Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1261 |
| ensemblid | ENSG00000144191.12 |
| hgncid | 2150 |
| symbol | CNGA3 |
| name | cyclic nucleotide gated channel subunit alpha 3 |
| refseq_nuc | NM_001298.3 |
| refseq_prot | NP_001289.1 |
| ensembl_nuc | ENST00000272602.7 |
| ensembl_prot | ENSP00000272602.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 98346456 |
| end | 98398601 |
| strand | + |
| ver | v1.2 |
| region | chr2:98346456-98398601 |
| region5000 | chr2:98341456-98403601 |
| regionname0 | CNGA3_chr2_98346456_98398601 |
| regionname5000 | CNGA3_chr2_98341456_98403601 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 694 | 315 | 64 | 62 | 140 | 15 | 32 | 97 | CNGA3_chr2_98341456_98403601 | CNGA3 | MAKIN others(689): Show |
chr2 | 98341456 | 98403601 |
| a0002 | 0/0 | 694 | 12 | 6 | 0 | 6 | 0 | 0 | 6 | CNGA3_chr2_98341456_98403601 | CNGA3 | MAKIN others(689): Show |
chr2 | 98341456 | 98403601 |
| a0003 | 0/0 | 694 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | MAKIN others(689): Show |
chr2 | 98341456 | 98403601 |
| a0004 | 0/0 | 694 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | MAKIN others(689): Show |
chr2 | 98341456 | 98403601 |
| a0005 | 0/0 | 694 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | MAKIN others(689): Show |
chr2 | 98341456 | 98403601 |
| a0006 | 0/0 | 694 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | MAKIN others(689): Show |
chr2 | 98341456 | 98403601 |
| a0007 | 0/0 | 694 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | MAKIN others(689): Show |
chr2 | 98341456 | 98403601 |
| a0008 | 0/0 | 694 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | MAKIN others(689): Show |
chr2 | 98341456 | 98403601 |
| a0009 | 0/0 | 694 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | MAKIN others(689): Show |
chr2 | 98341456 | 98403601 |
| a0010 | 0/0 | 694 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | MAKIN others(689): Show |
chr2 | 98341456 | 98403601 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2082 | 277 | 55 | 49 | 126 | 14 | 31 | CNGA3_chr2_98341456_98403601 | CNGA3 | ATGGC others(2077): Show |
chr2 | 98341456 | 98403601 | ||
| a0001c0002 | 0/0 | 2082 | 23 | 9 | 11 | 1 | 1 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | ATGGC others(2077): Show |
chr2 | 98341456 | 98403601 | ||
| a0001c0003 | 0/0 | 2082 | 11 | 0 | 0 | 11 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | ATGGC others(2077): Show |
chr2 | 98341456 | 98403601 | ||
| a0001c0012 | 0/0 | 2082 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | ATGGC others(2077): Show |
chr2 | 98341456 | 98403601 | ||
| a0001c0013 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | ATGGC others(2077): Show |
chr2 | 98341456 | 98403601 | ||
| a0001c0017 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | ATGGC others(2077): Show |
chr2 | 98341456 | 98403601 | ||
| a0001c0018 | 0/0 | 2082 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | ATGGC others(2077): Show |
chr2 | 98341456 | 98403601 | ||
| a0002c0004 | 0/0 | 2082 | 6 | 0 | 0 | 6 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | ATGGC others(2077): Show |
chr2 | 98341456 | 98403601 | ||
| a0002c0005 | 0/0 | 2082 | 4 | 4 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | ATGGC others(2077): Show |
chr2 | 98341456 | 98403601 | ||
| a0002c0006 | 0/0 | 2082 | 2 | 2 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | ATGGC others(2077): Show |
chr2 | 98341456 | 98403601 | ||
| a0003c0008 | 0/0 | 2082 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | ATGGC others(2077): Show |
chr2 | 98341456 | 98403601 | ||
| a0004c0007 | 0/0 | 2082 | 2 | 2 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | ATGGC others(2077): Show |
chr2 | 98341456 | 98403601 | ||
| a0005c0009 | 0/0 | 2082 | 2 | 2 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | ATGGC others(2077): Show |
chr2 | 98341456 | 98403601 | ||
| a0006c0015 | 0/0 | 2082 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | ATGGC others(2077): Show |
chr2 | 98341456 | 98403601 | ||
| a0007c0016 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | ATGGC others(2077): Show |
chr2 | 98341456 | 98403601 | ||
| a0008c0010 | 0/0 | 2082 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | ATGGC others(2077): Show |
chr2 | 98341456 | 98403601 | ||
| a0009c0011 | 0/0 | 2082 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | ATGGC others(2077): Show |
chr2 | 98341456 | 98403601 | ||
| a0010c0014 | 0/0 | 2082 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | ATGGC others(2077): Show |
chr2 | 98341456 | 98403601 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3547 | 258 | 42 | 47 | 122 | 14 | 31 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0001c0001t0002 | 0/0 | 3547 | 5 | 5 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0001c0001t0003 | 0/0 | 3547 | 6 | 5 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0001c0001t0004 | 0/0 | 3547 | 2 | 2 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0001c0001t0006 | 0/0 | 3547 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0001c0001t0007 | 0/0 | 3547 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0001c0001t0008 | 0/0 | 3547 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0001c0001t0009 | 0/0 | 3547 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0001c0001t0010 | 0/0 | 3534 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3529): Show |
chr2 | 98341456 | 98403601 |
| a0001c0001t0011 | 0/0 | 3547 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0001c0002t0001 | 0/0 | 3547 | 19 | 5 | 11 | 1 | 1 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0001c0002t0002 | 0/0 | 3547 | 3 | 3 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0001c0002t0005 | 0/0 | 3547 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0001c0003t0001 | 0/0 | 3547 | 11 | 0 | 0 | 11 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0001c0012t0001 | 0/0 | 3547 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0001c0013t0001 | 0/0 | 3547 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0001c0017t0001 | 0/0 | 3547 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0001c0018t0001 | 0/0 | 3547 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0002c0004t0002 | 0/0 | 3547 | 6 | 0 | 0 | 6 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0002c0005t0003 | 0/0 | 3547 | 4 | 4 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0002c0006t0003 | 0/0 | 3547 | 2 | 2 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0003c0008t0001 | 0/0 | 3547 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0004c0007t0001 | 0/0 | 3547 | 2 | 2 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0005c0009t0001 | 0/0 | 3547 | 2 | 2 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0006c0015t0001 | 0/0 | 3547 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0007c0016t0002 | 0/0 | 3547 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0008c0010t0001 | 0/0 | 3547 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0009c0011t0001 | 0/0 | 3547 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| a0010c0014t0002 | 0/0 | 3547 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | GGAAC others(3542): Show |
