Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57472 |
| ensemblid | ENSG00000113300.13 |
| hgncid | 14099 |
| symbol | CNOT6 |
| name | CCR4-NOT transcription complex subunit 6 |
| refseq_nuc | NM_001370472.1 |
| refseq_prot | NP_001357401.1 |
| ensembl_nuc | ENST00000261951.9 |
| ensembl_prot | ENSP00000261951.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 180494379 |
| end | 180578358 |
| strand | + |
| ver | v1.2 |
| region | chr5:180494379-180578358 |
| region5000 | chr5:180489379-180583358 |
| regionname0 | CNOT6_chr5_180494379_180578358 |
| regionname5000 | CNOT6_chr5_180489379_180583358 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 557 | 332 | 86 | 70 | 126 | 12 | 36 | 84 | CNOT6_chr5_180489379_180583358 | CNOT6 | MPKEK others(552): Show |
chr5 | 180489379 | 180583358 |
| a0002 | 0/0 | 557 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CNOT6_chr5_180489379_180583358 | CNOT6 | MPKEK others(552): Show |
chr5 | 180489379 | 180583358 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1671 | 294 | 57 | 63 | 126 | 12 | 35 | CNOT6_chr5_180489379_180583358 | CNOT6 | ATGCC others(1666): Show |
chr5 | 180489379 | 180583358 | ||
| a0001c0002 | 1/0 | 1671 | 35 | 26 | 7 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | ATGCC others(1666): Show |
chr5 | 180489379 | 180583358 | ||
| a0001c0003 | 0/0 | 1671 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | ATGCC others(1666): Show |
chr5 | 180489379 | 180583358 | ||
| a0001c0005 | 0/0 | 1671 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | ATGCC others(1666): Show |
chr5 | 180489379 | 180583358 | ||
| a0002c0004 | 0/0 | 1671 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | ATGCC others(1666): Show |
chr5 | 180489379 | 180583358 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6227 | 65 | 6 | 15 | 33 | 3 | 8 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6222): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0002 | 0/0 | 6221 | 44 | 1 | 5 | 35 | 2 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6216): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0003 | 0/0 | 6231 | 17 | 1 | 8 | 4 | 1 | 3 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6226): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0005 | 0/1 | 6223 | 5 | 1 | 0 | 2 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6218): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0006 | 0/0 | 6226 | 15 | 3 | 3 | 5 | 0 | 4 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6221): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0007 | 0/0 | 6222 | 13 | 0 | 1 | 12 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6217): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0008 | 0/0 | 6229 | 12 | 0 | 2 | 6 | 1 | 3 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6224): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0009 | 0/0 | 6233 | 10 | 1 | 0 | 5 | 0 | 4 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6228): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0010 | 0/0 | 6229 | 8 | 0 | 1 | 2 | 1 | 4 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6224): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0011 | 0/0 | 6227 | 6 | 6 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6222): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0012 | 0/0 | 6231 | 6 | 1 | 2 | 2 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6226): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0013 | 0/0 | 6225 | 6 | 4 | 2 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6220): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0014 | 0/0 | 6227 | 5 | 3 | 1 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6222): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0015 | 0/0 | 6226 | 5 | 4 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6221): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0016 | 0/0 | 6228 | 5 | 0 | 2 | 3 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6223): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0017 | 0/0 | 6225 | 5 | 5 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6220): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0018 | 0/0 | 6232 | 4 | 0 | 2 | 0 | 2 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6227): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0019 | 0/0 | 6223 | 4 | 0 | 0 | 4 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6218): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0021 | 0/0 | 6221 | 3 | 0 | 0 | 0 | 0 | 3 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6216): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0022 | 0/0 | 6227 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6222): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0023 | 0/0 | 6235 | 3 | 2 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6230): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0024 | 0/0 | 6220 | 3 | 0 | 2 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6215): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0025 | 0/0 | 6231 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6226): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0026 | 0/0 | 6229 | 2 | 1 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6224): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0027 | 0/0 | 6231 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6226): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0028 | 0/0 | 6235 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6230): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0029 | 0/0 | 6229 | 2 | 0 | 0 | 2 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6224): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0030 | 0/0 | 6232 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6227): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0031 | 0/0 | 6230 | 2 | 0 | 2 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6225): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0032 | 0/0 | 6218 | 2 | 0 | 1 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6213): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0033 | 0/0 | 6225 | 2 | 1 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6220): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0034 | 0/0 | 6204 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6199): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0035 | 0/0 | 6235 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6230): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0036 | 0/0 | 6233 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6228): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0037 | 0/0 | 6229 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6224): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0038 | 0/0 | 6233 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6228): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0039 | 0/0 | 6223 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6218): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0040 | 0/0 | 6223 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6218): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0041 | 0/0 | 6221 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6216): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0042 | 0/0 | 6221 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6216): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0043 | 0/0 | 6231 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6226): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0044 | 0/0 | 6230 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6225): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0045 | 0/0 | 6239 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6234): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0046 | 0/0 | 6227 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6222): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0047 | 0/0 | 6227 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6222): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0048 | 0/0 | 6227 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6222): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0049 | 0/0 | 6221 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6216): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0050 | 0/0 | 6221 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6216): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0051 | 0/0 | 6221 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6216): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0052 | 0/0 | 6221 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6216): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0053 | 0/0 | 6230 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6225): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0054 | 0/0 | 6226 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6221): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0055 | 0/0 | 6224 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6219): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0056 | 0/0 | 6229 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6224): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0057 | 0/0 | 6221 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6216): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0058 | 0/0 | 6221 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6216): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0059 | 0/0 | 6227 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6222): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0060 | 0/0 | 6223 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6218): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0061 | 0/0 | 6223 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6218): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0062 | 0/0 | 6223 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6218): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0063 | 0/0 | 6221 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6216): Show |
chr5 | 180489379 | 180583358 |
| a0001c0001t0064 | 0/0 | 6227 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6222): Show |
chr5 | 180489379 | 180583358 |
| a0001c0002t0002 | 0/0 | 6221 | 8 | 1 | 6 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6216): Show |
chr5 | 180489379 | 180583358 |
| a0001c0002t0004 | 1/0 | 6219 | 14 | 12 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6214): Show |
chr5 | 180489379 | 180583358 |
| a0001c0002t0005 | 0/0 | 6223 | 10 | 10 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6218): Show |
chr5 | 180489379 | 180583358 |
| a0001c0002t0020 | 0/0 | 6219 | 3 | 3 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6214): Show |
chr5 | 180489379 | 180583358 |
| a0001c0003t0022 | 0/0 | 6227 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6222): Show |
chr5 | 180489379 | 180583358 |
| a0001c0005t0004 | 0/0 | 6219 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6214): Show |
chr5 | 180489379 | 180583358 |
| a0002c0004t0001 | 0/0 | 6227 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6222): Show |
chr5 | 180489379 | 180583358 |
| a0002c0004t0004 | 0/0 | 6219 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | GAGGG others(6214): Show |
chr5 | 180489379 | 180583358 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0005g0100 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0005g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0006g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0007g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0008g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0009g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0010g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0010g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0010g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0010g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0010g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0010g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0010g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0010g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0011g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0011g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0011g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0011g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0011g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0012g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0012g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0012g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0012g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0012g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0012g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0013g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0013g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0013g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0013g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0013g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0013g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0014g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0014g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0014g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0014g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0014g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0015g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0015g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0015g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0015g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0015g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0016g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0016g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0016g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0016g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0016g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0017g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0017g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0017g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0017g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0017g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0018g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0018g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0018g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0018g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0019g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0019g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0019g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0019g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0021g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0021g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0021g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0022g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0023g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0023g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0023g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0024g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0024g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0024g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0025g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0025g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0026g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0026g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0027g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0027g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0028g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0028g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0029g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0029g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0030g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0030g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0031g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0031g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0032g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0032g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0033g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0033g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0034g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0035g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0036g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0037g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0038g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0039g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0040g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0041g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0042g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0043g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0044g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0045g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0046g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0047g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0048g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0049g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0050g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0051g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0052g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0053g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0054g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0055g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0056g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0057g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0058g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0059g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0060g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0061g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0062g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0063g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0001t0064g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0004g0253 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0020g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0020g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0002t0020g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0003t0022g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0003t0022g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0001c0005t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0002c0004t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| a0002c0004t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0018 | g0005 | EUR | GBR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0246 | EUR | GBR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | FIN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00280 | hp2 | a0001 | c0001 | t0014 | g0168 | EUR | FIN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00408 | hp1 | a0001 | c0001 | t0006 | g0122 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00544 | hp2 | a0001 | c0001 | t0012 | g0113 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00609 | hp1 | a0001 | c0001 | t0058 | g0094 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00609 | hp2 | a0001 | c0001 | t0007 | g0142 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00639 | hp1 | a0001 | c0001 | t0050 | g0088 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00639 | hp2 | a0001 | c0001 | t0014 | g0175 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00642 | hp2 | a0001 | c0001 | t0013 | g0254 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00673 | hp2 | a0001 | c0001 | t0008 | g0274 | EAS | CHS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0328 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00733 | hp2 | a0001 | c0001 | t0031 | g0134 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00735 | hp1 | a0001 | c0001 | t0055 | g0154 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00735 | hp2 | a0001 | c0001 | t0008 | g0296 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00738 | hp1 | a0001 | c0001 | t0018 | g0008 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00738 | hp2 | a0001 | c0001 | t0010 | g0199 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG00741 | hp2 | a0001 | c0001 | t0037 | g0172 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0030 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01074 | hp2 | a0001 | c0001 | t0031 | g0133 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01106 | hp1 | a0001 | c0002 | t0002 | g0031 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01109 | hp1 | a0001 | c0001 | t0030 | g0132 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01109 | hp2 | a0001 | c0001 | t0030 | g0153 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01167 | hp1 | a0001 | c0002 | t0004 | g0045 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01167 | hp2 | a0001 | c0001 | t0027 | g0191 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01168 | hp1 | a0001 | c0001 | t0016 | g0117 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01168 | hp2 | a0001 | c0001 | t0024 | g0119 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01169 | hp1 | a0001 | c0001 | t0016 | g0121 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01169 | hp2 | a0001 | c0001 | t0027 | g0187 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01243 | hp1 | a0001 | c0001 | t0015 | g0128 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01243 | hp2 | a0001 | c0001 | t0033 | g0074 | AMR | PUR | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01255 | hp2 | a0001 | c0001 | t0007 | g0126 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0040 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01257 | hp1 | a0001 | c0001 | t0032 | g0129 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0190 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0041 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01261 | hp1 | a0001 | c0001 | t0026 | g0222 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01346 | hp2 | a0001 | c0001 | t0024 | g0152 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01358 | hp1 | a0001 | c0001 | t0018 | g0007 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01361 | hp2 | a0001 | c0001 | t0048 | g0310 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0042 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0198 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0208 | EUR | IBS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0312 | EUR | IBS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01516 | hp1 | a0001 | c0001 | t0008 | g0316 | EUR | IBS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01516 | hp2 | a0001 | c0001 | t0010 | g0209 | EUR | IBS | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01884 | hp1 | a0001 | c0001 | t0026 | g0220 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01891 | hp1 | a0001 | c0001 | t0009 | g0211 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01891 | hp2 | a0001 | c0002 | t0005 | g0023 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01975 | hp1 | a0001 | c0001 | t0042 | g0072 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0021 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01978 | hp1 | a0001 | c0001 | t0013 | g0268 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01978 | hp2 | a0001 | c0001 | t0008 | g0295 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01981 | hp1 | a0001 | c0001 | t0006 | g0137 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01993 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02004 | hp1 | a0001 | c0001 | t0051 | g0096 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0138 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02015 | hp1 | a0001 | c0001 | t0007 | g0130 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02027 | hp1 | a0001 | c0001 | t0009 | g0011 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02027 | hp2 | a0001 | c0001 | t0008 | g0302 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02055 | hp1 | a0001 | c0001 | t0015 | g0013 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02055 | hp2 | a0001 | c0003 | t0022 | g0221 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02071 | hp2 | a0001 | c0001 | t0039 | g0103 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02074 | hp1 | a0001 | c0001 | t0035 | g0018 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02083 | hp1 | a0001 | c0001 | t0036 | g0193 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02132 | hp1 | a0001 | c0001 | t0056 | g0262 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02132 | hp2 | a0001 | c0001 | t0059 | g0299 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02148 | hp1 | a0001 | c0001 | t0054 | g0146 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0171 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | CDX | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | CDX | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | CDX | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CDX | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02257 | hp1 | a0001 | c0001 | t0014 | g0176 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02257 | hp2 | a0001 | c0001 | t0061 | g0004 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02258 | hp1 | a0001 | c0001 | t0062 | g0073 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02258 | hp2 | a0001 | c0001 | t0064 | g0164 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02273 | hp1 | a0001 | c0001 | t0012 | g0320 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02273 | hp2 | a0001 | c0001 | t0012 | g0244 | AMR | PEL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02280 | hp1 | a0001 | c0001 | t0046 | g0012 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02280 | hp2 | a0001 | c0002 | t0004 | g0036 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02451 | hp1 | a0001 | c0002 | t0004 | g0054 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02451 | hp2 | a0001 | c0001 | t0040 | g0101 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02523 | hp2 | a0001 | c0001 | t0007 | g0144 | EAS | KHV | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02572 | hp2 | a0001 | c0002 | t0005 | g0329 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02615 | hp1 | a0001 | c0002 | t0004 | g0032 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02615 | hp2 | a0001 | c0001 | t0053 | g0118 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02622 | hp1 | a0001 | c0001 | t0017 | g0165 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02622 | hp2 | a0001 | c0002 | t0005 | g0026 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02630 | hp1 | a0001 | c0001 | t0045 | g0331 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02630 | hp2 | a0001 | c0002 | t0002 | g0039 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02683 | hp1 | a0001 | c0001 | t0006 | g0125 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02683 | hp2 | a0001 | c0001 | t0010 | g0188 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02698 | hp1 | a0001 | c0002 | t0002 | g0048 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02717 | hp1 | a0001 | c0002 | t0005 | g0029 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02717 | hp2 | a0001 | c0001 | t0013 | g0104 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02723 | hp1 | a0001 | c0002 | t0020 | g0050 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02735 | hp1 | a0001 | c0001 | t0021 | g0160 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02738 | hp1 | a0001 | c0001 | t0008 | g0297 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02738 | hp2 | a0001 | c0001 | t0021 | g0161 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02809 | hp1 | a0001 | c0002 | t0020 | g0051 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02809 | hp2 | a0001 | c0001 | t0060 | g0003 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02818 | hp1 | a0001 | c0001 | t0011 | g0215 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02818 | hp2 | a0001 | c0001 | t0013 | g0105 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02886 | hp1 | a0001 | c0001 | t0012 | g0277 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02886 | hp2 | a0001 | c0002 | t0005 | g0024 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02895 | hp1 | a0001 | c0002 | t0005 | g0022 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02895 | hp2 | a0001 | c0001 | t0017 | g0166 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02896 | hp1 | a0001 | c0001 | t0017 | g0167 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0157 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02922 | hp1 | a0001 | c0002 | t0004 | g0049 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02922 | hp2 | a0001 | c0001 | t0025 | g0216 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02965 | hp1 | a0001 | c0001 | t0015 | g0116 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02965 | hp2 | a0001 | c0001 | t0011 | g0223 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02970 | hp1 | a0001 | c0002 | t0004 | g0047 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02970 | hp2 | a0001 | c0002 | t0004 | g0037 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02976 | hp1 | a0001 | c0001 | t0022 | g0224 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02976 | hp2 | a0001 | c0002 | t0005 | g0028 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0181 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03017 | hp2 | a0001 | c0001 | t0008 | g0294 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03098 | hp1 | a0001 | c0002 | t0004 | g0038 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03098 | hp2 | a0001 | c0001 | t0049 | g0332 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03130 | hp1 | a0001 | c0001 | t0017 | g0162 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03130 | hp2 | a0001 | c0001 | t0011 | g0001 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03139 | hp1 | a0001 | c0002 | t0004 | g0034 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03139 | hp2 | a0001 | c0001 | t0015 | g0127 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03195 | hp1 | a0001 | c0001 | t0025 | g0218 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03195 | hp2 | a0001 | c0001 | t0014 | g0203 | AFR | ESN | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03209 | hp1 | a0001 | c0002 | t0004 | g0046 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0131 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03225 | hp1 | a0001 | c0001 | t0011 | g0001 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0202 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03453 | hp1 | a0001 | c0001 | t0011 | g0214 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03453 | hp2 | a0001 | c0005 | t0004 | g0020 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03486 | hp1 | a0001 | c0002 | t0020 | g0052 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03486 | hp2 | a0001 | c0001 | t0011 | g0213 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03491 | hp1 | a0001 | c0001 | t0043 | g0205 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03491 | hp2 | a0001 | c0001 | t0009 | g0174 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03540 | hp1 | a0001 | c0001 | t0041 | g0102 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03540 | hp2 | a0001 | c0002 | t0004 | g0053 | AFR | GWD | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03579 | hp1 | a0001 | c0002 | t0005 | g0027 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0180 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03669 | hp2 | a0001 | c0001 | t0008 | g0227 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03704 | hp2 | a0001 | c0001 | t0009 | g0207 | SAS | PJL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03831 | hp1 | a0001 | c0001 | t0010 | g0183 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03831 | hp2 | a0001 | c0001 | t0021 | g0159 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0270 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03927 | hp1 | a0001 | c0001 | t0006 | g0323 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03942 | hp1 | a0001 | c0001 | t0009 | g0200 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03942 | hp2 | a0001 | c0001 | t0024 | g0158 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG04184 | hp1 | a0001 | c0001 | t0047 | g0238 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG04184 | hp2 | a0001 | c0001 | t0032 | g0155 | SAS | BEB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG04199 | hp1 | a0001 | c0001 | t0010 | g0210 | SAS | STU | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | STU | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG04204 | hp1 | a0001 | c0001 | t0009 | g0179 | SAS | STU | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | STU | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG04228 | hp2 | a0001 | c0001 | t0006 | g0151 | SAS | STU | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18612 | hp1 | a0001 | c0001 | t0028 | g0326 | EAS | CHB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18612 | hp2 | a0001 | c0001 | t0023 | g0010 | EAS | CHB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0196 | EAS | CHB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18747 | hp2 | a0001 | c0001 | t0016 | g0014 | EAS | CHB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18906 | hp1 | a0001 | c0001 | t0057 | g0055 | AFR | YRI | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18906 | hp2 | a0001 | c0001 | t0033 | g0095 | AFR | YRI | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18939 | hp2 | a0001 | c0001 | t0008 | g0286 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18941 | hp2 | a0001 | c0001 | t0052 | g0080 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18944 | hp1 | a0001 | c0001 | t0016 | g0330 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18944 | hp2 | a0001 | c0001 | t0008 | g0234 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18947 | hp1 | a0001 | c0001 | t0019 | g0284 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18950 | hp2 | a0001 | c0001 | t0007 | g0143 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18957 | hp2 | a0001 | c0001 | t0009 | g0015 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0114 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18961 | hp1 | a0001 | c0001 | t0009 | g0184 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18961 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18962 | hp2 | a0001 | c0001 | t0008 | g0263 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18963 | hp1 | a0001 | c0001 | t0007 | g0324 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18966 | hp1 | a0002 | c0004 | t0004 | g0249 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18966 | hp2 | a0001 | c0001 | t0007 | g0136 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18967 | hp2 | a0001 | c0001 | t0019 | g0291 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18968 | hp2 | a0001 | c0001 | t0016 | g0123 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18969 | hp1 | a0001 | c0001 | t0029 | g0288 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18969 | hp2 | a0002 | c0004 | t0001 | g0318 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18973 | hp1 | a0001 | c0001 | t0007 | g0150 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18977 | hp1 | a0001 | c0001 | t0009 | g0178 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18978 | hp1 | a0001 | c0001 | t0006 | g0147 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18980 | hp1 | a0001 | c0001 | t0010 | g0017 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18980 | hp2 | a0001 | c0001 | t0008 | g0283 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18982 | hp1 | a0001 | c0001 | t0029 | g0287 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18990 | hp1 | a0001 | c0001 | t0007 | g0141 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0148 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19004 | hp2 | a0001 | c0001 | t0034 | g0002 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19005 | hp2 | a0001 | c0001 | t0007 | g0156 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19012 | hp1 | a0001 | c0001 | t0007 | g0149 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19043 | hp1 | a0001 | c0001 | t0017 | g0163 | AFR | LWK | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0225 | AFR | LWK | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19054 | hp1 | a0001 | c0001 | t0007 | g0140 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19064 | hp1 | a0001 | c0001 | t0012 | g0261 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19064 | hp2 | a0001 | c0001 | t0006 | g0139 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19070 | hp2 | a0001 | c0001 | t0028 | g0242 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19077 | hp1 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19077 | hp2 | a0001 | c0001 | t0019 | g0255 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19080 | hp2 | a0001 | c0001 | t0007 | g0135 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19081 | hp1 | a0001 | c0001 | t0019 | g0256 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19081 | hp2 | a0001 | c0001 | t0006 | g0145 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19085 | hp1 | a0001 | c0001 | t0009 | g0016 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19090 | hp2 | a0001 | c0001 | t0010 | g0194 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19240 | hp1 | a0001 | c0001 | t0013 | g0108 | AFR | YRI | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA19240 | hp2 | a0001 | c0002 | t0004 | g0035 | AFR | YRI | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0124 | AFR | ASW | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20129 | hp2 | a0001 | c0001 | t0015 | g0120 | AFR | ASW | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0084 | EUR | TSI | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20752 | hp2 | a0001 | c0001 | t0012 | g0252 | EUR | TSI | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20805 | hp1 | a0001 | c0001 | t0018 | g0006 | EUR | TSI | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0082 | EUR | TSI | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20905 | hp1 | a0001 | c0001 | t0006 | g0322 | SAS | GIH | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20905 | hp2 | a0001 | c0001 | t0010 | g0195 | SAS | GIH | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01123 | hp1 | a0001 | c0001 | t0006 | g0009 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0044 | AMR | CLM | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02109 | hp1 | a0001 | c0001 | t0038 | g0217 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02109 | hp2 | a0001 | c0001 | t0023 | g0204 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02486 | hp1 | a0001 | c0002 | t0005 | g0025 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02486 | hp2 | a0001 | c0001 | t0044 | g0170 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0206 | AFR | ACB | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03471 | hp1 | a0001 | c0002 | t0004 | g0033 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG03471 | hp2 | a0001 | c0001 | t0063 | g0229 | AFR | MSL | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG06807 | hp1 | a0001 | c0001 | t0013 | g0107 | AFR | USA | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| HG06807 | hp2 | a0001 | c0003 | t0022 | g0219 | AFR | USA | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20300 | hp1 | a0001 | c0002 | t0005 | g0043 | AFR | USA | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA20300 | hp2 | a0001 | c0001 | t0014 | g0186 | AFR | USA | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | LWK | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| NA21309 | hp2 | a0001 | c0001 | t0023 | g0197 | AFR | LWK | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0005 | g0100 | REF | REF | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0004 | g0253 | REF | REF | CNOT6_chr5_180489379_180583358 | CNOT6 | chr5 | 180489379 | 180583358 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180529302 | C | T | 1 | a0002 | 2 | NA18966.hp1 NA18969.hp2 |
