| geneid | 1259 |
|---|---|
| ensemblid | ENSG00000198515.16 |
| hgncid | 2148 |
| symbol | CNGA1 |
| name | cyclic nucleotide gated channel subunit alpha 1 |
| refseq_nuc | NM_001379270.1 |
| refseq_prot | NP_001366199.1 |
| ensembl_nuc | ENST00000514170.7 |
| ensembl_prot | ENSP00000426862.3 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 47935977 |
| end | 48016681 |
| strand | - |
| ver | v1.2 |
| region | chr4:47935977-48016681 |
| region5000 | chr4:47930977-48021681 |
| regionname0 | CNGA1_chr4_47935977_48016681 |
| regionname5000 | CNGA1_chr4_47930977_48021681 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 686 | 270 | 69 | 56 | 102 | 16 | 25 | 75 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0002 | 0/0 | 686 | 93 | 20 | 8 | 55 | 0 | 10 | 46 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0003 | 0/0 | 686 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0004 | 0/0 | 686 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0005 | 0/0 | 686 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| 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 | 1/1 | 2061 | 250 | 57 | 51 | 102 | 15 | 23 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| c0002 | 0/0 | 2061 | 93 | 20 | 8 | 55 | 0 | 10 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| c0003 | 0/0 | 2061 | 13 | 12 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| c0004 | 0/0 | 2061 | 7 | 0 | 4 | 0 | 1 | 2 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| c0005 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| c0006 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| c0007 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| 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 | 866 | 154 | 22 | 39 | 61 | 13 | 18 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| t0002 | 1/0 | 866 | 110 | 39 | 8 | 57 | 0 | 5 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| t0003 | 0/0 | 866 | 66 | 19 | 6 | 38 | 0 | 3 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| t0004 | 0/0 | 866 | 17 | 1 | 6 | 2 | 3 | 5 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| t0005 | 0/0 | 866 | 6 | 6 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| t0006 | 0/0 | 866 | 5 | 0 | 5 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| t0007 | 0/0 | 866 | 3 | 0 | 0 | 0 | 0 | 3 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| t0008 | 0/0 | 866 | 2 | 2 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| t0009 | 0/0 | 866 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| t0010 | 0/0 | 866 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| t0011 | 0/0 | 866 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0282 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| 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 | 1/1 | 2061 | 250 | 57 | 51 | 102 | 15 | 23 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0001c0003 | 0/0 | 2061 | 13 | 12 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0001c0004 | 0/0 | 2061 | 7 | 0 | 4 | 0 | 1 | 2 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0002c0002 | 0/0 | 2061 | 93 | 20 | 8 | 55 | 0 | 10 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0003c0006 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0004c0005 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0005c0007 | 0/0 | 2061 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2926 | 142 | 21 | 34 | 60 | 12 | 14 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0001c0001t0002 | 1/0 | 2926 | 23 | 17 | 1 | 4 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0001c0001t0003 | 0/0 | 2926 | 54 | 10 | 5 | 36 | 0 | 3 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0001c0001t0004 | 0/0 | 2926 | 17 | 1 | 6 | 2 | 3 | 5 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0001c0001t0005 | 0/0 | 2926 | 6 | 6 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0001c0001t0006 | 0/0 | 2926 | 5 | 0 | 5 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0001c0001t0008 | 0/0 | 2926 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0001c0001t0009 | 0/0 | 2926 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0001c0001t0011 | 0/0 | 2926 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0001c0003t0001 | 0/0 | 2926 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0001c0003t0002 | 0/0 | 2926 | 3 | 3 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0001c0003t0003 | 0/0 | 2926 | 9 | 8 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0001c0004t0001 | 0/0 | 2926 | 7 | 0 | 4 | 0 | 1 | 2 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0002c0002t0001 | 0/0 | 2926 | 3 | 0 | 1 | 1 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0002c0002t0002 | 0/0 | 2926 | 84 | 19 | 7 | 53 | 0 | 5 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0002c0002t0003 | 0/0 | 2926 | 2 | 1 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0002c0002t0007 | 0/0 | 2926 | 3 | 0 | 0 | 0 | 0 | 3 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0002c0002t0010 | 0/0 | 2926 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0003c0006t0008 | 0/0 | 2926 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0004c0005t0003 | 0/0 | 2926 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| a0005c0007t0001 | 0/0 | 2926 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | copy fasta | chr4 | 47930977 | 48021681 |
| 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 | 3 | 0 | 0 | 3 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0282 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0105 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0005g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0005g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0005g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0006g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0006g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0006g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0006g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0006g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0011g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0003t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0003t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0003t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0003t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0003t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0003t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0003t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0003t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0003t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0003t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0003t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0003t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0003t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0004t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0004t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0004t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0004t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0004t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0004t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0007 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0007g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0007g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0007g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0010g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0003c0006t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0004c0005t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0005c0007t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0310 | EUR | GBR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0032 | EUR | GBR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00140 | hp1 | a0001 | c0004 | t0001 | g0220 | EUR | GBR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0302 | EUR | GBR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | FIN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0345 | EUR | FIN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0284 | EUR | FIN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | FIN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0166 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0172 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0211 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0031 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00642 | hp2 | a0001 | c0003 | t0003 | g0092 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00733 | hp1 | a0001 | c0004 | t0001 | g0216 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00733 | hp2 | a0001 | c0001 | t0006 | g0210 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0045 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0158 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0209 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0249 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0059 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01167 | hp2 | a0002 | c0002 | t0002 | g0128 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0040 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0340 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01243 | hp2 | a0001 | c0004 | t0001 | g0214 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01256 | hp1 | a0001 | c0004 | t0001 | g0321 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01257 | hp2 | a0001 | c0004 | t0001 | g0215 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0036 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0248 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0185 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0039 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0212 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0343 | EUR | IBS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01515 | hp2 | a0001 | c0001 | t0004 | g0069 | EUR | IBS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0033 | EUR | IBS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0232 | EUR | IBS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0131 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0125 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01891 | hp2 | a0001 | c0003 | t0003 | g0088 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0186 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0336 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0153 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0044 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0198 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0155 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0188 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0199 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02145 | hp1 | a0001 | c0003 | t0002 | g0122 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0142 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02257 | hp1 | a0001 | c0003 | t0003 | g0090 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0201 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02280 | hp1 | a0001 | c0003 | t0003 | g0020 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0174 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02451 | hp2 | a0001 | c0003 | t0002 | g0121 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0194 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0123 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02602 | hp1 | a0002 | c0002 | t0007 | g0095 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0046 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02615 | hp1 | a0002 | c0002 | t0002 | g0132 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0018 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02622 | hp1 | a0001 | c0003 | t0003 | g0091 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0124 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0148 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0332 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0037 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0146 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0016 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0112 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02723 | hp2 | a0001 | c0003 | t0003 | g0087 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02735 | hp1 | a0002 | c0002 | t0007 | g0096 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02809 | hp1 | a0003 | c0006 | t0008 | g0017 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02886 | hp1 | a0001 | c0003 | t0003 | g0075 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0200 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0140 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0203 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0169 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0084 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | ESN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | ESN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0093 | AFR | ESN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | ESN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0076 | AFR | ESN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | ESN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0150 | AFR | ESN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | MSL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03098 | hp2 | a0001 | c0003 | t0002 | g0120 | AFR | MSL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03130 | hp1 | a0002 | c0002 | t0002 | g0130 | AFR | ESN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | ESN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | MSL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03225 | hp1 | a0001 | c0003 | t0003 | g0089 | AFR | MSL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | MSL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0342 | AFR | MSL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0113 | AFR | MSL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0034 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03491 | hp2 | a0001 | c0004 | t0001 | g0233 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | ESN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ESN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | MSL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0097 | AFR | MSL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03654 | hp2 | a0002 | c0002 | t0007 | g0094 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03669 | hp1 | a0002 | c0002 | t0002 | g0129 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0145 | SAS | STU | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0061 | SAS | STU | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0181 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0056 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03831 | hp1 | a0005 | c0007 | t0001 | g0313 | SAS | BEB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0159 | SAS | BEB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03927 | hp1 | a0001 | c0004 | t0001 | g0208 | SAS | BEB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03927 | hp2 | a0001 | c0001 | t0011 | g0151 | SAS | BEB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG04184 | hp1 | a0001 | c0001 | t0004 | g0072 | SAS | BEB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG04184 | hp2 | a0002 | c0002 | t0010 | g0178 | SAS | BEB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0167 | SAS | STU | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0311 | SAS | STU | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0312 | SAS | STU | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0035 | SAS | STU | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | STU | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0068 | SAS | STU | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18522 | hp1 | a0002 | c0002 | t0002 | g0147 | AFR | YRI | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18522 | hp2 | a0001 | c0003 | t0003 | g0078 | AFR | YRI | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CHB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0161 | EAS | CHB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0183 | EAS | CHB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18906 | hp1 | a0002 | c0002 | t0002 | g0126 | AFR | YRI | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | YRI | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0189 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0176 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0175 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0180 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0193 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0202 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19000 | hp2 | a0002 | c0002 | t0002 | g0163 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0098 | AFR | LWK | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | LWK | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | LWK | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0010 | AFR | LWK | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0195 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0276 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0154 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19078 | hp1 | a0004 | c0005 | t0003 | g0071 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19081 | hp2 | a0002 | c0002 | t0003 | g0073 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19082 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0070 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0157 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0338 | AFR | YRI | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | YRI | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ASW | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ASW | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | TSI | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0330 | EUR | TSI | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0328 | EUR | TSI | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0333 | EUR | TSI | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | GIH | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | GIH | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0042 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0149 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0086 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | MSL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0108 | AFR | MSL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0083 | AFR | USA | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | USA | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | LWK | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA21309 | hp2 | a0002 | c0002 | t0003 | g0074 | AFR | LWK | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0282 | REF | REF | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0105 | REF | REF | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:47936809
|
G | A | 1 | a0004 | 1 | NA19078.hp1 | missense_variant | MODERATE | c.1673C>T | p.Thr558Met | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 11/11 | 2094/2926 | 1673/2061 | 558/686 | chr4 | 47936809 | ||
| chr4:47942048
|
T | A | 1 | a0003 | 1 | HG02809.hp1 | missense_variant | MODERATE | c.538A>T | p.Ile180Phe | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 9/11 | 959/2926 | 538/2061 | 180/686 | chr4 | 47942048 | ||
| chr4:47943278
|
C | T | 2 | a0002a0005 | 94 | HG00408.hp1 HG00423.hp2 HG01071.hp1 others(91): Show |
missense_variant | MODERATE | c.340G>A | p.Asp114Asn | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 8/11 | 761/2926 | 340/2061 | 114/686 | chr4 | 47943278 | ||
| chr4:47949867
|
G | C | 1 | a0005 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.253C>G | p.Leu85Val | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/11 | 674/2926 | 253/2061 | 85/686 | chr4 | 47949867 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:47936448
|
C | T | 1 | a0001c0003 | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
synonymous_variant | LOW | c.2034G>A | p.Ala678Ala | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 11/11 | 2455/2926 | 2034/2061 | 678/686 | chr4 | 47936448 | ||
| chr4:47936862
|
G | A | 1 | a0001c0004 | 7 | HG00140.hp1 HG00733.hp1 HG01243.hp2 others(4): Show |
synonymous_variant | LOW | c.1620C>T | p.Phe540Phe | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 11/11 | 2041/2926 | 1620/2061 | 540/686 | chr4 | 47936862 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:47936147
|
G | A | 1 | a0002c0002t0010 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*274C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 11/11 | 274 | chr4 | 47936147 | |||||
| chr4:47936359
|
T | A | 1 | a0001c0001t0011 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*62A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 11/11 | 62 | chr4 | 47936359 | |||||
| chr4:47981419
|
T | C | 1 | a0001c0001t0009 | 1 | HG02615.hp2 | 5_prime_UTR_variant | MODIFIER | c.-41A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/11 | 28730 | chr4 | 47981419 | |||||
| chr4:47981469
|
C | T | 1 | a0001c0001t0005 | 6 | HG01884.hp2 HG02895.hp2 HG02922.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-91G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/11 | 28780 | chr4 | 47981469 | |||||
| chr4:48010800
|
G | A | 5 | a0001c0001t0004a0001c0001t0006a0001c0001t0008others(2): Show | 25 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(22): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-129C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/11 | chr4 | 48010800 | ||||||
| chr4:48016491
|
G | T | 1 | a0002c0002t0007 | 3 | HG02602.hp1 HG02735.hp1 HG03654.hp2 |
5_prime_UTR_variant | MODIFIER | c.-231C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/11 | 63802 | chr4 | 48016491 | |||||
| chr4:48016512
|
T | C | 15 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(12): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
5_prime_UTR_variant | MODIFIER | c.-252A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/11 | 63823 | chr4 | 48016512 | |||||
| chr4:48016597
|
C | G | 5 | a0001c0001t0003a0001c0001t0004a0001c0003t0003others(2): Show | 83 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(80): Show |
5_prime_UTR_variant | MODIFIER | c.-337G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/11 | 63908 | chr4 | 48016597 | |||||
| chr4:48016655
|
C | T | 3 | a0001c0001t0008a0001c0001t0009a0003c0006t0008 | 3 | HG02615.hp2 HG02717.hp2 HG02809.hp1 |
5_prime_UTR_variant | MODIFIER | c.-395G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/11 | 63966 | chr4 | 48016655 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:47938173
|
CA | C | 241 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(238): Show | 254 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.653-345delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938173 | ||||||
| chr4:47938173
|
CAA | C | 53 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(50): Show | 58 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.653-346_653-345del others(2): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938173 | ||||||
| chr4:47938176
|
AAAAAAAA others(4): Show |
A | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.653-358_653-348del others(11): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938176 | ||||||
| chr4:47938177
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0003t0003g0092 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.653-358_653-349del others(10): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938177 | ||||||
| chr4:47938314
|
G | GAT | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.653-487_653-486dup others(2): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938314 | ||||||
| chr4:47938314
|
GAT | G | 299 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(296): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.653-487_653-486del others(2): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938314 | ||||||
| chr4:47938397
|
A | AT | 187 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(184): Show | 199 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.653-569dupA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938397 | ||||||
| chr4:47938397
|
A | ATT | 61 | a0001c0001t0001g0205a0001c0001t0001g0207a0001c0001t0001g0226others(58): Show | 66 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.653-570_653-569dup others(2): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938397 | ||||||
| chr4:47938397
|
AT | A | 51 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(48): Show | 53 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.653-569delA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938397 | ||||||
| chr4:47938537
|
C | T | 1 | a0001c0001t0001g0316 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.653-708G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938537 | ||||||
| chr4:47938538
|
A | G | 299 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(296): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.653-709T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938538 | ||||||
| chr4:47938681
|
G | A | 1 | a0002c0002t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.653-852C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938681 | ||||||
| chr4:47938914
|
A | AAAAG | 4 | a0002c0002t0002g0133a0002c0002t0002g0139a0002c0002t0002g0175others(1): Show | 4 | NA18974.hp2 NA19011.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.653-1089_653-1086d others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938914 | ||||||
| chr4:47938977
|
AAAAG | A | 16 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(13): Show | 16 | HG02109.hp1 HG02257.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.653-1152_653-1149d others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938977 | ||||||
| chr4:47938977
|
AAAAGAAA others(11): Show |
A | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.653-1166_653-1149d others(20): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938977 | ||||||
| chr4:47938978
|
AAAGAAAG others(32): Show |
A | 1 | a0002c0002t0002g0153 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.653-1188_653-1150d others(41): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938978 | ||||||
| chr4:47938983
|
AAGAAAGA others(3): Show |
A | 1 | a0001c0001t0001g0225 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.653-1164_653-1155d others(12): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938983 | ||||||
| chr4:47938991
|
AAG | A | 5 | a0001c0001t0001g0296a0001c0001t0004g0032a0001c0001t0004g0033others(2): Show | 5 | HG00099.hp2 HG00741.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.653-1164_653-1163d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938991 | ||||||
| chr4:47938993
|
G | GAA | 5 | a0001c0003t0003g0020a0001c0003t0003g0075a0001c0003t0003g0090others(2): Show | 5 | HG00642.hp2 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.653-1165_653-1164i others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938993 | ||||||
| chr4:47939013
|
G | A | 5 | a0001c0003t0003g0020a0001c0003t0003g0075a0001c0003t0003g0090others(2): Show | 5 | HG00642.hp2 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.653-1184C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47939013 | ||||||
| chr4:47939015
|
A | G | 5 | a0001c0003t0003g0020a0001c0003t0003g0075a0001c0003t0003g0090others(2): Show | 5 | HG00642.hp2 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.653-1186T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47939015 | ||||||
| chr4:47939017
|
GAAGA | G | 8 | a0001c0001t0008g0016a0001c0003t0001g0338a0001c0003t0002g0120others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.653-1192_653-1189d others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47939017 | ||||||
| chr4:47939020
|
G | A | 5 | a0001c0003t0003g0020a0001c0003t0003g0075a0001c0003t0003g0090others(2): Show | 5 | HG00642.hp2 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.653-1191C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47939020 | ||||||
| chr4:47939021
|
A | G | 5 | a0001c0003t0003g0020a0001c0003t0003g0075a0001c0003t0003g0090others(2): Show | 5 | HG00642.hp2 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.653-1192T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47939021 | ||||||
| chr4:47939240
|
G | A | 1 | a0002c0002t0002g0193 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.653-1411C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47939240 | ||||||
| chr4:47939241
|
