Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MKNNI others(681): Show |
chr4 | 47930977 | 48021681 |
| a0002 | 0/0 | 686 | 93 | 20 | 8 | 55 | 0 | 10 | 46 | CNGA1_chr4_47930977_48021681 | CNGA1 | MKNNI others(681): Show |
chr4 | 47930977 | 48021681 |
| a0003 | 0/0 | 686 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | MKNNI others(681): Show |
chr4 | 47930977 | 48021681 |
| a0004 | 0/0 | 686 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | MKNNI others(681): Show |
chr4 | 47930977 | 48021681 |
| a0005 | 0/0 | 686 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | MKNNI others(681): Show |
chr4 | 47930977 | 48021681 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2058 | 250 | 57 | 51 | 102 | 15 | 23 | CNGA1_chr4_47930977_48021681 | CNGA1 | ATGAA others(2053): Show |
chr4 | 47930977 | 48021681 | ||
| a0001c0003 | 0/0 | 2058 | 13 | 12 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | ATGAA others(2053): Show |
chr4 | 47930977 | 48021681 | ||
| a0001c0004 | 0/0 | 2058 | 7 | 0 | 4 | 0 | 1 | 2 | CNGA1_chr4_47930977_48021681 | CNGA1 | ATGAA others(2053): Show |
chr4 | 47930977 | 48021681 | ||
| a0002c0002 | 0/0 | 2058 | 93 | 20 | 8 | 55 | 0 | 10 | CNGA1_chr4_47930977_48021681 | CNGA1 | ATGAA others(2053): Show |
chr4 | 47930977 | 48021681 | ||
| a0003c0006 | 0/0 | 2058 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | ATGAA others(2053): Show |
chr4 | 47930977 | 48021681 | ||
| a0004c0007 | 0/0 | 2058 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | ATGAA others(2053): Show |
chr4 | 47930977 | 48021681 | ||
| a0005c0005 | 0/0 | 2058 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | ATGAA others(2053): Show |
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 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0001c0001t0002 | 1/0 | 2926 | 23 | 17 | 1 | 4 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0001c0001t0003 | 0/0 | 2926 | 54 | 10 | 5 | 36 | 0 | 3 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0001c0001t0004 | 0/0 | 2926 | 17 | 1 | 6 | 2 | 3 | 5 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0001c0001t0005 | 0/0 | 2926 | 6 | 6 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0001c0001t0006 | 0/0 | 2926 | 5 | 0 | 5 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0001c0001t0008 | 0/0 | 2926 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0001c0001t0009 | 0/0 | 2926 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0001c0001t0011 | 0/0 | 2926 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0001c0003t0001 | 0/0 | 2926 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0001c0003t0002 | 0/0 | 2926 | 3 | 3 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0001c0003t0003 | 0/0 | 2926 | 9 | 8 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0001c0004t0001 | 0/0 | 2926 | 7 | 0 | 4 | 0 | 1 | 2 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0002c0002t0001 | 0/0 | 2926 | 3 | 0 | 1 | 1 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0002c0002t0002 | 0/0 | 2926 | 84 | 19 | 7 | 53 | 0 | 5 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0002c0002t0003 | 0/0 | 2926 | 2 | 1 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0002c0002t0007 | 0/0 | 2926 | 3 | 0 | 0 | 0 | 0 | 3 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0002c0002t0010 | 0/0 | 2926 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0003c0006t0008 | 0/0 | 2926 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0004c0007t0001 | 0/0 | 2926 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| a0005c0005t0003 | 0/0 | 2926 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | AGCGC others(2921): Show |
chr4 | 47930977 | 48021681 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0269 | 0/1 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 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 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0321 | 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 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 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 |
| a0001c0001t0002g0113 | 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 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 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 |
| 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 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 1 | 0 | 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 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0004g0048 | 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 |
| a0001c0001t0005g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0005g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0006g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0006g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0006g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0006g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0006g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0009g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0001t0011g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0003t0001g0324 | 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 |
| a0001c0003t0003g0027 | 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 |
| a0001c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0004t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0004t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0004t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0004t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0004t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0001c0004t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0004 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0013 | 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 |
| a0002c0002t0002g0114 | 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 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 |
| a0002c0002t0002g0178 | 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 | 1 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | 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 |
| 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 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0002c0002t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| 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 |
| a0002c0002t0010g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0003c0006t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0004c0007t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| a0005c0005t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | g0299 | EUR | GBR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0036 | EUR | GBR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00140 | hp1 | a0001 | c0004 | t0001 | g0215 | EUR | GBR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0290 | EUR | GBR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0281 | EUR | FIN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0331 | EUR | FIN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0273 | EUR | FIN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0212 | EUR | FIN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00408 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0006 | 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 | g0167 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0257 | 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 | g0225 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0206 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00642 | hp1 | a0001 | c0001 | t0004 | g0035 | 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 | g0031 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00733 | hp1 | a0001 | c0004 | t0001 | g0211 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00733 | hp2 | a0001 | c0001 | t0006 | g0205 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0049 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0037 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01071 | hp1 | a0002 | c0002 | t0002 | g0155 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0332 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01109 | hp1 | a0001 | c0001 | t0006 | g0204 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0240 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0060 | 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 | g0295 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0059 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0046 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01243 | hp2 | a0001 | c0004 | t0001 | g0209 | 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 | g0277 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01256 | hp1 | a0001 | c0004 | t0001 | g0309 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01257 | hp2 | a0001 | c0004 | t0001 | g0210 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01346 | hp1 | a0001 | c0001 | t0006 | g0239 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0180 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01361 | hp1 | a0001 | c0001 | t0004 | g0044 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01433 | hp2 | a0001 | c0001 | t0006 | g0207 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0329 | 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 | g0038 | EUR | IBS | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0227 | 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 | g0015 | 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 | g0308 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0181 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0310 | 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 | g0323 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0289 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0151 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0193 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0153 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02055 | hp1 | a0002 | c0002 | t0002 | g0183 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02129 | hp1 | a0002 | c0002 | t0002 | g0194 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0231 | 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 | g0202 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0321 | 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 | g0285 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0196 | AMR | PEL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02280 | hp1 | a0001 | c0003 | t0003 | g0027 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0169 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0017 | 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 | g0112 | 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 | g0028 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0189 | EAS | KHV | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0232 | 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 | g0050 | 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 | g0025 | 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 | g0236 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0011 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0318 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0042 | 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 | g0023 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0113 | 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 | g0280 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02809 | hp1 | a0003 | c0006 | t0008 | g0024 | 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 | g0003 | 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 | g0195 | 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 | g0198 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0166 | 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 | g0015 | 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 | g0110 | 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 | g0148 | AFR | ESN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0235 | 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 | g0199 | AFR | GWD | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0016 | 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 | g0238 | AFR | ESN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0234 | 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 | g0007 | 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 | g0115 | AFR | MSL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0276 | 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 | g0328 | AFR | MSL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0114 | AFR | MSL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0039 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03491 | hp2 | a0001 | c0004 | t0001 | g0228 | 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 | g0111 | AFR | ESN | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0007 | 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 | g0214 | 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 | g0265 | 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 | g0302 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0176 | 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 | g0219 | SAS | PJL | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03831 | hp1 | a0004 | c0007 | t0001 | g0301 | SAS | BEB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0156 | SAS | BEB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03927 | hp1 | a0001 | c0004 | t0001 | g0203 | SAS | BEB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG03927 | hp2 | a0001 | c0001 | t0011 | g0149 | 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 | g0173 | SAS | BEB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0164 | SAS | STU | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | STU | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0300 | SAS | STU | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0040 | SAS | STU | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0220 | 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 | g0011 | 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 | g0270 | EAS | CHB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0158 | EAS | CHB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0178 | 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 | g0019 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0185 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0188 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0002 | 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 | g0242 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0019 | 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 | g0184 | 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 | g0221 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0165 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0174 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0171 | 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 | g0034 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18974 | hp2 | a0002 | c0002 | t0002 | g0170 | 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 | g0002 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0012 | 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 | g0002 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0004 | 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 | g0182 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0175 | 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 | g0029 | 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 | g0264 | 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 | g0013 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0033 | 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 | g0268 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0197 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0283 | 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 | g0297 | 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 | g0138 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0192 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0012 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0001 | 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 | g0266 | 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 | g0201 | AFR | LWK | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | LWK | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0016 | AFR | LWK | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19055 | hp1 | a0002 | c0002 | t0002 | g0168 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0177 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0160 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0186 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0293 | 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 | g0154 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19078 | hp1 | a0005 | c0005 | t0003 | g0071 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0150 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0009 | 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 | g0286 | 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 | g0306 | 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 | g0001 | 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 | g0001 | 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 | g0172 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0324 | AFR | YRI | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | ASW | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ASW | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | TSI | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0317 | EUR | TSI | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0319 | EUR | TSI | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | GIH | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | GIH | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG01123 | hp2 | a0001 | c0001 | t0004 | g0045 | 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 | g0200 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02486 | hp1 | a0002 | c0002 | t0002 | g0147 | AFR | ACB | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0237 | 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 | g0003 | 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 | g0282 | AFR | USA | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0043 | 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 | a0001 | c0001 | t0001 | g0269 | REF | REF | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0105 | REF | REF | CNGA1_chr4_47930977_48021681 | CNGA1 | chr4 | 47930977 | 48021681 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:47936809 | G | A | 1 | a0005 | 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 | a0002 a0004 |
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 | a0004 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0008 others(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 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(12): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): 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 | a0001c0001t0003 a0001c0001t0004 a0001c0003t0003 others(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 | a0001c0001t0008 a0001c0001t0009 a0003c0006t0008 |
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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:47938173 | CA | C | 232 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(229): Show |
253 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.653-345delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938173 | |||||||
| chr4:47938173 | CAA | C | 48 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(45): 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | 285 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(282): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): 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 | 178 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(175): Show |
198 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.653-569dupA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47938397 | |||||||
| chr4:47938397 | A | ATT | 56 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0221 others(53): 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 | 50 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0208 others(47): 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 | a0001c0001t0001g0303 | 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 | 285 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(282): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): 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 | a0002c0002t0002g0133 a0002c0002t0002g0139 a0002c0002t0002g0170 others(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 | a0001c0001t0002g0098 a0001c0001t0002g0099 a0001c0001t0002g0100 others(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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | a0002c0002t0002g0151 | 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 | a0001c0001t0001g0220 | 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 | a0001c0001t0001g0285 a0001c0001t0004g0036 a0001c0001t0004g0037 others(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 | a0001c0003t0003g0027 a0001c0003t0003g0075 a0001c0003t0003g0090 others(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 | a0001c0003t0003g0027 a0001c0003t0003g0075 a0001c0003t0003g0090 others(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 | a0001c0003t0003g0027 a0001c0003t0003g0075 a0001c0003t0003g0090 others(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 | a0001c0001t0008g0023 a0001c0003t0001g0324 a0001c0003t0002g0120 others(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 | a0001c0003t0003g0027 a0001c0003t0003g0075 a0001c0003t0003g0090 others(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 | a0001c0003t0003g0027 a0001c0003t0003g0075 a0001c0003t0003g0090 others(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 | a0002c0002t0002g0187 | 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 | a0002c0002t0002g0187 | 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 | 285 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(282): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.652+1176G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 10/10 | chr4 | 47939587 | |||||||
| chr4:47939614 | G | A | 52 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0208 others(49): 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 | 14 | a0002c0002t0002g0011 a0002c0002t0002g0097 a0002c0002t0002g0114 others(11): 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 | a0001c0001t0001g0297 | 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 | a0001c0001t0001g0302 | 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 | a0001c0001t0001g0304 | 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 | 285 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(282): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): 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 | a0001c0003t0002g0120 a0001c0003t0002g0121 a0001c0003t0002g0122 others(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 | 327 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(324): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): 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 | a0001c0001t0001g0219 | 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 | 290 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(287): Show |
323 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.545+28delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 9/10 | chr4 | 47942012 | |||||||
| chr4:47942030 | A | G | 4 | a0001c0001t0001g0248 a0001c0001t0001g0255 a0001c0001t0001g0257 others(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 | 67 | a0001c0001t0001g0003 a0001c0001t0001g0199 a0001c0001t0001g0200 others(64): 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 | 213 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0017 others(210): Show |
231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): 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 | a0001c0001t0001g0292 a0001c0003t0001g0324 a0001c0003t0002g0120 others(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 | a0001c0001t0001g0294 | 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 | a0001c0003t0001g0324 a0001c0003t0003g0027 a0001c0003t0003g0075 others(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 | a0001c0001t0004g0042 | 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 | a0001c0001t0003g0031 | 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 | a0002c0002t0001g0252 a0002c0002t0002g0137 a0002c0002t0002g0138 others(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 | 8 | a0001c0001t0001g0003 a0001c0001t0001g0232 a0001c0001t0001g0233 others(5): 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 | 289 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.437+345C>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 8/10 | chr4 | 47942836 | |||||||
| chr4:47942855 | C | G | 289 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.437+326G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 8/10 | chr4 | 47942855 | |||||||
| chr4:47942865 | C | T | 52 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0208 others(49): 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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | 289 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.288-26G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47943438 | |||||||
| chr4:47943653 | G | T | 52 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0208 others(49): 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 | a0001c0001t0001g0249 a0001c0001t0001g0280 a0001c0001t0001g0285 others(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 | 302 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(299): Show |
333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): Show |
intron_variant | MODIFIER | c.288-385G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47943797 | |||||||
| chr4:47943874 | C | T | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(163): Show |
179 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(176): 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 | a0001c0001t0003g0034 | 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 | a0001c0001t0001g0219 | 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 | a0001c0001t0004g0043 | 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 | 12 | a0001c0001t0001g0003 a0001c0001t0001g0232 a0001c0001t0001g0233 others(9): 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 | a0001c0001t0001g0287 | 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 | a0001c0001t0001g0272 | 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 | a0001c0001t0006g0204 | 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 | a0001c0001t0003g0049 | 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 | 289 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(286): Show |
320 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(317): 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 | a0001c0003t0001g0324 a0001c0003t0002g0120 a0001c0003t0002g0121 others(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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | a0001c0001t0001g0241 | 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 | a0001c0003t0001g0324 a0001c0003t0002g0120 a0001c0003t0002g0121 others(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 | a0002c0002t0001g0240 a0002c0002t0001g0300 a0002c0002t0002g0156 others(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 | 302 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(299): Show |
