| geneid | 1258 |
|---|---|
| ensemblid | ENSG00000070729.14 |
| hgncid | 2151 |
| symbol | CNGB1 |
| name | cyclic nucleotide gated channel subunit beta 1 |
| refseq_nuc | NM_001297.5 |
| refseq_prot | NP_001288.3 |
| ensembl_nuc | ENST00000251102.13 |
| ensembl_prot | ENSP00000251102.8 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 57882340 |
| end | 57971128 |
| strand | - |
| ver | v1.2 |
| region | chr16:57882340-57971128 |
| region5000 | chr16:57877340-57976128 |
| regionname0 | CNGB1_chr16_57882340_57971128 |
| regionname5000 | CNGB1_chr16_57877340_57976128 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 1251 | 183 | 26 | 30 | 99 | 9 | 19 | 72 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002 | 1/1 | 1251 | 56 | 14 | 6 | 27 | 1 | 6 | 20 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003 | 0/0 | 1251 | 21 | 1 | 9 | 8 | 0 | 3 | 4 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0004 | 0/0 | 1251 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0005 | 0/0 | 1251 | 7 | 0 | 3 | 1 | 2 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0006 | 0/0 | 1252 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0007 | 0/0 | 1251 | 6 | 1 | 1 | 4 | 0 | 0 | 4 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0008 | 0/0 | 1251 | 5 | 2 | 0 | 1 | 1 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0009 | 0/0 | 1251 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0010 | 0/0 | 1251 | 5 | 3 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0011 | 0/0 | 1251 | 4 | 1 | 2 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0012 | 0/0 | 1251 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0013 | 0/0 | 1251 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0014 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0015 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0016 | 0/0 | 1251 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0017 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0018 | 0/0 | 1251 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0019 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0020 | 0/0 | 1251 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0021 | 0/0 | 1251 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0022 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0023 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0024 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0025 | 0/0 | 122 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0026 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0027 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0028 | 0/0 | 1252 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0029 | 0/0 | 1252 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0030 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0031 | 0/0 | 1251 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0032 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0033 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0034 | 0/0 | 1251 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0035 | 0/0 | 1251 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0036 | 0/0 | 1251 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0037 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0038 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0039 | 0/0 | 1251 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0040 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0041 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0042 | 0/0 | 1247 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0043 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0044 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0045 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0046 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0047 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0048 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0049 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0050 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0051 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0052 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 3756 | 40 | 1 | 3 | 28 | 3 | 5 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0002 | 0/0 | 3756 | 36 | 3 | 10 | 16 | 1 | 6 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0003 | 0/0 | 3756 | 33 | 0 | 7 | 18 | 2 | 6 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0004 | 0/0 | 3756 | 30 | 3 | 2 | 23 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0005 | 0/0 | 3756 | 25 | 3 | 3 | 16 | 0 | 3 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0006 | 0/1 | 3756 | 16 | 2 | 2 | 9 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0007 | 0/0 | 3756 | 6 | 5 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0008 | 0/0 | 3756 | 6 | 0 | 2 | 4 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0009 | 0/0 | 3756 | 5 | 0 | 3 | 1 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0010 | 0/0 | 3756 | 5 | 3 | 0 | 0 | 2 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0011 | 1/0 | 3756 | 5 | 4 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0012 | 0/0 | 3756 | 4 | 1 | 2 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0013 | 0/0 | 3756 | 4 | 1 | 3 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0014 | 0/0 | 3756 | 3 | 3 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0015 | 0/0 | 3756 | 3 | 3 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0016 | 0/0 | 3756 | 3 | 3 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0017 | 0/0 | 3756 | 3 | 0 | 0 | 3 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0018 | 0/0 | 3756 | 3 | 0 | 0 | 3 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0019 | 0/0 | 3756 | 3 | 0 | 3 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0020 | 0/0 | 3756 | 3 | 1 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0021 | 0/0 | 3756 | 3 | 0 | 1 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0022 | 0/0 | 3756 | 3 | 2 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0023 | 0/0 | 3756 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0024 | 0/0 | 3756 | 2 | 0 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0025 | 0/0 | 3756 | 2 | 1 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0026 | 0/0 | 3756 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0027 | 0/0 | 3756 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0028 | 0/0 | 3756 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0029 | 0/0 | 3756 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0030 | 0/0 | 3756 | 2 | 0 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0031 | 0/0 | 3756 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0032 | 0/0 | 3756 | 2 | 0 | 0 | 0 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0033 | 0/0 | 3756 | 2 | 0 | 1 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0034 | 0/0 | 3756 | 2 | 0 | 0 | 0 | 2 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0035 | 0/0 | 3756 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0036 | 0/0 | 3756 | 2 | 0 | 1 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0037 | 0/0 | 3756 | 2 | 0 | 0 | 0 | 0 | 2 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0038 | 0/0 | 3756 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0039 | 0/0 | 3756 | 2 | 0 | 0 | 0 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0040 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0041 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0042 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0043 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0044 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0045 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0046 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0047 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0048 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0049 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0050 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0051 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0052 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0053 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0054 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0055 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0056 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0057 | 0/0 | 3744 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0058 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0059 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0060 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0061 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0062 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0063 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0064 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0065 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0066 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0067 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0068 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0069 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0070 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0071 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0072 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0073 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0074 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0075 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0076 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0077 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0078 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0079 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0080 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0081 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0082 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0083 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0084 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0085 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0086 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0087 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0088 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0089 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0090 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0091 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0092 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0093 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0094 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0095 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0096 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0097 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0098 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0099 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0100 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0101 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0102 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0103 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0104 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0105 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0106 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0107 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0108 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0109 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0110 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0111 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0112 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0113 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0114 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0115 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0116 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0117 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0118 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0119 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0120 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0121 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0122 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| c0123 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 1898 | 107 | 9 | 14 | 63 | 5 | 15 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0002 | 0/0 | 1901 | 54 | 7 | 10 | 27 | 2 | 8 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0003 | 1/0 | 1902 | 52 | 18 | 9 | 18 | 2 | 4 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0004 | 0/0 | 1898 | 17 | 15 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0005 | 0/0 | 1902 | 16 | 2 | 3 | 11 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0006 | 0/0 | 1899 | 15 | 1 | 2 | 9 | 1 | 2 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0007 | 0/0 | 1902 | 10 | 3 | 5 | 0 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0008 | 0/0 | 1898 | 8 | 0 | 3 | 0 | 4 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0009 | 0/0 | 1902 | 7 | 0 | 1 | 6 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0010 | 0/0 | 1902 | 6 | 3 | 0 | 3 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0011 | 0/0 | 1902 | 6 | 6 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0012 | 0/0 | 1901 | 5 | 0 | 1 | 0 | 3 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0013 | 0/0 | 1903 | 4 | 0 | 1 | 2 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0014 | 0/0 | 1903 | 4 | 0 | 1 | 3 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0015 | 0/0 | 1902 | 4 | 4 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0016 | 0/0 | 1898 | 4 | 4 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0017 | 0/0 | 1899 | 3 | 0 | 1 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0018 | 0/0 | 1903 | 3 | 3 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0019 | 0/0 | 1898 | 3 | 0 | 3 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0020 | 0/0 | 1902 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0021 | 0/0 | 1903 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0022 | 0/0 | 1903 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0023 | 0/0 | 1902 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0024 | 0/0 | 1898 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0025 | 0/0 | 1902 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0026 | 0/0 | 1903 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0027 | 0/0 | 1902 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0028 | 0/0 | 1902 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0029 | 0/0 | 1901 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0030 | 0/0 | 1898 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0031 | 0/0 | 1897 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0032 | 0/0 | 1898 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0033 | 0/0 | 1898 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0034 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0035 | 0/0 | 1904 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0036 | 0/0 | 1902 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0037 | 0/0 | 1888 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0038 | 0/0 | 1902 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0039 | 0/0 | 1903 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0040 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0041 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0042 | 0/0 | 1902 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0043 | 0/0 | 1904 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0044 | 0/0 | 1903 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0045 | 0/0 | 1898 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| t0046 | 0/0 | 1897 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0072 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0304 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 3756 | 40 | 1 | 3 | 28 | 3 | 5 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0002 | 0/0 | 3756 | 36 | 3 | 10 | 16 | 1 | 6 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0003 | 0/0 | 3756 | 33 | 0 | 7 | 18 | 2 | 6 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0004 | 0/0 | 3756 | 30 | 3 | 2 | 23 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0007 | 0/0 | 3756 | 6 | 5 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0013 | 0/0 | 3756 | 4 | 1 | 3 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0015 | 0/0 | 3756 | 3 | 3 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0016 | 0/0 | 3756 | 3 | 3 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0017 | 0/0 | 3756 | 3 | 0 | 0 | 3 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0018 | 0/0 | 3756 | 3 | 0 | 0 | 3 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0019 | 0/0 | 3756 | 3 | 0 | 3 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0027 | 0/0 | 3756 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0028 | 0/0 | 3756 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0029 | 0/0 | 3756 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0035 | 0/0 | 3756 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0041 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0042 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0053 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0066 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0068 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0070 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0073 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0096 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0097 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0099 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0103 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0005 | 0/0 | 3756 | 25 | 3 | 3 | 16 | 0 | 3 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0006 | 0/1 | 3756 | 16 | 2 | 2 | 9 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0011 | 1/0 | 3756 | 5 | 4 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0022 | 0/0 | 3756 | 3 | 2 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0037 | 0/0 | 3756 | 2 | 0 | 0 | 0 | 0 | 2 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0038 | 0/0 | 3756 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0109 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0113 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0114 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0008 | 0/0 | 3756 | 6 | 0 | 2 | 4 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0009 | 0/0 | 3756 | 5 | 0 | 3 | 1 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0012 | 0/0 | 3756 | 4 | 1 | 2 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0040 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0064 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0074 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0101 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0104 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0105 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0004c0014 | 0/0 | 3756 | 3 | 3 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0004c0044 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0004c0045 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0004c0046 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0004c0048 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0004c0049 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0005c0030 | 0/0 | 3756 | 2 | 0 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0005c0034 | 0/0 | 3756 | 2 | 0 | 0 | 0 | 2 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0005c0036 | 0/0 | 3756 | 2 | 0 | 1 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0005c0100 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0006c0081 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0006c0082 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0006c0083 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0006c0085 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0006c0086 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0006c0087 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0007c0020 | 0/0 | 3756 | 3 | 1 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0007c0021 | 0/0 | 3756 | 3 | 0 | 1 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0008c0025 | 0/0 | 3756 | 2 | 1 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0008c0032 | 0/0 | 3756 | 2 | 0 | 0 | 0 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0008c0054 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0009c0026 | 0/0 | 3756 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0009c0061 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0009c0077 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0009c0098 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0010c0010 | 0/0 | 3756 | 5 | 3 | 0 | 0 | 2 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0011c0033 | 0/0 | 3756 | 2 | 0 | 1 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0011c0058 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0011c0059 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0012c0115 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0012c0119 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0012c0120 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0012c0122 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0013c0024 | 0/0 | 3756 | 2 | 0 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0013c0091 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0014c0023 | 0/0 | 3756 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0015c0031 | 0/0 | 3756 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0016c0052 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0016c0090 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0017c0060 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0017c0062 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0018c0055 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0018c0102 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0019c0110 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0019c0112 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0020c0116 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0020c0118 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0021c0039 | 0/0 | 3756 | 2 | 0 | 0 | 0 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0022c0050 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0023c0043 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0024c0047 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0025c0051 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0026c0080 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0027c0078 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0028c0084 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0029c0088 | 0/0 | 3759 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0030c0092 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0031c0093 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0032c0075 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0033c0065 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0034c0095 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0035c0094 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0036c0067 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0037c0071 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0038c0056 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0039c0072 | 0/0 | 3756 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0040c0063 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0041c0069 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0042c0057 | 0/0 | 3744 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0043c0076 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0044c0089 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0045c0079 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0046c0107 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0047c0111 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0048c0117 | 0/0 | 3756 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0049c0108 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0050c0121 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0051c0123 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0052c0106 | 0/0 | 3756 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5653 | 20 | 0 | 1 | 14 | 1 | 4 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0001t0002 | 0/0 | 5656 | 7 | 1 | 0 | 5 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0001t0003 | 0/0 | 5657 | 3 | 0 | 0 | 3 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0001t0005 | 0/0 | 5657 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0001t0006 | 0/0 | 5654 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0001t0007 | 0/0 | 5657 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0001t0012 | 0/0 | 5656 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0001t0013 | 0/0 | 5658 | 2 | 0 | 1 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0001t0017 | 0/0 | 5654 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0001t0037 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0002t0001 | 0/0 | 5653 | 14 | 1 | 3 | 7 | 0 | 3 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0002t0002 | 0/0 | 5656 | 7 | 0 | 3 | 3 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0002t0003 | 0/0 | 5657 | 5 | 1 | 1 | 1 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0002t0005 | 0/0 | 5657 | 6 | 0 | 2 | 4 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0002t0007 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0002t0013 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0002t0022 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0002t0033 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0003t0001 | 0/0 | 5653 | 12 | 0 | 2 | 7 | 1 | 2 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0003t0002 | 0/0 | 5656 | 7 | 0 | 2 | 5 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0003t0003 | 0/0 | 5657 | 6 | 0 | 2 | 2 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0003t0005 | 0/0 | 5657 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0003t0006 | 0/0 | 5654 | 3 | 0 | 0 | 2 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0003t0012 | 0/0 | 5656 | 2 | 0 | 1 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0003t0032 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0004t0001 | 0/0 | 5653 | 14 | 0 | 0 | 13 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0004t0002 | 0/0 | 5656 | 4 | 0 | 0 | 4 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0004t0003 | 0/0 | 5657 | 4 | 0 | 0 | 4 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0004t0005 | 0/0 | 5657 | 2 | 0 | 1 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0004t0006 | 0/0 | 5654 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0004t0008 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0004t0014 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0004t0022 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0004t0031 | 0/0 | 5652 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0004t0035 | 0/0 | 5659 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0007t0002 | 0/0 | 5656 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0007t0003 | 0/0 | 5657 | 3 | 3 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0007t0004 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0007t0008 | 0/0 | 5653 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0013t0001 | 0/0 | 5653 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0013t0004 | 0/0 | 5653 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0013t0018 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0013t0019 | 0/0 | 5653 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0015t0001 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0015t0002 | 0/0 | 5656 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0015t0020 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0016t0004 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0016t0010 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0016t0046 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0017t0001 | 0/0 | 5653 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0017t0017 | 0/0 | 5654 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0018t0001 | 0/0 | 5653 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0018t0002 | 0/0 | 5656 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0019t0008 | 0/0 | 5653 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0019t0019 | 0/0 | 5653 | 2 | 0 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0027t0003 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0027t0040 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0028t0042 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0028t0044 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0029t0002 | 0/0 | 5656 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0035t0010 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0035t0028 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0041t0005 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0042t0011 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0053t0004 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0066t0001 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0068t0005 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0070t0007 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0073t0002 | 0/0 | 5656 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0096t0002 | 0/0 | 5656 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0097t0003 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0099t0001 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0001c0103t0029 | 0/0 | 5656 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0005t0001 | 0/0 | 5653 | 16 | 2 | 3 | 9 | 0 | 2 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0005t0002 | 0/0 | 5656 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0005t0003 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0005t0005 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0005t0006 | 0/0 | 5654 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0005t0008 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0005t0009 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0005t0041 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0006t0001 | 0/1 | 5653 | 7 | 0 | 1 | 5 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0006t0002 | 0/0 | 5656 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0006t0003 | 0/0 | 5657 | 3 | 0 | 1 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0006t0006 | 0/0 | 5654 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0006t0008 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0006t0013 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0006t0016 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0006t0021 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0011t0003 | 1/0 | 5657 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0011t0004 | 0/0 | 5653 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0011t0016 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0011t0018 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0022t0002 | 0/0 | 5656 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0022t0008 | 0/0 | 5653 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0022t0018 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0037t0003 | 0/0 | 5657 | 2 | 0 | 0 | 0 | 0 | 2 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0038t0003 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0038t0010 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0109t0004 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0113t0003 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0002c0114t0010 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0008t0002 | 0/0 | 5656 | 4 | 0 | 2 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0008t0003 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0008t0009 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0009t0006 | 0/0 | 5654 | 2 | 0 | 1 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0009t0007 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0009t0009 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0009t0039 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0012t0003 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0012t0007 | 0/0 | 5657 | 2 | 1 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0012t0014 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0040t0038 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0064t0017 | 0/0 | 5654 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0074t0009 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0101t0030 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0104t0007 | 0/0 | 5657 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0003c0105t0014 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0004c0014t0001 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0004c0014t0005 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0004c0014t0016 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0004c0044t0004 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0004c0045t0003 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0004c0046t0036 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0004c0048t0016 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0004c0049t0015 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0005c0030t0003 | 0/0 | 5657 | 2 | 0 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0005c0034t0012 | 0/0 | 5656 | 2 | 0 | 0 | 0 | 2 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0005c0036t0001 | 0/0 | 5653 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0005c0036t0002 | 0/0 | 5656 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0005c0100t0002 | 0/0 | 5656 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0006c0081t0021 | 0/0 | 5661 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0006c0082t0010 | 0/0 | 5660 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0006c0083t0043 | 0/0 | 5662 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0006c0085t0024 | 0/0 | 5656 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0006c0086t0003 | 0/0 | 5660 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0006c0087t0001 | 0/0 | 5656 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0007c0020t0007 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0007c0020t0009 | 0/0 | 5657 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0007c0021t0003 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0007c0021t0009 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0007c0021t0014 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0008c0025t0001 | 0/0 | 5653 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0008c0025t0023 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0008c0032t0002 | 0/0 | 5656 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0008c0032t0006 | 0/0 | 5654 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0008c0054t0002 | 0/0 | 5656 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0009c0026t0004 | 0/0 | 5653 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0009c0061t0004 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0009c0077t0004 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0009c0098t0003 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0010c0010t0003 | 0/0 | 5657 | 3 | 3 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0010c0010t0008 | 0/0 | 5653 | 2 | 0 | 0 | 0 | 2 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0011c0033t0001 | 0/0 | 5653 | 2 | 0 | 1 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0011c0058t0004 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0011c0059t0001 | 0/0 | 5653 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0012c0115t0045 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0012c0119t0023 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0012c0120t0003 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0012c0122t0003 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0013c0024t0002 | 0/0 | 5656 | 2 | 0 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0013c0091t0007 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0014c0023t0002 | 0/0 | 5656 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0015c0031t0004 | 0/0 | 5653 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0016c0052t0003 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0016c0090t0010 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0017c0060t0015 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0017c0062t0027 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0018c0055t0025 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0018c0102t0003 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0019c0110t0011 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0019c0112t0024 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0020c0116t0004 | 0/0 | 5653 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0020c0118t0001 | 0/0 | 5653 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0021c0039t0002 | 0/0 | 5656 | 2 | 0 | 0 | 0 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0022c0050t0003 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0023c0043t0011 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0024c0047t0034 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0025c0051t0001 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0026c0080t0015 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0027c0078t0011 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0028c0084t0003 | 0/0 | 5660 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0029c0088t0007 | 0/0 | 5660 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0030c0092t0001 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0031c0093t0001 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0032c0075t0001 | 0/0 | 5653 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0033c0065t0015 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0034c0095t0001 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0035c0094t0002 | 0/0 | 5656 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0036c0067t0002 | 0/0 | 5656 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0037c0071t0006 | 0/0 | 5654 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0038c0056t0011 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0039c0072t0001 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0040c0063t0020 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0041c0069t0001 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0042c0057t0002 | 0/0 | 5644 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0043c0076t0003 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0044c0089t0001 | 0/0 | 5653 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0045c0079t0006 | 0/0 | 5654 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0046c0107t0006 | 0/0 | 5654 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0047c0111t0003 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0048c0117t0026 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0049c0108t0004 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0050c0121t0011 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0051c0123t0003 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| a0052c0106t0002 | 0/0 | 5656 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | copy fasta | chr16 | 57877340 | 57976128 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0006g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0006g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0007g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0012g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0013g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0013g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0017g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0001t0037g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0007g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0013g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0022g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0002t0033g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0006g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0006g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0012g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0012g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0003t0032g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0008g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0014g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0022g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0031g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0004t0035g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0007t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0007t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0007t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0007t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0007t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0007t0008g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0013t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0013t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0013t0018g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0013t0019g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0015t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0015t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0015t0020g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0016t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0016t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0016t0046g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0017t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0017t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0017t0017g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0018t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0018t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0018t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0019t0008g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0019t0019g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0019t0019g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0027t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0027t0040g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0028t0042g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0028t0044g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0029t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0029t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0035t0010g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0035t0028g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0041t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0042t0011g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0053t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0066t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0068t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0070t0007g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0073t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0096t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0097t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0099t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0001c0103t0029g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0005g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0008g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0009g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0005t0041g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0006t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0006t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0006t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0006t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0006t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0006t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0006t0001g0304 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0006t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0006t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0006t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0006t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0006t0006g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0006t0008g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0006t0013g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0006t0016g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0006t0021g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0011t0003g0072 