C | T | 1 | a0002c0002t0002g0193 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.653-1412G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47939241 | ||||||
| chr4:47939587
|
C | T | 299 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(296): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.652+1176G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47939587 | ||||||
| chr4:47939614
|
G | A | 53 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(50): Show | 55 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(52): Show |
intron_variant | MODIFIER | c.652+1149C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47939614 | ||||||
| chr4:47939672
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.652+1091T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47939672 | ||||||
| chr4:47940048
|
T | C | 15 | a0002c0002t0002g0097a0002c0002t0002g0113a0002c0002t0002g0125others(12): Show | 15 | HG01167.hp2 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.652+715A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47940048 | ||||||
| chr4:47940056
|
T | C | 1 | a0001c0001t0001g0309 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.652+707A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47940056 | ||||||
| chr4:47940236
|
G | A | 1 | a0002c0002t0002g0141 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.652+527C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47940236 | ||||||
| chr4:47940744
|
C | A | 1 | a0001c0001t0001g0314 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.652+19G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47940744 | ||||||
| chr4:47941123
|
T | G | 1 | a0001c0001t0001g0315 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.546-254A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 9/10 | chr4 | 47941123 | ||||||
| chr4:47941296
|
G | C | 299 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(296): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.546-427C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 9/10 | chr4 | 47941296 | ||||||
| chr4:47941302
|
T | A | 1 | a0001c0001t0003g0066 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.546-433A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 9/10 | chr4 | 47941302 | ||||||
| chr4:47941308
|
C | CA | 4 | a0001c0003t0002g0120a0001c0003t0002g0121a0001c0003t0002g0122others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.546-440dupT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 9/10 | chr4 | 47941308 | ||||||
| chr4:47941330
|
A | T | 1 | a0001c0001t0002g0118 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.546-461T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 9/10 | chr4 | 47941330 | ||||||
| chr4:47941419
|
C | T | 342 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(339): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.546-550G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 9/10 | chr4 | 47941419 | ||||||
| chr4:47941481
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.545+560T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 9/10 | chr4 | 47941481 | ||||||
| chr4:47941500
|
T | C | 1 | a0001c0003t0002g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.545+541A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 9/10 | chr4 | 47941500 | ||||||
| chr4:47941547
|
G | A | 1 | a0001c0001t0003g0093 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.545+494C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 9/10 | chr4 | 47941547 | ||||||
| chr4:47942012
|
CA | C | 305 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(302): Show | 324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.545+28delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 9/10 | chr4 | 47942012 | ||||||
| chr4:47942030
|
A | G | 4 | a0001c0001t0001g0257a0001c0001t0001g0260a0001c0001t0001g0263others(1): Show | 4 | HG00558.hp2 HG00609.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.545+11T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 9/10 | chr4 | 47942030 | ||||||
| chr4:47942359
|
GTT | G | 75 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(72): Show | 80 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.438-213_438-212del others(2): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 8/10 | chr4 | 47942359 | ||||||
| chr4:47942359
|
GTTT | G | 219 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(216): Show | 232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.438-214_438-212del others(3): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 8/10 | chr4 | 47942359 | ||||||
| chr4:47942359
|
GTTTT | G | 19 | a0001c0001t0001g0304a0001c0003t0001g0338a0001c0003t0002g0120others(16): Show | 19 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.438-215_438-212del others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 8/10 | chr4 | 47942359 | ||||||
| chr4:47942415
|
TAAAGAGA others(6): Show |
T | 1 | a0001c0001t0001g0306 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.438-280_438-268del others(13): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 8/10 | chr4 | 47942415 | ||||||
| chr4:47942427
|
T | TA | 9 | a0001c0003t0001g0338a0001c0003t0003g0020a0001c0003t0003g0075others(6): Show | 9 | HG00642.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.438-280dupT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 8/10 | chr4 | 47942427 | ||||||
| chr4:47942517
|
C | A | 1 | a0001c0001t0004g0037 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.438-369G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 8/10 | chr4 | 47942517 | ||||||
| chr4:47942539
|
C | A | 1 | a0001c0001t0003g0024 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.438-391G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 8/10 | chr4 | 47942539 | ||||||
| chr4:47942753
|
C | T | 11 | a0002c0002t0001g0276a0002c0002t0002g0136a0002c0002t0002g0137others(8): Show | 11 | HG00423.hp2 HG03688.hp1 HG03704.hp2 others(8): Show |
intron_variant | MODIFIER | c.437+428G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 8/10 | chr4 | 47942753 | ||||||
| chr4:47942831
|
A | G | 11 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(8): Show | 11 | HG01243.hp1 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.437+350T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 8/10 | chr4 | 47942831 | ||||||
| chr4:47942836
|
G | T | 303 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(300): Show | 321 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.437+345C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 8/10 | chr4 | 47942836 | ||||||
| chr4:47942855
|
C | G | 303 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(300): Show | 321 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.437+326G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 8/10 | chr4 | 47942855 | ||||||
| chr4:47942865
|
C | T | 53 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(50): Show | 55 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(52): Show |
intron_variant | MODIFIER | c.437+316G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 8/10 | chr4 | 47942865 | ||||||
| chr4:47942889
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.437+292C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 8/10 | chr4 | 47942889 | ||||||
| chr4:47943311
|
A | C | 1 | a0002c0002t0002g0132 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.330-23T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 7/10 | chr4 | 47943311 | ||||||
| chr4:47943438
|
C | G | 303 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(300): Show | 321 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.288-26G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47943438 | ||||||
| chr4:47943653
|
G | T | 53 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(50): Show | 55 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(52): Show |
intron_variant | MODIFIER | c.288-241C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47943653 | ||||||
| chr4:47943716
|
G | C | 7 | a0001c0001t0001g0258a0001c0001t0001g0291a0001c0001t0001g0296others(4): Show | 7 | HG01515.hp1 HG01952.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.288-304C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47943716 | ||||||
| chr4:47943797
|
C | G | 316 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(313): Show | 334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.288-385G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47943797 | ||||||
| chr4:47943874
|
C | T | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(168): Show | 180 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.288-462G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47943874 | ||||||
| chr4:47943915
|
A | G | 1 | a0001c0001t0003g0030 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.288-503T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47943915 | ||||||
| chr4:47944187
|
A | AAGTATCA others(40): Show |
1 | a0001c0001t0001g0224 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.288-776_288-775ins others(47): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47944187 | ||||||
| chr4:47944215
|
G | A | 1 | a0001c0003t0003g0090 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.288-803C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47944215 | ||||||
| chr4:47944258
|
G | A | 1 | a0001c0001t0004g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.288-846C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47944258 | ||||||
| chr4:47944302
|
T | C | 15 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(12): Show | 17 | HG01243.hp1 HG01884.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.288-890A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47944302 | ||||||
| chr4:47944438
|
G | T | 1 | a0001c0001t0001g0299 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.288-1026C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47944438 | ||||||
| chr4:47944510
|
A | G | 1 | a0001c0001t0001g0283 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.288-1098T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47944510 | ||||||
| chr4:47944672
|
A | G | 1 | a0001c0001t0006g0209 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.288-1260T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47944672 | ||||||
| chr4:47944677
|
G | A | 1 | a0001c0001t0003g0080 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.288-1265C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47944677 | ||||||
| chr4:47944701
|
G | A | 1 | a0001c0001t0003g0045 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.288-1289C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47944701 | ||||||
| chr4:47944876
|
T | C | 1 | a0001c0001t0002g0099 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.288-1464A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47944876 | ||||||
| chr4:47945171
|
C | T | 303 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(300): Show | 321 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.288-1759G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47945171 | ||||||
| chr4:47945236
|
A | C | 13 | a0001c0003t0001g0338a0001c0003t0002g0120a0001c0003t0002g0121others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.288-1824T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47945236 | ||||||
| chr4:47945462
|
A | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.288-2050T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47945462 | ||||||
| chr4:47945518
|
A | G | 1 | a0001c0001t0001g0250 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.288-2106T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47945518 | ||||||
| chr4:47945558
|
G | A | 13 | a0001c0003t0001g0338a0001c0003t0002g0120a0001c0003t0002g0121others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.288-2146C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47945558 | ||||||
| chr4:47945644
|
C | T | 5 | a0002c0002t0001g0249a0002c0002t0001g0312a0002c0002t0002g0159others(2): Show | 5 | HG01109.hp2 HG03831.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.288-2232G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47945644 | ||||||
| chr4:47945976
|
T | C | 1 | a0001c0001t0003g0065 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.288-2564A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47945976 | ||||||
| chr4:47946247
|
T | C | 316 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(313): Show | 334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.288-2835A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47946247 | ||||||
| chr4:47946256
|
A | T | 1 | a0001c0001t0001g0236 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.288-2844T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47946256 | ||||||
| chr4:47946284
|
C | A | 1 | a0002c0002t0002g0153 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.288-2872G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47946284 | ||||||
| chr4:47946520
|
G | A | 1 | a0001c0001t0001g0284 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.288-3108C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47946520 | ||||||
| chr4:47946749
|
G | C | 68 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(65): Show | 72 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.287+3084C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47946749 | ||||||
| chr4:47946770
|
TTTTC | T | 27 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0001g0301others(24): Show | 28 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.287+3059_287+3062d others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47946770 | ||||||
| chr4:47946770
|
TTTTCTTT others(1): Show |
T | 316 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(313): Show | 334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.287+3055_287+3062d others(10): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47946770 | ||||||
| chr4:47946876
|
C | T | 1 | a0001c0003t0003g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.287+2957G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47946876 | ||||||
| chr4:47946878
|
A | G | 319 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(316): Show | 338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.287+2955T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47946878 | ||||||
| chr4:47947132
|
T | C | 13 | a0001c0003t0001g0338a0001c0003t0002g0120a0001c0003t0002g0121others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.287+2701A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47947132 | ||||||
| chr4:47947168
|
T | G | 3 | a0001c0001t0003g0022a0001c0001t0003g0025a0001c0001t0003g0026 | 3 | NA18987.hp2 NA19068.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.287+2665A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47947168 | ||||||
| chr4:47947613
|
T | C | 1 | a0001c0001t0003g0084 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.287+2220A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47947613 | ||||||
| chr4:47947628
|
C | T | 1 | a0001c0004t0001g0214 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.287+2205G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47947628 | ||||||
| chr4:47947634
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0271a0001c0001t0001g0272 | 4 | NA18957.hp2 NA18970.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.287+2199G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47947634 | ||||||
| chr4:47947936
|
G | C | 1 | a0001c0001t0002g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.287+1897C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47947936 | ||||||
| chr4:47948185
|
C | CA | 184 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(181): Show | 193 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.287+1647dupT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47948185 | ||||||
| chr4:47948229
|
G | A | 318 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(315): Show | 337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.287+1604C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47948229 | ||||||
| chr4:47948239
|
C | T | 68 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(65): Show | 72 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(69): Show |
intron_variant | MODIFIER | c.287+1594G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47948239 | ||||||
| chr4:47948288
|
C | A | 1 | a0002c0002t0007g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.287+1545G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47948288 | ||||||
| chr4:47948314
|
A | G | 1 | a0002c0002t0002g0175 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.287+1519T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47948314 | ||||||
| chr4:47948370
|
A | G | 171 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(168): Show | 180 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.287+1463T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47948370 | ||||||
| chr4:47948579
|
C | T | 1 | a0001c0001t0003g0093 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.287+1254G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47948579 | ||||||
| chr4:47948764
|
G | A | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.287+1069C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47948764 | ||||||
| chr4:47948883
|
T | C | 319 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(316): Show | 338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.287+950A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47948883 | ||||||
| chr4:47948905
|
T | C | 4 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0083others(1): Show | 4 | HG02559.hp1 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.287+928A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47948905 | ||||||
| chr4:47949032
|
C | A | 2 | a0002c0002t0002g0123a0002c0002t0002g0124 | 2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.287+801G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47949032 | ||||||
| chr4:47949099
|
G | T | 1 | a0001c0001t0009g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.287+734C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47949099 | ||||||
| chr4:47949176
|
C | A | 1 | a0001c0001t0001g0305 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.287+657G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47949176 | ||||||
| chr4:47949776
|
T | A | 1 | a0001c0001t0001g0213 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.287+57A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47949776 | ||||||
| chr4:47949928
|
G | A | 319 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(316): Show | 338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.225-33C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47949928 | ||||||
| chr4:47950062
|
A | G | 1 | a0001c0001t0003g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.225-167T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47950062 | ||||||
| chr4:47950067
|
T | C | 13 | a0001c0003t0001g0338a0001c0003t0002g0120a0001c0003t0002g0121others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.225-172A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47950067 | ||||||
| chr4:47950196
|
G | A | 306 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(303): Show | 325 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.225-301C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47950196 | ||||||
| chr4:47950225
|
C | A | 1 | a0002c0002t0002g0193 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.225-330G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47950225 | ||||||
| chr4:47950302
|
A | G | 13 | a0001c0003t0001g0338a0001c0003t0002g0120a0001c0003t0002g0121others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.225-407T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47950302 | ||||||
| chr4:47950402
|
A | C | 51 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(48): Show | 56 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.225-507T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47950402 | ||||||
| chr4:47950415
|
G | T | 13 | a0001c0003t0001g0338a0001c0003t0002g0120a0001c0003t0002g0121others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.225-520C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47950415 | ||||||
| chr4:47950423
|
C | A | 1 | a0001c0003t0001g0338 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.225-528G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47950423 | ||||||
| chr4:47950640
|
C | A | 13 | a0001c0003t0001g0338a0001c0003t0002g0120a0001c0003t0002g0121others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.224+713G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47950640 | ||||||
| chr4:47950659
|
A | G | 235 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(232): Show | 249 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.224+694T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47950659 | ||||||
| chr4:47950683
|
G | A | 13 | a0001c0003t0001g0338a0001c0003t0002g0120a0001c0003t0002g0121others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.224+670C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47950683 | ||||||
| chr4:47950916
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+437G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47950916 | ||||||
| chr4:47950930
|
A | C | 306 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(303): Show | 325 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.224+423T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47950930 | ||||||
| chr4:47951070
|
A | G | 306 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(303): Show | 325 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.224+283T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47951070 | ||||||
| chr4:47951130
|
T | C | 319 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(316): Show | 338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.224+223A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47951130 | ||||||
| chr4:47951273
|
G | A | 2 | a0002c0002t0002g0006a0002c0002t0002g0179 | 3 | NA18969.hp2 NA18979.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.224+80C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47951273 | ||||||
| chr4:47951293
|
C | T | 1 | a0002c0002t0002g0176 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.224+60G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47951293 | ||||||
| chr4:47951498
|
A | T | 319 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(316): Show | 338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.108-29T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 4/10 | chr4 | 47951498 | ||||||
| chr4:47951690
|
C | T | 13 | a0001c0003t0001g0338a0001c0003t0002g0120a0001c0003t0002g0121others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.108-221G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 4/10 | chr4 | 47951690 | ||||||
| chr4:47951718
|
T | A | 1 | a0001c0001t0004g0034 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.108-249A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 4/10 | chr4 | 47951718 | ||||||
| chr4:47951784
|
T | G | 1 | a0002c0002t0002g0155 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.108-315A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 4/10 | chr4 | 47951784 | ||||||
| chr4:47951825
|
G | A | 3 | a0002c0002t0002g0152a0002c0002t0002g0189a0002c0002t0002g0190 | 3 | NA18942.hp2 NA18963.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.108-356C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 4/10 | chr4 | 47951825 | ||||||
| chr4:47951860
|
C | T | 13 | a0001c0003t0001g0338a0001c0003t0002g0120a0001c0003t0002g0121others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.108-391G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 4/10 | chr4 | 47951860 | ||||||
| chr4:47952161
|
G | A | 37 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(34): Show | 43 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.107+422C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 4/10 | chr4 | 47952161 | ||||||
| chr4:47952208
|
C | CA | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(169): Show | 181 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.107+374dupT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 4/10 | chr4 | 47952208 | ||||||
| chr4:47952223
|
C | A | 1 | a0001c0001t0003g0083 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.107+360G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 4/10 | chr4 | 47952223 | ||||||
| chr4:47952368
|
A | AAAAT | 104 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(101): Show | 112 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.107+211_107+214dup others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 4/10 | chr4 | 47952368 | ||||||
| chr4:47952368
|
A | AAAATAAA others(1): Show |
5 | a0001c0001t0001g0256a0001c0001t0001g0267a0001c0004t0001g0214others(2): Show | 5 | HG00423.hp2 HG00733.hp1 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.107+207_107+214dup others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 4/10 | chr4 | 47952368 | ||||||
| chr4:47952368
|
AAAAT | A | 83 | a0001c0001t0001g0015a0001c0001t0001g0221a0001c0001t0001g0226others(80): Show | 89 | HG00099.hp1 HG00280.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.107+211_107+214del others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 4/10 | chr4 | 47952368 | ||||||
| chr4:47952368
|
AAAATAAA others(1): Show |
A | 4 | a0001c0001t0001g0238a0001c0001t0003g0077a0001c0001t0003g0079others(1): Show | 4 | HG02886.hp1 HG03453.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.107+207_107+214del others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 4/10 | chr4 | 47952368 | ||||||
| chr4:47952368
|
AAAATAAA others(5): Show |
A | 12 | a0001c0003t0001g0338a0001c0003t0002g0120a0001c0003t0002g0121others(9): Show | 12 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.107+203_107+214del others(12): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 4/10 | chr4 | 47952368 | ||||||
| chr4:47952432
|
C | T | 2 | a0001c0001t0001g0324a0001c0001t0001g0325 | 2 | HG01934.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.107+151G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 4/10 | chr4 | 47952432 | ||||||
| chr4:47952921
|
A | G | 320 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(317): Show | 339 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.-14-218T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47952921 | ||||||
| chr4:47953114
|
T | C | 1 | a0001c0001t0001g0265 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-14-411A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47953114 | ||||||
| chr4:47953741
|
T | C | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(179): Show | 191 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.-14-1038A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47953741 | ||||||
| chr4:47953814
|
C | T | 11 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(8): Show | 11 | HG01243.hp1 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-14-1111G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47953814 | ||||||
| chr4:47953895
|
GCCTTATG others(8): Show |
G | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(180): Show | 192 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.-14-1207_-14-1193d others(17): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47953895 | ||||||
| chr4:47953954
|
C | T | 1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-14-1251G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47953954 | ||||||
| chr4:47954062
|
C | T | 4 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0083others(1): Show | 4 | HG02559.hp1 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-14-1359G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47954062 | ||||||
| chr4:47954122
|
A | G | 319 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(316): Show | 338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.-14-1419T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47954122 | ||||||
| chr4:47954215
|
C | T | 86 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(83): Show | 91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.-14-1512G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47954215 | ||||||
| chr4:47954239
|
G | T | 1 | a0001c0001t0001g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-14-1536C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47954239 | ||||||
| chr4:47954261
|
A | T | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(166): Show | 178 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.-14-1558T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47954261 | ||||||
| chr4:47954351
|
G | A | 18 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(15): Show | 18 | HG01255.hp1 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-14-1648C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47954351 | ||||||