missense_variant | MODERATE | c.26C>T | p.Pro9Leu | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/12 | 413/6219 | 26/1674 | 9/557 | chr5 | 180529302 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180567099 | G | A | 1 | a0001c0003 | 2 | HG02055.hp2 HG06807.hp2 |
synonymous_variant | LOW | c.729G>A | p.Thr243Thr | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 8/12 | 1116/6219 | 729/1674 | 243/557 | chr5 | 180567099 | |||
| chr5:180569111 | C | T | 3 | a0001c0001 a0001c0003 a0002c0004 |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
splice_region_variant&synonymous_variant | LOW | c.1029C>T | p.Ser343Ser | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/12 | 1416/6219 | 1029/1674 | 343/557 | chr5 | 180569111 | |||
| chr5:180571372 | G | A | 1 | a0001c0005 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.1401G>A | p.Lys467Lys | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/12 | 1788/6219 | 1401/1674 | 467/557 | chr5 | 180571372 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180494391 | C | T | 1 | a0001c0001t0064 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-375C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/12 | 34886 | chr5 | 180494391 | ||||||
| chr5:180494461 | TGGCGGCG others(16): Show |
T | 1 | a0001c0001t0034 | 1 | NA19004.hp2 | 5_prime_UTR_variant | MODIFIER | c.-300_-278delGCGGCG others(17): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/12 | 34789 | INFO_REALIGN_3_PRIME | chr5 | 180494461 | |||||
| chr5:180494503 | C | T | 3 | a0001c0001t0033 a0001c0001t0062 a0001c0001t0063 |
4 | HG01243.hp2 HG02258.hp1 HG03471.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-263C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/12 | 34774 | chr5 | 180494503 | ||||||
| chr5:180494513 | A | C | 2 | a0001c0001t0017 a0001c0001t0064 |
6 | HG02258.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-253A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/12 | 34764 | chr5 | 180494513 | ||||||
| chr5:180494563 | G | A | 1 | a0001c0002t0020 | 3 | HG02723.hp1 HG02809.hp1 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-203G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/12 | 34714 | chr5 | 180494563 | ||||||
| chr5:180494726 | A | C | 2 | a0001c0001t0060 a0001c0001t0061 |
2 | HG02257.hp2 HG02809.hp2 |
5_prime_UTR_variant | MODIFIER | c.-40A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/12 | 34551 | chr5 | 180494726 | ||||||
| chr5:180574338 | A | G | 1 | a0001c0001t0059 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*138A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 138 | chr5 | 180574338 | ||||||
| chr5:180574389 | G | A | 1 | a0001c0001t0018 | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*189G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 189 | chr5 | 180574389 | ||||||
| chr5:180574659 | A | G | 1 | a0001c0001t0058 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*459A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 459 | chr5 | 180574659 | ||||||
| chr5:180574737 | A | T | 1 | a0001c0001t0018 | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*537A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 537 | chr5 | 180574737 | ||||||
| chr5:180574867 | G | C | 2 | a0001c0001t0035 a0001c0001t0036 |
2 | HG02074.hp1 HG02083.hp1 |
3_prime_UTR_variant | MODIFIER | c.*667G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 667 | chr5 | 180574867 | ||||||
| chr5:180574872 | C | T | 1 | a0001c0001t0057 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*672C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 672 | chr5 | 180574872 | ||||||
| chr5:180574938 | T | C | 1 | a0001c0001t0037 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*738T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 738 | chr5 | 180574938 | ||||||
| chr5:180574980 | C | G | 1 | a0001c0001t0056 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*780C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 780 | chr5 | 180574980 | ||||||
| chr5:180575181 | A | G | 1 | a0001c0002t0020 | 3 | HG02723.hp1 HG02809.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*981A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 981 | chr5 | 180575181 | ||||||
| chr5:180575433 | G | A | 8 | a0001c0001t0011 a0001c0001t0021 a0001c0001t0022 others(5): Show |
18 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1233G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 1233 | chr5 | 180575433 | ||||||
| chr5:180575452 | T | TTTG | 1 | a0001c0001t0018 | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1273_*1275dupGTT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 1276 | INFO_REALIGN_3_PRIME | chr5 | 180575452 | |||||
| chr5:180575820 | T | G | 1 | a0001c0001t0018 | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1620T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 1620 | chr5 | 180575820 | ||||||
| chr5:180575849 | A | C | 11 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0015 others(8): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1649A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 1649 | chr5 | 180575849 | ||||||
| chr5:180575883 | G | A | 3 | a0001c0001t0040 a0001c0001t0041 a0001c0001t0060 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1683G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 1683 | chr5 | 180575883 | ||||||
| chr5:180575892 | GT | G | 15 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0015 others(12): Show |
57 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1704delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 1704 | INFO_REALIGN_3_PRIME | chr5 | 180575892 | |||||
| chr5:180575938 | G | A | 1 | a0001c0001t0042 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1738G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 1738 | chr5 | 180575938 | ||||||
| chr5:180576085 | C | T | 11 | a0001c0001t0006 a0001c0001t0007 a0001c0001t0015 others(8): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1885C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 1885 | chr5 | 180576085 | ||||||
| chr5:180576146 | GT | G | 4 | a0001c0001t0018 a0001c0001t0040 a0001c0001t0041 others(1): Show |
7 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1955delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 1955 | INFO_REALIGN_3_PRIME | chr5 | 180576146 | |||||
| chr5:180576664 | A | G | 1 | a0001c0001t0052 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2464A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2464 | chr5 | 180576664 | ||||||
| chr5:180576827 | A | G | 1 | a0001c0001t0051 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2627A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2627 | chr5 | 180576827 | ||||||
| chr5:180576995 | A | G | 1 | a0001c0001t0011 | 6 | HG02818.hp1 HG02965.hp2 HG03130.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2795A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2795 | chr5 | 180576995 | ||||||
| chr5:180577054 | A | G | 1 | a0001c0001t0050 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2854A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2854 | chr5 | 180577054 | ||||||
| chr5:180577154 | T | A | 11 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0010 others(8): Show |
50 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*2954T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2954 | chr5 | 180577154 | ||||||
| chr5:180577163 | A | ATG | 12 | a0001c0001t0002 a0001c0001t0021 a0001c0001t0024 others(9): Show |
66 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*2995_*2996dupGT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | |||||
| chr5:180577163 | A | ATGTG | 8 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0019 others(5): Show |
35 | HG00609.hp2 HG01255.hp2 HG01891.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2993_*2996dupGTGT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | |||||
| chr5:180577163 | A | ATGTGTG | 6 | a0001c0001t0013 a0001c0001t0017 a0001c0001t0033 others(3): Show |
16 | HG00642.hp2 HG00735.hp1 HG01243.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2991_*2996dupGTGT others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | |||||
| chr5:180577163 | A | ATGTGTGT others(1): Show |
11 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0014 others(8): Show |
93 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*2989_*2996dupGTGT others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | |||||
| chr5:180577163 | A | ATGTGTGT others(3): Show |
6 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0016 others(3): Show |
29 | HG00673.hp2 HG00735.hp2 HG00738.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2987_*2996dupGTGT others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | |||||
| chr5:180577163 | A | ATGTGTGT others(5): Show |
1 | a0001c0001t0053 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2973_*2974insCGTG others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2974 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | |||||
| chr5:180577163 | A | ATGTGTGT others(5): Show |
5 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0027 others(2): Show |
28 | HG00544.hp2 HG00733.hp2 HG01071.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*2985_*2996dupGTGT others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | |||||
| chr5:180577163 | A | ATGTGTGT others(7): Show |
3 | a0001c0001t0009 a0001c0001t0030 a0001c0001t0036 |
13 | HG01109.hp1 HG01109.hp2 HG01891.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2983_*2996dupGTGT others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | |||||
| chr5:180577163 | A | ATGTGTGT others(9): Show |
3 | a0001c0001t0023 a0001c0001t0028 a0001c0001t0035 |
6 | HG02074.hp1 HG02109.hp2 NA18612.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2981_*2996dupGTGT others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | |||||
| chr5:180577163 | A | ATGTGTGT others(13): Show |
1 | a0001c0001t0045 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2977_*2996dupGTGT others(16): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | |||||
| chr5:180577163 | A | ATTGTGTG others(4): Show |
1 | a0001c0001t0044 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2964_*2965insTGTG others(7): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2965 | INFO_REALIGN_3_PRIME | chr5 | 180577163 | |||||
| chr5:180577166 | T | TGTGTGTG others(1): Show |
1 | a0001c0001t0015 | 5 | HG01243.hp1 HG02055.hp1 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2973_*2974insCGTG others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2974 | INFO_REALIGN_3_PRIME | chr5 | 180577166 | |||||
| chr5:180577173 | G | GTGTGTGT others(5): Show |
1 | a0001c0001t0018 | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2984_*2985insTTGT others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2985 | INFO_REALIGN_3_PRIME | chr5 | 180577173 | |||||
| chr5:180577191 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0038 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2996_*2997insGTGT others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577191 | |||||
| chr5:180577191 | G | GTGTGTGT others(5): Show |
1 | a0001c0001t0025 | 2 | HG02922.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2996_*2997insGTGT others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577191 | |||||
| chr5:180577191 | G | GTGTGTGT others(3): Show |
1 | a0001c0001t0026 | 2 | HG01261.hp1 HG01884.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2996_*2997insGTGT others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577191 | |||||
| chr5:180577191 | G | GTGTGTGT others(1): Show |
3 | a0001c0001t0011 a0001c0001t0022 a0001c0003t0022 |
9 | HG02055.hp2 HG02818.hp1 HG02965.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2996_*2997insGTTT others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | INFO_REALIGN_3_PRIME | chr5 | 180577191 | |||||
| chr5:180577197 | T | G | 1 | a0001c0001t0054 | 1 | HG02148.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2997T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 2997 | chr5 | 180577197 | ||||||
| chr5:180577322 | C | T | 1 | a0001c0001t0018 | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3122C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3122 | chr5 | 180577322 | ||||||
| chr5:180577347 | A | G | 1 | a0001c0001t0018 | 4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3147A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3147 | chr5 | 180577347 | ||||||
| chr5:180577499 | C | G | 1 | a0001c0001t0048 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3299C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3299 | chr5 | 180577499 | ||||||
| chr5:180577544 | G | A | 1 | a0001c0001t0046 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3344G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3344 | chr5 | 180577544 | ||||||
| chr5:180577671 | A | G | 1 | a0001c0001t0027 | 2 | HG01167.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3471A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3471 | chr5 | 180577671 | ||||||
| chr5:180577740 | C | T | 3 | a0001c0001t0017 a0001c0001t0033 a0001c0001t0064 |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3540C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3540 | chr5 | 180577740 | ||||||
| chr5:180577742 | A | C | 1 | a0001c0001t0043 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3542A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3542 | chr5 | 180577742 | ||||||
| chr5:180577831 | G | A | 1 | a0001c0001t0047 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3631G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3631 | chr5 | 180577831 | ||||||
| chr5:180577936 | C | T | 1 | a0001c0001t0019 | 4 | NA18947.hp1 NA18967.hp2 NA19077.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3736C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3736 | chr5 | 180577936 | ||||||
| chr5:180578180 | C | T | 1 | a0001c0001t0029 | 2 | NA18969.hp1 NA18982.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3980C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 3980 | chr5 | 180578180 | ||||||
| chr5:180578263 | T | C | 9 | a0001c0001t0011 a0001c0001t0021 a0001c0001t0022 others(6): Show |
19 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4063T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 12/12 | 4063 | chr5 | 180578263 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180494779 | C | T | 1 | a0001c0001t0049g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3+16C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180494779 | |||||||
| chr5:180494791 | C | T | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+28C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180494791 | |||||||
| chr5:180494803 | C | T | 1 | a0001c0001t0016g0330 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-3+40C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180494803 | |||||||
| chr5:180494907 | T | C | 7 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(4): Show |
7 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+144T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180494907 | |||||||
| chr5:180494915 | C | T | 1 | a0001c0002t0005g0329 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-3+152C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180494915 | |||||||
| chr5:180494935 | G | A | 227 | a0001c0001t0001g0067 a0001c0001t0001g0106 a0001c0001t0001g0169 others(224): Show |
228 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.-3+172G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180494935 | |||||||
| chr5:180494942 | G | GCCCCGGG others(6): Show |
2 | a0001c0001t0001g0327 a0001c0001t0001g0328 |
2 | HG00733.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-3+190_-3+202dupCG others(11): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180494942 | ||||||
| chr5:180494957 | C | G | 1 | a0001c0001t0005g0225 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-3+194C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180494957 | |||||||
| chr5:180494978 | G | C | 2 | a0001c0001t0001g0226 a0001c0001t0008g0227 |
2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-3+215G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180494978 | |||||||
| chr5:180495032 | C | A | 1 | a0001c0001t0006g0009 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-3+269C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495032 | |||||||
| chr5:180495143 | G | T | 1 | a0001c0001t0028g0326 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-3+380G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495143 | |||||||
| chr5:180495158 | G | A | 2 | a0001c0001t0009g0011 a0001c0001t0023g0010 |
2 | HG02027.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.-3+395G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495158 | |||||||
| chr5:180495180 | T | C | 2 | a0001c0001t0060g0003 a0001c0001t0061g0004 |
2 | HG02257.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-3+417T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495180 | |||||||
| chr5:180495218 | C | T | 13 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(10): Show |
14 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3+455C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495218 | |||||||
| chr5:180495256 | C | A | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-3+493C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495256 | |||||||
| chr5:180495284 | T | G | 1 | a0001c0001t0015g0013 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-3+521T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495284 | |||||||
| chr5:180495313 | A | G | 1 | a0001c0001t0003g0212 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-3+550A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495313 | |||||||
| chr5:180495506 | G | A | 1 | a0001c0001t0016g0014 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-3+743G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495506 | |||||||
| chr5:180495515 | T | G | 3 | a0001c0001t0009g0015 a0001c0001t0009g0016 a0001c0001t0010g0017 |
3 | NA18957.hp2 NA18980.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-3+752T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495515 | |||||||
| chr5:180495562 | C | T | 1 | a0001c0001t0009g0211 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-3+799C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495562 | |||||||
| chr5:180495565 | G | C | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+802G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495565 | |||||||
| chr5:180495883 | T | G | 1 | a0001c0001t0035g0018 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-3+1120T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495883 | |||||||
| chr5:180495904 | C | T | 58 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(55): Show |
58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+1141C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180495904 | |||||||
| chr5:180496174 | A | C | 3 | a0001c0001t0021g0159 a0001c0001t0021g0160 a0001c0001t0021g0161 |
3 | HG02735.hp1 HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-3+1411A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180496174 | |||||||
| chr5:180496261 | A | C | 31 | a0001c0001t0003g0189 a0001c0001t0003g0190 a0001c0001t0003g0192 others(28): Show |
31 | HG00738.hp2 HG01071.hp2 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.-3+1498A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180496261 | |||||||
| chr5:180496405 | C | T | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+1642C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180496405 | |||||||
| chr5:180496416 | G | A | 1 | a0001c0001t0002g0019 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-3+1653G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180496416 | |||||||
| chr5:180496549 | A | T | 1 | a0001c0001t0001g0325 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-3+1786A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180496549 | |||||||
| chr5:180496576 | C | T | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-3+1813C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180496576 | |||||||
| chr5:180496613 | G | T | 1 | a0001c0001t0002g0115 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-3+1850G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180496613 | |||||||
| chr5:180496615 | T | G | 1 | a0001c0001t0001g0228 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-3+1852T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180496615 | |||||||
| chr5:180497065 | C | A | 6 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(3): Show |
6 | HG02258.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+2302C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497065 | |||||||
| chr5:180497325 | C | CA | 157 | a0001c0001t0001g0067 a0001c0001t0001g0169 a0001c0001t0001g0226 others(154): Show |
158 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.-3+2579dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180497325 | ||||||
| chr5:180497325 | C | CAAAA | 46 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(43): Show |
46 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.-3+2576_-3+2579dup others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180497325 | ||||||
| chr5:180497354 | G | T | 1 | a0001c0001t0003g0208 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-3+2591G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497354 | |||||||
| chr5:180497384 | T | A | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+2621T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497384 | |||||||
| chr5:180497732 | C | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+2969C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497732 | |||||||
| chr5:180497772 | G | A | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-3+3009G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497772 | |||||||
| chr5:180497780 | A | T | 1 | a0001c0001t0001g0321 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-3+3017A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497780 | |||||||
| chr5:180497809 | C | T | 1 | a0001c0001t0061g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-3+3046C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497809 | |||||||
| chr5:180497845 | A | G | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-3+3082A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497845 | |||||||
| chr5:180497935 | C | T | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+3172C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497935 | |||||||
| chr5:180497992 | G | A | 1 | a0001c0001t0014g0168 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-3+3229G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180497992 | |||||||
| chr5:180498157 | G | A | 1 | a0001c0005t0004g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-3+3394G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498157 | |||||||
| chr5:180498212 | G | A | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+3449G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498212 | |||||||
| chr5:180498223 | T | G | 231 | a0001c0001t0001g0067 a0001c0001t0001g0106 a0001c0001t0001g0169 others(228): Show |
232 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.-3+3460T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498223 | |||||||
| chr5:180498283 | A | G | 17 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(14): Show |
18 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-3+3520A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498283 | |||||||
| chr5:180498329 | A | C | 1 | a0001c0001t0005g0225 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-3+3566A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498329 | |||||||
| chr5:180498350 | A | G | 230 | a0001c0001t0001g0067 a0001c0001t0001g0106 a0001c0001t0001g0169 others(227): Show |
231 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.-3+3587A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498350 | |||||||
| chr5:180498571 | A | G | 113 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(110): Show |
113 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.-3+3808A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498571 | |||||||
| chr5:180498759 | C | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+3996C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498759 | |||||||
| chr5:180498834 | A | G | 115 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(112): Show |
115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-3+4071A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498834 | |||||||
| chr5:180498878 | C | T | 1 | a0001c0001t0055g0154 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-3+4115C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498878 | |||||||
| chr5:180498946 | C | G | 3 | a0001c0001t0024g0152 a0001c0001t0024g0158 a0001c0001t0030g0153 |
3 | HG01109.hp2 HG01346.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-3+4183C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180498946 | |||||||
| chr5:180499010 | T | C | 231 | a0001c0001t0001g0067 a0001c0001t0001g0106 a0001c0001t0001g0169 others(228): Show |
232 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.-3+4247T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499010 | |||||||
| chr5:180499070 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-3+4307C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499070 | |||||||
| chr5:180499107 | T | TTGGATAT others(6): Show |
1 | a0001c0001t0001g0321 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-3+4346_-3+4358dup others(13): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180499107 | ||||||
| chr5:180499141 | A | G | 1 | a0001c0001t0009g0207 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-3+4378A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499141 | |||||||
| chr5:180499175 | A | G | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-3+4412A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499175 | |||||||
| chr5:180499274 | G | A | 1 | a0001c0005t0004g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-3+4511G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499274 | |||||||
| chr5:180499288 | T | C | 58 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(55): Show |
58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+4525T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499288 | |||||||
| chr5:180499403 | G | T | 1 | a0001c0001t0039g0103 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-3+4640G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499403 | |||||||
| chr5:180499429 | G | C | 58 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(55): Show |
58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+4666G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499429 | |||||||
| chr5:180499479 | G | A | 5 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(2): Show |
6 | HG02818.hp1 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+4716G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499479 | |||||||
| chr5:180499657 | C | G | 1 | a0002c0004t0001g0318 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-3+4894C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499657 | |||||||
| chr5:180499693 | G | A | 1 | a0001c0001t0016g0014 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-3+4930G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499693 | |||||||
| chr5:180499789 | A | G | 1 | a0001c0001t0005g0114 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-3+5026A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499789 | |||||||
| chr5:180499839 | T | C | 51 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(48): Show |
51 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.-3+5076T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499839 | |||||||
| chr5:180499908 | G | A | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+5145G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499908 | |||||||
| chr5:180499943 | T | C | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+5180T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499943 | |||||||
| chr5:180499957 | C | T | 1 | a0001c0001t0006g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-3+5194C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180499957 | |||||||
| chr5:180500060 | G | A | 58 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(55): Show |
58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+5297G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500060 | |||||||
| chr5:180500106 | T | C | 1 | a0001c0001t0002g0021 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-3+5343T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500106 | |||||||
| chr5:180500106 | TC | T | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+5349delC | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180500106 | ||||||
| chr5:180500146 | T | C | 9 | a0001c0002t0005g0022 a0001c0002t0005g0023 a0001c0002t0005g0024 others(6): Show |
9 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3+5383T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500146 | |||||||
| chr5:180500233 | C | G | 1 | a0001c0001t0003g0208 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-3+5470C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500233 | |||||||
| chr5:180500303 | G | C | 51 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(48): Show |
51 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.-3+5540G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500303 | |||||||
| chr5:180500337 | C | A | 2 | a0001c0001t0049g0332 a0001c0005t0004g0020 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-3+5574C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500337 | |||||||
| chr5:180500439 | TTC | T | 49 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(46): Show |
49 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.-3+5678_-3+5679del others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180500439 | ||||||
| chr5:180500441 | C | CT | 207 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(204): Show |
208 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.-3+5692dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180500441 | ||||||
| chr5:180500442 | T | C | 49 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(46): Show |
49 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.-3+5679T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500442 | |||||||
| chr5:180500444 | T | TC | 62 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(59): Show |
62 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.-3+5681_-3+5682ins others(1): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500444 | |||||||
| chr5:180500530 | C | T | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-3+5767C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500530 | |||||||
| chr5:180500673 | A | G | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+5910A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500673 | |||||||
| chr5:180500727 | A | G | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-3+5964A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500727 | |||||||
| chr5:180500743 | G | C | 170 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(167): Show |
171 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.-3+5980G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500743 | |||||||
| chr5:180500838 | A | G | 54 | a0001c0001t0001g0067 a0001c0001t0002g0019 a0001c0001t0002g0021 others(51): Show |
54 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.-3+6075A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500838 | |||||||
| chr5:180500849 | G | T | 68 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(65): Show |
69 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.-3+6086G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180500849 | |||||||
| chr5:180501173 | C | T | 1 | a0001c0001t0009g0184 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-3+6410C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180501173 | |||||||
| chr5:180501243 | C | T | 1 | a0001c0001t0006g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-3+6480C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180501243 | |||||||
| chr5:180501383 | C | T | 115 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(112): Show |
115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-3+6620C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180501383 | |||||||
| chr5:180501391 | C | T | 18 | a0001c0001t0006g0137 a0001c0001t0006g0138 a0001c0001t0006g0139 others(15): Show |
18 | HG00609.hp2 HG01981.hp1 HG02004.hp2 others(15): Show |
intron_variant | MODIFIER | c.-3+6628C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180501391 | |||||||
| chr5:180501530 | A | G | 1 | a0001c0001t0025g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-3+6767A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180501530 | |||||||
| chr5:180501760 | A | G | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-3+6997A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180501760 | |||||||
| chr5:180501809 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-3+7046C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180501809 | |||||||
| chr5:180501920 | G | A | 1 | a0001c0001t0005g0225 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-3+7157G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180501920 | |||||||
| chr5:180501939 | T | C | 2 | a0001c0002t0002g0030 a0001c0002t0002g0031 |
2 | HG01069.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-3+7176T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180501939 | |||||||
| chr5:180502078 | A | G | 2 | a0001c0001t0031g0133 a0001c0001t0031g0134 |
2 | HG00733.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.-3+7315A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502078 | |||||||
| chr5:180502105 | G | A | 17 | a0001c0001t0001g0067 a0001c0001t0002g0019 a0001c0001t0002g0056 others(14): Show |
17 | HG00423.hp1 HG00621.hp1 NA18939.hp1 others(14): Show |
intron_variant | MODIFIER | c.-3+7342G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502105 | |||||||
| chr5:180502114 | T | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+7351T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502114 | |||||||
| chr5:180502139 | G | A | 58 | a0001c0001t0001g0067 a0001c0001t0001g0106 a0001c0001t0002g0019 others(55): Show |
58 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.-3+7376G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502139 | |||||||
| chr5:180502192 | C | T | 13 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(10): Show |
14 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3+7429C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502192 | |||||||
| chr5:180502204 | C | G | 3 | a0001c0001t0030g0132 a0001c0001t0031g0133 a0001c0001t0031g0134 |
3 | HG00733.hp2 HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.-3+7441C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502204 | |||||||
| chr5:180502206 | A | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+7443A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502206 | |||||||
| chr5:180502258 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-3+7495C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502258 | |||||||
| chr5:180502308 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-3+7545C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502308 | |||||||
| chr5:180502343 | C | T | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+7580C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502343 | |||||||
| chr5:180502364 | TAGA | T | 8 | a0001c0001t0001g0106 a0001c0001t0013g0104 a0001c0001t0013g0105 others(5): Show |
8 | HG01884.hp2 HG02717.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+7611_-3+7613del others(3): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180502364 | ||||||
| chr5:180502386 | A | C | 1 | a0001c0001t0003g0206 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-3+7623A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502386 | |||||||
| chr5:180502496 | T | C | 1 | a0001c0002t0004g0032 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-3+7733T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502496 | |||||||
| chr5:180502553 | ATAG | A | 18 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(15): Show |
19 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-3+7794_-3+7796del others(3): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180502553 | ||||||
| chr5:180502560 | C | G | 1 | a0001c0001t0005g0225 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-3+7797C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502560 | |||||||
| chr5:180502677 | T | TTAGC | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+7917_-3+7918ins others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180502677 | ||||||
| chr5:180502700 | A | AT | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-3+7938dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180502700 | ||||||
| chr5:180502768 | C | G | 1 | a0001c0001t0008g0316 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-3+8005C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502768 | |||||||
| chr5:180502772 | CAG | C | 6 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(3): Show |
6 | HG02258.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+8013_-3+8014del others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180502772 | ||||||
| chr5:180502825 | G | A | 51 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(48): Show |
51 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.-3+8062G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502825 | |||||||
| chr5:180502896 | A | G | 1 | a0001c0002t0004g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-3+8133A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502896 | |||||||
| chr5:180502919 | C | G | 18 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(15): Show |
19 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-3+8156C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180502919 | |||||||
| chr5:180503098 | A | G | 1 | a0001c0001t0043g0205 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-3+8335A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503098 | |||||||
| chr5:180503106 | C | G | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-3+8343C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503106 | |||||||
| chr5:180503262 | C | CT | 55 | a0001c0001t0001g0169 a0001c0001t0001g0317 a0001c0001t0002g0070 others(52): Show |
55 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.-3+8516dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180503262 | ||||||
| chr5:180503407 | G | T | 58 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(55): Show |
58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+8644G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503407 | |||||||
| chr5:180503427 | C | G | 1 | a0001c0001t0003g0212 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-3+8664C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503427 | |||||||
| chr5:180503511 | T | C | 115 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(112): Show |
115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-3+8748T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503511 | |||||||
| chr5:180503512 | G | A | 1 | a0001c0001t0007g0135 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-3+8749G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503512 | |||||||
| chr5:180503516 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-3+8753C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503516 | |||||||