chr2 | 98341456 | 98403601 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 4 | 0 | 0 | 1 | 2 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0276 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0007g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0008g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0009g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0001t0011g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0002t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0003t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0012t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0013t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0017t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0001c0018t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0002c0004t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0002c0004t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0002c0004t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0002c0004t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0002c0004t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0002c0004t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0002c0005t0003g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0002c0005t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0002c0005t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0002c0005t0003g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0002c0006t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0002c0006t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0003c0008t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0003c0008t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0004c0007t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0004c0007t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0005c0009t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0005c0009t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0006c0015t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0007c0016t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0008c0010t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0009c0011t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| a0010c0014t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | GBR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0310 | EUR | GBR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0051 | EUR | GBR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00140 | hp2 | a0006 | c0015 | t0001 | g0120 | EUR | GBR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0078 | EUR | FIN | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | FIN | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00408 | hp1 | a0001 | c0003 | t0001 | g0106 | EAS | CHS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00408 | hp2 | a0001 | c0003 | t0001 | g0181 | EAS | CHS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00544 | hp2 | a0001 | c0003 | t0001 | g0159 | EAS | CHS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00558 | hp1 | a0007 | c0016 | t0002 | g0200 | EAS | CHS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00609 | hp1 | a0008 | c0010 | t0001 | g0145 | EAS | CHS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0077 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01243 | hp1 | a0001 | c0012 | t0001 | g0122 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | CLM | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | CLM | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0234 | AMR | CLM | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01358 | hp2 | a0001 | c0018 | t0001 | g0059 | AMR | CLM | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | CLM | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | IBS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | IBS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | ACB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02071 | hp1 | a0001 | c0003 | t0001 | g0140 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02129 | hp2 | a0001 | c0013 | t0001 | g0180 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CDX | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CDX | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CDX | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0060 | AFR | ACB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02300 | hp1 | a0001 | c0001 | t0009 | g0009 | AMR | PEL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0073 | AMR | PEL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02451 | hp2 | a0009 | c0011 | t0001 | g0035 | AFR | ACB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02523 | hp2 | a0003 | c0008 | t0001 | g0129 | EAS | KHV | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02647 | hp2 | a0002 | c0006 | t0003 | g0031 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02809 | hp1 | a0004 | c0007 | t0001 | g0071 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02895 | hp2 | a0004 | c0007 | t0001 | g0070 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02896 | hp2 | a0002 | c0005 | t0003 | g0164 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02897 | hp2 | a0002 | c0005 | t0003 | g0165 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ESN | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | ESN | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0046 | AFR | ESN | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | ESN | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02976 | hp1 | a0002 | c0006 | t0003 | g0030 | AFR | ESN | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02976 | hp2 | a0002 | c0005 | t0003 | g0306 | AFR | ESN | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03041 | hp2 | a0002 | c0005 | t0003 | g0233 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | MSL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | MSL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | MSL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | MSL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0028 | AFR | MSL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0047 | AFR | MSL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03579 | hp1 | a0005 | c0009 | t0001 | g0170 | AFR | MSL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0048 | AFR | MSL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0244 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | BEB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | STU | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0023 | SAS | STU | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | YRI | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | YRI | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | CHB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | CHB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | CHB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18944 | hp2 | a0002 | c0004 | t0002 | g0249 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18948 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18949 | hp1 | a0001 | c0003 | t0001 | g0291 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18950 | hp1 | a0002 | c0004 | t0002 | g0127 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18956 | hp2 | a0001 | c0003 | t0001 | g0193 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18959 | hp2 | a0001 | c0003 | t0001 | g0194 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18962 | hp1 | a0001 | c0003 | t0001 | g0095 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18970 | hp1 | a0001 | c0003 | t0001 | g0100 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18973 | hp1 | a0002 | c0004 | t0002 | g0098 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18983 | hp2 | a0001 | c0001 | t0007 | g0292 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18986 | hp1 | a0002 | c0004 | t0002 | g0126 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18989 | hp1 | a0001 | c0001 | t0011 | g0258 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19007 | hp2 | a0003 | c0008 | t0001 | g0250 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19010 | hp1 | a0002 | c0004 | t0002 | g0296 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | LWK | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19030 | hp2 | a0010 | c0014 | t0002 | g0260 | AFR | LWK | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19067 | hp1 | a0001 | c0003 | t0001 | g0086 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19068 | hp1 | a0001 | c0017 | t0001 | g0125 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19077 | hp1 | a0001 | c0001 | t0008 | g0101 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19088 | hp1 | a0002 | c0004 | t0002 | g0088 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19090 | hp1 | a0001 | c0003 | t0001 | g0309 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | YRI | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0219 | AFR | YRI | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | TSI | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0075 | EUR | TSI | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | GIH | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | GIH | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | MSL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG06807 | hp1 | a0001 | c0002 | t0005 | g0068 | AFR | USA | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| HG06807 | hp2 | a0005 | c0009 | t0001 | g0240 | AFR | USA | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | USA | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | USA | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | LWK | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | LWK | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0276 | REF | REF | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | CNGA3_chr2_98341456_98403601 | CNGA3 | chr2 | 98341456 | 98403601 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:98380312 | A | G | 1 | a0005 | 2 | HG03579.hp1 HG06807.hp2 |
missense_variant | MODERATE | c.353A>G | p.Gln118Arg | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/8 | 469/3547 | 353/2085 | 118/694 | chr2 | 98380312 | |||
| chr2:98380343 | C | G | 1 | a0007 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.384C>G | p.Asp128Glu | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/8 | 500/3547 | 384/2085 | 128/694 | chr2 | 98380343 | |||
| chr2:98389666 | C | T | 1 | a0006 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.458C>T | p.Thr153Met | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/8 | 574/3547 | 458/2085 | 153/694 | chr2 | 98389666 | |||
| chr2:98389679 | T | G | 1 | a0008 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.471T>G | p.Asp157Glu | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/8 | 587/3547 | 471/2085 | 157/694 | chr2 | 98389679 | |||
| chr2:98391889 | G | A | 2 | a0002 a0007 |
13 | HG00558.hp1 HG02647.hp2 HG02896.hp2 others(10): Show |
missense_variant | MODERATE | c.592G>A | p.Glu198Lys | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/8 | 708/3547 | 592/2085 | 198/694 | chr2 | 98391889 | |||
| chr2:98395910 | C | T | 1 | a0003 | 2 | HG02523.hp2 NA19007.hp2 |
missense_variant | MODERATE | c.740C>T | p.Thr247Met | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 8/8 | 856/3547 | 740/2085 | 247/694 | chr2 | 98395910 | |||
| chr2:98396078 | T | C | 1 | a0004 | 2 | HG02809.hp1 HG02895.hp2 |
missense_variant | MODERATE | c.908T>C | p.Ile303Thr | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 8/8 | 1024/3547 | 908/2085 | 303/694 | chr2 | 98396078 | |||
| chr2:98396513 | A | G | 1 | a0010 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1343A>G | p.Lys448Arg | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 8/8 | 1459/3547 | 1343/2085 | 448/694 | chr2 | 98396513 | |||
| chr2:98397138 | G | A | 1 | a0009 | 1 | HG02451.hp2 | missense_variant | MODERATE | c.1968G>A | p.Met656Ile | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 8/8 | 2084/3547 | 1968/2085 | 656/694 | chr2 | 98397138 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:98370047 | T | C | 2 | a0001c0002 a0002c0006 |
25 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(22): Show |
synonymous_variant | LOW | c.72T>C | p.Asp24Asp | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/8 | 188/3547 | 72/2085 | 24/694 | chr2 | 98370047 | |||
| chr2:98370056 | C | T | 1 | a0001c0018 | 1 | HG01358.hp2 | synonymous_variant | LOW | c.81C>T | p.Arg27Arg | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/8 | 197/3547 | 81/2085 | 27/694 | chr2 | 98370056 | |||
| chr2:98380184 | C | T | 1 | a0001c0017 | 1 | NA19068.hp1 | synonymous_variant | LOW | c.225C>T | p.Arg75Arg | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/8 | 341/3547 | 225/2085 | 75/694 | chr2 | 98380184 | |||
| chr2:98396796 | C | T | 2 | a0001c0003 a0001c0013 |
12 | HG00408.hp1 HG00408.hp2 HG00544.hp2 others(9): Show |
synonymous_variant | LOW | c.1626C>T | p.Ser542Ser | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 8/8 | 1742/3547 | 1626/2085 | 542/694 | chr2 | 98396796 | |||
| chr2:98396916 | C | T | 2 | a0002c0004 a0007c0016 |
7 | HG00558.hp1 NA18944.hp2 NA18950.hp1 others(4): Show |
synonymous_variant | LOW | c.1746C>T | p.Asp582Asp | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 8/8 | 1862/3547 | 1746/2085 | 582/694 | chr2 | 98396916 | |||
| chr2:98396937 | C | T | 1 | a0001c0013 | 1 | HG02129.hp2 | synonymous_variant | LOW | c.1767C>T | p.Thr589Thr | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 8/8 | 1883/3547 | 1767/2085 | 589/694 | chr2 | 98396937 | |||
| chr2:98396946 | C | T | 1 | a0001c0012 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.1776C>T | p.Pro592Pro | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 8/8 | 1892/3547 | 1776/2085 | 592/694 | chr2 | 98396946 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:98346499 | C | A | 1 | a0001c0002t0005 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-73C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/8 | 23477 | chr2 | 98346499 | ||||||
| chr2:98397298 | G | T | 1 | a0001c0001t0011 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*43G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 8/8 | 43 | chr2 | 98397298 | ||||||
| chr2:98397305 | G | A | 1 | a0001c0001t0006 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*50G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 8/8 | 50 | chr2 | 98397305 | ||||||
| chr2:98397460 | T | C | 1 | a0001c0001t0007 | 1 | NA18983.hp2 | 3_prime_UTR_variant | MODIFIER | c.*205T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 8/8 | 205 | chr2 | 98397460 | ||||||
| chr2:98397829 | C | T | 5 | a0001c0001t0002 a0001c0002t0002 a0002c0004t0002 others(2): Show |
16 | HG00558.hp1 HG01891.hp1 HG02818.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*574C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 8/8 | 574 | chr2 | 98397829 | ||||||
| chr2:98398093 | T | C | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0002t0002 others(5): Show |
28 | HG00558.hp1 HG01261.hp2 HG01891.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*838T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 8/8 | 838 | chr2 | 98398093 | ||||||
| chr2:98398151 | ATTAGGAA others(6): Show |
A | 1 | a0001c0001t0010 | 1 | NA18948.hp2 | 3_prime_UTR_variant | MODIFIER | c.*899_*911delAGGAAC others(7): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 8/8 | 899 | INFO_REALIGN_3_PRIME | chr2 | 98398151 | |||||
| chr2:98398432 | T | A | 1 | a0001c0001t0008 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1177T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 8/8 | 1177 | chr2 | 98398432 | ||||||
| chr2:98398525 | A | G | 1 | a0001c0001t0004 | 2 | HG02965.hp1 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1270A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 8/8 | 1270 | chr2 | 98398525 | ||||||