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0011t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0011t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0011t0016g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0011t0018g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0022t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0022t0008g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0022t0018g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0037t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0037t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0038t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0038t0010g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0109t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0113t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0002c0114t0010g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0008t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0008t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0008t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0008t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0008t0009g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0009t0006g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0009t0006g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0009t0007g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0009t0009g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0009t0039g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0012t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0012t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0012t0007g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0012t0014g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0040t0038g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0064t0017g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0074t0009g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0101t0030g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0104t0007g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0003c0105t0014g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0004c0014t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0004c0014t0005g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0004c0014t0016g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0004c0044t0004g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0004c0045t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0004c0046t0036g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0004c0048t0016g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0004c0049t0015g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0005c0030t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0005c0034t0012g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0005c0034t0012g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0005c0036t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0005c0036t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0005c0100t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0006c0081t0021g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0006c0082t0010g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0006c0083t0043g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0006c0085t0024g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0006c0086t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0006c0087t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0007c0020t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0007c0020t0009g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0007c0020t0009g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0007c0021t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0007c0021t0009g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0007c0021t0014g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0008c0025t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0008c0025t0023g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0008c0032t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0008c0032t0006g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0008c0054t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0009c0026t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0009c0026t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0009c0061t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0009c0077t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0009c0098t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0010c0010t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0010c0010t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0010c0010t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0010c0010t0008g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0010c0010t0008g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0011c0033t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0011c0033t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0011c0058t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0011c0059t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0012c0115t0045g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0012c0119t0023g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0012c0120t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0012c0122t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0013c0024t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0013c0024t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0013c0091t0007g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0014c0023t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0014c0023t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0015c0031t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0015c0031t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0016c0052t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0016c0090t0010g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0017c0060t0015g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0017c0062t0027g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0018c0055t0025g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0018c0102t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0019c0110t0011g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0019c0112t0024g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0020c0116t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0020c0118t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0021c0039t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0021c0039t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0022c0050t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0023c0043t0011g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0024c0047t0034g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0025c0051t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0026c0080t0015g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0027c0078t0011g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0028c0084t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0029c0088t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0030c0092t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0031c0093t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0032c0075t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0033c0065t0015g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0034c0095t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0035c0094t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0036c0067t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0037c0071t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0038c0056t0011g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0039c0072t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0040c0063t0020g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0041c0069t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0042c0057t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0043c0076t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0044c0089t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0045c0079t0006g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0046c0107t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0047c0111t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0048c0117t0026g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0049c0108t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0050c0121t0011g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0051c0123t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| a0052c0106t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0003 | g0222 | EUR | GBR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00099 | hp2 | a0001 | c0004 | t0008 | g0135 | EUR | GBR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | GBR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00140 | hp2 | a0001 | c0001 | t0012 | g0212 | EUR | GBR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00280 | hp1 | a0008 | c0032 | t0006 | g0221 | EUR | FIN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00280 | hp2 | a0034 | c0095 | t0001 | g0193 | EUR | FIN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00323 | hp1 | a0001 | c0096 | t0002 | g0293 | EUR | FIN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00323 | hp2 | a0021 | c0039 | t0002 | g0305 | EUR | FIN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00408 | hp1 | a0001 | c0003 | t0002 | g0201 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00408 | hp2 | a0001 | c0003 | t0006 | g0284 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00423 | hp1 | a0002 | c0005 | t0001 | g0027 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00423 | hp2 | a0002 | c0006 | t0006 | g0323 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00438 | hp1 | a0001 | c0097 | t0003 | g0231 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00438 | hp2 | a0001 | c0002 | t0005 | g0143 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00544 | hp1 | a0001 | c0002 | t0003 | g0031 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00544 | hp2 | a0001 | c0004 | t0001 | g0119 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00558 | hp1 | a0003 | c0008 | t0003 | g0145 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00558 | hp2 | a0001 | c0103 | t0029 | g0272 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00597 | hp2 | a0003 | c0105 | t0014 | g0298 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00639 | hp1 | a0020 | c0118 | t0001 | g0302 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00642 | hp1 | a0002 | c0006 | t0001 | g0071 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00642 | hp2 | a0003 | c0009 | t0007 | g0080 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00733 | hp1 | a0001 | c0003 | t0002 | g0191 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00733 | hp2 | a0001 | c0003 | t0012 | g0266 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00735 | hp1 | a0003 | c0009 | t0006 | g0217 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00735 | hp2 | a0001 | c0001 | t0037 | g0246 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00738 | hp1 | a0001 | c0013 | t0001 | g0306 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00738 | hp2 | a0001 | c0070 | t0007 | g0134 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00741 | hp1 | a0048 | c0117 | t0026 | g0186 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG00741 | hp2 | a0011 | c0059 | t0001 | g0123 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01069 | hp1 | a0005 | c0036 | t0002 | g0256 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01069 | hp2 | a0013 | c0024 | t0002 | g0170 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01070 | hp1 | a0020 | c0116 | t0004 | g0070 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01070 | hp2 | a0005 | c0030 | t0003 | g0001 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01071 | hp1 | a0005 | c0030 | t0003 | g0001 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01071 | hp2 | a0013 | c0024 | t0002 | g0169 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01074 | hp1 | a0001 | c0002 | t0007 | g0126 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01074 | hp2 | a0013 | c0091 | t0007 | g0268 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01081 | hp1 | a0001 | c0019 | t0008 | g0247 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0329 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01109 | hp1 | a0002 | c0006 | t0003 | g0022 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01109 | hp2 | a0012 | c0120 | t0003 | g0065 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01168 | hp1 | a0001 | c0007 | t0008 | g0356 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01168 | hp2 | a0001 | c0019 | t0019 | g0286 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01169 | hp1 | a0001 | c0019 | t0019 | g0299 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01175 | hp1 | a0045 | c0079 | t0006 | g0194 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01175 | hp2 | a0001 | c0004 | t0005 | g0127 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01243 | hp1 | a0011 | c0033 | t0001 | g0267 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0168 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01255 | hp1 | a0003 | c0012 | t0007 | g0167 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01255 | hp2 | a0001 | c0002 | t0005 | g0184 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01256 | hp1 | a0003 | c0008 | t0002 | g0002 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0214 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01258 | hp1 | a0003 | c0008 | t0002 | g0002 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0248 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01261 | hp1 | a0002 | c0005 | t0001 | g0016 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01261 | hp2 | a0001 | c0002 | t0002 | g0183 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01346 | hp1 | a0001 | c0003 | t0002 | g0244 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0124 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01358 | hp1 | a0002 | c0022 | t0008 | g0011 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01358 | hp2 | a0001 | c0013 | t0004 | g0308 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01361 | hp1 | a0003 | c0009 | t0039 | g0307 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01361 | hp2 | a0001 | c0001 | t0013 | g0251 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01433 | hp1 | a0001 | c0002 | t0005 | g0142 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01433 | hp2 | a0001 | c0013 | t0019 | g0213 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01496 | hp1 | a0002 | c0005 | t0001 | g0015 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01496 | hp2 | a0001 | c0003 | t0003 | g0296 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01515 | hp1 | a0001 | c0003 | t0001 | g0199 | EUR | IBS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01515 | hp2 | a0010 | c0010 | t0008 | g0090 | EUR | IBS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01516 | hp1 | a0001 | c0002 | t0003 | g0038 | EUR | IBS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01516 | hp2 | a0005 | c0034 | t0012 | g0255 | EUR | IBS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01517 | hp1 | a0010 | c0010 | t0008 | g0102 | EUR | IBS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01517 | hp2 | a0005 | c0034 | t0012 | g0292 | EUR | IBS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01884 | hp1 | a0041 | c0069 | t0001 | g0045 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01884 | hp2 | a0014 | c0023 | t0002 | g0347 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01891 | hp1 | a0009 | c0026 | t0004 | g0059 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01891 | hp2 | a0007 | c0020 | t0007 | g0007 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01934 | hp1 | a0003 | c0064 | t0017 | g0179 | AMR | PEL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01934 | hp2 | a0007 | c0021 | t0003 | g0105 | AMR | PEL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01978 | hp1 | a0003 | c0012 | t0003 | g0176 | AMR | PEL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01978 | hp2 | a0003 | c0074 | t0009 | g0177 | AMR | PEL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02015 | hp1 | a0001 | c0004 | t0001 | g0138 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02027 | hp1 | a0001 | c0018 | t0001 | g0263 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02027 | hp2 | a0001 | c0004 | t0001 | g0172 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02040 | hp2 | a0002 | c0005 | t0001 | g0319 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02055 | hp1 | a0002 | c0011 | t0004 | g0185 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02055 | hp2 | a0001 | c0041 | t0005 | g0028 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02056 | hp1 | a0001 | c0002 | t0005 | g0154 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02056 | hp2 | a0001 | c0004 | t0001 | g0174 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02071 | hp1 | a0001 | c0002 | t0013 | g0041 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02071 | hp2 | a0001 | c0073 | t0002 | g0132 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02074 | hp2 | a0002 | c0005 | t0006 | g0089 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02080 | hp1 | a0001 | c0018 | t0001 | g0297 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02080 | hp2 | a0001 | c0068 | t0005 | g0175 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02083 | hp1 | a0005 | c0036 | t0001 | g0355 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02083 | hp2 | a0002 | c0005 | t0001 | g0013 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02129 | hp2 | a0003 | c0008 | t0002 | g0131 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02132 | hp1 | a0002 | c0005 | t0001 | g0024 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02132 | hp2 | a0051 | c0123 | t0003 | g0085 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02135 | hp1 | a0001 | c0004 | t0003 | g0136 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02135 | hp2 | a0001 | c0003 | t0001 | g0259 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02145 | hp1 | a0009 | c0098 | t0003 | g0241 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02145 | hp2 | a0004 | c0014 | t0005 | g0346 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02148 | hp1 | a0002 | c0005 | t0001 | g0303 | AMR | PEL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0113 | AMR | PEL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02257 | hp1 | a0049 | c0108 | t0004 | g0061 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02257 | hp2 | a0001 | c0015 | t0001 | g0335 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02258 | hp1 | a0050 | c0121 | t0011 | g0315 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02258 | hp2 | a0030 | c0092 | t0001 | g0285 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02280 | hp1 | a0026 | c0080 | t0015 | g0188 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02280 | hp2 | a0006 | c0086 | t0003 | g0067 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02300 | hp1 | a0001 | c0003 | t0003 | g0215 | AMR | PEL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02300 | hp2 | a0001 | c0002 | t0002 | g0159 | AMR | PEL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02451 | hp1 | a0011 | c0058 | t0004 | g0140 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02451 | hp2 | a0012 | c0122 | t0003 | g0317 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02523 | hp1 | a0003 | c0040 | t0038 | g0203 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02572 | hp1 | a0004 | c0048 | t0016 | g0354 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02572 | hp2 | a0001 | c0016 | t0004 | g0313 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02615 | hp1 | a0019 | c0110 | t0011 | g0321 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02615 | hp2 | a0006 | c0083 | t0043 | g0063 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02622 | hp1 | a0001 | c0027 | t0040 | g0078 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02622 | hp2 | a0043 | c0076 | t0003 | g0055 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02630 | hp1 | a0002 | c0113 | t0003 | g0318 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02630 | hp2 | a0003 | c0012 | t0007 | g0048 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02647 | hp1 | a0001 | c0004 | t0022 | g0107 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02647 | hp2 | a0002 | c0011 | t0004 | g0066 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02698 | hp1 | a0001 | c0002 | t0003 | g0050 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02698 | hp2 | a0001 | c0004 | t0001 | g0153 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02717 | hp1 | a0047 | c0111 | t0003 | g0327 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02717 | hp2 | a0006 | c0082 | t0010 | g0337 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02723 | hp1 | a0001 | c0007 | t0003 | g0189 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02723 | hp2 | a0027 | c0078 | t0011 | g0353 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02735 | hp1 | a0002 | c0005 | t0001 | g0101 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02735 | hp2 | a0035 | c0094 | t0002 | g0295 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02738 | hp1 | a0001 | c0003 | t0006 | g0288 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0157 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02809 | hp1 | a0001 | c0016 | t0010 | g0057 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02809 | hp2 | a0002 | c0005 | t0001 | g0314 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02818 | hp1 | a0004 | c0014 | t0016 | g0326 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02818 | hp2 | a0006 | c0087 | t0001 | g0211 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02886 | hp1 | a0002 | c0005 | t0041 | g0068 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02886 | hp2 | a0008 | c0025 | t0023 | g0077 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02895 | hp1 | a0001 | c0007 | t0003 | g0004 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02895 | hp2 | a0010 | c0010 | t0003 | g0328 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02896 | hp1 | a0015 | c0031 | t0004 | g0333 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02896 | hp2 | a0001 | c0028 | t0044 | g0064 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02897 | hp1 | a0015 | c0031 | t0004 | g0334 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02897 | hp2 | a0010 | c0010 | t0003 | g0325 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02922 | hp1 | a0001 | c0053 | t0004 | g0200 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02922 | hp2 | a0001 | c0042 | t0011 | g0029 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02965 | hp1 | a0002 | c0006 | t0021 | g0187 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02965 | hp2 | a0001 | c0015 | t0002 | g0006 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02970 | hp1 | a0033 | c0065 | t0015 | g0043 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02970 | hp2 | a0004 | c0046 | t0036 | g0348 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02976 | hp1 | a0002 | c0022 | t0018 | g0112 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02976 | hp2 | a0001 | c0007 | t0002 | g0073 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03017 | hp1 | a0002 | c0037 | t0003 | g0023 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03017 | hp2 | a0003 | c0104 | t0007 | g0218 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03041 | hp1 | a0001 | c0015 | t0020 | g0336 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03041 | hp2 | a0001 | c0013 | t0018 | g0294 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03098 | hp1 | a0012 | c0115 | t0045 | g0111 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03098 | hp2 | a0009 | c0026 | t0004 | g0310 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03130 | hp1 | a0001 | c0007 | t0004 | g0046 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03130 | hp2 | a0028 | c0084 | t0003 | g0330 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03139 | hp1 | a0004 | c0049 | t0015 | g0344 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03139 | hp2 | a0025 | c0051 | t0001 | g0339 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03195 | hp1 | a0002 | c0109 | t0004 | g0108 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03195 | hp2 | a0023 | c0043 | t0011 | g0351 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03209 | hp2 | a0002 | c0006 | t0016 | g0110 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03225 | hp1 | a0004 | c0045 | t0003 | g0342 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03225 | hp2 | a0009 | c0061 | t0004 | g0049 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03239 | hp1 | a0042 | c0057 | t0002 | g0147 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03239 | hp2 | a0002 | c0005 | t0008 | g0025 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03453 | hp1 | a0029 | c0088 | t0007 | g0210 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03453 | hp2 | a0040 | c0063 | t0020 | g0009 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03486 | hp1 | a0001 | c0007 | t0003 | g0340 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03486 | hp2 | a0017 | c0062 | t0027 | g0324 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03491 | hp1 | a0001 | c0002 | t0001 | g0052 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03492 | hp2 | a0001 | c0003 | t0003 | g0265 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03516 | hp1 | a0006 | c0081 | t0021 | g0331 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03516 | hp2 | a0012 | c0119 | t0023 | g0091 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03579 | hp1 | a0009 | c0077 | t0004 | g0060 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03579 | hp2 | a0004 | c0014 | t0001 | g0345 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03654 | hp1 | a0031 | c0093 | t0001 | g0258 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03654 | hp2 | a0001 | c0002 | t0033 | g0053 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03669 | hp1 | a0005 | c0100 | t0002 | g0232 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0270 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03704 | hp1 | a0001 | c0003 | t0032 | g0109 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0039 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03710 | hp1 | a0001 | c0003 | t0012 | g0204 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03710 | hp2 | a0001 | c0003 | t0001 | g0253 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0312 | SAS | BEB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03831 | hp2 | a0002 | c0005 | t0001 | g0332 | SAS | BEB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03834 | hp1 | a0002 | c0006 | t0013 | g0083 | SAS | BEB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03942 | hp1 | a0039 | c0072 | t0001 | g0137 | SAS | BEB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03942 | hp2 | a0002 | c0037 | t0003 | g0092 | SAS | BEB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG04115 | hp1 | a0003 | c0009 | t0006 | g0289 | SAS | STU | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG04115 | hp2 | a0021 | c0039 | t0002 | g0086 | SAS | STU | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG04204 | hp1 | a0001 | c0066 | t0001 | g0130 | SAS | STU | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG04204 | hp2 | a0008 | c0032 | t0002 | g0269 | SAS | STU | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG04228 | hp2 | a0036 | c0067 | t0002 | g0051 | SAS | STU | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18747 | hp2 | a0002 | c0038 | t0010 | g0103 | EAS | CHB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18906 | hp1 | a0001 | c0027 | t0003 | g0058 | AFR | YRI | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18906 | hp2 | a0024 | c0047 | t0034 | g0350 | AFR | YRI | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18939 | hp1 | a0001 | c0017 | t0001 | g0114 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18939 | hp2 | a0001 | c0003 | t0002 | g0196 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18940 | hp1 | a0001 | c0004 | t0002 | g0156 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18940 | hp2 | a0007 | c0020 | t0009 | g0081 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0338 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18942 | hp2 | a0001 | c0003 | t0001 | g0202 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18943 | hp1 | a0001 | c0004 | t0001 | g0164 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18943 | hp2 | a0001 | c0003 | t0002 | g0229 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18944 | hp1 | a0001 | c0001 | t0013 | g0206 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18944 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18945 | hp1 | a0001 | c0004 | t0001 | g0133 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18945 | hp2 | a0002 | c0006 | t0002 | g0096 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18948 | hp1 | a0001 | c0017 | t0001 | g0139 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18954 | hp1 | a0002 | c0005 | t0002 | g0320 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18954 | hp2 | a0001 | c0001 | t0005 | g0274 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18956 | hp1 | a0001 | c0003 | t0005 | g0300 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18956 | hp2 | a0001 | c0004 | t0001 | g0150 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18957 | hp1 | a0001 | c0004 | t0001 | g0115 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18957 | hp2 | a0001 | c0003 | t0001 | g0278 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18959 | hp1 | a0002 | c0038 | t0003 | g0094 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18960 | hp1 | a0002 | c0005 | t0001 | g0014 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18962 | hp1 | a0001 | c0004 | t0031 | g0152 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18962 | hp2 | a0001 | c0018 | t0002 | g0254 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18966 | hp2 | a0002 | c0006 | t0001 | g0017 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18967 | hp1 | a0002 | c0005 | t0006 | g0097 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18967 | hp2 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18970 | hp2 | a0016 | c0052 | t0003 | g0180 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18972 | hp2 | a0001 | c0004 | t0001 | g0117 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0228 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18974 | hp2 | a0001 | c0004 | t0001 | g0165 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18977 | hp1 | a0001 | c0002 | t0005 | g0160 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18977 | hp2 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18980 | hp1 | a0007 | c0021 | t0014 | g0088 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18981 | hp1 | a0002 | c0005 | t0009 | g0104 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18981 | hp2 | a0001 | c0001 | t0005 | g0277 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18982 | hp1 | a0001 | c0029 | t0002 | g0163 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18982 | hp2 | a0001 | c0003 | t0006 | g0219 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18983 | hp1 | a0001 | c0004 | t0003 | g0037 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18983 | hp2 | a0001 | c0003 | t0001 | g0282 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18984 | hp1 | a0002 | c0006 | t0001 | g0095 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18984 | hp2 | a0001 | c0004 | t0003 | g0151 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18986 | hp2 | a0001 | c0001 | t0006 | g0226 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18989 | hp1 | a0007 | c0021 | t0009 | g0093 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18989 | hp2 | a0032 | c0075 | t0001 | g0144 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18994 | hp1 | a0001 | c0003 | t0002 | g0239 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18994 | hp2 | a0002 | c0005 | t0001 | g0026 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18998 | hp1 | a0001 | c0035 | t0028 | g0291 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18998 | hp2 | a0001 | c0002 | t0005 | g0129 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18999 | hp1 | a0001 | c0035 | t0010 | g0230 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19000 | hp2 | a0001 | c0029 | t0002 | g0034 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19002 | hp2 | a0037 | c0071 | t0006 | g0148 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19003 | hp1 | a0001 | c0004 | t0002 | g0178 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19003 | hp2 | a0001 | c0003 | t0001 | g0301 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19004 | hp1 | a0002 | c0005 | t0001 | g0021 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19004 | hp2 | a0001 | c0004 | t0003 | g0128 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19005 | hp1 | a0002 | c0005 | t0001 | g0098 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19005 | hp2 | a0003 | c0009 | t0009 | g0287 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19007 | hp1 | a0001 | c0004 | t0001 | g0118 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19007 | hp2 | a0008 | c0025 | t0001 | g0122 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19030 | hp1 | a0002 | c0022 | t0002 | g0074 | AFR | LWK | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19030 | hp2 | a0001 | c0002 | t0022 | g0062 | AFR | LWK | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19043 | hp1 | a0008 | c0054 | t0002 | g0044 | AFR | LWK | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19043 | hp2 | a0006 | c0085 | t0024 | g0209 | AFR | LWK | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19054 | hp2 | a0002 | c0005 | t0005 | g0322 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19056 | hp1 | a0016 | c0090 | t0010 | g0220 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19056 | hp2 | a0052 | c0106 | t0002 | g0075 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19057 | hp1 | a0002 | c0006 | t0001 | g0100 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19063 | hp1 | a0001 | c0003 | t0003 | g0198 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19064 | hp1 | a0001 | c0004 | t0002 | g0171 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19065 | hp2 | a0001 | c0004 | t0001 | g0166 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19066 | hp1 | a0001 | c0004 | t0001 | g0173 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19066 | hp2 | a0002 | c0005 | t0003 | g0106 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19067 | hp1 | a0001 | c0001 | t0017 | g0225 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19067 | hp2 | a0001 | c0017 | t0017 | g0033 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19068 | hp1 | a0046 | c0107 | t0006 | g0099 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19068 | hp2 | a0001 | c0001 | t0006 | g0242 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19074 | hp1 | a0001 | c0004 | t0002 | g0116 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19074 | hp2 | a0002 | c0006 | t0003 | g0076 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19077 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19077 | hp2 | a0002 | c0006 | t0001 | g0019 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19079 | hp1 | a0003 | c0012 | t0014 | g0158 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19079 | hp2 | a0002 | c0005 | t0002 | g0082 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19081 | hp1 | a0002 | c0006 | t0001 | g0020 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19081 | hp2 | a0001 | c0003 | t0005 | g0240 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19084 | hp1 | a0002 | c0006 | t0003 | g0012 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19087 | hp1 | a0001 | c0003 | t0002 | g0245 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19087 | hp2 | a0003 | c0008 | t0009 | g0146 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19088 | hp1 | a0001 | c0003 | t0003 | g0283 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19088 | hp2 | a0003 | c0008 | t0002 | g0120 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19090 | hp1 | a0001 | c0004 | t0005 | g0182 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19090 | hp2 | a0007 | c0020 | t0009 | g0018 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19240 | hp1 | a0002 | c0011 | t0016 | g0190 | AFR | YRI | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA19240 | hp2 | a0038 | c0056 | t0011 | g0047 | AFR | YRI | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | ASW | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA20129 | hp2 | a0001 | c0016 | t0046 | g0054 | AFR | ASW | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA20752 | hp1 | a0002 | c0006 | t0008 | g0084 | EUR | TSI | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA20752 | hp2 | a0001 | c0099 | t0001 | g0216 | EUR | TSI | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA20805 | hp1 | a0011 | c0033 | t0001 | g0249 | EUR | TSI | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA20805 | hp2 | a0001 | c0001 | t0007 | g0290 | EUR | TSI | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA20905 | hp1 | a0003 | c0101 | t0030 | g0264 | SAS | GIH | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0125 | SAS | GIH | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01123 | hp1 | a0001 | c0004 | t0014 | g0192 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG01123 | hp2 | a0018 | c0055 | t0025 | g0042 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02109 | hp1 | a0002 | c0005 | t0001 | g0316 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02109 | hp2 | a0002 | c0114 | t0010 | g0357 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02486 | hp1 | a0004 | c0044 | t0004 | g0343 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02486 | hp2 | a0019 | c0112 | t0024 | g0010 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02559 | hp1 | a0014 | c0023 | t0002 | g0349 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG02559 | hp2 | a0017 | c0060 | t0015 | g0005 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03471 | hp1 | a0010 | c0010 | t0003 | g0030 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG03471 | hp2 | a0001 | c0028 | t0042 | g0069 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG06807 | hp1 | a0002 | c0011 | t0018 | g0341 | AFR | USA | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| HG06807 | hp2 | a0018 | c0102 | t0003 | g0271 | AFR | USA | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18955 | hp1 | a0002 | c0005 | t0001 | g0087 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA18955 | hp2 | a0044 | c0089 | t0001 | g0257 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA20300 | hp1 | a0001 | c0004 | t0006 | g0149 | AFR | USA | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA20300 | hp2 | a0022 | c0050 | t0003 | g0352 | AFR | USA | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA21309 | hp1 | a0001 | c0002 | t0003 | g0008 | AFR | LWK | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| NA21309 | hp2 | a0001 | c0004 | t0035 | g0079 | AFR | LWK | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| homoSapiens_chm13v2 | hp1 | a0002 | c0006 | t0001 | g0304 | REF | REF | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| homoSapiens_grch38 | hp1 | a0002 | c0011 | t0003 | g0072 | REF | REF | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:57882340
|
A | T | 1 | a0003 | 1 | NA20905.hp1 | splice_region_variant | LOW | c.*1824T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | chr16 | 57882340 | ||||||
| chr16:57884336
|
G | C | 1 | a0039 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.3584C>G | p.Ser1195Cys | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 3661/5657 | 3584/3756 | 1195/1251 | chr16 | 57884336 | ||
| chr16:57884364
|
G | A | 4 | a0018a0022a0028others(1): Show | 5 | HG01123.hp2 HG02717.hp1 HG03130.hp2 others(2): Show |
missense_variant | MODERATE | c.3556C>T | p.Pro1186Ser | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 3633/5657 | 3556/3756 | 1186/1251 | chr16 | 57884364 | ||
| chr16:57884393
|
G | A | 3 | a0023a0038a0050 | 3 | HG02258.hp1 HG03195.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.3527C>T | p.Pro1176Leu | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 3604/5657 | 3527/3756 | 1176/1251 | chr16 | 57884393 | ||
| chr16:57884432
|
C | T | 1 | a0037 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.3488G>A | p.Gly1163Glu | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 3565/5657 | 3488/3756 | 1163/1251 | chr16 | 57884432 | ||
| chr16:57887977
|
C | T | 2 | a0024a0040 | 2 | HG03453.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.3340G>A | p.Ala1114Thr | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/33 | 3417/5657 | 3340/3756 | 1114/1251 | chr16 | 57887977 | ||
| chr16:57901538
|
G | A | 3 | a0005a0021a0034 | 10 | HG00280.hp2 HG00323.hp2 HG01069.hp1 others(7): Show |
missense_variant | MODERATE | c.2882C>T | p.Ala961Val | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 28/33 | 2959/5657 | 2882/3756 | 961/1251 | chr16 | 57901538 | ||
| chr16:57901539
|
C | A | 5 | a0009a0010a0012others(2): Show | 17 | HG01109.hp2 HG01515.hp2 HG01517.hp1 others(14): Show |
missense_variant | MODERATE | c.2881G>T | p.Ala961Ser | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 28/33 | 2958/5657 | 2881/3756 | 961/1251 | chr16 | 57901539 | ||
| chr16:57901566
|
C | T | 5 | a0017a0026a0033others(2): Show | 6 | HG00741.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
missense_variant | MODERATE | c.2854G>A | p.Val952Met | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 28/33 | 2931/5657 | 2854/3756 | 952/1251 | chr16 | 57901566 | ||
| chr16:57901567
|
G | T | 2 | a0025a0041 | 2 | HG01884.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.2853C>A | p.Asp951Glu | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 28/33 | 2930/5657 | 2853/3756 | 951/1251 | chr16 | 57901567 | ||
| chr16:57903884
|
T | C | 5 | a0003a0007a0013others(2): Show | 32 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(29): Show |
missense_variant | MODERATE | c.2732A>G | p.Lys911Arg | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/33 | 2809/5657 | 2732/3756 | 911/1251 | chr16 | 57903884 | ||
| chr16:57903971
|
A | G | 1 | a0036 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.2645T>C | p.Val882Ala | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/33 | 2722/5657 | 2645/3756 | 882/1251 | chr16 | 57903971 | ||
| chr16:57915320
|
G | T | 13 | a0008a0010a0011others(10): Show | 28 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(25): Show |
missense_variant | MODERATE | c.2233C>A | p.Leu745Ile | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/33 | 2310/5657 | 2233/3756 | 745/1251 | chr16 | 57915320 | ||
| chr16:57916139
|
C | T | 1 | a0033 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.2207G>A | p.Arg736His | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/33 | 2284/5657 | 2207/3756 | 736/1251 | chr16 | 57916139 | ||
| chr16:57920489
|
G | A | 1 | a0051 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.1699C>T | p.Arg567Trp | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/33 | 1776/5657 | 1699/3756 | 567/1251 | chr16 | 57920489 | ||
| chr16:57920517
|
GGCCGTGG others(5): Show |
G | 1 | a0042 | 1 | HG03239.hp1 | disruptive_inframe_deletion | MODERATE | c.1659_1670delGGCCTC others(6): Show |
p.Ala554_Ala557del | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/33 | 1747/5657 | 1659/3756 | 553/1251 | chr16 | 57920517 | ||
| chr16:57923285
|
G | A | 1 | a0032 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.1631C>T | p.Pro544Leu | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/33 | 1708/5657 | 1631/3756 | 544/1251 | chr16 | 57923285 | ||
| chr16:57923312
|
A | G | 10 | a0008a0010a0013others(7): Show | 21 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(18): Show |
missense_variant | MODERATE | c.1604T>C | p.Val535Ala | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/33 | 1681/5657 | 1604/3756 | 535/1251 | chr16 | 57923312 | ||
| chr16:57923336
|
G | A | 2 | a0029a0043 | 2 | HG02622.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.1580C>T | p.Ala527Val | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/33 | 1657/5657 | 1580/3756 | 527/1251 | chr16 | 57923336 | ||
| chr16:57931816
|
G | T | 2 | a0016a0046 | 3 | NA18970.hp2 NA19056.hp1 NA19068.hp1 |
missense_variant | MODERATE | c.1435C>A | p.Leu479Ile | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/33 | 1512/5657 | 1435/3756 | 479/1251 | chr16 | 57931816 | ||
| chr16:57940239
|
C | T | 2 | a0044a0052 | 2 | NA18955.hp2 NA19056.hp2 |
missense_variant | MODERATE | c.1204G>A | p.Asp402Asn | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 15/33 | 1281/5657 | 1204/3756 | 402/1251 | chr16 | 57940239 | ||
| chr16:57949370
|
T | TTCC | 3 | a0006a0028a0029 | 8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
disruptive_inframe_insertion | MODERATE | c.1101_1103dupGGA | p.Glu368dup | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/33 | 1180/5657 | 1103/3756 | 368/1251 | chr16 | 57949370 | ||
| chr16:57959937
|
C | T | 1 | a0045 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.712G>A | p.Gly238Ser | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/33 | 789/5657 | 712/3756 | 238/1251 | chr16 | 57959937 | ||
| chr16:57960014
|
G | A | 1 | a0027 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.635C>T | p.Thr212Ile | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/33 | 712/5657 | 635/3756 | 212/1251 | chr16 | 57960014 | ||
| chr16:57960015
|
T | A | 2 | a0015a0026 | 3 | HG02280.hp1 HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.634A>T | p.Thr212Ser | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/33 | 711/5657 | 634/3756 | 212/1251 | chr16 | 57960015 | ||
| chr16:57960054
|
G | A | 1 | a0026 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.595C>T | p.Arg199Cys | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/33 | 672/5657 | 595/3756 | 199/1251 | chr16 | 57960054 | ||
| chr16:57962583
|
A | C | 5 | a0004a0014a0023others(2): Show | 13 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(10): Show |
missense_variant | MODERATE | c.440T>G | p.Leu147Arg | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/33 | 517/5657 | 440/3756 | 147/1251 | chr16 | 57962583 | ||
| chr16:57962988
|
C | A | 1 | a0025 | 1 | HG03139.hp2 | stop_gained | HIGH | c.367G>T | p.Glu123* | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/33 | 444/5657 | 367/3756 | 123/1251 | chr16 | 57962988 | ||
| chr16:57963017
|
A | T | 1 | a0025 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.338T>A | p.Val113Glu | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/33 | 415/5657 | 338/3756 | 113/1251 | chr16 | 57963017 | ||
| chr16:57963056
|
C | T | 38 | a0001a0003a0004others(35): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
missense_variant | MODERATE | c.299G>A | p.Arg100His | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/33 | 376/5657 | 299/3756 | 100/1251 | chr16 | 57963056 | ||
| chr16:57964163
|
C | T | 5 | a0004a0014a0022others(2): Show | 13 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(10): Show |
missense_variant | MODERATE | c.257G>A | p.Arg86Gln | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/33 | 334/5657 | 257/3756 | 86/1251 | chr16 | 57964163 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:57887939
|
G | A | 8 | a0001c0029a0001c0035a0001c0073others(5): Show | 11 | HG02071.hp2 HG03239.hp1 HG04228.hp2 others(8): Show |
synonymous_variant | LOW | c.3378C>T | p.Gly1126Gly | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/33 | 3455/5657 | 3378/3756 | 1126/1251 | chr16 | 57887939 | ||
| chr16:57887987
|
G | A | 1 | a0001c0103 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.3330C>T | p.Asn1110Asn | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/33 | 3407/5657 | 3330/3756 | 1110/1251 | chr16 | 57887987 | ||
| chr16:57903853
|
G | A | 1 | a0004c0046 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.2763C>T | p.Tyr921Tyr | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/33 | 2840/5657 | 2763/3756 | 921/1251 | chr16 | 57903853 | ||
| chr16:57903952
|
G | C | 58 | a0001c0001a0001c0002a0001c0003others(55): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
synonymous_variant | LOW | c.2664C>G | p.Ala888Ala | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/33 | 2741/5657 | 2664/3756 | 888/1251 | chr16 | 57903952 | ||
| chr16:57903952
|
G | T | 34 | a0001c0015a0001c0028a0001c0053others(31): Show | 54 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(51): Show |
synonymous_variant | LOW | c.2664C>A | p.Ala888Ala | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/33 | 2741/5657 | 2664/3756 | 888/1251 | chr16 | 57903952 | ||
| chr16:57904851
|
A | G | 2 | a0001c0096a0005c0034 | 3 | HG00323.hp1 HG01516.hp2 HG01517.hp2 |
synonymous_variant | LOW | c.2517T>C | p.Ala839Ala | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/33 | 2594/5657 | 2517/3756 | 839/1251 | chr16 | 57904851 | ||
| chr16:57904854
|
A | G | 2 | a0001c0066a0002c0037 | 3 | HG03017.hp1 HG03942.hp2 HG04204.hp1 |
synonymous_variant | LOW | c.2514T>C | p.Phe838Phe | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/33 | 2591/5657 | 2514/3756 | 838/1251 | chr16 | 57904854 | ||
| chr16:57911764
|
G | A | 5 | a0001c0017a0001c0018a0003c0064others(2): Show | 9 | HG01934.hp1 HG01978.hp2 HG02027.hp1 others(6): Show |
synonymous_variant | LOW | c.2481C>T | p.Gly827Gly | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/33 | 2558/5657 | 2481/3756 | 827/1251 | chr16 | 57911764 | ||
| chr16:57916153
|
G | A | 36 | a0001c0001a0001c0004a0001c0019others(33): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
synonymous_variant | LOW | c.2193C>T | p.Asn731Asn | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/33 | 2270/5657 | 2193/3756 | 731/1251 | chr16 | 57916153 | ||
| chr16:57916165
|
G | A | 1 | a0003c0105 | 1 | HG00597.hp2 | synonymous_variant | LOW | c.2181C>T | p.Asp727Asp | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/33 | 2258/5657 | 2181/3756 | 727/1251 | chr16 | 57916165 | ||
| chr16:57919106
|
C | G | 13 | a0008c0025a0008c0032a0008c0054others(10): Show | 20 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
synonymous_variant | LOW | c.1950G>C | p.Pro650Pro | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/33 | 2027/5657 | 1950/3756 | 650/1251 | chr16 | 57919106 | ||
| chr16:57920544
|
A | G | 26 | a0001c0015a0001c0016a0001c0027others(23): Show | 35 | HG01123.hp2 HG01891.hp1 HG02055.hp2 others(32): Show |
splice_region_variant&synonymous_variant | LOW | c.1644T>C | p.Asp548Asp | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/33 | 1721/5657 | 1644/3756 | 548/1251 | chr16 | 57920544 | ||
| chr16:57931778
|
C | T | 3 | a0001c0053a0002c0109a0049c0108 | 3 | HG02257.hp1 HG02922.hp1 HG03195.hp1 |
synonymous_variant | LOW | c.1473G>A | p.Pro491Pro | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/33 | 1550/5657 | 1473/3756 | 491/1251 | chr16 | 57931778 | ||
| chr16:57939527
|
G | A | 1 | a0009c0077 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.1275C>T | p.Ala425Ala | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/33 | 1352/5657 | 1275/3756 | 425/1251 | chr16 | 57939527 | ||
| chr16:57960043
|