| chr5:180503540 | T | C | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+8777T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503540 | |||||||
| chr5:180503601 | C | CT | 14 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(11): Show |
14 | HG00621.hp2 HG00741.hp1 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.-3+8862dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180503601 | ||||||
| chr5:180503601 | C | CTTT | 35 | a0001c0001t0006g0122 a0001c0001t0006g0124 a0001c0001t0006g0125 others(32): Show |
35 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.-3+8860_-3+8862dup others(3): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180503601 | ||||||
| chr5:180503601 | C | CTTTT | 8 | a0001c0001t0006g0009 a0001c0001t0006g0131 a0001c0001t0006g0147 others(5): Show |
8 | HG01123.hp1 HG02015.hp1 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+8859_-3+8862dup others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180503601 | ||||||
| chr5:180503601 | CT | C | 69 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0001g0235 others(66): Show |
69 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.-3+8862delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180503601 | ||||||
| chr5:180503601 | CTT | C | 82 | a0001c0001t0001g0067 a0001c0001t0001g0106 a0001c0001t0001g0169 others(79): Show |
82 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.-3+8861_-3+8862del others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180503601 | ||||||
| chr5:180503601 | CTTT | C | 6 | a0001c0001t0002g0071 a0001c0001t0002g0098 a0001c0001t0027g0187 others(3): Show |
6 | HG01169.hp2 HG02071.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+8860_-3+8862del others(3): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180503601 | ||||||
| chr5:180503698 | C | T | 1 | a0001c0001t0001g0303 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-3+8935C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503698 | |||||||
| chr5:180503709 | G | A | 1 | a0001c0001t0061g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-3+8946G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180503709 | |||||||
| chr5:180504010 | G | A | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+9247G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180504010 | |||||||
| chr5:180504046 | A | C | 9 | a0001c0002t0005g0022 a0001c0002t0005g0023 a0001c0002t0005g0024 others(6): Show |
9 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3+9283A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180504046 | |||||||
| chr5:180504194 | A | C | 5 | a0001c0001t0001g0298 a0001c0001t0001g0300 a0001c0001t0001g0301 others(2): Show |
5 | HG00597.hp2 HG02015.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3+9431A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180504194 | |||||||
| chr5:180504403 | G | A | 4 | a0001c0001t0024g0119 a0001c0001t0024g0152 a0001c0001t0024g0158 others(1): Show |
4 | HG01109.hp2 HG01168.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+9640G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180504403 | |||||||
| chr5:180504491 | C | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+9728C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180504491 | |||||||
| chr5:180504502 | CG | C | 58 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(55): Show |
58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+9744delG | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180504502 | ||||||
| chr5:180504672 | A | G | 5 | a0001c0001t0008g0294 a0001c0001t0008g0295 a0001c0001t0008g0296 others(2): Show |
5 | HG00735.hp2 HG01516.hp1 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3+9909A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180504672 | |||||||
| chr5:180504902 | C | T | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+10139C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180504902 | |||||||
| chr5:180504955 | A | AT | 8 | a0001c0001t0001g0292 a0001c0001t0001g0293 a0001c0001t0001g0311 others(5): Show |
8 | HG01346.hp1 HG01515.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+10214dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180504955 | ||||||
| chr5:180504955 | A | ATTT | 11 | a0001c0001t0003g0208 a0001c0001t0009g0211 a0001c0001t0010g0209 others(8): Show |
11 | HG00738.hp1 HG01515.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.-3+10212_-3+10214d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180504955 | ||||||
| chr5:180504955 | A | ATTTT | 38 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(35): Show |
38 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.-3+10211_-3+10214d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180504955 | ||||||
| chr5:180504955 | A | ATTTTT | 12 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0006g0147 others(9): Show |
12 | HG01168.hp2 HG02027.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+10210_-3+10214d others(7): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180504955 | ||||||
| chr5:180504955 | A | ATTTTTT | 40 | a0001c0001t0003g0182 a0001c0001t0006g0122 a0001c0001t0006g0124 others(37): Show |
40 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.-3+10209_-3+10214d others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180504955 | ||||||
| chr5:180504955 | A | ATTTTTTT | 8 | a0001c0001t0006g0009 a0001c0001t0006g0131 a0001c0001t0006g0151 others(5): Show |
8 | HG01123.hp1 HG01257.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+10208_-3+10214d others(9): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180504955 | ||||||
| chr5:180504955 | AT | A | 100 | a0001c0001t0001g0067 a0001c0001t0001g0237 a0001c0001t0001g0239 others(97): Show |
101 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.-3+10214delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180504955 | ||||||
| chr5:180504955 | ATT | A | 15 | a0001c0001t0002g0021 a0001c0001t0002g0071 a0001c0001t0040g0101 others(12): Show |
15 | HG01069.hp1 HG01891.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.-3+10213_-3+10214d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180504955 | ||||||
| chr5:180505117 | C | T | 1 | a0001c0001t0061g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-3+10354C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505117 | |||||||
| chr5:180505126 | T | A | 1 | a0001c0001t0002g0071 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-3+10363T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505126 | |||||||
| chr5:180505162 | G | A | 2 | a0001c0001t0015g0116 a0001c0001t0015g0120 |
2 | HG02965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-3+10399G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505162 | |||||||
| chr5:180505251 | A | AT | 16 | a0001c0001t0001g0233 a0001c0001t0001g0235 a0001c0001t0001g0236 others(13): Show |
16 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.-3+10510dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505251 | ||||||
| chr5:180505251 | A | ATT | 44 | a0001c0001t0001g0314 a0001c0001t0006g0009 a0001c0001t0006g0122 others(41): Show |
44 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.-3+10509_-3+10510d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505251 | ||||||
| chr5:180505251 | A | ATTT | 6 | a0001c0001t0007g0150 a0001c0001t0015g0013 a0001c0001t0015g0127 others(3): Show |
6 | HG01243.hp1 HG02055.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3+10508_-3+10510d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505251 | ||||||
| chr5:180505251 | AT | A | 109 | a0001c0001t0001g0106 a0001c0001t0002g0019 a0001c0001t0002g0021 others(106): Show |
110 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.-3+10510delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505251 | ||||||
| chr5:180505251 | ATT | A | 57 | a0001c0001t0001g0169 a0001c0001t0002g0056 a0001c0001t0002g0071 others(54): Show |
57 | HG00280.hp2 HG00639.hp2 HG00741.hp2 others(54): Show |
intron_variant | MODIFIER | c.-3+10509_-3+10510d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505251 | ||||||
| chr5:180505281 | A | G | 52 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(49): Show |
52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-3+10518A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505281 | |||||||
| chr5:180505294 | C | T | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+10531C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505294 | |||||||
| chr5:180505301 | T | G | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+10538T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505301 | |||||||
| chr5:180505305 | G | A | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+10542G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505305 | |||||||
| chr5:180505307 | C | G | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+10544C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505307 | |||||||
| chr5:180505318 | C | T | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+10555C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505318 | |||||||
| chr5:180505324 | C | T | 2 | a0001c0001t0029g0287 a0001c0001t0029g0288 |
2 | NA18969.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-3+10561C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505324 | |||||||
| chr5:180505325 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-3+10562G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505325 | |||||||
| chr5:180505328 | T | C | 1 | a0001c0001t0028g0242 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-3+10565T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505328 | |||||||
| chr5:180505382 | A | C | 4 | a0001c0002t0004g0032 a0001c0002t0004g0045 a0001c0002t0004g0046 others(1): Show |
4 | HG01167.hp1 HG02615.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+10619A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505382 | |||||||
| chr5:180505422 | A | AT | 6 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(3): Show |
6 | HG02258.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+10667dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505422 | ||||||
| chr5:180505477 | C | G | 58 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(55): Show |
58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+10714C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505477 | |||||||
| chr5:180505547 | A | AT | 35 | a0001c0001t0001g0301 a0001c0001t0001g0314 a0001c0001t0001g0328 others(32): Show |
36 | HG00733.hp1 HG01243.hp2 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.-3+10802dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505547 | ||||||
| chr5:180505547 | A | ATT | 98 | a0001c0001t0001g0169 a0001c0001t0002g0019 a0001c0001t0002g0021 others(95): Show |
98 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.-3+10801_-3+10802d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505547 | ||||||
| chr5:180505547 | AT | A | 6 | a0001c0001t0001g0243 a0001c0001t0001g0245 a0001c0001t0012g0244 others(3): Show |
6 | HG00099.hp1 HG01358.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+10802delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505547 | ||||||
| chr5:180505601 | G | A | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-3+10838G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505601 | |||||||
| chr5:180505612 | ATC | A | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-3+10852_-3+10853d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180505612 | ||||||
| chr5:180505633 | C | T | 1 | a0001c0001t0026g0222 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-3+10870C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505633 | |||||||
| chr5:180505687 | A | C | 4 | a0001c0001t0021g0159 a0001c0001t0021g0160 a0001c0001t0021g0161 others(1): Show |
4 | HG02071.hp2 HG02735.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+10924A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505687 | |||||||
| chr5:180505843 | C | T | 1 | a0001c0001t0017g0162 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-3+11080C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505843 | |||||||
| chr5:180505943 | A | G | 2 | a0001c0001t0002g0230 a0001c0002t0004g0054 |
2 | HG02165.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-3+11180A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505943 | |||||||
| chr5:180505975 | A | G | 1 | a0001c0001t0012g0113 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-3+11212A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180505975 | |||||||
| chr5:180506000 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-3+11237G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180506000 | |||||||
| chr5:180506207 | G | C | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+11444G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180506207 | |||||||
| chr5:180506359 | A | G | 2 | a0001c0001t0040g0101 a0001c0001t0041g0102 |
2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-3+11596A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180506359 | |||||||
| chr5:180506650 | T | G | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-3+11887T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180506650 | |||||||
| chr5:180506758 | A | G | 3 | a0001c0002t0005g0027 a0001c0002t0005g0028 a0001c0002t0005g0029 |
3 | HG02717.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-3+11995A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180506758 | |||||||
| chr5:180506920 | G | C | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+12157G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180506920 | |||||||
| chr5:180507151 | A | G | 58 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(55): Show |
58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+12388A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180507151 | |||||||
| chr5:180507325 | TGTG | T | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-3+12567_-3+12569d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180507325 | ||||||
| chr5:180507399 | A | G | 1 | a0001c0001t0057g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-3+12636A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180507399 | |||||||
| chr5:180507463 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-3+12700G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180507463 | |||||||
| chr5:180507559 | G | A | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+12796G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180507559 | |||||||
| chr5:180507580 | G | C | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+12817G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180507580 | |||||||
| chr5:180507615 | AG | A | 58 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(55): Show |
58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+12853delG | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180507615 | |||||||
| chr5:180507735 | A | C | 1 | a0001c0001t0009g0184 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-3+12972A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180507735 | |||||||
| chr5:180507778 | C | T | 47 | a0001c0001t0001g0067 a0001c0001t0002g0019 a0001c0001t0002g0021 others(44): Show |
47 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.-3+13015C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180507778 | |||||||
| chr5:180507818 | A | AAGGTGAA others(244): Show |
49 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(46): Show |
49 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.-3+13058_-3+13308d others(253): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180507818 | ||||||
| chr5:180507818 | A | AAGGTGAA others(495): Show |
1 | a0001c0001t0007g0130 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-3+13308_-3+13309i others(504): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180507818 | ||||||
| chr5:180507994 | C | G | 58 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(55): Show |
58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+13231C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180507994 | |||||||
| chr5:180508192 | T | G | 58 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(55): Show |
58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+13429T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508192 | |||||||
| chr5:180508293 | G | A | 7 | a0001c0002t0002g0039 a0001c0002t0004g0033 a0001c0002t0004g0034 others(4): Show |
7 | HG02280.hp2 HG02630.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+13530G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508293 | |||||||
| chr5:180508312 | A | AATTTGTT others(11): Show |
1 | a0001c0001t0061g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-3+13551_-3+13568d others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180508312 | ||||||
| chr5:180508419 | C | G | 10 | a0001c0001t0006g0145 a0001c0001t0006g0147 a0001c0001t0007g0135 others(7): Show |
10 | HG00609.hp2 HG02055.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3+13656C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508419 | |||||||
| chr5:180508477 | A | G | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-3+13714A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508477 | |||||||
| chr5:180508512 | G | T | 1 | a0001c0001t0001g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-3+13749G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508512 | |||||||
| chr5:180508531 | C | T | 3 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0009g0179 |
3 | HG03017.hp1 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-3+13768C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508531 | |||||||
| chr5:180508543 | C | T | 8 | a0001c0001t0001g0285 a0001c0001t0001g0304 a0001c0001t0001g0306 others(5): Show |
8 | HG00741.hp1 HG01074.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+13780C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508543 | |||||||
| chr5:180508601 | C | T | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-3+13838C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508601 | |||||||
| chr5:180508710 | T | A | 1 | a0001c0001t0019g0291 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-3+13947T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508710 | |||||||
| chr5:180508712 | T | A | 1 | a0001c0001t0019g0291 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-3+13949T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508712 | |||||||
| chr5:180508718 | G | T | 1 | a0001c0001t0019g0291 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-3+13955G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508718 | |||||||
| chr5:180508720 | T | G | 1 | a0001c0001t0019g0291 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-3+13957T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508720 | |||||||
| chr5:180508722 | A | G | 1 | a0001c0001t0019g0291 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-3+13959A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508722 | |||||||
| chr5:180508723 | A | T | 1 | a0001c0001t0019g0291 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-3+13960A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508723 | |||||||
| chr5:180508725 | C | T | 1 | a0001c0001t0019g0291 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-3+13962C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508725 | |||||||
| chr5:180508726 | A | T | 1 | a0001c0001t0019g0291 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-3+13963A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508726 | |||||||
| chr5:180508763 | C | T | 1 | a0001c0001t0003g0181 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-3+14000C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508763 | |||||||
| chr5:180508814 | TA | T | 5 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(2): Show |
5 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+14053delA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180508814 | ||||||
| chr5:180508815 | A | T | 1 | a0001c0001t0019g0291 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-3+14052A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508815 | |||||||
| chr5:180508816 | A | T | 5 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(2): Show |
5 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+14053A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508816 | |||||||
| chr5:180508818 | T | A | 5 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(2): Show |
5 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+14055T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508818 | |||||||
| chr5:180508818 | T | TTTA | 99 | a0001c0001t0001g0067 a0001c0001t0002g0019 a0001c0001t0002g0056 others(96): Show |
100 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.-3+14070_-3+14072d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180508818 | ||||||
| chr5:180508830 | A | ATT | 9 | a0001c0001t0007g0135 a0001c0001t0014g0175 a0001c0001t0014g0176 others(6): Show |
9 | HG00639.hp2 HG02257.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3+14068_-3+14069d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180508830 | ||||||
| chr5:180508833 | A | ATT | 98 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(95): Show |
98 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.-3+14078_-3+14079d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180508833 | ||||||
| chr5:180508833 | A | ATTT | 16 | a0001c0001t0001g0106 a0001c0001t0002g0021 a0001c0001t0013g0104 others(13): Show |
16 | HG01884.hp2 HG01891.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.-3+14077_-3+14079d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180508833 | ||||||
| chr5:180508833 | A | T | 14 | a0001c0001t0001g0245 a0001c0001t0007g0135 a0001c0001t0014g0175 others(11): Show |
14 | HG00099.hp1 HG00639.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.-3+14070A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508833 | |||||||
| chr5:180508885 | T | C | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+14122T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508885 | |||||||
| chr5:180508916 | G | A | 58 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(55): Show |
58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+14153G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508916 | |||||||
| chr5:180508954 | C | G | 51 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(48): Show |
51 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.-3+14191C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180508954 | |||||||
| chr5:180509168 | G | T | 3 | a0001c0001t0022g0224 a0001c0003t0022g0219 a0001c0003t0022g0221 |
3 | HG02055.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-3+14405G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180509168 | |||||||
| chr5:180509315 | T | C | 53 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(50): Show |
53 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.-3+14552T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180509315 | |||||||
| chr5:180509424 | C | T | 1 | a0001c0001t0024g0119 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-3+14661C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180509424 | |||||||
| chr5:180509695 | G | A | 3 | a0001c0001t0003g0171 a0001c0001t0003g0182 a0001c0001t0003g0185 |
3 | HG01358.hp2 HG01993.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-3+14932G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180509695 | |||||||
| chr5:180509737 | G | A | 8 | a0001c0002t0002g0030 a0001c0002t0002g0031 a0001c0002t0002g0040 others(5): Show |
8 | HG01069.hp1 HG01106.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+14974G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180509737 | |||||||
| chr5:180509803 | A | G | 1 | a0001c0002t0004g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-3+15040A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180509803 | |||||||
| chr5:180509825 | GGT | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+15065_-3+15066d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180509825 | ||||||
| chr5:180509828 | G | GT | 17 | a0001c0001t0001g0317 a0001c0001t0001g0327 a0001c0001t0002g0070 others(14): Show |
17 | HG01106.hp2 HG01123.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.-3+15083dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180509828 | ||||||
| chr5:180509828 | GT | G | 54 | a0001c0001t0001g0248 a0001c0001t0002g0075 a0001c0001t0002g0076 others(51): Show |
54 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.-3+15083delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180509828 | ||||||
| chr5:180509846 | T | C | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-3+15083T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180509846 | |||||||
| chr5:180509876 | A | G | 1 | a0001c0001t0061g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-3+15113A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180509876 | |||||||
| chr5:180509911 | C | G | 2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG01952.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-3+15148C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180509911 | |||||||
| chr5:180510091 | G | A | 1 | a0001c0001t0049g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3+15328G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510091 | |||||||
| chr5:180510123 | C | T | 6 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(3): Show |
6 | HG02258.hp2 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+15360C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510123 | |||||||
| chr5:180510134 | C | CT | 25 | a0001c0001t0001g0226 a0001c0001t0001g0232 a0001c0001t0001g0236 others(22): Show |
25 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.-3+15406dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | C | CTT | 14 | a0001c0001t0001g0239 a0001c0001t0001g0278 a0001c0001t0001g0292 others(11): Show |
14 | HG01256.hp2 HG01258.hp1 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.-3+15405_-3+15406d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | C | CTTT | 13 | a0001c0001t0001g0303 a0001c0001t0002g0021 a0001c0001t0002g0058 others(10): Show |
13 | HG01069.hp1 HG01123.hp2 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.-3+15404_-3+15406d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | C | CTTTT | 30 | a0001c0001t0001g0067 a0001c0001t0001g0293 a0001c0001t0001g0312 others(27): Show |
30 | HG00423.hp1 HG00642.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.-3+15403_-3+15406d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | C | CTTTTT | 21 | a0001c0001t0001g0240 a0001c0001t0002g0019 a0001c0001t0002g0060 others(18): Show |
21 | HG00597.hp1 HG00639.hp1 HG01361.hp1 others(18): Show |
intron_variant | MODIFIER | c.-3+15402_-3+15406d others(7): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | C | CTTTTTT | 9 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0066 others(6): Show |
9 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(6): Show |
intron_variant | MODIFIER | c.-3+15401_-3+15406d others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | C | CTTTTTTT others(1): Show |
8 | a0001c0001t0001g0241 a0001c0001t0001g0279 a0001c0001t0001g0280 others(5): Show |
8 | HG01069.hp2 HG01071.hp1 HG01993.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+15399_-3+15406d others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | C | CTTTTTTT others(4): Show |
3 | a0001c0001t0002g0076 a0001c0001t0008g0283 a0001c0001t0058g0094 |
3 | HG00609.hp1 HG02723.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.-3+15396_-3+15406d others(13): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0321 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-3+15394_-3+15406d others(15): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | CT | C | 7 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0223 others(4): Show |
8 | HG01884.hp1 HG02965.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.-3+15406delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | CTTTTT | C | 9 | a0001c0001t0003g0196 a0001c0001t0003g0202 a0001c0001t0009g0011 others(6): Show |
9 | HG00099.hp1 HG00738.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.-3+15402_-3+15406d others(7): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | CTTTTTT | C | 33 | a0001c0001t0003g0171 a0001c0001t0003g0189 a0001c0001t0003g0190 others(30): Show |
33 | HG00738.hp2 HG01071.hp2 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.-3+15401_-3+15406d others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | CTTTTTTT | C | 49 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0173 others(46): Show |
49 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.-3+15400_-3+15406d others(9): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | CTTTTTTT others(1): Show |
C | 10 | a0001c0001t0006g0157 a0001c0001t0014g0168 a0001c0001t0014g0175 others(7): Show |
10 | HG00280.hp2 HG00639.hp2 HG01168.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3+15399_-3+15406d others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | CTTTTTTT others(3): Show |
C | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG02258.hp2 HG02622.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+15397_-3+15406d others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | CTTTTTTT others(4): Show |
C | 8 | a0001c0002t0005g0022 a0001c0002t0005g0023 a0001c0002t0005g0024 others(5): Show |
8 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+15396_-3+15406d others(13): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0049g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3+15395_-3+15406d others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | CTTTTTTT others(6): Show |
C | 7 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0315 others(4): Show |
7 | HG00544.hp1 HG00544.hp2 HG00621.hp2 others(4): Show |
intron_variant | MODIFIER | c.-3+15394_-3+15406d others(15): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0021g0159 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-3+15393_-3+15406d others(16): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | CTTTTTTT others(8): Show |
C | 5 | a0001c0001t0001g0106 a0001c0001t0001g0247 a0001c0001t0013g0105 others(2): Show |
5 | HG01884.hp2 HG02818.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+15392_-3+15406d others(17): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0001g0248 a0001c0001t0013g0104 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-3+15391_-3+15406d others(18): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | CTTTTTTT others(10): Show |
C | 2 | a0002c0004t0001g0318 a0002c0004t0004g0249 |
2 | NA18966.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-3+15390_-3+15406d others(19): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510134 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0057g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-3+15389_-3+15406d others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180510134 | ||||||
| chr5:180510179 | T | C | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+15416T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510179 | |||||||
| chr5:180510231 | G | C | 115 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(112): Show |
115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-3+15468G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510231 | |||||||
| chr5:180510474 | A | G | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+15711A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510474 | |||||||
| chr5:180510560 | G | A | 5 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(2): Show |
6 | HG02818.hp1 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+15797G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510560 | |||||||
| chr5:180510661 | C | T | 58 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(55): Show |
58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+15898C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510661 | |||||||
| chr5:180510665 | A | G | 1 | a0001c0001t0016g0330 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-3+15902A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510665 | |||||||
| chr5:180510749 | G | C | 2 | a0001c0001t0025g0216 a0001c0001t0038g0217 |
2 | HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-3+15986G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510749 | |||||||
| chr5:180510854 | G | C | 1 | a0001c0001t0023g0204 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-3+16091G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180510854 | |||||||
| chr5:180511094 | C | T | 4 | a0001c0001t0014g0168 a0001c0001t0014g0175 a0001c0001t0014g0176 others(1): Show |
4 | HG00280.hp2 HG00639.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+16331C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511094 | |||||||
| chr5:180511121 | G | A | 2 | a0001c0001t0010g0188 a0001c0001t0010g0195 |
2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-3+16358G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511121 | |||||||
| chr5:180511186 | A | T | 161 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(158): Show |
161 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.-3+16423A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511186 | |||||||
| chr5:180511298 | T | C | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-3+16535T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511298 | |||||||
| chr5:180511317 | A | C | 1 | a0001c0001t0017g0167 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-3+16554A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511317 | |||||||
| chr5:180511382 | C | T | 58 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(55): Show |
58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-3+16619C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511382 | |||||||
| chr5:180511670 | T | C | 1 | a0001c0001t0016g0330 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-3+16907T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511670 | |||||||
| chr5:180511732 | C | T | 1 | a0001c0001t0006g0323 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-3+16969C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511732 | |||||||
| chr5:180511808 | G | A | 49 | a0001c0001t0001g0067 a0001c0001t0002g0019 a0001c0001t0002g0021 others(46): Show |
49 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.-3+17045G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511808 | |||||||
| chr5:180511856 | A | G | 3 | a0001c0002t0005g0027 a0001c0002t0005g0028 a0001c0002t0005g0029 |
3 | HG02717.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-3+17093A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511856 | |||||||
| chr5:180511869 | A | T | 3 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0009g0179 |
3 | HG03017.hp1 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-3+17106A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511869 | |||||||
| chr5:180511876 | C | T | 1 | a0001c0001t0007g0141 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-3+17113C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511876 | |||||||
| chr5:180511884 | G | A | 161 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(158): Show |
161 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.-3+17121G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511884 | |||||||
| chr5:180511899 | G | A | 51 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(48): Show |
51 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.-3+17136G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180511899 | |||||||
| chr5:180512191 | G | A | 1 | a0001c0001t0017g0163 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-2-17084G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180512191 | |||||||
| chr5:180512349 | G | C | 1 | a0001c0001t0018g0005 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-2-16926G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180512349 | |||||||
| chr5:180512394 | G | A | 9 | a0001c0002t0005g0022 a0001c0002t0005g0023 a0001c0002t0005g0024 others(6): Show |
9 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-16881G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180512394 | |||||||
| chr5:180512658 | G | A | 6 | a0001c0001t0003g0171 a0001c0001t0003g0180 a0001c0001t0003g0181 others(3): Show |
6 | HG01358.hp2 HG01993.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-16617G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180512658 | |||||||
| chr5:180512744 | G | T | 1 | a0001c0001t0032g0129 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.-2-16531G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180512744 | |||||||
| chr5:180512789 | G | A | 9 | a0001c0002t0005g0022 a0001c0002t0005g0023 a0001c0002t0005g0024 others(6): Show |
9 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-2-16486G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180512789 | |||||||
| chr5:180512926 | T | A | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-2-16349T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180512926 | |||||||
| chr5:180512958 | C | T | 2 | a0001c0001t0001g0311 a0001c0003t0022g0221 |
2 | HG02055.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.-2-16317C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180512958 | |||||||
| chr5:180512991 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2-16284G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180512991 | |||||||
| chr5:180513035 | A | G | 2 | a0001c0001t0001g0240 a0001c0001t0001g0312 |
2 | HG01515.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-2-16240A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180513035 | |||||||
| chr5:180513036 | C | A | 1 | a0001c0005t0004g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-2-16239C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180513036 | |||||||
| chr5:180513044 | C | T | 58 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(55): Show |
58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-2-16231C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180513044 | |||||||
| chr5:180513091 | A | G | 296 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(293): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-2-16184A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180513091 | |||||||
| chr5:180513221 | T | A | 1 | a0001c0001t0013g0254 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-2-16054T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180513221 | |||||||
| chr5:180513228 | C | T | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-2-16047C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180513228 | |||||||
| chr5:180513410 | G | A | 2 | a0001c0001t0001g0237 a0001c0001t0001g0271 |
2 | NA19075.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-2-15865G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180513410 | |||||||
| chr5:180513520 | C | G | 1 | a0001c0001t0002g0086 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-2-15755C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180513520 | |||||||
| chr5:180513673 | TTTTATTT others(5): Show |
T | 58 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(55): Show |
58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-2-15586_-2-15575d others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180513673 | ||||||
| chr5:180513699 | T | TTATTTAT others(9): Show |
4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-15575_-2-15574i others(18): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180513699 | ||||||
| chr5:180513699 | T | TTTTA | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-15560_-2-15557d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180513699 | ||||||
| chr5:180513896 | G | A | 2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG01952.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-2-15379G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180513896 | |||||||
| chr5:180514070 | C | G | 1 | a0001c0001t0006g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-2-15205C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514070 | |||||||