| chr2:98398540 | A | C | 1 | a0001c0001t0009 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1285A>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 8/8 | 1285 | chr2 | 98398540 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:98346570 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-38+36T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98346570 | |||||||
| chr2:98346954 | A | G | 1 | a0001c0001t0001g0310 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-38+420A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98346954 | |||||||
| chr2:98346983 | C | T | 1 | a0001c0003t0001g0309 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-38+449C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98346983 | |||||||
| chr2:98347019 | G | C | 11 | a0001c0001t0001g0027 a0001c0002t0001g0002 a0001c0002t0001g0022 others(8): Show |
13 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.-38+485G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98347019 | |||||||
| chr2:98347087 | G | A | 2 | a0001c0001t0001g0032 a0001c0001t0001g0033 |
2 | HG02602.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.-38+553G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98347087 | |||||||
| chr2:98347334 | C | A | 9 | a0001c0001t0001g0021 a0001c0001t0001g0034 a0001c0001t0001g0036 others(6): Show |
9 | HG02055.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.-38+800C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98347334 | |||||||
| chr2:98347457 | C | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-38+923C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98347457 | |||||||
| chr2:98347545 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-38+1011G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98347545 | |||||||
| chr2:98347657 | C | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-38+1123C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98347657 | |||||||
| chr2:98347921 | T | C | 1 | a0001c0001t0001g0045 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-38+1387T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98347921 | |||||||
| chr2:98347955 | G | C | 3 | a0001c0002t0001g0047 a0001c0002t0002g0046 a0001c0002t0002g0048 |
3 | HG02965.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-38+1421G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98347955 | |||||||
| chr2:98347995 | T | C | 98 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(95): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-38+1461T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98347995 | |||||||
| chr2:98348003 | G | C | 98 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(95): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-38+1469G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98348003 | |||||||
| chr2:98348089 | C | T | 1 | a0001c0001t0001g0308 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-38+1555C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98348089 | |||||||
| chr2:98348188 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0050 others(7): Show |
11 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.-38+1654G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98348188 | |||||||
| chr2:98348273 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-38+1739C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98348273 | |||||||
| chr2:98348466 | A | G | 1 | a0001c0001t0001g0307 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-38+1932A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98348466 | |||||||
| chr2:98348515 | G | A | 7 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(4): Show |
7 | HG01358.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+1981G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98348515 | |||||||
| chr2:98348543 | C | G | 9 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(6): Show |
9 | HG01243.hp1 HG01358.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.-38+2009C>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98348543 | |||||||
| chr2:98348581 | A | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0050 others(7): Show |
11 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.-38+2047A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98348581 | |||||||
| chr2:98348617 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-38+2083C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98348617 | |||||||
| chr2:98348650 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-38+2116G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98348650 | |||||||
| chr2:98348795 | T | A | 1 | a0001c0001t0001g0067 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-38+2261T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98348795 | |||||||
| chr2:98348916 | G | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0303 a0001c0001t0001g0304 others(2): Show |
7 | HG01167.hp2 HG02280.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+2382G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98348916 | |||||||
| chr2:98348947 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
5 | HG00140.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38+2413C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98348947 | |||||||
| chr2:98349049 | T | G | 7 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(4): Show |
7 | HG01358.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+2515T>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98349049 | |||||||
| chr2:98349110 | T | C | 98 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(95): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.-38+2576T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98349110 | |||||||
| chr2:98349147 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0050 others(7): Show |
11 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.-38+2613G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98349147 | |||||||
| chr2:98349155 | C | A | 1 | a0001c0001t0001g0124 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-38+2621C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98349155 | |||||||
| chr2:98349667 | C | A | 13 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0001g0121 others(10): Show |
14 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.-38+3133C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98349667 | |||||||
| chr2:98349810 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-38+3276G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98349810 | |||||||
| chr2:98349863 | A | C | 2 | a0001c0001t0001g0117 a0001c0001t0002g0116 |
2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-38+3329A>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98349863 | |||||||
| chr2:98349900 | G | A | 3 | a0001c0017t0001g0125 a0002c0004t0002g0126 a0002c0004t0002g0127 |
3 | NA18950.hp1 NA18986.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-38+3366G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98349900 | |||||||
| chr2:98349994 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0050 others(7): Show |
11 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.-38+3460C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98349994 | |||||||
| chr2:98350019 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0050 others(7): Show |
11 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.-38+3485G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98350019 | |||||||
| chr2:98350025 | C | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0300 a0001c0001t0001g0301 others(1): Show |
4 | HG00639.hp1 HG01175.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+3491C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98350025 | |||||||