T | C | 1 | a0045c0079 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.606A>G | p.Glu202Glu | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/33 | 683/5657 | 606/3756 | 202/1251 | chr16 | 57960043 | ||
| chr16:57962570
|
G | A | 8 | a0006c0081a0006c0082a0006c0083others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
synonymous_variant | LOW | c.453C>T | p.Asp151Asp | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/33 | 530/5657 | 453/3756 | 151/1251 | chr16 | 57962570 | ||
| chr16:57962864
|
C | A | 1 | a0025c0051 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.390G>T | p.Gly130Gly | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/33 | 467/5657 | 390/3756 | 130/1251 | chr16 | 57962864 | ||
| chr16:57962980
|
C | A | 1 | a0025c0051 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.375G>T | p.Pro125Pro | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/33 | 452/5657 | 375/3756 | 125/1251 | chr16 | 57962980 | ||
| chr16:57963028
|
G | A | 29 | a0001c0001a0001c0003a0001c0013others(26): Show | 116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
synonymous_variant | LOW | c.327C>T | p.Gly109Gly | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/33 | 404/5657 | 327/3756 | 109/1251 | chr16 | 57963028 | ||
| chr16:57967164
|
C | T | 2 | a0001c0041a0001c0042 | 2 | HG02055.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.123G>A | p.Pro41Pro | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/33 | 200/5657 | 123/3756 | 41/1251 | chr16 | 57967164 | ||
| chr16:57967197
|
C | T | 1 | a0003c0040 | 1 | HG02523.hp1 | synonymous_variant | LOW | c.90G>A | p.Glu30Glu | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/33 | 167/5657 | 90/3756 | 30/1251 | chr16 | 57967197 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:57882384
|
A | G | 1 | a0004c0046t0036 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1780T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1780 | chr16 | 57882384 | |||||
| chr16:57882484
|
A | G | 1 | a0001c0003t0032 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1680T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1680 | chr16 | 57882484 | |||||
| chr16:57882493
|
T | C | 2 | a0001c0013t0019a0001c0019t0019 | 3 | HG01168.hp2 HG01169.hp1 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1671A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1671 | chr16 | 57882493 | |||||
| chr16:57882646
|
A | C | 3 | a0001c0015t0020a0024c0047t0034a0040c0063t0020 | 3 | HG03041.hp1 HG03453.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1518T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1518 | chr16 | 57882646 | |||||
| chr16:57882702
|
T | C | 10 | a0001c0004t0014a0002c0005t0009a0003c0008t0009others(7): Show | 11 | HG00597.hp2 HG01123.hp1 HG01978.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1462A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1462 | chr16 | 57882702 | |||||
| chr16:57882735
|
A | G | 1 | a0017c0062t0027 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1429T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1429 | chr16 | 57882735 | |||||
| chr16:57882782
|
C | CT | 35 | a0001c0001t0005a0001c0001t0006a0001c0001t0013others(32): Show | 49 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1381dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1381 | chr16 | 57882782 | |||||
| chr16:57882784
|
T | C | 1 | a0018c0055t0025 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1380A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1380 | chr16 | 57882784 | |||||
| chr16:57882799
|
C | CT | 11 | a0001c0001t0017a0001c0004t0035a0001c0013t0018others(8): Show | 11 | HG01934.hp1 HG02615.hp2 HG02896.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1364dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1364 | chr16 | 57882799 | |||||
| chr16:57882799
|
CT | C | 40 | a0001c0001t0002a0001c0001t0005a0001c0001t0012others(37): Show | 79 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1364delA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1364 | chr16 | 57882799 | |||||
| chr16:57882833
|
A | G | 1 | a0003c0040t0038 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1331T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1331 | chr16 | 57882833 | |||||
| chr16:57882872
|
T | G | 24 | a0001c0007t0004a0001c0013t0004a0001c0013t0019others(21): Show | 28 | HG01070.hp1 HG01168.hp2 HG01169.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1292A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1292 | chr16 | 57882872 | |||||
| chr16:57882923
|
A | G | 1 | a0012c0115t0045 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1241T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1241 | chr16 | 57882923 | |||||
| chr16:57882931
|
A | G | 32 | a0001c0007t0004a0001c0013t0004a0001c0013t0019others(29): Show | 36 | HG01070.hp1 HG01168.hp2 HG01169.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1233T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1233 | chr16 | 57882931 | |||||
| chr16:57882936
|
G | C | 8 | a0001c0003t0032a0001c0004t0008a0001c0007t0008others(5): Show | 9 | HG00099.hp2 HG01081.hp1 HG01168.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1228C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1228 | chr16 | 57882936 | |||||
| chr16:57882973
|
C | T | 2 | a0006c0085t0024a0019c0112t0024 | 2 | HG02486.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1191G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1191 | chr16 | 57882973 | |||||
| chr16:57883022
|
T | C | 1 | a0001c0002t0033 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1142A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1142 | chr16 | 57883022 | |||||
| chr16:57883108
|
T | C | 7 | a0001c0002t0022a0001c0004t0022a0001c0013t0018others(4): Show | 7 | HG02647.hp1 HG02886.hp2 HG02976.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1056A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1056 | chr16 | 57883108 | |||||
| chr16:57883210
|
A | G | 3 | a0001c0015t0020a0024c0047t0034a0040c0063t0020 | 3 | HG03041.hp1 HG03453.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*954T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 954 | chr16 | 57883210 | |||||
| chr16:57883245
|
C | T | 52 | a0001c0001t0001a0001c0001t0006a0001c0001t0017others(49): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*919G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 919 | chr16 | 57883245 | |||||
| chr16:57883246
|
G | T | 4 | a0002c0006t0016a0002c0011t0016a0004c0014t0016others(1): Show | 4 | HG02572.hp1 HG02818.hp1 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*918C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 918 | chr16 | 57883246 | |||||
| chr16:57883256
|
CCTTT | C | 24 | a0001c0007t0004a0001c0013t0004a0001c0013t0019others(21): Show | 28 | HG01070.hp1 HG01168.hp2 HG01169.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*904_*907delAAAG | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 904 | chr16 | 57883256 | |||||
| chr16:57883269
|
TTTTG | T | 52 | a0001c0001t0001a0001c0001t0006a0001c0001t0017others(49): Show | 138 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*891_*894delCAAA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 891 | chr16 | 57883269 | |||||
| chr16:57883328
|
G | A | 51 | a0001c0001t0002a0001c0001t0005a0001c0001t0012others(48): Show | 90 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*836C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 836 | chr16 | 57883328 | |||||
| chr16:57883416
|
ATGTGAAC others(3): Show |
A | 1 | a0001c0001t0037 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*738_*747delGTGGTT others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 738 | chr16 | 57883416 | |||||
| chr16:57883489
|
C | T | 3 | a0001c0001t0012a0001c0003t0012a0005c0034t0012 | 5 | HG00140.hp2 HG00733.hp2 HG01516.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*675G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 675 | chr16 | 57883489 | |||||
| chr16:57883569
|
G | C | 21 | a0001c0001t0007a0001c0002t0007a0001c0004t0014others(18): Show | 23 | HG00597.hp2 HG00642.hp2 HG00738.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*595C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 595 | chr16 | 57883569 | |||||
| chr16:57883671
|
G | A | 7 | a0001c0027t0040a0001c0042t0011a0019c0110t0011others(4): Show | 7 | HG02258.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*493C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 493 | chr16 | 57883671 | |||||
| chr16:57883843
|
C | G | 2 | a0001c0035t0028a0001c0103t0029 | 2 | HG00558.hp2 NA18998.hp1 |
3_prime_UTR_variant | MODIFIER | c.*321G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 321 | chr16 | 57883843 | |||||
| chr16:57883854
|
A | G | 26 | a0001c0007t0004a0001c0013t0004a0001c0013t0019others(23): Show | 30 | HG01070.hp1 HG01168.hp2 HG01169.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*310T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 310 | chr16 | 57883854 | |||||
| chr16:57883883
|
A | G | 2 | a0017c0062t0027a0048c0117t0026 | 2 | HG00741.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*281T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 281 | chr16 | 57883883 | |||||
| chr16:57883920
|
T | C | 8 | a0001c0028t0042a0001c0028t0044a0002c0005t0041others(5): Show | 8 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*244A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 244 | chr16 | 57883920 | |||||
| chr16:57883995
|
G | T | 1 | a0018c0055t0025 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*169C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 169 | chr16 | 57883995 | |||||
| chr16:57884131
|
T | C | 24 | a0001c0007t0004a0001c0013t0004a0001c0013t0019others(21): Show | 28 | HG01070.hp1 HG01168.hp2 HG01169.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*33A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 33 | chr16 | 57884131 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:57884580
|
G | T | 5 | a0001c0004t0003g0151a0001c0097t0003g0231a0002c0006t0003g0022others(2): Show | 5 | HG00438.hp1 HG00558.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.3463-123C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57884580 | ||||||
| chr16:57884643
|
G | A | 1 | a0033c0065t0015g0043 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3463-186C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57884643 | ||||||
| chr16:57884665
|
T | A | 12 | a0001c0007t0002g0073a0001c0096t0002g0293a0005c0036t0002g0256others(9): Show | 12 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.3463-208A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57884665 | ||||||
| chr16:57884705
|
T | A | 1 | a0001c0001t0001g0279 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3463-248A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57884705 | ||||||
| chr16:57884863
|
C | T | 14 | a0001c0007t0002g0073a0001c0041t0005g0028a0001c0096t0002g0293others(11): Show | 14 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.3463-406G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57884863 | ||||||
| chr16:57884869
|
T | C | 28 | a0001c0007t0004g0046a0001c0013t0004g0308a0001c0013t0019g0213others(25): Show | 28 | HG01070.hp1 HG01168.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.3463-412A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57884869 | ||||||
| chr16:57884963
|
G | C | 15 | a0001c0007t0002g0073a0001c0041t0005g0028a0001c0096t0002g0293others(12): Show | 15 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.3463-506C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57884963 | ||||||
| chr16:57885130
|
C | T | 225 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(222): Show | 226 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.3463-673G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885130 | ||||||
| chr16:57885137
|
C | T | 22 | a0001c0001t0007g0290a0001c0002t0007g0126a0001c0004t0014g0192others(19): Show | 22 | HG00597.hp2 HG00642.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.3463-680G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885137 | ||||||
| chr16:57885212
|
G | A | 1 | a0048c0117t0026g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3463-755C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885212 | ||||||
| chr16:57885224
|
C | T | 1 | a0003c0009t0006g0217 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3463-767G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885224 | ||||||
| chr16:57885505
|
CTTTCCTT others(13): Show |
C | 2 | a0028c0084t0003g0330a0047c0111t0003g0327 | 2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3463-1068_3463-104 others(24): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885505 | ||||||
| chr16:57885525
|
T | C | 1 | a0001c0003t0001g0197 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.3463-1068A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885525 | ||||||
| chr16:57885543
|
TTCTTTCC others(7): Show |
T | 2 | a0001c0007t0004g0046a0002c0011t0004g0185 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3463-1100_3463-108 others(18): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885543 | ||||||
| chr16:57885557
|
C | CCT | 7 | a0001c0015t0002g0006a0001c0016t0010g0057a0001c0073t0002g0132others(4): Show | 7 | HG00323.hp1 HG01069.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.3463-1102_3463-110 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | ||||||
| chr16:57885557
|
C | CCTCT | 14 | a0001c0001t0002g0250a0001c0001t0005g0274a0001c0001t0012g0212others(11): Show | 14 | HG00140.hp2 HG00733.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.3463-1104_3463-110 others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | ||||||
| chr16:57885557
|
C | CCTCTCT | 27 | a0001c0001t0002g0252a0001c0001t0002g0273a0001c0001t0002g0309others(24): Show | 27 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.3463-1106_3463-110 others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | ||||||
| chr16:57885557
|
C | CCTCTCTC others(1): Show |
13 | a0001c0001t0002g0223a0001c0001t0002g0312a0001c0002t0005g0143others(10): Show | 13 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.3463-1108_3463-110 others(12): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | ||||||
| chr16:57885557
|
C | CCTCTCTC others(3): Show |
10 | a0001c0001t0002g0238a0001c0002t0002g0183a0001c0004t0005g0127others(7): Show | 11 | HG01175.hp2 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.3463-1110_3463-110 others(14): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | ||||||
| chr16:57885557
|
C | CCTCTCTC others(5): Show |
7 | a0001c0001t0003g0224a0001c0002t0002g0124a0001c0003t0002g0196others(4): Show | 7 | HG01346.hp1 HG01346.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.3463-1112_3463-110 others(16): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | ||||||
| chr16:57885557
|
C | CCTCTCTC others(7): Show |
13 | a0001c0002t0003g0031a0001c0002t0003g0038a0001c0002t0005g0184others(10): Show | 14 | HG00544.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.3463-1114_3463-110 others(18): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | ||||||
| chr16:57885557
|
C | CCTCTCTC others(9): Show |
7 | a0001c0001t0013g0206a0001c0002t0003g0050a0001c0002t0005g0142others(4): Show | 7 | HG00099.hp1 HG01433.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.3463-1116_3463-110 others(20): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | ||||||
| chr16:57885557
|
C | CCTCTCTC others(11): Show |
3 | a0001c0003t0003g0198a0002c0006t0013g0083a0002c0038t0003g0094 | 3 | HG03834.hp1 NA18959.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.3463-1118_3463-110 others(22): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | ||||||
| chr16:57885557
|
C | CCTCTCTC others(13): Show |
10 | a0001c0001t0001g0262a0001c0001t0003g0208a0001c0002t0002g0157others(7): Show | 10 | HG02145.hp1 HG02738.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.3463-1120_3463-110 others(24): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | ||||||
| chr16:57885557
|
C | CCTCTCTC others(15): Show |
3 | a0001c0002t0003g0113a0001c0002t0013g0041a0010c0010t0003g0030 | 3 | HG02071.hp1 HG02148.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3463-1122_3463-110 others(26): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | ||||||
| chr16:57885557
|
C | CCTCTCTC others(17): Show |
2 | a0001c0001t0013g0251a0012c0122t0003g0317 | 2 | HG01361.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3463-1101_3463-110 others(28): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | ||||||
| chr16:57885557
|
C | CCTCTCTC others(21): Show |
2 | a0006c0086t0003g0067a0012c0120t0003g0065 | 2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.3463-1101_3463-110 others(32): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | ||||||
| chr16:57885557
|
C | CCTCTCTC others(23): Show |
1 | a0008c0032t0002g0269 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3463-1101_3463-110 others(34): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | ||||||
| chr16:57885557
|
C | CTCTCTCT others(8): Show |
1 | a0001c0003t0002g0201 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3463-1101_3463-110 others(19): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | ||||||
| chr16:57885576
|
C | CTCTT | 3 | a0002c0005t0001g0024a0019c0110t0011g0321a0027c0078t0011g0353 | 3 | HG02132.hp1 HG02615.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3463-1123_3463-112 others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885576 | ||||||
| chr16:57885576
|
CTCTT | C | 123 | a0001c0001t0001g0195a0001c0001t0001g0205a0001c0001t0001g0207others(120): Show | 123 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.3463-1123_3463-112 others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885576 | ||||||
| chr16:57885576
|
CTCTTTCT others(1): Show |
C | 34 | a0001c0002t0003g0008a0001c0007t0003g0004a0001c0007t0003g0340others(31): Show | 34 | HG01070.hp1 HG01123.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.3463-1127_3463-112 others(12): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885576 | ||||||
| chr16:57885576
|
CTCTTTCT others(5): Show |
C | 10 | a0001c0028t0044g0064a0004c0049t0015g0344a0006c0083t0043g0063others(7): Show | 10 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.3463-1131_3463-112 others(16): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885576 | ||||||
| chr16:57885576
|
CTCTTTCT others(9): Show |
C | 3 | a0024c0047t0034g0350a0040c0063t0020g0009a0045c0079t0006g0194 | 3 | HG01175.hp1 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3463-1135_3463-112 others(20): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885576 | ||||||
| chr16:57885578
|
CTT | C | 4 | a0001c0001t0037g0246a0001c0013t0018g0294a0002c0011t0018g0341others(1): Show | 4 | HG00735.hp2 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3463-1123_3463-112 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885578 | ||||||
| chr16:57885578
|
CTTTCTT | C | 4 | a0002c0011t0016g0190a0003c0008t0009g0146a0007c0021t0014g0088others(1): Show | 4 | HG02257.hp1 NA18980.hp1 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.3463-1127_3463-112 others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885578 | ||||||
| chr16:57885578
|
CTTTCTTT others(3): Show |
C | 23 | a0001c0001t0007g0290a0001c0002t0007g0126a0001c0004t0014g0192others(20): Show | 23 | HG00597.hp2 HG00642.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.3463-1131_3463-112 others(14): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885578 | ||||||
| chr16:57885578
|
CTTTCTTT others(7): Show |
C | 7 | a0001c0004t0003g0151a0001c0097t0003g0231a0002c0006t0003g0022others(4): Show | 7 | HG00438.hp1 HG00558.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.3463-1135_3463-112 others(18): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885578 | ||||||
| chr16:57885580
|
T | C | 126 | a0001c0001t0001g0262a0001c0001t0002g0223a0001c0001t0002g0238others(123): Show | 128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.3463-1123A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885580 | ||||||
| chr16:57885584
|
T | C | 128 | a0001c0001t0001g0262a0001c0001t0002g0223a0001c0001t0002g0238others(125): Show | 130 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.3463-1127A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885584 | ||||||
| chr16:57885584
|
TTC | T | 3 | a0001c0004t0001g0165a0002c0005t0001g0087a0046c0107t0006g0099 | 3 | NA18955.hp1 NA18974.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.3463-1129_3463-112 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885584 | ||||||
| chr16:57885588
|
T | C | 157 | a0001c0001t0001g0262a0001c0001t0002g0223a0001c0001t0002g0238others(154): Show | 159 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.3463-1131A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885588 | ||||||
| chr16:57885592
|
T | C | 133 | a0001c0001t0001g0262a0001c0001t0002g0223a0001c0001t0002g0238others(130): Show | 135 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.3463-1135A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885592 | ||||||
| chr16:57885595
|
T | TCTCTCTC others(8): Show |
1 | a0002c0006t0003g0012 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3463-1139_3463-113 others(19): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885595 | ||||||
| chr16:57885607
|
T | C | 11 | a0001c0028t0044g0064a0004c0049t0015g0344a0006c0083t0043g0063others(8): Show | 11 | HG01123.hp2 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.3463-1150A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885607 | ||||||
| chr16:57885696
|
C | G | 3 | a0001c0013t0018g0294a0002c0011t0018g0341a0002c0022t0018g0112 | 3 | HG02976.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3463-1239G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885696 | ||||||
| chr16:57885750
|
T | C | 6 | a0001c0028t0044g0064a0004c0049t0015g0344a0006c0083t0043g0063others(3): Show | 6 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3463-1293A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885750 | ||||||
| chr16:57885805
|
G | A | 5 | a0001c0004t0003g0151a0001c0097t0003g0231a0002c0006t0003g0022others(2): Show | 5 | HG00438.hp1 HG00558.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.3463-1348C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885805 | ||||||
| chr16:57885814
|
A | G | 41 | a0001c0007t0004g0046a0001c0013t0004g0308a0001c0013t0019g0213others(38): Show | 41 | HG01070.hp1 HG01123.hp2 HG01168.hp2 others(38): Show |
intron_variant | MODIFIER | c.3463-1357T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885814 | ||||||
| chr16:57885830
|
G | A | 5 | a0001c0002t0001g0056a0002c0005t0001g0314a0002c0005t0001g0316others(2): Show | 5 | HG02109.hp1 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3463-1373C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885830 | ||||||
| chr16:57886002
|
A | G | 11 | a0001c0028t0044g0064a0004c0049t0015g0344a0006c0083t0043g0063others(8): Show | 11 | HG01123.hp2 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.3463-1545T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886002 | ||||||
| chr16:57886173
|
T | C | 5 | a0001c0002t0003g0008a0001c0007t0003g0004a0001c0007t0003g0340others(2): Show | 5 | HG02622.hp2 HG02895.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3462+1682A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886173 | ||||||
| chr16:57886212
|
G | A | 1 | a0002c0006t0003g0076 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3462+1643C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886212 | ||||||
| chr16:57886265
|
A | C | 1 | a0006c0081t0021g0331 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3462+1590T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886265 | ||||||
| chr16:57886485
|
T | C | 2 | a0001c0001t0001g0205a0002c0005t0006g0089 | 2 | HG02015.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.3462+1370A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886485 | ||||||
| chr16:57886557
|
C | T | 39 | a0001c0001t0001g0262a0001c0001t0003g0208a0001c0001t0003g0224others(36): Show | 40 | HG00544.hp1 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.3462+1298G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886557 | ||||||
| chr16:57886707
|
TCCTAAAG others(5): Show |
T | 28 | a0001c0007t0004g0046a0001c0013t0004g0308a0001c0013t0019g0213others(25): Show | 28 | HG01070.hp1 HG01168.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.3462+1136_3462+114 others(16): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886707 | ||||||
| chr16:57886798
|
T | C | 1 | a0046c0107t0006g0099 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3462+1057A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886798 | ||||||
| chr16:57886864
|
C | T | 342 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(339): Show | 344 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.3462+991G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886864 | ||||||
| chr16:57886998
|
C | T | 1 | a0001c0003t0003g0296 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3462+857G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886998 | ||||||
| chr16:57887062
|
A | C | 83 | a0001c0001t0007g0290a0001c0002t0001g0125a0001c0002t0007g0126others(80): Show | 83 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.3462+793T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887062 | ||||||
| chr16:57887212
|
A | G | 237 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(234): Show | 238 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.3462+643T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887212 | ||||||
| chr16:57887542
|
A | G | 1 | a0007c0021t0009g0093 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3462+313T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887542 | ||||||
| chr16:57887588
|
G | A | 204 | a0001c0001t0001g0003a0001c0001t0001g0207a0001c0001t0001g0227others(201): Show | 205 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.3462+267C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887588 | ||||||
| chr16:57887600
|
C | T | 1 | a0009c0098t0003g0241 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3462+255G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887600 | ||||||
| chr16:57887652
|
G | A | 116 | a0001c0001t0001g0003a0001c0001t0001g0207a0001c0001t0001g0227others(113): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.3462+203C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887652 | ||||||
| chr16:57887718
|
C | A | 1 | a0018c0102t0003g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3462+137G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887718 | ||||||
| chr16:57887729
|
T | C | 12 | a0001c0007t0003g0189a0001c0013t0018g0294a0002c0005t0041g0068others(9): Show | 12 | HG00741.hp2 HG01109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.3462+126A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887729 | ||||||
| chr16:57887748
|
G | C | 1 | a0001c0001t0001g0280 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3462+107C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887748 | ||||||
| chr16:57887848
|
A | G | 132 | a0001c0001t0001g0195a0001c0001t0001g0205a0001c0001t0001g0236others(129): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
splice_region_variant&intron_variant | LOW | c.3462+7T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887848 | ||||||
| chr16:57888097
|
G | T | 4 | a0001c0002t0003g0008a0001c0007t0003g0340a0004c0046t0036g0348others(1): Show | 4 | HG02622.hp2 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3243-23C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888097 | ||||||
| chr16:57888180
|
T | G | 41 | a0001c0001t0012g0212a0001c0002t0001g0052a0001c0002t0002g0157others(38): Show | 41 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.3243-106A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888180 | ||||||
| chr16:57888362
|
C | T | 1 | a0001c0053t0004g0200 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3243-288G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888362 | ||||||
| chr16:57888363
|
G | A | 1 | a0019c0110t0011g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3243-289C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888363 | ||||||
| chr16:57888467
|
GTC | G | 55 | a0001c0007t0003g0189a0001c0013t0018g0294a0001c0015t0001g0335others(52): Show | 56 | HG00597.hp2 HG00642.hp2 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.3243-395_3243-394d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888467 | ||||||
| chr16:57888562
|
T | C | 3 | a0002c0109t0004g0108a0024c0047t0034g0350a0040c0063t0020g0009 | 3 | HG03195.hp1 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3243-488A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888562 | ||||||
| chr16:57888625
|
A | G | 1 | a0001c0001t0001g0275 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3243-551T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888625 | ||||||
| chr16:57888653
|
T | C | 3 | a0001c0013t0018g0294a0002c0011t0018g0341a0002c0022t0018g0112 | 3 | HG02976.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3243-579A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888653 | ||||||
| chr16:57888690
|
G | A | 5 | a0001c0001t0001g0234a0002c0005t0001g0015a0002c0005t0001g0016others(2): Show | 5 | HG00639.hp2 HG00642.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.3243-616C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888690 | ||||||
| chr16:57888757
|
C | CT | 76 | a0001c0001t0007g0290a0001c0001t0012g0212a0001c0002t0001g0052others(73): Show | 77 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.3243-684dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888757 | ||||||
| chr16:57888918
|
C | T | 4 | a0001c0007t0003g0189a0001c0042t0011g0029a0024c0047t0034g0350others(1): Show | 4 | HG02723.hp1 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3243-844G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888918 | ||||||
| chr16:57889044
|
C | T | 250 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(247): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.3243-970G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889044 | ||||||
| chr16:57889209
|
C | T | 1 | a0001c0002t0001g0052 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3243-1135G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889209 | ||||||
| chr16:57889210
|
T | C | 15 | a0001c0004t0035g0079a0001c0015t0020g0336a0001c0028t0044g0064others(12): Show | 15 | HG00438.hp1 HG00741.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.3243-1136A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889210 | ||||||
| chr16:57889487
|
T | C | 13 | a0001c0004t0035g0079a0001c0015t0020g0336a0001c0028t0044g0064others(10): Show | 13 | HG01884.hp1 HG02451.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.3243-1413A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889487 | ||||||
| chr16:57889546
|
A | G | 1 | a0019c0110t0011g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3243-1472T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889546 | ||||||
| chr16:57889556
|
C | T | 2 | a0001c0041t0005g0028a0002c0022t0002g0074 | 2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3243-1482G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889556 | ||||||
| chr16:57889557
|
G | A | 1 | a0001c0002t0001g0162 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3243-1483C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889557 | ||||||
| chr16:57889573
|
G | C | 12 | a0001c0015t0001g0335a0001c0016t0046g0054a0001c0028t0042g0069others(9): Show | 12 | HG02257.hp1 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.3243-1499C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889573 | ||||||
| chr16:57889613
|
T | C | 1 | a0001c0003t0001g0199 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3243-1539A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889613 | ||||||
| chr16:57889755
|
C | G | 51 | a0001c0001t0002g0238a0001c0001t0002g0252a0001c0001t0002g0273others(48): Show | 51 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.3243-1681G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889755 | ||||||
| chr16:57889894
|
A | G | 1 | a0001c0027t0040g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3243-1820T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889894 | ||||||
| chr16:57889987
|
C | T | 1 | a0003c0008t0002g0131 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3243-1913G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889987 | ||||||
| chr16:57889998
|
A | G | 2 | a0017c0062t0027g0324a0048c0117t0026g0186 | 2 | HG00741.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3243-1924T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889998 | ||||||
| chr16:57890141
|
C | G | 1 | a0011c0059t0001g0123 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3243-2067G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890141 | ||||||
| chr16:57890247
|
G | A | 1 | a0018c0102t0003g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3243-2173C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890247 | ||||||
| chr16:57890339
|
C | T | 2 | a0004c0049t0015g0344a0026c0080t0015g0188 | 2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3243-2265G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890339 | ||||||
| chr16:57890360
|
C | A | 2 | a0024c0047t0034g0350a0040c0063t0020g0009 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3243-2286G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890360 | ||||||
| chr16:57890471
|
T | C | 1 | a0001c0002t0001g0039 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3243-2397A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890471 | ||||||
| chr16:57890496
|
C | A | 55 | a0001c0001t0012g0212a0001c0003t0012g0266a0001c0007t0002g0073others(52): Show | 55 | HG00140.hp2 HG00438.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.3243-2422G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890496 | ||||||
| chr16:57890528
|
C | T | 1 | a0001c0001t0005g0277 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3243-2454G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890528 | ||||||
| chr16:57890653
|
T | C | 96 | a0001c0001t0007g0290a0001c0001t0012g0212a0001c0002t0001g0052others(93): Show | 97 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.3243-2579A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890653 | ||||||
| chr16:57890798
|
T | C | 2 | a0017c0062t0027g0324a0048c0117t0026g0186 | 2 | HG00741.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3243-2724A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890798 | ||||||
| chr16:57890917
|
A | G | 1 | a0003c0012t0014g0158 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3243-2843T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890917 | ||||||
| chr16:57890946
|
C | T | 12 | a0001c0015t0001g0335a0001c0016t0046g0054a0001c0028t0042g0069others(9): Show | 12 | HG02257.hp1 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.3243-2872G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890946 | ||||||
| chr16:57890976
|
C | T | 1 | a0001c0029t0002g0163 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3243-2902G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890976 | ||||||
| chr16:57891025
|
G | A | 3 | a0011c0058t0004g0140a0028c0084t0003g0330a0047c0111t0003g0327 | 3 | HG02451.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3243-2951C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57891025 | ||||||
| chr16:57891089
|
C | A | 1 | a0001c0002t0001g0052 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3243-3015G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57891089 | ||||||
| chr16:57891250
|
C | T | 1 | a0001c0003t0001g0228 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3243-3176G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57891250 | ||||||
| chr16:57891351
|
T | C | 6 | a0001c0001t0001g0237a0001c0002t0001g0329a0001c0002t0033g0053others(3): Show | 6 | HG00280.hp1 HG00639.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.3243-3277A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57891351 | ||||||
| chr16:57891356
|
G | A | 26 | a0001c0013t0018g0294a0001c0015t0001g0335a0001c0016t0010g0057others(23): Show | 26 | HG00438.hp1 HG02109.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.3243-3282C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57891356 | ||||||
| chr16:57891625
|
T | C | 67 | a0001c0001t0012g0212a0001c0002t0001g0052a0001c0002t0002g0157others(64): Show | 67 | HG00140.hp2 HG00438.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.3243-3551A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57891625 | ||||||
| chr16:57891800
|
A | G | 97 | a0001c0001t0007g0290a0001c0001t0012g0212a0001c0002t0001g0052others(94): Show | 98 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.3243-3726T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57891800 | ||||||
| chr16:57891842
|
C | T | 12 | a0001c0015t0001g0335a0001c0016t0046g0054a0001c0028t0042g0069others(9): Show | 12 | HG02257.hp1 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.3243-3768G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57891842 | ||||||
| chr16:57891901
|
C | T | 2 | a0001c0007t0004g0046a0002c0011t0004g0185 | 2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3243-3827G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57891901 | ||||||
| chr16:57892072
|
C | CA | 38 | a0001c0001t0012g0212a0001c0002t0001g0039a0001c0002t0002g0157others(35): Show | 38 | HG00140.hp2 HG00438.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.3243-3999dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892072 | ||||||
| chr16:57892072
|
C | CAA | 33 | a0001c0001t0007g0290a0001c0002t0001g0052a0001c0035t0010g0230others(30): Show | 34 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.3243-4000_3243-399 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892072 | ||||||
| chr16:57892072
|
CA | C | 150 | a0001c0001t0001g0003a0001c0001t0001g0205a0001c0001t0001g0260others(147): Show | 151 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.3243-3999delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892072 | ||||||
| chr16:57892072
|
CAA | C | 6 | a0017c0060t0015g0005a0024c0047t0034g0350a0026c0080t0015g0188others(3): Show | 6 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3243-4000_3243-399 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892072 | ||||||
| chr16:57892128
|
G | T | 1 | a0018c0055t0025g0042 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3243-4054C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892128 | ||||||
| chr16:57892160
|
A | T | 198 | a0001c0001t0001g0262a0001c0001t0001g0279a0001c0001t0002g0238others(195): Show | 199 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.3243-4086T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892160 | ||||||
| chr16:57892178
|
C | T | 1 | a0001c0004t0003g0037 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3243-4104G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892178 | ||||||
| chr16:57892262
|
G | A | 2 | a0001c0027t0003g0058a0006c0086t0003g0067 | 2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3243-4188C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892262 | ||||||
| chr16:57892265
|
G | A | 97 | a0001c0001t0007g0290a0001c0001t0012g0212a0001c0002t0001g0052others(94): Show | 98 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.3243-4191C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892265 | ||||||
| chr16:57892267
|
A | G | 97 | a0001c0001t0007g0290a0001c0001t0012g0212a0001c0002t0001g0052others(94): Show | 98 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.3243-4193T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892267 | ||||||
| chr16:57892288
|
C | T | 5 | a0004c0049t0015g0344a0017c0060t0015g0005a0026c0080t0015g0188others(2): Show | 5 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.3243-4214G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892288 | ||||||
| chr16:57892314
|
A | G | 16 | a0001c0004t0035g0079a0001c0016t0010g0057a0002c0005t0041g0068others(13): Show | 16 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.3243-4240T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892314 | ||||||
| chr16:57892336
|
C | T | 19 | a0001c0001t0001g0262a0001c0001t0001g0279a0001c0001t0003g0224others(16): Show | 19 | HG00544.hp1 HG00609.hp1 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.3243-4262G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892336 | ||||||
| chr16:57892423
|
C | T | 1 | a0002c0113t0003g0318 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3243-4349G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892423 | ||||||
| chr16:57892466
|
G | A | 3 | a0001c0013t0018g0294a0002c0011t0018g0341a0002c0022t0018g0112 | 3 | HG02976.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3243-4392C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892466 | ||||||
| chr16:57892526
|
T | C | 3 | a0001c0016t0010g0057a0002c0114t0010g0357a0006c0082t0010g0337 | 3 | HG02109.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3243-4452A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892526 | ||||||
| chr16:57892631
|
T | C | 1 | a0001c0001t0013g0251 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3243-4557A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892631 | ||||||
| chr16:57892637
|
C | T | 3 | a0001c0013t0018g0294a0002c0011t0018g0341a0002c0022t0018g0112 | 3 | HG02976.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3243-4563G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892637 | ||||||
| chr16:57892656
|
CA | C | 40 | a0001c0001t0012g0212a0001c0002t0001g0052a0001c0002t0002g0157others(37): Show | 40 | HG00140.hp2 HG00733.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.3243-4583delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892656 | ||||||
| chr16:57892665
|
C | A | 62 | a0001c0001t0012g0212a0001c0002t0001g0052a0001c0002t0002g0157others(59): Show | 62 | HG00140.hp2 HG00438.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.3243-4591G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892665 | ||||||
| chr16:57892769
|
C | G | 67 | a0001c0001t0012g0212a0001c0002t0001g0052a0001c0002t0002g0157others(64): Show | 67 | HG00140.hp2 HG00438.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.3242+4628G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892769 | ||||||
| chr16:57892855
|
C | A | 1 | a0001c0007t0003g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3242+4542G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892855 | ||||||
| chr16:57892915
|
G | A | 1 | a0039c0072t0001g0137 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3242+4482C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892915 | ||||||
| chr16:57892943
|
G | A | 16 | a0001c0013t0018g0294a0001c0016t0010g0057a0002c0005t0041g0068others(13): Show | 16 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.3242+4454C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892943 | ||||||
| chr16:57892955
|
C | T | 1 | a0006c0081t0021g0331 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3242+4442G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892955 | ||||||
| chr16:57893010
|
T | C | 3 | a0001c0013t0018g0294a0002c0011t0018g0341a0002c0022t0018g0112 | 3 | HG02976.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3242+4387A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893010 | ||||||
| chr16:57893053
|
T | G | 49 | a0001c0001t0012g0212a0001c0002t0001g0052a0001c0002t0002g0157others(46): Show | 49 | HG00140.hp2 HG00438.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.3242+4344A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893053 | ||||||
| chr16:57893217
|
C | T | 18 | a0001c0004t0035g0079a0001c0013t0018g0294a0001c0016t0010g0057others(15): Show | 18 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.3242+4180G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893217 | ||||||
| chr16:57893264
|
T | C | 2 | a0025c0051t0001g0339a0041c0069t0001g0045 | 2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3242+4133A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893264 | ||||||
| chr16:57893317
|
C | A | 1 | a0001c0003t0032g0109 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3242+4080G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893317 | ||||||
| chr16:57893369
|
G | A | 2 | a0001c0042t0011g0029a0001c0068t0005g0175 | 2 | HG02080.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3242+4028C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893369 | ||||||
| chr16:57893387
|
G | T | 1 | a0001c0003t0001g0282 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3242+4010C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893387 | ||||||
| chr16:57893413
|
C | T | 3 | a0001c0002t0001g0052a0001c0002t0002g0157a0039c0072t0001g0137 | 3 | HG02738.hp2 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.3242+3984G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893413 | ||||||
| chr16:57893414
|
G | A | 3 | a0001c0016t0010g0057a0002c0114t0010g0357a0006c0082t0010g0337 | 3 | HG02109.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3242+3983C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893414 | ||||||
| chr16:57893432
|
C | A | 18 | a0001c0004t0035g0079a0001c0013t0018g0294a0001c0016t0010g0057others(15): Show | 18 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.3242+3965G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893432 | ||||||
| chr16:57893475
|
C | T | 1 | a0004c0014t0001g0345 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3242+3922G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893475 | ||||||
| chr16:57893614
|
A | G | 2 | a0001c0001t0001g0205a0002c0005t0006g0089 | 2 | HG02015.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.3242+3783T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893614 | ||||||
| chr16:57893630
|
T | C | 47 | a0001c0001t0012g0212a0001c0002t0001g0052a0001c0002t0002g0157others(44): Show | 47 | HG00140.hp2 HG00733.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.3242+3767A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893630 | ||||||
| chr16:57893671
|
G | T | 5 | a0001c0013t0018g0294a0002c0011t0018g0341a0002c0022t0018g0112others(2): Show | 5 | HG02976.hp1 HG03041.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3242+3726C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893671 | ||||||
| chr16:57893763
|
G | A | 3 | a0001c0001t0001g0261a0001c0004t0001g0150a0008c0025t0001g0122 | 3 | NA18956.hp2 NA19007.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.3242+3634C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893763 | ||||||
| chr16:57893822
|
T | A | 2 | a0024c0047t0034g0350a0040c0063t0020g0009 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3242+3575A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893822 | ||||||
| chr16:57893830
|
A | C | 1 | a0002c0005t0041g0068 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3242+3567T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893830 | ||||||
| chr16:57893850
|
C | A | 3 | a0010c0010t0008g0090a0010c0010t0008g0102a0030c0092t0001g0285 | 3 | HG01515.hp2 HG01517.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.3242+3547G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893850 | ||||||
| chr16:57893879
|
C | G | 5 | a0001c0013t0018g0294a0002c0011t0018g0341a0002c0022t0018g0112others(2): Show | 5 | HG02976.hp1 HG03041.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3242+3518G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893879 | ||||||
| chr16:57893895
|
C | A | 1 | a0002c0005t0001g0332 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3242+3502G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893895 | ||||||
| chr16:57894027
|
G | A | 47 | a0001c0001t0012g0212a0001c0002t0001g0052a0001c0002t0002g0157others(44): Show | 47 | HG00140.hp2 HG00733.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.3242+3370C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894027 | ||||||
| chr16:57894040
|
G | A | 1 | a0001c0007t0003g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3242+3357C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894040 | ||||||
| chr16:57894225
|
G | A | 2 | a0018c0102t0003g0271a0022c0050t0003g0352 | 2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3242+3172C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894225 | ||||||
| chr16:57894252
|