| chr4:47954417
|
C | T | 13 | a0001c0003t0001g0338a0001c0003t0002g0120a0001c0003t0002g0121others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-14-1714G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47954417 | ||||||
| chr4:47954539
|
A | G | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(179): Show | 191 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.-14-1836T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47954539 | ||||||
| chr4:47954674
|
A | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-1971T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47954674 | ||||||
| chr4:47954793
|
C | T | 1 | a0001c0001t0001g0316 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-14-2090G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47954793 | ||||||
| chr4:47954808
|
G | T | 1 | a0002c0002t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-14-2105C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47954808 | ||||||
| chr4:47954810
|
G | T | 2 | a0002c0002t0002g0138a0002c0002t0002g0173 | 2 | NA18957.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-14-2107C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47954810 | ||||||
| chr4:47954899
|
C | T | 55 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(52): Show | 57 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.-14-2196G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47954899 | ||||||
| chr4:47955024
|
C | CA | 119 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(116): Show | 122 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.-14-2322dupT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955024 | ||||||
| chr4:47955074
|
G | A | 319 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(316): Show | 338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.-14-2371C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955074 | ||||||
| chr4:47955081
|
A | T | 78 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(75): Show | 86 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.-14-2378T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955081 | ||||||
| chr4:47955147
|
C | A | 60 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(57): Show | 65 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.-14-2444G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955147 | ||||||
| chr4:47955173
|
CTTTTT | C | 24 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(21): Show | 24 | HG00423.hp1 HG01255.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-14-2475_-14-2471d others(7): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955173 | ||||||
| chr4:47955173
|
CTTTTTT | C | 50 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(47): Show | 55 | HG00609.hp2 HG00621.hp1 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.-14-2476_-14-2471d others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955173 | ||||||
| chr4:47955173
|
CTTTTTTT | C | 104 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(101): Show | 107 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.-14-2477_-14-2471d others(9): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955173 | ||||||
| chr4:47955173
|
CTTTTTTT others(3): Show |
C | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-14-2480_-14-2471d others(12): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955173 | ||||||
| chr4:47955184
|
T | C | 2 | a0001c0001t0001g0251a0001c0001t0001g0252 | 2 | NA18747.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.-14-2481A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955184 | ||||||
| chr4:47955185
|
T | C | 1 | a0002c0002t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-14-2482A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955185 | ||||||
| chr4:47955259
|
T | C | 1 | a0002c0002t0010g0178 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-14-2556A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955259 | ||||||
| chr4:47955343
|
T | C | 321 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(318): Show | 340 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.-14-2640A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955343 | ||||||
| chr4:47955374
|
G | C | 1 | a0001c0001t0003g0060 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-14-2671C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955374 | ||||||
| chr4:47955694
|
G | A | 60 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(57): Show | 65 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.-14-2991C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955694 | ||||||
| chr4:47955713
|
G | C | 1 | a0001c0001t0001g0223 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-14-3010C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955713 | ||||||
| chr4:47955966
|
G | A | 1 | a0001c0001t0004g0035 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-14-3263C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955966 | ||||||
| chr4:47955989
|
G | A | 1 | a0001c0001t0001g0286 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-14-3286C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955989 | ||||||
| chr4:47956127
|
G | A | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-3424C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47956127 | ||||||
| chr4:47956270
|
G | A | 55 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(52): Show | 57 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.-14-3567C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47956270 | ||||||
| chr4:47956358
|
A | G | 1 | a0001c0001t0001g0015 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-14-3655T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47956358 | ||||||
| chr4:47956600
|
A | G | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-3897T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47956600 | ||||||
| chr4:47956662
|
C | T | 105 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(102): Show | 108 | HG00408.hp1 HG00423.hp2 HG01071.hp1 others(105): Show |
intron_variant | MODIFIER | c.-14-3959G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47956662 | ||||||
| chr4:47956752
|
A | G | 63 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(60): Show | 68 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.-14-4049T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47956752 | ||||||
| chr4:47956927
|
A | AT | 6 | a0001c0001t0001g0327a0001c0001t0001g0328a0001c0001t0001g0329others(3): Show | 6 | HG01070.hp2 HG01074.hp1 HG02698.hp1 others(3): Show |
intron_variant | MODIFIER | c.-14-4225dupA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47956927 | ||||||
| chr4:47956927
|
A | ATT | 10 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0240others(7): Show | 10 | HG01243.hp1 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-4226_-14-4225d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47956927 | ||||||
| chr4:47956955
|
A | G | 63 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(60): Show | 68 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.-14-4252T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47956955 | ||||||
| chr4:47956974
|
C | T | 4 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0203others(1): Show | 6 | HG01884.hp2 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-4271G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47956974 | ||||||
| chr4:47957005
|
T | C | 315 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(312): Show | 333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.-14-4302A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47957005 | ||||||
| chr4:47957086
|
A | C | 1 | a0002c0002t0002g0144 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-14-4383T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47957086 | ||||||
| chr4:47957111
|
T | C | 1 | a0001c0001t0002g0102 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-14-4408A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47957111 | ||||||
| chr4:47957155
|
C | T | 60 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(57): Show | 65 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.-14-4452G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47957155 | ||||||
| chr4:47957380
|
T | G | 4 | a0001c0003t0002g0120a0001c0003t0002g0121a0001c0003t0002g0122others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-4677A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47957380 | ||||||
| chr4:47957711
|
G | T | 3 | a0001c0001t0001g0275a0002c0002t0002g0184a0002c0002t0002g0202 | 3 | NA18994.hp1 NA19068.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.-14-5008C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47957711 | ||||||
| chr4:47957892
|
AT | A | 59 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(56): Show | 62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.-14-5190delA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47957892 | ||||||
| chr4:47957892
|
ATT | A | 119 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(116): Show | 122 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(119): Show |
intron_variant | MODIFIER | c.-14-5191_-14-5190d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47957892 | ||||||
| chr4:47957892
|
ATTT | A | 64 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(61): Show | 69 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-14-5192_-14-5190d others(5): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47957892 | ||||||
| chr4:47957934
|
G | A | 197 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(194): Show | 212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): Show |
intron_variant | MODIFIER | c.-14-5231C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47957934 | ||||||
| chr4:47958483
|
G | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-5780C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47958483 | ||||||
| chr4:47958571
|
G | A | 1 | a0001c0001t0001g0319 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-14-5868C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47958571 | ||||||
| chr4:47958586
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-14-5883G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47958586 | ||||||
| chr4:47958621
|
CA | C | 140 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(137): Show | 151 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.-14-5919delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47958621 | ||||||
| chr4:47958872
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-14-6169A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47958872 | ||||||
| chr4:47959114
|
G | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(130): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.-14-6411C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47959114 | ||||||
| chr4:47959198
|
C | T | 1 | a0001c0001t0001g0332 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-14-6495G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47959198 | ||||||
| chr4:47959333
|
A | T | 1 | a0001c0003t0003g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-14-6630T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47959333 | ||||||
| chr4:47959429
|
GA | G | 55 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(52): Show | 57 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.-14-6727delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47959429 | ||||||
| chr4:47959570
|
A | G | 50 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(47): Show | 55 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.-14-6867T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47959570 | ||||||
| chr4:47959573
|
G | C | 4 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0203others(1): Show | 6 | HG01884.hp2 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-14-6870C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47959573 | ||||||
| chr4:47959598
|
ACACT | A | 3 | a0001c0001t0001g0257a0001c0001t0001g0263a0001c0001t0003g0067 | 3 | HG00609.hp1 NA18975.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.-14-6899_-14-6896d others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47959598 | ||||||
| chr4:47959669
|
G | A | 59 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(56): Show | 64 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.-14-6966C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47959669 | ||||||
| chr4:47959726
|
C | T | 59 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(56): Show | 64 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.-14-7023G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47959726 | ||||||
| chr4:47959844
|
G | A | 1 | a0002c0002t0002g0097 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-14-7141C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47959844 | ||||||
| chr4:47959861
|
C | T | 2 | a0001c0001t0001g0228a0001c0001t0001g0347 | 2 | HG02080.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.-14-7158G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47959861 | ||||||
| chr4:47959927
|
T | C | 2 | a0001c0001t0005g0010a0001c0001t0005g0203 | 3 | HG02895.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-14-7224A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47959927 | ||||||
| chr4:47959927
|
TTGGA | T | 10 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0240others(7): Show | 10 | HG01243.hp1 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-7228_-14-7225d others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47959927 | ||||||
| chr4:47959932
|
T | C | 10 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0240others(7): Show | 10 | HG01243.hp1 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-7229A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47959932 | ||||||
| chr4:47959935
|
C | T | 10 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0240others(7): Show | 10 | HG01243.hp1 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-7232G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47959935 | ||||||
| chr4:47960046
|
A | T | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(193): Show | 211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.-14-7343T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47960046 | ||||||
| chr4:47960061
|
A | T | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(130): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.-14-7358T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47960061 | ||||||
| chr4:47960132
|
A | G | 1 | a0001c0003t0003g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-14-7429T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47960132 | ||||||
| chr4:47960155
|
A | C | 1 | a0001c0001t0001g0273 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-14-7452T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47960155 | ||||||
| chr4:47960221
|
C | T | 1 | a0001c0001t0003g0056 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-14-7518G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47960221 | ||||||
| chr4:47960326
|
A | G | 1 | a0001c0001t0001g0223 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-14-7623T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47960326 | ||||||
| chr4:47960497
|
G | A | 55 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(52): Show | 57 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.-14-7794C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47960497 | ||||||
| chr4:47960647
|
T | A | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(130): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.-14-7944A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47960647 | ||||||
| chr4:47960704
|
A | G | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(130): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.-14-8001T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47960704 | ||||||
| chr4:47960722
|
A | AC | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(130): Show | 143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.-14-8020_-14-8019i others(3): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47960722 | ||||||
| chr4:47960917
|
T | G | 3 | a0001c0001t0006g0210a0001c0001t0006g0211a0001c0001t0006g0212 | 3 | HG00639.hp2 HG00733.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-14-8214A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47960917 | ||||||
| chr4:47960924
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-8221C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47960924 | ||||||
| chr4:47960960
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-14-8257C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47960960 | ||||||
| chr4:47961076
|
G | T | 55 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(52): Show | 57 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(54): Show |
intron_variant | MODIFIER | c.-14-8373C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47961076 | ||||||
| chr4:47961163
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-14-8460G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47961163 | ||||||
| chr4:47961292
|
A | G | 1 | a0001c0001t0001g0015 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-14-8589T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47961292 | ||||||
| chr4:47961302
|
G | C | 1 | a0001c0001t0002g0118 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-14-8599C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47961302 | ||||||
| chr4:47961652
|
C | G | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(193): Show | 211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.-14-8949G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47961652 | ||||||
| chr4:47961672
|
G | A | 2 | a0001c0001t0005g0009a0001c0001t0005g0342 | 3 | HG01884.hp2 HG02922.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-14-8969C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47961672 | ||||||
| chr4:47961721
|
G | C | 196 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(193): Show | 211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.-14-9018C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47961721 | ||||||
| chr4:47961774
|
T | C | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(129): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.-14-9071A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47961774 | ||||||
| chr4:47961810
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-9107G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47961810 | ||||||
| chr4:47961970
|
G | A | 1 | a0001c0001t0001g0337 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-14-9267C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47961970 | ||||||
| chr4:47962073
|
C | T | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-14-9370G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962073 | ||||||
| chr4:47962082
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-14-9379C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962082 | ||||||
| chr4:47962160
|
A | G | 2 | a0001c0001t0003g0058a0001c0001t0003g0059 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-14-9457T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962160 | ||||||
| chr4:47962276
|
G | T | 2 | a0002c0002t0002g0130a0002c0002t0002g0131 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-14-9573C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962276 | ||||||
| chr4:47962277
|
G | C | 2 | a0002c0002t0002g0130a0002c0002t0002g0131 | 2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-14-9574C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962277 | ||||||
| chr4:47962343
|
C | CA | 22 | a0001c0001t0001g0207a0001c0001t0001g0226a0001c0001t0001g0227others(19): Show | 22 | HG00621.hp1 HG01891.hp2 HG02080.hp2 others(19): Show |
intron_variant | MODIFIER | c.-14-9641dupT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962343 | ||||||
| chr4:47962343
|
CA | C | 36 | a0001c0001t0001g0011a0001c0001t0001g0213a0001c0001t0001g0217others(33): Show | 37 | HG00323.hp2 HG00639.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.-14-9641delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962343 | ||||||
| chr4:47962343
|
CAA | C | 30 | a0001c0001t0001g0015a0001c0001t0001g0237a0001c0001t0001g0238others(27): Show | 31 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(28): Show |
intron_variant | MODIFIER | c.-14-9642_-14-9641d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962343 | ||||||
| chr4:47962343
|
CAAA | C | 66 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(63): Show | 74 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.-14-9643_-14-9641d others(5): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962343 | ||||||
| chr4:47962422
|
GA | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(128): Show | 141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.-14-9720delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962422 | ||||||
| chr4:47962438
|
C | T | 1 | a0002c0002t0002g0145 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-14-9735G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962438 | ||||||
| chr4:47962516
|
G | A | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(126): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-14-9813C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962516 | ||||||
| chr4:47962540
|
T | C | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(126): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-14-9837A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962540 | ||||||
| chr4:47962565
|
TCAGGTTC others(3): Show |
T | 1 | a0001c0001t0002g0118 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-14-9872_-14-9863d others(12): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962565 | ||||||
| chr4:47962569
|
G | A | 53 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(50): Show | 55 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(52): Show |
intron_variant | MODIFIER | c.-14-9866C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962569 | ||||||
| chr4:47962694
|
C | T | 10 | a0001c0001t0003g0093a0001c0003t0001g0338a0001c0003t0003g0020others(7): Show | 10 | HG00642.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-9991G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962694 | ||||||
| chr4:47962707
|
G | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(58): Show | 67 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.-14-10004C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962707 | ||||||
| chr4:47962749
|
A | T | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-14-10046T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962749 | ||||||
| chr4:47962837
|
G | T | 1 | a0003c0006t0008g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-14-10134C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962837 | ||||||
| chr4:47962854
|
G | A | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-14-10151C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962854 | ||||||
| chr4:47962877
|
C | T | 1 | a0002c0002t0002g0191 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-14-10174G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962877 | ||||||
| chr4:47962960
|
GA | G | 5 | a0001c0001t0002g0103a0001c0001t0002g0107a0001c0001t0002g0108others(2): Show | 5 | HG01255.hp1 HG02109.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-14-10258delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962960 | ||||||
| chr4:47962962
|
AT | A | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-14-10260delA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962962 | ||||||
| chr4:47963485
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-14-10782G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47963485 | ||||||
| chr4:47963530
|
T | C | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(126): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-14-10827A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47963530 | ||||||
| chr4:47963634
|
A | C | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(126): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-14-10931T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47963634 | ||||||
| chr4:47963642
|
A | G | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(126): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-14-10939T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47963642 | ||||||
| chr4:47963886
|
A | C | 1 | a0001c0001t0001g0306 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-14-11183T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47963886 | ||||||
| chr4:47964199
|
C | T | 1 | a0001c0001t0003g0045 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-14-11496G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47964199 | ||||||
| chr4:47964523
|
T | C | 10 | a0001c0001t0003g0093a0001c0003t0001g0338a0001c0003t0003g0020others(7): Show | 10 | HG00642.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-14-11820A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47964523 | ||||||
| chr4:47964619
|
G | A | 317 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(314): Show | 335 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.-14-11916C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47964619 | ||||||
| chr4:47964703
|
C | T | 1 | a0001c0001t0004g0031 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-14-12000G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47964703 | ||||||
| chr4:47964800
|
T | C | 1 | a0001c0001t0003g0079 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-14-12097A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47964800 | ||||||
| chr4:47964856
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-14-12153C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47964856 | ||||||
| chr4:47964906
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0271a0001c0001t0001g0272 | 4 | NA18957.hp2 NA18970.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-12203G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47964906 | ||||||
| chr4:47964945
|
C | T | 2 | a0001c0001t0003g0063a0001c0001t0003g0064 | 2 | HG00423.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-14-12242G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47964945 | ||||||
| chr4:47964957
|
C | T | 1 | a0002c0002t0002g0192 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-14-12254G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47964957 | ||||||
| chr4:47965047
|
T | C | 1 | a0001c0001t0003g0080 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-14-12344A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47965047 | ||||||
| chr4:47965145
|
C | T | 14 | a0001c0001t0002g0196a0002c0002t0002g0133a0002c0002t0002g0139others(11): Show | 14 | HG01346.hp2 HG01943.hp1 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.-14-12442G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47965145 | ||||||
| chr4:47965163
|
C | T | 8 | a0002c0002t0002g0136a0002c0002t0002g0137a0002c0002t0002g0156others(5): Show | 8 | HG00423.hp2 NA18612.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.-14-12460G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47965163 | ||||||
| chr4:47965186
|
T | G | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-14-12483A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47965186 | ||||||
| chr4:47965194
|
A | G | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(126): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-14-12491T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47965194 | ||||||
| chr4:47965330
|
T | C | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-12627A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47965330 | ||||||
| chr4:47965429
|
C | CT | 7 | a0001c0001t0001g0268a0001c0003t0003g0089a0001c0003t0003g0090others(4): Show | 7 | HG00642.hp2 HG02257.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-14-12727dupA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47965429 | ||||||
| chr4:47965429
|
CT | C | 54 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(51): Show | 57 | HG00423.hp1 HG00621.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.-14-12727delA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47965429 | ||||||
| chr4:47965482
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-12779C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47965482 | ||||||
| chr4:47965576
|
A | G | 317 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(314): Show | 335 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.-14-12873T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47965576 | ||||||
| chr4:47965588
|
G | A | 1 | a0001c0001t0004g0072 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-14-12885C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47965588 | ||||||
| chr4:47965690
|