| chr2:98350134 | G | A | 11 | a0001c0001t0001g0027 a0001c0002t0001g0002 a0001c0002t0001g0022 others(8): Show |
13 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.-38+3600G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98350134 | |||||||
| chr2:98350245 | T | G | 96 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(93): Show |
103 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-38+3711T>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98350245 | |||||||
| chr2:98350253 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0050 others(7): Show |
11 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.-38+3719G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98350253 | |||||||
| chr2:98350651 | C | T | 53 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(50): Show |
55 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.-38+4117C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98350651 | |||||||
| chr2:98350659 | G | T | 11 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0293 others(8): Show |
11 | HG00423.hp2 HG02056.hp1 NA18940.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38+4125G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98350659 | |||||||
| chr2:98350791 | T | G | 31 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0069 others(28): Show |
35 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-38+4257T>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98350791 | |||||||
| chr2:98350920 | C | T | 31 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0069 others(28): Show |
35 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-38+4386C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98350920 | |||||||
| chr2:98350980 | C | T | 1 | a0001c0001t0001g0288 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-38+4446C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98350980 | |||||||
| chr2:98351011 | A | G | 31 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0069 others(28): Show |
35 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-38+4477A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98351011 | |||||||
| chr2:98351038 | C | G | 1 | a0001c0001t0001g0288 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-38+4504C>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98351038 | |||||||
| chr2:98351074 | A | T | 12 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0050 others(9): Show |
13 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.-38+4540A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98351074 | |||||||
| chr2:98351082 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-38+4548T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98351082 | |||||||
| chr2:98351237 | C | T | 31 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0069 others(28): Show |
35 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-38+4703C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98351237 | |||||||
| chr2:98351261 | G | A | 1 | a0003c0008t0001g0129 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-38+4727G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98351261 | |||||||
| chr2:98351274 | C | T | 1 | a0006c0015t0001g0120 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-38+4740C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98351274 | |||||||
| chr2:98351352 | G | A | 44 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(41): Show |
46 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.-38+4818G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98351352 | |||||||
| chr2:98351428 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-38+4894G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98351428 | |||||||
| chr2:98351428 | G | T | 31 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0069 others(28): Show |
35 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-38+4894G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98351428 | |||||||
| chr2:98351571 | C | A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | NA18967.hp1 NA19005.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-38+5037C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98351571 | |||||||
| chr2:98351698 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-38+5164T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98351698 | |||||||
| chr2:98351762 | C | T | 46 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(43): Show |
48 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.-38+5228C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98351762 | |||||||
| chr2:98351972 | T | C | 31 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0069 others(28): Show |
35 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-38+5438T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98351972 | |||||||
| chr2:98351973 | G | A | 1 | a0001c0002t0005g0068 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-38+5439G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98351973 | |||||||
| chr2:98352034 | T | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02155.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-38+5500T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98352034 | |||||||
| chr2:98352276 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-38+5742C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98352276 | |||||||
| chr2:98352277 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0002g0116 |
2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-38+5743G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98352277 | |||||||
| chr2:98352306 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-38+5772T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98352306 | |||||||
| chr2:98352360 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-38+5826G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98352360 | |||||||
| chr2:98352433 | T | A | 3 | a0001c0002t0001g0047 a0001c0002t0002g0046 a0001c0002t0002g0048 |
3 | HG02965.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-38+5899T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98352433 | |||||||
| chr2:98352683 | G | A | 4 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
4 | HG02071.hp1 HG02135.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+6149G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98352683 | |||||||
| chr2:98353023 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-38+6489G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98353023 | |||||||
| chr2:98353063 | G | A | 13 | a0001c0001t0001g0069 a0001c0001t0001g0078 a0001c0001t0001g0121 others(10): Show |
14 | HG00280.hp2 HG00735.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.-38+6529G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98353063 | |||||||
| chr2:98353102 | T | G | 31 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0069 others(28): Show |
35 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-38+6568T>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98353102 | |||||||
| chr2:98353155 | T | C | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 |
3 | HG00140.hp1 HG00323.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-38+6621T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98353155 | |||||||
| chr2:98353247 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-38+6713T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98353247 | |||||||
| chr2:98353269 | C | CCTAA | 31 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0069 others(28): Show |
35 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-38+6737_-38+6740d others(6): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98353269 | ||||||