333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): 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 | a0001c0001t0001g0231 | 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 | a0002c0002t0002g0151 | 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 | a0001c0001t0001g0273 | 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 | 64 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(61): 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 | 26 | a0001c0001t0001g0007 a0001c0001t0001g0289 a0001c0001t0003g0066 others(23): 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 | 302 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(299): Show |
333 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(330): 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 | 304 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(301): Show |
337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): 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 | a0001c0003t0001g0324 a0001c0003t0002g0120 a0001c0003t0002g0121 others(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 | 2 | a0001c0001t0003g0009 a0001c0001t0003g0029 |
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 | a0001c0004t0001g0209 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0266 a0001c0001t0001g0267 |
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 | a0001c0001t0002g0110 | 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 | 179 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(176): Show |
192 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.287+1647dupT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47948185 | |||||||
| chr4:47948229 | G | A | 303 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(300): Show |
336 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.287+1604C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 6/10 | chr4 | 47948229 | |||||||
| chr4:47948239 | C | T | 64 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(61): 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 | a0002c0002t0002g0170 | 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 | 166 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(163): Show |
179 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(176): 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | 304 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(301): Show |
337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): 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 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 others(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 | a0002c0002t0002g0123 a0002c0002t0002g0124 |
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 | a0001c0001t0009g0025 | 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 | a0001c0001t0001g0293 | 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 | a0001c0001t0001g0208 | 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 | 304 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(301): Show |
337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): 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 | a0001c0003t0001g0324 a0001c0003t0002g0120 a0001c0003t0002g0121 others(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 | 291 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(288): Show |
324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): 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 | a0002c0002t0002g0187 | 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 | a0001c0003t0001g0324 a0001c0003t0002g0120 a0001c0003t0002g0121 others(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 | 46 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(43): 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 | a0001c0003t0001g0324 a0001c0003t0002g0120 a0001c0003t0002g0121 others(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 | a0001c0003t0001g0324 | 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 | a0001c0003t0001g0324 a0001c0003t0002g0120 a0001c0003t0002g0121 others(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 | 225 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(222): Show |
248 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(245): 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 | a0001c0003t0001g0324 a0001c0003t0002g0120 a0001c0003t0002g0121 others(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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | 291 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(288): Show |
324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.224+423T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47950930 | |||||||
| chr4:47951070 | A | G | 291 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(288): Show |
324 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(321): Show |
intron_variant | MODIFIER | c.224+283T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 5/10 | chr4 | 47951070 | |||||||
| chr4:47951130 | T | C | 304 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(301): Show |
337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): 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 | a0002c0002t0002g0012 a0002c0002t0002g0174 |
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 | a0002c0002t0002g0171 | 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 | 304 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(301): Show |
337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): 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 | a0001c0003t0001g0324 a0001c0003t0002g0120 a0001c0003t0002g0121 others(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 | a0001c0001t0004g0039 | 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 | a0002c0002t0002g0153 | 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 | a0002c0002t0002g0150 a0002c0002t0002g0184 a0002c0002t0002g0185 |
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 | a0001c0003t0001g0324 a0001c0003t0002g0120 a0001c0003t0002g0121 others(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 | 35 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(32): Show |
42 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.107+422C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 4/10 | chr4 | 47952161 | |||||||
| chr4:47952208 | C | CA | 167 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(164): Show |
180 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(177): 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 | 100 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(97): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(108): 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 | a0001c0001t0001g0246 a0001c0001t0001g0260 a0001c0004t0001g0209 others(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 | 77 | a0001c0001t0001g0021 a0001c0001t0001g0216 a0001c0001t0001g0221 others(74): 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 | a0001c0001t0001g0233 a0001c0001t0003g0077 a0001c0001t0003g0079 others(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 | a0001c0003t0001g0324 a0001c0003t0002g0120 a0001c0003t0002g0121 others(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 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
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 | 305 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(302): Show |
338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): 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 | a0001c0001t0001g0262 | 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 | 177 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(174): Show |
190 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.-14-1038A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47953741 | |||||||
| chr4:47953814 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0232 a0001c0001t0001g0233 others(5): 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 | 178 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(175): Show |
191 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(188): 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 | a0002c0002t0002g0177 | 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 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 others(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 | 304 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(301): Show |
337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.-14-1419T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47954122 | |||||||
| chr4:47954215 | C | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0017 others(78): 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 | a0001c0001t0001g0199 | 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 | 164 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(161): Show |
177 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(174): 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 | a0001c0001t0002g0098 a0001c0001t0002g0099 a0001c0001t0002g0100 others(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 | a0001c0003t0001g0324 a0001c0003t0002g0120 a0001c0003t0002g0121 others(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 | 177 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(174): Show |
190 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.-14-1836T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47954539 | |||||||
| chr4:47954674 | A | T | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | a0001c0001t0001g0303 | 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 | a0002c0002t0002g0136 a0002c0002t0002g0168 |
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 | 54 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0208 others(51): 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 | 117 | a0001c0001t0002g0098 a0001c0001t0002g0099 a0001c0001t0002g0100 others(114): 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 | 304 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(301): Show |
337 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.-14-2371C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955074 | |||||||
| chr4:47955081 | A | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
85 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.-14-2378T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47955081 | |||||||
| chr4:47955147 | C | A | 55 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(52): 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 | a0001c0001t0002g0098 a0001c0001t0002g0099 a0001c0001t0002g0100 others(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 | 45 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(42): 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 | 102 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(99): 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 | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): 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 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
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 | a0002c0002t0010g0173 | 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 | 306 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(303): Show |
339 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(336): 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 | a0001c0001t0003g0058 | 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 | 55 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(52): 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 | a0001c0001t0001g0218 | 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 | a0001c0001t0004g0040 | 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 | a0001c0001t0001g0275 | 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | 54 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0208 others(51): 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | 103 | a0001c0001t0002g0098 a0001c0001t0002g0099 a0001c0001t0002g0100 others(100): 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 | 58 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(55): 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 | 5 | a0001c0001t0001g0022 a0001c0001t0001g0315 a0001c0001t0001g0316 others(2): 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 | 7 | a0001c0001t0001g0003 a0001c0001t0001g0232 a0001c0001t0001g0234 others(4): 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 | 58 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(55): 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0198 others(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 | 301 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(298): Show |
332 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(329): 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 | 55 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(52): 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 | a0001c0003t0002g0120 a0001c0003t0002g0121 a0001c0003t0002g0122 others(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 | a0001c0001t0001g0251 a0002c0002t0002g0179 a0002c0002t0002g0197 |
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 | 57 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0021 others(54): 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 | 117 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(114): 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 | 59 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(56): 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 | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(182): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0307 | 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 | a0001c0001t0001g0272 | 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 | 132 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(129): Show |
150 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.-14-5919delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47958621 | |||||||