C | G | 317 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(314): Show | 335 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.-14-12987G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47965690 | ||||||
| chr4:47965838
|
T | C | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-14-13135A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47965838 | ||||||
| chr4:47965923
|
GA | G | 320 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(317): Show | 339 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.-14-13221delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47965923 | ||||||
| chr4:47965957
|
T | C | 1 | a0001c0001t0003g0093 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-14-13254A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47965957 | ||||||
| chr4:47966053
|
T | G | 1 | a0001c0001t0009g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-14-13350A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47966053 | ||||||
| chr4:47966082
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-14-13379C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47966082 | ||||||
| chr4:47966202
|
T | G | 1 | a0001c0001t0001g0303 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-14-13499A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47966202 | ||||||
| chr4:47966212
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-14-13509C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47966212 | ||||||
| chr4:47966223
|
G | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-14-13520C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47966223 | ||||||
| chr4:47966540
|
G | A | 1 | a0001c0001t0002g0119 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-14-13837C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47966540 | ||||||
| chr4:47966688
|
C | T | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-14-13985G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47966688 | ||||||
| chr4:47967211
|
G | A | 1 | a0002c0002t0002g0132 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-15+14182C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47967211 | ||||||
| chr4:47967219
|
C | G | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+14174G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47967219 | ||||||
| chr4:47967359
|
A | G | 1 | a0001c0001t0001g0268 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-15+14034T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47967359 | ||||||
| chr4:47967733
|
C | T | 4 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0203others(1): Show | 6 | HG01884.hp2 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+13660G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47967733 | ||||||
| chr4:47967736
|
T | C | 2 | a0001c0001t0005g0010a0001c0001t0005g0203 | 3 | HG02895.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-15+13657A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47967736 | ||||||
| chr4:47967806
|
G | A | 1 | a0001c0003t0003g0078 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-15+13587C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47967806 | ||||||
| chr4:47968148
|
C | G | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-15+13245G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47968148 | ||||||
| chr4:47968183
|
T | A | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(191): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.-15+13210A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47968183 | ||||||
| chr4:47968333
|
T | A | 197 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(194): Show | 213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.-15+13060A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47968333 | ||||||
| chr4:47968441
|
C | T | 1 | a0001c0001t0001g0319 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-15+12952G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47968441 | ||||||
| chr4:47968485
|
AGGT | A | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+12905_-15+1290 others(7): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47968485 | ||||||
| chr4:47968703
|
A | T | 1 | a0002c0002t0002g0144 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-15+12690T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47968703 | ||||||
| chr4:47968717
|
C | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+12676G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47968717 | ||||||
| chr4:47968766
|
A | C | 4 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0203others(1): Show | 6 | HG01884.hp2 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15+12627T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47968766 | ||||||
| chr4:47968983
|
T | C | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(126): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-15+12410A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47968983 | ||||||
| chr4:47969030
|
GC | G | 10 | a0001c0001t0003g0093a0001c0003t0001g0338a0001c0003t0003g0020others(7): Show | 10 | HG00642.hp2 HG01891.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-15+12362delG | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47969030 | ||||||
| chr4:47969075
|
T | C | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+12318A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47969075 | ||||||
| chr4:47969404
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-15+11989C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47969404 | ||||||
| chr4:47969480
|
G | T | 1 | a0001c0001t0003g0022 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-15+11913C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47969480 | ||||||
| chr4:47969570
|
A | T | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(126): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-15+11823T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47969570 | ||||||
| chr4:47969693
|
C | T | 1 | a0001c0001t0001g0286 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-15+11700G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47969693 | ||||||
| chr4:47969840
|
G | A | 61 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0196others(58): Show | 64 | HG00408.hp1 HG00558.hp1 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.-15+11553C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47969840 | ||||||
| chr4:47969910
|
A | C | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(126): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-15+11483T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47969910 | ||||||
| chr4:47969975
|
A | T | 1 | a0001c0001t0001g0238 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-15+11418T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47969975 | ||||||
| chr4:47970031
|
A | G | 2 | a0001c0001t0003g0030a0001c0001t0003g0060 | 2 | NA18972.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.-15+11362T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47970031 | ||||||
| chr4:47970255
|
C | T | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(126): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-15+11138G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47970255 | ||||||
| chr4:47970327
|
C | T | 1 | a0001c0001t0003g0082 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-15+11066G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47970327 | ||||||
| chr4:47970341
|
C | G | 7 | a0001c0003t0001g0338a0001c0003t0003g0020a0001c0003t0003g0075others(4): Show | 7 | HG00642.hp2 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-15+11052G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47970341 | ||||||
| chr4:47970363
|
T | A | 1 | a0001c0001t0001g0296 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-15+11030A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47970363 | ||||||
| chr4:47970591
|
G | A | 1 | a0001c0001t0006g0248 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-15+10802C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47970591 | ||||||
| chr4:47970650
|
T | TA | 69 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(66): Show | 75 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.-15+10742dupT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47970650 | ||||||
| chr4:47970650
|
T | TAA | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(122): Show | 134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.-15+10741_-15+1074 others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47970650 | ||||||
| chr4:47970722
|
C | G | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(126): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-15+10671G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47970722 | ||||||
| chr4:47970833
|
GA | G | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(126): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-15+10559delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47970833 | ||||||
| chr4:47971014
|
G | A | 109 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(106): Show | 112 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.-15+10379C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971014 | ||||||
| chr4:47971019
|
C | T | 1 | a0001c0001t0002g0119 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-15+10374G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971019 | ||||||
| chr4:47971090
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-15+10303G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971090 | ||||||
| chr4:47971093
|
G | A | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(126): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-15+10300C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971093 | ||||||
| chr4:47971154
|
G | A | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-15+10239C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971154 | ||||||
| chr4:47971168
|
T | TTG | 13 | a0001c0001t0001g0223a0001c0001t0002g0119a0001c0001t0003g0076others(10): Show | 15 | HG01123.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-15+10223_-15+1022 others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971168 | ||||||
| chr4:47971168
|
T | TTGTG | 45 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(42): Show | 48 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.-15+10221_-15+1022 others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971168 | ||||||
| chr4:47971168
|
T | TTGTGTG | 19 | a0001c0001t0001g0341a0001c0001t0003g0002a0001c0001t0003g0046others(16): Show | 21 | HG00609.hp2 HG01993.hp1 HG02300.hp2 others(18): Show |
intron_variant | MODIFIER | c.-15+10219_-15+1022 others(10): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971168 | ||||||
| chr4:47971168
|
T | TTGTGTGT others(3): Show |
1 | a0001c0003t0002g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-15+10215_-15+1022 others(14): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971168 | ||||||
| chr4:47971168
|
T | TTGTGTGT others(5): Show |
1 | a0001c0001t0003g0061 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-15+10213_-15+1022 others(16): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971168 | ||||||
| chr4:47971168
|
TTG | T | 16 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(13): Show | 16 | HG01243.hp1 HG01261.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.-15+10223_-15+1022 others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971168 | ||||||
| chr4:47971168
|
TTGTG | T | 89 | a0001c0001t0002g0118a0001c0001t0002g0170a0001c0001t0002g0171others(86): Show | 92 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-15+10221_-15+1022 others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971168 | ||||||
| chr4:47971168
|
TTGTGTG | T | 18 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(15): Show | 18 | HG01255.hp1 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15+10219_-15+1022 others(10): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971168 | ||||||
| chr4:47971205
|
G | A | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-15+10188C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971205 | ||||||
| chr4:47971217
|
T | G | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(191): Show | 209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.-15+10176A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971217 | ||||||
| chr4:47971249
|
G | C | 1 | a0001c0001t0002g0118 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-15+10144C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971249 | ||||||
| chr4:47971492
|
T | C | 1 | a0001c0001t0004g0031 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-15+9901A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971492 | ||||||
| chr4:47971608
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+9785C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971608 | ||||||
| chr4:47971668
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-15+9725G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971668 | ||||||
| chr4:47971669
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-15+9724C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971669 | ||||||
| chr4:47971841
|
C | T | 1 | a0001c0001t0002g0111 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-15+9552G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971841 | ||||||
| chr4:47971893
|
A | AAAAC | 102 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(99): Show | 105 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.-15+9496_-15+9499d others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971893 | ||||||
| chr4:47971902
|
AAACAAAC others(8): Show |
A | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(61): Show | 72 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.-15+9476_-15+9490d others(17): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971902 | ||||||
| chr4:47971904
|
A | ACAAG | 3 | a0002c0002t0002g0142a0002c0002t0002g0193a0002c0002t0002g0201 | 3 | HG02148.hp2 HG02273.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.-15+9488_-15+9489i others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971904 | ||||||
| chr4:47971914
|
AAAC | A | 64 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(61): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-15+9476_-15+9478d others(5): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971914 | ||||||
| chr4:47972057
|
C | T | 1 | a0002c0002t0002g0143 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-15+9336G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47972057 | ||||||
| chr4:47972082
|
T | C | 2 | a0002c0002t0001g0312a0005c0007t0001g0313 | 2 | HG03831.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-15+9311A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47972082 | ||||||
| chr4:47972093
|
A | G | 1 | a0002c0002t0002g0180 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-15+9300T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47972093 | ||||||
| chr4:47972574
|
C | T | 1 | a0001c0001t0004g0036 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-15+8819G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47972574 | ||||||
| chr4:47972581
|
T | G | 1 | a0001c0001t0003g0084 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.-15+8812A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47972581 | ||||||
| chr4:47972894
|
C | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+8499G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47972894 | ||||||
| chr4:47973004
|
C | T | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(126): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-15+8389G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973004 | ||||||
| chr4:47973066
|
C | CT | 88 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(85): Show | 91 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(88): Show |
intron_variant | MODIFIER | c.-15+8326dupA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973066 | ||||||
| chr4:47973066
|
C | CTT | 160 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(157): Show | 170 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.-15+8325_-15+8326d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973066 | ||||||
| chr4:47973066
|
C | CTTT | 13 | a0001c0001t0001g0207a0001c0001t0001g0237a0001c0001t0001g0347others(10): Show | 13 | HG00423.hp2 HG02083.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.-15+8324_-15+8326d others(5): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973066 | ||||||
| chr4:47973104
|
G | T | 3 | a0001c0001t0001g0258a0001c0001t0001g0291a0001c0001t0001g0343 | 3 | HG01515.hp1 HG02735.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-15+8289C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973104 | ||||||
| chr4:47973145
|
G | A | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+8248C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973145 | ||||||
| chr4:47973149
|
C | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-15+8244G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973149 | ||||||
| chr4:47973203
|
G | T | 4 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0083others(1): Show | 4 | HG02559.hp1 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+8190C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973203 | ||||||
| chr4:47973204
|
A | T | 4 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0083others(1): Show | 4 | HG02559.hp1 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+8189T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973204 | ||||||
| chr4:47973205
|
TTAAAG | T | 4 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0003g0083others(1): Show | 4 | HG02559.hp1 HG02897.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15+8183_-15+8187d others(7): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973205 | ||||||
| chr4:47973218
|
C | A | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-15+8175G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973218 | ||||||
| chr4:47973292
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-15+8101C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973292 | ||||||
| chr4:47973314
|
G | A | 1 | a0001c0001t0001g0325 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-15+8079C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973314 | ||||||
| chr4:47973368
|
G | A | 3 | a0002c0002t0002g0125a0002c0002t0002g0146a0002c0002t0002g0188 | 3 | HG01891.hp1 HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-15+8025C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973368 | ||||||
| chr4:47973477
|
C | T | 320 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(317): Show | 339 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.-15+7916G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973477 | ||||||
| chr4:47973502
|
G | A | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-15+7891C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973502 | ||||||
| chr4:47973703
|
T | C | 6 | a0001c0003t0001g0338a0001c0003t0003g0075a0001c0003t0003g0089others(3): Show | 6 | HG00642.hp2 HG02257.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+7690A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973703 | ||||||
| chr4:47973787
|
G | A | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(192): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.-15+7606C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973787 | ||||||
| chr4:47973886
|
T | C | 125 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0098others(122): Show | 129 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.-15+7507A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973886 | ||||||
| chr4:47973931
|
A | G | 10 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0240others(7): Show | 10 | HG01243.hp1 HG02486.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.-15+7462T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973931 | ||||||
| chr4:47973986
|
A | G | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-15+7407T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973986 | ||||||
| chr4:47973998
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA19004.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-15+7395C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973998 | ||||||
| chr4:47974047
|
G | A | 3 | a0001c0001t0004g0038a0001c0001t0004g0068a0001c0001t0004g0072 | 3 | HG04184.hp1 HG04228.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-15+7346C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974047 | ||||||
| chr4:47974067
|
T | TGTAG | 10 | a0002c0002t0002g0155a0002c0002t0002g0168a0002c0002t0002g0176others(7): Show | 10 | HG02040.hp2 HG02273.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15+7325_-15+7326i others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974067 | ||||||
| chr4:47974067
|
TCTAG | T | 48 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0102others(45): Show | 50 | HG00408.hp1 HG00423.hp2 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.-15+7322_-15+7325d others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974067 | ||||||
| chr4:47974067
|
TCTAGATA others(1): Show |
T | 24 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0107others(21): Show | 25 | HG01071.hp1 HG01255.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-15+7318_-15+7325d others(10): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974067 | ||||||
| chr4:47974067
|
TCTAGATA others(5): Show |
T | 6 | a0001c0001t0002g0099a0002c0002t0002g0097a0002c0002t0002g0126others(3): Show | 6 | HG02280.hp2 HG03579.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+7314_-15+7325d others(14): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974067 | ||||||
| chr4:47974068
|
C | A | 12 | a0001c0001t0002g0171a0002c0002t0002g0155a0002c0002t0002g0168others(9): Show | 12 | HG02040.hp2 HG02273.hp2 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.-15+7325G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974068 | ||||||
| chr4:47974068
|
C | CTAGA | 23 | a0001c0001t0001g0221a0001c0001t0001g0237a0001c0001t0001g0243others(20): Show | 23 | HG00280.hp1 HG00642.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.-15+7321_-15+7324d others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974068 | ||||||
| chr4:47974068
|
C | CTAGATAG others(1): Show |
3 | a0001c0001t0001g0293a0001c0003t0003g0087a0005c0007t0001g0313 | 3 | HG02723.hp2 HG03831.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-15+7317_-15+7324d others(10): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974068 | ||||||
| chr4:47974068
|
C | G | 19 | a0001c0001t0002g0098a0001c0001t0002g0104a0001c0001t0002g0170others(16): Show | 19 | HG00558.hp1 HG01109.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.-15+7325G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974068 | ||||||
| chr4:47974068
|
CTAGA | C | 82 | a0001c0001t0001g0205a0001c0001t0001g0217a0001c0001t0001g0223others(79): Show | 87 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.-15+7321_-15+7324d others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974068 | ||||||
| chr4:47974068
|
CTAGATAG others(1): Show |
C | 23 | a0001c0001t0001g0011a0001c0001t0001g0204a0001c0001t0001g0213others(20): Show | 24 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.-15+7317_-15+7324d others(10): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974068 | ||||||
| chr4:47974068
|
CTAGATAG others(5): Show |
C | 22 | a0001c0001t0001g0206a0001c0001t0001g0218a0001c0001t0001g0224others(19): Show | 22 | HG00280.hp2 HG01070.hp2 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.-15+7313_-15+7324d others(14): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974068 | ||||||
| chr4:47974068
|
CTAGATAG others(9): Show |
C | 40 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(37): Show | 47 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-15+7309_-15+7324d others(18): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974068 | ||||||
| chr4:47974068
|
CTAGATAG others(13): Show |
C | 5 | a0001c0001t0001g0265a0001c0001t0005g0009a0001c0001t0005g0010others(2): Show | 7 | HG01884.hp2 HG02895.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+7305_-15+7324d others(22): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974068 | ||||||
| chr4:47974068
|
CTAGATAG others(21): Show |
C | 1 | a0001c0001t0001g0231 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-15+7297_-15+7324d others(30): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974068 | ||||||
| chr4:47974072
|
A | G | 48 | a0001c0001t0002g0100a0001c0001t0002g0101a0001c0001t0002g0102others(45): Show | 50 | HG00408.hp1 HG00423.hp2 HG01167.hp2 others(47): Show |
intron_variant | MODIFIER | c.-15+7321T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974072 | ||||||
| chr4:47974076
|
A | G | 24 | a0001c0001t0002g0103a0001c0001t0002g0106a0001c0001t0002g0107others(21): Show | 25 | HG01071.hp1 HG01255.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-15+7317T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974076 | ||||||
| chr4:47974080
|
A | G | 6 | a0001c0001t0002g0099a0002c0002t0002g0097a0002c0002t0002g0126others(3): Show | 6 | HG02280.hp2 HG03579.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15+7313T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974080 | ||||||
| chr4:47974174
|
G | A | 1 | a0001c0001t0003g0064 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-15+7219C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974174 | ||||||
| chr4:47974205
|
A | AC | 323 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(320): Show | 342 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(339): Show |
intron_variant | MODIFIER | c.-15+7187dupG | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974205 | ||||||
| chr4:47974371
|
CAA | C | 89 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0196others(86): Show | 92 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.-15+7020_-15+7021d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974371 | ||||||
| chr4:47974519
|
T | G | 8 | a0001c0001t0001g0259a0001c0001t0001g0327a0001c0001t0001g0328others(5): Show | 8 | HG00280.hp2 HG01070.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15+6874A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974519 | ||||||
| chr4:47974709
|
G | GT | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(141): Show | 154 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.-15+6683dupA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974709 | ||||||
| chr4:47974709
|
G | GTT | 6 | a0001c0001t0001g0014a0001c0001t0001g0244a0001c0001t0001g0297others(3): Show | 7 | HG00140.hp1 HG00140.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+6682_-15+6683d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974709 | ||||||
| chr4:47975006
|
A | G | 1 | a0001c0001t0001g0345 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-15+6387T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47975006 | ||||||
| chr4:47975008
|
T | G | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-15+6385A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47975008 | ||||||
| chr4:47975143
|
C | G | 1 | a0001c0001t0002g0118 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-15+6250G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47975143 | ||||||
| chr4:47975161
|
G | A | 54 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(51): Show | 56 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.-15+6232C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47975161 | ||||||
| chr4:47975166
|
TAAAATTG others(15): Show |
T | 2 | a0001c0003t0003g0087a0001c0003t0003g0088 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-15+6205_-15+6226d others(24): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47975166 | ||||||
| chr4:47975176
|
A | G | 1 | a0001c0001t0001g0317 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-15+6217T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47975176 | ||||||
| chr4:47975216
|
T | C | 1 | a0002c0002t0002g0176 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-15+6177A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47975216 | ||||||
| chr4:47975222
|
G | A | 1 | a0001c0001t0001g0334 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-15+6171C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47975222 | ||||||
| chr4:47975237
|
C | A | 1 | a0001c0001t0001g0219 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-15+6156G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47975237 | ||||||
| chr4:47975276
|
A | T | 1 | a0001c0001t0001g0334 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-15+6117T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47975276 | ||||||
| chr4:47975413
|
T | C | 1 | a0001c0004t0001g0214 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-15+5980A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47975413 | ||||||
| chr4:47975584