| chr2:98353302 | A | G | 3 | a0001c0002t0001g0047 a0001c0002t0002g0046 a0001c0002t0002g0048 |
3 | HG02965.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-38+6768A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98353302 | |||||||
| chr2:98353308 | AT | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0050 others(6): Show |
10 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38+6778delT | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98353308 | ||||||
| chr2:98353538 | C | A | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 |
3 | HG02135.hp1 NA18965.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-38+7004C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98353538 | |||||||
| chr2:98353658 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-38+7124C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98353658 | |||||||
| chr2:98353715 | T | A | 2 | a0001c0001t0001g0123 a0001c0012t0001g0122 |
2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-38+7181T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98353715 | |||||||
| chr2:98353883 | T | A | 2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-38+7349T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98353883 | |||||||
| chr2:98353892 | C | T | 31 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0069 others(28): Show |
35 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-38+7358C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98353892 | |||||||
| chr2:98354260 | G | A | 11 | a0001c0001t0001g0027 a0001c0002t0001g0002 a0001c0002t0001g0022 others(8): Show |
13 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.-38+7726G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98354260 | |||||||
| chr2:98354319 | T | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
5 | HG00140.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38+7785T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98354319 | |||||||
| chr2:98354428 | C | A | 31 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0069 others(28): Show |
35 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-38+7894C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98354428 | |||||||
| chr2:98354453 | C | CT | 31 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0069 others(28): Show |
35 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-38+7923dupT | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98354453 | ||||||
| chr2:98354627 | A | G | 2 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
2 | NA18959.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.-38+8093A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98354627 | |||||||
| chr2:98354793 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-38+8259T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98354793 | |||||||
| chr2:98354960 | C | A | 2 | a0001c0001t0001g0117 a0001c0001t0002g0116 |
2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-38+8426C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98354960 | |||||||
| chr2:98355026 | T | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
5 | HG00140.hp2 HG01257.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38+8492T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98355026 | |||||||
| chr2:98355099 | G | A | 1 | a0001c0002t0001g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-38+8565G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98355099 | |||||||
| chr2:98355179 | C | CT | 26 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0078 others(23): Show |
30 | HG00140.hp2 HG00280.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-38+8649dupT | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98355179 | ||||||
| chr2:98355248 | G | A | 15 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0058 others(12): Show |
15 | HG01358.hp2 HG01891.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-38+8714G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98355248 | |||||||
| chr2:98355328 | T | C | 6 | a0001c0001t0001g0027 a0001c0002t0001g0002 a0001c0002t0001g0023 others(3): Show |
8 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38+8794T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98355328 | |||||||
| chr2:98355396 | A | G | 1 | a0001c0001t0003g0041 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-38+8862A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98355396 | |||||||
| chr2:98355543 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-38+9009A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98355543 | |||||||
| chr2:98355556 | T | TA | 9 | a0001c0001t0001g0021 a0001c0001t0001g0034 a0001c0001t0001g0036 others(6): Show |
9 | HG02055.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-38+9026dupA | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98355556 | ||||||
| chr2:98355565 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-38+9031T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98355565 | |||||||
| chr2:98355579 | T | TA | 4 | a0001c0001t0001g0069 a0001c0001t0001g0121 a0004c0007t0001g0070 others(1): Show |
4 | HG02809.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+9049dupA | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98355579 | ||||||
| chr2:98355603 | C | T | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | NA18940.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.-38+9069C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98355603 | |||||||
| chr2:98355799 | A | G | 4 | a0001c0001t0001g0069 a0001c0001t0001g0121 a0004c0007t0001g0070 others(1): Show |
4 | HG02809.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-38+9265A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98355799 | |||||||
| chr2:98355855 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-38+9321T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98355855 | |||||||
| chr2:98356161 | T | C | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-38+9627T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98356161 | |||||||
| chr2:98356184 | A | G | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | NA18960.hp1 NA18972.hp1 NA18978.hp1 |
intron_variant | MODIFIER | c.-38+9650A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98356184 | |||||||
| chr2:98356202 | A | G | 6 | a0001c0002t0001g0002 a0001c0002t0001g0023 a0001c0002t0001g0024 others(3): Show |
8 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38+9668A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98356202 | |||||||
| chr2:98356224 | G | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0142 a0001c0001t0001g0154 |
3 | HG00280.hp2 HG01261.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-38+9690G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98356224 | |||||||
| chr2:98356251 | T | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0142 a0001c0001t0001g0154 |
3 | HG00280.hp2 HG01261.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.-38+9717T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98356251 | |||||||
| chr2:98356340 | GTCTGAGA others(8): Show |
G | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-38+9816_-38+9830d others(17): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98356340 | ||||||
| chr2:98356377 | C | A | 12 | a0001c0001t0001g0014 a0001c0001t0001g0065 a0001c0001t0001g0066 others(9): Show |
13 | HG02027.hp1 HG02109.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.-38+9843C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98356377 | |||||||
| chr2:98356433 | C | T | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | NA18965.hp2 NA18968.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.-38+9899C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98356433 | |||||||