| chr4:47958872 | T | C | 1 | a0001c0001t0001g0287 | 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 | 126 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(123): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): 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 | a0001c0001t0001g0318 | 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 | 54 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0208 others(51): 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 | 45 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(42): 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0198 others(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 | a0001c0001t0001g0248 a0001c0001t0001g0257 a0001c0001t0003g0067 |
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 | 54 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(51): 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 | 54 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(51): 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 | a0001c0001t0001g0223 a0001c0001t0001g0333 |
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 | a0001c0001t0005g0016 a0001c0001t0005g0198 |
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 | 7 | a0001c0001t0001g0003 a0001c0001t0001g0232 a0001c0001t0001g0234 others(4): 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 | 7 | a0001c0001t0001g0003 a0001c0001t0001g0232 a0001c0001t0001g0234 others(4): 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 | 7 | a0001c0001t0001g0003 a0001c0001t0001g0232 a0001c0001t0001g0234 others(4): 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 | 184 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(181): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.-14-7343T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47960046 | |||||||
| chr4:47960061 | A | T | 126 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(123): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): 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 | a0001c0001t0001g0268 | 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 | a0001c0001t0001g0218 | 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 | 54 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0208 others(51): 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 | 126 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(123): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.-14-7944A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47960647 | |||||||
| chr4:47960704 | A | G | 126 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(123): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.-14-8001T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47960704 | |||||||
| chr4:47960722 | A | AC | 126 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(123): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): 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 | a0001c0001t0006g0205 a0001c0001t0006g0206 a0001c0001t0006g0207 |
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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | a0001c0001t0001g0243 | 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 | 54 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0208 others(51): 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 | a0001c0001t0001g0199 | 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 | a0001c0001t0001g0021 | 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 | 184 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(181): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): 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 | a0001c0001t0005g0015 a0001c0001t0005g0328 |
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 | 184 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(181): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.-14-9018C>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47961721 | |||||||
| chr4:47961774 | T | C | 125 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.-14-9071A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47961774 | |||||||
| chr4:47961810 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | a0001c0001t0001g0323 | 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 | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | a0001c0001t0001g0223 | 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 | a0001c0001t0003g0059 a0001c0001t0003g0060 |
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 | a0002c0002t0002g0130 a0002c0002t0002g0131 |
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 | a0002c0002t0002g0130 a0002c0002t0002g0131 |
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 | 21 | a0001c0001t0001g0201 a0001c0001t0001g0221 a0001c0001t0001g0222 others(18): 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 | a0001c0001t0001g0017 a0001c0001t0001g0208 a0001c0001t0001g0212 others(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 | 26 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0232 others(23): 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 | 63 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(60): Show |
73 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(70): 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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): 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 | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.-14-9813C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962516 | |||||||
| chr4:47962540 | T | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): 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 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0208 others(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 | a0001c0001t0003g0093 a0001c0003t0001g0324 a0001c0003t0003g0027 others(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 | 58 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(55): Show |
66 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.-14-10004C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47962707 | |||||||
| chr4:47962749 | A | T | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | a0003c0006t0008g0024 | 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 | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | a0002c0002t0002g0186 | 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 | a0001c0001t0002g0103 a0001c0001t0002g0107 a0001c0001t0002g0108 others(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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | a0001c0001t0001g0220 | 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 | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.-14-10827A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47963530 | |||||||
| chr4:47963634 | A | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.-14-10931T>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47963634 | |||||||
| chr4:47963642 | A | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): 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 | a0001c0001t0001g0294 | 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 | a0001c0001t0003g0049 | 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 | a0001c0001t0003g0093 a0001c0003t0001g0324 a0001c0003t0003g0027 others(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 | 303 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(300): Show |
334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): 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 | a0001c0001t0004g0035 | 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 | a0001c0001t0001g0260 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0266 a0001c0001t0001g0267 |
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 | a0001c0001t0003g0063 a0001c0001t0003g0064 |
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 | a0002c0002t0002g0188 | 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 | a0001c0001t0002g0191 a0002c0002t0002g0133 a0002c0002t0002g0139 others(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 | a0002c0002t0002g0137 a0002c0002t0002g0138 a0002c0002t0002g0154 others(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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0261 a0001c0003t0003g0089 a0001c0003t0003g0090 others(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 | 52 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(49): 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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | 303 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(300): Show |
334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): 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 | 303 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(300): Show |
334 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.-14-12987G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47965690 | |||||||
| chr4:47965838 | T | C | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 305 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(302): Show |
338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): 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 | a0001c0001t0009g0025 | 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 | a0001c0001t0001g0244 | 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 | a0001c0001t0001g0291 | 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0261 | 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0198 others(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 | a0001c0001t0005g0016 a0001c0001t0005g0198 |
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 | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | 183 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.-15+13210A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47968183 | |||||||
| chr4:47968333 | T | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(182): Show |
212 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(209): 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 | a0001c0001t0001g0307 | 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0198 others(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 | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): 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 | a0001c0001t0003g0093 a0001c0003t0001g0324 a0001c0003t0003g0027 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0272 | 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 | a0001c0001t0003g0029 | 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 | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): 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 | a0001c0001t0001g0275 | 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 | 59 | a0001c0001t0002g0014 a0001c0001t0002g0191 a0001c0001t0011g0149 others(56): 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 | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0003g0034 a0001c0001t0003g0058 |
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 | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): 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 | a0001c0003t0001g0324 a0001c0003t0003g0027 a0001c0003t0003g0075 others(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 | a0001c0001t0001g0285 | 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 | a0001c0001t0006g0239 | 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 | 64 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(61): 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 | 119 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): 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 | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.-15+10671G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47970722 | |||||||
| chr4:47970833 | GA | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.-15+10559delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47970833 | |||||||
| chr4:47971014 | G | A | 106 | a0001c0001t0002g0014 a0001c0001t0002g0098 a0001c0001t0002g0099 others(103): 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 | a0001c0001t0001g0236 | 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 | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.-15+10300C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47971093 | |||||||
| chr4:47971154 | G | A | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | a0001c0001t0001g0218 a0001c0001t0002g0119 a0001c0001t0003g0076 others(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 | 43 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(40): 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 | 16 | a0001c0001t0001g0327 a0001c0001t0003g0001 a0001c0001t0003g0010 others(13): 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 | 13 | a0001c0001t0001g0003 a0001c0001t0001g0232 a0001c0001t0001g0233 others(10): 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 | 87 | a0001c0001t0002g0014 a0001c0001t0002g0118 a0001c0001t0002g0191 others(84): 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 | a0001c0001t0002g0098 a0001c0001t0002g0099 a0001c0001t0002g0100 others(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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 183 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): 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 | a0001c0001t0004g0035 | 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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | a0001c0001t0001g0226 | 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 | a0001c0001t0002g0112 | 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 | 99 | a0001c0001t0002g0014 a0001c0001t0002g0098 a0001c0001t0002g0099 others(96): 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 | 61 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(58): Show |
71 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(68): 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 | a0002c0002t0002g0142 a0002c0002t0002g0187 a0002c0002t0002g0196 |