|
C | T | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-15+5809G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47975584 | ||||||
| chr4:47975592
|
C | T | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-15+5801G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47975592 | ||||||
| chr4:47976050
|
A | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG02132.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-15+5343T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976050 | ||||||
| chr4:47976149
|
G | GTA | 3 | a0001c0001t0004g0034a0001c0001t0004g0035a0001c0001t0006g0248 | 3 | HG01346.hp1 HG03491.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-15+5242_-15+5243d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976149 | ||||||
| chr4:47976149
|
GTA | G | 3 | a0001c0001t0001g0204a0001c0001t0008g0016a0003c0006t0008g0017 | 3 | HG02717.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-15+5242_-15+5243d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976149 | ||||||
| chr4:47976149
|
GTATA | G | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG02109.hp2 HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-15+5240_-15+5243d others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976149 | ||||||
| chr4:47976149
|
GTATATAT others(1): Show |
G | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-15+5236_-15+5243d others(10): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976149 | ||||||
| chr4:47976153
|
ATATATAT others(121): Show |
A | 12 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086others(9): Show | 13 | HG00642.hp2 HG01891.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15+5112_-15+5239d others(2): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976153 | ||||||
| chr4:47976155
|
ATATATAT others(119): Show |
A | 1 | a0001c0001t0002g0118 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-15+5112_-15+5237d others(2): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976155 | ||||||
| chr4:47976157
|
ATATATAT others(117): Show |
A | 78 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(75): Show | 80 | HG00408.hp1 HG00558.hp1 HG01071.hp1 others(77): Show |
intron_variant | MODIFIER | c.-15+5112_-15+5235d others(2): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976157 | ||||||
| chr4:47976159
|
ATATATAT others(115): Show |
A | 15 | a0001c0001t0002g0102a0001c0001t0002g0196a0002c0002t0002g0125others(12): Show | 15 | HG01167.hp2 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-15+5112_-15+5233d others(2): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976159 | ||||||
| chr4:47976161
|
ATATATAT others(73): Show |
A | 5 | a0001c0001t0003g0024a0001c0001t0003g0080a0001c0001t0003g0082others(2): Show | 5 | HG00673.hp1 HG02559.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15+5152_-15+5231d others(82): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976161 | ||||||
| chr4:47976161
|
ATATATAT others(113): Show |
A | 2 | a0001c0001t0003g0076a0002c0002t0002g0097 | 2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-15+5112_-15+5231d others(2): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976161 | ||||||
| chr4:47976163
|
ATATATAT others(71): Show |
A | 50 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(47): Show | 55 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.-15+5152_-15+5229d others(80): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976163 | ||||||
| chr4:47976164
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-15+5229A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976164 | ||||||
| chr4:47976165
|
ATATATAC others(69): Show |
A | 2 | a0001c0001t0001g0236a0001c0001t0003g0056 | 2 | HG02132.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-15+5152_-15+5227d others(78): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976165 | ||||||
| chr4:47976167
|
ATATACAC others(67): Show |
A | 1 | a0001c0001t0003g0070 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-15+5152_-15+5225d others(76): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976167 | ||||||
| chr4:47976172
|
CACATACA others(115): Show |
C | 4 | a0001c0003t0002g0120a0001c0003t0002g0121a0001c0003t0002g0122others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+5099_-15+5220d others(2): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976172 | ||||||
| chr4:47976178
|
CAT | C | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+5213_-15+5214d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976178 | ||||||
| chr4:47976199
|
GTA | G | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-15+5192_-15+5193d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976199 | ||||||
| chr4:47976218
|
TACATATA others(115): Show |
T | 14 | a0002c0002t0002g0006a0002c0002t0002g0127a0002c0002t0002g0134others(11): Show | 15 | HG00423.hp2 NA18612.hp2 NA18944.hp2 others(12): Show |
intron_variant | MODIFIER | c.-15+5053_-15+5174d others(2): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976218 | ||||||
| chr4:47976220
|
CATATATA others(77): Show |
C | 2 | a0001c0001t0003g0079a0001c0001t0003g0081 | 2 | HG02922.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-15+5089_-15+5172d others(86): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976220 | ||||||
| chr4:47976241
|
GTATATAT others(95): Show |
G | 77 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(74): Show | 85 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.-15+5050_-15+5151d others(2): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976241 | ||||||
| chr4:47976254
|
C | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+5139G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976254 | ||||||
| chr4:47976256
|
CAT | C | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+5135_-15+5136d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976256 | ||||||
| chr4:47976264
|
TATATATA others(43): Show |
T | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+5079_-15+5128d others(52): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976264 | ||||||
| chr4:47976281
|
GTA | G | 3 | a0001c0001t0001g0011a0001c0001t0001g0217a0001c0001t0001g0232 | 4 | HG00323.hp2 HG01361.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+5110_-15+5111d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976281 | ||||||
| chr4:47976281
|
GTATATAT others(55): Show |
G | 50 | a0001c0001t0001g0015a0001c0001t0001g0213a0001c0001t0001g0218others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.-15+5050_-15+5111d others(64): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976281 | ||||||
| chr4:47976294
|
T | C | 6 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0011g0151others(3): Show | 7 | HG00558.hp1 HG02040.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+5099A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976294 | ||||||
| chr4:47976302
|
CAT | C | 57 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(54): Show | 62 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.-15+5089_-15+5090d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976302 | ||||||
| chr4:47976312
|
T | C | 1 | a0001c0001t0001g0294 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-15+5081A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976312 | ||||||
| chr4:47976323
|
GTATATAT others(13): Show |
G | 3 | a0001c0001t0001g0011a0001c0001t0001g0217a0001c0001t0001g0232 | 4 | HG00323.hp2 HG01361.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+5050_-15+5069d others(22): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976323 | ||||||
| chr4:47976325
|
A | G | 1 | a0001c0001t0003g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-15+5068T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976325 | ||||||
| chr4:47976338
|
C | T | 1 | a0001c0001t0003g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-15+5055G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976338 | ||||||
| chr4:47976340
|
CAT | C | 64 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(61): Show | 69 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-15+5051_-15+5052d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976340 | ||||||
| chr4:47976342
|
T | C | 1 | a0001c0001t0003g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-15+5051A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976342 | ||||||
| chr4:47976354
|
T | G | 1 | a0001c0001t0001g0012 | 2 | NA18939.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-15+5039A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976354 | ||||||
| chr4:47976386
|
G | C | 1 | a0001c0004t0001g0214 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-15+5007C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976386 | ||||||
| chr4:47976533
|
C | T | 1 | a0001c0001t0001g0286 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-15+4860G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976533 | ||||||
| chr4:47976566
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-15+4827G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976566 | ||||||
| chr4:47976652
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-15+4741C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976652 | ||||||
| chr4:47976920
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-15+4473T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976920 | ||||||
| chr4:47976979
|
T | C | 2 | a0001c0003t0003g0087a0001c0003t0003g0088 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-15+4414A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47976979 | ||||||
| chr4:47977046
|
A | C | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(126): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-15+4347T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47977046 | ||||||
| chr4:47977046
|
A | T | 1 | a0001c0001t0001g0333 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-15+4347T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47977046 | ||||||
| chr4:47977163
|
C | T | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-15+4230G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47977163 | ||||||
| chr4:47977165
|
G | A | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-15+4228C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47977165 | ||||||
| chr4:47977808
|
T | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA19004.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-15+3585A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47977808 | ||||||
| chr4:47977828
|
A | AT | 257 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(254): Show | 271 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(268): Show |
intron_variant | MODIFIER | c.-15+3564dupA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47977828 | ||||||
| chr4:47977890
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-15+3503C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47977890 | ||||||
| chr4:47977895
|
C | T | 2 | a0001c0001t0004g0034a0001c0001t0004g0035 | 2 | HG03491.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-15+3498G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47977895 | ||||||
| chr4:47977983
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-15+3410G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47977983 | ||||||
| chr4:47978115
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-15+3278G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47978115 | ||||||
| chr4:47978268
|
T | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+3125A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47978268 | ||||||
| chr4:47978390
|
A | G | 4 | a0001c0003t0002g0120a0001c0003t0002g0121a0001c0003t0002g0122others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+3003T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47978390 | ||||||
| chr4:47978413
|
C | T | 1 | a0001c0001t0003g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-15+2980G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47978413 | ||||||
| chr4:47978449
|
G | A | 2 | a0001c0001t0001g0287a0001c0001t0001g0288 | 2 | HG01255.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.-15+2944C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47978449 | ||||||
| chr4:47978790
|
C | G | 1 | a0001c0001t0003g0048 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-15+2603G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47978790 | ||||||
| chr4:47978834
|
T | C | 1 | a0002c0002t0002g0172 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-15+2559A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47978834 | ||||||
| chr4:47978864
|
TA | T | 48 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(45): Show | 53 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.-15+2528delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47978864 | ||||||
| chr4:47978881
|
T | C | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-15+2512A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47978881 | ||||||
| chr4:47979220
|
C | A | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-15+2173G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47979220 | ||||||
| chr4:47979228
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-15+2165C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47979228 | ||||||
| chr4:47979320
|
C | CA | 108 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(105): Show | 111 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.-15+2072dupT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47979320 | ||||||
| chr4:47979320
|
C | CAA | 7 | a0001c0001t0001g0326a0001c0001t0002g0114a0002c0002t0002g0149others(4): Show | 7 | HG02040.hp1 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15+2071_-15+2072d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47979320 | ||||||
| chr4:47979320
|
CA | C | 62 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(59): Show | 70 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.-15+2072delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47979320 | ||||||
| chr4:47979320
|
CAA | C | 126 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0205others(123): Show | 133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.-15+2071_-15+2072d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47979320 | ||||||
| chr4:47979348
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-15+2045G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47979348 | ||||||
| chr4:47979499
|
T | A | 66 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(63): Show | 71 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.-15+1894A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47979499 | ||||||
| chr4:47979646
|
T | C | 2 | a0001c0003t0003g0087a0001c0003t0003g0088 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-15+1747A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47979646 | ||||||
| chr4:47979652
|
A | G | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(192): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.-15+1741T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47979652 | ||||||
| chr4:47979813
|
C | T | 1 | a0001c0001t0003g0047 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-15+1580G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47979813 | ||||||
| chr4:47979936
|
T | C | 2 | a0001c0001t0002g0112a0002c0002t0002g0113 | 2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-15+1457A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47979936 | ||||||
| chr4:47979980
|
C | G | 1 | a0001c0001t0001g0230 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-15+1413G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47979980 | ||||||
| chr4:47980058
|
G | A | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-15+1335C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47980058 | ||||||
| chr4:47980066
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+1327A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47980066 | ||||||
| chr4:47980472
|
CT | C | 233 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(230): Show | 247 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.-15+920delA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47980472 | ||||||
| chr4:47980472
|
CTT | C | 11 | a0001c0001t0001g0314a0001c0001t0002g0114a0002c0002t0002g0133others(8): Show | 11 | HG02015.hp1 HG02602.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15+919_-15+920del others(2): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47980472 | ||||||
| chr4:47980476
|
T | C | 1 | a0001c0001t0001g0256 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-15+917A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47980476 | ||||||
| chr4:47980477
|
T | C | 131 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(128): Show | 142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.-15+916A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47980477 | ||||||
| chr4:47980478
|
T | C | 1 | a0001c0001t0001g0314 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-15+915A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47980478 | ||||||
| chr4:47980481
|
T | C | 1 | a0001c0001t0003g0067 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-15+912A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47980481 | ||||||
| chr4:47980521
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+872G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47980521 | ||||||
| chr4:47980550
|
C | T | 1 | a0001c0004t0001g0216 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-15+843G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47980550 | ||||||
| chr4:47980558
|
T | A | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(58): Show | 67 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.-15+835A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47980558 | ||||||
| chr4:47980805
|
G | A | 1 | a0001c0001t0003g0079 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-15+588C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47980805 | ||||||
| chr4:47980834
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-15+559C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47980834 | ||||||
| chr4:47980883
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-15+510C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47980883 | ||||||
| chr4:47980892
|
A | AATCTCTT others(14): Show |
191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(188): Show | 206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.-15+480_-15+500dup others(21): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47980892 | ||||||
| chr4:47980905
|
C | CACTTATT others(14): Show |
4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-15+487_-15+488ins others(21): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47980905 | ||||||
| chr4:47981326
|
G | A | 26 | a0001c0001t0003g0066a0001c0001t0004g0031a0001c0001t0004g0032others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-15+67C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47981326 | ||||||
| chr4:47981601
|
G | A | 2 | a0001c0001t0001g0346a0001c0001t0003g0079 | 2 | HG01074.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-122-101C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47981601 | ||||||
| chr4:47981675
|
A | G | 1 | a0001c0001t0001g0296 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.-122-175T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47981675 | ||||||
| chr4:47981697
|
G | C | 13 | a0001c0001t0003g0093a0001c0003t0001g0338a0001c0003t0002g0120others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-122-197C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47981697 | ||||||
| chr4:47981698
|
T | A | 13 | a0001c0001t0003g0093a0001c0003t0001g0338a0001c0003t0002g0120others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-122-198A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47981698 | ||||||
| chr4:47981714
|
T | C | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-122-214A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47981714 | ||||||
| chr4:47981764
|
C | T | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-264G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47981764 | ||||||
| chr4:47981837
|
G | C | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122-337C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47981837 | ||||||
| chr4:47981946
|
A | T | 1 | a0001c0001t0001g0326 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-122-446T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47981946 | ||||||
| chr4:47981947
|
T | C | 1 | a0001c0004t0001g0220 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-122-447A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47981947 | ||||||
| chr4:47981959
|
C | G | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-459G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47981959 | ||||||
| chr4:47981972
|
A | G | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-122-472T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47981972 | ||||||
| chr4:47982059
|
G | A | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(192): Show | 210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.-122-559C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982059 | ||||||
| chr4:47982070
|
A | G | 1 | a0001c0001t0002g0112 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-122-570T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982070 | ||||||
| chr4:47982142
|
A | G | 4 | a0001c0001t0003g0001a0001c0001t0003g0023a0001c0001t0003g0028others(1): Show | 6 | NA18944.hp1 NA18952.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-122-642T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982142 | ||||||
| chr4:47982241
|
A | G | 12 | a0001c0001t0001g0298a0001c0001t0001g0300a0001c0001t0001g0304others(9): Show | 12 | HG00741.hp1 HG01934.hp1 HG01943.hp2 others(9): Show |
intron_variant | MODIFIER | c.-122-741T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982241 | ||||||
| chr4:47982280
|
A | G | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122-780T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982280 | ||||||
| chr4:47982354
|
T | C | 1 | a0002c0002t0002g0141 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-122-854A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982354 | ||||||
| chr4:47982398
|
G | A | 2 | a0001c0001t0003g0080a0002c0002t0003g0074 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-122-898C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982398 | ||||||
| chr4:47982412
|
T | C | 108 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0205others(105): Show | 114 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.-122-912A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982412 | ||||||
| chr4:47982548
|
G | A | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-122-1048C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982548 | ||||||
| chr4:47982618
|
T | C | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-1118A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982618 | ||||||
| chr4:47982696
|
C | T | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-122-1196G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982696 | ||||||
| chr4:47982721
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-122-1221A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982721 | ||||||
| chr4:47982807
|
G | T | 1 | a0001c0001t0001g0270 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-122-1307C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982807 | ||||||
| chr4:47982824
|
A | C | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122-1324T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982824 | ||||||
| chr4:47982836
|
G | A | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122-1336C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982836 | ||||||
| chr4:47982844
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-122-1344C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982844 | ||||||
| chr4:47982860
|
A | C | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-122-1360T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982860 | ||||||
| chr4:47982906
|
G | A | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-122-1406C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982906 | ||||||
| chr4:47982929
|
C | G | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-1429G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982929 | ||||||
| chr4:47982935
|
G | A | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-1435C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47982935 | ||||||
| chr4:47983203
|
T | C | 328 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(325): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.-122-1703A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47983203 | ||||||
| chr4:47983243
|
G | A | 1 | a0001c0001t0001g0238 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-122-1743C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47983243 | ||||||
| chr4:47983252
|
CT | C | 57 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(54): Show | 63 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.-122-1753delA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47983252 | ||||||
| chr4:47983281
|
C | A | 238 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(235): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-122-1781G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47983281 | ||||||
| chr4:47983450
|
G | A | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-1950C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47983450 | ||||||
| chr4:47983554
|
C | A | 26 | a0001c0001t0003g0066a0001c0001t0004g0031a0001c0001t0004g0032others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-122-2054G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47983554 | ||||||
| chr4:47983571
|
C | A | 26 | a0001c0001t0003g0066a0001c0001t0004g0031a0001c0001t0004g0032others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-122-2071G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47983571 | ||||||
| chr4:47983604
|
C | A | 1 | a0001c0001t0002g0111 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-122-2104G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47983604 | ||||||
| chr4:47983607
|
A | C | 2 | a0002c0002t0002g0143a0002c0002t0002g0144 | 2 | NA18954.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-122-2107T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47983607 | ||||||
| chr4:47983615
|
TAAAAGA | T | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-2121_-122-211 others(10): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47983615 | ||||||
| chr4:47983615
|
TAAAAGAA others(5): Show |
T | 2 | a0001c0001t0001g0280a0001c0001t0001g0281 | 2 | HG02080.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.-122-2127_-122-211 others(16): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47983615 | ||||||
| chr4:47984071
|
C | T | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-122-2571G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984071 | ||||||
| chr4:47984491
|
G | A | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-122-2991C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984491 | ||||||
| chr4:47984602
|
G | A | 1 | a0001c0004t0001g0233 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-122-3102C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984602 | ||||||
| chr4:47984640
|
T | TA | 5 | a0001c0001t0002g0118a0001c0001t0004g0069a0001c0003t0002g0120others(2): Show | 5 | HG01515.hp2 HG02145.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-122-3141dupT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984640 | ||||||
| chr4:47984640
|
T | TAA | 10 | a0001c0001t0004g0033a0001c0001t0004g0040a0001c0001t0004g0042others(7): Show | 10 | HG00639.hp2 HG01123.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-122-3142_-122-314 others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984640 | ||||||
| chr4:47984647
|
A | AAAATATA others(5): Show |
1 | a0001c0001t0004g0031 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-122-3148_-122-314 others(16): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984647 | ||||||
| chr4:47984647
|
A | AT | 4 | a0001c0001t0003g0093a0001c0003t0001g0338a0001c0003t0003g0087others(1): Show | 4 | HG01891.hp2 HG02723.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-122-3148_-122-314 others(5): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984647 | ||||||
| chr4:47984647
|
A | T | 1 | a0001c0001t0003g0057 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-122-3147T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984647 | ||||||
| chr4:47984647
|
AAT | A | 10 | a0001c0001t0001g0285a0001c0001t0001g0287a0001c0001t0001g0288others(7): Show | 10 | HG00280.hp2 HG00735.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.-122-3149_-122-314 others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984647 | ||||||