C | A | 5 | a0001c0004t0035g0079a0002c0005t0041g0068a0002c0006t0021g0187others(2): Show | 5 | HG02886.hp1 HG02965.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.3242+3145G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894252 | ||||||
| chr16:57894310
|
A | C | 1 | a0007c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3087T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894310 | ||||||
| chr16:57894311
|
A | T | 1 | a0007c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3086T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894311 | ||||||
| chr16:57894314
|
G | A | 1 | a0007c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3083C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894314 | ||||||
| chr16:57894315
|
T | C | 1 | a0007c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3082A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894315 | ||||||
| chr16:57894316
|
T | A | 1 | a0007c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3081A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894316 | ||||||
| chr16:57894318
|
G | A | 1 | a0007c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3079C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894318 | ||||||
| chr16:57894320
|
G | T | 1 | a0007c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3077C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894320 | ||||||
| chr16:57894321
|
C | G | 1 | a0007c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3076G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894321 | ||||||
| chr16:57894322
|
T | A | 1 | a0007c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3075A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894322 | ||||||
| chr16:57894323
|
G | T | 1 | a0007c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3074C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894323 | ||||||
| chr16:57894325
|
G | T | 1 | a0007c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3072C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894325 | ||||||
| chr16:57894384
|
T | C | 2 | a0018c0102t0003g0271a0022c0050t0003g0352 | 2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3242+3013A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894384 | ||||||
| chr16:57894417
|
G | A | 90 | a0001c0001t0007g0290a0001c0001t0012g0212a0001c0002t0001g0052others(87): Show | 91 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.3242+2980C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894417 | ||||||
| chr16:57894497
|
A | ATGCCTGT others(6): Show |
2 | a0024c0047t0034g0350a0040c0063t0020g0009 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3242+2899_3242+290 others(17): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894497 | ||||||
| chr16:57894498
|
G | A | 2 | a0024c0047t0034g0350a0040c0063t0020g0009 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3242+2899C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894498 | ||||||
| chr16:57894516
|
A | G | 67 | a0001c0001t0012g0212a0001c0002t0001g0052a0001c0002t0002g0157others(64): Show | 67 | HG00140.hp2 HG00438.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.3242+2881T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894516 | ||||||
| chr16:57894559
|
C | A | 1 | a0001c0097t0003g0231 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3242+2838G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894559 | ||||||
| chr16:57894643
|
G | A | 27 | a0001c0001t0007g0290a0003c0008t0002g0002a0003c0008t0003g0145others(24): Show | 28 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.3242+2754C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894643 | ||||||
| chr16:57894823
|
A | G | 1 | a0002c0005t0001g0101 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3242+2574T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894823 | ||||||
| chr16:57894875
|
A | G | 2 | a0017c0062t0027g0324a0048c0117t0026g0186 | 2 | HG00741.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3242+2522T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894875 | ||||||
| chr16:57895021
|
T | C | 1 | a0018c0102t0003g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3242+2376A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895021 | ||||||
| chr16:57895028
|
AG | A | 23 | a0001c0007t0004g0046a0001c0007t0008g0356a0001c0013t0004g0308others(20): Show | 23 | HG00738.hp2 HG01070.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.3242+2368delC | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895028 | ||||||
| chr16:57895033
|
C | A | 1 | a0001c0007t0003g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3242+2364G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895033 | ||||||
| chr16:57895221
|
A | G | 2 | a0001c0097t0003g0231a0002c0037t0003g0023 | 2 | HG00438.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.3242+2176T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895221 | ||||||
| chr16:57895272
|
C | A | 8 | a0001c0002t0022g0062a0001c0004t0022g0107a0001c0027t0040g0078others(5): Show | 8 | HG02258.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.3242+2125G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895272 | ||||||
| chr16:57895368
|
C | T | 1 | a0002c0005t0041g0068 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3242+2029G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895368 | ||||||
| chr16:57895398
|
G | A | 1 | a0001c0015t0020g0336 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3242+1999C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895398 | ||||||
| chr16:57895438
|
G | T | 4 | a0001c0001t0003g0208a0001c0001t0005g0277a0001c0001t0013g0206others(1): Show | 4 | NA18944.hp1 NA18962.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.3242+1959C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895438 | ||||||
| chr16:57895540
|
A | C | 2 | a0001c0002t0001g0125a0001c0003t0001g0270 | 2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.3242+1857T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895540 | ||||||
| chr16:57895549
|
T | TTA | 18 | a0001c0015t0020g0336a0001c0028t0044g0064a0001c0097t0003g0231others(15): Show | 18 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.3242+1847_3242+184 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895549 | ||||||
| chr16:57895551
|
T | A | 30 | a0001c0004t0035g0079a0001c0015t0020g0336a0001c0028t0044g0064others(27): Show | 30 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.3242+1846A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895551 | ||||||
| chr16:57895551
|
T | TTA | 18 | a0001c0001t0007g0290a0003c0008t0002g0002a0003c0009t0006g0289others(15): Show | 19 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.3242+1844_3242+184 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895551 | ||||||
| chr16:57895553
|
A | T | 2 | a0001c0015t0001g0335a0001c0028t0042g0069 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3242+1844T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895553 | ||||||
| chr16:57895959
|
A | G | 2 | a0002c0011t0016g0190a0004c0048t0016g0354 | 2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3242+1438T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895959 | ||||||
| chr16:57896041
|
G | A | 27 | a0001c0001t0007g0290a0003c0008t0002g0002a0003c0008t0003g0145others(24): Show | 28 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.3242+1356C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896041 | ||||||
| chr16:57896110
|
A | G | 3 | a0011c0058t0004g0140a0028c0084t0003g0330a0047c0111t0003g0327 | 3 | HG02451.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3242+1287T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896110 | ||||||
| chr16:57896291
|
G | A | 23 | a0001c0007t0004g0046a0001c0007t0008g0356a0001c0013t0004g0308others(20): Show | 23 | HG00738.hp2 HG01070.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.3242+1106C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896291 | ||||||
| chr16:57896429
|
T | C | 1 | a0001c0013t0001g0306 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3242+968A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896429 | ||||||
| chr16:57896485
|
G | T | 1 | a0002c0005t0001g0013 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3242+912C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896485 | ||||||
| chr16:57896497
|
G | A | 3 | a0001c0016t0010g0057a0002c0114t0010g0357a0006c0082t0010g0337 | 3 | HG02109.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3242+900C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896497 | ||||||
| chr16:57896503
|
A | G | 33 | a0001c0007t0002g0073a0001c0007t0003g0189a0001c0015t0001g0335others(30): Show | 33 | HG00438.hp1 HG00741.hp2 HG01515.hp2 others(30): Show |
intron_variant | MODIFIER | c.3242+894T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896503 | ||||||
| chr16:57896574
|
G | A | 2 | a0003c0012t0007g0048a0007c0020t0007g0007 | 2 | HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3242+823C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896574 | ||||||
| chr16:57896593
|
A | G | 1 | a0001c0001t0001g0279 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3242+804T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896593 | ||||||
| chr16:57896621
|
G | A | 31 | a0001c0007t0002g0073a0001c0007t0003g0189a0001c0015t0001g0335others(28): Show | 31 | HG00741.hp2 HG01515.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.3242+776C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896621 | ||||||
| chr16:57896641
|
A | G | 5 | a0004c0049t0015g0344a0017c0060t0015g0005a0026c0080t0015g0188others(2): Show | 5 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.3242+756T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896641 | ||||||
| chr16:57896713
|
A | AAAAT | 61 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0207others(58): Show | 62 | HG00099.hp2 HG00140.hp2 HG01074.hp2 others(59): Show |
intron_variant | MODIFIER | c.3242+680_3242+683d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896713 | ||||||
| chr16:57896713
|
A | AAAATAAA others(1): Show |
3 | a0003c0104t0007g0218a0010c0010t0003g0030a0012c0115t0045g0111 | 3 | HG03017.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3242+676_3242+683d others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896713 | ||||||
| chr16:57896713
|
A | AAAATAAA others(5): Show |
1 | a0001c0007t0003g0004 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3242+672_3242+683d others(14): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896713 | ||||||
| chr16:57896713
|
AAAAT | A | 138 | a0001c0001t0001g0205a0001c0001t0001g0227a0001c0001t0001g0234others(135): Show | 139 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.3242+680_3242+683d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896713 | ||||||
| chr16:57896713
|
AAAATAAA others(1): Show |
A | 19 | a0001c0001t0003g0224a0001c0001t0013g0206a0001c0002t0001g0125others(16): Show | 19 | HG00733.hp1 HG01255.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.3242+676_3242+683d others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896713 | ||||||
| chr16:57896713
|
AAAATAAA others(5): Show |
A | 5 | a0001c0003t0001g0278a0001c0007t0003g0189a0001c0097t0003g0231others(2): Show | 5 | HG00438.hp1 HG02723.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3242+672_3242+683d others(14): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896713 | ||||||
| chr16:57896713
|
AAAATAAA others(13): Show |
A | 1 | a0004c0014t0005g0346 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3242+664_3242+683d others(22): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896713 | ||||||
| chr16:57896713
|
AAAATAAA others(17): Show |
A | 2 | a0017c0062t0027g0324a0048c0117t0026g0186 | 2 | HG00741.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3242+660_3242+683d others(26): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896713 | ||||||
| chr16:57896761
|
T | A | 4 | a0001c0002t0007g0126a0001c0003t0003g0296a0001c0017t0001g0139others(1): Show | 4 | HG00280.hp2 HG01074.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.3242+636A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896761 | ||||||
| chr16:57896778
|
A | G | 1 | a0011c0059t0001g0123 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3242+619T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896778 | ||||||
| chr16:57896993
|
G | A | 1 | a0008c0054t0002g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3242+404C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896993 | ||||||
| chr16:57897032
|
A | T | 31 | a0001c0007t0002g0073a0001c0007t0003g0189a0001c0015t0001g0335others(28): Show | 31 | HG00741.hp2 HG01515.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.3242+365T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57897032 | ||||||
| chr16:57897039
|
C | G | 2 | a0001c0028t0044g0064a0006c0083t0043g0063 | 2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.3242+358G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57897039 | ||||||
| chr16:57897050
|
C | T | 51 | a0001c0004t0035g0079a0001c0007t0002g0073a0001c0007t0003g0189others(48): Show | 51 | HG00438.hp1 HG00741.hp2 HG01515.hp2 others(48): Show |
intron_variant | MODIFIER | c.3242+347G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57897050 | ||||||
| chr16:57897117
|
T | C | 13 | a0001c0001t0012g0212a0001c0002t0001g0052a0001c0002t0002g0157others(10): Show | 13 | HG00140.hp2 HG00733.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.3242+280A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57897117 | ||||||
| chr16:57897145
|
T | A | 6 | a0001c0015t0020g0336a0001c0028t0044g0064a0006c0083t0043g0063others(3): Show | 6 | HG02451.hp1 HG02615.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3242+252A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57897145 | ||||||
| chr16:57897294
|
G | C | 3 | a0001c0013t0018g0294a0002c0011t0018g0341a0002c0022t0018g0112 | 3 | HG02976.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3242+103C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57897294 | ||||||
| chr16:57897301
|
C | CA | 27 | a0001c0004t0003g0151a0001c0007t0002g0073a0001c0015t0001g0335others(24): Show | 27 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.3242+95dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57897301 | ||||||
| chr16:57897301
|
CA | C | 37 | a0001c0001t0007g0290a0001c0002t0003g0008a0001c0016t0010g0057others(34): Show | 38 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.3242+95delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57897301 | ||||||
| chr16:57897329
|
C | G | 50 | a0001c0001t0002g0238a0001c0001t0002g0252a0001c0001t0002g0309others(47): Show | 50 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.3242+68G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57897329 | ||||||
| chr16:57898001
|
C | T | 1 | a0001c0002t0001g0039 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2977-87G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898001 | ||||||
| chr16:57898154
|
A | G | 24 | a0001c0007t0004g0046a0001c0007t0008g0356a0001c0013t0004g0308others(21): Show | 24 | HG00738.hp2 HG01070.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.2977-240T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898154 | ||||||
| chr16:57898383
|
C | T | 1 | a0003c0012t0007g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2977-469G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898383 | ||||||
| chr16:57898384
|
CT | C | 44 | a0001c0007t0002g0073a0001c0013t0018g0294a0001c0015t0001g0335others(41): Show | 44 | HG00438.hp1 HG00741.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.2977-471delA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898384 | ||||||
| chr16:57898504
|
A | G | 5 | a0004c0049t0015g0344a0017c0060t0015g0005a0026c0080t0015g0188others(2): Show | 5 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2977-590T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898504 | ||||||
| chr16:57898521
|
G | A | 2 | a0001c0097t0003g0231a0002c0037t0003g0023 | 2 | HG00438.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2977-607C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898521 | ||||||
| chr16:57898540
|
C | T | 1 | a0002c0005t0001g0098 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2977-626G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898540 | ||||||
| chr16:57898577
|
G | A | 2 | a0024c0047t0034g0350a0040c0063t0020g0009 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2977-663C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898577 | ||||||
| chr16:57898636
|
G | A | 24 | a0001c0007t0002g0073a0001c0015t0001g0335a0001c0015t0020g0336others(21): Show | 24 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.2977-722C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898636 | ||||||
| chr16:57898838
|
G | A | 1 | a0003c0101t0030g0264 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2977-924C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898838 | ||||||
| chr16:57898879
|
C | T | 1 | a0002c0006t0003g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2977-965G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898879 | ||||||
| chr16:57898887
|
C | T | 1 | a0001c0001t0037g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2977-973G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898887 | ||||||
| chr16:57898930
|
A | G | 1 | a0003c0012t0003g0176 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2977-1016T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898930 | ||||||
| chr16:57899049
|
A | C | 1 | a0016c0052t0003g0180 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2977-1135T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899049 | ||||||
| chr16:57899050
|
A | G | 26 | a0001c0007t0002g0073a0001c0015t0001g0335a0001c0015t0020g0336others(23): Show | 26 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.2977-1136T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899050 | ||||||
| chr16:57899162
|
G | A | 8 | a0001c0004t0035g0079a0001c0016t0010g0057a0002c0005t0041g0068others(5): Show | 8 | HG02109.hp2 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2977-1248C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899162 | ||||||
| chr16:57899221
|
A | C | 1 | a0002c0038t0003g0094 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2977-1307T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899221 | ||||||
| chr16:57899232
|
C | T | 5 | a0003c0009t0006g0289a0003c0009t0007g0080a0003c0009t0039g0307others(2): Show | 5 | HG00642.hp2 HG01074.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.2977-1318G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899232 | ||||||
| chr16:57899241
|
A | G | 1 | a0016c0052t0003g0180 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2977-1327T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899241 | ||||||
| chr16:57899282
|
G | C | 2 | a0024c0047t0034g0350a0040c0063t0020g0009 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2977-1368C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899282 | ||||||
| chr16:57899322
|
GAAA | G | 74 | a0001c0001t0007g0290a0001c0001t0012g0212a0001c0003t0012g0266others(71): Show | 75 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.2977-1411_2977-140 others(7): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899322 | ||||||
| chr16:57899330
|
A | T | 262 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(259): Show | 264 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.2977-1416T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899330 | ||||||
| chr16:57899330
|
AAAT | A | 9 | a0001c0007t0002g0073a0001c0015t0001g0335a0001c0028t0042g0069others(6): Show | 9 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2977-1419_2977-141 others(7): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899330 | ||||||
| chr16:57899333
|
T | A | 1 | a0017c0060t0015g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2977-1419A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899333 | ||||||
| chr16:57899351
|
A | G | 1 | a0001c0027t0040g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2977-1437T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899351 | ||||||
| chr16:57899362
|
G | A | 150 | a0001c0001t0001g0195a0001c0001t0001g0205a0001c0001t0001g0236others(147): Show | 151 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.2977-1448C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899362 | ||||||
| chr16:57899497
|
G | A | 3 | a0001c0013t0018g0294a0002c0011t0018g0341a0002c0022t0018g0112 | 3 | HG02976.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2977-1583C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899497 | ||||||
| chr16:57899572
|
G | A | 1 | a0001c0004t0022g0107 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2977-1658C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899572 | ||||||
| chr16:57899588
|
C | T | 3 | a0001c0068t0005g0175a0001c0097t0003g0231a0002c0037t0003g0023 | 3 | HG00438.hp1 HG02080.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.2977-1674G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899588 | ||||||
| chr16:57899612
|
C | G | 2 | a0010c0010t0008g0090a0010c0010t0008g0102 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2977-1698G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899612 | ||||||
| chr16:57899616
|
GGA | G | 8 | a0001c0004t0035g0079a0001c0016t0010g0057a0002c0005t0041g0068others(5): Show | 8 | HG02109.hp2 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2977-1704_2977-170 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899616 | ||||||
| chr16:57899627
|
G | A | 1 | a0002c0006t0003g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2977-1713C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899627 | ||||||
| chr16:57899643
|
T | TAAAC | 32 | a0001c0001t0007g0290a0001c0068t0005g0175a0001c0097t0003g0231others(29): Show | 33 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2976+1705_2976+170 others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899643 | ||||||
| chr16:57899643
|
TAAAC | T | 8 | a0001c0004t0035g0079a0001c0016t0010g0057a0002c0005t0041g0068others(5): Show | 8 | HG02109.hp2 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2976+1705_2976+170 others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899643 | ||||||
| chr16:57899683
|
G | A | 21 | a0001c0007t0002g0073a0001c0015t0001g0335a0001c0028t0042g0069others(18): Show | 21 | HG00741.hp2 HG02055.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.2976+1669C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899683 | ||||||
| chr16:57899722
|
T | C | 1 | a0001c0001t0002g0238 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2976+1630A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899722 | ||||||
| chr16:57899839
|
C | T | 19 | a0001c0001t0001g0262a0001c0001t0001g0279a0001c0001t0003g0224others(16): Show | 19 | HG00544.hp1 HG00609.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.2976+1513G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899839 | ||||||
| chr16:57899867
|
T | C | 34 | a0001c0001t0007g0290a0001c0068t0005g0175a0001c0097t0003g0231others(31): Show | 35 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.2976+1485A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899867 | ||||||
| chr16:57899892
|
C | T | 2 | a0001c0018t0001g0263a0002c0005t0003g0106 | 2 | HG02027.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2976+1460G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899892 | ||||||
| chr16:57899895
|
G | T | 1 | a0001c0001t0006g0226 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2976+1457C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899895 | ||||||
| chr16:57899919
|
G | A | 15 | a0009c0026t0004g0059a0009c0026t0004g0310a0009c0061t0004g0049others(12): Show | 15 | HG01109.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2976+1433C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899919 | ||||||
| chr16:57900043
|
G | A | 1 | a0039c0072t0001g0137 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2976+1309C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57900043 | ||||||
| chr16:57900176
|
C | T | 1 | a0001c0003t0003g0265 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2976+1176G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57900176 | ||||||
| chr16:57900346
|
C | G | 2 | a0018c0102t0003g0271a0022c0050t0003g0352 | 2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2976+1006G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57900346 | ||||||
| chr16:57900499
|
G | A | 1 | a0005c0036t0002g0256 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2976+853C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57900499 | ||||||
| chr16:57900594
|
A | G | 1 | a0001c0042t0011g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2976+758T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57900594 | ||||||
| chr16:57900859
|
G | GA | 11 | a0001c0003t0005g0300a0001c0003t0006g0288a0001c0004t0001g0117others(8): Show | 11 | HG00438.hp1 HG00741.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.2976+492dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57900859 | ||||||
| chr16:57900870
|
A | C | 2 | a0001c0041t0005g0028a0002c0022t0002g0074 | 2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2976+482T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57900870 | ||||||
| chr16:57900921
|
A | C | 6 | a0017c0060t0015g0005a0017c0062t0027g0324a0026c0080t0015g0188others(3): Show | 6 | HG00741.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2976+431T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57900921 | ||||||
| chr16:57901059
|
TG | T | 303 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(300): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.2976+292delC | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57901059 | ||||||
| chr16:57901066
|
G | T | 2 | a0001c0001t0003g0208a0001c0001t0013g0206 | 2 | NA18944.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2976+286C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57901066 | ||||||
| chr16:57901067
|
G | A | 2 | a0001c0003t0001g0202a0001c0004t0001g0173 | 2 | NA18942.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2976+285C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57901067 | ||||||
| chr16:57901181
|
T | C | 315 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(312): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.2976+171A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57901181 | ||||||
| chr16:57901251
|
T | A | 3 | a0001c0042t0011g0029a0018c0102t0003g0271a0022c0050t0003g0352 | 3 | HG02922.hp2 HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2976+101A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57901251 | ||||||
| chr16:57901252
|
C | A | 3 | a0001c0042t0011g0029a0018c0102t0003g0271a0022c0050t0003g0352 | 3 | HG02922.hp2 HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2976+100G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57901252 | ||||||
| chr16:57901307
|
G | A | 1 | a0001c0013t0019g0213 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2976+45C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57901307 | ||||||
| chr16:57901327
|
C | T | 17 | a0009c0026t0004g0059a0009c0026t0004g0310a0009c0061t0004g0049others(14): Show | 17 | HG01109.hp2 HG01515.hp2 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.2976+25G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57901327 | ||||||
| chr16:57901344
|
C | G | 1 | a0001c0003t0002g0201 | 1 | HG00408.hp1 | splice_region_variant&intron_variant | LOW | c.2976+8G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57901344 | ||||||
| chr16:57901462
|
C | A | 1 | a0001c0004t0022g0107 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2893-27G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 28/32 | chr16 | 57901462 | ||||||
| chr16:57901473
|
A | C | 1 | a0001c0002t0022g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2893-38T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 28/32 | chr16 | 57901473 | ||||||
| chr16:57901476
|
T | C | 2 | a0002c0006t0016g0110a0004c0014t0016g0326 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2893-41A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 28/32 | chr16 | 57901476 | ||||||
| chr16:57901479
|
G | T | 1 | a0001c0002t0022g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2893-44C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 28/32 | chr16 | 57901479 | ||||||
| chr16:57901522
|
G | A | 15 | a0009c0026t0004g0059a0009c0026t0004g0310a0009c0061t0004g0049others(12): Show | 15 | HG01109.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.2892+6C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 28/32 | chr16 | 57901522 | ||||||
| chr16:57901662
|
C | T | 1 | a0002c0005t0001g0014 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2795-37G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57901662 | ||||||
| chr16:57901680
|
T | A | 5 | a0001c0004t0035g0079a0002c0005t0041g0068a0002c0006t0013g0083others(2): Show | 5 | HG02886.hp1 HG02965.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.2795-55A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57901680 | ||||||
| chr16:57901722
|
A | G | 1 | a0036c0067t0002g0051 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2795-97T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57901722 | ||||||
| chr16:57901940
|
C | T | 1 | a0002c0006t0008g0084 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2795-315G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57901940 | ||||||
| chr16:57901975
|
T | G | 6 | a0017c0060t0015g0005a0017c0062t0027g0324a0026c0080t0015g0188others(3): Show | 6 | HG00741.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2795-350A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57901975 | ||||||
| chr16:57902066
|
T | TTTG | 15 | a0009c0026t0004g0059a0009c0026t0004g0310a0009c0061t0004g0049others(12): Show | 15 | HG01109.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2795-444_2795-442d others(5): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902066 | ||||||
| chr16:57902066
|
TTTG | T | 4 | a0001c0004t0022g0107a0001c0013t0018g0294a0002c0011t0018g0341others(1): Show | 4 | HG02647.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2795-444_2795-442d others(5): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902066 | ||||||
| chr16:57902186
|
T | C | 5 | a0001c0004t0035g0079a0002c0005t0041g0068a0002c0006t0013g0083others(2): Show | 5 | HG02886.hp1 HG02965.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.2795-561A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902186 | ||||||
| chr16:57902230
|
G | T | 307 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(304): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.2795-605C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902230 | ||||||
| chr16:57902259
|
C | T | 2 | a0018c0102t0003g0271a0022c0050t0003g0352 | 2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2795-634G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902259 | ||||||
| chr16:57902263
|
G | T | 1 | a0001c0003t0032g0109 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2795-638C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902263 | ||||||
| chr16:57902308
|
T | G | 3 | a0023c0043t0011g0351a0038c0056t0011g0047a0050c0121t0011g0315 | 3 | HG02258.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2795-683A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902308 | ||||||
| chr16:57902346
|
C | T | 303 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(300): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.2795-721G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902346 | ||||||
| chr16:57902461
|
G | A | 1 | a0001c0002t0003g0050 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2795-836C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902461 | ||||||
| chr16:57902477
|
T | A | 1 | a0007c0021t0003g0105 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2795-852A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902477 | ||||||
| chr16:57902691
|
C | T | 2 | a0001c0001t0002g0312a0002c0037t0003g0092 | 2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2795-1066G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902691 | ||||||
| chr16:57902712
|
G | A | 12 | a0001c0068t0005g0175a0001c0097t0003g0231a0002c0037t0003g0023others(9): Show | 12 | HG00438.hp1 HG01515.hp2 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.2795-1087C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902712 | ||||||
| chr16:57902714
|
G | A | 12 | a0001c0068t0005g0175a0001c0097t0003g0231a0002c0037t0003g0023others(9): Show | 12 | HG00438.hp1 HG01515.hp2 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.2795-1089C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902714 | ||||||
| chr16:57902888
|
C | A | 11 | a0001c0068t0005g0175a0001c0097t0003g0231a0002c0037t0003g0023others(8): Show | 11 | HG00438.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.2794+934G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902888 | ||||||
| chr16:57902928
|
A | T | 1 | a0001c0001t0012g0212 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2794+894T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902928 | ||||||
| chr16:57902948
|
G | A | 1 | a0001c0042t0011g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2794+874C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902948 | ||||||
| chr16:57902978
|
T | A | 1 | a0001c0070t0007g0134 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2794+844A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902978 | ||||||
| chr16:57902983
|
G | A | 1 | a0001c0002t0001g0162 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2794+839C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902983 | ||||||
| chr16:57902998
|
G | A | 1 | a0002c0006t0003g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2794+824C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902998 | ||||||
| chr16:57903089
|
G | A | 12 | a0001c0068t0005g0175a0001c0097t0003g0231a0002c0037t0003g0023others(9): Show | 12 | HG00438.hp1 HG01123.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.2794+733C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903089 | ||||||
| chr16:57903133
|
G | A | 1 | a0001c0002t0001g0155 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2794+689C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903133 | ||||||
| chr16:57903185
|
C | CT | 14 | a0001c0001t0002g0223a0001c0001t0002g0312a0001c0004t0001g0174others(11): Show | 14 | HG00423.hp1 HG00597.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.2794+636dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903185 | ||||||
| chr16:57903185
|
C | CTT | 14 | a0001c0002t0001g0052a0001c0004t0035g0079a0002c0006t0013g0083others(11): Show | 14 | HG00741.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2794+635_2794+636d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903185 | ||||||
| chr16:57903185
|
C | CTTT | 9 | a0001c0013t0018g0294a0001c0068t0005g0175a0001c0097t0003g0231others(6): Show | 9 | HG00438.hp1 HG02080.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.2794+634_2794+636d others(5): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903185 | ||||||
| chr16:57903187
|
T | C | 1 | a0001c0003t0001g0278 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2794+635A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903187 | ||||||
| chr16:57903246
|
C | T | 8 | a0005c0030t0003g0001a0005c0034t0012g0255a0005c0034t0012g0292others(5): Show | 9 | HG00280.hp2 HG00323.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.2794+576G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903246 | ||||||
| chr16:57903289
|
C | T | 4 | a0001c0068t0005g0175a0001c0097t0003g0231a0002c0037t0003g0023others(1): Show | 4 | HG00438.hp1 HG02080.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.2794+533G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903289 | ||||||
| chr16:57903349
|
A | T | 2 | a0002c0006t0016g0110a0004c0014t0016g0326 | 2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2794+473T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903349 | ||||||
| chr16:57903537
|
C | T | 56 | a0001c0001t0001g0260a0001c0001t0002g0238a0001c0001t0002g0273others(53): Show | 56 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.2794+285G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903537 | ||||||
| chr16:57903551
|
T | C | 4 | a0001c0015t0002g0006a0002c0109t0004g0108a0004c0014t0005g0346others(1): Show | 4 | HG02145.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2794+271A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903551 | ||||||
| chr16:57903589
|
C | G | 2 | a0014c0023t0002g0347a0014c0023t0002g0349 | 2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2794+233G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903589 | ||||||
| chr16:57903705
|
G | A | 1 | a0001c0002t0002g0157 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2794+117C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903705 | ||||||
| chr16:57903711
|
G | A | 2 | a0017c0062t0027g0324a0048c0117t0026g0186 | 2 | HG00741.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2794+111C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903711 | ||||||
| chr16:57903755
|
T | G | 12 | a0001c0003t0001g0228a0001c0004t0035g0079a0001c0017t0001g0114others(9): Show | 12 | HG00438.hp1 HG02080.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.2794+67A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903755 | ||||||
| chr16:57903991
|
G | A | 257 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(254): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.2635-10C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57903991 | ||||||
| chr16:57904035
|
C | T | 5 | a0001c0015t0001g0335a0001c0015t0002g0006a0001c0028t0042g0069others(2): Show | 5 | HG02257.hp2 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2635-54G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904035 | ||||||
| chr16:57904098
|
G | C | 1 | a0001c0004t0001g0117 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2635-117C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904098 | ||||||
| chr16:57904099
|
C | G | 1 | a0001c0004t0001g0117 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2635-118G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904099 | ||||||
| chr16:57904099
|
C | T | 1 | a0001c0004t0001g0115 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2635-118G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904099 | ||||||
| chr16:57904296
|
C | T | 1 | a0012c0115t0045g0111 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2635-315G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904296 | ||||||
| chr16:57904305
|
T | C | 284 | a0001c0001t0001g0003a0001c0001t0001g0205a0001c0001t0001g0207others(281): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.2635-324A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904305 | ||||||
| chr16:57904333
|
A | G | 6 | a0001c0035t0010g0230a0001c0103t0029g0272a0002c0038t0003g0094others(3): Show | 6 | HG00558.hp2 NA18747.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.2635-352T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904333 | ||||||
| chr16:57904360
|
C | T | 1 | a0001c0016t0004g0313 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2634+374G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904360 | ||||||
| chr16:57904361
|
G | A | 2 | a0001c0097t0003g0231a0036c0067t0002g0051 | 2 | HG00438.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2634+373C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904361 | ||||||
| chr16:57904503
|
G | A | 66 | a0001c0001t0001g0207a0001c0001t0001g0261a0001c0001t0001g0275others(63): Show | 66 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.2634+231C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904503 | ||||||
| chr16:57904568
|
C | G | 2 | a0009c0026t0004g0059a0009c0077t0004g0060 | 2 | HG01891.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2634+166G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904568 | ||||||
| chr16:57904577
|
G | A | 1 | a0001c0004t0005g0127 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2634+157C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904577 | ||||||
| chr16:57904600
|
T | C | 2 | a0001c0015t0020g0336a0001c0027t0040g0078 | 2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2634+134A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904600 | ||||||
| chr16:57904724
|
G | C | 1 | a0001c0003t0003g0198 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2634+10C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904724 | ||||||
| chr16:57904729
|
G | A | 1 | a0002c0005t0006g0089 | 1 | HG02074.hp2 | splice_region_variant&intron_variant | LOW | c.2634+5C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904729 | ||||||
| chr16:57905094
|
G | A | 2 | a0001c0002t0001g0125a0001c0066t0001g0130 | 2 | HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2493-219C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905094 | ||||||
| chr16:57905270
|
G | A | 1 | a0001c0002t0001g0125 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2493-395C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905270 | ||||||
| chr16:57905305
|
G | A | 3 | a0001c0001t0001g0234a0002c0005t0001g0015a0002c0005t0001g0016 | 3 | HG00639.hp2 HG01261.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2493-430C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905305 | ||||||
| chr16:57905361
|
GA | G | 37 | a0001c0001t0001g0243a0001c0001t0037g0246a0001c0002t0001g0052others(34): Show | 37 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.2493-487delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905361 | ||||||
| chr16:57905394
|
C | T | 41 | a0001c0001t0001g0207a0001c0001t0001g0279a0001c0001t0001g0280others(38): Show | 41 | HG00099.hp2 HG00408.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.2493-519G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905394 | ||||||
| chr16:57905400
|
C | T | 6 | a0001c0015t0001g0335a0001c0016t0046g0054a0002c0109t0004g0108others(3): Show | 6 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2493-525G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905400 | ||||||
| chr16:57905434
|
G | A | 1 | a0003c0101t0030g0264 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2493-559C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905434 | ||||||
| chr16:57905484
|
G | A | 4 | a0004c0046t0036g0348a0010c0010t0003g0325a0010c0010t0003g0328others(1): Show | 4 | HG02717.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2493-609C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905484 | ||||||
| chr16:57905644
|
C | T | 1 | a0001c0018t0001g0263 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2493-769G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905644 | ||||||
| chr16:57905645
|
G | A | 1 | a0001c0002t0001g0039 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2493-770C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905645 | ||||||
| chr16:57905680
|
G | T | 1 | a0018c0055t0025g0042 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2493-805C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905680 | ||||||
| chr16:57905829
|
C | T | 39 | a0001c0002t0002g0161a0001c0002t0002g0183a0001c0002t0005g0184others(36): Show | 39 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.2493-954G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905829 | ||||||
| chr16:57905845
|
C | G | 10 | a0001c0004t0001g0164a0001c0017t0001g0114a0001c0017t0001g0139others(7): Show | 10 | HG01934.hp1 HG02027.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.2493-970G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905845 | ||||||
| chr16:57905998
|
G | A | 1 | a0001c0004t0001g0165 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2493-1123C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905998 | ||||||
| chr16:57906000
|
C | T | 1 | a0011c0033t0001g0249 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2493-1125G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906000 | ||||||
| chr16:57906066
|
C | G | 159 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.2493-1191G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906066 | ||||||
| chr16:57906184
|
G | A | 3 | a0002c0006t0021g0187a0002c0109t0004g0108a0002c0114t0010g0357 | 3 | HG02109.hp2 HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2493-1309C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906184 | ||||||
| chr16:57906213
|
C | T | 1 | a0004c0014t0005g0346 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2493-1338G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906213 | ||||||
| chr16:57906215
|
C | T | 3 | a0001c0002t0003g0038a0001c0002t0003g0050a0001c0003t0003g0222 | 3 | HG00099.hp1 HG01516.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2493-1340G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906215 | ||||||
| chr16:57906264
|
T | C | 1 | a0001c0053t0004g0200 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2493-1389A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906264 | ||||||
| chr16:57906277
|
A | C | 1 | a0001c0053t0004g0200 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2493-1402T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906277 | ||||||
| chr16:57906284
|
A | G | 45 | a0001c0001t0001g0207a0001c0001t0001g0279a0001c0001t0001g0280others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.2493-1409T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906284 | ||||||
| chr16:57906317
|
G | A | 24 | a0001c0002t0002g0183a0001c0002t0005g0184a0001c0013t0019g0213others(21): Show | 24 | HG00280.hp1 HG00639.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.2493-1442C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906317 | ||||||
| chr16:57906323
|
G | A | 1 | a0001c0002t0001g0329 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2493-1448C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906323 | ||||||
| chr16:57906381
|
C | T | 32 | a0001c0002t0001g0056a0001c0002t0003g0008a0001c0004t0022g0107others(29): Show | 32 | HG01123.hp2 HG01884.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.2493-1506G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906381 | ||||||
| chr16:57906440
|
G | A | 7 | a0001c0017t0001g0114a0001c0017t0001g0139a0001c0018t0001g0263others(4): Show | 7 | HG01934.hp1 HG01978.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.2493-1565C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906440 | ||||||
| chr16:57906442
|
C | T | 2 | a0003c0104t0007g0218a0036c0067t0002g0051 | 2 | HG03017.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2493-1567G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906442 | ||||||
| chr16:57906443
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2493-1568C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906443 | ||||||
| chr16:57906449
|
T | C | 2 | a0002c0006t0021g0187a0002c0114t0010g0357 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2493-1574A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906449 | ||||||
| chr16:57907059
|
C | T | 1 | a0018c0102t0003g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2493-2184G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907059 | ||||||
| chr16:57907123
|
G | A | 257 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(254): Show | 260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.2493-2248C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907123 | ||||||
| chr16:57907148
|
C | T | 1 | a0001c0002t0001g0125 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2493-2273G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907148 | ||||||
| chr16:57907166
|
G | A | 19 | a0001c0001t0001g0207a0001c0001t0002g0250a0001c0001t0003g0208others(16): Show | 19 | HG00099.hp2 HG00738.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.2493-2291C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907166 | ||||||
| chr16:57907190
|
T | C | 219 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(216): Show | 222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.2493-2315A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907190 | ||||||
| chr16:57907197
|
C | A | 1 | a0018c0055t0025g0042 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2493-2322G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907197 | ||||||
| chr16:57907264
|
C | T | 2 | a0001c0016t0004g0313a0001c0016t0010g0057 | 2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2493-2389G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907264 | ||||||