| chr5:180514165 | C | T | 1 | a0001c0001t0023g0204 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-2-15110C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514165 | |||||||
| chr5:180514180 | T | C | 1 | a0001c0001t0001g0239 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-2-15095T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514180 | |||||||
| chr5:180514190 | G | A | 115 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(112): Show |
115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-2-15085G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514190 | |||||||
| chr5:180514195 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-2-15080G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514195 | |||||||
| chr5:180514242 | T | C | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-2-15033T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514242 | |||||||
| chr5:180514274 | C | A | 58 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(55): Show |
58 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(55): Show |
intron_variant | MODIFIER | c.-2-15001C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514274 | |||||||
| chr5:180514284 | T | G | 4 | a0001c0001t0019g0255 a0001c0001t0019g0256 a0001c0001t0019g0284 others(1): Show |
4 | NA18947.hp1 NA18967.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-14991T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514284 | |||||||
| chr5:180514295 | G | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0226 a0001c0001t0001g0228 others(97): Show |
100 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.-2-14980G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514295 | |||||||
| chr5:180514401 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-2-14874G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514401 | |||||||
| chr5:180514409 | G | A | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-14866G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514409 | |||||||
| chr5:180514643 | G | A | 1 | a0001c0001t0008g0283 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-2-14632G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514643 | |||||||
| chr5:180514646 | T | C | 115 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(112): Show |
115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-2-14629T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514646 | |||||||
| chr5:180514728 | G | A | 1 | a0001c0001t0008g0295 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-2-14547G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180514728 | |||||||
| chr5:180514872 | G | GA | 4 | a0001c0001t0033g0074 a0001c0001t0033g0095 a0001c0001t0062g0073 others(1): Show |
4 | HG01243.hp2 HG02258.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-14396dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180514872 | ||||||
| chr5:180515256 | CA | C | 54 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(51): Show |
54 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.-2-14008delA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180515256 | ||||||
| chr5:180515395 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0226 a0001c0001t0001g0228 others(97): Show |
100 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.-2-13880C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180515395 | |||||||
| chr5:180515452 | ATAGT | A | 103 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(100): Show |
103 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.-2-13819_-2-13816d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180515452 | ||||||
| chr5:180515464 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0226 a0001c0001t0001g0228 others(98): Show |
101 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.-2-13811G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180515464 | |||||||
| chr5:180515660 | A | G | 2 | a0001c0001t0025g0216 a0001c0001t0038g0217 |
2 | HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-2-13615A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180515660 | |||||||
| chr5:180515687 | G | A | 1 | a0001c0001t0049g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-2-13588G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180515687 | |||||||
| chr5:180515714 | C | T | 3 | a0001c0001t0006g0145 a0001c0001t0006g0147 a0001c0001t0007g0135 |
3 | NA18978.hp1 NA19080.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-2-13561C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180515714 | |||||||
| chr5:180515762 | T | G | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-13513T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180515762 | |||||||
| chr5:180515914 | A | T | 1 | a0001c0001t0009g0184 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-2-13361A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180515914 | |||||||
| chr5:180516182 | A | AT | 53 | a0001c0001t0001g0067 a0001c0001t0001g0305 a0001c0001t0001g0321 others(50): Show |
53 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.-2-13076dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180516182 | ||||||
| chr5:180516182 | AT | A | 106 | a0001c0001t0001g0169 a0001c0001t0001g0233 a0001c0001t0001g0235 others(103): Show |
106 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.-2-13076delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180516182 | ||||||
| chr5:180516182 | ATT | A | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-13077_-2-13076d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180516182 | ||||||
| chr5:180516205 | G | A | 2 | a0002c0004t0001g0318 a0002c0004t0004g0249 |
2 | NA18966.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.-2-13070G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516205 | |||||||
| chr5:180516292 | T | C | 3 | a0001c0001t0001g0258 a0001c0001t0012g0252 a0001c0001t0012g0320 |
3 | HG02273.hp1 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-2-12983T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516292 | |||||||
| chr5:180516310 | G | A | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-2-12965G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516310 | |||||||
| chr5:180516329 | G | A | 3 | a0001c0001t0001g0002 a0001c0001t0034g0002 a0001c0001t0045g0331 |
3 | HG02630.hp1 NA19004.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.-2-12946G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516329 | |||||||
| chr5:180516380 | A | C | 1 | a0001c0001t0002g0061 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-2-12895A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516380 | |||||||
| chr5:180516423 | G | A | 119 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(116): Show |
119 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.-2-12852G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516423 | |||||||
| chr5:180516502 | G | T | 1 | a0001c0001t0016g0330 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-2-12773G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516502 | |||||||
| chr5:180516584 | A | T | 115 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(112): Show |
115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-2-12691A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516584 | |||||||
| chr5:180516587 | C | T | 1 | a0001c0002t0004g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-2-12688C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516587 | |||||||
| chr5:180516634 | A | T | 57 | a0001c0001t0001g0067 a0001c0001t0001g0106 a0001c0001t0002g0019 others(54): Show |
57 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.-2-12641A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516634 | |||||||
| chr5:180516709 | T | C | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-12566T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516709 | |||||||
| chr5:180516774 | C | A | 1 | a0001c0001t0002g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-2-12501C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516774 | |||||||
| chr5:180516790 | T | C | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-12485T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516790 | |||||||
| chr5:180516816 | C | T | 1 | a0001c0003t0022g0221 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-2-12459C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516816 | |||||||
| chr5:180516955 | A | G | 36 | a0001c0001t0006g0137 a0001c0001t0006g0138 a0001c0001t0006g0139 others(33): Show |
36 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.-2-12320A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516955 | |||||||
| chr5:180516978 | C | T | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-12297C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180516978 | |||||||
| chr5:180517005 | A | AG | 8 | a0001c0001t0001g0259 a0001c0001t0001g0306 a0001c0001t0003g0185 others(5): Show |
8 | HG00741.hp1 HG00741.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-12265dupG | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180517005 | ||||||
| chr5:180517082 | T | C | 3 | a0001c0001t0022g0224 a0001c0003t0022g0219 a0001c0003t0022g0221 |
3 | HG02055.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-2-12193T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517082 | |||||||
| chr5:180517276 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-2-11999G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517276 | |||||||
| chr5:180517310 | G | A | 101 | a0001c0001t0001g0002 a0001c0001t0001g0226 a0001c0001t0001g0228 others(98): Show |
101 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.-2-11965G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517310 | |||||||
| chr5:180517363 | A | G | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-11912A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517363 | |||||||
| chr5:180517684 | C | G | 6 | a0001c0001t0005g0114 a0001c0001t0005g0270 a0001c0001t0019g0255 others(3): Show |
6 | HG03834.hp2 NA18947.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-11591C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517684 | |||||||
| chr5:180517782 | TC | T | 61 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(58): Show |
61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.-2-11491delC | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180517782 | ||||||
| chr5:180517821 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-2-11454C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517821 | |||||||
| chr5:180517841 | C | T | 2 | a0001c0001t0013g0107 a0001c0001t0013g0108 |
2 | HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2-11434C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517841 | |||||||
| chr5:180517879 | A | T | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-2-11396A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517879 | |||||||
| chr5:180517892 | G | C | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-2-11383G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517892 | |||||||
| chr5:180517939 | C | T | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-11336C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517939 | |||||||
| chr5:180517965 | G | A | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-11310G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180517965 | |||||||
| chr5:180518008 | CCCTCTCT others(3): Show |
C | 112 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(109): Show |
112 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.-2-11265_-2-11256d others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180518008 | ||||||
| chr5:180518042 | C | T | 1 | a0001c0001t0028g0326 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-2-11233C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518042 | |||||||
| chr5:180518094 | T | C | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-11181T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518094 | |||||||
| chr5:180518251 | T | C | 1 | a0001c0001t0006g0131 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-2-11024T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518251 | |||||||
| chr5:180518259 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-2-11016C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518259 | |||||||
| chr5:180518334 | G | A | 115 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(112): Show |
115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-2-10941G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518334 | |||||||
| chr5:180518336 | C | G | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-10939C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518336 | |||||||
| chr5:180518504 | T | G | 14 | a0001c0001t0003g0189 a0001c0001t0003g0190 a0001c0001t0003g0201 others(11): Show |
14 | HG00738.hp2 HG01071.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-10771T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518504 | |||||||
| chr5:180518589 | G | A | 1 | a0001c0001t0063g0229 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-2-10686G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518589 | |||||||
| chr5:180518801 | C | T | 2 | a0001c0001t0003g0171 a0001c0001t0003g0185 |
2 | HG01993.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-2-10474C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518801 | |||||||
| chr5:180518827 | C | T | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-2-10448C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518827 | |||||||
| chr5:180518865 | C | CT | 5 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(2): Show |
6 | HG02818.hp1 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-10408dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180518865 | ||||||
| chr5:180518933 | G | A | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-10342G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180518933 | |||||||
| chr5:180519059 | A | G | 61 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(58): Show |
61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.-2-10216A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519059 | |||||||
| chr5:180519077 | A | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-10198A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519077 | |||||||
| chr5:180519108 | G | A | 5 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(2): Show |
5 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-10167G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519108 | |||||||
| chr5:180519289 | G | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-9986G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519289 | |||||||
| chr5:180519311 | T | C | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-9964T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519311 | |||||||
| chr5:180519496 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-2-9779G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519496 | |||||||
| chr5:180519505 | T | C | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-9770T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519505 | |||||||
| chr5:180519560 | T | C | 3 | a0001c0001t0001g0233 a0001c0001t0001g0236 a0001c0001t0008g0234 |
3 | NA18944.hp2 NA18959.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.-2-9715T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519560 | |||||||
| chr5:180519762 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-2-9513G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519762 | |||||||
| chr5:180519766 | C | CT | 60 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(57): Show |
60 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.-2-9497dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180519766 | ||||||
| chr5:180519766 | CT | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0226 a0001c0001t0001g0228 others(99): Show |
102 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.-2-9497delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180519766 | ||||||
| chr5:180519806 | A | G | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-9469A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519806 | |||||||
| chr5:180519833 | C | CTT | 51 | a0001c0001t0001g0067 a0001c0001t0001g0278 a0001c0001t0002g0019 others(48): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.-2-9428_-2-9427dup others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180519833 | ||||||
| chr5:180519833 | CT | C | 105 | a0001c0001t0001g0169 a0001c0001t0001g0233 a0001c0001t0002g0177 others(102): Show |
105 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.-2-9427delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180519833 | ||||||
| chr5:180519833 | CTT | C | 10 | a0001c0001t0015g0127 a0001c0001t0015g0128 a0001c0001t0017g0162 others(7): Show |
10 | HG01243.hp1 HG01243.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-9428_-2-9427del others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180519833 | ||||||
| chr5:180519941 | C | T | 1 | a0001c0001t0009g0184 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-2-9334C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519941 | |||||||
| chr5:180519974 | T | C | 1 | a0001c0001t0023g0204 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-2-9301T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180519974 | |||||||
| chr5:180520061 | T | G | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-9214T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180520061 | |||||||
| chr5:180520073 | A | G | 1 | a0001c0002t0004g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-2-9202A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180520073 | |||||||
| chr5:180520151 | T | G | 3 | a0001c0001t0025g0216 a0001c0001t0026g0222 a0001c0001t0038g0217 |
3 | HG01261.hp1 HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-2-9124T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180520151 | |||||||
| chr5:180520185 | A | G | 2 | a0001c0001t0001g0241 a0001c0001t0001g0282 |
2 | NA18941.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-2-9090A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180520185 | |||||||
| chr5:180520251 | AAAGAGTT others(7): Show |
A | 52 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(49): Show |
52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.-2-9012_-2-8999del others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180520251 | ||||||
| chr5:180520469 | C | A | 1 | a0001c0001t0009g0015 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-2-8806C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180520469 | |||||||
| chr5:180520851 | T | A | 330 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(327): Show |
331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.-2-8424T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180520851 | |||||||
| chr5:180520873 | C | T | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-8402C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180520873 | |||||||
| chr5:180521008 | A | G | 1 | a0001c0001t0057g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-2-8267A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180521008 | |||||||
| chr5:180521067 | G | A | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-8208G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180521067 | |||||||
| chr5:180521547 | A | C | 1 | a0001c0001t0005g0225 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-2-7728A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180521547 | |||||||
| chr5:180521558 | T | A | 2 | a0001c0001t0005g0225 a0001c0002t0002g0044 |
2 | HG01123.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-2-7717T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180521558 | |||||||
| chr5:180521748 | G | A | 115 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(112): Show |
115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-2-7527G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180521748 | |||||||
| chr5:180521754 | A | G | 1 | a0001c0001t0019g0256 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.-2-7521A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180521754 | |||||||
| chr5:180521874 | C | G | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2-7401C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180521874 | |||||||
| chr5:180522029 | A | G | 6 | a0001c0001t0003g0192 a0001c0001t0003g0196 a0001c0001t0003g0289 others(3): Show |
6 | HG02027.hp1 NA18612.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-7246A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522029 | |||||||
| chr5:180522041 | T | G | 1 | a0001c0002t0004g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-2-7234T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522041 | |||||||
| chr5:180522090 | G | T | 1 | a0001c0001t0003g0208 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-2-7185G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522090 | |||||||
| chr5:180522109 | TTATCTGT others(13): Show |
T | 1 | a0002c0004t0004g0249 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-2-7156_-2-7137del others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180522109 | ||||||
| chr5:180522156 | C | T | 1 | a0001c0001t0025g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-2-7119C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522156 | |||||||
| chr5:180522256 | T | C | 1 | a0001c0001t0021g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-2-7019T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522256 | |||||||
| chr5:180522297 | T | G | 78 | a0001c0001t0001g0002 a0001c0001t0001g0226 a0001c0001t0001g0228 others(75): Show |
78 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.-2-6978T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522297 | |||||||
| chr5:180522304 | G | T | 1 | a0001c0001t0006g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-2-6971G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522304 | |||||||
| chr5:180522316 | T | C | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-6959T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522316 | |||||||
| chr5:180522366 | G | A | 4 | a0001c0001t0001g0298 a0001c0001t0001g0300 a0001c0001t0008g0302 others(1): Show |
4 | HG00597.hp2 HG02027.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-6909G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522366 | |||||||
| chr5:180522532 | TGTTA | T | 3 | a0001c0001t0030g0132 a0001c0001t0031g0133 a0001c0001t0031g0134 |
3 | HG00733.hp2 HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.-2-6739_-2-6736del others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180522532 | ||||||
| chr5:180522797 | C | T | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-2-6478C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522797 | |||||||
| chr5:180522804 | G | C | 1 | a0001c0001t0001g0243 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-2-6471G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522804 | |||||||
| chr5:180522831 | C | T | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-6444C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522831 | |||||||
| chr5:180522907 | C | T | 1 | a0001c0001t0025g0218 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-2-6368C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522907 | |||||||
| chr5:180522923 | G | A | 2 | a0001c0001t0040g0101 a0001c0001t0041g0102 |
2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-6352G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180522923 | |||||||
| chr5:180523023 | A | G | 50 | a0001c0001t0001g0067 a0001c0001t0002g0019 a0001c0001t0002g0021 others(47): Show |
50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.-2-6252A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180523023 | |||||||
| chr5:180523066 | G | A | 1 | a0001c0005t0004g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-2-6209G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180523066 | |||||||
| chr5:180523220 | G | A | 1 | a0001c0001t0001g0245 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-2-6055G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180523220 | |||||||
| chr5:180523301 | T | C | 3 | a0001c0001t0025g0216 a0001c0001t0026g0222 a0001c0001t0038g0217 |
3 | HG01261.hp1 HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-2-5974T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180523301 | |||||||
| chr5:180523448 | C | G | 2 | a0001c0001t0006g0139 a0001c0001t0006g0148 |
2 | NA18995.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-2-5827C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180523448 | |||||||
| chr5:180523452 | A | AT | 55 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(52): Show |
55 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.-2-5820dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180523452 | ||||||
| chr5:180523726 | C | T | 1 | a0001c0001t0006g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-2-5549C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180523726 | |||||||
| chr5:180523776 | G | T | 3 | a0001c0001t0009g0015 a0001c0001t0009g0016 a0001c0001t0010g0017 |
3 | NA18957.hp2 NA18980.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-2-5499G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180523776 | |||||||
| chr5:180523873 | G | A | 3 | a0001c0002t0005g0027 a0001c0002t0005g0028 a0001c0002t0005g0029 |
3 | HG02717.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-2-5402G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180523873 | |||||||
| chr5:180524180 | C | A | 4 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0063 others(1): Show |
4 | NA18955.hp2 NA18960.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-5095C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524180 | |||||||
| chr5:180524183 | T | C | 1 | a0001c0001t0041g0102 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-2-5092T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524183 | |||||||
| chr5:180524250 | T | A | 1 | a0001c0001t0041g0102 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-2-5025T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524250 | |||||||
| chr5:180524273 | G | A | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-5002G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524273 | |||||||
| chr5:180524366 | C | G | 1 | a0001c0001t0030g0132 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-2-4909C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524366 | |||||||
| chr5:180524405 | T | G | 2 | a0001c0001t0006g0139 a0001c0001t0006g0148 |
2 | NA18995.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-2-4870T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524405 | |||||||
| chr5:180524574 | C | T | 115 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(112): Show |
115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-2-4701C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524574 | |||||||
| chr5:180524789 | A | G | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-2-4486A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524789 | |||||||
| chr5:180524801 | C | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-4474C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524801 | |||||||
| chr5:180524994 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-2-4281G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180524994 | |||||||
| chr5:180525057 | GTGTT | G | 58 | a0001c0001t0001g0067 a0001c0001t0001g0106 a0001c0001t0002g0019 others(55): Show |
58 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.-2-4213_-2-4210del others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180525057 | ||||||
| chr5:180525080 | AT | A | 5 | a0001c0001t0001g0106 a0001c0001t0013g0104 a0001c0001t0013g0105 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-4188delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180525080 | ||||||
| chr5:180525114 | A | C | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-4161A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525114 | |||||||
| chr5:180525275 | G | A | 1 | a0001c0001t0024g0158 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-2-4000G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525275 | |||||||
| chr5:180525431 | C | T | 1 | a0001c0001t0061g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-2-3844C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525431 | |||||||
| chr5:180525437 | G | T | 1 | a0001c0001t0006g0145 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-2-3838G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525437 | |||||||
| chr5:180525442 | G | A | 5 | a0001c0001t0001g0106 a0001c0001t0013g0104 a0001c0001t0013g0105 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-3833G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525442 | |||||||
| chr5:180525538 | C | CA | 11 | a0001c0001t0001g0247 a0001c0001t0001g0305 a0001c0001t0002g0078 others(8): Show |
11 | HG01069.hp2 HG01167.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2-3720dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180525538 | ||||||
| chr5:180525538 | CA | C | 12 | a0001c0001t0001g0169 a0001c0001t0002g0060 a0001c0001t0002g0071 others(9): Show |
12 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-3720delA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180525538 | ||||||
| chr5:180525543 | A | C | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-3732A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525543 | |||||||
| chr5:180525634 | G | A | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-3641G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525634 | |||||||
| chr5:180525727 | A | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-3548A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525727 | |||||||
| chr5:180525811 | G | A | 1 | a0001c0001t0003g0289 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-2-3464G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525811 | |||||||
| chr5:180525822 | C | T | 1 | a0001c0001t0010g0194 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-2-3453C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525822 | |||||||
| chr5:180525828 | C | T | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-2-3447C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525828 | |||||||
| chr5:180525881 | C | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-3394C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525881 | |||||||
| chr5:180525920 | T | TA | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-3355_-2-3354ins others(1): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525920 | |||||||
| chr5:180525921 | T | A | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.-2-3354T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180525921 | |||||||
| chr5:180525921 | T | TA | 7 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(4): Show |
7 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-3345dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180525921 | ||||||
| chr5:180526047 | C | T | 2 | a0001c0001t0007g0149 a0001c0001t0007g0150 |
2 | NA18973.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-2-3228C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180526047 | |||||||
| chr5:180526048 | C | G | 296 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(293): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.-2-3227C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180526048 | |||||||
| chr5:180526053 | A | G | 1 | a0001c0001t0003g0206 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-2-3222A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180526053 | |||||||
| chr5:180526078 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0282 |
2 | NA18941.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.-2-3197C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180526078 | |||||||
| chr5:180526226 | TGA | T | 61 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(58): Show |
61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.-2-3044_-2-3043del others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180526226 | ||||||
| chr5:180526275 | T | C | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-3000T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180526275 | |||||||
| chr5:180526402 | G | A | 1 | a0001c0001t0007g0130 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-2-2873G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180526402 | |||||||
| chr5:180526617 | C | A | 1 | a0001c0001t0009g0200 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-2-2658C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180526617 | |||||||
| chr5:180526646 | T | G | 61 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(58): Show |
61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.-2-2629T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180526646 | |||||||
| chr5:180526883 | CT | C | 118 | a0001c0001t0001g0169 a0001c0001t0001g0235 a0001c0001t0002g0177 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-2-2375delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180526883 | ||||||
| chr5:180526982 | C | T | 2 | a0001c0001t0013g0107 a0001c0001t0013g0108 |
2 | HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-2-2293C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180526982 | |||||||
| chr5:180527092 | C | G | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2-2183C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527092 | |||||||
| chr5:180527232 | C | A | 1 | a0001c0001t0001g0304 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-2-2043C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527232 | |||||||
| chr5:180527284 | T | G | 20 | a0001c0001t0001g0241 a0001c0001t0001g0265 a0001c0001t0001g0266 others(17): Show |
20 | HG00423.hp2 HG00642.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.-2-1991T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527284 | |||||||
| chr5:180527352 | A | G | 2 | a0001c0001t0001g0169 a0001c0001t0002g0177 |
2 | NA18955.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-2-1923A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527352 | |||||||
| chr5:180527394 | G | A | 61 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(58): Show |
61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.-2-1881G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527394 | |||||||
| chr5:180527406 | G | A | 17 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(14): Show |
18 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-2-1869G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527406 | |||||||
| chr5:180527615 | A | C | 17 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(14): Show |
18 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-2-1660A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527615 | |||||||
| chr5:180527687 | G | A | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1588G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527687 | |||||||
| chr5:180527840 | C | T | 1 | a0001c0002t0005g0329 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-2-1435C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527840 | |||||||
| chr5:180527896 | C | G | 1 | a0001c0001t0039g0103 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-2-1379C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527896 | |||||||
| chr5:180527936 | G | A | 1 | a0001c0001t0007g0144 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-2-1339G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527936 | |||||||
| chr5:180527937 | T | C | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-2-1338T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527937 | |||||||
| chr5:180527994 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-2-1281C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180527994 | |||||||
| chr5:180528073 | C | T | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-2-1202C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180528073 | |||||||
| chr5:180528089 | A | AT | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-2-1186_-2-1185ins others(1): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180528089 | |||||||
| chr5:180528144 | A | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-1131A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180528144 | |||||||
| chr5:180528303 | A | AT | 3 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0009g0179 |
3 | HG03017.hp1 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-2-970dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180528303 | ||||||
| chr5:180528398 | C | T | 1 | a0001c0001t0006g0131 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-2-877C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180528398 | |||||||
| chr5:180528644 | C | T | 1 | a0001c0001t0007g0140 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-2-631C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180528644 | |||||||
| chr5:180528798 | T | G | 1 | a0001c0001t0024g0152 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-2-477T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180528798 | |||||||
| chr5:180528876 | T | G | 53 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(50): Show |
53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.-2-399T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180528876 | |||||||
| chr5:180528933 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-2-342G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180528933 | |||||||
| chr5:180529037 | C | T | 2 | a0001c0001t0001g0248 a0001c0001t0045g0331 |
2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-2-238C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180529037 | |||||||
| chr5:180529042 | G | C | 115 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(112): Show |
115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.-2-233G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180529042 | |||||||
| chr5:180529082 | G | A | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-193G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | chr5 | 180529082 | |||||||
| chr5:180529144 | G | GC | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-2-129dupC | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180529144 | ||||||
| chr5:180529197 | C | CA | 23 | a0001c0001t0001g0279 a0001c0001t0006g0137 a0001c0001t0006g0323 others(20): Show |
24 | HG01884.hp1 HG01981.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.-2-62dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180529197 | ||||||
| chr5:180529197 | C | CAAA | 53 | a0001c0001t0002g0177 a0001c0001t0003g0171 a0001c0001t0003g0173 others(50): Show |
53 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.-2-64_-2-62dupAAA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr5 | 180529197 | ||||||
| chr5:180529622 | C | A | 52 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(49): Show |
52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.112+234C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180529622 | |||||||
| chr5:180529629 | C | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+241C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180529629 | |||||||
| chr5:180529948 | T | C | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+560T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180529948 | |||||||
| chr5:180529952 | A | G | 2 | a0001c0001t0003g0173 a0001c0001t0037g0172 |
2 | HG00741.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.112+564A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180529952 | |||||||
| chr5:180530182 | G | T | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+794G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180530182 | |||||||
| chr5:180530283 | G | A | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+895G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180530283 | |||||||
| chr5:180530400 | T | A | 1 | a0002c0004t0001g0318 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.112+1012T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180530400 | |||||||