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 | 61 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(58): 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 | a0002c0002t0001g0300 a0004c0007t0001g0301 |
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 | a0002c0002t0002g0175 | 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 | a0001c0001t0004g0041 | 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.-15+8389G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973004 | |||||||
| chr4:47973066 | C | CT | 87 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0021 others(84): 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 | 149 | a0001c0001t0001g0003 a0001c0001t0001g0199 a0001c0001t0001g0200 others(146): 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 | a0001c0001t0001g0201 a0001c0001t0001g0232 a0001c0001t0001g0333 others(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 | a0001c0001t0001g0249 a0001c0001t0001g0280 a0001c0001t0001g0329 |
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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): 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 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 others(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 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 others(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 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0003g0083 others(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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): 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 | a0001c0001t0001g0313 | 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 | a0002c0002t0002g0125 a0002c0002t0002g0146 a0002c0002t0002g0183 |
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 | 305 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(302): Show |
338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.-15+7916G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973477 | |||||||
| chr4:47973502 | G | A | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | a0001c0003t0001g0324 a0001c0003t0003g0075 a0001c0003t0003g0089 others(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 | 184 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(181): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.-15+7606C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47973787 | |||||||
| chr4:47973886 | T | C | 121 | a0001c0001t0001g0007 a0001c0001t0002g0014 a0001c0001t0002g0098 others(118): 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 | 7 | a0001c0001t0001g0003 a0001c0001t0001g0232 a0001c0001t0001g0234 others(4): 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 | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
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 | a0001c0001t0004g0043 a0001c0001t0004g0068 a0001c0001t0004g0072 |
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 | a0002c0002t0002g0153 a0002c0002t0002g0165 a0002c0002t0002g0171 others(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 | 47 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0102 others(44): 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 | 23 | a0001c0001t0002g0103 a0001c0001t0002g0106 a0001c0001t0002g0107 others(20): 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 | a0001c0001t0002g0099 a0002c0002t0002g0097 a0002c0002t0002g0126 others(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 | a0001c0001t0002g0014 a0002c0002t0002g0153 a0002c0002t0002g0165 others(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 | 22 | a0001c0001t0001g0003 a0001c0001t0001g0216 a0001c0001t0001g0232 others(19): 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 | a0001c0001t0001g0282 a0001c0003t0003g0087 a0004c0007t0001g0301 |
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 | a0001c0001t0002g0014 a0001c0001t0002g0098 a0001c0001t0002g0104 others(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 | 81 | a0001c0001t0001g0003 a0001c0001t0001g0200 a0001c0001t0001g0212 others(78): 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 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0199 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0022 others(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 | 39 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(36): Show |
46 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(43): 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 | a0001c0001t0001g0262 a0001c0001t0005g0015 a0001c0001t0005g0016 others(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 | a0001c0001t0001g0226 | 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 | 47 | a0001c0001t0002g0100 a0001c0001t0002g0101 a0001c0001t0002g0102 others(44): 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 | 23 | a0001c0001t0002g0103 a0001c0001t0002g0106 a0001c0001t0002g0107 others(20): 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 | a0001c0001t0002g0099 a0002c0002t0002g0097 a0002c0002t0002g0126 others(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 | 308 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(305): Show |
341 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.-15+7187dupG | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974205 | |||||||
| chr4:47974371 | CAA | C | 86 | a0001c0001t0002g0014 a0001c0001t0002g0191 a0001c0001t0011g0149 others(83): 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 | 7 | a0001c0001t0001g0022 a0001c0001t0001g0254 a0001c0001t0001g0315 others(4): 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 | 138 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
153 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.-15+6683dupA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47974709 | |||||||
| chr4:47974709 | G | GTT | 5 | a0001c0001t0001g0007 a0001c0001t0001g0236 a0001c0001t0001g0290 others(2): 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 | a0001c0001t0001g0331 | 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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): 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 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0208 others(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 | a0001c0003t0003g0087 a0001c0003t0003g0088 |
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 | a0001c0001t0001g0305 | 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 | a0002c0002t0002g0171 | 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 | a0001c0001t0001g0320 | 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 | a0001c0001t0001g0214 | 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 | a0001c0001t0001g0320 | 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 | a0001c0004t0001g0209 | 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 | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
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 | a0001c0001t0004g0039 a0001c0001t0004g0040 a0001c0001t0006g0239 |
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 | a0001c0001t0001g0199 a0001c0001t0008g0023 a0003c0006t0008g0024 |
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 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 |
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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): 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 | 11 | a0001c0001t0001g0007 a0001c0001t0003g0086 a0001c0001t0003g0093 others(8): 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 | 76 | a0001c0001t0002g0014 a0001c0001t0002g0098 a0001c0001t0002g0099 others(73): 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 | 14 | a0001c0001t0002g0102 a0001c0001t0002g0191 a0002c0002t0002g0011 others(11): 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 | a0001c0001t0003g0031 a0001c0001t0003g0080 a0001c0001t0003g0082 others(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 | a0001c0001t0003g0076 a0002c0002t0002g0097 |
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 | 45 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(42): 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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0231 a0001c0001t0003g0056 |
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 | a0001c0003t0002g0120 a0001c0003t0002g0121 a0001c0003t0002g0122 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): 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 | a0002c0002t0002g0012 a0002c0002t0002g0127 a0002c0002t0002g0134 others(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 | a0001c0001t0003g0079 a0001c0001t0003g0081 |
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 | 71 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
84 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(81): 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0212 a0001c0001t0001g0227 |
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 | a0001c0001t0001g0021 a0001c0001t0001g0208 a0001c0001t0001g0213 others(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 | 5 | a0001c0001t0002g0014 a0001c0001t0011g0149 a0002c0002t0002g0013 others(2): 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 | 52 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(49): 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 | a0001c0001t0001g0283 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0212 a0001c0001t0001g0227 |
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 | 59 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(56): 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 | a0001c0001t0001g0019 | 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 | a0001c0004t0001g0209 | 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 | a0001c0001t0001g0275 | 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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): 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 | a0001c0001t0001g0255 | 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 | a0001c0003t0003g0087 a0001c0003t0003g0088 |
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 | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): 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 | a0001c0001t0001g0319 | 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 | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | a0001c0001t0001g0278 a0001c0001t0001g0279 |
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 | 247 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(244): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.-15+3564dupA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47977828 | |||||||
| chr4:47977890 | G | A | 1 | a0001c0001t0001g0261 | 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 | a0001c0001t0004g0039 a0001c0001t0004g0040 |
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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): 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 | a0001c0001t0001g0266 | 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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | a0001c0003t0002g0120 a0001c0003t0002g0121 a0001c0003t0002g0122 others(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 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
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 | a0001c0001t0003g0052 | 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 | a0002c0002t0002g0167 | 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 | 43 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(40): 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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-15+2512A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47978881 | |||||||
| chr4:47979220 | C | A | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | a0001c0001t0001g0284 | 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 | 105 | a0001c0001t0002g0014 a0001c0001t0002g0098 a0001c0001t0002g0099 others(102): 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 | a0001c0001t0001g0314 a0001c0001t0002g0115 a0002c0002t0002g0147 others(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 | 59 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(56): Show |
69 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(66): Show |
intron_variant | MODIFIER | c.-15+2072delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47979320 | |||||||
| chr4:47979320 | CAA | C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0021 others(115): 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 | 61 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(58): 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 | a0001c0003t0003g0087 a0001c0003t0003g0088 |
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 | 184 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(181): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): 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 | a0001c0001t0003g0051 | 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 | a0001c0001t0002g0113 a0002c0002t0002g0114 |
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 | a0001c0001t0001g0225 | 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 | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | 223 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(220): Show |
246 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.-15+920delA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 3/10 | chr4 | 47980472 | |||||||
| chr4:47980472 | CTT | C | 11 | a0001c0001t0001g0302 a0001c0001t0002g0115 a0002c0002t0002g0133 others(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 | a0001c0001t0001g0246 | 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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
141 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(138): 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 | a0001c0001t0001g0302 | 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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | a0001c0004t0001g0211 | 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 | 58 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(55): Show |