| chr2:98356447 | A | T | 1 | a0001c0002t0001g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-38+9913A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98356447 | |||||||
| chr2:98356499 | C | T | 64 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(61): Show |
71 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-38+9965C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98356499 | |||||||
| chr2:98356539 | A | T | 1 | a0001c0001t0001g0297 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-38+10005A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98356539 | |||||||
| chr2:98356540 | G | C | 1 | a0001c0001t0001g0297 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-38+10006G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98356540 | |||||||
| chr2:98356574 | C | A | 1 | a0001c0003t0001g0159 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-38+10040C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98356574 | |||||||
| chr2:98356721 | C | A | 3 | a0001c0001t0001g0069 a0004c0007t0001g0070 a0004c0007t0001g0071 |
3 | HG02809.hp1 HG02895.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-38+10187C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98356721 | |||||||
| chr2:98356809 | C | A | 1 | a0001c0002t0002g0028 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-38+10275C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98356809 | |||||||
| chr2:98356837 | A | C | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-38+10303A>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98356837 | |||||||
| chr2:98357013 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-38+10479C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98357013 | |||||||
| chr2:98357017 | G | C | 1 | a0001c0001t0001g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-38+10483G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98357017 | |||||||
| chr2:98357163 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-38+10629T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98357163 | |||||||
| chr2:98357232 | A | G | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-38+10698A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98357232 | |||||||
| chr2:98357284 | G | A | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-38+10750G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98357284 | |||||||
| chr2:98357475 | G | A | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-38+10941G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98357475 | |||||||
| chr2:98357531 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-38+10997C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98357531 | |||||||
| chr2:98357662 | G | A | 54 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(51): Show |
59 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-38+11128G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98357662 | |||||||
| chr2:98357665 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0081 a0001c0001t0001g0082 others(4): Show |
7 | HG00741.hp1 HG01243.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38+11131G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98357665 | |||||||
| chr2:98357721 | G | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0065 a0001c0001t0001g0066 others(10): Show |
14 | HG02027.hp1 HG02109.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.-38+11187G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98357721 | |||||||
| chr2:98357926 | T | G | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-38+11392T>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98357926 | |||||||
| chr2:98358104 | T | C | 1 | a0001c0001t0001g0289 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-38+11570T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98358104 | |||||||
| chr2:98358114 | A | G | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-38+11580A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98358114 | |||||||
| chr2:98358272 | A | G | 1 | a0001c0001t0001g0308 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-37-11667A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98358272 | |||||||
| chr2:98358352 | A | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 |
4 | HG01257.hp2 HG01258.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-11587A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98358352 | |||||||
| chr2:98358395 | T | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG00639.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-37-11544T>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98358395 | |||||||
| chr2:98358654 | A | T | 108 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(105): Show |
117 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.-37-11285A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98358654 | |||||||
| chr2:98358750 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-37-11189G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98358750 | |||||||
| chr2:98358767 | GAGTT | G | 13 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(10): Show |
14 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(11): Show |
intron_variant | MODIFIER | c.-37-11170_-37-1116 others(8): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98358767 | ||||||
| chr2:98358802 | T | C | 2 | a0002c0005t0003g0164 a0002c0005t0003g0165 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-37-11137T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98358802 | |||||||
| chr2:98358831 | T | C | 57 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(54): Show |
63 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-37-11108T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98358831 | |||||||
| chr2:98358894 | G | A | 3 | a0001c0001t0001g0290 a0001c0003t0001g0159 a0001c0003t0001g0291 |
3 | HG00423.hp2 HG00544.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.-37-11045G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98358894 | |||||||
| chr2:98359006 | A | C | 57 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(54): Show |
63 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.-37-10933A>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98359006 | |||||||
| chr2:98359225 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-37-10714A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98359225 | |||||||
| chr2:98359396 | A | G | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-37-10543A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98359396 | |||||||
| chr2:98359443 | T | C | 104 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(101): Show |
113 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.-37-10496T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98359443 | |||||||
| chr2:98359522 | A | C | 104 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(101): Show |
113 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.-37-10417A>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98359522 | |||||||
| chr2:98359676 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 |
4 | HG01257.hp2 HG01258.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-10263C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98359676 | |||||||
| chr2:98359730 | C | T | 1 | a0001c0001t0003g0064 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-37-10209C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98359730 | |||||||
| chr2:98359776 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-37-10163C>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98359776 | |||||||
| chr2:98359842 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-37-10097G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98359842 | |||||||