| chr16:57907373
|
A | T | 1 | a0005c0036t0001g0355 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2493-2498T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907373 | ||||||
| chr16:57907390
|
T | TG | 29 | a0001c0042t0011g0029a0008c0025t0001g0122a0008c0025t0023g0077others(26): Show | 29 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.2493-2516dupC | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907390 | ||||||
| chr16:57907433
|
T | A | 1 | a0001c0003t0003g0222 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2493-2558A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907433 | ||||||
| chr16:57907434
|
A | T | 1 | a0001c0003t0003g0222 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2493-2559T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907434 | ||||||
| chr16:57907493
|
C | T | 127 | a0001c0001t0001g0233a0001c0002t0001g0032a0001c0002t0001g0035others(124): Show | 127 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.2493-2618G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907493 | ||||||
| chr16:57907524
|
T | A | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2493-2649A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907524 | ||||||
| chr16:57908034
|
G | A | 2 | a0002c0005t0001g0024a0002c0011t0018g0341 | 2 | HG02132.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2493-3159C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908034 | ||||||
| chr16:57908068
|
TTTTGTAG others(4): Show |
T | 7 | a0001c0002t0003g0008a0001c0028t0044g0064a0009c0061t0004g0049others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2493-3204_2493-319 others(15): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908068 | ||||||
| chr16:57908088
|
C | G | 220 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(217): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2493-3213G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908088 | ||||||
| chr16:57908089
|
C | T | 1 | a0040c0063t0020g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2493-3214G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908089 | ||||||
| chr16:57908090
|
C | T | 1 | a0009c0026t0004g0310 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2493-3215G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908090 | ||||||
| chr16:57908211
|
G | A | 1 | a0001c0003t0005g0240 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2493-3336C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908211 | ||||||
| chr16:57908228
|
C | A | 37 | a0001c0002t0022g0062a0001c0015t0002g0006a0001c0027t0003g0058others(34): Show | 37 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.2493-3353G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908228 | ||||||
| chr16:57908329
|
C | T | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2492+3424G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908329 | ||||||
| chr16:57908505
|
A | G | 5 | a0001c0007t0003g0004a0001c0007t0004g0046a0001c0028t0042g0069others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2492+3248T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908505 | ||||||
| chr16:57908573
|
T | C | 220 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(217): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2492+3180A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908573 | ||||||
| chr16:57908695
|
C | T | 212 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(209): Show | 215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.2492+3058G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908695 | ||||||
| chr16:57908721
|
G | A | 4 | a0001c0002t0022g0062a0003c0012t0007g0048a0012c0119t0023g0091others(1): Show | 4 | HG02280.hp1 HG02630.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2492+3032C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908721 | ||||||
| chr16:57908808
|
G | A | 165 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(162): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.2492+2945C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908808 | ||||||
| chr16:57908833
|
G | A | 6 | a0001c0002t0003g0008a0001c0028t0044g0064a0009c0061t0004g0049others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2492+2920C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908833 | ||||||
| chr16:57908886
|
A | C | 1 | a0001c0002t0022g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2492+2867T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908886 | ||||||
| chr16:57908962
|
C | A | 220 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(217): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2492+2791G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908962 | ||||||
| chr16:57909001
|
T | C | 220 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(217): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2492+2752A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909001 | ||||||
| chr16:57909002
|
G | A | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2492+2751C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909002 | ||||||
| chr16:57909126
|
G | A | 1 | a0043c0076t0003g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2492+2627C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909126 | ||||||
| chr16:57909212
|
G | A | 4 | a0002c0005t0005g0322a0003c0008t0003g0145a0003c0008t0009g0146others(1): Show | 4 | HG00558.hp1 NA18980.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.2492+2541C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909212 | ||||||
| chr16:57909216
|
T | C | 220 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(217): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2492+2537A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909216 | ||||||
| chr16:57909244
|
A | G | 220 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(217): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2492+2509T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909244 | ||||||
| chr16:57909372
|
TTAAG | T | 14 | a0001c0007t0003g0004a0001c0007t0004g0046a0001c0016t0046g0054others(11): Show | 14 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2492+2377_2492+238 others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909372 | ||||||
| chr16:57909403
|
CT | C | 11 | a0001c0002t0001g0035a0001c0002t0002g0036a0001c0002t0003g0031others(8): Show | 11 | HG00438.hp1 HG00544.hp1 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.2492+2349delA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909403 | ||||||
| chr16:57909413
|
C | T | 220 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(217): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2492+2340G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909413 | ||||||
| chr16:57909462
|
T | C | 16 | a0001c0001t0001g0207a0001c0001t0001g0279a0001c0001t0001g0280others(13): Show | 16 | HG00099.hp2 HG00609.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.2492+2291A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909462 | ||||||
| chr16:57909478
|
C | T | 2 | a0006c0083t0043g0063a0006c0085t0024g0209 | 2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2492+2275G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909478 | ||||||
| chr16:57909491
|
T | C | 1 | a0043c0076t0003g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2492+2262A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909491 | ||||||
| chr16:57909494
|
T | C | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2492+2259A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909494 | ||||||
| chr16:57909576
|
A | G | 6 | a0001c0016t0046g0054a0002c0109t0004g0108a0004c0014t0005g0346others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2492+2177T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909576 | ||||||
| chr16:57909586
|
G | A | 6 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0002g0273others(3): Show | 6 | NA18947.hp1 NA18948.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.2492+2167C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909586 | ||||||
| chr16:57909614
|
C | A | 1 | a0043c0076t0003g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2492+2139G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909614 | ||||||
| chr16:57909624
|
T | A | 220 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(217): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2492+2129A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909624 | ||||||
| chr16:57909760
|
C | T | 6 | a0001c0002t0003g0008a0001c0028t0044g0064a0009c0061t0004g0049others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2492+1993G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909760 | ||||||
| chr16:57909772
|
T | C | 1 | a0001c0003t0012g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2492+1981A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909772 | ||||||
| chr16:57909803
|
C | T | 220 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(217): Show | 223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2492+1950G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909803 | ||||||
| chr16:57909834
|
C | A | 1 | a0001c0001t0002g0223 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2492+1919G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909834 | ||||||
| chr16:57909923
|
G | A | 205 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(202): Show | 208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.2492+1830C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909923 | ||||||
| chr16:57909942
|
G | A | 1 | a0002c0006t0021g0187 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2492+1811C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909942 | ||||||
| chr16:57910038
|
C | T | 219 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(216): Show | 222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.2492+1715G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910038 | ||||||
| chr16:57910252
|
G | A | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2492+1501C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910252 | ||||||
| chr16:57910313
|
C | T | 219 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(216): Show | 222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.2492+1440G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910313 | ||||||
| chr16:57910318
|
A | C | 188 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(185): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.2492+1435T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910318 | ||||||
| chr16:57910411
|
A | G | 228 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(225): Show | 231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.2492+1342T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910411 | ||||||
| chr16:57910462
|
C | T | 188 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(185): Show | 191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.2492+1291G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910462 | ||||||
| chr16:57910519
|
C | T | 8 | a0001c0001t0001g0234a0001c0001t0007g0290a0001c0001t0013g0251others(5): Show | 8 | HG00639.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2492+1234G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910519 | ||||||
| chr16:57910555
|
T | G | 216 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(213): Show | 219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.2492+1198A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910555 | ||||||
| chr16:57910561
|
A | G | 1 | a0002c0022t0018g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2492+1192T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910561 | ||||||
| chr16:57910571
|
G | A | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2492+1182C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910571 | ||||||
| chr16:57910601
|
T | G | 2 | a0008c0032t0002g0269a0013c0091t0007g0268 | 2 | HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2492+1152A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910601 | ||||||
| chr16:57910644
|
G | A | 1 | a0001c0004t0001g0138 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2492+1109C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910644 | ||||||
| chr16:57910667
|
C | T | 35 | a0001c0002t0022g0062a0001c0042t0011g0029a0003c0012t0007g0048others(32): Show | 35 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.2492+1086G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910667 | ||||||
| chr16:57910672
|
C | A | 1 | a0002c0114t0010g0357 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2492+1081G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910672 | ||||||
| chr16:57910673
|
C | CT | 164 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(161): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.2492+1079dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910673 | ||||||
| chr16:57910673
|
C | CTT | 13 | a0001c0001t0001g0207a0001c0001t0001g0279a0001c0004t0001g0150others(10): Show | 13 | HG00609.hp1 HG01175.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.2492+1078_2492+107 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910673 | ||||||
| chr16:57910673
|
C | CTTT | 6 | a0001c0016t0046g0054a0002c0109t0004g0108a0004c0014t0005g0346others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2492+1077_2492+107 others(7): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910673 | ||||||
| chr16:57910673
|
C | T | 1 | a0002c0006t0021g0187 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2492+1080G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910673 | ||||||
| chr16:57910673
|
CTTTT | C | 30 | a0001c0042t0011g0029a0008c0025t0001g0122a0008c0025t0023g0077others(27): Show | 30 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.2492+1076_2492+107 others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910673 | ||||||
| chr16:57910695
|
T | C | 31 | a0001c0042t0011g0029a0008c0025t0001g0122a0008c0025t0023g0077others(28): Show | 31 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2492+1058A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910695 | ||||||
| chr16:57910707
|
A | AT | 31 | a0001c0042t0011g0029a0008c0025t0001g0122a0008c0025t0023g0077others(28): Show | 31 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2492+1045dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910707 | ||||||
| chr16:57910709
|
T | G | 1 | a0021c0039t0002g0086 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2492+1044A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910709 | ||||||
| chr16:57910752
|
A | T | 2 | a0002c0006t0021g0187a0002c0114t0010g0357 | 2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2492+1001T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910752 | ||||||
| chr16:57910794
|
T | A | 31 | a0001c0042t0011g0029a0008c0025t0001g0122a0008c0025t0023g0077others(28): Show | 31 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2492+959A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910794 | ||||||
| chr16:57910860
|
A | G | 31 | a0001c0042t0011g0029a0008c0025t0001g0122a0008c0025t0023g0077others(28): Show | 31 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2492+893T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910860 | ||||||
| chr16:57911119
|
A | G | 207 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(204): Show | 210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.2492+634T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911119 | ||||||
| chr16:57911131
|
G | A | 9 | a0001c0017t0001g0114a0001c0017t0001g0139a0001c0017t0017g0033others(6): Show | 9 | HG01934.hp1 HG01978.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.2492+622C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911131 | ||||||
| chr16:57911177
|
G | C | 206 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(203): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.2492+576C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911177 | ||||||
| chr16:57911186
|
C | A | 1 | a0001c0003t0001g0278 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2492+567G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911186 | ||||||
| chr16:57911226
|
C | T | 27 | a0001c0002t0001g0056a0001c0004t0022g0107a0001c0015t0001g0335others(24): Show | 27 | HG01123.hp2 HG02055.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.2492+527G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911226 | ||||||
| chr16:57911251
|
G | A | 1 | a0001c0007t0008g0356 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2492+502C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911251 | ||||||
| chr16:57911275
|
A | G | 206 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(203): Show | 209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.2492+478T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911275 | ||||||
| chr16:57911287
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2492+466G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911287 | ||||||
| chr16:57911311
|
A | G | 236 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(233): Show | 239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.2492+442T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911311 | ||||||
| chr16:57911364
|
T | C | 236 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(233): Show | 239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.2492+389A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911364 | ||||||
| chr16:57911374
|
C | T | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2492+379G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911374 | ||||||
| chr16:57911433
|
T | C | 236 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(233): Show | 239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.2492+320A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911433 | ||||||
| chr16:57911455
|
A | G | 1 | a0001c0003t0001g0199 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2492+298T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911455 | ||||||
| chr16:57911456
|
G | GTTTTTTT others(184): Show |
1 | a0001c0001t0001g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2492+296_2492+297i others(193): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911456 | ||||||
| chr16:57911477
|
T | C | 1 | a0001c0001t0001g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2492+276A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911477 | ||||||
| chr16:57911494
|
G | A | 1 | a0001c0001t0001g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2492+259C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911494 | ||||||
| chr16:57911509
|
T | G | 1 | a0001c0001t0001g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2492+244A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911509 | ||||||
| chr16:57911634
|
G | A | 2 | a0001c0003t0002g0196a0001c0003t0002g0229 | 2 | NA18939.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.2492+119C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911634 | ||||||
| chr16:57911692
|
C | T | 1 | a0001c0004t0002g0116 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2492+61G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911692 | ||||||
| chr16:57911734
|
G | C | 1 | a0001c0003t0002g0244 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2492+19C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911734 | ||||||
| chr16:57911909
|
C | T | 1 | a0006c0083t0043g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2370-34G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57911909 | ||||||
| chr16:57911973
|
G | A | 2 | a0001c0004t0001g0165a0002c0005t0001g0026 | 2 | NA18974.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2370-98C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57911973 | ||||||
| chr16:57912029
|
G | A | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2370-154C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912029 | ||||||
| chr16:57912056
|
A | C | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2370-181T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912056 | ||||||
| chr16:57912110
|
ATG | A | 50 | a0001c0002t0001g0056a0001c0002t0003g0008a0001c0004t0022g0107others(47): Show | 50 | HG01123.hp2 HG01884.hp2 HG01934.hp1 others(47): Show |
intron_variant | MODIFIER | c.2370-237_2370-236d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912110 | ||||||
| chr16:57912174
|
G | A | 49 | a0001c0002t0001g0056a0001c0002t0003g0008a0001c0004t0022g0107others(46): Show | 49 | HG01123.hp2 HG01884.hp2 HG01934.hp1 others(46): Show |
intron_variant | MODIFIER | c.2370-299C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912174 | ||||||
| chr16:57912410
|
A | G | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2369+520T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912410 | ||||||
| chr16:57912478
|
C | T | 6 | a0001c0002t0003g0008a0001c0028t0044g0064a0009c0061t0004g0049others(3): Show | 6 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2369+452G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912478 | ||||||
| chr16:57912493
|
C | T | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2369+437G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912493 | ||||||
| chr16:57912571
|
G | GTT | 4 | a0002c0109t0004g0108a0002c0113t0003g0318a0006c0081t0021g0331others(1): Show | 4 | HG02630.hp1 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2369+357_2369+358d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912571 | ||||||
| chr16:57912572
|
T | TTG | 10 | a0002c0005t0001g0314a0002c0005t0001g0316a0002c0006t0001g0071others(7): Show | 10 | HG00642.hp1 HG01109.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2369+356_2369+357d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912572 | ||||||
| chr16:57912572
|
TTGTGTGT others(3): Show |
T | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2369+348_2369+357d others(12): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912572 | ||||||
| chr16:57912574
|
G | T | 46 | a0001c0002t0001g0056a0001c0002t0003g0008a0001c0004t0022g0107others(43): Show | 46 | HG01123.hp2 HG01884.hp2 HG01934.hp1 others(43): Show |
intron_variant | MODIFIER | c.2369+356C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912574 | ||||||
| chr16:57912584
|
G | T | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2369+346C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912584 | ||||||
| chr16:57912657
|
T | C | 6 | a0001c0003t0005g0300a0001c0004t0001g0174a0001c0004t0003g0037others(3): Show | 6 | HG02056.hp2 HG02071.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.2369+273A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912657 | ||||||
| chr16:57912677
|
G | C | 2 | a0001c0001t0012g0212a0002c0022t0008g0011 | 2 | HG00140.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2369+253C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912677 | ||||||
| chr16:57912680
|
T | G | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2369+250A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912680 | ||||||
| chr16:57912715
|
G | A | 1 | a0001c0001t0001g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2369+215C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912715 | ||||||
| chr16:57913033
|
A | T | 60 | a0001c0002t0001g0056a0001c0002t0003g0008a0001c0002t0022g0062others(57): Show | 60 | HG01123.hp2 HG01884.hp2 HG01934.hp1 others(57): Show |
intron_variant | MODIFIER | c.2305-39T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913033 | ||||||
| chr16:57913055
|
G | A | 1 | a0001c0096t0002g0293 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2305-61C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913055 | ||||||
| chr16:57913068
|
G | A | 8 | a0001c0002t0001g0162a0001c0002t0005g0160a0001c0003t0001g0197others(5): Show | 8 | NA18942.hp2 NA18957.hp2 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.2305-74C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913068 | ||||||
| chr16:57913069
|
A | G | 237 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(234): Show | 240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.2305-75T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913069 | ||||||
| chr16:57913110
|
C | T | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2305-116G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913110 | ||||||
| chr16:57913276
|
T | C | 61 | a0001c0002t0001g0056a0001c0002t0003g0008a0001c0002t0022g0062others(58): Show | 61 | HG01123.hp2 HG01884.hp2 HG01934.hp1 others(58): Show |
intron_variant | MODIFIER | c.2305-282A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913276 | ||||||
| chr16:57913402
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2305-408C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913402 | ||||||
| chr16:57913474
|
T | A | 60 | a0001c0002t0001g0056a0001c0002t0003g0008a0001c0002t0022g0062others(57): Show | 60 | HG01123.hp2 HG01884.hp2 HG01934.hp1 others(57): Show |
intron_variant | MODIFIER | c.2305-480A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913474 | ||||||
| chr16:57913619
|
T | G | 49 | a0001c0002t0003g0008a0001c0002t0022g0062a0001c0004t0022g0107others(46): Show | 49 | HG01123.hp2 HG01884.hp2 HG02055.hp1 others(46): Show |
intron_variant | MODIFIER | c.2305-625A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913619 | ||||||
| chr16:57913640
|
A | T | 59 | a0001c0002t0003g0008a0001c0002t0022g0062a0001c0004t0022g0107others(56): Show | 59 | HG01123.hp2 HG01884.hp2 HG01934.hp1 others(56): Show |
intron_variant | MODIFIER | c.2305-646T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913640 | ||||||
| chr16:57913828
|
G | A | 1 | a0005c0030t0003g0001 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2305-834C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913828 | ||||||
| chr16:57913853
|
A | G | 1 | a0001c0003t0002g0191 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2305-859T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913853 | ||||||
| chr16:57914012
|
T | C | 177 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(174): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.2305-1018A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914012 | ||||||
| chr16:57914070
|
G | A | 177 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(174): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.2305-1076C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914070 | ||||||
| chr16:57914146
|
A | G | 177 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(174): Show | 180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.2304+1103T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914146 | ||||||
| chr16:57914154
|
C | T | 1 | a0034c0095t0001g0193 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2304+1095G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914154 | ||||||
| chr16:57914332
|
T | C | 11 | a0001c0002t0003g0008a0001c0007t0003g0004a0001c0007t0004g0046others(8): Show | 11 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2304+917A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914332 | ||||||
| chr16:57914409
|
G | A | 14 | a0001c0002t0003g0008a0001c0007t0003g0004a0001c0007t0004g0046others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.2304+840C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914409 | ||||||
| chr16:57914467
|
C | T | 1 | a0001c0013t0001g0306 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2304+782G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914467 | ||||||
| chr16:57914519
|
C | T | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2304+730G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914519 | ||||||
| chr16:57914639
|
G | T | 47 | a0001c0002t0003g0008a0001c0004t0022g0107a0001c0007t0003g0004others(44): Show | 47 | HG01123.hp2 HG01884.hp2 HG01934.hp1 others(44): Show |
intron_variant | MODIFIER | c.2304+610C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914639 | ||||||
| chr16:57914708
|
A | G | 1 | a0002c0006t0008g0084 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2304+541T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914708 | ||||||
| chr16:57914917
|
A | C | 1 | a0017c0060t0015g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2304+332T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914917 | ||||||
| chr16:57914933
|
T | TG | 178 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(175): Show | 181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.2304+315dupC | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914933 | ||||||
| chr16:57914939
|
G | A | 178 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(175): Show | 181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.2304+310C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914939 | ||||||
| chr16:57915169
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2304+80C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57915169 | ||||||
| chr16:57915347
|
G | A | 182 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(179): Show | 185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2218-12C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915347 | ||||||
| chr16:57915370
|
G | A | 1 | a0021c0039t0002g0305 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2218-35C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915370 | ||||||
| chr16:57915456
|
G | A | 2 | a0003c0009t0009g0287a0052c0106t0002g0075 | 2 | NA19005.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2218-121C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915456 | ||||||
| chr16:57915487
|
C | T | 4 | a0001c0015t0002g0006a0001c0027t0003g0058a0004c0014t0001g0345others(1): Show | 4 | HG02965.hp2 HG03579.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2218-152G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915487 | ||||||
| chr16:57915552
|
A | G | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2218-217T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915552 | ||||||
| chr16:57915724
|
C | T | 3 | a0001c0053t0004g0200a0002c0109t0004g0108a0027c0078t0011g0353 | 3 | HG02723.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2218-389G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915724 | ||||||
| chr16:57915730
|
C | G | 1 | a0001c0041t0005g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2218-395G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915730 | ||||||
| chr16:57915770
|
A | G | 1 | a0001c0001t0003g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2217+359T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915770 | ||||||
| chr16:57915779
|
A | G | 276 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(273): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.2217+350T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915779 | ||||||
| chr16:57915897
|
C | CA | 79 | a0001c0001t0001g0003a0001c0002t0001g0035a0001c0002t0001g0039others(76): Show | 80 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.2217+231dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915897 | ||||||
| chr16:57915897
|
C | CAA | 32 | a0001c0007t0003g0004a0001c0007t0004g0046a0001c0015t0002g0006others(29): Show | 32 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.2217+230_2217+231d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915897 | ||||||
| chr16:57915909
|
A | AG | 5 | a0001c0002t0003g0008a0001c0028t0044g0064a0009c0061t0004g0049others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2217+219_2217+220i others(3): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915909 | ||||||
| chr16:57916000
|
C | T | 9 | a0002c0005t0001g0314a0002c0005t0001g0316a0012c0120t0003g0065others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2217+129G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57916000 | ||||||
| chr16:57916039
|
A | G | 2 | a0008c0032t0006g0221a0030c0092t0001g0285 | 2 | HG00280.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2217+90T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57916039 | ||||||
| chr16:57916101
|
C | T | 1 | a0001c0007t0003g0340 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2217+28G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57916101 | ||||||
| chr16:57916118
|
C | T | 1 | a0011c0033t0001g0267 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2217+11G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57916118 | ||||||
| chr16:57916220
|
C | T | 1 | a0006c0086t0003g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2167-41G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57916220 | ||||||
| chr16:57916274
|
G | C | 275 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(272): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.2167-95C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57916274 | ||||||
| chr16:57916366
|
C | T | 126 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(123): Show | 126 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2167-187G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57916366 | ||||||
| chr16:57916590
|
C | T | 5 | a0004c0045t0003g0342a0004c0046t0036g0348a0015c0031t0004g0333others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2167-411G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57916590 | ||||||
| chr16:57916732
|
G | A | 1 | a0002c0005t0001g0024 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2166+536C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57916732 | ||||||
| chr16:57916748
|
G | A | 1 | a0001c0013t0001g0306 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2166+520C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57916748 | ||||||
| chr16:57916855
|
C | T | 101 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(98): Show | 101 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.2166+413G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57916855 | ||||||
| chr16:57916884
|
G | T | 1 | a0001c0002t0002g0159 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2166+384C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57916884 | ||||||
| chr16:57917081
|
G | A | 100 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(97): Show | 100 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.2166+187C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57917081 | ||||||
| chr16:57917202
|
T | C | 4 | a0001c0003t0001g0253a0001c0013t0004g0308a0003c0009t0007g0080others(1): Show | 4 | HG00642.hp2 HG01358.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.2166+66A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57917202 | ||||||
| chr16:57917212
|
G | T | 1 | a0002c0006t0021g0187 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2166+56C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57917212 | ||||||
| chr16:57917490
|
T | G | 101 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(98): Show | 101 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1958-14A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917490 | ||||||
| chr16:57917514
|
C | T | 13 | a0001c0002t0003g0008a0001c0028t0044g0064a0002c0005t0001g0314others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1958-38G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917514 | ||||||
| chr16:57917517
|
G | A | 135 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(132): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1958-41C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917517 | ||||||
| chr16:57917597
|
A | AGT | 144 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1958-123_1958-122d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917597 | ||||||
| chr16:57917604
|
G | GTGTA | 4 | a0001c0001t0005g0277a0002c0005t0001g0314a0002c0005t0001g0316others(1): Show | 4 | HG02109.hp1 HG02809.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1958-129_1958-128i others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917604 | ||||||
| chr16:57917606
|
A | G | 109 | a0001c0001t0005g0277a0001c0002t0001g0035a0001c0002t0001g0039others(106): Show | 109 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1958-130T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917606 | ||||||
| chr16:57917608
|
G | A | 103 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(100): Show | 103 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1958-132C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917608 | ||||||
| chr16:57917620
|
G | A | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1958-144C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917620 | ||||||
| chr16:57917620
|
G | GTGTA | 9 | a0001c0002t0003g0008a0001c0028t0044g0064a0009c0061t0004g0049others(6): Show | 9 | HG01109.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1958-145_1958-144i others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917620 | ||||||
| chr16:57917620
|
GTA | G | 3 | a0001c0053t0004g0200a0002c0109t0004g0108a0027c0078t0011g0353 | 3 | HG02723.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1958-146_1958-145d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917620 | ||||||
| chr16:57917622
|
A | G | 4 | a0001c0007t0003g0004a0001c0028t0042g0069a0002c0011t0004g0185others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1958-146T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917622 | ||||||
| chr16:57917627
|
T | C | 10 | a0001c0002t0003g0008a0001c0028t0044g0064a0002c0006t0021g0187others(7): Show | 10 | HG01109.hp2 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1958-151A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917627 | ||||||
| chr16:57917627
|
T | TACAC | 4 | a0002c0005t0001g0314a0002c0005t0001g0316a0033c0065t0015g0043others(1): Show | 4 | HG01884.hp1 HG02109.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1958-155_1958-152d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917627 | ||||||
| chr16:57917627
|
TAC | T | 68 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(65): Show | 68 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1958-153_1958-152d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917627 | ||||||
| chr16:57917627
|
TACAC | T | 21 | a0001c0001t0002g0252a0001c0001t0037g0246a0001c0004t0001g0117others(18): Show | 21 | HG00280.hp1 HG00735.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1958-155_1958-152d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917627 | ||||||
| chr16:57917627
|
TACACACA others(3): Show |
T | 5 | a0004c0045t0003g0342a0004c0046t0036g0348a0015c0031t0004g0333others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1958-161_1958-152d others(12): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917627 | ||||||
| chr16:57917629
|
C | T | 14 | a0001c0003t0005g0300a0001c0007t0003g0004a0001c0017t0001g0114others(11): Show | 14 | HG01934.hp1 HG02055.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1958-153G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917629 | ||||||
| chr16:57917631
|
C | T | 36 | a0001c0003t0005g0300a0001c0007t0003g0004a0001c0015t0001g0335others(33): Show | 36 | HG01123.hp2 HG01891.hp1 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.1958-155G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917631 | ||||||
| chr16:57917633
|
C | T | 18 | a0008c0025t0001g0122a0008c0025t0023g0077a0008c0032t0002g0269others(15): Show | 18 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1958-157G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917633 | ||||||
| chr16:57917635
|
C | T | 18 | a0008c0025t0001g0122a0008c0025t0023g0077a0008c0032t0002g0269others(15): Show | 18 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1958-159G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917635 | ||||||
| chr16:57917639
|
C | T | 5 | a0004c0045t0003g0342a0004c0046t0036g0348a0015c0031t0004g0333others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1958-163G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917639 | ||||||
| chr16:57917742
|
G | T | 2 | a0006c0083t0043g0063a0006c0085t0024g0209 | 2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1958-266C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917742 | ||||||
| chr16:57917801
|
TA | T | 154 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(151): Show | 157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1958-326delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917801 | ||||||
| chr16:57917955
|
A | G | 2 | a0020c0118t0001g0302a0045c0079t0006g0194 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1958-479T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917955 | ||||||
| chr16:57918038
|
C | CATGG | 29 | a0001c0001t0001g0003a0001c0002t0001g0056a0001c0002t0003g0008others(26): Show | 30 | HG00280.hp1 HG00639.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1958-566_1958-563d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918038 | ||||||
| chr16:57918038
|
C | CATGGATG others(1): Show |
6 | a0008c0054t0002g0044a0010c0010t0008g0090a0010c0010t0008g0102others(3): Show | 6 | HG01515.hp2 HG01517.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1958-570_1958-563d others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918038 | ||||||
| chr16:57918038
|
CATGG | C | 40 | a0001c0002t0003g0038a0001c0002t0003g0050a0001c0002t0003g0113others(37): Show | 40 | HG00099.hp1 HG00597.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.1958-566_1958-563d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918038 | ||||||
| chr16:57918038
|
CATGGATG others(5): Show |
C | 1 | a0001c0096t0002g0293 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1958-574_1958-563d others(14): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918038 | ||||||
| chr16:57918038
|
CATGGATG others(9): Show |
C | 1 | a0001c0003t0003g0198 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1958-578_1958-563d others(18): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918038 | ||||||
| chr16:57918108
|
G | GTTAT | 226 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(223): Show | 229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1958-636_1958-633d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918108 | ||||||
| chr16:57918108
|
G | GTTATTTA others(1): Show |
5 | a0001c0001t0005g0277a0002c0005t0001g0101a0002c0005t0009g0104others(2): Show | 5 | HG01884.hp2 HG02735.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.1958-640_1958-633d others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918108 | ||||||
| chr16:57918108
|
GTTATTTA others(1): Show |
G | 44 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(41): Show | 44 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.1958-640_1958-633d others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918108 | ||||||
| chr16:57918108
|
GTTATTTA others(5): Show |
G | 1 | a0006c0085t0024g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1958-644_1958-633d others(14): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918108 | ||||||
| chr16:57918148
|
C | T | 5 | a0004c0045t0003g0342a0004c0046t0036g0348a0015c0031t0004g0333others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1958-672G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918148 | ||||||
| chr16:57918178
|
T | G | 4 | a0001c0007t0003g0004a0001c0028t0042g0069a0002c0011t0004g0185others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1958-702A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918178 | ||||||
| chr16:57918348
|
G | A | 1 | a0027c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1957+751C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918348 | ||||||
| chr16:57918368
|
C | T | 1 | a0019c0110t0011g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1957+731G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918368 | ||||||
| chr16:57918426
|
C | T | 1 | a0002c0006t0021g0187 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1957+673G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918426 | ||||||
| chr16:57918443
|
C | A | 1 | a0001c0003t0012g0266 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1957+656G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918443 | ||||||
| chr16:57918458
|
A | C | 1 | a0011c0058t0004g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1957+641T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918458 | ||||||
| chr16:57918520
|
T | C | 1 | a0001c0001t0003g0311 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1957+579A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918520 | ||||||
| chr16:57918557
|
C | T | 1 | a0003c0074t0009g0177 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1957+542G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918557 | ||||||
| chr16:57918601
|
G | T | 1 | a0001c0003t0003g0265 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1957+498C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918601 | ||||||
| chr16:57918652
|
G | A | 1 | a0003c0064t0017g0179 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1957+447C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918652 | ||||||
| chr16:57918773
|
C | G | 2 | a0004c0014t0005g0346a0004c0044t0004g0343 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1957+326G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918773 | ||||||
| chr16:57918779
|
A | G | 6 | a0001c0004t0002g0116a0001c0004t0002g0156a0001c0004t0005g0182others(3): Show | 6 | NA18940.hp1 NA18955.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.1957+320T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918779 | ||||||
| chr16:57918966
|
A | G | 135 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(132): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1957+133T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918966 | ||||||
| chr16:57919031
|
C | T | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1957+68G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57919031 | ||||||
| chr16:57919410
|
T | C | 170 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(167): Show | 173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1802-156A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919410 | ||||||
| chr16:57919476
|
G | A | 34 | a0001c0003t0005g0300a0001c0015t0001g0335a0001c0015t0002g0006others(31): Show | 34 | HG01123.hp2 HG01891.hp1 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.1802-222C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919476 | ||||||
| chr16:57919549
|
G | A | 7 | a0001c0002t0003g0008a0001c0007t0003g0189a0001c0028t0044g0064others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1802-295C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919549 | ||||||
| chr16:57919581
|
C | A | 18 | a0001c0002t0003g0008a0001c0007t0003g0004a0001c0007t0003g0189others(15): Show | 18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1802-327G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919581 | ||||||
| chr16:57919709
|
A | T | 20 | a0008c0025t0001g0122a0008c0025t0023g0077a0008c0032t0002g0269others(17): Show | 20 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1802-455T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919709 | ||||||
| chr16:57919718
|
T | A | 1 | a0003c0008t0002g0131 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1802-464A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919718 | ||||||
| chr16:57919811
|
G | T | 20 | a0008c0025t0001g0122a0008c0025t0023g0077a0008c0032t0002g0269others(17): Show | 20 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1802-557C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919811 | ||||||
| chr16:57919815
|
A | G | 5 | a0001c0002t0003g0008a0001c0028t0044g0064a0009c0061t0004g0049others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1802-561T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919815 | ||||||
| chr16:57919819
|
T | C | 46 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(43): Show | 46 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1802-565A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919819 | ||||||
| chr16:57919868
|
C | T | 1 | a0018c0102t0003g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1801+519G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919868 | ||||||
| chr16:57920161
|
G | C | 34 | a0001c0004t0035g0079a0001c0015t0001g0335a0001c0015t0002g0006others(31): Show | 34 | HG01123.hp2 HG01891.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1801+226C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57920161 | ||||||
| chr16:57920218
|
C | T | 4 | a0001c0007t0003g0004a0001c0028t0042g0069a0002c0011t0004g0185others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1801+169G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57920218 | ||||||
| chr16:57920364
|