66 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(63): 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 | a0001c0001t0001g0236 | 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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): 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 |
180 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(177): Show |
205 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(202): 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0003g0066 a0001c0001t0004g0035 a0001c0001t0004g0036 others(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 | a0001c0001t0001g0332 a0001c0001t0003g0079 |
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 | a0001c0001t0001g0285 | 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 | a0001c0001t0003g0093 a0001c0003t0001g0324 a0001c0003t0002g0120 others(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 | a0001c0001t0003g0093 a0001c0003t0001g0324 a0001c0003t0002g0120 others(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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-122-214A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47981714 | |||||||
| chr4:47981764 | C | T | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0314 | 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 | a0001c0004t0001g0215 | 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-122-472T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47981972 | |||||||
| chr4:47982059 | G | A | 184 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(181): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): 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 | a0001c0001t0002g0113 | 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 | 3 | a0001c0001t0003g0002 a0001c0001t0003g0030 a0001c0001t0003g0033 |
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 | a0001c0001t0001g0286 a0001c0001t0001g0288 a0001c0001t0001g0292 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0003g0080 a0002c0002t0003g0074 |
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 | 102 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0200 others(99): 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 | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | a0001c0001t0001g0271 | 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 | a0001c0001t0001g0264 | 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0277 | 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 | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 313 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(310): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): 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 | a0001c0001t0001g0233 | 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 | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(51): Show |
62 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.-122-1753delA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47983252 | |||||||
| chr4:47983281 | C | A | 226 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-122-1781G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47983281 | |||||||
| chr4:47983450 | G | A | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | a0001c0001t0003g0066 a0001c0001t0004g0035 a0001c0001t0004g0036 others(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 | a0001c0001t0003g0066 a0001c0001t0004g0035 a0001c0001t0004g0036 others(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 | a0001c0001t0002g0112 | 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 | a0002c0002t0002g0143 a0002c0002t0002g0144 |
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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
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 | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | a0001c0004t0001g0228 | 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 | a0001c0001t0002g0118 a0001c0001t0004g0069 a0001c0003t0002g0120 others(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 | a0001c0001t0004g0038 a0001c0001t0004g0045 a0001c0001t0004g0046 others(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 | a0001c0001t0004g0035 | 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 | a0001c0001t0003g0093 a0001c0003t0001g0324 a0001c0003t0003g0087 others(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 | a0001c0001t0001g0274 a0001c0001t0001g0276 a0001c0001t0001g0277 others(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 | 16 | a0001c0001t0001g0007 a0001c0001t0003g0076 a0001c0001t0003g0079 others(13): 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 | 202 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0017 others(199): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.-122-3149A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47984649 | |||||||
| chr4:47984651 | T | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0274 others(16): 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 | a0001c0001t0001g0317 | 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 | 46 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(43): Show |
54 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(51): 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 | a0001c0001t0001g0273 | 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 | a0001c0001t0003g0093 a0001c0001t0006g0205 a0001c0003t0001g0324 others(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 | a0001c0001t0001g0017 a0001c0001t0001g0208 a0001c0001t0001g0212 others(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 | 12 | a0001c0001t0001g0003 a0001c0001t0001g0232 a0001c0001t0001g0234 others(9): 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 | 59 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(56): 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 | a0001c0001t0001g0233 | 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 | 22 | a0001c0001t0001g0007 a0001c0001t0001g0316 a0001c0001t0001g0317 others(19): 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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | a0001c0001t0003g0030 | 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0002g0118 a0001c0001t0003g0093 a0001c0001t0006g0205 others(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 | a0001c0001t0003g0066 a0001c0001t0004g0036 a0001c0001t0004g0037 others(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 | 75 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0200 others(72): 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 | a0001c0001t0001g0318 | 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 | a0001c0001t0001g0318 | 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 | 48 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(45): 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 | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | 8 | a0001c0001t0001g0003 a0001c0001t0001g0232 a0001c0001t0001g0233 others(5): 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | 102 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0200 others(99): 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 | a0001c0001t0001g0291 | 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 | a0001c0001t0003g0093 a0001c0003t0003g0087 a0001c0003t0003g0088 others(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 | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | a0001c0003t0003g0087 a0001c0003t0003g0088 a0001c0003t0003g0089 others(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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 95 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0200 others(92): 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 | a0001c0001t0003g0066 a0001c0001t0004g0035 a0001c0001t0004g0036 others(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 | 102 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0200 others(99): 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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): 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 | a0001c0001t0002g0113 a0001c0001t0002g0115 a0002c0002t0002g0114 |
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 | a0001c0001t0003g0026 | 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 | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | a0001c0001t0003g0093 a0001c0003t0001g0324 a0001c0003t0002g0120 others(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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | a0001c0001t0001g0284 | 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 | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | a0002c0002t0002g0193 | 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): 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 | a0001c0001t0003g0093 a0001c0003t0001g0324 a0001c0003t0003g0075 others(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 | a0002c0002t0002g0148 | 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 | 58 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(55): Show |
66 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(63): 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 | a0002c0002t0002g0181 | 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 | a0001c0001t0001g0330 | 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.-122-7482T>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47988982 | |||||||
| chr4:47988983 | A | T | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): 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 | a0001c0001t0001g0297 a0001c0001t0001g0305 a0001c0001t0001g0326 |
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 | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | a0001c0003t0002g0120 a0001c0003t0002g0121 |
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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0198 others(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 | 222 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(219): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): 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 | a0001c0001t0003g0066 a0001c0001t0004g0035 a0001c0001t0004g0036 others(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 | a0001c0001t0001g0326 | 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 | a0001c0001t0001g0326 | 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 | a0001c0001t0005g0016 a0001c0001t0005g0198 |
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 | a0001c0001t0001g0283 | 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 | 225 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): 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 | a0001c0001t0002g0110 | 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 | 102 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0200 others(99): 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 | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | 313 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(310): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): 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 | a0001c0001t0004g0043 | 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 | 160 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(157): Show |
180 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(177): 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 | a0001c0001t0004g0036 a0001c0001t0004g0037 a0001c0001t0004g0038 others(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 | a0001c0001t0001g0216 a0001c0004t0001g0210 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0208 others(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 | a0001c0001t0001g0287 | 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 | 226 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-122-9187A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47990687 | |||||||
| chr4:47990696 | T | C | 313 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(310): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): 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 | a0002c0002t0002g0123 a0002c0002t0002g0124 |
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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | a0001c0001t0003g0066 a0001c0001t0004g0035 a0001c0001t0004g0036 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | 102 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0200 others(99): 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 | a0001c0001t0006g0239 | 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 | a0001c0001t0003g0066 a0001c0001t0004g0035 a0001c0001t0004g0036 others(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 | a0005c0005t0003g0071 | 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | a0001c0001t0009g0025 | 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 | a0001c0001t0001g0258 | 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 | a0002c0002t0002g0143 a0002c0002t0002g0144 |
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 | a0001c0001t0003g0093 a0001c0003t0001g0324 a0001c0003t0002g0120 others(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 | a0001c0001t0001g0286 | 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 | 7 | a0002c0002t0002g0011 a0002c0002t0002g0125 a0002c0002t0002g0126 others(4): 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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-122-10177G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991677 | |||||||
| chr4:47991760 | A | G | 226 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-122-10260T>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47991760 | |||||||