| chr4:47984648
|
AT | A | 17 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0076others(14): Show | 18 | HG00642.hp2 HG02257.hp1 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.-122-3149delA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984648 | ||||||
| chr4:47984649
|
T | A | 207 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(204): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.-122-3149A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984649 | ||||||
| chr4:47984651
|
T | A | 20 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0285others(17): Show | 21 | HG00280.hp2 HG00735.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.-122-3151A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984651 | ||||||
| chr4:47984653
|
T | A | 1 | a0001c0001t0001g0328 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-122-3153A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984653 | ||||||
| chr4:47984661
|
TATAC | T | 49 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(46): Show | 55 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-122-3165_-122-316 others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984661 | ||||||
| chr4:47984661
|
TATACACA others(7): Show |
T | 1 | a0001c0001t0001g0284 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-122-3175_-122-316 others(18): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984661 | ||||||
| chr4:47984663
|
T | C | 9 | a0001c0001t0003g0093a0001c0001t0006g0210a0001c0003t0001g0338others(6): Show | 9 | HG00733.hp2 HG01891.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.-122-3163A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984663 | ||||||
| chr4:47984663
|
TAC | T | 50 | a0001c0001t0001g0011a0001c0001t0001g0213a0001c0001t0001g0217others(47): Show | 51 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.-122-3165_-122-316 others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984663 | ||||||
| chr4:47984663
|
TACAC | T | 14 | a0001c0001t0001g0237a0001c0001t0001g0239a0001c0001t0001g0240others(11): Show | 16 | HG01243.hp1 HG01884.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.-122-3167_-122-316 others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984663 | ||||||
| chr4:47984663
|
TACACACA others(3): Show |
T | 64 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(61): Show | 69 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-122-3173_-122-316 others(14): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984663 | ||||||
| chr4:47984663
|
TACACACA others(7): Show |
T | 1 | a0001c0001t0001g0238 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-122-3177_-122-316 others(18): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984663 | ||||||
| chr4:47984665
|
C | T | 23 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0001g0327others(20): Show | 24 | HG00099.hp2 HG00741.hp2 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.-122-3165G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984665 | ||||||
| chr4:47984667
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122-3167G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984667 | ||||||
| chr4:47984673
|
C | T | 1 | a0001c0001t0003g0028 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-122-3173G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984673 | ||||||
| chr4:47984675
|
C | T | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-3175G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984675 | ||||||
| chr4:47984677
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-122-3177G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984677 | ||||||
| chr4:47984691
|
C | T | 11 | a0001c0001t0002g0118a0001c0001t0003g0093a0001c0001t0006g0210others(8): Show | 11 | HG00642.hp2 HG00733.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-122-3191G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984691 | ||||||
| chr4:47984693
|
C | CATAT | 24 | a0001c0001t0003g0066a0001c0001t0004g0032a0001c0001t0004g0034others(21): Show | 24 | HG00099.hp2 HG00639.hp2 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.-122-3197_-122-319 others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984693 | ||||||
| chr4:47984693
|
C | T | 81 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0205others(78): Show | 87 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.-122-3193G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984693 | ||||||
| chr4:47984705
|
A | T | 1 | a0001c0001t0001g0332 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-122-3205T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984705 | ||||||
| chr4:47984706
|
T | A | 1 | a0001c0001t0001g0332 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-122-3206A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984706 | ||||||
| chr4:47984968
|
C | T | 1 | a0001c0001t0003g0080 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-122-3468G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984968 | ||||||
| chr4:47985741
|
C | T | 53 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(50): Show | 58 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-122-4241G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47985741 | ||||||
| chr4:47985760
|
A | AC | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-122-4261dupG | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47985760 | ||||||
| chr4:47985765
|
C | T | 11 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(8): Show | 11 | HG01243.hp1 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-122-4265G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47985765 | ||||||
| chr4:47985768
|
A | C | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-4268T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47985768 | ||||||
| chr4:47985770
|
A | G | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-122-4270T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47985770 | ||||||
| chr4:47985919
|
C | A | 108 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0205others(105): Show | 114 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.-122-4419G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47985919 | ||||||
| chr4:47986061
|
A | G | 1 | a0001c0001t0001g0303 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-122-4561T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47986061 | ||||||
| chr4:47986615
|
A | G | 7 | a0001c0001t0003g0093a0001c0003t0003g0087a0001c0003t0003g0088others(4): Show | 7 | HG00642.hp2 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-122-5115T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47986615 | ||||||
| chr4:47986642
|
T | C | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-122-5142A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47986642 | ||||||
| chr4:47986745
|
A | T | 6 | a0001c0003t0003g0087a0001c0003t0003g0088a0001c0003t0003g0089others(3): Show | 6 | HG00642.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-122-5245T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47986745 | ||||||
| chr4:47986966
|
A | G | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-5466T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47986966 | ||||||
| chr4:47986974
|
ATTGTG | A | 98 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0205others(95): Show | 102 | HG00099.hp2 HG00423.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.-122-5479_-122-547 others(9): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47986974 | ||||||
| chr4:47986980
|
T | C | 26 | a0001c0001t0003g0066a0001c0001t0004g0031a0001c0001t0004g0032others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-122-5480A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47986980 | ||||||
| chr4:47987105
|
T | TAGAA | 108 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0205others(105): Show | 114 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.-122-5609_-122-560 others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47987105 | ||||||
| chr4:47987468
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-122-5968C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47987468 | ||||||
| chr4:47987522
|
T | C | 3 | a0001c0001t0002g0112a0001c0001t0002g0114a0002c0002t0002g0113 | 3 | HG02723.hp1 HG03225.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-122-6022A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47987522 | ||||||
| chr4:47987556
|
A | C | 1 | a0001c0001t0003g0019 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-122-6056T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47987556 | ||||||
| chr4:47987643
|
T | TTA | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-122-6144_-122-614 others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47987643 | ||||||
| chr4:47987646
|
G | T | 13 | a0001c0001t0003g0093a0001c0003t0001g0338a0001c0003t0002g0120others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-122-6146C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47987646 | ||||||
| chr4:47987665
|
A | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122-6165T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47987665 | ||||||
| chr4:47987776
|
G | A | 1 | a0001c0001t0001g0295 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-122-6276C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47987776 | ||||||
| chr4:47987783
|
G | A | 1 | a0001c0001t0003g0079 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-122-6283C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47987783 | ||||||
| chr4:47987817
|
A | C | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-122-6317T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47987817 | ||||||
| chr4:47987857
|
C | A | 1 | a0002c0002t0002g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-122-6357G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47987857 | ||||||
| chr4:47988079
|
G | A | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122-6579C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47988079 | ||||||
| chr4:47988177
|
G | A | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-122-6677C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47988177 | ||||||
| chr4:47988509
|
C | T | 9 | a0001c0001t0003g0093a0001c0003t0001g0338a0001c0003t0003g0075others(6): Show | 9 | HG00642.hp2 HG01891.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-122-7009G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47988509 | ||||||
| chr4:47988518
|
G | A | 1 | a0002c0002t0002g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-122-7018C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47988518 | ||||||
| chr4:47988792
|
A | C | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(58): Show | 67 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.-122-7292T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47988792 | ||||||
| chr4:47988800
|
T | C | 1 | a0002c0002t0002g0186 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-122-7300A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47988800 | ||||||
| chr4:47988803
|
C | T | 1 | a0001c0001t0001g0344 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-122-7303G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47988803 | ||||||
| chr4:47988977
|
GT | G | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-7478delA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47988977 | ||||||
| chr4:47988981
|
T | A | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-122-7481A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47988981 | ||||||
| chr4:47988982
|
A | T | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(126): Show | 139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-122-7482T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47988982 | ||||||
| chr4:47988983
|
A | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-122-7483T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47988983 | ||||||
| chr4:47988984
|
A | T | 3 | a0001c0001t0001g0309a0001c0001t0001g0317a0001c0001t0001g0340 | 3 | HG01192.hp1 HG02055.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.-122-7484T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47988984 | ||||||
| chr4:47988999
|
T | A | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-122-7499A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47988999 | ||||||
| chr4:47989208
|
T | C | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-122-7708A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47989208 | ||||||
| chr4:47989256
|
T | C | 2 | a0001c0003t0002g0120a0001c0003t0002g0121 | 2 | HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-122-7756A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47989256 | ||||||
| chr4:47989498
|
CT | C | 4 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0203others(1): Show | 6 | HG01884.hp2 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-122-7999delA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47989498 | ||||||
| chr4:47989499
|
T | C | 234 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(231): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.-122-7999A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47989499 | ||||||
| chr4:47989552
|
A | G | 26 | a0001c0001t0003g0066a0001c0001t0004g0031a0001c0001t0004g0032others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-122-8052T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47989552 | ||||||
| chr4:47989648
|
T | A | 1 | a0001c0001t0001g0340 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-122-8148A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47989648 | ||||||
| chr4:47989662
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-122-8162C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47989662 | ||||||
| chr4:47989673
|
GGGAAGCT others(372): Show |
G | 1 | a0001c0001t0003g0076 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-122-8552_-122-817 others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47989673 | ||||||
| chr4:47989684
|
G | A | 2 | a0001c0001t0005g0010a0001c0001t0005g0203 | 3 | HG02895.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-122-8184C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47989684 | ||||||
| chr4:47989785
|
T | C | 1 | a0001c0001t0003g0067 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-122-8285A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47989785 | ||||||
| chr4:47989826
|
T | A | 1 | a0001c0001t0001g0294 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-122-8326A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47989826 | ||||||
| chr4:47989865
|
A | G | 237 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(234): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-122-8365T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47989865 | ||||||
| chr4:47990003
|
A | G | 1 | a0001c0001t0003g0077 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-122-8503T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990003 | ||||||
| chr4:47990040
|
T | C | 1 | a0001c0001t0002g0115 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-122-8540A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990040 | ||||||
| chr4:47990165
|
T | C | 108 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0205others(105): Show | 114 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.-122-8665A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990165 | ||||||
| chr4:47990166
|
G | A | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-122-8666C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990166 | ||||||
| chr4:47990194
|
G | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122-8694C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990194 | ||||||
| chr4:47990268
|
A | G | 328 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(325): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.-122-8768T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990268 | ||||||
| chr4:47990387
|
C | T | 1 | a0001c0001t0004g0038 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-122-8887G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990387 | ||||||
| chr4:47990399
|
T | C | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(166): Show | 181 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.-122-8899A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990399 | ||||||
| chr4:47990431
|
A | C | 4 | a0001c0001t0004g0032a0001c0001t0004g0033a0001c0001t0004g0041others(1): Show | 4 | HG00099.hp2 HG00741.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122-8931T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990431 | ||||||
| chr4:47990475
|
G | A | 2 | a0001c0001t0001g0221a0001c0004t0001g0215 | 2 | HG01256.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.-122-8975C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990475 | ||||||
| chr4:47990582
|
G | A | 54 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(51): Show | 56 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.-122-9082C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990582 | ||||||
| chr4:47990591
|
T | C | 1 | a0001c0001t0001g0299 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-122-9091A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990591 | ||||||
| chr4:47990673
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-122-9173G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990673 | ||||||
| chr4:47990677
|
G | A | 1 | a0001c0003t0002g0122 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-122-9177C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990677 | ||||||
| chr4:47990687
|
T | C | 238 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(235): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-122-9187A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990687 | ||||||
| chr4:47990696
|
T | C | 328 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(325): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.-122-9196A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990696 | ||||||
| chr4:47990770
|
C | G | 2 | a0002c0002t0002g0123a0002c0002t0002g0124 | 2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-122-9270G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990770 | ||||||
| chr4:47990804
|
C | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122-9304G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990804 | ||||||
| chr4:47990836
|
A | T | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-122-9336T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990836 | ||||||
| chr4:47990881
|
C | T | 26 | a0001c0001t0003g0066a0001c0001t0004g0031a0001c0001t0004g0032others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-122-9381G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990881 | ||||||
| chr4:47990901
|
T | C | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122-9401A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990901 | ||||||
| chr4:47991018
|
A | G | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-122-9518T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991018 | ||||||
| chr4:47991059
|
C | A | 108 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0205others(105): Show | 114 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.-122-9559G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991059 | ||||||
| chr4:47991073
|
C | A | 1 | a0001c0001t0006g0248 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-122-9573G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991073 | ||||||
| chr4:47991073
|
C | T | 25 | a0001c0001t0003g0066a0001c0001t0004g0031a0001c0001t0004g0032others(22): Show | 25 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.-122-9573G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991073 | ||||||
| chr4:47991087
|
T | C | 1 | a0004c0005t0003g0071 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-122-9587A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991087 | ||||||
| chr4:47991152
|
C | G | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-9652G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991152 | ||||||
| chr4:47991159
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122-9659G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991159 | ||||||
| chr4:47991208
|
C | T | 1 | a0001c0001t0009g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-122-9708G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991208 | ||||||
| chr4:47991292
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-122-9792G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991292 | ||||||
| chr4:47991349
|
T | C | 2 | a0002c0002t0002g0143a0002c0002t0002g0144 | 2 | NA18954.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.-122-9849A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991349 | ||||||
| chr4:47991513
|
GTT | G | 13 | a0001c0001t0003g0093a0001c0003t0001g0338a0001c0003t0002g0120others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-122-10015_-122-10 others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991513 | ||||||
| chr4:47991603
|
C | T | 1 | a0001c0001t0001g0298 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-122-10103G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991603 | ||||||
| chr4:47991665
|
G | T | 8 | a0002c0002t0002g0125a0002c0002t0002g0126a0002c0002t0002g0146others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-122-10165C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991665 | ||||||
| chr4:47991677
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-122-10177G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991677 | ||||||
| chr4:47991760
|
A | G | 238 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(235): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-122-10260T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991760 | ||||||
| chr4:47991898
|
T | G | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-122-10398A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991898 | ||||||
| chr4:47991998
|
G | A | 1 | a0001c0001t0006g0209 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-122-10498C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991998 | ||||||
| chr4:47992059
|
G | T | 1 | a0001c0003t0003g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-122-10559C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992059 | ||||||
| chr4:47992131
|
T | A | 1 | a0003c0006t0008g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-122-10631A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992131 | ||||||
| chr4:47992393
|
G | T | 1 | a0001c0001t0001g0263 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-122-10893C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992393 | ||||||
| chr4:47992431
|
T | TAA | 64 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(61): Show | 69 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.-122-10933_-122-10 others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992431 | ||||||
| chr4:47992440
|
G | C | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-10940C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992440 | ||||||
| chr4:47992441
|
T | G | 238 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(235): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-122-10941A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992441 | ||||||
| chr4:47992640
|
T | G | 2 | a0001c0001t0003g0080a0002c0002t0003g0074 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-122-11140A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992640 | ||||||
| chr4:47992656
|
T | A | 59 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(56): Show | 65 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.-122-11156A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992656 | ||||||
| chr4:47992657
|
A | ATTAT | 75 | a0001c0001t0001g0015a0001c0001t0001g0225a0001c0001t0001g0237others(72): Show | 77 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.-122-11161_-122-11 others(10): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992657 | ||||||
| chr4:47992657
|
A | ATTATTTA others(1): Show |
62 | a0001c0001t0001g0011a0001c0001t0001g0217a0001c0001t0001g0218others(59): Show | 65 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.-122-11165_-122-11 others(14): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992657 | ||||||
| chr4:47992657
|
A | ATTATTTA others(5): Show |
21 | a0001c0001t0001g0213a0001c0001t0001g0223a0001c0001t0001g0234others(18): Show | 21 | HG00741.hp1 HG01123.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.-122-11169_-122-11 others(18): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992657 | ||||||
| chr4:47992657
|
A | T | 59 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(56): Show | 65 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.-122-11157T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992657 | ||||||
| chr4:47992657
|
ATTATTTA others(1): Show |
A | 29 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0066others(26): Show | 30 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.-122-11165_-122-11 others(14): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992657 | ||||||
| chr4:47992749
|
G | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122-11249C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992749 | ||||||
| chr4:47992779
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0001g0325 | 2 | HG01934.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-122-11279C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992779 | ||||||
| chr4:47992796
|
T | C | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-11296A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992796 | ||||||
| chr4:47992833
|
T | C | 1 | a0002c0002t0002g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-122-11333A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992833 | ||||||
| chr4:47992983
|
T | C | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-122-11483A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992983 | ||||||
| chr4:47993020
|
C | G | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-122-11520G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47993020 | ||||||
| chr4:47993220
|
G | A | 1 | a0001c0001t0001g0314 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-122-11720C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47993220 | ||||||
| chr4:47993220
|
G | T | 1 | a0001c0001t0001g0224 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-122-11720C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47993220 | ||||||
| chr4:47993324
|
T | C | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-11824A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47993324 | ||||||
| chr4:47993389
|
T | C | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-122-11889A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47993389 | ||||||
| chr4:47993457
|
T | A | 1 | a0001c0001t0002g0196 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-122-11957A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47993457 | ||||||
| chr4:47993887
|
C | T | 1 | a0001c0001t0003g0063 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-122-12387G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47993887 | ||||||
| chr4:47993888
|
G | A | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-122-12388C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47993888 | ||||||
| chr4:47993966
|
T | A | 4 | a0001c0001t0004g0038a0001c0001t0004g0039a0001c0001t0004g0040others(1): Show | 4 | HG01123.hp2 HG01175.hp1 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-122-12466A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47993966 | ||||||
| chr4:47994535
|
C | A | 4 | a0001c0001t0001g0300a0001c0001t0001g0315a0001c0001t0001g0316others(1): Show | 4 | HG00741.hp1 HG01934.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122-13035G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47994535 | ||||||
| chr4:47994561
|
C | T | 7 | a0001c0001t0003g0093a0001c0003t0003g0087a0001c0003t0003g0088others(4): Show | 7 | HG00642.hp2 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-122-13061G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47994561 | ||||||
| chr4:47994591
|
A | G | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-13091T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47994591 | ||||||
| chr4:47994742
|
G | C | 53 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(50): Show | 58 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-122-13242C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47994742 | ||||||
| chr4:47994817
|
C | G | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-13317G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47994817 | ||||||
| chr4:47994929
|
A | G | 1 | a0001c0001t0001g0269 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-122-13429T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47994929 | ||||||
