| chr12:70352394
|
A | G | 1 | a0001c0001t0001g0198 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1537-1435A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352394 | ||||||
| chr12:70352502
|
G | A | 14 | a0000c0003t0002g0229a0000c0003t0002g0230a0001c0002t0002g0228others(11): Show | 14 | HG00621.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1537-1327G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352502 | ||||||
| chr12:70352623
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0188 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1537-1206A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352623 | ||||||
| chr12:70352633
|
T | C | 3 | a0001c0002t0004g0232a0001c0002t0004g0238a0001c0002t0004g0239 | 3 | NA18941.hp2 NA18945.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1537-1196T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352633 | ||||||
| chr12:70352819
|
G | T | 1 | a0001c0002t0002g0234 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1537-1010G>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352819 | ||||||
| chr12:70352829
|
T | A | 10 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(7): Show | 10 | HG00733.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1537-1000T>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70352829 | ||||||
| chr12:70353075
|
C | CT | 16 | a0000c0003t0001g0020a0000c0003t0001g0033a0000c0003t0001g0049others(13): Show | 16 | HG00438.hp1 HG01934.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.1537-738dupT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 70353075 | |||||
| chr12:70353075
|
CT | C | 9 | a0001c0001t0001g0016a0001c0001t0001g0218a0001c0001t0001g0220others(6): Show | 9 | HG00733.hp1 HG00738.hp2 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.1537-738delT | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr12 | 70353075 | |||||
| chr12:70353079
|
T | G | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1537-750T>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70353079 | ||||||
| chr12:70353096
|
G | A | 12 | a0000c0003t0001g0179a0000c0003t0001g0185a0001c0001t0001g0174others(9): Show | 12 | HG00741.hp2 HG01167.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.1537-733G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70353096 | ||||||
| chr12:70353218
|
G | A | 33 | a0001c0002t0001g0248a0001c0002t0001g0265a0001c0002t0003g0241others(30): Show | 33 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1537-611G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70353218 | ||||||
| chr12:70353230
|
G | A | 37 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(34): Show | 37 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1537-599G>A | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70353230 | ||||||
| chr12:70353430
|
C | T | 37 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(34): Show | 37 | HG00323.hp1 HG00609.hp1 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.1537-399C>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70353430 | ||||||
| chr12:70353463
|
A | T | 2 | a0001c0002t0001g0080a0001c0002t0001g0092 | 2 | HG02080.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.1537-366A>T | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70353463 | ||||||
| chr12:70353520
|
A | G | 4 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0112others(1): Show | 4 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1537-309A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70353520 | ||||||
| chr12:70353673
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1537-156A>G | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70353673 | ||||||
| chr12:70353719
|
T | C | 1 | a0000c0003t0001g0057 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1537-110T>C | CNOT2 | ENSG00000111596.14 | transcript | ENST00000229195.8 | protein_coding | 15/15 | chr12 | 70353719 |