A | G | 247 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(244): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1801+23T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57920364 | ||||||
| chr16:57920585
|
A | C | 1 | a0003c0008t0002g0131 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1644-41T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57920585 | ||||||
| chr16:57920621
|
G | A | 10 | a0011c0033t0001g0249a0011c0033t0001g0267a0011c0058t0004g0140others(7): Show | 10 | HG00280.hp2 HG00639.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.1644-77C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57920621 | ||||||
| chr16:57920693
|
C | T | 1 | a0001c0013t0018g0294 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1644-149G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57920693 | ||||||
| chr16:57920892
|
A | T | 1 | a0001c0001t0002g0309 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1644-348T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57920892 | ||||||
| chr16:57920910
|
G | A | 1 | a0034c0095t0001g0193 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1644-366C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57920910 | ||||||
| chr16:57921082
|
A | G | 42 | a0001c0002t0022g0062a0001c0007t0004g0046a0001c0015t0001g0335others(39): Show | 42 | HG01123.hp2 HG01891.hp1 HG02055.hp2 others(39): Show |
intron_variant | MODIFIER | c.1644-538T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921082 | ||||||
| chr16:57921125
|
C | CT | 47 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(44): Show | 47 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.1644-582dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921125 | ||||||
| chr16:57921125
|
CT | C | 7 | a0001c0016t0046g0054a0001c0053t0004g0200a0002c0109t0004g0108others(4): Show | 7 | HG02145.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1644-582delA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921125 | ||||||
| chr16:57921177
|
T | G | 100 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(97): Show | 103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.1644-633A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921177 | ||||||
| chr16:57921196
|
C | A | 30 | a0001c0002t0022g0062a0001c0007t0004g0046a0001c0015t0001g0335others(27): Show | 30 | HG01123.hp2 HG01891.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1644-652G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921196 | ||||||
| chr16:57921198
|
G | A | 2 | a0001c0004t0022g0107a0002c0022t0018g0112 | 2 | HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1644-654C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921198 | ||||||
| chr16:57921217
|
C | CT | 36 | a0001c0001t0002g0250a0001c0002t0001g0181a0001c0002t0002g0161others(33): Show | 36 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(33): Show |
intron_variant | MODIFIER | c.1644-674dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921217 | ||||||
| chr16:57921217
|
CT | C | 78 | a0001c0001t0001g0227a0001c0001t0006g0226a0001c0001t0012g0212others(75): Show | 78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.1644-674delA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921217 | ||||||
| chr16:57921317
|
G | A | 20 | a0008c0025t0001g0122a0008c0025t0023g0077a0008c0032t0002g0269others(17): Show | 20 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1644-773C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921317 | ||||||
| chr16:57921370
|
C | T | 29 | a0001c0002t0022g0062a0001c0007t0004g0046a0001c0015t0001g0335others(26): Show | 29 | HG01123.hp2 HG01891.hp1 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1644-826G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921370 | ||||||
| chr16:57921452
|
C | G | 1 | a0006c0086t0003g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1644-908G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921452 | ||||||
| chr16:57921489
|
T | C | 11 | a0001c0002t0001g0181a0001c0003t0005g0300a0001c0017t0001g0114others(8): Show | 11 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1644-945A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921489 | ||||||
| chr16:57921682
|
A | G | 11 | a0001c0002t0001g0181a0001c0003t0005g0300a0001c0017t0001g0114others(8): Show | 11 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1644-1138T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921682 | ||||||
| chr16:57921709
|
A | G | 36 | a0001c0002t0022g0062a0001c0007t0004g0046a0001c0015t0001g0335others(33): Show | 36 | HG01123.hp2 HG01891.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1644-1165T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921709 | ||||||
| chr16:57921788
|
C | G | 36 | a0001c0002t0022g0062a0001c0007t0004g0046a0001c0015t0001g0335others(33): Show | 36 | HG01123.hp2 HG01891.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1644-1244G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921788 | ||||||
| chr16:57921799
|
G | A | 10 | a0001c0001t0001g0195a0001c0001t0001g0275a0001c0001t0001g0276others(7): Show | 10 | HG00099.hp2 HG00738.hp2 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.1644-1255C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921799 | ||||||
| chr16:57921850
|
C | A | 1 | a0041c0069t0001g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1644-1306G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921850 | ||||||
| chr16:57921912
|
A | G | 46 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(43): Show | 46 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1643+1361T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921912 | ||||||
| chr16:57921986
|
A | G | 1 | a0012c0115t0045g0111 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1643+1287T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921986 | ||||||
| chr16:57922021
|
G | A | 1 | a0001c0004t0005g0182 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1643+1252C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922021 | ||||||
| chr16:57922107
|
G | A | 46 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(43): Show | 46 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1643+1166C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922107 | ||||||
| chr16:57922279
|
G | T | 1 | a0001c0007t0003g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1643+994C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922279 | ||||||
| chr16:57922289
|
C | G | 258 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(255): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1643+984G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922289 | ||||||
| chr16:57922327
|
G | A | 34 | a0001c0002t0022g0062a0001c0007t0004g0046a0001c0015t0001g0335others(31): Show | 34 | HG01123.hp2 HG01891.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.1643+946C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922327 | ||||||
| chr16:57922413
|
C | CTCTT | 118 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(115): Show | 121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.1643+856_1643+859d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922413 | ||||||
| chr16:57922413
|
CTCTT | C | 6 | a0001c0007t0003g0340a0003c0040t0038g0203a0004c0048t0016g0354others(3): Show | 6 | HG02523.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1643+856_1643+859d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922413 | ||||||
| chr16:57922427
|
C | CT | 4 | a0001c0007t0003g0189a0001c0053t0004g0200a0002c0109t0004g0108others(1): Show | 4 | HG02723.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1643+845dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922427 | ||||||
| chr16:57922427
|
C | CTTT | 12 | a0001c0002t0022g0062a0001c0007t0004g0046a0001c0042t0011g0029others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1643+843_1643+845d others(5): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922427 | ||||||
| chr16:57922427
|
C | CTTTTT | 16 | a0001c0015t0001g0335a0001c0015t0002g0006a0001c0015t0020g0336others(13): Show | 16 | HG01123.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1643+845_1643+846i others(7): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922427 | ||||||
| chr16:57922431
|
C | CT | 7 | a0001c0003t0001g0199a0001c0003t0001g0282a0001c0003t0003g0283others(4): Show | 7 | HG01515.hp1 HG02895.hp1 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.1643+841dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922431 | ||||||
| chr16:57922431
|
C | CTTTTT | 11 | a0001c0002t0001g0181a0001c0003t0005g0300a0001c0017t0001g0114others(8): Show | 11 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1643+837_1643+841d others(7): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922431 | ||||||
| chr16:57922431
|
C | T | 38 | a0001c0002t0022g0062a0001c0007t0003g0189a0001c0007t0004g0046others(35): Show | 38 | HG01123.hp2 HG01891.hp1 HG02055.hp2 others(35): Show |
intron_variant | MODIFIER | c.1643+842G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922431 | ||||||
| chr16:57922709
|
A | G | 39 | a0001c0002t0022g0062a0001c0004t0035g0079a0001c0007t0004g0046others(36): Show | 39 | HG01123.hp2 HG01891.hp1 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.1643+564T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922709 | ||||||
| chr16:57922711
|
G | A | 3 | a0001c0053t0004g0200a0002c0109t0004g0108a0027c0078t0011g0353 | 3 | HG02723.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1643+562C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922711 | ||||||
| chr16:57922771
|
C | T | 1 | a0005c0030t0003g0001 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1643+502G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922771 | ||||||
| chr16:57922839
|
C | T | 4 | a0001c0007t0002g0073a0002c0006t0021g0187a0002c0011t0016g0190others(1): Show | 4 | HG02965.hp1 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1643+434G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922839 | ||||||
| chr16:57922863
|
C | CT | 47 | a0001c0001t0002g0309a0001c0002t0001g0181a0001c0002t0022g0062others(44): Show | 47 | HG01123.hp2 HG01891.hp1 HG01934.hp1 others(44): Show |
intron_variant | MODIFIER | c.1643+409dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922863 | ||||||
| chr16:57923050
|
G | A | 7 | a0001c0002t0003g0008a0001c0007t0003g0189a0001c0028t0044g0064others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1643+223C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57923050 | ||||||
| chr16:57923090
|
A | T | 37 | a0001c0002t0022g0062a0001c0007t0004g0046a0001c0015t0001g0335others(34): Show | 37 | HG01123.hp2 HG01891.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1643+183T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57923090 | ||||||
| chr16:57923165
|
A | C | 1 | a0002c0005t0001g0087 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1643+108T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57923165 | ||||||
| chr16:57923214
|
C | T | 20 | a0008c0025t0001g0122a0008c0025t0023g0077a0008c0032t0002g0269others(17): Show | 20 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1643+59G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57923214 | ||||||
| chr16:57923218
|
A | G | 2 | a0020c0118t0001g0302a0045c0079t0006g0194 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1643+55T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57923218 | ||||||
| chr16:57923229
|
T | TC | 11 | a0001c0002t0001g0181a0001c0003t0005g0300a0001c0017t0001g0114others(8): Show | 11 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1643+43dupG | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57923229 | ||||||
| chr16:57923234
|
G | C | 258 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(255): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1643+39C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57923234 | ||||||
| chr16:57923235
|
C | T | 7 | a0001c0002t0003g0008a0001c0007t0003g0189a0001c0028t0044g0064others(4): Show | 7 | HG01884.hp2 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1643+38G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57923235 | ||||||
| chr16:57923259
|
CA | C | 22 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(19): Show | 22 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.1643+13delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57923259 | ||||||
| chr16:57923545
|
C | T | 11 | a0001c0002t0001g0181a0001c0003t0005g0300a0001c0017t0001g0114others(8): Show | 11 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1536-165G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57923545 | ||||||
| chr16:57923882
|
C | T | 1 | a0001c0042t0011g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1536-502G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57923882 | ||||||
| chr16:57923897
|
C | A | 1 | a0001c0001t0013g0251 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1536-517G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57923897 | ||||||
| chr16:57924027
|
A | G | 2 | a0020c0118t0001g0302a0045c0079t0006g0194 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1536-647T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57924027 | ||||||
| chr16:57924255
|
C | T | 57 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(54): Show | 57 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1536-875G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57924255 | ||||||
| chr16:57924540
|
A | G | 5 | a0004c0045t0003g0342a0004c0046t0036g0348a0015c0031t0004g0333others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1536-1160T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57924540 | ||||||
| chr16:57924620
|
A | G | 1 | a0018c0055t0025g0042 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1536-1240T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57924620 | ||||||
| chr16:57924660
|
AC | A | 5 | a0001c0002t0003g0008a0001c0028t0044g0064a0009c0061t0004g0049others(2): Show | 5 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1536-1281delG | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57924660 | ||||||
| chr16:57924683
|
T | C | 2 | a0001c0004t0022g0107a0002c0022t0018g0112 | 2 | HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1536-1303A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57924683 | ||||||
| chr16:57924693
|
C | T | 7 | a0001c0016t0046g0054a0001c0053t0004g0200a0002c0109t0004g0108others(4): Show | 7 | HG02145.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1536-1313G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57924693 | ||||||
| chr16:57924952
|
G | C | 1 | a0040c0063t0020g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1536-1572C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57924952 | ||||||
| chr16:57924966
|
G | A | 1 | a0001c0002t0001g0155 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1536-1586C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57924966 | ||||||
| chr16:57925079
|
T | C | 219 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(216): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1536-1699A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925079 | ||||||
| chr16:57925146
|
G | T | 1 | a0001c0002t0001g0125 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1536-1766C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925146 | ||||||
| chr16:57925191
|
T | C | 58 | a0001c0002t0022g0062a0001c0007t0004g0046a0001c0015t0001g0335others(55): Show | 58 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(55): Show |
intron_variant | MODIFIER | c.1536-1811A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925191 | ||||||
| chr16:57925196
|
T | A | 1 | a0001c0001t0001g0205 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1536-1816A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925196 | ||||||
| chr16:57925223
|
A | G | 60 | a0001c0002t0022g0062a0001c0004t0035g0079a0001c0007t0003g0004others(57): Show | 60 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1536-1843T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925223 | ||||||
| chr16:57925334
|
G | A | 66 | a0001c0002t0001g0181a0001c0002t0003g0008a0001c0002t0022g0062others(63): Show | 66 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(63): Show |
intron_variant | MODIFIER | c.1536-1954C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925334 | ||||||
| chr16:57925433
|
G | A | 4 | a0001c0028t0044g0064a0009c0061t0004g0049a0014c0023t0002g0347others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536-2053C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925433 | ||||||
| chr16:57925471
|
G | A | 2 | a0001c0004t0035g0079a0002c0022t0002g0074 | 2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1536-2091C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925471 | ||||||
| chr16:57925499
|
C | T | 1 | a0001c0013t0019g0213 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1536-2119G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925499 | ||||||
| chr16:57925500
|
G | A | 1 | a0002c0037t0003g0023 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1536-2120C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925500 | ||||||
| chr16:57925689
|
A | T | 4 | a0001c0007t0002g0073a0002c0006t0021g0187a0002c0011t0016g0190others(1): Show | 4 | HG02965.hp1 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536-2309T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925689 | ||||||
| chr16:57925700
|
T | TC | 87 | a0001c0001t0001g0003a0001c0001t0001g0227a0001c0001t0001g0237others(84): Show | 90 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1536-2321_1536-232 others(5): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925700 | ||||||
| chr16:57925765
|
G | A | 1 | a0009c0077t0004g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1536-2385C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925765 | ||||||
| chr16:57925915
|
T | A | 4 | a0001c0028t0044g0064a0009c0061t0004g0049a0014c0023t0002g0347others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536-2535A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925915 | ||||||
| chr16:57925964
|
C | A | 249 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(246): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1536-2584G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925964 | ||||||
| chr16:57925978
|
G | A | 1 | a0049c0108t0004g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1536-2598C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925978 | ||||||
| chr16:57926253
|
C | A | 1 | a0001c0004t0022g0107 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1536-2873G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926253 | ||||||
| chr16:57926324
|
C | T | 24 | a0001c0002t0022g0062a0001c0007t0003g0004a0001c0007t0004g0046others(21): Show | 24 | HG02055.hp1 HG02280.hp1 HG02559.hp2 others(21): Show |
intron_variant | MODIFIER | c.1536-2944G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926324 | ||||||
| chr16:57926341
|
T | G | 4 | a0001c0002t0001g0181a0001c0018t0002g0254a0002c0006t0002g0096others(1): Show | 4 | HG02074.hp1 NA18945.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536-2961A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926341 | ||||||
| chr16:57926351
|
G | A | 8 | a0001c0053t0004g0200a0002c0113t0003g0318a0006c0081t0021g0331others(5): Show | 8 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1536-2971C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926351 | ||||||
| chr16:57926380
|
G | T | 95 | a0001c0001t0001g0003a0001c0001t0001g0227a0001c0001t0001g0237others(92): Show | 98 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1536-3000C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926380 | ||||||
| chr16:57926595
|
C | T | 92 | a0001c0001t0001g0195a0001c0001t0001g0205a0001c0001t0001g0207others(89): Show | 92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.1536-3215G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926595 | ||||||
| chr16:57926633
|
A | G | 34 | a0001c0002t0003g0008a0001c0015t0001g0335a0001c0015t0020g0336others(31): Show | 34 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1536-3253T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926633 | ||||||
| chr16:57926715
|
T | C | 42 | a0001c0002t0003g0008a0001c0002t0007g0126a0001c0015t0001g0335others(39): Show | 42 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.1536-3335A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926715 | ||||||
| chr16:57926737
|
T | C | 1 | a0001c0002t0001g0162 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1536-3357A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926737 | ||||||
| chr16:57926910
|
G | A | 1 | a0002c0005t0009g0104 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1536-3530C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926910 | ||||||
| chr16:57926921
|
A | G | 1 | a0003c0012t0007g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1536-3541T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926921 | ||||||
| chr16:57926932
|
A | ACCATTG | 6 | a0001c0053t0004g0200a0002c0109t0004g0108a0004c0014t0005g0346others(3): Show | 6 | HG02145.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1536-3558_1536-355 others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926932 | ||||||
| chr16:57926971
|
C | T | 1 | a0001c0002t0002g0157 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1536-3591G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926971 | ||||||
| chr16:57927154
|
A | G | 1 | a0001c0004t0001g0117 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1536-3774T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927154 | ||||||
| chr16:57927189
|
G | A | 2 | a0001c0007t0003g0340a0008c0032t0002g0269 | 2 | HG03486.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1536-3809C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927189 | ||||||
| chr16:57927368
|
C | T | 1 | a0003c0009t0039g0307 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1536-3988G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927368 | ||||||
| chr16:57927403
|
C | A | 2 | a0011c0033t0001g0267a0048c0117t0026g0186 | 2 | HG00741.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1536-4023G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927403 | ||||||
| chr16:57927411
|
T | A | 4 | a0001c0028t0044g0064a0009c0061t0004g0049a0014c0023t0002g0347others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536-4031A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927411 | ||||||
| chr16:57927522
|
T | C | 3 | a0001c0028t0044g0064a0014c0023t0002g0347a0014c0023t0002g0349 | 3 | HG01884.hp2 HG02559.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1536-4142A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927522 | ||||||
| chr16:57927746
|
C | A | 32 | a0001c0002t0003g0008a0001c0015t0001g0335a0001c0015t0020g0336others(29): Show | 32 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1535+3970G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927746 | ||||||
| chr16:57927777
|
C | T | 3 | a0001c0002t0001g0056a0001c0027t0003g0058a0009c0077t0004g0060 | 3 | HG03209.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1535+3939G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927777 | ||||||
| chr16:57927842
|
C | T | 32 | a0001c0002t0003g0008a0001c0015t0001g0335a0001c0015t0020g0336others(29): Show | 32 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1535+3874G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927842 | ||||||
| chr16:57927867
|
G | C | 1 | a0003c0074t0009g0177 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1535+3849C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927867 | ||||||
| chr16:57927903
|
G | A | 8 | a0001c0027t0040g0078a0001c0028t0044g0064a0001c0053t0004g0200others(5): Show | 8 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1535+3813C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927903 | ||||||
| chr16:57928158
|
C | T | 88 | a0001c0001t0001g0195a0001c0001t0001g0205a0001c0001t0001g0234others(85): Show | 88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.1535+3558G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57928158 | ||||||
| chr16:57928583
|
G | C | 2 | a0001c0007t0003g0340a0025c0051t0001g0339 | 2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1535+3133C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57928583 | ||||||
| chr16:57928647
|
T | G | 115 | a0001c0001t0001g0195a0001c0001t0001g0205a0001c0001t0001g0207others(112): Show | 115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.1535+3069A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57928647 | ||||||
| chr16:57928729
|
G | C | 15 | a0001c0001t0001g0227a0001c0001t0006g0226a0001c0004t0005g0127others(12): Show | 16 | HG00423.hp1 HG00558.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.1535+2987C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57928729 | ||||||
| chr16:57928905
|
C | A | 8 | a0002c0005t0001g0314a0002c0005t0001g0316a0012c0120t0003g0065others(5): Show | 8 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1535+2811G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57928905 | ||||||
| chr16:57928919
|
A | G | 1 | a0001c0053t0004g0200 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1535+2797T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57928919 | ||||||
| chr16:57928989
|
G | A | 1 | a0011c0033t0001g0249 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1535+2727C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57928989 | ||||||
| chr16:57929178
|
G | A | 15 | a0001c0002t0022g0062a0001c0004t0022g0107a0001c0007t0004g0046others(12): Show | 15 | HG02280.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.1535+2538C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929178 | ||||||
| chr16:57929262
|
G | A | 5 | a0001c0007t0003g0004a0001c0015t0002g0006a0001c0028t0042g0069others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1535+2454C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929262 | ||||||
| chr16:57929268
|
T | G | 11 | a0001c0002t0001g0181a0001c0003t0005g0300a0001c0004t0005g0182others(8): Show | 11 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1535+2448A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929268 | ||||||
| chr16:57929277
|
C | A | 2 | a0001c0053t0004g0200a0002c0109t0004g0108 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1535+2439G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929277 | ||||||
| chr16:57929308
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1535+2408T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929308 | ||||||
| chr16:57929337
|
T | A | 1 | a0001c0018t0001g0263 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1535+2379A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929337 | ||||||
| chr16:57929476
|
G | GGAGAGAG others(1): Show |
216 | a0001c0001t0001g0195a0001c0001t0001g0205a0001c0001t0001g0207others(213): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1535+2232_1535+223 others(12): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929476 | ||||||
| chr16:57929476
|
G | GGAGAGAG others(3): Show |
5 | a0001c0007t0003g0004a0001c0015t0002g0006a0001c0028t0042g0069others(2): Show | 5 | HG02055.hp2 HG02559.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1535+2230_1535+223 others(14): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929476 | ||||||
| chr16:57929476
|
G | GGAGAGAG others(5): Show |
4 | a0001c0015t0001g0335a0001c0015t0020g0336a0002c0011t0004g0185others(1): Show | 4 | HG02055.hp1 HG02257.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1535+2228_1535+223 others(16): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929476 | ||||||
| chr16:57929514
|
A | G | 109 | a0001c0001t0001g0195a0001c0001t0001g0205a0001c0001t0001g0207others(106): Show | 109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.1535+2202T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929514 | ||||||
| chr16:57929654
|
C | A | 1 | a0001c0002t0001g0052 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1535+2062G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929654 | ||||||
| chr16:57929710
|
T | C | 6 | a0001c0007t0003g0189a0002c0113t0003g0318a0006c0081t0021g0331others(3): Show | 6 | HG02630.hp1 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1535+2006A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929710 | ||||||
| chr16:57929818
|
C | T | 1 | a0001c0002t0001g0162 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1535+1898G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929818 | ||||||
| chr16:57929932
|
T | A | 109 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(106): Show | 110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.1535+1784A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929932 | ||||||
| chr16:57929935
|
A | G | 5 | a0001c0053t0004g0200a0002c0109t0004g0108a0004c0014t0005g0346others(2): Show | 5 | HG02145.hp2 HG02257.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1535+1781T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929935 | ||||||
| chr16:57930074
|
G | C | 143 | a0001c0001t0005g0277a0001c0002t0001g0035a0001c0002t0001g0039others(140): Show | 143 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1535+1642C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930074 | ||||||
| chr16:57930184
|
A | T | 11 | a0001c0002t0022g0062a0001c0004t0022g0107a0001c0007t0004g0046others(8): Show | 11 | HG02280.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1535+1532T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930184 | ||||||
| chr16:57930185
|
T | A | 5 | a0001c0007t0003g0004a0001c0015t0002g0006a0001c0028t0042g0069others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1535+1531A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930185 | ||||||
| chr16:57930194
|
A | C | 1 | a0001c0001t0001g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1535+1522T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930194 | ||||||
| chr16:57930247
|
G | A | 1 | a0022c0050t0003g0352 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1535+1469C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930247 | ||||||
| chr16:57930388
|
G | A | 1 | a0001c0027t0040g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1535+1328C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930388 | ||||||
| chr16:57930403
|
G | A | 3 | a0001c0003t0003g0265a0001c0003t0003g0296a0001c0003t0012g0266 | 3 | HG00733.hp2 HG01496.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1535+1313C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930403 | ||||||
| chr16:57930457
|
G | A | 11 | a0001c0002t0001g0181a0001c0003t0005g0300a0001c0004t0005g0182others(8): Show | 11 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1535+1259C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930457 | ||||||
| chr16:57930496
|
A | G | 1 | a0005c0100t0002g0232 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1535+1220T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930496 | ||||||
| chr16:57930525
|
A | G | 178 | a0001c0001t0001g0003a0001c0001t0001g0207a0001c0001t0001g0279others(175): Show | 179 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(176): Show |
intron_variant | MODIFIER | c.1535+1191T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930525 | ||||||
| chr16:57930538
|
G | A | 11 | a0001c0002t0001g0181a0001c0003t0005g0300a0001c0004t0005g0182others(8): Show | 11 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1535+1178C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930538 | ||||||
| chr16:57930575
|
G | C | 1 | a0001c0029t0002g0034 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1535+1141C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930575 | ||||||
| chr16:57930582
|
G | A | 1 | a0001c0001t0002g0250 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1535+1134C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930582 | ||||||
| chr16:57930611
|
T | G | 1 | a0037c0071t0006g0148 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1535+1105A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930611 | ||||||
| chr16:57930702
|
A | G | 2 | a0011c0058t0004g0140a0011c0059t0001g0123 | 2 | HG00741.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1535+1014T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930702 | ||||||
| chr16:57930941
|
G | A | 4 | a0001c0015t0002g0006a0001c0028t0042g0069a0002c0011t0004g0185others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1535+775C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930941 | ||||||
| chr16:57930999
|
A | G | 11 | a0001c0002t0001g0181a0001c0003t0005g0300a0001c0004t0005g0182others(8): Show | 11 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1535+717T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930999 | ||||||
| chr16:57931010
|
T | A | 1 | a0001c0003t0005g0240 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1535+706A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57931010 | ||||||
| chr16:57931011
|
A | T | 1 | a0016c0090t0010g0220 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1535+705T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57931011 | ||||||
| chr16:57931253
|
A | C | 10 | a0001c0002t0001g0181a0001c0003t0005g0300a0001c0004t0005g0182others(7): Show | 10 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.1535+463T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57931253 | ||||||
| chr16:57931261
|
T | C | 1 | a0011c0058t0004g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1535+455A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57931261 | ||||||
| chr16:57931264
|
T | C | 1 | a0002c0022t0002g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1535+452A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57931264 | ||||||
| chr16:57931351
|
C | T | 2 | a0020c0118t0001g0302a0045c0079t0006g0194 | 2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1535+365G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57931351 | ||||||
| chr16:57931392
|
C | T | 3 | a0001c0001t0001g0227a0001c0001t0006g0226a0003c0008t0002g0120 | 3 | NA18959.hp2 NA18986.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1535+324G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57931392 | ||||||
| chr16:57931541
|
G | T | 4 | a0001c0001t0001g0236a0001c0001t0001g0262a0001c0001t0002g0252others(1): Show | 4 | NA18972.hp1 NA18980.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1535+175C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57931541 | ||||||
| chr16:57931881
|
G | T | 2 | a0003c0104t0007g0218a0036c0067t0002g0051 | 2 | HG03017.hp2 HG04228.hp2 |
splice_region_variant&intron_variant | LOW | c.1373-3C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57931881 | ||||||
| chr16:57931889
|
G | T | 10 | a0001c0002t0001g0181a0001c0003t0005g0300a0001c0004t0005g0182others(7): Show | 10 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.1373-11C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57931889 | ||||||
| chr16:57931938
|
C | T | 7 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0002g0273others(4): Show | 7 | NA18947.hp1 NA18948.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.1373-60G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57931938 | ||||||
| chr16:57932014
|
C | A | 3 | a0001c0053t0004g0200a0002c0109t0004g0108a0049c0108t0004g0061 | 3 | HG02257.hp1 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1373-136G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932014 | ||||||
| chr16:57932036
|
G | T | 13 | a0001c0015t0001g0335a0001c0015t0020g0336a0001c0016t0046g0054others(10): Show | 13 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1373-158C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932036 | ||||||
| chr16:57932219
|
A | G | 2 | a0001c0007t0003g0189a0017c0062t0027g0324 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1373-341T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932219 | ||||||
| chr16:57932250
|
C | A | 51 | a0001c0001t0001g0237a0001c0001t0005g0277a0001c0002t0001g0035others(48): Show | 52 | HG00544.hp1 HG00609.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.1373-372G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932250 | ||||||
| chr16:57932262
|
C | T | 1 | a0001c0013t0019g0213 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1373-384G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932262 | ||||||
| chr16:57932400
|
C | CT | 36 | a0001c0002t0003g0008a0001c0004t0001g0117a0001c0004t0001g0150others(33): Show | 36 | HG00280.hp1 HG00642.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.1373-523dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932400 | ||||||
| chr16:57932400
|
CT | C | 13 | a0001c0003t0005g0300a0001c0003t0006g0288a0001c0004t0005g0182others(10): Show | 13 | HG01934.hp1 HG02080.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.1373-523delA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932400 | ||||||
| chr16:57932400
|
CTT | C | 55 | a0001c0001t0001g0237a0001c0001t0005g0277a0001c0002t0001g0035others(52): Show | 56 | HG00544.hp1 HG00609.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1373-524_1373-523d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932400 | ||||||
| chr16:57932400
|
CTTTTTTT others(3): Show |
C | 1 | a0002c0006t0008g0084 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1373-532_1373-523d others(12): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932400 | ||||||
| chr16:57932551
|
C | T | 1 | a0003c0105t0014g0298 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1373-673G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932551 | ||||||
| chr16:57932684
|
C | A | 4 | a0001c0001t0001g0236a0001c0001t0001g0262a0001c0001t0002g0252others(1): Show | 4 | NA18972.hp1 NA18980.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1373-806G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932684 | ||||||
| chr16:57932723
|
G | A | 5 | a0001c0004t0035g0079a0002c0005t0001g0101a0002c0022t0002g0074others(2): Show | 5 | HG02109.hp2 HG02735.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1373-845C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932723 | ||||||
| chr16:57932772
|
G | A | 13 | a0001c0015t0001g0335a0001c0015t0020g0336a0001c0016t0046g0054others(10): Show | 13 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1373-894C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932772 | ||||||
| chr16:57932832
|
G | A | 4 | a0001c0002t0003g0008a0008c0054t0002g0044a0019c0112t0024g0010others(1): Show | 4 | HG02486.hp2 HG03195.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1373-954C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932832 | ||||||
| chr16:57932909
|
T | C | 5 | a0001c0004t0035g0079a0002c0005t0001g0101a0002c0022t0002g0074others(2): Show | 5 | HG02109.hp2 HG02735.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1373-1031A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932909 | ||||||
| chr16:57932932
|
G | T | 10 | a0001c0002t0001g0181a0001c0003t0005g0300a0001c0004t0005g0182others(7): Show | 10 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.1373-1054C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932932 | ||||||
| chr16:57932935
|
G | A | 49 | a0001c0001t0001g0237a0001c0001t0005g0277a0001c0002t0001g0035others(46): Show | 50 | HG00544.hp1 HG00609.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.1373-1057C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932935 | ||||||
| chr16:57932939
|
G | A | 1 | a0001c0003t0001g0248 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1373-1061C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932939 | ||||||
| chr16:57932980
|
T | C | 1 | a0030c0092t0001g0285 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1373-1102A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932980 | ||||||
| chr16:57933224
|
G | A | 1 | a0012c0120t0003g0065 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1373-1346C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933224 | ||||||
| chr16:57933288
|
T | C | 73 | a0001c0002t0001g0056a0001c0002t0001g0181a0001c0002t0003g0008others(70): Show | 73 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(70): Show |
intron_variant | MODIFIER | c.1373-1410A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933288 | ||||||
| chr16:57933314
|
T | C | 290 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(287): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1373-1436A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933314 | ||||||
| chr16:57933315
|
C | T | 4 | a0002c0113t0003g0318a0006c0081t0021g0331a0009c0026t0004g0310others(1): Show | 4 | HG02630.hp1 HG03098.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1373-1437G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933315 | ||||||
| chr16:57933682
|
A | G | 13 | a0001c0015t0001g0335a0001c0015t0020g0336a0001c0016t0046g0054others(10): Show | 13 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1373-1804T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933682 | ||||||
| chr16:57933724
|
C | CT | 14 | a0001c0016t0004g0313a0002c0005t0001g0101a0002c0005t0001g0314others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1373-1847dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933724 | ||||||
| chr16:57933724
|
C | CTT | 9 | a0001c0002t0001g0181a0001c0004t0005g0182a0001c0017t0001g0114others(6): Show | 9 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.1373-1848_1373-184 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933724 | ||||||
| chr16:57933724
|
CT | C | 247 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(244): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.1373-1847delA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933724 | ||||||
| chr16:57933754
|
G | A | 3 | a0001c0007t0003g0189a0017c0062t0027g0324a0027c0078t0011g0353 | 3 | HG02723.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1373-1876C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933754 | ||||||
| chr16:57933795
|
T | A | 3 | a0006c0082t0010g0337a0018c0055t0025g0042a0038c0056t0011g0047 | 3 | HG01123.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1373-1917A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933795 | ||||||
| chr16:57934004
|
T | C | 2 | a0002c0006t0003g0022a0035c0094t0002g0295 | 2 | HG01109.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1373-2126A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934004 | ||||||
| chr16:57934028
|
G | A | 4 | a0002c0113t0003g0318a0006c0081t0021g0331a0009c0026t0004g0310others(1): Show | 4 | HG02630.hp1 HG03098.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1373-2150C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934028 | ||||||
| chr16:57934389
|
G | A | 3 | a0001c0017t0001g0114a0001c0017t0001g0139a0003c0064t0017g0179 | 3 | HG01934.hp1 NA18939.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1373-2511C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934389 | ||||||
| chr16:57934413
|
C | T | 1 | a0031c0093t0001g0258 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1373-2535G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934413 | ||||||
| chr16:57934576
|
T | C | 1 | a0019c0110t0011g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1373-2698A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934576 | ||||||
| chr16:57934695
|
G | A | 1 | a0027c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1373-2817C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934695 | ||||||
| chr16:57934788
|
C | G | 1 | a0001c0002t0007g0126 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1373-2910G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934788 | ||||||
| chr16:57934854
|
G | A | 2 | a0001c0003t0003g0296a0001c0003t0012g0266 | 2 | HG00733.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1373-2976C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934854 | ||||||
| chr16:57934881
|
C | T | 10 | a0001c0002t0001g0181a0001c0003t0005g0300a0001c0004t0005g0182others(7): Show | 10 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.1373-3003G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934881 | ||||||
| chr16:57934913
|
C | T | 25 | a0001c0001t0001g0003a0001c0001t0001g0279a0001c0001t0001g0280others(22): Show | 26 | HG00609.hp1 HG02015.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.1373-3035G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934913 | ||||||
| chr16:57934956
|
C | A | 1 | a0002c0011t0018g0341 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1373-3078G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934956 | ||||||
| chr16:57934956
|
C | CA | 79 | a0001c0001t0002g0252a0001c0002t0001g0056a0001c0002t0002g0157others(76): Show | 79 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(76): Show |
intron_variant | MODIFIER | c.1373-3079dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934956 | ||||||
| chr16:57935036
|
A | T | 10 | a0001c0002t0001g0181a0001c0003t0005g0300a0001c0004t0005g0182others(7): Show | 10 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.1373-3158T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935036 | ||||||
| chr16:57935062
|
A | G | 1 | a0031c0093t0001g0258 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1373-3184T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935062 | ||||||
| chr16:57935103
|
G | A | 3 | a0001c0016t0004g0313a0001c0016t0010g0057a0009c0026t0004g0059 | 3 | HG01891.hp1 HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1373-3225C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935103 | ||||||
| chr16:57935112
|
C | A | 5 | a0001c0007t0003g0004a0001c0015t0002g0006a0001c0028t0042g0069others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1373-3234G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935112 | ||||||
| chr16:57935402
|
G | A | 1 | a0011c0033t0001g0267 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1373-3524C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935402 | ||||||
| chr16:57935572
|
C | T | 1 | a0018c0102t0003g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1373-3694G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935572 | ||||||
| chr16:57935605
|
G | A | 1 | a0018c0102t0003g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1373-3727C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935605 | ||||||
| chr16:57935642
|
C | T | 5 | a0001c0007t0003g0189a0001c0019t0019g0286a0001c0019t0019g0299others(2): Show | 5 | HG01168.hp2 HG01169.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1373-3764G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935642 | ||||||
| chr16:57935652
|
C | A | 2 | a0001c0004t0001g0118a0001c0029t0002g0163 | 2 | NA18982.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1373-3774G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935652 | ||||||
| chr16:57935653
|
A | C | 88 | a0001c0001t0001g0237a0001c0001t0005g0277a0001c0002t0001g0035others(85): Show | 89 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.1373-3775T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935653 | ||||||
| chr16:57935756
|
C | CT | 70 | a0001c0002t0001g0181a0001c0002t0003g0008a0001c0002t0022g0062others(67): Show | 70 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(67): Show |
intron_variant | MODIFIER | c.1372+3673dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935756 | ||||||
| chr16:57935756
|
C | CTT | 11 | a0001c0002t0001g0056a0001c0007t0003g0340a0001c0016t0004g0313others(8): Show | 11 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1372+3672_1372+367 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935756 | ||||||
| chr16:57936014
|
A | G | 1 | a0001c0004t0001g0117 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1372+3416T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936014 | ||||||
| chr16:57936047
|
G | A | 13 | a0001c0004t0035g0079a0001c0053t0004g0200a0002c0005t0001g0314others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1372+3383C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936047 | ||||||
| chr16:57936168
|
G | A | 3 | a0001c0004t0035g0079a0002c0022t0002g0074a0002c0114t0010g0357 | 3 | HG02109.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1372+3262C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936168 | ||||||
| chr16:57936367
|
G | A | 9 | a0002c0005t0001g0314a0002c0005t0001g0316a0002c0109t0004g0108others(6): Show | 9 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1372+3063C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936367 | ||||||
| chr16:57936610
|
T | G | 2 | a0001c0003t0003g0198a0001c0003t0006g0284 | 2 | HG00408.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1372+2820A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936610 | ||||||