| chr4:47994939
|
C | A | 1 | a0002c0002t0002g0177 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-122-13439G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47994939 | ||||||
| chr4:47994942
|
G | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG02109.hp2 HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-122-13442C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47994942 | ||||||
| chr4:47995191
|
TC | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-122-13692delG | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47995191 | ||||||
| chr4:47995236
|
A | G | 54 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(51): Show | 56 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.-122-13736T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47995236 | ||||||
| chr4:47995429
|
A | G | 108 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0205others(105): Show | 114 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.-122-13929T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47995429 | ||||||
| chr4:47995463
|
A | G | 1 | a0002c0002t0002g0156 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-122-13963T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47995463 | ||||||
| chr4:47995516
|
GCTAT | G | 44 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0001g0334others(41): Show | 45 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.-122-14020_-122-14 others(10): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47995516 | ||||||
| chr4:47995555
|
A | AT | 183 | a0001c0001t0001g0011a0001c0001t0001g0014a0001c0001t0001g0015others(180): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.-122-14056dupA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47995555 | ||||||
| chr4:47995555
|
A | ATT | 53 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(50): Show | 59 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(56): Show |
intron_variant | MODIFIER | c.-122-14057_-122-14 others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47995555 | ||||||
| chr4:47995575
|
A | G | 4 | a0001c0003t0002g0120a0001c0003t0002g0121a0001c0003t0002g0122others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-122-14075T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47995575 | ||||||
| chr4:47995628
|
CT | C | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-14129delA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47995628 | ||||||
| chr4:47995703
|
G | A | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-122-14203C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47995703 | ||||||
| chr4:47995818
|
C | A | 1 | a0001c0001t0002g0118 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-122-14318G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47995818 | ||||||
| chr4:47995871
|
G | A | 1 | a0001c0001t0001g0345 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-122-14371C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47995871 | ||||||
| chr4:47995906
|
T | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0269a0001c0001t0001g0270 | 5 | HG00408.hp2 HG02071.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.-122-14406A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47995906 | ||||||
| chr4:47996285
|
C | A | 1 | a0002c0002t0002g0132 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-123+14509G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47996285 | ||||||
| chr4:47996480
|
G | T | 1 | a0002c0002t0002g0181 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-123+14314C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47996480 | ||||||
| chr4:47996482
|
A | G | 1 | a0001c0003t0001g0338 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-123+14312T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47996482 | ||||||
| chr4:47996790
|
T | A | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-123+14004A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47996790 | ||||||
| chr4:47996917
|
T | C | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-123+13877A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47996917 | ||||||
| chr4:47996940
|
C | T | 1 | a0001c0003t0003g0075 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-123+13854G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47996940 | ||||||
| chr4:47997045
|
G | A | 2 | a0002c0002t0002g0199a0002c0002t0010g0178 | 2 | HG02129.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-123+13749C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47997045 | ||||||
| chr4:47997075
|
T | C | 1 | a0002c0002t0002g0197 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-123+13719A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47997075 | ||||||
| chr4:47997084
|
T | C | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-123+13710A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47997084 | ||||||
| chr4:47997095
|
G | A | 2 | a0001c0001t0001g0234a0001c0001t0006g0209 | 2 | HG01109.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-123+13699C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47997095 | ||||||
| chr4:47997428
|
A | G | 1 | a0002c0002t0007g0094 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-123+13366T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47997428 | ||||||
| chr4:47997688
|
G | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-123+13106C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47997688 | ||||||
| chr4:47997702
|
C | T | 238 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(235): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-123+13092G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47997702 | ||||||
| chr4:47997709
|
T | C | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-123+13085A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47997709 | ||||||
| chr4:47997722
|
A | C | 238 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(235): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-123+13072T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47997722 | ||||||
| chr4:47997981
|
A | G | 2 | a0001c0003t0003g0087a0001c0003t0003g0088 | 2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-123+12813T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47997981 | ||||||
| chr4:47998372
|
C | T | 2 | a0001c0001t0001g0262a0001c0001t0001g0289 | 2 | NA19004.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-123+12422G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47998372 | ||||||
| chr4:47998380
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-123+12414C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47998380 | ||||||
| chr4:47998441
|
T | C | 2 | a0001c0001t0001g0317a0001c0001t0001g0340 | 2 | HG01192.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-123+12353A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47998441 | ||||||
| chr4:47998467
|
C | T | 7 | a0001c0001t0001g0293a0001c0001t0001g0302a0001c0001t0001g0319others(4): Show | 7 | HG00140.hp2 HG01074.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.-123+12327G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47998467 | ||||||
| chr4:47998533
|
G | A | 2 | a0001c0001t0001g0301a0001c0003t0003g0020 | 2 | HG01993.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-123+12261C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47998533 | ||||||
| chr4:47998570
|
T | G | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-123+12224A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47998570 | ||||||
| chr4:47998620
|
CA | C | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-123+12173delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47998620 | ||||||
| chr4:47998771
|
C | T | 238 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(235): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-123+12023G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47998771 | ||||||
| chr4:47998798
|
A | T | 17 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(14): Show | 18 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-123+11996T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47998798 | ||||||
| chr4:47998937
|
ATTTAATG others(29): Show |
A | 1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-123+11821_-123+11 others(42): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47998937 | ||||||
| chr4:47999036
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-123+11758G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47999036 | ||||||
| chr4:47999108
|
G | A | 108 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0205others(105): Show | 114 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.-123+11686C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47999108 | ||||||
| chr4:47999115
|
GAGAA | G | 13 | a0001c0001t0003g0093a0001c0003t0001g0338a0001c0003t0002g0120others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-123+11675_-123+11 others(10): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47999115 | ||||||
| chr4:47999323
|
T | A | 26 | a0001c0001t0003g0066a0001c0001t0004g0031a0001c0001t0004g0032others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-123+11471A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47999323 | ||||||
| chr4:47999332
|
G | A | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-123+11462C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47999332 | ||||||
| chr4:47999360
|
G | T | 1 | a0002c0002t0002g0155 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-123+11434C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47999360 | ||||||
| chr4:47999610
|
C | T | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-123+11184G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47999610 | ||||||
| chr4:47999772
|
G | A | 13 | a0001c0001t0003g0093a0001c0003t0001g0338a0001c0003t0002g0120others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-123+11022C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47999772 | ||||||
| chr4:47999990
|
G | GA | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-123+10803dupT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47999990 | ||||||
| chr4:48000137
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-123+10657A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48000137 | ||||||
| chr4:48000179
|
G | A | 108 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0205others(105): Show | 114 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.-123+10615C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48000179 | ||||||
| chr4:48000310
|
A | G | 43 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(40): Show | 44 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.-123+10484T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48000310 | ||||||
| chr4:48000374
|
G | GT | 98 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(95): Show | 103 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.-123+10419dupA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48000374 | ||||||
| chr4:48000465
|
T | G | 108 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0205others(105): Show | 114 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.-123+10329A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48000465 | ||||||
| chr4:48000532
|
C | T | 26 | a0001c0001t0003g0066a0001c0001t0004g0031a0001c0001t0004g0032others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-123+10262G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48000532 | ||||||
| chr4:48000535
|
A | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-123+10259T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48000535 | ||||||
| chr4:48000595
|
C | T | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-123+10199G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48000595 | ||||||
| chr4:48000609
|
C | T | 54 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(51): Show | 56 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.-123+10185G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48000609 | ||||||
| chr4:48000638
|
G | C | 1 | a0002c0002t0002g0179 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-123+10156C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48000638 | ||||||
| chr4:48000669
|
C | T | 26 | a0001c0001t0003g0066a0001c0001t0004g0031a0001c0001t0004g0032others(23): Show | 26 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.-123+10125G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48000669 | ||||||
| chr4:48000740
|
GC | G | 230 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(227): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.-123+10053delG | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48000740 | ||||||
| chr4:48000741
|
C | G | 4 | a0001c0001t0001g0206a0001c0001t0001g0261a0001c0001t0003g0019others(1): Show | 4 | HG00621.hp2 HG02145.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-123+10053G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48000741 | ||||||
| chr4:48000803
|
A | G | 1 | a0001c0001t0004g0031 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-123+9991T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48000803 | ||||||
| chr4:48000837
|
A | T | 1 | a0001c0001t0001g0335 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-123+9957T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48000837 | ||||||
| chr4:48000917
|
C | T | 1 | a0002c0002t0002g0154 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-123+9877G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48000917 | ||||||
| chr4:48001099
|
T | C | 1 | a0001c0001t0005g0342 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-123+9695A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48001099 | ||||||
| chr4:48001207
|
T | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0271a0001c0001t0001g0272others(1): Show | 5 | NA18957.hp2 NA18970.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.-123+9587A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48001207 | ||||||
| chr4:48001217
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-123+9577C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48001217 | ||||||
| chr4:48001328
|
G | C | 4 | a0001c0003t0002g0120a0001c0003t0002g0121a0001c0003t0002g0122others(1): Show | 4 | HG02145.hp1 HG02451.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-123+9466C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48001328 | ||||||
| chr4:48001359
|
C | T | 25 | a0001c0001t0004g0031a0001c0001t0004g0032a0001c0001t0004g0033others(22): Show | 25 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.-123+9435G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48001359 | ||||||
| chr4:48001422
|
T | C | 1 | a0002c0002t0002g0145 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-123+9372A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48001422 | ||||||
| chr4:48001473
|
A | G | 2 | a0001c0001t0003g0083a0001c0001t0003g0084 | 2 | HG02897.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-123+9321T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48001473 | ||||||
| chr4:48001580
|
T | C | 1 | a0001c0003t0003g0092 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-123+9214A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48001580 | ||||||
| chr4:48001863
|
T | C | 1 | a0001c0001t0001g0273 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-123+8931A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48001863 | ||||||
| chr4:48001998
|
AACATTAT others(4): Show |
A | 69 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(66): Show | 74 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.-123+8785_-123+879 others(15): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48001998 | ||||||
| chr4:48002041
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-123+8753C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48002041 | ||||||
| chr4:48002122
|
C | T | 8 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(5): Show | 8 | HG01884.hp1 HG02109.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-123+8672G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48002122 | ||||||
| chr4:48002129
|
C | T | 2 | a0001c0001t0001g0292a0001c0001t0001g0333 | 2 | HG00280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-123+8665G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48002129 | ||||||
| chr4:48002518
|
T | C | 1 | a0002c0002t0002g0180 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-123+8276A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48002518 | ||||||
| chr4:48002584
|
T | TAGTA | 111 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0205others(108): Show | 117 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.-123+8209_-123+821 others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48002584 | ||||||
| chr4:48002633
|
C | A | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-123+8161G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48002633 | ||||||
| chr4:48002683
|
CA | C | 83 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(80): Show | 88 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.-123+8110delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48002683 | ||||||
| chr4:48002683
|
CAA | C | 116 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(113): Show | 126 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.-123+8109_-123+811 others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48002683 | ||||||
| chr4:48002693
|
A | C | 13 | a0001c0001t0003g0093a0001c0003t0001g0338a0001c0003t0002g0120others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-123+8101T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48002693 | ||||||
| chr4:48002694
|
A | C | 62 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(59): Show | 67 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.-123+8100T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48002694 | ||||||
| chr4:48002699
|
AC | A | 32 | a0001c0001t0003g0093a0001c0001t0004g0031a0001c0001t0004g0032others(29): Show | 32 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-123+8094delG | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48002699 | ||||||
| chr4:48002700
|
C | A | 7 | a0001c0001t0002g0118a0001c0001t0004g0041a0001c0001t0004g0042others(4): Show | 7 | HG00741.hp2 HG01123.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.-123+8094G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48002700 | ||||||
| chr4:48002897
|
A | T | 1 | a0001c0001t0001g0226 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-123+7897T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48002897 | ||||||
| chr4:48003078
|
T | C | 242 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(239): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-123+7716A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48003078 | ||||||
| chr4:48003154
|
T | C | 2 | a0001c0001t0003g0063a0001c0001t0003g0064 | 2 | HG00423.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-123+7640A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48003154 | ||||||
| chr4:48003235
|
T | C | 2 | a0001c0001t0003g0063a0001c0001t0003g0064 | 2 | HG00423.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.-123+7559A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48003235 | ||||||
| chr4:48003238
|
A | G | 54 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(51): Show | 56 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(53): Show |
intron_variant | MODIFIER | c.-123+7556T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48003238 | ||||||
| chr4:48003480
|
C | T | 3 | a0001c0003t0002g0120a0001c0003t0002g0121a0001c0003t0002g0122 | 3 | HG02145.hp1 HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-123+7314G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48003480 | ||||||
| chr4:48003489
|
C | T | 1 | a0001c0001t0002g0118 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-123+7305G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48003489 | ||||||
| chr4:48003516
|
G | A | 77 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(74): Show | 85 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.-123+7278C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48003516 | ||||||
| chr4:48003627
|
C | G | 1 | a0001c0001t0008g0016 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-123+7167G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48003627 | ||||||
| chr4:48003646
|
G | C | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-123+7148C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48003646 | ||||||
| chr4:48003737
|
A | G | 111 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0205others(108): Show | 117 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(114): Show |
intron_variant | MODIFIER | c.-123+7057T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48003737 | ||||||
| chr4:48003741
|
T | C | 1 | a0002c0002t0002g0180 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-123+7053A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48003741 | ||||||
| chr4:48003750
|
C | A | 1 | a0002c0002t0002g0181 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-123+7044G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48003750 | ||||||
| chr4:48003938
|
C | A | 1 | a0001c0001t0002g0118 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-123+6856G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48003938 | ||||||
| chr4:48003970
|
G | A | 1 | a0001c0003t0001g0338 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-123+6824C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48003970 | ||||||
| chr4:48004041
|
C | T | 53 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(50): Show | 58 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-123+6753G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004041 | ||||||
| chr4:48004212
|
C | T | 1 | a0001c0001t0001g0344 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-123+6582G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004212 | ||||||
| chr4:48004323
|
G | A | 4 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0203others(1): Show | 6 | HG01884.hp2 HG02895.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-123+6471C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004323 | ||||||
| chr4:48004354
|
A | G | 1 | a0002c0002t0002g0153 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-123+6440T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004354 | ||||||
| chr4:48004603
|
T | TTAGCCCC others(6): Show |
1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-123+6190_-123+619 others(17): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004603 | ||||||
| chr4:48004720
|
G | C | 53 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(50): Show | 58 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-123+6074C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004720 | ||||||
| chr4:48004737
|
C | CCCCCCCC others(5): Show |
1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-123+6056_-123+605 others(16): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004737 | ||||||
| chr4:48004742
|
A | C | 1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-123+6052T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004742 | ||||||
| chr4:48004745
|
A | C | 1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-123+6049T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004745 | ||||||
| chr4:48004746
|
A | C | 1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-123+6048T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004746 | ||||||
| chr4:48004747
|
G | C | 1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-123+6047C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004747 | ||||||
| chr4:48004748
|
T | G | 1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-123+6046A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004748 | ||||||
| chr4:48004752
|
T | A | 1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-123+6042A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004752 | ||||||
| chr4:48004753
|
T | A | 1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-123+6041A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004753 | ||||||
| chr4:48004755
|
T | A | 1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-123+6039A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004755 | ||||||
| chr4:48004757
|
T | A | 1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-123+6037A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004757 | ||||||
| chr4:48004758
|
A | C | 1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-123+6036T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004758 | ||||||
| chr4:48004759
|
T | A | 1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-123+6035A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004759 | ||||||
| chr4:48004761
|
T | C | 1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-123+6033A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004761 | ||||||
| chr4:48004763
|
A | C | 1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-123+6031T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004763 | ||||||
| chr4:48004764
|
A | C | 1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-123+6030T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004764 | ||||||
| chr4:48004765
|
T | C | 1 | a0002c0002t0002g0182 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-123+6029A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004765 | ||||||
| chr4:48004870
|
G | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG02109.hp2 HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-123+5924C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004870 | ||||||
| chr4:48004877
|
G | T | 1 | a0002c0002t0002g0152 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-123+5917C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004877 | ||||||
| chr4:48004946
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-123+5848C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48004946 | ||||||
| chr4:48005105
|
A | ATTAT | 131 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(128): Show | 141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.-123+5685_-123+568 others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48005105 | ||||||
| chr4:48005105
|
A | ATTATTTA others(1): Show |
33 | a0001c0001t0001g0205a0001c0001t0001g0226a0001c0001t0001g0228others(30): Show | 33 | HG00423.hp1 HG00558.hp2 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.-123+5681_-123+568 others(12): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48005105 | ||||||
| chr4:48005105
|
A | ATTATTTA others(5): Show |
35 | a0001c0001t0001g0227a0001c0001t0003g0001a0001c0001t0003g0002others(32): Show | 40 | HG00609.hp2 HG00673.hp1 HG02523.hp1 others(37): Show |
intron_variant | MODIFIER | c.-123+5677_-123+568 others(16): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48005105 | ||||||
| chr4:48005126
|
T | TTATG | 42 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(39): Show | 43 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.-123+5667_-123+566 others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48005126 | ||||||
| chr4:48005228
|
C | G | 1 | a0001c0001t0001g0015 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-123+5566G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48005228 | ||||||
| chr4:48005265
|
G | A | 1 | a0001c0001t0006g0212 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-123+5529C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48005265 | ||||||
| chr4:48005501
|
T | C | 1 | a0001c0001t0003g0065 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-123+5293A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48005501 | ||||||
| chr4:48005688
|
C | A | 1 | a0001c0001t0002g0118 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-123+5106G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48005688 | ||||||
| chr4:48005714
|
G | A | 1 | a0001c0001t0001g0286 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-123+5080C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48005714 | ||||||
| chr4:48005902
|
A | G | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-123+4892T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48005902 | ||||||
| chr4:48005988
|
C | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0206a0001c0001t0001g0207 | 3 | HG02109.hp2 HG02145.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-123+4806G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48005988 | ||||||
| chr4:48006153
|
TCTCC | T | 7 | a0001c0001t0001g0256a0001c0001t0001g0274a0001c0001t0001g0275others(4): Show | 7 | NA18969.hp1 NA18985.hp2 NA18999.hp2 others(4): Show |
intron_variant | MODIFIER | c.-123+4637_-123+464 others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48006153 | ||||||
| chr4:48006157
|
C | T | 55 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(52): Show | 63 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.-123+4637G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48006157 | ||||||