| chr4:47991898 | T | G | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): 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 | a0001c0001t0006g0204 | 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 | a0003c0006t0008g0024 | 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 | a0001c0001t0001g0257 | 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 | 59 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(56): 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 226 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): 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 | a0001c0001t0003g0080 a0002c0002t0003g0074 |
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 | 56 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(53): Show |
64 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.-122-11156A>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992656 | |||||||
| chr4:47992657 | A | ATTAT | 73 | a0001c0001t0001g0021 a0001c0001t0001g0220 a0001c0001t0001g0232 others(70): 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 |
58 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0212 others(55): 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 | a0001c0001t0001g0208 a0001c0001t0001g0218 a0001c0001t0001g0229 others(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 | 56 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(53): Show |
64 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(61): 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 | 28 | a0001c0001t0001g0007 a0001c0001t0003g0066 a0001c0001t0003g0086 others(25): 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0312 a0001c0001t0001g0313 |
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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-122-11483A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47992983 | |||||||
| chr4:47993020 | C | G | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | a0001c0001t0001g0302 | 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 | a0001c0001t0001g0219 | 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): 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 | a0001c0001t0002g0191 | 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 | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | a0001c0001t0004g0043 a0001c0001t0004g0044 a0001c0001t0004g0045 others(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 | a0001c0001t0001g0288 a0001c0001t0001g0303 a0001c0001t0001g0304 others(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 | a0001c0001t0003g0093 a0001c0003t0003g0087 a0001c0003t0003g0088 others(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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 48 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(45): 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | a0001c0001t0001g0263 | 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 | a0002c0002t0002g0172 | 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 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 |
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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-122-13692delG | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47995191 | |||||||
| chr4:47995236 | A | G | 54 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0208 others(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 | 102 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0200 others(99): 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 | a0002c0002t0002g0154 | 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 | 43 | a0001c0001t0001g0007 a0001c0001t0001g0320 a0001c0001t0002g0118 others(40): 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 | 172 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0017 others(169): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.-122-14056dupA | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47995555 | |||||||
| chr4:47995555 | A | ATT | 52 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(49): 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 | a0001c0003t0002g0120 a0001c0003t0002g0121 a0001c0003t0002g0122 others(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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | a0001c0001t0001g0331 | 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 | a0001c0001t0001g0006 a0001c0001t0001g0263 a0001c0001t0001g0264 |
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 | a0002c0002t0002g0176 | 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 | a0001c0003t0001g0324 | 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 | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | a0002c0002t0002g0194 a0002c0002t0010g0173 |
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 | a0002c0002t0002g0192 | 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 | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | a0001c0001t0001g0229 a0001c0001t0006g0204 |
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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | 226 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-123+13092G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47997702 | |||||||
| chr4:47997709 | T | C | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | 226 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): 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 | a0001c0003t0003g0087 a0001c0003t0003g0088 |
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 | a0001c0001t0001g0256 a0001c0001t0001g0278 |
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 | a0001c0001t0001g0238 | 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 | a0001c0001t0001g0305 a0001c0001t0001g0326 |
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 | a0001c0001t0001g0282 a0001c0001t0001g0290 a0001c0001t0001g0307 others(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 | a0001c0001t0001g0289 a0001c0003t0003g0027 |
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 | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | 226 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-123+12023G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47998771 | |||||||
| chr4:47998798 | A | T | 16 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0086 others(13): 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 | a0002c0002t0002g0177 | 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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-123+11758G>A | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 47999036 | |||||||
| chr4:47999108 | G | A | 102 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0200 others(99): 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 | a0001c0001t0003g0093 a0001c0003t0001g0324 a0001c0003t0002g0120 others(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 | a0001c0001t0003g0066 a0001c0001t0004g0035 a0001c0001t0004g0036 others(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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | a0002c0002t0002g0153 | 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 | 124 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): 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 | a0001c0001t0003g0093 a0001c0003t0001g0324 a0001c0003t0002g0120 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | 102 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0200 others(99): 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 | 42 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0066 others(39): 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 | 93 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(90): 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 | 102 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0200 others(99): 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 | a0001c0001t0003g0066 a0001c0001t0004g0035 a0001c0001t0004g0036 others(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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0208 others(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 | a0002c0002t0002g0174 | 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 | a0001c0001t0003g0066 a0001c0001t0004g0035 a0001c0001t0004g0036 others(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 | 218 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(215): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.-123+10053delG | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48000740 | |||||||
| chr4:48000741 | C | G | 4 | a0001c0001t0001g0202 a0001c0001t0001g0265 a0001c0001t0003g0026 others(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 | a0001c0001t0004g0035 | 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 | a0001c0001t0001g0321 | 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 | a0002c0002t0002g0152 | 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 | a0001c0001t0005g0328 | 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 | a0001c0001t0001g0020 a0001c0001t0001g0266 a0001c0001t0001g0267 others(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 | a0001c0001t0001g0243 | 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 | a0001c0003t0002g0120 a0001c0003t0002g0121 a0001c0003t0002g0122 others(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 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0004g0037 others(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 | a0001c0001t0003g0083 a0001c0001t0003g0084 |
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 | a0001c0001t0001g0268 | 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 | 64 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(61): 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 | a0001c0001t0001g0244 | 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0281 a0001c0001t0001g0319 |
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 | a0002c0002t0002g0175 | 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 | 105 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0200 others(102): 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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | 75 | a0001c0001t0001g0003 a0001c0001t0001g0199 a0001c0001t0001g0200 others(72): 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 | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0017 others(110): Show |
125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): 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 | a0001c0001t0003g0093 a0001c0003t0001g0324 a0001c0003t0002g0120 others(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 | 57 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(54): 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 | a0001c0001t0003g0093 a0001c0001t0004g0035 a0001c0001t0004g0036 others(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 | a0001c0001t0002g0118 a0001c0001t0004g0037 a0001c0001t0004g0045 others(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 | a0001c0001t0001g0221 | 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 | 230 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(227): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): 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 | a0001c0001t0003g0063 a0001c0001t0003g0064 |
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 | a0001c0001t0003g0063 a0001c0001t0003g0064 |
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 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0208 others(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 | a0001c0003t0002g0120 a0001c0003t0002g0121 a0001c0003t0002g0122 |
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 | 71 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
84 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(81): 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 | a0001c0001t0008g0023 | 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 | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | 105 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0200 others(102): 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 | a0002c0002t0002g0175 | 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 | a0002c0002t0002g0176 | 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 | a0001c0003t0001g0324 | 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 | 48 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(45): 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 | a0001c0001t0001g0330 | 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0198 others(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 | a0002c0002t0002g0151 | 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 | a0002c0002t0002g0177 | 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 | 48 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(45): 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 | a0002c0002t0002g0177 | 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 | a0002c0002t0002g0177 | 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 | a0002c0002t0002g0177 | 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 | a0002c0002t0002g0177 | 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 | a0002c0002t0002g0177 | 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 | a0002c0002t0002g0177 | 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 | a0002c0002t0002g0177 | 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 | a0002c0002t0002g0177 | 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 | a0002c0002t0002g0177 | 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 | a0002c0002t0002g0177 | 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 | a0002c0002t0002g0177 | 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 | a0002c0002t0002g0177 | 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 | a0002c0002t0002g0177 | 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 | a0002c0002t0002g0177 | 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 | a0002c0002t0002g0177 | 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 | a0002c0002t0002g0177 | 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 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 |