| chr5:180530492 | G | A | 3 | a0001c0001t0001g0258 a0001c0001t0012g0252 a0001c0001t0012g0320 |
3 | HG02273.hp1 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.112+1104G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180530492 | |||||||
| chr5:180530561 | C | CT | 42 | a0001c0001t0002g0057 a0001c0001t0003g0189 a0001c0001t0003g0190 others(39): Show |
42 | HG00621.hp1 HG00738.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.112+1191dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180530561 | ||||||
| chr5:180530561 | CT | C | 12 | a0001c0001t0001g0233 a0001c0001t0001g0235 a0001c0001t0001g0264 others(9): Show |
12 | HG00099.hp1 HG01069.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.112+1191delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180530561 | ||||||
| chr5:180530716 | C | T | 296 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(293): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.112+1328C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180530716 | |||||||
| chr5:180530721 | G | T | 1 | a0001c0001t0039g0103 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.112+1333G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180530721 | |||||||
| chr5:180530781 | G | A | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.112+1393G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180530781 | |||||||
| chr5:180530865 | A | T | 1 | a0001c0001t0001g0306 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.112+1477A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180530865 | |||||||
| chr5:180530874 | G | A | 1 | a0001c0001t0003g0196 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.112+1486G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180530874 | |||||||
| chr5:180531044 | C | T | 5 | a0001c0001t0003g0206 a0001c0001t0018g0005 a0001c0001t0018g0006 others(2): Show |
5 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+1656C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531044 | |||||||
| chr5:180531107 | GGGCAGAG others(87): Show |
G | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.112+1747_112+1840d others(96): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180531107 | ||||||
| chr5:180531143 | T | C | 65 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(62): Show |
65 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.112+1755T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531143 | |||||||
| chr5:180531190 | G | GGGCGGCT others(33): Show |
5 | a0001c0001t0001g0106 a0001c0001t0013g0104 a0001c0001t0013g0105 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.112+1841_112+1842i others(42): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180531190 | ||||||
| chr5:180531230 | G | T | 6 | a0001c0001t0001g0106 a0001c0001t0005g0225 a0001c0001t0013g0104 others(3): Show |
6 | HG01884.hp2 HG02717.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.112+1842G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531230 | |||||||
| chr5:180531234 | G | A | 61 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(58): Show |
61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.112+1846G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531234 | |||||||
| chr5:180531241 | G | A | 159 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(156): Show |
159 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.112+1853G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531241 | |||||||
| chr5:180531273 | T | C | 115 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(112): Show |
115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.112+1885T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531273 | |||||||
| chr5:180531274 | G | A | 61 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(58): Show |
61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.112+1886G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531274 | |||||||
| chr5:180531283 | G | A | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.112+1895G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531283 | |||||||
| chr5:180531287 | C | T | 115 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(112): Show |
115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.112+1899C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531287 | |||||||
| chr5:180531305 | C | CG | 12 | a0001c0001t0002g0092 a0001c0001t0002g0098 a0001c0001t0003g0185 others(9): Show |
12 | HG00438.hp2 HG01361.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.112+1921dupG | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180531305 | ||||||
| chr5:180531305 | C | T | 1 | a0001c0001t0002g0063 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.112+1917C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531305 | |||||||
| chr5:180531318 | G | A | 52 | a0001c0001t0001g0067 a0001c0001t0002g0019 a0001c0001t0002g0021 others(49): Show |
52 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.112+1930G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531318 | |||||||
| chr5:180531429 | C | T | 1 | a0001c0001t0001g0319 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.112+2041C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531429 | |||||||
| chr5:180531430 | G | A | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.112+2042G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531430 | |||||||
| chr5:180531470 | G | A | 18 | a0001c0001t0001g0067 a0001c0001t0002g0019 a0001c0001t0002g0056 others(15): Show |
18 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(15): Show |
intron_variant | MODIFIER | c.112+2082G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531470 | |||||||
| chr5:180531470 | G | T | 1 | a0001c0001t0049g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.112+2082G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531470 | |||||||
| chr5:180531520 | GGCTCCTC others(32): Show |
G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+2142_112+2180d others(41): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180531520 | ||||||
| chr5:180531532 | C | T | 111 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(108): Show |
111 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.112+2144C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531532 | |||||||
| chr5:180531539 | G | A | 1 | a0001c0001t0001g0319 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.112+2151G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531539 | |||||||
| chr5:180531577 | C | CG | 11 | a0001c0001t0001g0306 a0001c0001t0002g0079 a0001c0001t0002g0098 others(8): Show |
11 | HG00544.hp2 HG00735.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.112+2193dupG | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180531577 | ||||||
| chr5:180531586 | G | A | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.112+2198G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531586 | |||||||
| chr5:180531732 | C | T | 2 | a0001c0001t0062g0073 a0001c0001t0063g0229 |
2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.112+2344C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531732 | |||||||
| chr5:180531744 | A | T | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.112+2356A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531744 | |||||||
| chr5:180531768 | G | T | 2 | a0001c0001t0040g0101 a0001c0001t0041g0102 |
2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.112+2380G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531768 | |||||||
| chr5:180531803 | C | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+2415C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531803 | |||||||
| chr5:180531803 | C | T | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.112+2415C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531803 | |||||||
| chr5:180531827 | T | C | 4 | a0001c0001t0021g0159 a0001c0001t0021g0160 a0001c0001t0021g0161 others(1): Show |
4 | HG02071.hp2 HG02735.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+2439T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531827 | |||||||
| chr5:180531948 | C | T | 1 | a0001c0001t0015g0120 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.112+2560C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531948 | |||||||
| chr5:180531984 | G | A | 61 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(58): Show |
61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.112+2596G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531984 | |||||||
| chr5:180531992 | G | A | 58 | a0001c0001t0001g0067 a0001c0001t0001g0106 a0001c0001t0002g0019 others(55): Show |
58 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.112+2604G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180531992 | |||||||
| chr5:180532021 | A | G | 2 | a0001c0001t0003g0198 a0001c0001t0023g0197 |
2 | HG01433.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.112+2633A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532021 | |||||||
| chr5:180532063 | G | A | 20 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(17): Show |
20 | HG00280.hp2 HG00639.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.112+2675G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532063 | |||||||
| chr5:180532149 | A | C | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+2761A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532149 | |||||||
| chr5:180532220 | G | A | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.112+2832G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532220 | |||||||
| chr5:180532327 | C | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+2939C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532327 | |||||||
| chr5:180532486 | T | C | 2 | a0001c0001t0001g0237 a0001c0001t0001g0271 |
2 | NA19075.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.112+3098T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532486 | |||||||
| chr5:180532519 | G | C | 61 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(58): Show |
61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.112+3131G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532519 | |||||||
| chr5:180532602 | G | T | 1 | a0001c0001t0017g0167 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.112+3214G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532602 | |||||||
| chr5:180532708 | A | C | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+3320A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532708 | |||||||
| chr5:180532834 | T | C | 2 | a0001c0001t0002g0021 a0001c0001t0042g0072 |
2 | HG01975.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.112+3446T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532834 | |||||||
| chr5:180532979 | A | G | 52 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(49): Show |
52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.112+3591A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180532979 | |||||||
| chr5:180533034 | T | C | 2 | a0001c0001t0040g0101 a0001c0001t0041g0102 |
2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.112+3646T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533034 | |||||||
| chr5:180533227 | T | C | 20 | a0001c0001t0001g0241 a0001c0001t0001g0265 a0001c0001t0001g0266 others(17): Show |
20 | HG00423.hp2 HG00642.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.112+3839T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533227 | |||||||
| chr5:180533311 | C | CAT | 28 | a0001c0001t0001g0228 a0001c0001t0001g0235 a0001c0001t0001g0237 others(25): Show |
28 | HG00544.hp2 HG00558.hp2 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.112+3923_112+3924i others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533311 | |||||||
| chr5:180533311 | C | CATAT | 3 | a0001c0001t0001g0250 a0001c0001t0001g0259 a0001c0001t0001g0271 |
3 | HG00544.hp1 HG03927.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.112+3923_112+3924i others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533311 | |||||||
| chr5:180533311 | C | CATATAT | 3 | a0001c0001t0001g0317 a0001c0001t0005g0114 a0002c0004t0004g0249 |
3 | HG02572.hp1 NA18960.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.112+3923_112+3924i others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533311 | |||||||
| chr5:180533311 | C | CATATATA others(3): Show |
1 | a0001c0001t0001g0315 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.112+3923_112+3924i others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533311 | |||||||
| chr5:180533311 | C | CATATATA others(13): Show |
1 | a0001c0001t0001g0226 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.112+3923_112+3924i others(22): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533311 | |||||||
| chr5:180533311 | CCT | C | 3 | a0001c0001t0001g0240 a0001c0001t0001g0264 a0001c0001t0001g0276 |
3 | HG00558.hp1 HG02559.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.112+3924_112+3925d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533311 | |||||||
| chr5:180533312 | C | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0226 a0001c0001t0001g0228 others(93): Show |
96 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.112+3924C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533312 | |||||||
| chr5:180533312 | C | CTA | 3 | a0001c0001t0002g0063 a0001c0001t0057g0055 a0001c0005t0004g0020 |
3 | HG03453.hp2 NA18906.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.112+3954_112+3955d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATA | 11 | a0001c0001t0002g0230 a0001c0001t0005g0225 a0001c0002t0002g0040 others(8): Show |
11 | HG01256.hp2 HG01258.hp1 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.112+3952_112+3955d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATATA | 6 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0002t0002g0030 others(3): Show |
6 | HG01069.hp1 HG01106.hp1 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.112+3950_112+3955d others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATATAT others(3): Show |
8 | a0001c0001t0002g0077 a0001c0001t0002g0079 a0001c0001t0002g0086 others(5): Show |
8 | HG00438.hp1 HG03704.hp1 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.112+3946_112+3955d others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATATAT others(5): Show |
9 | a0001c0001t0002g0021 a0001c0001t0002g0078 a0001c0001t0002g0082 others(6): Show |
9 | HG00438.hp2 HG00639.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.112+3944_112+3955d others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATATAT others(7): Show |
2 | a0001c0001t0002g0019 a0001c0001t0002g0081 |
2 | HG00642.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.112+3942_112+3955d others(16): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATATAT others(9): Show |
3 | a0001c0001t0001g0106 a0001c0001t0002g0071 a0001c0001t0013g0105 |
3 | HG01884.hp2 HG02818.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.112+3940_112+3955d others(18): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATATAT others(11): Show |
3 | a0001c0001t0013g0104 a0001c0001t0013g0107 a0001c0001t0013g0108 |
3 | HG02717.hp2 HG06807.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.112+3938_112+3955d others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATATAT others(15): Show |
1 | a0001c0001t0002g0091 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.112+3934_112+3955d others(24): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATATAT others(17): Show |
2 | a0001c0001t0002g0068 a0001c0001t0002g0069 |
2 | NA18939.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.112+3932_112+3955d others(26): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATATAT others(19): Show |
3 | a0001c0001t0002g0057 a0001c0001t0002g0062 a0001c0001t0002g0087 |
3 | HG00621.hp1 HG02165.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.112+3930_112+3955d others(28): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATATAT others(21): Show |
3 | a0001c0001t0002g0065 a0001c0001t0002g0066 a0001c0001t0058g0094 |
3 | HG00609.hp1 NA18947.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.112+3928_112+3955d others(30): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATATAT others(23): Show |
1 | a0001c0001t0002g0060 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.112+3926_112+3955d others(32): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATATAT others(25): Show |
3 | a0001c0001t0002g0056 a0001c0001t0002g0061 a0001c0001t0002g0109 |
3 | NA18955.hp2 NA19012.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.112+3955_112+3956i others(34): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATATAT others(27): Show |
3 | a0001c0001t0002g0064 a0001c0001t0002g0098 a0001c0001t0002g0231 |
3 | HG00597.hp1 HG02071.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.112+3955_112+3956i others(36): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATATAT others(29): Show |
1 | a0001c0001t0001g0067 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.112+3955_112+3956i others(38): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATATAT others(31): Show |
1 | a0001c0001t0002g0059 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.112+3955_112+3956i others(40): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATATAT others(33): Show |
1 | a0001c0001t0002g0070 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.112+3955_112+3956i others(42): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATATGT others(21): Show |
1 | a0001c0001t0002g0075 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.112+3929_112+3930i others(30): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | C | CTATATGT others(43): Show |
1 | a0001c0001t0002g0076 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.112+3929_112+3930i others(52): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | CTA | C | 5 | a0001c0001t0017g0167 a0001c0001t0025g0218 a0001c0001t0026g0222 others(2): Show |
5 | HG01261.hp1 HG02257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+3954_112+3955d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | CTATA | C | 13 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(10): Show |
13 | HG01243.hp2 HG01884.hp1 HG02071.hp2 others(10): Show |
intron_variant | MODIFIER | c.112+3952_112+3955d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | CTATATA | C | 13 | a0001c0001t0002g0097 a0001c0001t0002g0112 a0001c0001t0011g0001 others(10): Show |
14 | HG01256.hp1 HG01361.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.112+3950_112+3955d others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | CTATATAT others(9): Show |
C | 52 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(49): Show |
52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.112+3940_112+3955d others(18): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533312 | CTATATAT others(11): Show |
C | 7 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(4): Show |
7 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+3938_112+3955d others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533312 | ||||||
| chr5:180533331 | TATATATA | T | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.112+3944_112+3950d others(9): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533331 | |||||||
| chr5:180533339 | T | C | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.112+3951T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533339 | |||||||
| chr5:180533341 | T | C | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.112+3953T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533341 | |||||||
| chr5:180533651 | G | A | 4 | a0001c0001t0021g0159 a0001c0001t0021g0160 a0001c0001t0021g0161 others(1): Show |
4 | HG02071.hp2 HG02735.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+4263G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533651 | |||||||
| chr5:180533756 | T | C | 52 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(49): Show |
52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.112+4368T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533756 | |||||||
| chr5:180533771 | A | G | 1 | a0001c0002t0002g0048 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.112+4383A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533771 | |||||||
| chr5:180533901 | TC | T | 7 | a0001c0001t0002g0087 a0001c0001t0002g0089 a0001c0001t0002g0091 others(4): Show |
7 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+4515delC | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180533901 | ||||||
| chr5:180533932 | G | A | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+4544G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180533932 | |||||||
| chr5:180534082 | G | A | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.112+4694G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534082 | |||||||
| chr5:180534243 | A | C | 2 | a0001c0001t0003g0202 a0001c0001t0003g0206 |
2 | HG02559.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.112+4855A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534243 | |||||||
| chr5:180534383 | T | G | 1 | a0001c0001t0026g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.112+4995T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534383 | |||||||
| chr5:180534464 | G | A | 2 | a0001c0002t0004g0033 a0001c0002t0004g0047 |
2 | HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.112+5076G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534464 | |||||||
| chr5:180534502 | A | G | 53 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(50): Show |
53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.112+5114A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534502 | |||||||
| chr5:180534507 | C | T | 52 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(49): Show |
52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.112+5119C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534507 | |||||||
| chr5:180534589 | C | A | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+5201C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534589 | |||||||
| chr5:180534612 | GGGGGTCC others(189): Show |
G | 3 | a0001c0001t0001g0243 a0001c0001t0001g0273 a0001c0001t0001g0314 |
3 | NA18978.hp2 NA19005.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.112+5271_112+5466d others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180534612 | ||||||
| chr5:180534612 | GGGGGTCC others(238): Show |
G | 9 | a0001c0002t0005g0022 a0001c0002t0005g0023 a0001c0002t0005g0024 others(6): Show |
9 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.112+5438_112+5682d others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180534612 | ||||||
| chr5:180534612 | GGGGGTCC others(287): Show |
G | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.112+5271_112+5564d others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180534612 | ||||||
| chr5:180534619 | C | T | 1 | a0001c0001t0022g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.112+5231C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534619 | |||||||
| chr5:180534659 | G | C | 60 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(57): Show |
60 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.112+5271G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534659 | |||||||
| chr5:180534659 | GCTGGGGT others(42): Show |
G | 53 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(50): Show |
53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.112+5467_112+5515d others(51): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180534659 | ||||||
| chr5:180534667 | C | T | 60 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(57): Show |
60 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.112+5279C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534667 | |||||||
| chr5:180534702 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.112+5314G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534702 | |||||||
| chr5:180534708 | C | G | 9 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(6): Show |
9 | HG00099.hp1 HG00738.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.112+5320C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534708 | |||||||
| chr5:180534748 | G | A | 5 | a0001c0001t0010g0183 a0001c0001t0014g0168 a0001c0001t0014g0175 others(2): Show |
5 | HG00280.hp2 HG00639.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+5360G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534748 | |||||||
| chr5:180534757 | C | G | 60 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(57): Show |
60 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.112+5369C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534757 | |||||||
| chr5:180534757 | CCTGGGGT others(140): Show |
C | 1 | a0001c0001t0018g0007 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.112+5516_112+5662d others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180534757 | ||||||
| chr5:180534806 | CCTGGGGT others(91): Show |
C | 3 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0008 |
3 | HG00099.hp1 HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.112+5516_112+5613d others(100): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180534806 | ||||||
| chr5:180534814 | C | T | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.112+5426C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534814 | |||||||
| chr5:180534826 | CGGAATCC others(238): Show |
C | 60 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(57): Show |
60 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.112+5472_112+5716d others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180534826 | ||||||
| chr5:180534848 | C | T | 1 | a0001c0001t0006g0138 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.112+5460C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534848 | |||||||
| chr5:180534865 | G | A | 2 | a0001c0001t0001g0236 a0001c0001t0008g0234 |
2 | NA18944.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.112+5477G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534865 | |||||||
| chr5:180534882 | C | T | 154 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(151): Show |
154 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.112+5494C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534882 | |||||||
| chr5:180534914 | G | A | 2 | a0001c0001t0001g0240 a0001c0001t0001g0312 |
2 | HG01515.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.112+5526G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534914 | |||||||
| chr5:180534953 | C | G | 3 | a0001c0001t0002g0086 a0001c0001t0002g0099 a0001c0001t0002g0115 |
3 | HG00438.hp1 HG02135.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.112+5565C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180534953 | |||||||
| chr5:180535002 | C | G | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.112+5614C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535002 | |||||||
| chr5:180535022 | CGGAATCC others(42): Show |
C | 53 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(50): Show |
53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.112+5668_112+5716d others(51): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535022 | ||||||
| chr5:180535071 | T | C | 5 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(2): Show |
5 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+5683T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535071 | |||||||
| chr5:180535111 | A | C | 10 | a0001c0002t0004g0032 a0001c0002t0004g0037 a0001c0002t0004g0045 others(7): Show |
10 | HG01167.hp1 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.112+5723A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535111 | |||||||
| chr5:180535141 | A | G | 1 | a0001c0001t0040g0101 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.112+5753A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535141 | |||||||
| chr5:180535180 | G | C | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+5792G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535180 | |||||||
| chr5:180535206 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.112+5818C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535206 | |||||||
| chr5:180535237 | C | T | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+5849C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535237 | |||||||
| chr5:180535314 | G | A | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.112+5926G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535314 | |||||||
| chr5:180535319 | C | A | 61 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(58): Show |
61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.112+5931C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535319 | |||||||
| chr5:180535366 | A | G | 1 | a0001c0001t0057g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.112+5978A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535366 | |||||||
| chr5:180535521 | G | A | 1 | a0001c0001t0053g0118 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.112+6133G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535521 | |||||||
| chr5:180535707 | T | C | 2 | a0001c0002t0004g0053 a0001c0002t0004g0054 |
2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.112+6319T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535707 | |||||||
| chr5:180535811 | G | A | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+6423G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535811 | |||||||
| chr5:180535915 | G | A | 1 | a0001c0001t0009g0179 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.112+6527G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535915 | |||||||
| chr5:180535951 | A | G | 1 | a0001c0001t0002g0083 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.112+6563A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535951 | |||||||
| chr5:180535959 | T | C | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+6571T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535959 | |||||||
| chr5:180535988 | G | GT | 44 | a0001c0001t0002g0019 a0001c0001t0002g0021 a0001c0001t0002g0056 others(41): Show |
45 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.112+6629dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535988 | ||||||
| chr5:180535988 | G | GTT | 15 | a0001c0001t0001g0067 a0001c0001t0002g0058 a0001c0001t0002g0063 others(12): Show |
15 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(12): Show |
intron_variant | MODIFIER | c.112+6628_112+6629d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535988 | ||||||
| chr5:180535988 | GT | G | 21 | a0001c0001t0008g0302 a0001c0001t0026g0220 a0001c0001t0062g0073 others(18): Show |
21 | HG01167.hp1 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.112+6629delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535988 | ||||||
| chr5:180535988 | GTT | G | 25 | a0001c0001t0001g0226 a0001c0001t0001g0237 a0001c0001t0001g0240 others(22): Show |
25 | HG00544.hp2 HG00621.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.112+6628_112+6629d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535988 | ||||||
| chr5:180535988 | GTTT | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0228 a0001c0001t0001g0232 others(69): Show |
72 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.112+6627_112+6629d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535988 | ||||||
| chr5:180535988 | GTTTTT | G | 13 | a0001c0001t0002g0177 a0001c0001t0003g0171 a0001c0001t0003g0173 others(10): Show |
13 | HG00733.hp2 HG01243.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.112+6625_112+6629d others(7): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535988 | ||||||
| chr5:180535988 | GTTTTTT | G | 70 | a0001c0001t0001g0169 a0001c0001t0003g0180 a0001c0001t0003g0181 others(67): Show |
70 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.112+6624_112+6629d others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535988 | ||||||
| chr5:180535988 | GTTTTTTT | G | 28 | a0001c0001t0003g0189 a0001c0001t0003g0198 a0001c0001t0003g0201 others(25): Show |
28 | HG00738.hp2 HG01071.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.112+6623_112+6629d others(9): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535988 | ||||||
| chr5:180535988 | GTTTTTTT others(11): Show |
G | 1 | a0001c0001t0060g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.112+6612_112+6629d others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180535988 | ||||||
| chr5:180535992 | T | G | 1 | a0001c0001t0001g0248 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.112+6604T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180535992 | |||||||
| chr5:180536017 | T | G | 49 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(46): Show |
49 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.112+6629T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536017 | |||||||
| chr5:180536027 | A | G | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+6639A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536027 | |||||||
| chr5:180536029 | T | C | 1 | a0001c0001t0003g0192 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.112+6641T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536029 | |||||||
| chr5:180536034 | T | C | 306 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(303): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.112+6646T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536034 | |||||||
| chr5:180536127 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.112+6739C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536127 | |||||||
| chr5:180536171 | AT | A | 296 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(293): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.112+6792delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180536171 | ||||||
| chr5:180536190 | G | A | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+6802G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536190 | |||||||
| chr5:180536239 | T | G | 4 | a0001c0001t0007g0136 a0001c0001t0007g0142 a0001c0001t0007g0143 others(1): Show |
4 | HG00609.hp2 HG02523.hp2 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+6851T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536239 | |||||||
| chr5:180536240 | C | T | 4 | a0001c0001t0024g0119 a0001c0001t0024g0152 a0001c0001t0024g0158 others(1): Show |
4 | HG01109.hp2 HG01168.hp2 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+6852C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536240 | |||||||
| chr5:180536244 | C | T | 1 | a0001c0001t0002g0056 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.112+6856C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536244 | |||||||
| chr5:180536316 | T | G | 53 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(50): Show |
53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.112+6928T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536316 | |||||||
| chr5:180536353 | C | A | 1 | a0001c0001t0061g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.112+6965C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536353 | |||||||
| chr5:180536572 | A | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+7184A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536572 | |||||||
| chr5:180536636 | G | A | 1 | a0001c0001t0003g0196 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.112+7248G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536636 | |||||||
| chr5:180536636 | G | T | 1 | a0001c0001t0015g0128 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.112+7248G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180536636 | |||||||
| chr5:180537039 | C | A | 1 | a0001c0001t0057g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.112+7651C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180537039 | |||||||
| chr5:180537047 | C | T | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.112+7659C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180537047 | |||||||
| chr5:180537137 | T | C | 1 | a0001c0001t0026g0222 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.112+7749T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180537137 | |||||||
| chr5:180537526 | C | T | 7 | a0001c0001t0002g0087 a0001c0001t0002g0089 a0001c0001t0002g0091 others(4): Show |
7 | HG00408.hp2 HG00438.hp2 HG00609.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+8138C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180537526 | |||||||
| chr5:180537527 | G | A | 1 | a0001c0002t0005g0026 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.112+8139G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180537527 | |||||||
| chr5:180537800 | C | G | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.112+8412C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180537800 | |||||||
| chr5:180537804 | C | CT | 208 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(205): Show |
208 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.112+8430dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180537804 | ||||||
| chr5:180537804 | C | CTT | 19 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(16): Show |
20 | HG01243.hp2 HG01261.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.112+8429_112+8430d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180537804 | ||||||
| chr5:180537804 | CT | C | 54 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(51): Show |
54 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.112+8430delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180537804 | ||||||
| chr5:180537910 | T | G | 1 | a0001c0005t0004g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.112+8522T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180537910 | |||||||
| chr5:180537926 | T | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+8538T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180537926 | |||||||
| chr5:180538034 | C | CT | 7 | a0001c0001t0018g0005 a0001c0001t0018g0007 a0001c0001t0018g0008 others(4): Show |
7 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+8668dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538034 | ||||||
| chr5:180538034 | CT | C | 272 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(269): Show |
273 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.112+8668delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538034 | ||||||
| chr5:180538034 | CTT | C | 17 | a0001c0001t0001g0233 a0001c0001t0002g0079 a0001c0001t0002g0097 others(14): Show |
17 | HG00733.hp2 HG01243.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.112+8667_112+8668d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538034 | ||||||
| chr5:180538106 | T | C | 52 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(49): Show |
52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.112+8718T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538106 | |||||||
| chr5:180538149 | C | T | 1 | a0001c0001t0002g0058 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.112+8761C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538149 | |||||||
| chr5:180538300 | G | A | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+8912G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538300 | |||||||
| chr5:180538355 | T | TA | 61 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(58): Show |
61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.112+8973dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538355 | ||||||
| chr5:180538414 | G | A | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.112+9026G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538414 | |||||||
| chr5:180538466 | A | G | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+9078A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538466 | |||||||
| chr5:180538545 | G | A | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.112+9157G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538545 | |||||||
| chr5:180538585 | G | A | 1 | a0001c0001t0026g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.112+9197G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538585 | |||||||
| chr5:180538637 | A | G | 52 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(49): Show |