| chr4:48006218
|
T | C | 5 | a0002c0002t0002g0117a0002c0002t0002g0183a0002c0002t0002g0184others(2): Show | 5 | HG02027.hp2 NA18747.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.-123+4576A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48006218 | ||||||
| chr4:48006291
|
T | C | 238 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(235): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-123+4503A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48006291 | ||||||
| chr4:48006292
|
G | A | 4 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(1): Show | 4 | HG02080.hp1 HG02129.hp2 NA18612.hp1 others(1): Show |
intron_variant | MODIFIER | c.-123+4502C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48006292 | ||||||
| chr4:48006359
|
T | C | 13 | a0001c0001t0003g0093a0001c0003t0001g0338a0001c0003t0002g0120others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-123+4435A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48006359 | ||||||
| chr4:48006419
|
G | A | 1 | a0003c0006t0008g0017 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-123+4375C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48006419 | ||||||
| chr4:48006455
|
T | A | 1 | a0001c0001t0004g0044 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-123+4339A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48006455 | ||||||
| chr4:48006529
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-123+4265G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48006529 | ||||||
| chr4:48006531
|
G | A | 6 | a0001c0001t0001g0293a0001c0001t0001g0319a0001c0001t0001g0320others(3): Show | 6 | HG01074.hp2 HG01256.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.-123+4263C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48006531 | ||||||
| chr4:48006630
|
ATT | A | 42 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(39): Show | 43 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.-123+4162_-123+416 others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48006630 | ||||||
| chr4:48006648
|
G | C | 1 | a0001c0001t0001g0229 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-123+4146C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48006648 | ||||||
| chr4:48006652
|
C | T | 1 | a0001c0001t0006g0209 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-123+4142G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48006652 | ||||||
| chr4:48006830
|
C | G | 1 | a0001c0001t0001g0254 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-123+3964G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48006830 | ||||||
| chr4:48006903
|
A | G | 107 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0205others(104): Show | 113 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.-123+3891T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48006903 | ||||||
| chr4:48007040
|
T | A | 1 | a0001c0001t0001g0284 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-123+3754A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48007040 | ||||||
| chr4:48007101
|
C | T | 238 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(235): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-123+3693G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48007101 | ||||||
| chr4:48007140
|
C | A | 1 | a0001c0001t0002g0116 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-123+3654G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48007140 | ||||||
| chr4:48007176
|
T | C | 1 | a0001c0001t0001g0290 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-123+3618A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48007176 | ||||||
| chr4:48007291
|
C | G | 238 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(235): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-123+3503G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48007291 | ||||||
| chr4:48007341
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0003g0086 | 4 | HG02559.hp2 HG03209.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-123+3453A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48007341 | ||||||
| chr4:48007669
|
TA | T | 239 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(236): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.-123+3124delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48007669 | ||||||
| chr4:48007685
|
A | T | 1 | a0001c0001t0001g0300 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-123+3109T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48007685 | ||||||
| chr4:48007921
|
C | G | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-123+2873G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48007921 | ||||||
| chr4:48008172
|
T | TAA | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-123+2620_-123+262 others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48008172 | ||||||
| chr4:48008255
|
T | A | 1 | a0001c0001t0001g0230 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-123+2539A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48008255 | ||||||
| chr4:48008372
|
C | T | 1 | a0002c0002t0002g0127 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-123+2422G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48008372 | ||||||
| chr4:48008470
|
C | T | 2 | a0001c0001t0003g0081a0001c0001t0003g0082 | 2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-123+2324G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48008470 | ||||||
| chr4:48008516
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-123+2278T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48008516 | ||||||
| chr4:48008529
|
A | G | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-123+2265T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48008529 | ||||||
| chr4:48008572
|
G | T | 42 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(39): Show | 43 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.-123+2222C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48008572 | ||||||
| chr4:48008599
|
C | G | 2 | a0001c0001t0008g0016a0003c0006t0008g0017 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.-123+2195G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48008599 | ||||||
| chr4:48008609
|
TC | T | 42 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(39): Show | 43 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.-123+2184delG | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48008609 | ||||||
| chr4:48008618
|
ATCTG | A | 42 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(39): Show | 43 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.-123+2172_-123+217 others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48008618 | ||||||
| chr4:48008705
|
A | G | 13 | a0001c0001t0003g0093a0001c0003t0001g0338a0001c0003t0002g0120others(10): Show | 13 | HG00642.hp2 HG01891.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.-123+2089T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48008705 | ||||||
| chr4:48008859
|
C | T | 90 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0196others(87): Show | 93 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.-123+1935G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48008859 | ||||||
| chr4:48009006
|
GGTTTA | G | 131 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(128): Show | 141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.-123+1783_-123+178 others(9): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009006 | ||||||
| chr4:48009195
|
A | G | 328 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(325): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.-123+1599T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009195 | ||||||
| chr4:48009310
|
C | T | 1 | a0001c0001t0001g0299 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-123+1484G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009310 | ||||||
| chr4:48009322
|
C | T | 25 | a0001c0001t0004g0031a0001c0001t0004g0032a0001c0001t0004g0033others(22): Show | 25 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.-123+1472G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009322 | ||||||
| chr4:48009327
|
G | A | 1 | a0002c0002t0007g0096 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-123+1467C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009327 | ||||||
| chr4:48009390
|
G | A | 1 | a0001c0001t0001g0223 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-123+1404C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009390 | ||||||
| chr4:48009456
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-123+1338C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009456 | ||||||
| chr4:48009456
|
G | C | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-123+1338C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009456 | ||||||
| chr4:48009464
|
C | CA | 61 | a0001c0001t0001g0011a0001c0001t0001g0015a0001c0001t0001g0213others(58): Show | 63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.-123+1329dupT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009464 | ||||||
| chr4:48009464
|
C | CAA | 62 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(59): Show | 67 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.-123+1328_-123+132 others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009464 | ||||||
| chr4:48009517
|
T | C | 1 | a0001c0001t0001g0285 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-123+1277A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009517 | ||||||
| chr4:48009662
|
T | C | 2 | a0001c0001t0004g0043a0001c0001t0004g0044 | 2 | HG02027.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-123+1132A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009662 | ||||||
| chr4:48009665
|
G | C | 1 | a0001c0001t0003g0093 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-123+1129C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009665 | ||||||
| chr4:48009724
|
A | C | 1 | a0001c0004t0001g0208 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-123+1070T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009724 | ||||||
| chr4:48009795
|
G | A | 238 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(235): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-123+999C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009795 | ||||||
| chr4:48009799
|
C | T | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-123+995G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009799 | ||||||
| chr4:48009808
|
A | G | 8 | a0002c0002t0002g0125a0002c0002t0002g0126a0002c0002t0002g0146others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-123+986T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009808 | ||||||
| chr4:48009820
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-123+974T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009820 | ||||||
| chr4:48009930
|
A | G | 65 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(62): Show | 70 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.-123+864T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009930 | ||||||
| chr4:48009976
|
C | T | 1 | a0001c0001t0003g0070 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-123+818G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009976 | ||||||
| chr4:48010025
|
T | C | 42 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(39): Show | 43 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.-123+769A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48010025 | ||||||
| chr4:48010326
|
T | C | 6 | a0001c0003t0003g0087a0001c0003t0003g0088a0001c0003t0003g0089others(3): Show | 6 | HG00642.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-123+468A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48010326 | ||||||
| chr4:48010499
|
G | A | 2 | a0002c0002t0002g0185a0002c0002t0002g0186 | 2 | HG01346.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.-123+295C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48010499 | ||||||
| chr4:48010623
|
T | C | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-123+171A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48010623 | ||||||
| chr4:48010660
|
G | A | 61 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(58): Show | 66 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.-123+134C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48010660 | ||||||
| chr4:48011084
|
CT | C | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0001g0344 | 3 | NA19004.hp1 NA19007.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-222-192delA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48011084 | ||||||
| chr4:48011220
|
G | A | 42 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(39): Show | 43 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.-222-327C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48011220 | ||||||
| chr4:48011299
|
G | GA | 106 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0205others(103): Show | 112 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.-222-407dupT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48011299 | ||||||
| chr4:48011312
|
T | TA | 60 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(57): Show | 65 | HG00423.hp1 HG00609.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.-222-420dupT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48011312 | ||||||
| chr4:48011342
|
G | A | 1 | a0001c0001t0001g0340 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-222-449C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48011342 | ||||||
| chr4:48011342
|
G | GA | 45 | a0001c0001t0001g0014a0001c0001t0001g0204a0001c0001t0001g0205others(42): Show | 46 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.-222-450dupT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48011342 | ||||||
| chr4:48011380
|
C | T | 1 | a0001c0001t0001g0238 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-222-487G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48011380 | ||||||
| chr4:48011404
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-222-511A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48011404 | ||||||
| chr4:48011412
|
T | TAC | 80 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(77): Show | 88 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.-222-521_-222-520d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48011412 | ||||||
| chr4:48011412
|
TAC | T | 41 | a0001c0001t0001g0014a0001c0001t0001g0297a0001c0001t0002g0118others(38): Show | 42 | HG00099.hp2 HG00639.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.-222-521_-222-520d others(4): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48011412 | ||||||
| chr4:48011412
|
TACACAC | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-222-525_-222-520d others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48011412 | ||||||
| chr4:48011587
|
G | A | 1 | a0001c0001t0001g0225 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-222-694C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48011587 | ||||||
| chr4:48011700
|
A | G | 1 | a0004c0005t0003g0071 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-222-807T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48011700 | ||||||
| chr4:48011773
|
A | G | 220 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(217): Show | 236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.-222-880T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48011773 | ||||||
| chr4:48012163
|
T | C | 2 | a0001c0001t0004g0068a0001c0001t0004g0072 | 2 | HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-222-1270A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012163 | ||||||
| chr4:48012215
|
T | A | 1 | a0001c0001t0003g0077 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-222-1322A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012215 | ||||||
| chr4:48012216
|
C | T | 1 | a0001c0001t0003g0077 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-222-1323G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012216 | ||||||
| chr4:48012403
|
G | A | 1 | a0002c0002t0002g0187 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-222-1510C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012403 | ||||||
| chr4:48012463
|
G | C | 58 | a0001c0001t0001g0341a0001c0001t0003g0001a0001c0001t0003g0002others(55): Show | 63 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.-222-1570C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012463 | ||||||
| chr4:48012558
|
C | CT | 57 | a0001c0001t0002g0099a0001c0001t0002g0102a0001c0001t0002g0103others(54): Show | 60 | HG00408.hp1 HG00423.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.-222-1666dupA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012558 | ||||||
| chr4:48012558
|
C | CTT | 25 | a0001c0001t0002g0098a0002c0002t0002g0123a0002c0002t0002g0124others(22): Show | 25 | HG01167.hp2 HG01884.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-222-1667_-222-166 others(6): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012558 | ||||||
| chr4:48012558
|
C | CTTTTTTT others(9): Show |
2 | a0001c0001t0003g0076a0001c0003t0003g0075 | 2 | HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-222-1681_-222-166 others(20): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012558 | ||||||
| chr4:48012558
|
CTTTT | C | 12 | a0001c0001t0001g0237a0001c0001t0001g0254a0001c0001t0001g0255others(9): Show | 12 | HG00280.hp1 HG00280.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.-222-1669_-222-166 others(8): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012558 | ||||||
| chr4:48012558
|
CTTTTT | C | 97 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(94): Show | 105 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.-222-1670_-222-166 others(9): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012558 | ||||||
| chr4:48012558
|
CTTTTTT | C | 12 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(9): Show | 12 | HG01192.hp1 HG01943.hp2 HG01993.hp1 others(9): Show |
intron_variant | MODIFIER | c.-222-1671_-222-166 others(10): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012558 | ||||||
| chr4:48012558
|
CTTTTTTT others(2): Show |
C | 12 | a0001c0001t0003g0001a0001c0001t0003g0005a0001c0001t0003g0021others(9): Show | 15 | HG00673.hp1 HG02523.hp1 NA18939.hp2 others(12): Show |
intron_variant | MODIFIER | c.-222-1674_-222-166 others(13): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012558 | ||||||
| chr4:48012558
|
CTTTTTTT others(3): Show |
C | 53 | a0001c0001t0003g0002a0001c0001t0003g0019a0001c0001t0003g0045others(50): Show | 55 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.-222-1675_-222-166 others(14): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012558 | ||||||
| chr4:48012558
|
CTTTTTTT others(4): Show |
C | 33 | a0001c0001t0001g0011a0001c0001t0001g0213a0001c0001t0001g0217others(30): Show | 34 | HG00140.hp1 HG00323.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.-222-1676_-222-166 others(15): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012558 | ||||||
| chr4:48012558
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0232a0001c0001t0001g0253a0001c0004t0001g0233 | 3 | HG01261.hp1 HG01517.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.-222-1677_-222-166 others(16): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012558 | ||||||
| chr4:48012558
|
CTTTTTTT others(7): Show |
C | 8 | a0001c0001t0003g0086a0001c0001t0003g0093a0001c0003t0003g0087others(5): Show | 8 | HG00642.hp2 HG01891.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-222-1679_-222-166 others(18): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012558 | ||||||
| chr4:48012558
|
CTTTTTTT others(9): Show |
C | 1 | a0002c0002t0002g0199 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-222-1681_-222-166 others(20): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012558 | ||||||
| chr4:48012648
|
TTGATCAA others(23): Show |
T | 34 | a0001c0001t0001g0011a0001c0001t0001g0213a0001c0001t0001g0217others(31): Show | 35 | HG00140.hp1 HG00323.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.-222-1785_-222-175 others(34): Show |
CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012648 | ||||||
| chr4:48012748
|
C | T | 48 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(45): Show | 54 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.-222-1855G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012748 | ||||||
| chr4:48012821
|
G | A | 3 | a0001c0001t0003g0081a0001c0001t0003g0082a0001c0001t0005g0342 | 3 | HG02559.hp1 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-222-1928C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012821 | ||||||
| chr4:48012842
|
C | T | 2 | a0002c0002t0002g0123a0002c0002t0002g0124 | 2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.-222-1949G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012842 | ||||||
| chr4:48012896
|
C | T | 1 | a0002c0002t0003g0074 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-222-2003G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012896 | ||||||
| chr4:48012955
|
C | CA | 7 | a0001c0001t0001g0234a0001c0001t0004g0072a0001c0003t0002g0120others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.-222-2063dupT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012955 | ||||||
| chr4:48012960
|
A | C | 124 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(121): Show | 134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.-222-2067T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012960 | ||||||
| chr4:48012966
|
A | C | 1 | a0001c0004t0001g0208 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-222-2073T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48012966 | ||||||
| chr4:48013018
|
A | G | 237 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(234): Show | 253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-222-2125T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48013018 | ||||||
| chr4:48013026
|
T | G | 1 | a0001c0001t0001g0343 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-222-2133A>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48013026 | ||||||
| chr4:48013143
|
C | G | 34 | a0001c0001t0001g0011a0001c0001t0001g0213a0001c0001t0001g0217others(31): Show | 35 | HG00140.hp1 HG00323.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.-222-2250G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48013143 | ||||||
| chr4:48013243
|
G | T | 1 | a0001c0001t0001g0250 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-222-2350C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48013243 | ||||||
| chr4:48013272
|
C | A | 1 | a0001c0001t0001g0344 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-222-2379G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48013272 | ||||||
| chr4:48013277
|
A | G | 1 | a0002c0002t0002g0117 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-222-2384T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48013277 | ||||||
| chr4:48013288
|
C | T | 7 | a0001c0001t0003g0086a0001c0003t0003g0087a0001c0003t0003g0088others(4): Show | 7 | HG00642.hp2 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-222-2395G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48013288 | ||||||
| chr4:48013701
|
G | A | 1 | a0001c0001t0001g0345 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-223+2782C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48013701 | ||||||
| chr4:48014171
|
T | C | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG02132.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.-223+2312A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48014171 | ||||||
| chr4:48014260
|
G | A | 2 | a0001c0001t0003g0083a0001c0001t0003g0084 | 2 | HG02897.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-223+2223C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48014260 | ||||||
| chr4:48014304
|
A | C | 1 | a0001c0001t0003g0019 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-223+2179T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48014304 | ||||||
| chr4:48014421
|
GA | G | 109 | a0001c0001t0001g0011a0001c0001t0001g0213a0001c0001t0001g0217others(106): Show | 115 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-223+2061delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48014421 | ||||||
| chr4:48014423
|
A | G | 59 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0005others(56): Show | 64 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.-223+2060T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48014423 | ||||||
| chr4:48014453
|
C | A | 125 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0012others(122): Show | 135 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.-223+2030G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48014453 | ||||||
| chr4:48014737
|
A | G | 1 | a0001c0001t0002g0102 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-223+1746T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48014737 | ||||||
| chr4:48014858
|
A | G | 109 | a0001c0001t0001g0011a0001c0001t0001g0213a0001c0001t0001g0217others(106): Show | 115 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-223+1625T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48014858 | ||||||
| chr4:48014868
|
T | A | 1 | a0002c0002t0002g0201 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-223+1615A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48014868 | ||||||
| chr4:48014892
|
G | A | 1 | a0002c0002t0002g0202 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-223+1591C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48014892 | ||||||
| chr4:48015035
|
G | A | 2 | a0001c0001t0003g0083a0001c0001t0003g0084 | 2 | HG02897.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-223+1448C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48015035 | ||||||
| chr4:48015212
|
G | A | 328 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(325): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.-223+1271C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48015212 | ||||||
| chr4:48015213
|
C | G | 4 | a0001c0001t0002g0098a0001c0001t0002g0099a0001c0001t0002g0100others(1): Show | 4 | HG02257.hp2 HG02818.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-223+1270G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48015213 | ||||||
| chr4:48015551
|
C | T | 1 | a0001c0001t0006g0248 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-223+932G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48015551 | ||||||
| chr4:48015605
|
C | T | 11 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0239others(8): Show | 11 | HG01243.hp1 HG02486.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.-223+878G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48015605 | ||||||
| chr4:48015622
|
A | G | 31 | a0001c0001t0001g0011a0001c0001t0001g0213a0001c0001t0001g0217others(28): Show | 32 | HG00140.hp1 HG00323.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.-223+861T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48015622 | ||||||
| chr4:48015863
|
G | T | 1 | a0002c0002t0002g0097 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-223+620C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48015863 | ||||||
| chr4:48015957
|
T | A | 1 | a0001c0001t0001g0346 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-223+526A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48015957 | ||||||
| chr4:48016153
|
C | T | 109 | a0001c0001t0001g0011a0001c0001t0001g0213a0001c0001t0001g0217others(106): Show | 115 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-223+330G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48016153 | ||||||
| chr4:48016183
|
G | C | 1 | a0001c0001t0003g0085 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-223+300C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48016183 | ||||||
| chr4:48016212
|
A | G | 109 | a0001c0001t0001g0011a0001c0001t0001g0213a0001c0001t0001g0217others(106): Show | 115 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.-223+271T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48016212 | ||||||
| chr4:48016279
|
G | T | 4 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG02109.hp2 HG02145.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.-223+204C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48016279 | ||||||
| chr4:48016311
|
C | T | 70 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0005others(67): Show | 75 | HG00099.hp2 HG00423.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.-223+172G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48016311 | ||||||
| chr4:48016359
|
C | G | 3 | a0001c0001t0005g0009a0001c0001t0005g0010a0001c0001t0005g0203 | 5 | HG01884.hp2 HG02895.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-223+124G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48016359 | ||||||
| chr4:48016443
|
C | A | 1 | a0001c0001t0001g0347 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-223+40G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48016443 |