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 | a0002c0002t0002g0150 | 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 | a0001c0001t0001g0255 | 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 | 125 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): 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 | a0001c0001t0001g0200 a0001c0001t0001g0221 a0001c0001t0001g0223 others(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 |
30 | a0001c0001t0001g0222 a0001c0001t0003g0001 a0001c0001t0003g0002 others(27): 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 | 41 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0086 others(38): 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 | a0001c0001t0001g0021 | 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 | a0001c0001t0006g0207 | 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 | a0001c0001t0001g0275 | 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 | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 |
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 | 6 | a0001c0001t0001g0018 a0001c0001t0001g0246 a0001c0001t0001g0250 others(3): 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 | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0019 others(50): Show |
62 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(59): 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 | a0002c0002t0002g0117 a0002c0002t0002g0178 a0002c0002t0002g0179 others(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 | 226 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-123+4503A>G | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48006291 | |||||||
| chr4:48006292 | G | A | 3 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0001g0272 |
3 | HG02080.hp1 HG02129.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.-123+4502C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48006292 | |||||||
| chr4:48006359 | T | C | 13 | a0001c0001t0003g0093 a0001c0003t0001g0324 a0001c0003t0002g0120 others(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 | a0003c0006t0008g0024 | 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 | a0001c0001t0004g0048 | 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 | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | a0001c0001t0001g0282 a0001c0001t0001g0307 a0001c0001t0001g0308 others(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 | 41 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0086 others(38): 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0006g0204 | 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 | a0001c0001t0001g0245 | 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 | 101 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0200 others(98): 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 | a0001c0001t0001g0273 | 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 | 226 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): 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 | a0001c0001t0001g0279 | 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 | 226 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-123+3503G>C | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48007291 | |||||||
| chr4:48007341 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0003g0086 |
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 | 227 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(224): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.-123+3124delT | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48007669 | |||||||
| chr4:48007685 | A | T | 1 | a0001c0001t0001g0288 | 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | a0001c0001t0001g0225 | 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 | a0001c0001t0003g0081 a0001c0001t0003g0082 |
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 | a0001c0001t0001g0199 | 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 | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | 41 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0086 others(38): 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 | a0001c0001t0008g0023 a0003c0006t0008g0024 |
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 | 41 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0086 others(38): 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 | 41 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0086 others(38): 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 | a0001c0001t0003g0093 a0001c0003t0001g0324 a0001c0003t0002g0120 others(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 | 87 | a0001c0001t0002g0014 a0001c0001t0002g0191 a0001c0001t0011g0149 others(84): 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 | 125 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(122): Show |
140 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(137): 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 | 313 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(310): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): 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 | a0001c0001t0001g0287 | 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 | a0001c0001t0004g0035 a0001c0001t0004g0036 a0001c0001t0004g0037 others(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 | a0001c0001t0001g0218 | 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 | a0001c0001t0001g0219 | 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0208 others(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 | 57 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(54): 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 | a0001c0001t0001g0274 | 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 | a0001c0001t0004g0047 a0001c0001t0004g0048 |
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 | a0001c0004t0001g0203 | 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 | 226 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.-123+999C>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 2/10 | chr4 | 48009795 | |||||||
| chr4:48009799 | C | T | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | 7 | a0002c0002t0002g0011 a0002c0002t0002g0125 a0002c0002t0002g0126 others(4): 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 | a0001c0001t0001g0221 | 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 | 60 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(57): 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 | 41 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0086 others(38): 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 | a0001c0003t0003g0087 a0001c0003t0003g0088 a0001c0003t0003g0089 others(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 | a0002c0002t0002g0180 a0002c0002t0002g0181 |
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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | 56 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(53): 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 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0330 |
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 | 41 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0086 others(38): 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 | 100 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0200 others(97): 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 | 55 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(52): 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 | a0001c0001t0001g0326 | 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 | 44 | a0001c0001t0001g0007 a0001c0001t0001g0199 a0001c0001t0001g0200 others(41): 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0284 | 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 | 74 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
87 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(84): 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 | 40 | a0001c0001t0001g0007 a0001c0001t0002g0118 a0001c0001t0003g0086 others(37): 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0220 | 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 | a0005c0005t0003g0071 | 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 | 208 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(205): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): 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 | a0001c0001t0004g0068 a0001c0001t0004g0072 |
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 | a0002c0002t0002g0182 | 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 | 53 | a0001c0001t0001g0327 a0001c0001t0003g0001 a0001c0001t0003g0002 others(50): 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 | 54 | a0001c0001t0002g0014 a0001c0001t0002g0099 a0001c0001t0002g0102 others(51): 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 | a0001c0001t0002g0098 a0002c0002t0002g0123 a0002c0002t0002g0124 others(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 | a0001c0001t0003g0076 a0001c0003t0003g0075 |
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 | a0001c0001t0001g0232 a0001c0001t0001g0245 a0001c0001t0001g0246 others(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 | 90 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): Show |
104 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(101): 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | 10 | a0001c0001t0003g0002 a0001c0001t0003g0008 a0001c0001t0003g0009 others(7): 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 | 50 | a0001c0001t0003g0001 a0001c0001t0003g0010 a0001c0001t0003g0026 others(47): 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 | a0001c0001t0001g0017 a0001c0001t0001g0208 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0227 a0001c0001t0001g0244 a0001c0004t0001g0228 |
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 | a0001c0001t0003g0086 a0001c0001t0003g0093 a0001c0003t0003g0087 others(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 | a0002c0002t0002g0194 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0208 a0001c0001t0001g0212 others(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 | 46 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0018 others(43): Show |
53 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(50): 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 | a0001c0001t0003g0081 a0001c0001t0003g0082 a0001c0001t0005g0328 |
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 | a0002c0002t0002g0123 a0002c0002t0002g0124 |
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 | a0001c0001t0001g0229 a0001c0001t0004g0072 a0001c0003t0002g0120 others(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 | 117 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
133 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(130): 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 | a0001c0004t0001g0203 | 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 | 225 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): 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 | a0001c0001t0001g0329 | 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 | a0001c0001t0001g0017 a0001c0001t0001g0208 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0330 | 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 | a0001c0001t0003g0086 a0001c0003t0003g0087 a0001c0003t0003g0088 others(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 | a0001c0001t0001g0331 | 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 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
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 | a0001c0001t0003g0083 a0001c0001t0003g0084 |
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 | a0001c0001t0003g0026 | 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 | 104 | a0001c0001t0001g0017 a0001c0001t0001g0208 a0001c0001t0001g0212 others(101): 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 | 54 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(51): 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 | 118 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(131): 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 | 104 | a0001c0001t0001g0017 a0001c0001t0001g0208 a0001c0001t0001g0212 others(101): 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 | a0002c0002t0002g0196 | 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 | a0002c0002t0002g0197 | 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 | a0001c0001t0003g0083 a0001c0001t0003g0084 |
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 | 313 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(310): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): 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 | a0001c0001t0002g0098 a0001c0001t0002g0099 a0001c0001t0002g0100 others(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 | a0001c0001t0006g0239 | 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 | 8 | a0001c0001t0001g0003 a0001c0001t0001g0232 a0001c0001t0001g0233 others(5): 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 | a0001c0001t0001g0017 a0001c0001t0001g0208 a0001c0001t0001g0212 others(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 | a0001c0001t0001g0332 | 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 | 104 | a0001c0001t0001g0017 a0001c0001t0001g0208 a0001c0001t0001g0212 others(101): 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 | 104 | a0001c0001t0001g0017 a0001c0001t0001g0208 a0001c0001t0001g0212 others(101): 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 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0201 others(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 | 65 | a0001c0001t0003g0001 a0001c0001t0003g0002 a0001c0001t0003g0008 others(62): 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 | a0001c0001t0005g0015 a0001c0001t0005g0016 a0001c0001t0005g0198 |
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 | a0001c0001t0001g0333 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-223+40G>T | CNGA1 | ENSG00000198515.16 | transcript | ENST00000514170.7 | protein_coding | 1/10 | chr4 | 48016443 |