| chr16:57936652
|
C | T | 1 | a0001c0027t0040g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1372+2778G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936652 | ||||||
| chr16:57936653
|
G | A | 8 | a0001c0001t0001g0234a0001c0001t0007g0290a0001c0001t0013g0251others(5): Show | 8 | HG00639.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1372+2777C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936653 | ||||||
| chr16:57936675
|
C | T | 1 | a0001c0027t0040g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1372+2755G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936675 | ||||||
| chr16:57936799
|
C | A | 3 | a0001c0007t0003g0189a0017c0062t0027g0324a0018c0102t0003g0271 | 3 | HG02723.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1372+2631G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936799 | ||||||
| chr16:57936799
|
C | CA | 65 | a0001c0001t0001g0237a0001c0001t0005g0277a0001c0002t0001g0035others(62): Show | 66 | HG00544.hp1 HG00609.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.1372+2630dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936799 | ||||||
| chr16:57936799
|
C | CAA | 23 | a0001c0002t0003g0008a0001c0015t0001g0335a0001c0015t0020g0336others(20): Show | 23 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.1372+2629_1372+263 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936799 | ||||||
| chr16:57936801
|
A | AAC | 37 | a0001c0002t0001g0056a0001c0002t0022g0062a0001c0004t0022g0107others(34): Show | 37 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1372+2628_1372+262 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936801 | ||||||
| chr16:57936961
|
A | G | 133 | a0001c0001t0001g0237a0001c0001t0005g0277a0001c0002t0001g0035others(130): Show | 134 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.1372+2469T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936961 | ||||||
| chr16:57937154
|
C | T | 1 | a0001c0001t0002g0312 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1372+2276G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57937154 | ||||||
| chr16:57937281
|
A | G | 309 | a0001c0001t0001g0195a0001c0001t0001g0205a0001c0001t0001g0207others(306): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1372+2149T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57937281 | ||||||
| chr16:57937709
|
T | C | 1 | a0001c0013t0001g0306 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1372+1721A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57937709 | ||||||
| chr16:57937716
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1372+1714C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57937716 | ||||||
| chr16:57938017
|
C | T | 124 | a0001c0001t0001g0237a0001c0001t0002g0312a0001c0001t0005g0277others(121): Show | 125 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1372+1413G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938017 | ||||||
| chr16:57938042
|
G | C | 1 | a0002c0022t0002g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1372+1388C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938042 | ||||||
| chr16:57938045
|
C | T | 14 | a0001c0004t0022g0107a0001c0007t0003g0189a0001c0053t0004g0200others(11): Show | 14 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1372+1385G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938045 | ||||||
| chr16:57938254
|
T | C | 73 | a0001c0001t0001g0237a0001c0001t0002g0312a0001c0001t0005g0277others(70): Show | 74 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1372+1176A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938254 | ||||||
| chr16:57938382
|
G | C | 7 | a0001c0002t0001g0056a0001c0007t0003g0189a0001c0027t0003g0058others(4): Show | 7 | HG01891.hp1 HG02723.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1372+1048C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938382 | ||||||
| chr16:57938388
|
T | C | 1 | a0032c0075t0001g0144 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1372+1042A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938388 | ||||||
| chr16:57938416
|
C | T | 1 | a0027c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1372+1014G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938416 | ||||||
| chr16:57938596
|
G | A | 1 | a0006c0083t0043g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1372+834C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938596 | ||||||
| chr16:57938643
|
TG | T | 10 | a0001c0004t0022g0107a0002c0005t0001g0314a0002c0005t0001g0316others(7): Show | 10 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1372+786delC | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938643 | ||||||
| chr16:57938736
|
G | A | 4 | a0008c0032t0002g0269a0008c0032t0006g0221a0013c0091t0007g0268others(1): Show | 4 | HG00280.hp1 HG01074.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+694C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938736 | ||||||
| chr16:57939013
|
C | T | 1 | a0001c0001t0037g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1372+417G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57939013 | ||||||
| chr16:57939099
|
A | T | 2 | a0009c0061t0004g0049a0014c0023t0002g0347 | 2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1372+331T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57939099 | ||||||
| chr16:57939164
|
T | C | 87 | a0001c0001t0001g0003a0001c0001t0001g0207a0001c0001t0001g0237others(84): Show | 89 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1372+266A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57939164 | ||||||
| chr16:57939173
|
G | C | 1 | a0006c0086t0003g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1372+257C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57939173 | ||||||
| chr16:57939237
|
T | A | 1 | a0002c0114t0010g0357 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1372+193A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57939237 | ||||||
| chr16:57939315
|
G | C | 1 | a0001c0066t0001g0130 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1372+115C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57939315 | ||||||
| chr16:57940020
|
C | T | 4 | a0002c0006t0001g0095a0002c0006t0001g0100a0002c0038t0003g0094others(1): Show | 4 | NA18959.hp1 NA18984.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1209+214G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 15/32 | chr16 | 57940020 | ||||||
| chr16:57940085
|
G | A | 108 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(105): Show | 109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1209+149C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 15/32 | chr16 | 57940085 | ||||||
| chr16:57940173
|
C | T | 1 | a0002c0005t0001g0101 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1209+61G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 15/32 | chr16 | 57940173 | ||||||
| chr16:57940336
|
G | A | 143 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(140): Show | 144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1122-15C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940336 | ||||||
| chr16:57940339
|
G | A | 2 | a0001c0007t0003g0189a0017c0062t0027g0324 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1122-18C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940339 | ||||||
| chr16:57940371
|
TA | T | 4 | a0001c0007t0003g0340a0001c0007t0008g0356a0002c0011t0004g0185others(1): Show | 4 | HG01168.hp1 HG02055.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-51delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940371 | ||||||
| chr16:57940418
|
G | A | 4 | a0001c0007t0003g0340a0001c0007t0008g0356a0002c0011t0004g0185others(1): Show | 4 | HG01168.hp1 HG02055.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-97C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940418 | ||||||
| chr16:57940490
|
C | A | 1 | a0001c0002t0002g0121 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1122-169G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940490 | ||||||
| chr16:57940534
|
C | A | 3 | a0001c0007t0002g0073a0004c0014t0005g0346a0004c0044t0004g0343 | 3 | HG02145.hp2 HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1122-213G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940534 | ||||||
| chr16:57940711
|
A | G | 1 | a0002c0006t0008g0084 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1122-390T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940711 | ||||||
| chr16:57940775
|
A | G | 12 | a0001c0001t0007g0290a0001c0001t0012g0212a0001c0002t0001g0329others(9): Show | 12 | HG00140.hp2 HG00642.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1122-454T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940775 | ||||||
| chr16:57940781
|
C | A | 10 | a0001c0002t0001g0056a0001c0007t0003g0340a0001c0007t0008g0356others(7): Show | 10 | HG01168.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1122-460G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940781 | ||||||
| chr16:57940838
|
C | T | 2 | a0002c0005t0001g0101a0002c0037t0003g0092 | 2 | HG02735.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1122-517G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940838 | ||||||
| chr16:57940895
|
G | C | 1 | a0004c0045t0003g0342 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1122-574C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940895 | ||||||
| chr16:57940937
|
G | A | 26 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(23): Show | 26 | HG00544.hp1 HG00609.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.1122-616C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940937 | ||||||
| chr16:57940972
|
C | T | 3 | a0001c0013t0018g0294a0009c0098t0003g0241a0018c0102t0003g0271 | 3 | HG02145.hp1 HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1122-651G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940972 | ||||||
| chr16:57941035
|
G | T | 1 | a0027c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1122-714C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941035 | ||||||
| chr16:57941274
|
C | T | 1 | a0027c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1122-953G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941274 | ||||||
| chr16:57941276
|
A | C | 1 | a0001c0003t0006g0219 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1122-955T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941276 | ||||||
| chr16:57941311
|
G | A | 40 | a0001c0001t0001g0207a0001c0001t0002g0250a0001c0001t0003g0208others(37): Show | 40 | HG00099.hp2 HG00423.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1122-990C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941311 | ||||||
| chr16:57941493
|
C | T | 1 | a0001c0066t0001g0130 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1122-1172G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941493 | ||||||
| chr16:57941598
|
T | C | 1 | a0001c0003t0001g0197 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1122-1277A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941598 | ||||||
| chr16:57941657
|
T | C | 17 | a0001c0007t0003g0004a0001c0015t0002g0006a0002c0006t0006g0323others(14): Show | 17 | HG00423.hp2 HG02559.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1122-1336A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941657 | ||||||
| chr16:57941661
|
C | T | 13 | a0002c0006t0006g0323a0004c0014t0001g0345a0004c0014t0016g0326others(10): Show | 13 | HG00423.hp2 HG02559.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1122-1340G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941661 | ||||||
| chr16:57941674
|
C | A | 31 | a0001c0002t0001g0056a0001c0007t0003g0004a0001c0007t0003g0189others(28): Show | 31 | HG00423.hp2 HG01891.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.1122-1353G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941674 | ||||||
| chr16:57941713
|
G | T | 7 | a0002c0005t0001g0314a0002c0005t0001g0316a0002c0006t0016g0110others(4): Show | 7 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1122-1392C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941713 | ||||||
| chr16:57941720
|
G | A | 36 | a0001c0002t0001g0056a0001c0007t0003g0004a0001c0007t0003g0189others(33): Show | 36 | HG00423.hp2 HG01168.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1122-1399C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941720 | ||||||
| chr16:57941819
|
T | C | 3 | a0001c0041t0005g0028a0002c0109t0004g0108a0026c0080t0015g0188 | 3 | HG02055.hp2 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1122-1498A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941819 | ||||||
| chr16:57941836
|
TTTTA | T | 6 | a0001c0007t0004g0046a0001c0028t0044g0064a0001c0042t0011g0029others(3): Show | 6 | HG01884.hp1 HG02896.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1122-1519_1122-151 others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941836 | ||||||
| chr16:57941863
|
T | C | 1 | a0001c0003t0002g0191 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1122-1542A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941863 | ||||||
| chr16:57942014
|
G | T | 1 | a0002c0011t0004g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1122-1693C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942014 | ||||||
| chr16:57942028
|
T | TGTTTG | 3 | a0001c0041t0005g0028a0002c0109t0004g0108a0026c0080t0015g0188 | 3 | HG02055.hp2 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1122-1712_1122-170 others(9): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942028 | ||||||
| chr16:57942256
|
G | A | 1 | a0006c0083t0043g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1122-1935C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942256 | ||||||
| chr16:57942429
|
T | C | 1 | a0001c0004t0001g0119 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1122-2108A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942429 | ||||||
| chr16:57942561
|
G | A | 14 | a0001c0002t0001g0032a0002c0006t0006g0323a0004c0014t0001g0345others(11): Show | 14 | HG00423.hp2 HG01169.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1122-2240C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942561 | ||||||
| chr16:57942563
|
C | T | 30 | a0001c0002t0001g0056a0001c0007t0003g0340a0001c0007t0008g0356others(27): Show | 30 | HG00423.hp2 HG01168.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1122-2242G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942563 | ||||||
| chr16:57942653
|
G | A | 6 | a0001c0002t0001g0056a0001c0016t0010g0057a0001c0027t0003g0058others(3): Show | 6 | HG01891.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1122-2332C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942653 | ||||||
| chr16:57942682
|
C | T | 13 | a0002c0006t0006g0323a0004c0014t0001g0345a0004c0014t0016g0326others(10): Show | 13 | HG00423.hp2 HG02559.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1122-2361G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942682 | ||||||
| chr16:57942862
|
C | CA | 28 | a0001c0001t0013g0251a0001c0002t0005g0154a0001c0004t0001g0117others(25): Show | 28 | HG00423.hp2 HG00735.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.1122-2542dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942862 | ||||||
| chr16:57942862
|
CA | C | 7 | a0001c0004t0002g0178a0001c0029t0002g0034a0002c0005t0003g0106others(4): Show | 7 | HG02055.hp1 HG02723.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.1122-2542delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942862 | ||||||
| chr16:57942862
|
CAA | C | 32 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(29): Show | 32 | HG00544.hp1 HG00609.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.1122-2543_1122-254 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942862 | ||||||
| chr16:57942870
|
A | G | 1 | a0001c0013t0001g0306 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1122-2549T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942870 | ||||||
| chr16:57942893
|
T | C | 2 | a0001c0028t0042g0069a0024c0047t0034g0350 | 2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1122-2572A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942893 | ||||||
| chr16:57942952
|
A | G | 6 | a0001c0007t0003g0004a0001c0015t0002g0006a0001c0016t0046g0054others(3): Show | 6 | HG02559.hp2 HG02622.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1122-2631T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942952 | ||||||
| chr16:57943123
|
A | G | 1 | a0027c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1122-2802T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57943123 | ||||||
| chr16:57943243
|
G | A | 26 | a0001c0001t0012g0212a0001c0003t0001g0214a0001c0003t0003g0215others(23): Show | 26 | HG00140.hp2 HG00423.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1122-2922C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57943243 | ||||||
| chr16:57943348
|
C | CGT | 6 | a0001c0007t0003g0340a0001c0007t0008g0356a0001c0015t0001g0335others(3): Show | 6 | HG01168.hp1 HG02257.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1122-3028_1122-302 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57943348 | ||||||
| chr16:57943437
|
C | T | 1 | a0001c0001t0017g0225 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1122-3116G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57943437 | ||||||
| chr16:57943546
|
T | C | 1 | a0001c0041t0005g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1122-3225A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57943546 | ||||||
| chr16:57943854
|
G | A | 12 | a0002c0005t0001g0098a0002c0005t0003g0106a0002c0005t0006g0097others(9): Show | 12 | NA18940.hp2 NA18945.hp2 NA18959.hp1 others(9): Show |
intron_variant | MODIFIER | c.1122-3533C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57943854 | ||||||
| chr16:57943921
|
T | C | 1 | a0002c0038t0010g0103 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1122-3600A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57943921 | ||||||
| chr16:57944036
|
T | C | 3 | a0001c0002t0003g0008a0002c0011t0004g0066a0002c0022t0002g0074 | 3 | HG02647.hp2 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1122-3715A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944036 | ||||||
| chr16:57944077
|
G | A | 63 | a0001c0002t0001g0039a0001c0002t0001g0052a0001c0002t0001g0056others(60): Show | 63 | HG00423.hp2 HG00738.hp1 HG01168.hp1 others(60): Show |
intron_variant | MODIFIER | c.1122-3756C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944077 | ||||||
| chr16:57944343
|
AAGGAG | A | 3 | a0001c0007t0002g0073a0004c0014t0005g0346a0004c0044t0004g0343 | 3 | HG02145.hp2 HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1122-4027_1122-402 others(9): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944343 | ||||||
| chr16:57944633
|
C | T | 1 | a0001c0041t0005g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1122-4312G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944633 | ||||||
| chr16:57944737
|
T | C | 17 | a0001c0002t0001g0056a0001c0007t0003g0004a0001c0007t0003g0189others(14): Show | 17 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1122-4416A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944737 | ||||||
| chr16:57944744
|
C | T | 2 | a0001c0016t0046g0054a0043c0076t0003g0055 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1122-4423G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944744 | ||||||
| chr16:57944786
|
T | A | 1 | a0001c0003t0003g0198 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1122-4465A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944786 | ||||||
| chr16:57944825
|
A | G | 21 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(18): Show | 21 | HG00544.hp1 HG00609.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.1122-4504T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944825 | ||||||
| chr16:57944916
|
T | G | 1 | a0002c0006t0006g0323 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1121+4437A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944916 | ||||||
| chr16:57944951
|
T | TA | 74 | a0001c0001t0001g0237a0001c0001t0003g0208a0001c0001t0006g0242others(71): Show | 74 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1121+4401dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944951 | ||||||
| chr16:57944951
|
T | TAA | 14 | a0001c0002t0001g0162a0001c0002t0001g0329a0001c0004t0005g0182others(11): Show | 14 | HG01081.hp2 HG01175.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1121+4400_1121+440 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944951 | ||||||
| chr16:57944951
|
TA | T | 11 | a0001c0001t0002g0252a0001c0003t0001g0278a0001c0003t0003g0296others(8): Show | 11 | HG01070.hp1 HG01496.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1121+4401delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944951 | ||||||
| chr16:57944951
|
TAAAAAAA | T | 37 | a0001c0004t0001g0153a0002c0005t0001g0015a0002c0005t0001g0016others(34): Show | 37 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.1121+4395_1121+440 others(11): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944951 | ||||||
| chr16:57945241
|
A | G | 2 | a0001c0003t0005g0300a0001c0018t0001g0297 | 2 | HG02080.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1121+4112T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945241 | ||||||
| chr16:57945316
|
T | C | 1 | a0009c0061t0004g0049 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1121+4037A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945316 | ||||||
| chr16:57945351
|
G | C | 4 | a0001c0007t0003g0004a0001c0015t0002g0006a0017c0060t0015g0005others(1): Show | 4 | HG02559.hp2 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+4002C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945351 | ||||||
| chr16:57945428
|
G | A | 1 | a0002c0011t0004g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1121+3925C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945428 | ||||||
| chr16:57945508
|
T | C | 1 | a0027c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1121+3845A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945508 | ||||||
| chr16:57945615
|
G | C | 30 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(27): Show | 30 | HG00544.hp1 HG00609.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.1121+3738C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945615 | ||||||
| chr16:57945692
|
A | G | 8 | a0002c0005t0001g0314a0002c0005t0001g0316a0002c0006t0016g0110others(5): Show | 8 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1121+3661T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945692 | ||||||
| chr16:57945733
|
C | T | 16 | a0002c0011t0004g0185a0002c0109t0004g0108a0004c0014t0001g0345others(13): Show | 16 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1121+3620G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945733 | ||||||
| chr16:57945789
|
G | A | 1 | a0001c0003t0012g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1121+3564C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945789 | ||||||
| chr16:57945877
|
G | T | 17 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(14): Show | 17 | HG00544.hp1 HG00609.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1121+3476C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945877 | ||||||
| chr16:57946004
|
A | T | 7 | a0001c0001t0001g0234a0001c0001t0002g0250a0001c0001t0013g0251others(4): Show | 7 | HG00639.hp2 HG00735.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121+3349T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946004 | ||||||
| chr16:57946006
|
G | T | 3 | a0001c0001t0001g0205a0001c0001t0001g0233a0001c0003t0002g0245 | 3 | HG02015.hp2 NA18747.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1121+3347C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946006 | ||||||
| chr16:57946106
|
G | T | 1 | a0001c0007t0003g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1121+3247C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946106 | ||||||
| chr16:57946260
|
T | G | 8 | a0006c0081t0021g0331a0006c0082t0010g0337a0006c0083t0043g0063others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1121+3093A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946260 | ||||||
| chr16:57946347
|
G | A | 1 | a0001c0001t0002g0309 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1121+3006C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946347 | ||||||
| chr16:57946387
|
G | A | 1 | a0050c0121t0011g0315 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1121+2966C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946387 | ||||||
| chr16:57946398
|
C | T | 31 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(28): Show | 31 | HG00544.hp1 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.1121+2955G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946398 | ||||||
| chr16:57946424
|
C | T | 1 | a0049c0108t0004g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1121+2929G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946424 | ||||||
| chr16:57946449
|
G | A | 2 | a0007c0020t0007g0007a0049c0108t0004g0061 | 2 | HG01891.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1121+2904C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946449 | ||||||
| chr16:57946680
|
C | T | 1 | a0002c0006t0013g0083 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1121+2673G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946680 | ||||||
| chr16:57946800
|
G | T | 12 | a0001c0001t0007g0290a0001c0001t0012g0212a0001c0002t0001g0329others(9): Show | 12 | HG00140.hp2 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.1121+2553C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946800 | ||||||
| chr16:57946876
|
T | C | 8 | a0006c0081t0021g0331a0006c0082t0010g0337a0006c0083t0043g0063others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1121+2477A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946876 | ||||||
| chr16:57946907
|
G | A | 1 | a0001c0007t0003g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1121+2446C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946907 | ||||||
| chr16:57946962
|
C | T | 1 | a0048c0117t0026g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1121+2391G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946962 | ||||||
| chr16:57947101
|
G | C | 3 | a0001c0004t0001g0165a0002c0005t0001g0024a0002c0005t0001g0026 | 3 | HG02132.hp1 NA18974.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1121+2252C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947101 | ||||||
| chr16:57947123
|
C | A | 1 | a0001c0029t0002g0163 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1121+2230G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947123 | ||||||
| chr16:57947145
|
A | G | 1 | a0001c0001t0001g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1121+2208T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947145 | ||||||
| chr16:57947162
|
A | ATG | 8 | a0006c0081t0021g0331a0006c0082t0010g0337a0006c0083t0043g0063others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1121+2189_1121+219 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947162 | ||||||
| chr16:57947314
|
G | T | 1 | a0049c0108t0004g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1121+2039C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947314 | ||||||
| chr16:57947331
|
G | A | 1 | a0046c0107t0006g0099 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1121+2022C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947331 | ||||||
| chr16:57947411
|
T | G | 1 | a0002c0005t0006g0089 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1121+1942A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947411 | ||||||
| chr16:57947452
|
G | A | 3 | a0001c0004t0003g0136a0001c0004t0008g0135a0001c0070t0007g0134 | 3 | HG00099.hp2 HG00738.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1121+1901C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947452 | ||||||
| chr16:57947488
|
A | G | 1 | a0001c0004t0001g0119 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1121+1865T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947488 | ||||||
| chr16:57947981
|
T | G | 1 | a0039c0072t0001g0137 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1121+1372A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947981 | ||||||
| chr16:57948051
|
C | T | 1 | a0001c0003t0001g0199 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1121+1302G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948051 | ||||||
| chr16:57948053
|
C | T | 1 | a0001c0004t0001g0117 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1121+1300G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948053 | ||||||
| chr16:57948174
|
A | C | 175 | a0001c0001t0001g0207a0001c0001t0003g0208a0001c0001t0013g0206others(172): Show | 175 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.1121+1179T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948174 | ||||||
| chr16:57948179
|
A | G | 1 | a0001c0029t0002g0163 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1121+1174T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948179 | ||||||
| chr16:57948220
|
C | T | 1 | a0026c0080t0015g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1121+1133G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948220 | ||||||
| chr16:57948252
|
T | C | 12 | a0004c0014t0001g0345a0004c0014t0005g0346a0004c0014t0016g0326others(9): Show | 12 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1121+1101A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948252 | ||||||
| chr16:57948256
|
A | G | 1 | a0002c0006t0021g0187 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1121+1097T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948256 | ||||||
| chr16:57948313
|
CTTCTT | C | 30 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(27): Show | 30 | HG00544.hp1 HG00609.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.1121+1035_1121+103 others(9): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948313 | ||||||
| chr16:57948316
|
CTT | C | 251 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(248): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1121+1035_1121+103 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948316 | ||||||
| chr16:57948319
|
T | C | 2 | a0003c0008t0003g0145a0003c0008t0009g0146 | 2 | HG00558.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1121+1034A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948319 | ||||||
| chr16:57948321
|
T | C | 7 | a0001c0001t0002g0238a0001c0003t0001g0228a0001c0003t0002g0196others(4): Show | 7 | NA18939.hp2 NA18943.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121+1032A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948321 | ||||||
| chr16:57948407
|
G | A | 8 | a0001c0002t0001g0056a0001c0016t0010g0057a0001c0027t0003g0058others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1121+946C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948407 | ||||||
| chr16:57948432
|
G | A | 92 | a0001c0001t0001g0207a0001c0001t0003g0208a0001c0001t0013g0206others(89): Show | 92 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.1121+921C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948432 | ||||||
| chr16:57948533
|
C | G | 3 | a0001c0007t0003g0004a0001c0015t0002g0006a0017c0060t0015g0005 | 3 | HG02559.hp2 HG02895.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1121+820G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948533 | ||||||
| chr16:57948562
|
C | A | 1 | a0003c0008t0002g0002 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1121+791G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948562 | ||||||
| chr16:57948693
|
C | T | 1 | a0001c0001t0007g0290 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1121+660G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948693 | ||||||
| chr16:57948740
|
A | G | 139 | a0001c0001t0001g0207a0001c0001t0003g0208a0001c0001t0013g0206others(136): Show | 139 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.1121+613T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948740 | ||||||
| chr16:57948755
|
G | A | 2 | a0010c0010t0008g0090a0010c0010t0008g0102 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1121+598C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948755 | ||||||
| chr16:57948833
|
G | A | 1 | a0002c0011t0004g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1121+520C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948833 | ||||||
| chr16:57949054
|
G | A | 1 | a0001c0002t0003g0031 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1121+299C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57949054 | ||||||
| chr16:57949131
|
T | TG | 5 | a0001c0003t0001g0270a0001c0004t0001g0138a0007c0020t0007g0007others(2): Show | 5 | HG01891.hp2 HG02015.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1121+221dupC | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57949131 | ||||||
| chr16:57949133
|
T | A | 1 | a0007c0020t0007g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1121+220A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57949133 | ||||||
| chr16:57949133
|
T | G | 278 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(275): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.1121+220A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57949133 | ||||||
| chr16:57949134
|
G | C | 5 | a0001c0002t0001g0040a0001c0003t0001g0199a0001c0013t0018g0294others(2): Show | 5 | HG00609.hp2 HG01515.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121+219C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57949134 | ||||||
| chr16:57949324
|
G | A | 2 | a0001c0004t0001g0117a0042c0057t0002g0147 | 2 | HG03239.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1121+29C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57949324 | ||||||
| chr16:57949447
|
G | A | 2 | a0015c0031t0004g0333a0015c0031t0004g0334 | 2 | HG02896.hp1 HG02897.hp1 |
splice_region_variant&intron_variant | LOW | c.1035-8C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 13/32 | chr16 | 57949447 | ||||||
| chr16:57949664
|
T | C | 1 | a0009c0077t0004g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1035-225A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 13/32 | chr16 | 57949664 | ||||||
| chr16:57949778
|
A | T | 5 | a0002c0005t0041g0068a0002c0006t0016g0110a0002c0114t0010g0357others(2): Show | 5 | HG02109.hp2 HG02486.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1035-339T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 13/32 | chr16 | 57949778 | ||||||
| chr16:57949807
|
C | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(108): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1035-368G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 13/32 | chr16 | 57949807 | ||||||
| chr16:57949808
|
G | A | 1 | a0001c0002t0005g0154 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1035-369C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 13/32 | chr16 | 57949808 | ||||||
| chr16:57949850
|
T | C | 1 | a0001c0103t0029g0272 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1035-411A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 13/32 | chr16 | 57949850 | ||||||
| chr16:57949859
|
A | G | 1 | a0001c0002t0001g0329 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1035-420T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 13/32 | chr16 | 57949859 | ||||||
| chr16:57949887
|
G | A | 1 | a0001c0002t0005g0129 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1035-448C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 13/32 | chr16 | 57949887 | ||||||
| chr16:57949999
|
A | G | 105 | a0001c0001t0001g0207a0001c0001t0003g0208a0001c0001t0013g0206others(102): Show | 105 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.1034+382T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 13/32 | chr16 | 57949999 | ||||||
| chr16:57950575
|
G | A | 1 | a0027c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.875-35C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950575 | ||||||
| chr16:57950579
|
G | A | 354 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(351): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.875-39C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950579 | ||||||
| chr16:57950606
|
C | CCAGGGAG others(4): Show |
36 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(33): Show | 36 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.875-77_875-67dupCA others(9): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950606 | ||||||
| chr16:57950675
|
TG | T | 8 | a0006c0081t0021g0331a0006c0082t0010g0337a0006c0083t0043g0063others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.875-136delC | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950675 | ||||||
| chr16:57950785
|
G | A | 9 | a0001c0001t0001g0195a0001c0001t0001g0275a0001c0001t0001g0276others(6): Show | 9 | NA18947.hp1 NA18948.hp2 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.875-245C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950785 | ||||||
| chr16:57950810
|
G | T | 6 | a0001c0007t0003g0340a0001c0007t0008g0356a0001c0015t0001g0335others(3): Show | 6 | HG01168.hp1 HG02257.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.875-270C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950810 | ||||||
| chr16:57950818
|
C | A | 1 | a0037c0071t0006g0148 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.875-278G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950818 | ||||||
| chr16:57950818
|
C | T | 1 | a0049c0108t0004g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.875-278G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950818 | ||||||
| chr16:57950944
|
TTGTCCTG others(3): Show |
T | 6 | a0001c0002t0001g0056a0001c0016t0010g0057a0001c0027t0003g0058others(3): Show | 6 | HG01891.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.875-414_875-405del others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950944 | ||||||
| chr16:57950986
|
T | C | 10 | a0001c0007t0003g0189a0001c0053t0004g0200a0002c0005t0001g0314others(7): Show | 10 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.875-446A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950986 | ||||||
| chr16:57950991
|
A | G | 101 | a0001c0001t0001g0207a0001c0001t0003g0208a0001c0001t0013g0206others(98): Show | 101 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.875-451T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950991 | ||||||
| chr16:57951014
|
G | T | 1 | a0001c0003t0032g0109 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.875-474C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57951014 | ||||||
| chr16:57951194
|
G | C | 1 | a0027c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.875-654C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57951194 | ||||||
| chr16:57951436
|
C | G | 1 | a0022c0050t0003g0352 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.875-896G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57951436 | ||||||
| chr16:57951538
|
T | G | 2 | a0002c0022t0018g0112a0002c0113t0003g0318 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.875-998A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57951538 | ||||||
| chr16:57951938
|
A | T | 8 | a0006c0081t0021g0331a0006c0082t0010g0337a0006c0083t0043g0063others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.875-1398T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57951938 | ||||||
| chr16:57951957
|
C | T | 27 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(24): Show | 27 | HG00544.hp1 HG00609.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.875-1417G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57951957 | ||||||
| chr16:57951958
|
T | C | 9 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0281others(6): Show | 9 | HG00408.hp2 HG00609.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.875-1418A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57951958 | ||||||
| chr16:57951981
|
T | A | 1 | a0030c0092t0001g0285 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.875-1441A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57951981 | ||||||
| chr16:57952060
|
C | G | 144 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(141): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.875-1520G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952060 | ||||||
| chr16:57952141
|
G | A | 1 | a0008c0025t0001g0122 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.875-1601C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952141 | ||||||
| chr16:57952230
|
C | A | 5 | a0001c0002t0001g0056a0001c0016t0010g0057a0001c0027t0003g0058others(2): Show | 5 | HG01891.hp1 HG02809.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.875-1690G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952230 | ||||||
| chr16:57952301
|
G | A | 1 | a0001c0028t0044g0064 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.875-1761C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952301 | ||||||
| chr16:57952311
|
T | C | 4 | a0001c0007t0003g0004a0001c0015t0002g0006a0017c0060t0015g0005others(1): Show | 4 | HG02559.hp2 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.875-1771A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952311 | ||||||
| chr16:57952333
|
G | A | 5 | a0001c0004t0006g0149a0003c0008t0002g0002a0010c0010t0008g0090others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.875-1793C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952333 | ||||||
| chr16:57952493
|
C | CT | 131 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(128): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.875-1954dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952493 | ||||||
| chr16:57952493
|
C | CTT | 30 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237others(27): Show | 30 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.875-1955_875-1954d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952493 | ||||||
| chr16:57952493
|
CT | C | 21 | a0001c0002t0007g0126a0001c0004t0001g0150a0001c0004t0001g0153others(18): Show | 21 | HG01069.hp2 HG01074.hp1 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.875-1954delA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952493 | ||||||
| chr16:57952493
|
CTT | C | 68 | a0001c0004t0001g0165a0002c0005t0001g0013a0002c0005t0001g0014others(65): Show | 68 | HG00323.hp2 HG00423.hp1 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.875-1955_875-1954d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952493 | ||||||
| chr16:57952493
|
CTTT | C | 8 | a0002c0005t0001g0026a0002c0006t0001g0100a0002c0006t0006g0323others(5): Show | 8 | HG00423.hp2 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.875-1956_875-1954d others(5): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952493 | ||||||
| chr16:57952660
|
C | T | 1 | a0001c0002t0033g0053 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.875-2120G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952660 | ||||||
| chr16:57952875
|
T | TCTG | 11 | a0001c0007t0003g0189a0001c0053t0004g0200a0002c0005t0001g0314others(8): Show | 11 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.875-2338_875-2336d others(5): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952875 | ||||||
| chr16:57952880
|
A | C | 11 | a0001c0007t0003g0189a0001c0053t0004g0200a0002c0005t0001g0314others(8): Show | 11 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.875-2340T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952880 | ||||||
| chr16:57952958
|
G | C | 8 | a0006c0081t0021g0331a0006c0082t0010g0337a0006c0083t0043g0063others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.875-2418C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952958 | ||||||
| chr16:57952976
|
G | A | 1 | a0002c0022t0008g0011 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.875-2436C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952976 | ||||||
| chr16:57953019
|
C | T | 8 | a0001c0002t0001g0056a0001c0016t0010g0057a0001c0027t0003g0058others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.875-2479G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953019 | ||||||
| chr16:57953031
|
C | G | 6 | a0001c0007t0003g0340a0001c0007t0008g0356a0001c0015t0001g0335others(3): Show | 6 | HG01168.hp1 HG02257.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.875-2491G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953031 | ||||||
| chr16:57953033
|
G | T | 83 | a0001c0004t0001g0165a0002c0005t0001g0013a0002c0005t0001g0014others(80): Show | 83 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.875-2493C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953033 | ||||||
| chr16:57953061
|
G | A | 2 | a0015c0031t0004g0333a0015c0031t0004g0334 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.875-2521C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953061 | ||||||
| chr16:57953100
|
G | A | 8 | a0006c0081t0021g0331a0006c0082t0010g0337a0006c0083t0043g0063others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.875-2560C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953100 | ||||||
| chr16:57953268
|
C | T | 2 | a0002c0022t0018g0112a0002c0113t0003g0318 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.875-2728G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953268 | ||||||
| chr16:57953306
|
C | T | 2 | a0002c0022t0018g0112a0002c0113t0003g0318 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.875-2766G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953306 | ||||||
| chr16:57953419
|
C | T | 1 | a0001c0003t0012g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.875-2879G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953419 | ||||||
| chr16:57953493
|
T | TA | 91 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(88): Show | 91 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.875-2954dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953493 | ||||||
| chr16:57953493
|
T | TAA | 14 | a0001c0007t0003g0189a0001c0007t0003g0340a0001c0007t0008g0356others(11): Show | 14 | HG00423.hp1 HG01168.hp1 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.875-2955_875-2954d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953493 | ||||||
| chr16:57953493
|
TA | T | 32 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0002t0001g0056others(29): Show | 32 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.875-2954delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953493 | ||||||
| chr16:57953555
|
G | A | 3 | a0001c0001t0007g0290a0001c0013t0004g0308a0003c0009t0039g0307 | 3 | HG01358.hp2 HG01361.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.875-3015C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953555 | ||||||
| chr16:57953791
|
C | T | 1 | a0001c0002t0005g0154 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.875-3251G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953791 | ||||||
| chr16:57953793
|
G | A | 12 | a0004c0014t0001g0345a0004c0014t0005g0346a0004c0014t0016g0326others(9): Show | 12 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.875-3253C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953793 | ||||||
| chr16:57953865
|
C | A | 75 | a0001c0004t0001g0165a0002c0005t0001g0013a0002c0005t0001g0014others(72): Show | 75 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.875-3325G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953865 | ||||||
| chr16:57953888
|
G | GA | 9 | a0002c0005t0001g0332a0006c0081t0021g0331a0006c0082t0010g0337others(6): Show | 9 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.875-3349dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953888 | ||||||
| chr16:57953892
|
A | G | 24 | a0001c0002t0001g0056a0001c0007t0003g0004a0001c0015t0002g0006others(21): Show | 24 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.875-3352T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953892 | ||||||
| chr16:57954281
|
C | T | 3 | a0002c0005t0001g0015a0002c0005t0001g0016a0018c0055t0025g0042 | 3 | HG01123.hp2 HG01261.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.874+3060G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57954281 | ||||||
| chr16:57954429
|
C | T | 258 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(255): Show | 261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.874+2912G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57954429 | ||||||
| chr16:57954447
|
T | G | 1 | a0001c0002t0001g0329 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.874+2894A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57954447 | ||||||
| chr16:57954560
|
C | A | 3 | a0004c0048t0016g0354a0014c0023t0002g0349a0023c0043t0011g0351 | 3 | HG02559.hp1 HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.874+2781G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57954560 | ||||||