52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.112+9249A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538637 | |||||||
| chr5:180538685 | G | GGTATATA others(3): Show |
3 | a0001c0001t0001g0282 a0001c0001t0012g0320 a0001c0001t0061g0004 |
3 | HG02257.hp2 HG02273.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.112+9298_112+9307d others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538685 | ||||||
| chr5:180538685 | GGTATATA others(3): Show |
G | 2 | a0001c0001t0003g0173 a0001c0001t0003g0289 |
2 | HG01934.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.112+9298_112+9307d others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538685 | |||||||
| chr5:180538685 | GGTATATA others(5): Show |
G | 59 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(56): Show |
59 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.112+9298_112+9309d others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538685 | |||||||
| chr5:180538686 | G | GTA | 5 | a0001c0001t0001g0106 a0001c0001t0005g0225 a0001c0001t0013g0104 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+9327_112+9328d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | ||||||
| chr5:180538686 | G | GTATA | 3 | a0001c0001t0013g0105 a0001c0001t0062g0073 a0001c0001t0063g0229 |
3 | HG02258.hp1 HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.112+9325_112+9328d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | ||||||
| chr5:180538686 | G | GTATATAT others(1): Show |
3 | a0001c0002t0005g0023 a0001c0002t0005g0028 a0001c0002t0005g0029 |
3 | HG01891.hp2 HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.112+9321_112+9328d others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | ||||||
| chr5:180538686 | G | GTATATAT others(3): Show |
2 | a0001c0001t0002g0115 a0001c0002t0005g0025 |
2 | HG02135.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.112+9319_112+9328d others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | ||||||
| chr5:180538686 | G | GTATATAT others(5): Show |
2 | a0001c0002t0005g0022 a0001c0002t0005g0027 |
2 | HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.112+9317_112+9328d others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | ||||||
| chr5:180538686 | G | GTATATAT others(7): Show |
19 | a0001c0001t0002g0019 a0001c0001t0002g0058 a0001c0001t0002g0059 others(16): Show |
19 | HG00597.hp1 HG00639.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.112+9315_112+9328d others(16): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | ||||||
| chr5:180538686 | G | GTATATAT others(9): Show |
12 | a0001c0001t0001g0067 a0001c0001t0002g0021 a0001c0001t0002g0056 others(9): Show |
12 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.112+9313_112+9328d others(18): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | ||||||
| chr5:180538686 | G | GTATATAT others(11): Show |
8 | a0001c0001t0002g0070 a0001c0001t0002g0076 a0001c0001t0002g0086 others(5): Show |
8 | HG02165.hp1 HG02165.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.112+9311_112+9328d others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | ||||||
| chr5:180538686 | G | GTATATAT others(13): Show |
4 | a0001c0001t0002g0083 a0001c0001t0002g0089 a0001c0001t0002g0093 others(1): Show |
4 | HG02004.hp1 NA18968.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.112+9309_112+9328d others(22): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | ||||||
| chr5:180538686 | G | GTATATAT others(15): Show |
1 | a0001c0001t0002g0075 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.112+9307_112+9328d others(24): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | ||||||
| chr5:180538686 | G | GTATATAT others(17): Show |
2 | a0001c0001t0002g0077 a0001c0001t0002g0085 |
2 | HG03704.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.112+9305_112+9328d others(26): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | ||||||
| chr5:180538686 | G | GTATATAT others(19): Show |
5 | a0001c0001t0002g0065 a0001c0001t0002g0092 a0001c0001t0002g0099 others(2): Show |
5 | HG00438.hp1 HG00438.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.112+9303_112+9328d others(28): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | ||||||
| chr5:180538686 | G | GTATATAT others(23): Show |
1 | a0001c0001t0058g0094 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.112+9299_112+9328d others(32): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | ||||||
| chr5:180538686 | G | GTATATAT others(29): Show |
1 | a0001c0001t0002g0063 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.112+9328_112+9329i others(38): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | ||||||
| chr5:180538686 | GTA | G | 20 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0046g0012 others(17): Show |
20 | HG01069.hp1 HG01106.hp1 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.112+9327_112+9328d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | ||||||
| chr5:180538686 | GTATATAT others(3): Show |
G | 1 | a0001c0001t0021g0159 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.112+9319_112+9328d others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | ||||||
| chr5:180538686 | GTATATAT others(5): Show |
G | 54 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(51): Show |
54 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.112+9317_112+9328d others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | ||||||
| chr5:180538686 | GTATATAT others(11): Show |
G | 13 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(10): Show |
14 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.112+9311_112+9328d others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538686 | ||||||
| chr5:180538688 | A | ATATATAT others(1): Show |
20 | a0001c0001t0001g0258 a0001c0001t0001g0264 a0001c0001t0001g0265 others(17): Show |
20 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.112+9307_112+9308i others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538688 | ||||||
| chr5:180538690 | A | ATATATG | 76 | a0001c0001t0001g0002 a0001c0001t0001g0226 a0001c0001t0001g0228 others(73): Show |
76 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.112+9307_112+9308i others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538690 | ||||||
| chr5:180538713 | T | TATATATA others(9): Show |
1 | a0001c0001t0060g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.112+9328_112+9329i others(18): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180538713 | ||||||
| chr5:180538717 | C | T | 1 | a0001c0001t0061g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.112+9329C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538717 | |||||||
| chr5:180538909 | C | T | 1 | a0001c0001t0061g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.112+9521C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180538909 | |||||||
| chr5:180539019 | CA | C | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.112+9637delA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539019 | ||||||
| chr5:180539067 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.112+9679C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539067 | |||||||
| chr5:180539121 | G | A | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.112+9733G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539121 | |||||||
| chr5:180539173 | C | CA | 6 | a0001c0001t0001g0300 a0001c0001t0001g0314 a0001c0001t0008g0302 others(3): Show |
6 | HG00597.hp2 HG02027.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.112+9803dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539173 | ||||||
| chr5:180539173 | C | CAA | 56 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(53): Show |
56 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.112+9802_112+9803d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539173 | ||||||
| chr5:180539173 | C | CAAA | 47 | a0001c0001t0003g0173 a0001c0001t0006g0124 a0001c0001t0006g0125 others(44): Show |
47 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.112+9801_112+9803d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539173 | ||||||
| chr5:180539173 | C | CAAAA | 11 | a0001c0001t0006g0122 a0001c0001t0006g0147 a0001c0001t0016g0123 others(8): Show |
11 | HG00408.hp1 HG01243.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.112+9800_112+9803d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539173 | ||||||
| chr5:180539243 | G | A | 1 | a0001c0001t0006g0131 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.112+9855G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539243 | |||||||
| chr5:180539272 | C | T | 1 | a0001c0002t0004g0035 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.112+9884C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539272 | |||||||
| chr5:180539295 | C | A | 3 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0008 |
3 | HG00099.hp1 HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.112+9907C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539295 | |||||||
| chr5:180539295 | C | CA | 61 | a0001c0001t0001g0300 a0001c0001t0002g0063 a0001c0001t0006g0009 others(58): Show |
61 | HG00408.hp1 HG00597.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.112+9916dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539295 | ||||||
| chr5:180539298 | A | AC | 52 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(49): Show |
52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.112+9910_112+9911i others(3): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539298 | |||||||
| chr5:180539322 | T | C | 53 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(50): Show |
53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.112+9934T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539322 | |||||||
| chr5:180539413 | G | C | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.112+10025G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539413 | |||||||
| chr5:180539548 | GTTCTTTT others(6): Show |
G | 1 | a0001c0001t0011g0001 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.112+10163_112+1017 others(17): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539548 | ||||||
| chr5:180539548 | GTTCTTTT others(7): Show |
G | 3 | a0001c0001t0011g0223 a0001c0001t0025g0216 a0001c0001t0038g0217 |
3 | HG02109.hp1 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.112+10163_112+1017 others(18): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539548 | ||||||
| chr5:180539548 | GTTCTTTT others(8): Show |
G | 2 | a0001c0001t0011g0213 a0001c0001t0011g0215 |
2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.112+10163_112+1017 others(19): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539548 | ||||||
| chr5:180539548 | GTTCTTTT others(21): Show |
G | 2 | a0001c0001t0001g0169 a0001c0001t0002g0177 |
2 | NA18955.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.112+10163_112+1019 others(32): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539548 | ||||||
| chr5:180539548 | GTTCTTTT others(22): Show |
G | 1 | a0001c0001t0011g0214 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.112+10163_112+1019 others(33): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539548 | ||||||
| chr5:180539551 | C | T | 1 | a0001c0001t0026g0222 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.112+10163C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539551 | |||||||
| chr5:180539551 | CTTTTTTT others(4): Show |
C | 2 | a0001c0002t0002g0044 a0001c0002t0020g0051 |
2 | HG01123.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.112+10209_112+1021 others(15): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(5): Show |
C | 3 | a0001c0002t0002g0030 a0001c0002t0002g0031 a0001c0002t0020g0050 |
3 | HG01069.hp1 HG01106.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.112+10208_112+1021 others(16): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(6): Show |
C | 2 | a0001c0002t0002g0040 a0001c0002t0002g0041 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.112+10207_112+1021 others(17): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(7): Show |
C | 2 | a0001c0001t0021g0159 a0001c0001t0039g0103 |
2 | HG02071.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.112+10206_112+1021 others(18): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0021g0160 a0001c0001t0025g0218 |
2 | HG02735.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.112+10204_112+1021 others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.112+10201_112+1021 others(23): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0035g0018 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.112+10200_112+1021 others(24): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0036g0193 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.112+10199_112+1021 others(25): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(15): Show |
C | 3 | a0001c0001t0010g0194 a0001c0001t0013g0254 a0001c0001t0014g0203 |
3 | HG00642.hp2 HG03195.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.112+10198_112+1021 others(26): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(16): Show |
C | 15 | a0001c0001t0005g0114 a0001c0001t0009g0011 a0001c0001t0009g0016 others(12): Show |
15 | HG00280.hp2 HG00639.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.112+10197_112+1021 others(27): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(17): Show |
C | 17 | a0001c0001t0001g0260 a0001c0001t0003g0171 a0001c0001t0003g0182 others(14): Show |
17 | HG00741.hp2 HG01257.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.112+10196_112+1021 others(28): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(18): Show |
C | 33 | a0001c0001t0001g0245 a0001c0001t0001g0266 a0001c0001t0001g0279 others(30): Show |
33 | HG00438.hp1 HG00738.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.112+10195_112+1021 others(29): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(19): Show |
C | 69 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(66): Show |
69 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.112+10194_112+1021 others(30): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(20): Show |
C | 84 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0001g0232 others(81): Show |
84 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.112+10193_112+1021 others(31): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(21): Show |
C | 17 | a0001c0001t0002g0109 a0001c0001t0006g0009 a0001c0001t0006g0122 others(14): Show |
17 | HG00408.hp1 HG01109.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.112+10192_112+1021 others(32): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(22): Show |
C | 35 | a0001c0001t0006g0125 a0001c0001t0006g0131 a0001c0001t0006g0137 others(32): Show |
35 | HG00609.hp2 HG00733.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.112+10191_112+1021 others(33): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(23): Show |
C | 3 | a0001c0001t0006g0322 a0001c0001t0032g0129 a0001c0002t0002g0042 |
3 | HG01257.hp1 HG01433.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.112+10190_112+1021 others(34): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(24): Show |
C | 9 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 others(6): Show |
9 | HG01167.hp1 HG02451.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.112+10189_112+1021 others(35): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(26): Show |
C | 1 | a0001c0002t0004g0053 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.112+10187_112+1021 others(37): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(29): Show |
C | 1 | a0001c0001t0049g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.112+10184_112+1021 others(40): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(30): Show |
C | 3 | a0001c0001t0022g0224 a0001c0003t0022g0219 a0001c0003t0022g0221 |
3 | HG02055.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.112+10183_112+1021 others(41): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(31): Show |
C | 1 | a0001c0001t0002g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.112+10182_112+1021 others(42): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(33): Show |
C | 9 | a0001c0002t0005g0022 a0001c0002t0005g0023 a0001c0002t0005g0024 others(6): Show |
9 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.112+10180_112+1021 others(44): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539551 | CTTTTTTT others(37): Show |
C | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.112+10176_112+1021 others(48): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180539551 | ||||||
| chr5:180539564 | T | G | 1 | a0001c0001t0011g0001 | 2 | HG03130.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.112+10176T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539564 | |||||||
| chr5:180539565 | T | G | 3 | a0001c0001t0011g0223 a0001c0001t0025g0216 a0001c0001t0038g0217 |
3 | HG02109.hp1 HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.112+10177T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539565 | |||||||
| chr5:180539566 | T | G | 2 | a0001c0001t0011g0213 a0001c0001t0011g0215 |
2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.112+10178T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539566 | |||||||
| chr5:180539580 | T | G | 1 | a0001c0001t0011g0214 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.112+10192T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539580 | |||||||
| chr5:180539663 | T | C | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.113-10268T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539663 | |||||||
| chr5:180539673 | T | C | 20 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(17): Show |
20 | HG00280.hp2 HG00639.hp2 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.113-10258T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539673 | |||||||
| chr5:180539694 | A | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-10237A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539694 | |||||||
| chr5:180539714 | C | T | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.113-10217C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539714 | |||||||
| chr5:180539750 | C | T | 2 | a0001c0001t0009g0211 a0001c0001t0010g0210 |
2 | HG01891.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.113-10181C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539750 | |||||||
| chr5:180539791 | G | T | 3 | a0001c0001t0008g0263 a0001c0001t0029g0287 a0001c0001t0029g0288 |
3 | NA18962.hp2 NA18969.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.113-10140G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539791 | |||||||
| chr5:180539825 | A | G | 48 | a0001c0001t0001g0067 a0001c0001t0002g0019 a0001c0001t0002g0021 others(45): Show |
48 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.113-10106A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539825 | |||||||
| chr5:180539831 | C | T | 1 | a0001c0001t0002g0085 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.113-10100C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539831 | |||||||
| chr5:180539833 | C | T | 1 | a0001c0005t0004g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.113-10098C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539833 | |||||||
| chr5:180539836 | G | A | 1 | a0001c0001t0009g0200 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.113-10095G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539836 | |||||||
| chr5:180539836 | G | C | 1 | a0001c0001t0014g0203 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.113-10095G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539836 | |||||||
| chr5:180539841 | G | A | 2 | a0001c0001t0045g0331 a0001c0001t0049g0332 |
2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.113-10090G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539841 | |||||||
| chr5:180539955 | T | C | 1 | a0001c0005t0004g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.113-9976T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180539955 | |||||||
| chr5:180540171 | A | C | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-9760A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180540171 | |||||||
| chr5:180540386 | A | G | 2 | a0001c0002t0004g0034 a0001c0002t0004g0035 |
2 | HG03139.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.113-9545A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180540386 | |||||||
| chr5:180540423 | C | G | 159 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(156): Show |
159 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.113-9508C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180540423 | |||||||
| chr5:180540473 | C | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-9458C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180540473 | |||||||
| chr5:180540509 | A | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0226 a0001c0001t0001g0228 others(97): Show |
100 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.113-9422A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180540509 | |||||||
| chr5:180540738 | C | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-9193C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180540738 | |||||||
| chr5:180540803 | C | A | 115 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(112): Show |
115 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.113-9128C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180540803 | |||||||
| chr5:180541076 | A | G | 3 | a0001c0001t0006g0137 a0001c0001t0006g0138 a0001c0001t0054g0146 |
3 | HG01981.hp1 HG02004.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.113-8855A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541076 | |||||||
| chr5:180541142 | AT | A | 6 | a0001c0001t0001g0311 a0001c0001t0002g0069 a0001c0001t0009g0178 others(3): Show |
6 | HG00738.hp1 HG01169.hp1 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-8775delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180541142 | ||||||
| chr5:180541285 | C | T | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.113-8646C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541285 | |||||||
| chr5:180541348 | A | G | 1 | a0001c0001t0009g0184 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.113-8583A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541348 | |||||||
| chr5:180541381 | C | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-8550C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541381 | |||||||
| chr5:180541440 | A | ATTTT | 31 | a0001c0001t0001g0169 a0001c0001t0003g0173 a0001c0001t0003g0180 others(28): Show |
31 | HG00639.hp2 HG01167.hp2 HG01169.hp2 others(28): Show |
intron_variant | MODIFIER | c.113-8491_113-8490i others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541440 | |||||||
| chr5:180541440 | A | ATTTTT | 19 | a0001c0001t0002g0177 a0001c0001t0003g0171 a0001c0001t0003g0196 others(16): Show |
19 | HG00408.hp1 HG00735.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.113-8491_113-8490i others(7): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541440 | |||||||
| chr5:180541440 | A | ATTTTTT | 29 | a0001c0001t0003g0182 a0001c0001t0003g0189 a0001c0001t0003g0190 others(26): Show |
29 | HG00280.hp2 HG00609.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.113-8491_113-8490i others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541440 | |||||||
| chr5:180541440 | A | ATTTTTTT | 16 | a0001c0001t0006g0009 a0001c0001t0006g0147 a0001c0001t0006g0148 others(13): Show |
16 | HG00738.hp2 HG01123.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.113-8491_113-8490i others(9): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541440 | |||||||
| chr5:180541440 | A | ATTTTTTT others(1): Show |
6 | a0001c0001t0006g0322 a0001c0001t0017g0163 a0001c0001t0017g0166 others(3): Show |
6 | HG01109.hp1 HG02258.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-8491_113-8490i others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541440 | |||||||
| chr5:180541440 | A | ATTTTTTT others(3): Show |
5 | a0001c0001t0006g0151 a0001c0001t0006g0323 a0001c0001t0031g0134 others(2): Show |
5 | HG00733.hp2 HG01243.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-8491_113-8490i others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541440 | |||||||
| chr5:180541440 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0024g0152 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.113-8491_113-8490i others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541440 | |||||||
| chr5:180541441 | A | AT | 73 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0001g0236 others(70): Show |
74 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.113-8462dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180541441 | ||||||
| chr5:180541441 | A | ATT | 24 | a0001c0001t0001g0067 a0001c0001t0002g0057 a0001c0001t0002g0059 others(21): Show |
24 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(21): Show |
intron_variant | MODIFIER | c.113-8463_113-8462d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180541441 | ||||||
| chr5:180541441 | A | T | 113 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(110): Show |
113 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.113-8490A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541441 | |||||||
| chr5:180541613 | T | C | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-8318T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541613 | |||||||
| chr5:180541614 | G | A | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-8317G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541614 | |||||||
| chr5:180541635 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0305 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.113-8296G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541635 | |||||||
| chr5:180541674 | G | C | 8 | a0001c0002t0002g0030 a0001c0002t0002g0031 a0001c0002t0002g0040 others(5): Show |
8 | HG01069.hp1 HG01106.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.113-8257G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541674 | |||||||
| chr5:180541758 | AT | A | 6 | a0001c0001t0001g0237 a0001c0001t0001g0271 a0001c0001t0002g0083 others(3): Show |
6 | HG01256.hp2 HG02896.hp2 NA18942.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-8159delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180541758 | ||||||
| chr5:180541847 | G | T | 1 | a0001c0001t0017g0162 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.113-8084G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541847 | |||||||
| chr5:180541858 | A | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-8073A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541858 | |||||||
| chr5:180541899 | C | A | 61 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(58): Show |
61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.113-8032C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541899 | |||||||
| chr5:180541914 | G | A | 2 | a0001c0001t0009g0211 a0001c0001t0010g0210 |
2 | HG01891.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.113-8017G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541914 | |||||||
| chr5:180541986 | C | G | 61 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(58): Show |
61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.113-7945C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180541986 | |||||||
| chr5:180542167 | C | T | 1 | a0001c0001t0013g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.113-7764C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542167 | |||||||
| chr5:180542179 | T | C | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.113-7752T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542179 | |||||||
| chr5:180542208 | TAGGTTTT others(4): Show |
T | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.113-7709_113-7699d others(13): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180542208 | ||||||
| chr5:180542261 | C | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-7670C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542261 | |||||||
| chr5:180542293 | C | T | 1 | a0001c0001t0013g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.113-7638C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542293 | |||||||
| chr5:180542355 | C | T | 52 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(49): Show |
52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.113-7576C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542355 | |||||||
| chr5:180542390 | G | A | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.113-7541G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542390 | |||||||
| chr5:180542394 | A | AGC | 3 | a0001c0001t0002g0058 a0001c0001t0002g0062 a0001c0001t0002g0109 |
3 | NA18955.hp2 NA18960.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.113-7536_113-7535d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180542394 | ||||||
| chr5:180542560 | C | T | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.113-7371C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542560 | |||||||
| chr5:180542596 | C | A | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-7335C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542596 | |||||||
| chr5:180542654 | G | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-7277G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542654 | |||||||
| chr5:180542751 | T | A | 1 | a0001c0001t0047g0238 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.113-7180T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542751 | |||||||
| chr5:180542823 | T | A | 4 | a0001c0001t0014g0168 a0001c0001t0014g0175 a0001c0001t0014g0176 others(1): Show |
4 | HG00280.hp2 HG00639.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-7108T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542823 | |||||||
| chr5:180542882 | G | C | 3 | a0001c0001t0030g0132 a0001c0001t0031g0133 a0001c0001t0031g0134 |
3 | HG00733.hp2 HG01074.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.113-7049G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180542882 | |||||||
| chr5:180543120 | A | G | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-6811A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543120 | |||||||
| chr5:180543121 | C | T | 53 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(50): Show |
53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.113-6810C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543121 | |||||||
| chr5:180543141 | C | T | 2 | a0001c0001t0002g0021 a0001c0001t0042g0072 |
2 | HG01975.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.113-6790C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543141 | |||||||
| chr5:180543186 | G | A | 1 | a0001c0001t0013g0254 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.113-6745G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543186 | |||||||
| chr5:180543335 | AG | A | 53 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(50): Show |
53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.113-6594delG | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180543335 | ||||||
| chr5:180543351 | A | G | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-6580A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543351 | |||||||
| chr5:180543527 | T | C | 53 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(50): Show |
53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.113-6404T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543527 | |||||||
| chr5:180543536 | G | A | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-6395G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543536 | |||||||
| chr5:180543596 | A | G | 1 | a0001c0001t0028g0326 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.113-6335A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543596 | |||||||
| chr5:180543645 | T | C | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-6286T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543645 | |||||||
| chr5:180543681 | A | G | 1 | a0001c0001t0006g0137 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.113-6250A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543681 | |||||||
| chr5:180543741 | T | G | 1 | a0001c0001t0002g0081 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.113-6190T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543741 | |||||||
| chr5:180543765 | C | G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0226 a0001c0001t0001g0228 others(97): Show |
100 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.113-6166C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543765 | |||||||
| chr5:180543828 | T | G | 1 | a0001c0001t0023g0204 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.113-6103T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543828 | |||||||
| chr5:180543936 | A | C | 1 | a0001c0001t0001g0312 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.113-5995A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543936 | |||||||
| chr5:180543951 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.113-5980C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180543951 | |||||||
| chr5:180544036 | C | T | 1 | a0001c0001t0009g0174 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.113-5895C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544036 | |||||||
| chr5:180544052 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.113-5879C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544052 | |||||||
| chr5:180544136 | T | C | 1 | a0001c0001t0017g0165 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.113-5795T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544136 | |||||||
| chr5:180544235 | A | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-5696A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544235 | |||||||
| chr5:180544305 | G | A | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-5626G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544305 | |||||||
| chr5:180544339 | A | C | 1 | a0001c0001t0006g0124 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.113-5592A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544339 | |||||||
| chr5:180544409 | A | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-5522A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544409 | |||||||
| chr5:180544463 | C | T | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-5468C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544463 | |||||||
| chr5:180544486 | C | A | 61 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(58): Show |
61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.113-5445C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544486 | |||||||
| chr5:180544532 | C | T | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-5399C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544532 | |||||||
| chr5:180544559 | T | C | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-5372T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544559 | |||||||
| chr5:180544604 | T | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-5327T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544604 | |||||||
| chr5:180544831 | C | T | 53 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(50): Show |
53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.113-5100C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180544831 | |||||||
| chr5:180545067 | C | T | 1 | a0001c0001t0003g0212 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.113-4864C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180545067 | |||||||
| chr5:180545124 | CT | C | 52 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(49): Show |
52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.113-4805delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180545124 | ||||||
| chr5:180545459 | C | T | 53 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(50): Show |
53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.113-4472C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180545459 | |||||||
| chr5:180545499 | T | C | 114 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(111): Show |
114 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.113-4432T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180545499 | |||||||
| chr5:180545571 | G | C | 1 | a0001c0001t0010g0188 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.113-4360G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180545571 | |||||||
| chr5:180545732 | A | T | 1 | a0001c0001t0001g0321 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.113-4199A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180545732 | |||||||
| chr5:180545734 | A | T | 1 | a0001c0001t0001g0321 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.113-4197A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180545734 | |||||||
| chr5:180545781 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.113-4150A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180545781 | |||||||
| chr5:180546031 | C | CT | 53 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(50): Show |
53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.113-3891dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180546031 | ||||||
| chr5:180546053 | G | T | 6 | a0001c0001t0003g0171 a0001c0001t0003g0180 a0001c0001t0003g0181 others(3): Show |
6 | HG01358.hp2 HG01993.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.113-3878G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180546053 | |||||||
| chr5:180546105 | A | G | 1 | a0001c0001t0014g0203 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.113-3826A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180546105 | |||||||
| chr5:180546642 | T | A | 61 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(58): Show |
61 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(58): Show |
intron_variant | MODIFIER | c.113-3289T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180546642 | |||||||
| chr5:180546663 | C | T | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-3268C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180546663 | |||||||
| chr5:180546770 | A | G | 2 | a0002c0004t0001g0318 a0002c0004t0004g0249 |
2 | NA18966.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.113-3161A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180546770 | |||||||
| chr5:180546865 | G | C | 3 | a0001c0001t0006g0151 a0001c0001t0006g0322 a0001c0001t0006g0323 |
3 | HG03927.hp1 HG04228.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.113-3066G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180546865 | |||||||
| chr5:180547071 | C | A | 1 | a0001c0001t0005g0270 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.113-2860C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547071 | |||||||
| chr5:180547097 | G | C | 1 | a0001c0001t0006g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.113-2834G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547097 | |||||||
| chr5:180547221 | G | GTACAT | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-2708_113-2707i others(7): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr5 | 180547221 | ||||||
| chr5:180547245 | C | T | 100 | a0001c0001t0001g0002 a0001c0001t0001g0226 a0001c0001t0001g0228 others(97): Show |
100 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.113-2686C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547245 | |||||||
| chr5:180547388 | C | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-2543C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547388 | |||||||
| chr5:180547390 | G | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-2541G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547390 | |||||||
| chr5:180547393 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.113-2538G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547393 | |||||||
| chr5:180547402 | C | A | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.113-2529C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547402 | |||||||
| chr5:180547479 | C | T | 99 | a0001c0001t0001g0002 a0001c0001t0001g0226 a0001c0001t0001g0228 others(96): Show |
99 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.113-2452C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547479 | |||||||