| chr16:57954582
|
C | T | 80 | a0001c0002t0001g0032a0001c0002t0001g0125a0001c0002t0001g0141others(77): Show | 82 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.874+2759G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57954582 | ||||||
| chr16:57954731
|
TTGGTGTC others(24): Show |
T | 2 | a0002c0005t0001g0015a0002c0005t0001g0016 | 2 | HG01261.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.874+2579_874+2609d others(33): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57954731 | ||||||
| chr16:57954801
|
T | C | 1 | a0021c0039t0002g0305 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.874+2540A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57954801 | ||||||
| chr16:57954893
|
A | G | 6 | a0002c0005t0001g0314a0002c0005t0001g0316a0002c0011t0018g0341others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.874+2448T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57954893 | ||||||
| chr16:57954959
|
C | T | 4 | a0001c0007t0003g0004a0001c0015t0002g0006a0017c0060t0015g0005others(1): Show | 4 | HG02559.hp2 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.874+2382G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57954959 | ||||||
| chr16:57955077
|
T | C | 1 | a0002c0011t0004g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.874+2264A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57955077 | ||||||
| chr16:57955169
|
A | C | 1 | a0002c0011t0004g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.874+2172T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57955169 | ||||||
| chr16:57955259
|
G | C | 1 | a0001c0001t0001g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.874+2082C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57955259 | ||||||
| chr16:57955277
|
G | A | 1 | a0002c0037t0003g0092 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.874+2064C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57955277 | ||||||
| chr16:57955387
|
C | T | 8 | a0006c0081t0021g0331a0006c0082t0010g0337a0006c0083t0043g0063others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.874+1954G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57955387 | ||||||
| chr16:57955413
|
G | T | 6 | a0001c0002t0001g0056a0001c0016t0010g0057a0001c0027t0003g0058others(3): Show | 6 | HG01891.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.874+1928C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57955413 | ||||||
| chr16:57955890
|
T | G | 1 | a0035c0094t0002g0295 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.874+1451A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57955890 | ||||||
| chr16:57956070
|
A | G | 1 | a0002c0109t0004g0108 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.874+1271T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956070 | ||||||
| chr16:57956173
|
G | A | 1 | a0001c0003t0005g0300 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.874+1168C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956173 | ||||||
| chr16:57956247
|
T | C | 9 | a0002c0005t0001g0098a0002c0005t0006g0097a0002c0006t0001g0095others(6): Show | 9 | NA18945.hp2 NA18959.hp1 NA18967.hp1 others(6): Show |
intron_variant | MODIFIER | c.874+1094A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956247 | ||||||
| chr16:57956275
|
G | A | 10 | a0001c0002t0001g0056a0001c0016t0010g0057a0001c0016t0046g0054others(7): Show | 10 | HG01891.hp1 HG02055.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.874+1066C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956275 | ||||||
| chr16:57956331
|
A | G | 10 | a0001c0002t0001g0056a0001c0016t0010g0057a0001c0016t0046g0054others(7): Show | 10 | HG01891.hp1 HG02055.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.874+1010T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956331 | ||||||
| chr16:57956492
|
C | T | 1 | a0027c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.874+849G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956492 | ||||||
| chr16:57956532
|
G | A | 8 | a0006c0081t0021g0331a0006c0082t0010g0337a0006c0083t0043g0063others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.874+809C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956532 | ||||||
| chr16:57956556
|
G | T | 2 | a0002c0022t0018g0112a0002c0113t0003g0318 | 2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.874+785C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956556 | ||||||
| chr16:57956560
|
A | G | 1 | a0001c0017t0001g0114 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.874+781T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956560 | ||||||
| chr16:57956578
|
A | G | 143 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(140): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.874+763T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956578 | ||||||
| chr16:57956630
|
A | G | 12 | a0004c0014t0001g0345a0004c0014t0005g0346a0004c0014t0016g0326others(9): Show | 12 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.874+711T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956630 | ||||||
| chr16:57956746
|
C | G | 1 | a0003c0074t0009g0177 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.874+595G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956746 | ||||||
| chr16:57956837
|
G | A | 10 | a0001c0002t0001g0056a0001c0016t0010g0057a0001c0016t0046g0054others(7): Show | 10 | HG01891.hp1 HG02055.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.874+504C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956837 | ||||||
| chr16:57956927
|
G | A | 3 | a0002c0011t0004g0185a0017c0062t0027g0324a0027c0078t0011g0353 | 3 | HG02055.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.874+414C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956927 | ||||||
| chr16:57956956
|
A | C | 114 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(111): Show | 115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.874+385T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956956 | ||||||
| chr16:57957113
|
A | G | 116 | a0001c0002t0001g0056a0001c0004t0001g0165a0001c0007t0003g0189others(113): Show | 116 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.874+228T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57957113 | ||||||
| chr16:57957218
|
TG | T | 6 | a0001c0002t0001g0056a0001c0016t0010g0057a0001c0027t0003g0058others(3): Show | 6 | HG01891.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.874+122delC | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57957218 | ||||||
| chr16:57957219
|
GC | G | 263 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(260): Show | 264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.874+121delG | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57957219 | ||||||
| chr16:57957220
|
C | T | 6 | a0001c0002t0001g0056a0001c0016t0010g0057a0001c0027t0003g0058others(3): Show | 6 | HG01891.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.874+121G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57957220 | ||||||
| chr16:57957224
|
C | G | 1 | a0001c0002t0007g0126 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.874+117G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57957224 | ||||||
| chr16:57957413
|
C | T | 238 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(235): Show | 241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.838-36G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57957413 | ||||||
| chr16:57957456
|
A | G | 1 | a0001c0004t0001g0164 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.838-79T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57957456 | ||||||
| chr16:57957479
|
G | A | 1 | a0001c0053t0004g0200 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.838-102C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57957479 | ||||||
| chr16:57957550
|
G | C | 3 | a0001c0004t0035g0079a0001c0027t0040g0078a0008c0025t0023g0077 | 3 | HG02622.hp1 HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.838-173C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57957550 | ||||||
| chr16:57957555
|
G | A | 4 | a0001c0016t0046g0054a0001c0041t0005g0028a0001c0042t0011g0029others(1): Show | 4 | HG02055.hp2 HG02622.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.838-178C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57957555 | ||||||
| chr16:57957598
|
G | A | 3 | a0001c0004t0001g0115a0001c0004t0001g0164a0001c0004t0001g0166 | 3 | NA18943.hp1 NA18957.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.838-221C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57957598 | ||||||
| chr16:57957631
|
A | G | 1 | a0026c0080t0015g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.838-254T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57957631 | ||||||
| chr16:57957777
|
A | G | 1 | a0001c0007t0002g0073 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.838-400T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57957777 | ||||||
| chr16:57958165
|
C | A | 12 | a0004c0014t0001g0345a0004c0014t0005g0346a0004c0014t0016g0326others(9): Show | 12 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.837+245G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57958165 | ||||||
| chr16:57958198
|
G | A | 1 | a0002c0011t0004g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.837+212C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57958198 | ||||||
| chr16:57958215
|
T | A | 141 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(138): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.837+195A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57958215 | ||||||
| chr16:57958325
|
G | GGGTCCCT others(34): Show |
115 | a0001c0002t0001g0056a0001c0004t0001g0165a0001c0007t0003g0189others(112): Show | 115 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.837+84_837+85insTG others(39): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57958325 | ||||||
| chr16:57958508
|
G | A | 1 | a0001c0035t0028g0291 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.762-23C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958508 | ||||||
| chr16:57958520
|
G | A | 17 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(14): Show | 17 | HG00544.hp1 HG00609.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.762-35C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958520 | ||||||
| chr16:57958549
|
G | A | 6 | a0002c0005t0001g0314a0002c0005t0001g0316a0002c0011t0018g0341others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.762-64C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958549 | ||||||
| chr16:57958595
|
C | G | 29 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(26): Show | 29 | HG00544.hp1 HG00609.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.762-110G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958595 | ||||||
| chr16:57958627
|
C | G | 1 | a0001c0097t0003g0231 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.762-142G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958627 | ||||||
| chr16:57958650
|
C | T | 7 | a0001c0007t0003g0189a0001c0007t0003g0340a0001c0007t0008g0356others(4): Show | 7 | HG01168.hp1 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.762-165G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958650 | ||||||
| chr16:57958677
|
G | T | 1 | a0001c0035t0010g0230 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.762-192C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958677 | ||||||
| chr16:57958699
|
C | T | 1 | a0001c0003t0002g0201 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.762-214G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958699 | ||||||
| chr16:57958712
|
C | T | 1 | a0002c0011t0004g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.762-227G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958712 | ||||||
| chr16:57958718
|
C | T | 95 | a0001c0002t0001g0032a0001c0002t0001g0125a0001c0002t0001g0141others(92): Show | 97 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.762-233G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958718 | ||||||
| chr16:57958729
|
G | A | 1 | a0001c0002t0001g0125 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.762-244C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958729 | ||||||
| chr16:57958849
|
A | G | 240 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(237): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.762-364T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958849 | ||||||
| chr16:57958921
|
C | CT | 79 | a0001c0002t0001g0141a0001c0002t0001g0155a0001c0002t0001g0162others(76): Show | 81 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.762-437dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958921 | ||||||
| chr16:57958921
|
C | CTT | 7 | a0001c0002t0001g0125a0001c0002t0002g0124a0001c0007t0002g0073others(4): Show | 7 | HG01255.hp1 HG01346.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.762-438_762-437dup others(2): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958921 | ||||||
| chr16:57958921
|
CT | C | 151 | a0001c0001t0001g0195a0001c0001t0001g0207a0001c0001t0001g0227others(148): Show | 151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.762-437delA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958921 | ||||||
| chr16:57958921
|
CTT | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0205a0001c0002t0001g0052others(10): Show | 14 | HG00323.hp1 HG01358.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.762-438_762-437del others(2): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958921 | ||||||
| chr16:57959004
|
T | C | 3 | a0002c0011t0004g0066a0002c0022t0002g0074a0002c0109t0004g0108 | 3 | HG02647.hp2 HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.762-519A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959004 | ||||||
| chr16:57959131
|
C | T | 1 | a0002c0005t0001g0332 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.762-646G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959131 | ||||||
| chr16:57959149
|
T | C | 1 | a0002c0038t0010g0103 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.762-664A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959149 | ||||||
| chr16:57959384
|
C | T | 1 | a0003c0009t0007g0080 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.761+504G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959384 | ||||||
| chr16:57959397
|
T | C | 1 | a0002c0005t0001g0332 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.761+491A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959397 | ||||||
| chr16:57959435
|
G | T | 3 | a0015c0031t0004g0333a0015c0031t0004g0334a0026c0080t0015g0188 | 3 | HG02280.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.761+453C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959435 | ||||||
| chr16:57959454
|
A | G | 8 | a0006c0081t0021g0331a0006c0082t0010g0337a0006c0083t0043g0063others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.761+434T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959454 | ||||||
| chr16:57959566
|
C | A | 142 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(139): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.761+322G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959566 | ||||||
| chr16:57959588
|
C | T | 1 | a0022c0050t0003g0352 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.761+300G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959588 | ||||||
| chr16:57959605
|
AAAAC | A | 179 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(176): Show | 180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.761+279_761+282del others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959605 | ||||||
| chr16:57959605
|
AAAACAAA others(1): Show |
A | 85 | a0001c0002t0001g0032a0001c0002t0001g0125a0001c0002t0001g0141others(82): Show | 87 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.761+275_761+282del others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959605 | ||||||
| chr16:57959697
|
C | T | 1 | a0007c0021t0003g0105 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.761+191G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959697 | ||||||
| chr16:57959723
|
T | C | 2 | a0001c0004t0001g0165a0002c0005t0001g0026 | 2 | NA18974.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.761+165A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959723 | ||||||
| chr16:57959866
|
C | T | 1 | a0002c0109t0004g0108 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.761+22G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959866 | ||||||
| chr16:57959873
|
T | C | 2 | a0004c0046t0036g0348a0014c0023t0002g0347 | 2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.761+15A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959873 | ||||||
| chr16:57960148
|
G | C | 1 | a0002c0006t0006g0323 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.584-83C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 9/32 | chr16 | 57960148 | ||||||
| chr16:57960331
|
C | A | 143 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(140): Show | 144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.583+151G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 9/32 | chr16 | 57960331 | ||||||
| chr16:57960437
|
C | T | 14 | a0002c0005t0001g0332a0002c0006t0006g0323a0004c0014t0001g0345others(11): Show | 14 | HG00423.hp2 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.583+45G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 9/32 | chr16 | 57960437 | ||||||
| chr16:57960438
|
G | A | 1 | a0001c0015t0002g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.583+44C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 9/32 | chr16 | 57960438 | ||||||
| chr16:57960591
|
C | T | 13 | a0002c0005t0001g0332a0004c0014t0001g0345a0004c0014t0005g0346others(10): Show | 13 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.535-61G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 8/32 | chr16 | 57960591 | ||||||
| chr16:57960711
|
A | T | 3 | a0001c0001t0001g0227a0001c0001t0006g0226a0001c0003t0002g0191 | 3 | HG00733.hp1 NA18959.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.534+129T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 8/32 | chr16 | 57960711 | ||||||
| chr16:57960764
|
G | C | 1 | a0001c0003t0003g0296 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.534+76C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 8/32 | chr16 | 57960764 | ||||||
| chr16:57960820
|
C | T | 80 | a0001c0002t0001g0032a0001c0002t0001g0125a0001c0002t0001g0141others(77): Show | 82 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.534+20G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 8/32 | chr16 | 57960820 | ||||||
| chr16:57960833
|
G | C | 8 | a0006c0081t0021g0331a0006c0082t0010g0337a0006c0083t0043g0063others(5): Show | 8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.534+7C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 8/32 | chr16 | 57960833 | ||||||
| chr16:57961175
|
C | T | 1 | a0022c0050t0003g0352 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.459-260G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961175 | ||||||
| chr16:57961208
|
C | T | 3 | a0001c0001t0002g0223a0001c0001t0003g0224a0001c0001t0017g0225 | 3 | HG00597.hp1 NA18960.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.459-293G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961208 | ||||||
| chr16:57961394
|
C | G | 1 | a0002c0011t0004g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.459-479G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961394 | ||||||
| chr16:57961422
|
A | C | 1 | a0020c0118t0001g0302 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.459-507T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961422 | ||||||
| chr16:57961497
|
G | C | 12 | a0004c0014t0001g0345a0004c0014t0005g0346a0004c0014t0016g0326others(9): Show | 12 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.459-582C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961497 | ||||||
| chr16:57961518
|
G | A | 21 | a0001c0007t0003g0189a0001c0007t0003g0340a0001c0007t0008g0356others(18): Show | 21 | HG00423.hp2 HG01168.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.459-603C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961518 | ||||||
| chr16:57961550
|
C | T | 1 | a0001c0003t0003g0222 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.459-635G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961550 | ||||||
| chr16:57961631
|
G | GGAAT | 62 | a0001c0002t0001g0125a0001c0002t0001g0141a0001c0002t0001g0168others(59): Show | 64 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.459-720_459-717dup others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961631 | ||||||
| chr16:57961631
|
G | GGAATGAA others(1): Show |
8 | a0001c0002t0002g0121a0001c0004t0001g0115a0001c0004t0001g0118others(5): Show | 8 | HG00544.hp2 HG00741.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.459-724_459-717dup others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961631 | ||||||
| chr16:57961631
|
GGAAT | G | 132 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(129): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.459-720_459-717del others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961631 | ||||||
| chr16:57961631
|
GGAATGAA others(1): Show |
G | 33 | a0001c0002t0001g0035a0001c0002t0001g0039a0001c0002t0001g0040others(30): Show | 33 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.459-724_459-717del others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961631 | ||||||
| chr16:57961631
|
GGAATGAA others(5): Show |
G | 2 | a0002c0011t0004g0185a0006c0086t0003g0067 | 2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.459-728_459-717del others(12): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961631 | ||||||
| chr16:57961666
|
A | G | 1 | a0003c0104t0007g0218 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.459-751T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961666 | ||||||
| chr16:57961670
|
G | A | 1 | a0001c0004t0001g0166 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.459-755C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961670 | ||||||
| chr16:57962059
|
G | A | 4 | a0001c0002t0001g0168a0003c0012t0007g0167a0013c0024t0002g0169others(1): Show | 4 | HG01069.hp2 HG01071.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.458+506C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57962059 | ||||||
| chr16:57962266
|
T | C | 2 | a0001c0004t0001g0172a0001c0004t0002g0171 | 2 | HG02027.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.458+299A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57962266 | ||||||
| chr16:57962366
|
C | A | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.458+199G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57962366 | ||||||
| chr16:57962367
|
A | T | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.458+198T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57962367 | ||||||
| chr16:57962487
|
C | G | 1 | a0001c0001t0001g0195 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.458+78G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57962487 | ||||||
| chr16:57962488
|
C | T | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.458+77G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57962488 | ||||||
| chr16:57962659
|
C | A | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413-49G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962659 | ||||||
| chr16:57962661
|
C | A | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413-51G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962661 | ||||||
| chr16:57962665
|
C | A | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413-55G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962665 | ||||||
| chr16:57962667
|
C | T | 1 | a0001c0002t0003g0031 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.413-57G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962667 | ||||||
| chr16:57962670
|
G | T | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413-60C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962670 | ||||||
| chr16:57962690
|
C | T | 2 | a0002c0006t0006g0323a0002c0011t0004g0185 | 2 | HG00423.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.413-80G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962690 | ||||||
| chr16:57962707
|
C | A | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413-97G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962707 | ||||||
| chr16:57962711
|
G | A | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413-101C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962711 | ||||||
| chr16:57962717
|
A | C | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413-107T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962717 | ||||||
| chr16:57962744
|
C | A | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.412+98G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962744 | ||||||
| chr16:57962780
|
C | G | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.412+62G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962780 | ||||||
| chr16:57962790
|
C | T | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.412+52G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962790 | ||||||
| chr16:57962798
|
C | A | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.412+44G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962798 | ||||||
| chr16:57962808
|
G | A | 1 | a0001c0028t0042g0069 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.412+34C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962808 | ||||||
| chr16:57962834
|
G | T | 2 | a0002c0006t0006g0323a0025c0051t0001g0339 | 2 | HG00423.hp2 HG03139.hp2 |
splice_region_variant&intron_variant | LOW | c.412+8C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962834 | ||||||
| chr16:57962835
|
T | G | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | splice_region_variant&intron_variant | LOW | c.412+7A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962835 | ||||||
| chr16:57962931
|
C | A | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.381+43G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/32 | chr16 | 57962931 | ||||||
| chr16:57962941
|
C | T | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.381+33G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/32 | chr16 | 57962941 | ||||||
| chr16:57962943
|
C | A | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.381+31G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/32 | chr16 | 57962943 | ||||||
| chr16:57962944
|
G | C | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.381+30C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/32 | chr16 | 57962944 | ||||||
| chr16:57962946
|
C | G | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.381+28G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/32 | chr16 | 57962946 | ||||||
| chr16:57962948
|
C | A | 2 | a0001c0003t0001g0301a0025c0051t0001g0339 | 2 | HG03139.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.381+26G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/32 | chr16 | 57962948 | ||||||
| chr16:57962963
|
C | A | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.381+11G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/32 | chr16 | 57962963 | ||||||
| chr16:57962964
|
C | A | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.381+10G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/32 | chr16 | 57962964 | ||||||
| chr16:57962969
|
A | T | 1 | a0025c0051t0001g0339 | 1 | HG03139.hp2 | splice_region_variant&intron_variant | LOW | c.381+5T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/32 | chr16 | 57962969 | ||||||
| chr16:57963122
|
C | T | 13 | a0004c0014t0001g0345a0004c0014t0005g0346a0004c0014t0016g0326others(10): Show | 13 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.291-58G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963122 | ||||||
| chr16:57963373
|
G | A | 1 | a0026c0080t0015g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.291-309C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963373 | ||||||
| chr16:57963545
|
A | T | 6 | a0001c0001t0012g0212a0001c0003t0001g0214a0001c0003t0003g0215others(3): Show | 6 | HG00140.hp2 HG00735.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.291-481T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963545 | ||||||
| chr16:57963596
|
G | A | 1 | a0006c0083t0043g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.291-532C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963596 | ||||||
| chr16:57963596
|
G | C | 1 | a0002c0005t0005g0322 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.291-532C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963596 | ||||||
| chr16:57963605
|
G | T | 274 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(271): Show | 275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.290+525C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963605 | ||||||
| chr16:57963612
|
T | C | 2 | a0001c0004t0001g0173a0001c0004t0014g0192 | 2 | HG01123.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.290+518A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963612 | ||||||
| chr16:57963615
|
C | G | 1 | a0006c0083t0043g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.290+515G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963615 | ||||||
| chr16:57963689
|
A | C | 259 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(256): Show | 262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.290+441T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963689 | ||||||
| chr16:57963725
|
C | T | 7 | a0006c0081t0021g0331a0006c0082t0010g0337a0006c0083t0043g0063others(4): Show | 7 | HG02615.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.290+405G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963725 | ||||||
| chr16:57963752
|
A | G | 29 | a0001c0002t0001g0032a0001c0002t0001g0035a0001c0002t0001g0039others(26): Show | 29 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.290+378T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963752 | ||||||
| chr16:57964074
|
G | T | 1 | a0001c0007t0002g0073 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.290+56C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57964074 | ||||||
| chr16:57964075
|
G | T | 1 | a0001c0007t0002g0073 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.290+55C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57964075 | ||||||
| chr16:57964220
|
A | G | 7 | a0006c0081t0021g0331a0006c0082t0010g0337a0006c0083t0043g0063others(4): Show | 7 | HG02615.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.218-18T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 3/32 | chr16 | 57964220 | ||||||
| chr16:57964441
|
C | T | 255 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(252): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.217+46G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 3/32 | chr16 | 57964441 | ||||||
| chr16:57964639
|
A | G | 19 | a0001c0002t0001g0032a0001c0002t0001g0035a0001c0002t0001g0039others(16): Show | 19 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.160-95T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57964639 | ||||||
| chr16:57964734
|
G | A | 7 | a0006c0081t0021g0331a0006c0082t0010g0337a0006c0083t0043g0063others(4): Show | 7 | HG02615.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-190C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57964734 | ||||||
| chr16:57964742
|
C | T | 6 | a0001c0007t0003g0340a0001c0007t0008g0356a0001c0015t0001g0335others(3): Show | 6 | HG01168.hp1 HG02257.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-198G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57964742 | ||||||
| chr16:57964856
|
A | G | 1 | a0045c0079t0006g0194 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.160-312T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57964856 | ||||||
| chr16:57964869
|
A | G | 6 | a0001c0002t0001g0056a0001c0016t0010g0057a0001c0027t0003g0058others(3): Show | 6 | HG01891.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-325T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57964869 | ||||||
| chr16:57964884
|
G | C | 1 | a0001c0004t0001g0174 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.160-340C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57964884 | ||||||
| chr16:57964936
|
T | C | 175 | a0001c0002t0001g0032a0001c0002t0001g0035a0001c0002t0001g0039others(172): Show | 177 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.160-392A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57964936 | ||||||
| chr16:57965123
|
TACTC | T | 261 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(258): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.160-583_160-580del others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965123 | ||||||
| chr16:57965228
|
TAC | T | 278 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(275): Show | 279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.160-686_160-685del others(2): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965228 | ||||||
| chr16:57965281
|
A | T | 1 | a0001c0002t0001g0338 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.160-737T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965281 | ||||||
| chr16:57965299
|
A | G | 7 | a0001c0007t0003g0340a0001c0007t0008g0356a0001c0015t0001g0335others(4): Show | 7 | HG01168.hp1 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-755T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965299 | ||||||
| chr16:57965318
|
C | T | 1 | a0002c0005t0001g0332 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.160-774G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965318 | ||||||
| chr16:57965332
|
C | T | 76 | a0001c0002t0001g0125a0001c0002t0001g0141a0001c0002t0001g0155others(73): Show | 78 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.160-788G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965332 | ||||||
| chr16:57965338
|
T | G | 5 | a0001c0002t0001g0056a0001c0016t0010g0057a0001c0027t0003g0058others(2): Show | 5 | HG01891.hp1 HG02809.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.160-794A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965338 | ||||||
| chr16:57965340
|
T | A | 1 | a0001c0002t0003g0050 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.160-796A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965340 | ||||||
| chr16:57965403
|
G | A | 1 | a0001c0001t0002g0309 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.160-859C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965403 | ||||||
| chr16:57965497
|
G | A | 182 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(179): Show | 183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.160-953C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965497 | ||||||
| chr16:57965616
|
G | A | 120 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(117): Show | 121 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.160-1072C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965616 | ||||||
| chr16:57965657
|
T | TACACATA others(6): Show |
172 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(169): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.160-1114_160-1113i others(15): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965657 | ||||||
| chr16:57965718
|
TCAGA | T | 28 | a0001c0002t0001g0032a0001c0002t0001g0035a0001c0002t0001g0039others(25): Show | 28 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.160-1178_160-1175d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965718 | ||||||
| chr16:57965867
|
T | A | 172 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(169): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.159+1261A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965867 | ||||||
| chr16:57965907
|
G | A | 1 | a0001c0003t0032g0109 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.159+1221C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965907 | ||||||
| chr16:57966117
|
C | T | 1 | a0001c0028t0042g0069 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.159+1011G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57966117 | ||||||
| chr16:57966259
|
A | G | 188 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(185): Show | 189 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.159+869T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57966259 | ||||||
| chr16:57966320
|
A | G | 3 | a0001c0001t0001g0207a0001c0001t0003g0208a0001c0001t0013g0206 | 3 | NA18944.hp1 NA19002.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.159+808T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57966320 | ||||||
| chr16:57966449
|
T | C | 1 | a0006c0086t0003g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.159+679A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57966449 | ||||||
| chr16:57966623
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.159+505T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57966623 | ||||||
| chr16:57966675
|
A | G | 1 | a0001c0003t0012g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.159+453T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57966675 | ||||||
| chr16:57966810
|
C | T | 76 | a0001c0002t0001g0125a0001c0002t0001g0141a0001c0002t0001g0155others(73): Show | 78 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.159+318G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57966810 | ||||||
| chr16:57967096
|
C | T | 13 | a0004c0014t0001g0345a0004c0014t0005g0346a0004c0014t0016g0326others(10): Show | 13 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+32G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57967096 | ||||||
| chr16:57967412
|
G | A | 1 | a0017c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-8-118C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967412 | ||||||
| chr16:57967485
|
G | C | 1 | a0001c0068t0005g0175 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-8-191C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967485 | ||||||
| chr16:57967514
|
C | T | 1 | a0014c0023t0002g0349 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-8-220G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967514 | ||||||
| chr16:57967520
|
C | T | 1 | a0001c0003t0001g0202 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-8-226G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967520 | ||||||
| chr16:57967626
|
G | T | 170 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(167): Show | 171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-8-332C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967626 | ||||||
| chr16:57967726
|
T | C | 1 | a0012c0122t0003g0317 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-8-432A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967726 | ||||||
| chr16:57967757
|
T | C | 2 | a0007c0020t0007g0007a0049c0108t0004g0061 | 2 | HG01891.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-8-463A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967757 | ||||||
| chr16:57967779
|
G | A | 1 | a0005c0030t0003g0001 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-8-485C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967779 | ||||||
| chr16:57967814
|
G | A | 172 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(169): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.-8-520C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967814 | ||||||
| chr16:57967924
|
A | C | 2 | a0001c0015t0001g0335a0001c0015t0020g0336 | 2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-8-630T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967924 | ||||||
| chr16:57968006
|
C | T | 1 | a0002c0022t0008g0011 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-8-712G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968006 | ||||||
| chr16:57968025
|
G | A | 172 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(169): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.-8-731C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968025 | ||||||
| chr16:57968133
|
G | A | 1 | a0007c0021t0003g0105 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-8-839C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968133 | ||||||
| chr16:57968150
|
A | G | 1 | a0001c0004t0001g0117 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-8-856T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968150 | ||||||
| chr16:57968211
|
A | T | 2 | a0015c0031t0004g0333a0015c0031t0004g0334 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-8-917T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968211 | ||||||
| chr16:57968228
|
T | A | 1 | a0026c0080t0015g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-8-934A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968228 | ||||||
| chr16:57968465
|
C | G | 76 | a0001c0002t0001g0125a0001c0002t0001g0141a0001c0002t0001g0155others(73): Show | 78 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-8-1171G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968465 | ||||||
| chr16:57968499
|
A | T | 1 | a0001c0003t0002g0201 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-8-1205T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968499 | ||||||
| chr16:57968606
|
ACTAATTG others(3): Show |
A | 144 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(141): Show | 145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.-8-1322_-8-1313del others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968606 | ||||||
| chr16:57968633
|
A | G | 3 | a0007c0020t0007g0007a0017c0062t0027g0324a0049c0108t0004g0061 | 3 | HG01891.hp2 HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-8-1339T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968633 | ||||||
| chr16:57968865
|
T | TA | 20 | a0001c0001t0002g0312a0001c0001t0003g0311a0001c0002t0001g0181others(17): Show | 20 | HG00423.hp1 HG00423.hp2 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-1572dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968865 | ||||||
| chr16:57968865
|
TA | T | 30 | a0001c0001t0001g0195a0001c0003t0001g0197a0001c0003t0001g0199others(27): Show | 30 | HG01515.hp1 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.-8-1572delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968865 | ||||||
| chr16:57968865
|
TAA | T | 32 | a0001c0002t0001g0032a0001c0002t0001g0035a0001c0002t0001g0039others(29): Show | 32 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.-8-1573_-8-1572del others(2): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968865 | ||||||
| chr16:57968866
|
A | T | 2 | a0001c0016t0046g0054a0043c0076t0003g0055 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-8-1572T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968866 | ||||||
| chr16:57968961
|
T | C | 177 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(174): Show | 178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.-8-1667A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968961 | ||||||
| chr16:57969017
|
A | C | 1 | a0005c0030t0003g0001 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-8-1723T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969017 | ||||||
| chr16:57969200
|
G | A | 169 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(166): Show | 170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.-9+1860C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969200 | ||||||
| chr16:57969230
|
C | T | 3 | a0002c0011t0004g0066a0002c0022t0002g0074a0006c0086t0003g0067 | 3 | HG02280.hp2 HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-9+1830G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969230 | ||||||
| chr16:57969240
|
A | G | 1 | a0001c0017t0001g0114 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-9+1820T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969240 | ||||||
| chr16:57969288
|
T | C | 282 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(279): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-9+1772A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969288 | ||||||
| chr16:57969327
|
CA | C | 6 | a0002c0005t0001g0314a0002c0005t0001g0316a0002c0011t0018g0341others(3): Show | 6 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+1732delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969327 | ||||||
| chr16:57969478
|
C | T | 1 | a0034c0095t0001g0193 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-9+1582G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969478 | ||||||
| chr16:57969479
|
G | A | 2 | a0001c0002t0002g0183a0001c0002t0005g0184 | 2 | HG01255.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-9+1581C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969479 | ||||||
| chr16:57969575
|
C | A | 1 | a0002c0005t0001g0332 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-9+1485G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969575 | ||||||
| chr16:57969749
|
C | T | 9 | a0001c0007t0003g0340a0001c0007t0008g0356a0001c0015t0001g0335others(6): Show | 9 | HG01168.hp1 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+1311G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969749 | ||||||
| chr16:57969839
|
T | C | 134 | a0001c0001t0001g0195a0001c0001t0001g0205a0001c0001t0001g0207others(131): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-9+1221A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969839 | ||||||
| chr16:57969921
|
A | G | 137 | a0001c0001t0001g0195a0001c0001t0001g0205a0001c0001t0001g0207others(134): Show | 137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.-9+1139T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969921 | ||||||
| chr16:57970152
|
A | G | 1 | a0001c0007t0002g0073 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-9+908T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970152 | ||||||
| chr16:57970177
|
C | T | 6 | a0001c0002t0003g0008a0001c0007t0003g0004a0001c0015t0002g0006others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+883G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970177 | ||||||
| chr16:57970275
|
C | T | 76 | a0001c0001t0001g0003a0001c0002t0001g0125a0001c0002t0001g0141others(73): Show | 79 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.-9+785G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970275 | ||||||
| chr16:57970280
|
C | T | 1 | a0002c0022t0018g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-9+780G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970280 | ||||||
| chr16:57970343
|
T | C | 1 | a0001c0002t0001g0338 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-9+717A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970343 | ||||||
| chr16:57970372
|
C | T | 44 | a0001c0003t0032g0109a0001c0004t0022g0107a0001c0004t0035g0079others(41): Show | 44 | HG00642.hp2 HG01109.hp2 HG01515.hp2 others(41): Show |
intron_variant | MODIFIER | c.-9+688G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970372 | ||||||
| chr16:57970456
|
G | A | 310 | a0001c0001t0001g0003a0001c0001t0001g0195a0001c0001t0001g0205others(307): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.-9+604C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970456 | ||||||
| chr16:57970621
|
G | A | 16 | a0001c0007t0003g0340a0002c0011t0018g0341a0004c0014t0001g0345others(13): Show | 16 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9+439C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970621 | ||||||
| chr16:57970765
|
G | A | 1 | a0005c0036t0001g0355 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-9+295C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970765 | ||||||
| chr16:57970785
|
A | G | 6 | a0001c0028t0042g0069a0001c0028t0044g0064a0002c0005t0041g0068others(3): Show | 6 | HG01109.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+275T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970785 | ||||||
| chr16:57970865
|
T | A | 2 | a0001c0007t0008g0356a0002c0114t0010g0357 | 2 | HG01168.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-9+195A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970865 | ||||||
| chr16:57970889
|
T | C | 7 | a0001c0002t0003g0008a0001c0007t0003g0004a0001c0015t0002g0006others(4): Show | 7 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+171A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970889 | ||||||
| chr16:57970928
|
A | G | 53 | a0001c0002t0001g0032a0001c0002t0001g0035a0001c0002t0001g0039others(50): Show | 53 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.-9+132T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970928 | ||||||
| chr16:57971023
|
C | T | 7 | a0001c0002t0003g0008a0001c0007t0003g0004a0001c0015t0002g0006others(4): Show | 7 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+37G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57971023 |