| chr5:180547609 | C | T | 1 | a0001c0001t0047g0238 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.113-2322C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547609 | |||||||
| chr5:180547671 | G | A | 118 | a0001c0001t0001g0169 a0001c0001t0002g0177 a0001c0001t0003g0171 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.113-2260G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547671 | |||||||
| chr5:180547692 | T | C | 1 | a0001c0001t0001g0308 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.113-2239T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547692 | |||||||
| chr5:180547696 | T | A | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.113-2235T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547696 | |||||||
| chr5:180547799 | G | A | 1 | a0001c0001t0055g0154 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.113-2132G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547799 | |||||||
| chr5:180547817 | G | T | 119 | a0001c0001t0001g0169 a0001c0001t0001g0292 a0001c0001t0002g0177 others(116): Show |
119 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.113-2114G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547817 | |||||||
| chr5:180547890 | T | C | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.113-2041T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547890 | |||||||
| chr5:180547975 | C | G | 1 | a0001c0001t0061g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.113-1956C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180547975 | |||||||
| chr5:180548104 | T | C | 316 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(313): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.113-1827T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180548104 | |||||||
| chr5:180548149 | A | AAG | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.113-1782_113-1781i others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180548149 | |||||||
| chr5:180548178 | A | G | 1 | a0001c0001t0001g0325 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.113-1753A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180548178 | |||||||
| chr5:180548236 | C | T | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.113-1695C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180548236 | |||||||
| chr5:180548385 | C | T | 53 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(50): Show |
53 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.113-1546C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180548385 | |||||||
| chr5:180548619 | T | C | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.113-1312T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180548619 | |||||||
| chr5:180548673 | G | C | 1 | a0001c0002t0004g0032 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.113-1258G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180548673 | |||||||
| chr5:180548792 | C | T | 15 | a0001c0002t0002g0030 a0001c0002t0002g0031 a0001c0002t0002g0039 others(12): Show |
15 | HG01069.hp1 HG01106.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.113-1139C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180548792 | |||||||
| chr5:180548828 | T | A | 2 | a0001c0001t0001g0169 a0001c0001t0002g0177 |
2 | NA18955.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.113-1103T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180548828 | |||||||
| chr5:180549012 | T | C | 3 | a0001c0001t0001g0243 a0001c0001t0001g0273 a0001c0001t0001g0314 |
3 | NA18978.hp2 NA19005.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.113-919T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549012 | |||||||
| chr5:180549038 | AAAGGTCT others(21): Show |
A | 1 | a0001c0001t0049g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.113-892_113-865del others(28): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549038 | |||||||
| chr5:180549067 | C | T | 1 | a0001c0001t0049g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.113-864C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549067 | |||||||
| chr5:180549201 | G | C | 1 | a0001c0001t0037g0172 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.113-730G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549201 | |||||||
| chr5:180549334 | T | G | 1 | a0001c0002t0004g0053 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.113-597T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549334 | |||||||
| chr5:180549375 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.113-556C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549375 | |||||||
| chr5:180549376 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.113-555A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549376 | |||||||
| chr5:180549387 | T | C | 1 | a0001c0002t0005g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.113-544T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549387 | |||||||
| chr5:180549389 | C | T | 4 | a0001c0002t0004g0032 a0001c0002t0004g0037 a0001c0002t0004g0045 others(1): Show |
4 | HG01167.hp1 HG02615.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.113-542C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549389 | |||||||
| chr5:180549396 | C | T | 2 | a0001c0001t0006g0322 a0001c0001t0006g0323 |
2 | HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.113-535C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549396 | |||||||
| chr5:180549472 | A | G | 5 | a0001c0001t0002g0019 a0001c0001t0002g0057 a0001c0001t0002g0061 others(2): Show |
5 | HG00621.hp1 NA18973.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.113-459A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549472 | |||||||
| chr5:180549476 | C | G | 1 | a0001c0001t0017g0167 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.113-455C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549476 | |||||||
| chr5:180549600 | GATCACGC others(4): Show |
G | 1 | a0001c0001t0001g0235 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.113-330_113-320del others(11): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549600 | |||||||
| chr5:180549628 | A | G | 2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG01952.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.113-303A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549628 | |||||||
| chr5:180549636 | G | A | 3 | a0001c0001t0025g0216 a0001c0001t0026g0222 a0001c0001t0038g0217 |
3 | HG01261.hp1 HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.113-295G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549636 | |||||||
| chr5:180549646 | T | C | 3 | a0001c0001t0016g0117 a0001c0001t0016g0121 a0001c0001t0050g0088 |
3 | HG00639.hp1 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.113-285T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549646 | |||||||
| chr5:180549819 | T | A | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.113-112T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549819 | |||||||
| chr5:180549905 | C | T | 1 | a0001c0001t0002g0065 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.113-26C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 2/11 | chr5 | 180549905 | |||||||
| chr5:180550388 | G | T | 116 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(113): Show |
116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.299+271G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180550388 | |||||||
| chr5:180550608 | T | C | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.299+491T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180550608 | |||||||
| chr5:180550868 | G | A | 1 | a0001c0001t0006g0139 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.299+751G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180550868 | |||||||
| chr5:180551115 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.299+998G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551115 | |||||||
| chr5:180551181 | C | CA | 9 | a0001c0001t0001g0300 a0001c0001t0001g0314 a0001c0001t0002g0111 others(6): Show |
9 | HG00099.hp1 HG00597.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.299+1079dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 180551181 | ||||||
| chr5:180551198 | C | T | 1 | a0001c0001t0007g0126 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.299+1081C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551198 | |||||||
| chr5:180551286 | G | A | 6 | a0001c0001t0001g0266 a0001c0001t0001g0280 a0001c0001t0001g0281 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.299+1169G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551286 | |||||||
| chr5:180551351 | T | C | 102 | a0001c0001t0001g0002 a0001c0001t0001g0169 a0001c0001t0001g0226 others(99): Show |
102 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.299+1234T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551351 | |||||||
| chr5:180551425 | T | G | 1 | a0001c0001t0032g0129 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.299+1308T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551425 | |||||||
| chr5:180551580 | T | A | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.299+1463T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551580 | |||||||
| chr5:180551663 | C | G | 3 | a0001c0001t0003g0192 a0001c0001t0009g0011 a0001c0001t0023g0010 |
3 | HG02027.hp1 NA18612.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.299+1546C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551663 | |||||||
| chr5:180551716 | A | C | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.299+1599A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551716 | |||||||
| chr5:180551761 | A | G | 2 | a0001c0001t0001g0325 a0001c0001t0011g0215 |
2 | HG02818.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.300-1625A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551761 | |||||||
| chr5:180551794 | A | T | 49 | a0001c0001t0001g0241 a0001c0001t0001g0282 a0001c0001t0006g0009 others(46): Show |
49 | HG00408.hp1 HG00609.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.300-1592A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551794 | |||||||
| chr5:180551796 | G | T | 49 | a0001c0001t0001g0241 a0001c0001t0001g0282 a0001c0001t0006g0009 others(46): Show |
49 | HG00408.hp1 HG00609.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.300-1590G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551796 | |||||||
| chr5:180551891 | C | T | 12 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 others(9): Show |
12 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.300-1495C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551891 | |||||||
| chr5:180551926 | A | G | 8 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(5): Show |
9 | HG02451.hp2 HG02809.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.300-1460A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180551926 | |||||||
| chr5:180552067 | C | T | 1 | a0001c0001t0049g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.300-1319C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552067 | |||||||
| chr5:180552075 | G | A | 1 | a0001c0002t0004g0049 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.300-1311G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552075 | |||||||
| chr5:180552120 | C | T | 3 | a0001c0001t0021g0159 a0001c0001t0021g0160 a0001c0001t0021g0161 |
3 | HG02735.hp1 HG02738.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.300-1266C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552120 | |||||||
| chr5:180552348 | G | C | 105 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(102): Show |
105 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.300-1038G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552348 | |||||||
| chr5:180552377 | A | C | 1 | a0001c0001t0002g0109 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.300-1009A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552377 | |||||||
| chr5:180552382 | A | G | 3 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0215 |
3 | HG02818.hp1 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.300-1004A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552382 | |||||||
| chr5:180552391 | GCA | G | 51 | a0001c0001t0001g0067 a0001c0001t0002g0019 a0001c0001t0002g0021 others(48): Show |
51 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.300-991_300-990del others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 180552391 | ||||||
| chr5:180552399 | T | C | 1 | a0001c0001t0001g0311 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.300-987T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552399 | |||||||
| chr5:180552407 | C | T | 112 | a0001c0001t0001g0300 a0001c0001t0003g0171 a0001c0001t0003g0173 others(109): Show |
112 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.300-979C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552407 | |||||||
| chr5:180552424 | A | G | 5 | a0001c0001t0001g0303 a0001c0001t0002g0071 a0001c0001t0002g0090 others(2): Show |
5 | HG02083.hp2 NA18942.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.300-962A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552424 | |||||||
| chr5:180552426 | A | G | 5 | a0001c0001t0001g0303 a0001c0001t0002g0071 a0001c0001t0002g0090 others(2): Show |
5 | HG02083.hp2 NA18942.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.300-960A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552426 | |||||||
| chr5:180552427 | G | A | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.300-959G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552427 | |||||||
| chr5:180552430 | T | A | 5 | a0001c0001t0001g0303 a0001c0001t0002g0071 a0001c0001t0002g0090 others(2): Show |
5 | HG02083.hp2 NA18942.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.300-956T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552430 | |||||||
| chr5:180552434 | G | T | 1 | a0001c0001t0061g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.300-952G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552434 | |||||||
| chr5:180552437 | C | T | 9 | a0001c0001t0002g0019 a0001c0001t0002g0057 a0001c0001t0002g0061 others(6): Show |
9 | HG00621.hp1 HG02486.hp2 HG03491.hp1 others(6): Show |
intron_variant | MODIFIER | c.300-949C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552437 | |||||||
| chr5:180552438 | G | A | 4 | a0001c0001t0019g0255 a0001c0001t0019g0256 a0001c0001t0019g0284 others(1): Show |
4 | NA18947.hp1 NA18967.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.300-948G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552438 | |||||||
| chr5:180552443 | C | T | 289 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(286): Show |
289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.300-943C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552443 | |||||||
| chr5:180552458 | G | A | 56 | a0001c0001t0001g0106 a0001c0001t0002g0084 a0001c0001t0006g0009 others(53): Show |
56 | HG00408.hp1 HG00609.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.300-928G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552458 | |||||||
| chr5:180552502 | T | A | 1 | a0001c0001t0009g0207 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.300-884T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552502 | |||||||
| chr5:180552504 | G | A | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.300-882G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552504 | |||||||
| chr5:180552514 | C | T | 1 | a0001c0001t0009g0207 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.300-872C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552514 | |||||||
| chr5:180552515 | A | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0169 a0001c0001t0001g0226 others(110): Show |
113 | HG00280.hp1 HG00423.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.300-871A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552515 | |||||||
| chr5:180552519 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.300-867A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552519 | |||||||
| chr5:180552577 | C | T | 3 | a0001c0001t0003g0171 a0001c0001t0003g0182 a0001c0001t0003g0185 |
3 | HG01358.hp2 HG01993.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.300-809C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552577 | |||||||
| chr5:180552580 | A | G | 50 | a0001c0001t0001g0067 a0001c0001t0002g0019 a0001c0001t0002g0021 others(47): Show |
50 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.300-806A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552580 | |||||||
| chr5:180552601 | G | A | 2 | a0001c0001t0010g0188 a0001c0001t0010g0195 |
2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.300-785G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552601 | |||||||
| chr5:180552611 | A | T | 4 | a0001c0001t0002g0087 a0001c0001t0002g0089 a0001c0001t0002g0092 others(1): Show |
4 | HG00438.hp2 HG02165.hp2 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.300-775A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552611 | |||||||
| chr5:180552625 | A | G | 1 | a0001c0001t0039g0103 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.300-761A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552625 | |||||||
| chr5:180552627 | T | C | 125 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(122): Show |
125 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.300-759T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552627 | |||||||
| chr5:180552628 | G | A | 1 | a0001c0001t0039g0103 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.300-758G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552628 | |||||||
| chr5:180552645 | C | CA | 116 | a0001c0001t0001g0002 a0001c0001t0001g0273 a0001c0001t0001g0293 others(113): Show |
116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.300-726dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 180552645 | ||||||
| chr5:180552836 | CTGT | C | 51 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(48): Show |
51 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.300-548_300-546del others(3): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 180552836 | ||||||
| chr5:180552887 | T | C | 2 | a0001c0001t0035g0018 a0001c0001t0036g0193 |
2 | HG02074.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.300-499T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180552887 | |||||||
| chr5:180552970 | A | ATCATTTC others(325): Show |
2 | a0001c0002t0004g0033 a0001c0002t0004g0047 |
2 | HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.300-400_300-399ins others(332): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 180552970 | ||||||
| chr5:180552970 | A | ATCATTTC others(338): Show |
1 | a0001c0002t0004g0036 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.300-400_300-399ins others(345): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 180552970 | ||||||
| chr5:180552970 | A | ATCATTTC others(346): Show |
1 | a0001c0002t0004g0038 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.300-400_300-399ins others(353): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 180552970 | ||||||
| chr5:180552970 | A | ATCATTTC others(361): Show |
1 | a0001c0002t0002g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.300-400_300-399ins others(368): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr5 | 180552970 | ||||||
| chr5:180553066 | C | T | 10 | a0001c0002t0004g0032 a0001c0002t0004g0037 a0001c0002t0004g0045 others(7): Show |
10 | HG01167.hp1 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.300-320C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180553066 | |||||||
| chr5:180553118 | G | A | 3 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0008 |
3 | HG00099.hp1 HG00738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.300-268G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180553118 | |||||||
| chr5:180553171 | A | G | 1 | a0001c0001t0010g0209 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.300-215A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180553171 | |||||||
| chr5:180553211 | T | C | 1 | a0001c0001t0057g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.300-175T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180553211 | |||||||
| chr5:180553215 | A | C | 110 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(107): Show |
110 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.300-171A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180553215 | |||||||
| chr5:180553251 | G | A | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.300-135G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180553251 | |||||||
| chr5:180553302 | T | A | 110 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(107): Show |
110 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.300-84T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180553302 | |||||||
| chr5:180553378 | A | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.300-8A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 3/11 | chr5 | 180553378 | |||||||
| chr5:180553527 | A | G | 117 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(114): Show |
117 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.385+56A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180553527 | |||||||
| chr5:180553661 | CT | C | 7 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(4): Show |
7 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.385+199delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180553661 | ||||||
| chr5:180553676 | GGA | G | 4 | a0001c0001t0019g0255 a0001c0001t0019g0256 a0001c0001t0019g0284 others(1): Show |
4 | NA18947.hp1 NA18967.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+206_385+207del others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180553676 | |||||||
| chr5:180553711 | A | G | 117 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(114): Show |
117 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.385+240A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180553711 | |||||||
| chr5:180553844 | A | G | 3 | a0001c0001t0001g0243 a0001c0001t0001g0273 a0001c0001t0001g0314 |
3 | NA18978.hp2 NA19005.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.385+373A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180553844 | |||||||
| chr5:180553847 | T | C | 5 | a0001c0001t0001g0298 a0001c0001t0001g0300 a0001c0001t0001g0301 others(2): Show |
5 | HG00597.hp2 HG02015.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+376T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180553847 | |||||||
| chr5:180553941 | G | A | 1 | a0001c0001t0009g0174 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.385+470G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180553941 | |||||||
| chr5:180554054 | C | G | 1 | a0001c0001t0001g0226 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.385+583C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554054 | |||||||
| chr5:180554124 | T | G | 3 | a0001c0002t0005g0027 a0001c0002t0005g0028 a0001c0002t0005g0029 |
3 | HG02717.hp1 HG02976.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.385+653T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554124 | |||||||
| chr5:180554168 | A | G | 2 | a0001c0001t0016g0117 a0001c0001t0016g0121 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.385+697A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554168 | |||||||
| chr5:180554330 | C | T | 117 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(114): Show |
117 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.385+859C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554330 | |||||||
| chr5:180554417 | TA | T | 269 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(266): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.385+962delA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180554417 | ||||||
| chr5:180554417 | TAAAAA | T | 14 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(11): Show |
15 | HG01261.hp1 HG01884.hp1 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.385+958_385+962del others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180554417 | ||||||
| chr5:180554487 | T | C | 1 | a0001c0001t0001g0317 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.385+1016T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554487 | |||||||
| chr5:180554517 | G | GT | 59 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(56): Show |
59 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.385+1054dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180554517 | ||||||
| chr5:180554517 | G | GTT | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.385+1053_385+1054d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180554517 | ||||||
| chr5:180554517 | G | GTTT | 49 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(46): Show |
49 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.385+1052_385+1054d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180554517 | ||||||
| chr5:180554557 | C | T | 52 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(49): Show |
52 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.385+1086C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554557 | |||||||
| chr5:180554603 | T | TG | 292 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(289): Show |
293 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.385+1132_385+1133i others(3): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554603 | |||||||
| chr5:180554604 | T | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+1133T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554604 | |||||||
| chr5:180554632 | A | G | 1 | a0001c0001t0006g0125 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.385+1161A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554632 | |||||||
| chr5:180554938 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.385+1467A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554938 | |||||||
| chr5:180554950 | G | A | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.385+1479G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180554950 | |||||||
| chr5:180555010 | C | CT | 6 | a0001c0001t0002g0070 a0001c0001t0007g0144 a0001c0001t0009g0174 others(3): Show |
6 | HG01243.hp1 HG02280.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.385+1553dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180555010 | ||||||
| chr5:180555111 | A | C | 118 | a0001c0001t0001g0285 a0001c0001t0001g0304 a0001c0001t0001g0306 others(115): Show |
118 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.385+1640A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180555111 | |||||||
| chr5:180555151 | T | C | 306 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(303): Show |
307 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.385+1680T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180555151 | |||||||
| chr5:180555278 | G | A | 305 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(302): Show |
306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.385+1807G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180555278 | |||||||
| chr5:180555281 | A | G | 111 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(108): Show |
111 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.385+1810A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180555281 | |||||||
| chr5:180555423 | G | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+1952G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180555423 | |||||||
| chr5:180555459 | A | C | 118 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(115): Show |
118 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.385+1988A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180555459 | |||||||
| chr5:180555935 | G | A | 2 | a0001c0001t0003g0212 a0001c0001t0009g0178 |
2 | NA18977.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.385+2464G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180555935 | |||||||
| chr5:180556221 | C | T | 113 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(110): Show |
113 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.385+2750C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556221 | |||||||
| chr5:180556367 | A | G | 1 | a0001c0001t0061g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.385+2896A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556367 | |||||||
| chr5:180556600 | T | C | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.385+3129T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556600 | |||||||
| chr5:180556602 | T | C | 110 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(107): Show |
110 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.385+3131T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556602 | |||||||
| chr5:180556618 | G | T | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.385+3147G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556618 | |||||||
| chr5:180556661 | A | G | 1 | a0001c0001t0049g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.385+3190A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556661 | |||||||
| chr5:180556748 | C | T | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.385+3277C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556748 | |||||||
| chr5:180556776 | C | T | 1 | a0001c0002t0004g0053 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.385+3305C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556776 | |||||||
| chr5:180556779 | C | T | 1 | a0001c0001t0002g0063 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.385+3308C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556779 | |||||||
| chr5:180556895 | G | A | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.385+3424G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556895 | |||||||
| chr5:180556942 | C | T | 2 | a0001c0001t0002g0075 a0001c0001t0002g0076 |
2 | HG01952.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.385+3471C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556942 | |||||||
| chr5:180556943 | G | A | 1 | a0001c0001t0002g0068 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.385+3472G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180556943 | |||||||
| chr5:180556955 | C | CA | 12 | a0001c0001t0005g0114 a0001c0001t0005g0270 a0001c0001t0018g0005 others(9): Show |
12 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.385+3499dupA | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180556955 | ||||||
| chr5:180557108 | G | A | 1 | a0001c0001t0011g0214 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.385+3637G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557108 | |||||||
| chr5:180557360 | A | ACCAGCAG others(6): Show |
116 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(113): Show |
116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.385+3889_385+3890i others(15): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557360 | |||||||
| chr5:180557361 | A | G | 116 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(113): Show |
116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.385+3890A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557361 | |||||||
| chr5:180557485 | A | G | 52 | a0001c0001t0002g0070 a0001c0001t0006g0009 a0001c0001t0006g0122 others(49): Show |
52 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.385+4014A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557485 | |||||||
| chr5:180557612 | G | A | 1 | a0001c0001t0001g0312 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.385+4141G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557612 | |||||||
| chr5:180557625 | A | C | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.385+4154A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557625 | |||||||
| chr5:180557678 | G | T | 1 | a0001c0002t0005g0027 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.385+4207G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557678 | |||||||
| chr5:180557748 | G | C | 101 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(98): Show |
101 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.385+4277G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557748 | |||||||
| chr5:180557848 | A | G | 51 | a0001c0001t0001g0319 a0001c0001t0003g0171 a0001c0001t0003g0173 others(48): Show |
51 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.385+4377A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557848 | |||||||
| chr5:180557874 | T | C | 5 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(2): Show |
6 | HG02818.hp1 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.385+4403T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557874 | |||||||
| chr5:180557905 | TTTTG | T | 46 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(43): Show |
46 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.385+4436_385+4439d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180557905 | ||||||
| chr5:180557921 | C | T | 1 | a0001c0001t0007g0143 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.385+4450C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557921 | |||||||
| chr5:180557952 | A | T | 2 | a0001c0001t0016g0117 a0001c0001t0016g0121 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.385+4481A>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180557952 | |||||||
| chr5:180558155 | G | A | 1 | a0001c0001t0048g0310 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.385+4684G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558155 | |||||||
| chr5:180558276 | T | C | 1 | a0001c0005t0004g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.385+4805T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558276 | |||||||
| chr5:180558277 | G | A | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.385+4806G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558277 | |||||||
| chr5:180558333 | T | C | 121 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(118): Show |
121 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.385+4862T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558333 | |||||||
| chr5:180558451 | G | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+4980G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558451 | |||||||
| chr5:180558465 | C | T | 1 | a0001c0002t0005g0024 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.385+4994C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558465 | |||||||
| chr5:180558496 | C | T | 10 | a0001c0002t0004g0032 a0001c0002t0004g0037 a0001c0002t0004g0045 others(7): Show |
10 | HG01167.hp1 HG02451.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.385+5025C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558496 | |||||||
| chr5:180558510 | T | TAA | 50 | a0001c0001t0003g0171 a0001c0001t0006g0009 a0001c0001t0006g0122 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.385+5049_385+5050d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180558510 | ||||||
| chr5:180558510 | T | TAAA | 48 | a0001c0001t0003g0173 a0001c0001t0003g0180 a0001c0001t0003g0181 others(45): Show |
48 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.385+5048_385+5050d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180558510 | ||||||
| chr5:180558521 | A | AAC | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.385+5050_385+5051i others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558521 | |||||||
| chr5:180558522 | C | A | 116 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(113): Show |
116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.385+5051C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558522 | |||||||
| chr5:180558549 | A | G | 1 | a0001c0001t0044g0170 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.385+5078A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558549 | |||||||
| chr5:180558588 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.385+5117C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558588 | |||||||
| chr5:180558620 | G | GCT | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.385+5150_385+5151d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180558620 | ||||||
| chr5:180558622 | T | TC | 62 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(59): Show |
62 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.385+5151_385+5152i others(3): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558622 | |||||||
| chr5:180558623 | T | C | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+5152T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558623 | |||||||
| chr5:180558804 | TTTATTTG others(4): Show |
T | 109 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(106): Show |
109 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.385+5336_385+5346d others(13): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180558804 | ||||||
| chr5:180558831 | C | T | 1 | a0001c0001t0046g0012 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.385+5360C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558831 | |||||||
| chr5:180558834 | G | A | 1 | a0001c0001t0035g0018 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.385+5363G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558834 | |||||||
| chr5:180558863 | C | T | 2 | a0001c0001t0062g0073 a0001c0001t0063g0229 |
2 | HG02258.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.385+5392C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558863 | |||||||
| chr5:180558909 | G | T | 1 | a0001c0001t0002g0093 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.385+5438G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558909 | |||||||
| chr5:180558934 | C | T | 51 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(48): Show |
51 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.385+5463C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558934 | |||||||
| chr5:180558962 | T | C | 49 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(46): Show |
49 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.385+5491T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180558962 | |||||||
| chr5:180559567 | G | T | 4 | a0001c0002t0004g0032 a0001c0002t0004g0037 a0001c0002t0004g0045 others(1): Show |
4 | HG01167.hp1 HG02615.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-4922G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180559567 | |||||||
| chr5:180559694 | A | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-4795A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180559694 | |||||||
| chr5:180559950 | A | AT | 58 | a0001c0001t0001g0067 a0001c0001t0001g0233 a0001c0001t0001g0245 others(55): Show |
58 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.386-4523dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180559950 | ||||||
| chr5:180559980 | G | C | 2 | a0001c0002t0004g0033 a0001c0002t0004g0047 |
2 | HG02970.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.386-4509G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180559980 | |||||||
| chr5:180560009 | C | T | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.386-4480C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560009 | |||||||
| chr5:180560147 | A | G | 3 | a0001c0001t0006g0137 a0001c0001t0006g0138 a0001c0001t0054g0146 |
3 | HG01981.hp1 HG02004.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.386-4342A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560147 | |||||||
| chr5:180560266 | C | T | 9 | a0001c0002t0005g0022 a0001c0002t0005g0023 a0001c0002t0005g0024 others(6): Show |
9 | HG01891.hp2 HG02486.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.386-4223C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560266 | |||||||
| chr5:180560583 | G | C | 1 | a0001c0001t0001g0319 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.386-3906G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560583 | |||||||
| chr5:180560631 | G | A | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.386-3858G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560631 | |||||||
| chr5:180560768 | C | A | 1 | a0001c0001t0010g0183 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.386-3721C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560768 | |||||||
| chr5:180560818 | C | T | 17 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(14): Show |
18 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.386-3671C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560818 | |||||||
| chr5:180560919 | T | G | 58 | a0001c0001t0006g0122 a0001c0001t0006g0124 a0001c0001t0006g0125 others(55): Show |
58 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(55): Show |
intron_variant | MODIFIER | c.386-3570T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560919 | |||||||
| chr5:180560922 | G | T | 135 | a0001c0001t0001g0002 a0001c0001t0001g0106 a0001c0001t0001g0169 others(132): Show |
135 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.386-3567G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560922 | |||||||
| chr5:180560937 | T | G | 50 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(47): Show |
50 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.386-3552T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560937 | |||||||
| chr5:180560964 | A | ATCAG | 304 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(301): Show |
305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.386-3522_386-3521i others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180560964 | ||||||
| chr5:180560964 | A | G | 1 | a0001c0001t0002g0065 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.386-3525A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180560964 | |||||||
| chr5:180561064 | C | T | 1 | a0001c0001t0049g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.386-3425C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561064 | |||||||
| chr5:180561240 | C | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-3249C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561240 | |||||||
| chr5:180561276 | T | G | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.386-3213T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561276 | |||||||
| chr5:180561277 | A | G | 102 | a0001c0001t0001g0002 a0001c0001t0001g0169 a0001c0001t0001g0226 others(99): Show |
102 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.386-3212A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561277 | |||||||
| chr5:180561283 | C | T | 296 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(293): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.386-3206C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561283 | |||||||
| chr5:180561356 | T | TTG | 106 | a0001c0001t0001g0002 a0001c0001t0001g0228 a0001c0001t0001g0232 others(103): Show |
107 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.386-3097_386-3096d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | ||||||
| chr5:180561356 | T | TTGTG | 47 | a0001c0001t0001g0169 a0001c0001t0001g0233 a0001c0001t0001g0239 others(44): Show |
47 | HG00280.hp2 HG00544.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.386-3099_386-3096d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | ||||||
| chr5:180561356 | T | TTGTGTG | 41 | a0001c0001t0001g0067 a0001c0001t0001g0106 a0001c0001t0001g0226 others(38): Show |
41 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.386-3101_386-3096d others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | ||||||
| chr5:180561356 | T | TTGTGTGT others(1): Show |
16 | a0001c0001t0001g0250 a0001c0001t0001g0260 a0001c0001t0001g0300 others(13): Show |
16 | HG00544.hp1 HG00597.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.386-3103_386-3096d others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | ||||||
| chr5:180561356 | T | TTGTGTGT others(3): Show |
6 | a0001c0001t0002g0057 a0001c0001t0002g0070 a0001c0001t0002g0098 others(3): Show |
6 | HG00609.hp1 HG00621.hp1 HG02071.hp1 others(3): Show |
intron_variant | MODIFIER | c.386-3105_386-3096d others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | ||||||
| chr5:180561356 | T | TTGTGTGT others(7): Show |
2 | a0001c0001t0002g0078 a0001c0001t0005g0225 |
2 | HG02523.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.386-3109_386-3096d others(16): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | ||||||
| chr5:180561356 | T | TTGTGTGT others(9): Show |
3 | a0001c0001t0002g0079 a0001c0001t0002g0111 a0001c0001t0052g0080 |
3 | NA18941.hp2 NA18991.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.386-3111_386-3096d others(18): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | ||||||
| chr5:180561356 | T | TTGTGTGT others(11): Show |
1 | a0001c0001t0002g0083 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.386-3113_386-3096d others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | ||||||
| chr5:180561356 | TTG | T | 3 | a0001c0001t0001g0235 a0001c0001t0036g0193 a0001c0002t0004g0054 |
3 | HG02083.hp1 HG02155.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.386-3097_386-3096d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | ||||||
| chr5:180561356 | TTGTG | T | 3 | a0001c0001t0007g0149 a0001c0001t0007g0150 a0001c0001t0008g0263 |
3 | NA18962.hp2 NA18973.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.386-3099_386-3096d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | ||||||
| chr5:180561356 | TTGTGTG | T | 49 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(46): Show |
49 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.386-3101_386-3096d others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | ||||||
| chr5:180561356 | TTGTGTGT others(1): Show |
T | 11 | a0001c0001t0006g0157 a0001c0001t0016g0117 a0001c0001t0016g0121 others(8): Show |
11 | HG01168.hp1 HG01169.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.386-3103_386-3096d others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | ||||||
| chr5:180561356 | TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0061g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.386-3107_386-3096d others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180561356 | ||||||
| chr5:180561695 | C | T | 2 | a0001c0001t0010g0188 a0001c0001t0010g0195 |
2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.386-2794C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561695 | |||||||
| chr5:180561711 | G | A | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.386-2778G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561711 | |||||||
| chr5:180561770 | T | C | 1 | a0001c0001t0007g0150 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.386-2719T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561770 | |||||||
| chr5:180561881 | C | G | 1 | a0001c0001t0005g0225 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.386-2608C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561881 | |||||||
| chr5:180561943 | G | C | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.386-2546G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180561943 | |||||||
| chr5:180562165 | G | A | 116 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(113): Show |
116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.386-2324G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562165 | |||||||
| chr5:180562178 | T | A | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.386-2311T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562178 | |||||||
| chr5:180562462 | C | T | 1 | a0001c0001t0063g0229 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.386-2027C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562462 | |||||||
| chr5:180562469 | G | A | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-2020G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562469 | |||||||
| chr5:180562512 | G | A | 1 | a0001c0001t0061g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.386-1977G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562512 | |||||||
| chr5:180562516 | G | A | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-1973G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562516 | |||||||
| chr5:180562542 | C | T | 1 | a0001c0001t0057g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.386-1947C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562542 | |||||||
| chr5:180562555 | G | A | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.386-1934G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562555 | |||||||
| chr5:180562556 | C | T | 1 | a0001c0001t0045g0331 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.386-1933C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562556 | |||||||
| chr5:180562664 | C | T | 13 | a0001c0001t0001g0228 a0001c0001t0001g0245 a0001c0001t0001g0250 others(10): Show |
13 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.386-1825C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562664 | |||||||
| chr5:180562773 | T | C | 17 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(14): Show |
18 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.386-1716T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562773 | |||||||
| chr5:180562871 | T | C | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.386-1618T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180562871 | |||||||
| chr5:180563048 | A | G | 117 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(114): Show |
117 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.386-1441A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563048 | |||||||
| chr5:180563062 | G | A | 1 | a0001c0002t0004g0053 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.386-1427G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563062 | |||||||
| chr5:180563107 | G | A | 2 | a0001c0001t0025g0216 a0001c0001t0038g0217 |
2 | HG02109.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.386-1382G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563107 | |||||||
| chr5:180563216 | A | AT | 110 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(107): Show |
110 | HG00408.hp1 HG00609.hp2 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.386-1256dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180563216 | ||||||
| chr5:180563217 | T | A | 6 | a0001c0001t0001g0266 a0001c0001t0001g0280 a0001c0001t0001g0281 others(3): Show |
6 | HG01069.hp2 HG01071.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.386-1272T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563217 | |||||||
| chr5:180563247 | G | A | 1 | a0001c0001t0060g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.386-1242G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563247 | |||||||
| chr5:180563380 | G | GT | 6 | a0001c0001t0010g0183 a0001c0001t0010g0194 a0001c0001t0014g0203 others(3): Show |
6 | HG02738.hp2 HG03195.hp2 HG03831.hp1 others(3): Show |
intron_variant | MODIFIER | c.386-1100dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180563380 | ||||||
| chr5:180563400 | GC | G | 293 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(290): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.386-1088delC | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563400 | |||||||
| chr5:180563401 | C | T | 3 | a0001c0001t0001g0237 a0001c0001t0003g0198 a0001c0001t0023g0197 |
3 | HG01433.hp2 NA19075.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.386-1088C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563401 | |||||||
| chr5:180563411 | C | A | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-1078C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563411 | |||||||
| chr5:180563416 | A | G | 117 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(114): Show |
117 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.386-1073A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563416 | |||||||
| chr5:180563433 | G | A | 1 | a0001c0001t0002g0059 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.386-1056G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563433 | |||||||
| chr5:180563478 | G | A | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-1011G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563478 | |||||||
| chr5:180563522 | A | G | 117 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(114): Show |
117 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.386-967A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563522 | |||||||
| chr5:180563580 | C | A | 1 | a0001c0001t0003g0180 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.386-909C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563580 | |||||||
| chr5:180563633 | G | C | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.386-856G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563633 | |||||||
| chr5:180563846 | T | C | 117 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(114): Show |
117 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.386-643T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563846 | |||||||
| chr5:180563882 | C | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-607C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563882 | |||||||
| chr5:180563903 | T | C | 1 | a0001c0001t0010g0188 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.386-586T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563903 | |||||||
| chr5:180563925 | G | A | 1 | a0001c0001t0061g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.386-564G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563925 | |||||||
| chr5:180563926 | C | T | 1 | a0001c0001t0061g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.386-563C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563926 | |||||||
| chr5:180563933 | A | AT | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.386-550dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr5 | 180563933 | ||||||
| chr5:180563980 | C | T | 3 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0009g0179 |
3 | HG03017.hp1 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.386-509C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180563980 | |||||||
| chr5:180564040 | T | A | 1 | a0001c0001t0061g0004 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.386-449T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180564040 | |||||||
| chr5:180564099 | C | T | 2 | a0001c0001t0040g0101 a0001c0001t0041g0102 |
2 | HG02451.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.386-390C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180564099 | |||||||
| chr5:180564162 | G | A | 1 | a0001c0001t0010g0183 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.386-327G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180564162 | |||||||
| chr5:180564238 | A | G | 1 | a0001c0001t0003g0202 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.386-251A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180564238 | |||||||
| chr5:180564276 | C | A | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.386-213C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180564276 | |||||||
| chr5:180564366 | AGTCTGAC others(8): Show |
A | 19 | a0001c0001t0003g0189 a0001c0001t0003g0190 a0001c0001t0003g0196 others(16): Show |
19 | HG00738.hp2 HG01071.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.386-122_386-108del others(15): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180564366 | |||||||
| chr5:180564401 | T | C | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-88T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 4/11 | chr5 | 180564401 | |||||||
| chr5:180564633 | G | A | 1 | a0001c0001t0001g0233 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.490+40G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 5/11 | chr5 | 180564633 | |||||||
| chr5:180564750 | A | G | 1 | a0001c0002t0004g0034 | 1 | HG03139.hp1 | splice_region_variant&intron_variant | LOW | c.559+7A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180564750 | |||||||
| chr5:180564841 | A | G | 117 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(114): Show |
117 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.559+98A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180564841 | |||||||
| chr5:180564886 | C | A | 5 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(2): Show |
6 | HG02818.hp1 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.559+143C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180564886 | |||||||
| chr5:180564946 | A | G | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.559+203A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180564946 | |||||||
| chr5:180564959 | C | T | 116 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(113): Show |
116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.559+216C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180564959 | |||||||
| chr5:180565218 | T | G | 1 | a0001c0001t0001g0309 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.559+475T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565218 | |||||||
| chr5:180565566 | C | T | 116 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(113): Show |
116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.560-254C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565566 | |||||||
| chr5:180565571 | C | T | 17 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(14): Show |
18 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.560-249C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565571 | |||||||
| chr5:180565582 | C | T | 116 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(113): Show |
116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.560-238C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565582 | |||||||
| chr5:180565609 | G | A | 1 | a0001c0001t0021g0160 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.560-211G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565609 | |||||||
| chr5:180565629 | T | G | 1 | a0001c0001t0006g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.560-191T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565629 | |||||||
| chr5:180565633 | C | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.560-187C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565633 | |||||||
| chr5:180565642 | C | T | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.560-178C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565642 | |||||||
| chr5:180565645 | G | C | 1 | a0001c0001t0001g0251 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.560-175G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565645 | |||||||
| chr5:180565708 | T | A | 1 | a0001c0001t0017g0166 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.560-112T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565708 | |||||||
| chr5:180565795 | A | G | 1 | a0001c0001t0032g0155 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.560-25A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 6/11 | chr5 | 180565795 | |||||||
| chr5:180566024 | G | A | 1 | a0001c0001t0003g0202 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.717+47G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | chr5 | 180566024 | |||||||
| chr5:180566123 | C | T | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.717+146C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | chr5 | 180566123 | |||||||
| chr5:180566172 | C | A | 1 | a0001c0001t0006g0131 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.717+195C>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | chr5 | 180566172 | |||||||
| chr5:180566273 | C | T | 1 | a0001c0001t0030g0153 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.717+296C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | chr5 | 180566273 | |||||||
| chr5:180566295 | T | C | 1 | a0001c0001t0006g0151 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.717+318T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | chr5 | 180566295 | |||||||
| chr5:180566443 | T | C | 1 | a0001c0001t0001g0325 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.717+466T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | chr5 | 180566443 | |||||||
| chr5:180566596 | G | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.718-492G>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | chr5 | 180566596 | |||||||
| chr5:180566640 | C | CT | 24 | a0001c0001t0002g0019 a0001c0001t0002g0062 a0001c0001t0002g0064 others(21): Show |
24 | HG00408.hp2 HG00642.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.718-421dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr5 | 180566640 | ||||||
| chr5:180566640 | CT | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0169 a0001c0001t0001g0226 others(93): Show |
96 | HG00099.hp2 HG00280.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.718-421delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr5 | 180566640 | ||||||
| chr5:180566640 | CTT | C | 46 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0266 others(43): Show |
46 | HG00738.hp2 HG00741.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.718-422_718-421del others(2): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr5 | 180566640 | ||||||
| chr5:180566640 | CTTT | C | 14 | a0001c0001t0009g0015 a0001c0001t0014g0168 a0001c0001t0014g0175 others(11): Show |
14 | HG00280.hp2 HG00639.hp2 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.718-423_718-421del others(3): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr5 | 180566640 | ||||||
| chr5:180566640 | CTTTT | C | 6 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(3): Show |
6 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-424_718-421del others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr5 | 180566640 | ||||||
| chr5:180566640 | CTTTTTTT others(3): Show |
C | 50 | a0001c0001t0001g0317 a0001c0001t0006g0009 a0001c0001t0006g0122 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.718-430_718-421del others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr5 | 180566640 | ||||||
| chr5:180566719 | G | C | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.718-369G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | chr5 | 180566719 | |||||||
| chr5:180566813 | T | C | 296 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0106 others(293): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.718-275T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 7/11 | chr5 | 180566813 | |||||||
| chr5:180567252 | C | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.872+10C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 8/11 | chr5 | 180567252 | |||||||
| chr5:180567581 | A | G | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.873-268A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 8/11 | chr5 | 180567581 | |||||||
| chr5:180567727 | G | A | 1 | a0001c0001t0017g0162 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.873-122G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 8/11 | chr5 | 180567727 | |||||||
| chr5:180568091 | A | G | 1 | a0001c0002t0005g0329 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1027+88A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568091 | |||||||
| chr5:180568230 | C | CT | 100 | a0001c0001t0001g0002 a0001c0001t0001g0169 a0001c0001t0001g0226 others(97): Show |
100 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.1027+242dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr5 | 180568230 | ||||||
| chr5:180568230 | CT | C | 9 | a0001c0001t0005g0225 a0001c0001t0011g0213 a0001c0001t0013g0104 others(6): Show |
9 | HG02451.hp2 HG02717.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1027+242delT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr5 | 180568230 | ||||||
| chr5:180568230 | CTT | C | 108 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(105): Show |
108 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.1027+241_1027+242d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr5 | 180568230 | ||||||
| chr5:180568234 | T | G | 1 | a0001c0001t0017g0166 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1027+231T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568234 | |||||||
| chr5:180568397 | C | G | 13 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(10): Show |
14 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1027+394C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568397 | |||||||
| chr5:180568401 | T | G | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1027+398T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568401 | |||||||
| chr5:180568493 | A | G | 2 | a0001c0001t0029g0287 a0001c0001t0029g0288 |
2 | NA18969.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1027+490A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568493 | |||||||
| chr5:180568546 | C | T | 1 | a0001c0001t0049g0332 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1027+543C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568546 | |||||||
| chr5:180568633 | A | G | 1 | a0001c0005t0004g0020 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1028-477A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568633 | |||||||
| chr5:180568823 | A | G | 1 | a0001c0001t0006g0157 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1028-287A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568823 | |||||||
| chr5:180568844 | G | A | 116 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(113): Show |
116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1028-266G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568844 | |||||||
| chr5:180568852 | G | A | 3 | a0001c0001t0022g0224 a0001c0003t0022g0219 a0001c0003t0022g0221 |
3 | HG02055.hp2 HG02976.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1028-258G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568852 | |||||||
| chr5:180568865 | C | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1028-245C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180568865 | |||||||
| chr5:180569009 | T | G | 2 | a0001c0002t0002g0030 a0001c0002t0002g0031 |
2 | HG01069.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1028-101T>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180569009 | |||||||
| chr5:180569031 | T | C | 1 | a0001c0001t0026g0220 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1028-79T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 9/11 | chr5 | 180569031 | |||||||
| chr5:180569381 | A | G | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1258+41A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180569381 | |||||||
| chr5:180569513 | C | T | 4 | a0001c0002t0004g0032 a0001c0002t0004g0037 a0001c0002t0004g0045 others(1): Show |
4 | HG01167.hp1 HG02615.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1258+173C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180569513 | |||||||
| chr5:180569529 | TGAG | T | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1258+193_1258+195d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr5 | 180569529 | ||||||
| chr5:180569550 | T | C | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1258+210T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180569550 | |||||||
| chr5:180569598 | G | A | 9 | a0001c0001t0006g0145 a0001c0001t0006g0147 a0001c0001t0007g0135 others(6): Show |
9 | HG00609.hp2 HG02523.hp2 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.1258+258G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180569598 | |||||||
| chr5:180569864 | C | T | 3 | a0001c0001t0011g0213 a0001c0001t0011g0214 a0001c0001t0011g0215 |
3 | HG02818.hp1 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1258+524C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180569864 | |||||||
| chr5:180569875 | G | A | 116 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(113): Show |
116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1258+535G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180569875 | |||||||
| chr5:180569962 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0012g0277 |
2 | HG02886.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1258+622C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180569962 | |||||||
| chr5:180570014 | C | T | 1 | a0001c0001t0030g0153 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1258+674C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570014 | |||||||
| chr5:180570046 | A | C | 50 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(47): Show |
50 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.1258+706A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570046 | |||||||
| chr5:180570086 | C | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0169 a0001c0001t0001g0226 others(99): Show |
102 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1258+746C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570086 | |||||||
| chr5:180570099 | C | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1258+759C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570099 | |||||||
| chr5:180570114 | T | C | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1258+774T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570114 | |||||||
| chr5:180570156 | G | C | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1258+816G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570156 | |||||||
| chr5:180570251 | G | A | 4 | a0001c0001t0014g0168 a0001c0001t0014g0175 a0001c0001t0014g0176 others(1): Show |
4 | HG00280.hp2 HG00639.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1258+911G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570251 | |||||||
| chr5:180570625 | A | G | 57 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(54): Show |
57 | HG00099.hp1 HG00408.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1259-605A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570625 | |||||||
| chr5:180570640 | A | G | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1259-590A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570640 | |||||||
| chr5:180570701 | A | G | 5 | a0001c0001t0011g0001 a0001c0001t0011g0213 a0001c0001t0011g0214 others(2): Show |
6 | HG02818.hp1 HG02965.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1259-529A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570701 | |||||||
| chr5:180570777 | G | A | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1259-453G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570777 | |||||||
| chr5:180570783 | C | T | 1 | a0001c0001t0057g0055 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1259-447C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 10/11 | chr5 | 180570783 | |||||||
| chr5:180571454 | C | T | 116 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(113): Show |
116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1461+22C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180571454 | |||||||
| chr5:180571569 | C | T | 1 | a0001c0001t0062g0073 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1461+137C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180571569 | |||||||
| chr5:180571683 | G | A | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1461+251G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180571683 | |||||||
| chr5:180571722 | C | T | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1461+290C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180571722 | |||||||
| chr5:180571805 | C | T | 50 | a0001c0001t0006g0009 a0001c0001t0006g0122 a0001c0001t0006g0124 others(47): Show |
50 | HG00408.hp1 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1461+373C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180571805 | |||||||
| chr5:180571968 | AAAT | A | 116 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(113): Show |
116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1461+540_1461+542d others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180571968 | ||||||
| chr5:180572060 | A | C | 4 | a0001c0001t0014g0168 a0001c0001t0014g0175 a0001c0001t0014g0176 others(1): Show |
4 | HG00280.hp2 HG00639.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1461+628A>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180572060 | |||||||
| chr5:180572070 | T | C | 1 | a0001c0001t0028g0242 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1461+638T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180572070 | |||||||
| chr5:180572251 | G | A | 2 | a0001c0001t0006g0322 a0001c0001t0006g0323 |
2 | HG03927.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1461+819G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180572251 | |||||||
| chr5:180572480 | G | A | 2 | a0001c0001t0009g0015 a0001c0001t0010g0017 |
2 | NA18957.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1461+1048G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180572480 | |||||||
| chr5:180572509 | C | T | 2 | a0001c0001t0003g0198 a0001c0001t0023g0197 |
2 | HG01433.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1461+1077C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180572509 | |||||||
| chr5:180572639 | T | A | 8 | a0001c0001t0017g0162 a0001c0001t0017g0163 a0001c0001t0017g0165 others(5): Show |
8 | HG01243.hp2 HG02258.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1461+1207T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180572639 | |||||||
| chr5:180572698 | C | T | 4 | a0001c0001t0018g0005 a0001c0001t0018g0006 a0001c0001t0018g0007 others(1): Show |
4 | HG00099.hp1 HG00738.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.1461+1266C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180572698 | |||||||
| chr5:180572715 | C | CT | 59 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(56): Show |
59 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.1462-1263dupT | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180572715 | ||||||
| chr5:180572824 | G | A | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1462-1164G>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180572824 | |||||||
| chr5:180572965 | C | G | 1 | a0001c0001t0009g0184 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1462-1023C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180572965 | |||||||
| chr5:180573090 | A | G | 116 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(113): Show |
116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1462-898A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573090 | |||||||
| chr5:180573188 | T | A | 12 | a0001c0001t0001g0228 a0001c0001t0001g0245 a0001c0001t0001g0250 others(9): Show |
12 | HG00544.hp1 HG00558.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.1462-800T>A | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573188 | |||||||
| chr5:180573220 | C | G | 116 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(113): Show |
116 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1462-768C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573220 | |||||||
| chr5:180573552 | A | AGT | 5 | a0001c0001t0062g0073 a0001c0001t0063g0229 a0001c0002t0005g0027 others(2): Show |
5 | HG02258.hp1 HG02717.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1462-387_1462-386d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573552 | ||||||
| chr5:180573552 | AGT | A | 9 | a0001c0002t0002g0030 a0001c0002t0002g0031 a0001c0002t0002g0039 others(6): Show |
9 | HG01069.hp1 HG01106.hp1 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.1462-387_1462-386d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573552 | ||||||
| chr5:180573552 | AGTGT | A | 9 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0048 others(6): Show |
9 | HG01167.hp1 HG01256.hp2 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1462-389_1462-386d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573552 | ||||||
| chr5:180573552 | AGTGTGTG others(1): Show |
A | 3 | a0001c0002t0004g0032 a0001c0002t0004g0037 a0001c0002t0004g0046 |
3 | HG02615.hp1 HG02970.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1462-393_1462-386d others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573552 | ||||||
| chr5:180573574 | TGTGTGTG others(27): Show |
T | 3 | a0001c0001t0040g0101 a0001c0001t0041g0102 a0001c0001t0060g0003 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1462-411_1462-378d others(36): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573574 | ||||||
| chr5:180573582 | TGTGTGTG others(15): Show |
T | 4 | a0001c0001t0019g0255 a0001c0001t0019g0256 a0001c0001t0019g0284 others(1): Show |
4 | NA18947.hp1 NA18967.hp2 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.1462-403_1462-382d others(24): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573582 | ||||||
| chr5:180573586 | TGTGTGTG others(11): Show |
T | 2 | a0001c0001t0008g0296 a0001c0001t0014g0203 |
2 | HG00735.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1462-399_1462-382d others(20): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573586 | ||||||
| chr5:180573590 | TGTGTGTG others(7): Show |
T | 16 | a0001c0001t0001g0272 a0001c0001t0007g0140 a0001c0001t0010g0183 others(13): Show |
16 | HG01261.hp1 HG02074.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.1462-395_1462-382d others(16): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573590 | ||||||
| chr5:180573592 | TGTGTGTG others(5): Show |
T | 44 | a0001c0001t0001g0067 a0001c0001t0001g0233 a0001c0001t0001g0264 others(41): Show |
44 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(41): Show |
intron_variant | MODIFIER | c.1462-393_1462-382d others(14): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573592 | ||||||
| chr5:180573594 | TGTGTGTG others(3): Show |
T | 59 | a0001c0001t0001g0245 a0001c0001t0001g0298 a0001c0001t0001g0317 others(56): Show |
59 | HG00408.hp2 HG00609.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.1462-391_1462-382d others(12): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573594 | ||||||
| chr5:180573596 | TGTGTGTC others(1): Show |
T | 52 | a0001c0001t0001g0106 a0001c0001t0001g0169 a0001c0001t0001g0228 others(49): Show |
52 | HG00099.hp1 HG00544.hp1 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.1462-389_1462-382d others(10): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573596 | ||||||
| chr5:180573598 | TGTGTCC | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0237 a0001c0001t0001g0246 others(63): Show |
66 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1462-387_1462-382d others(8): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573598 | ||||||
| chr5:180573600 | TGTCC | T | 26 | a0001c0001t0001g0232 a0001c0001t0001g0241 a0001c0001t0001g0243 others(23): Show |
26 | HG00438.hp1 HG00438.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.1462-371_1462-368d others(6): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573600 | ||||||
| chr5:180573601 | G | C | 2 | a0001c0002t0002g0040 a0001c0002t0002g0041 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1462-387G>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573601 | |||||||
| chr5:180573602 | T | C | 2 | a0001c0002t0002g0040 a0001c0002t0002g0041 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1462-386T>C | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573602 | |||||||
| chr5:180573602 | TCC | T | 24 | a0001c0001t0001g0226 a0001c0001t0001g0236 a0001c0001t0001g0240 others(21): Show |
24 | HG00544.hp2 HG01074.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1462-385_1462-384d others(4): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573602 | |||||||
| chr5:180573603 | C | G | 11 | a0001c0001t0002g0058 a0001c0001t0002g0109 a0001c0001t0002g0177 others(8): Show |
11 | HG00642.hp2 HG01361.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1462-385C>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573603 | |||||||
| chr5:180573604 | C | T | 11 | a0001c0001t0002g0058 a0001c0001t0002g0109 a0001c0001t0002g0177 others(8): Show |
11 | HG00642.hp2 HG01361.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.1462-384C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573604 | |||||||
| chr5:180573608 | C | T | 50 | a0001c0001t0003g0171 a0001c0001t0003g0173 a0001c0001t0003g0180 others(47): Show |
50 | HG00280.hp2 HG00639.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.1462-380C>T | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573608 | |||||||
| chr5:180573706 | A | G | 1 | a0001c0001t0060g0003 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1462-282A>G | CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | chr5 | 180573706 | |||||||
| chr5:180573881 | TTGTTC | T | 8 | a0001c0002t0002g0030 a0001c0002t0002g0031 a0001c0002t0002g0040 others(5): Show |
8 | HG01069.hp1 HG01106.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.1462-96_1462-92del others(5): Show |
CNOT6 | ENSG00000113300.13 | transcript | ENST00000261951.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr5 | 180573881 |