| chr2:98359879 | G | T | 64 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(61): Show |
71 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-37-10060G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98359879 | |||||||
| chr2:98359913 | T | C | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-37-10026T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98359913 | |||||||
| chr2:98359917 | G | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0275 |
2 | HG02735.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-37-10022G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98359917 | |||||||
| chr2:98360070 | A | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0062 a0001c0001t0002g0063 |
3 | HG01891.hp1 HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-37-9869A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98360070 | |||||||
| chr2:98360269 | G | T | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-37-9670G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98360269 | |||||||
| chr2:98360315 | C | T | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-37-9624C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98360315 | |||||||
| chr2:98360316 | A | T | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-37-9623A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98360316 | |||||||
| chr2:98360352 | T | C | 3 | a0001c0001t0001g0040 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02647.hp1 HG02717.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.-37-9587T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98360352 | |||||||
| chr2:98360359 | A | T | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-37-9580A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98360359 | |||||||
| chr2:98360424 | G | T | 62 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
68 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.-37-9515G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98360424 | |||||||
| chr2:98360553 | A | G | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-37-9386A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98360553 | |||||||
| chr2:98360554 | A | G | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-37-9385A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98360554 | |||||||
| chr2:98360555 | G | T | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-37-9384G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98360555 | |||||||
| chr2:98360647 | A | G | 65 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(62): Show |
72 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-37-9292A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98360647 | |||||||
| chr2:98360891 | C | T | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-9048C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98360891 | |||||||
| chr2:98360927 | A | T | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-9012A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98360927 | |||||||
| chr2:98360935 | T | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0065 a0001c0001t0001g0066 others(10): Show |
14 | HG02027.hp1 HG02109.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.-37-9004T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98360935 | |||||||
| chr2:98360991 | T | G | 2 | a0001c0001t0001g0123 a0001c0012t0001g0122 |
2 | HG01243.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.-37-8948T>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98360991 | |||||||
| chr2:98360996 | TTTTTA | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 |
4 | HG01257.hp2 HG01258.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-8919_-37-8915d others(7): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98360996 | ||||||
| chr2:98360997 | TTTTATTT others(17): Show |
T | 22 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0022 others(19): Show |
25 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-37-8923_-37-8900d others(26): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98360997 | ||||||
| chr2:98361013 | T | G | 13 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0058 others(10): Show |
13 | HG01358.hp2 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-37-8926T>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98361013 | |||||||
| chr2:98361050 | G | T | 6 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0001c0002t0002g0046 others(3): Show |
6 | HG02647.hp2 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-8889G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98361050 | |||||||
| chr2:98361124 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-37-8815A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98361124 | |||||||
| chr2:98361137 | A | G | 37 | a0001c0001t0001g0012 a0001c0001t0001g0019 a0001c0001t0001g0020 others(34): Show |
43 | HG00438.hp2 HG00735.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-37-8802A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98361137 | |||||||
| chr2:98361298 | G | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-8641G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98361298 | |||||||
| chr2:98361510 | T | A | 40 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(37): Show |
43 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.-37-8429T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98361510 | |||||||
| chr2:98361606 | A | G | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-8333A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98361606 | |||||||
| chr2:98361659 | G | A | 17 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(14): Show |
18 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(15): Show |
intron_variant | MODIFIER | c.-37-8280G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98361659 | |||||||
| chr2:98361704 | C | CT | 31 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0042 others(28): Show |
33 | HG00280.hp2 HG00597.hp1 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.-37-8214dupT | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98361704 | ||||||
| chr2:98361704 | CT | C | 23 | a0001c0001t0001g0169 a0001c0002t0001g0002 a0001c0002t0001g0008 others(20): Show |
26 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.-37-8214delT | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98361704 | ||||||
| chr2:98361704 | CTT | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(2): Show |
6 | HG01257.hp1 HG01257.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-8215_-37-8214d others(4): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98361704 | ||||||
| chr2:98361732 | G | T | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-8207G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98361732 | |||||||
| chr2:98361733 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0002g0116 |
2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-37-8206A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98361733 | |||||||
| chr2:98361747 | G | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-8192G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98361747 | |||||||
| chr2:98361770 | C | T | 13 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0058 others(10): Show |
13 | HG01358.hp2 HG01891.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-37-8169C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98361770 | |||||||
| chr2:98361833 | G | T | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-8106G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98361833 | |||||||
| chr2:98362173 | C | CT | 40 | a0001c0001t0001g0012 a0001c0001t0001g0027 a0001c0001t0001g0082 others(37): Show |
44 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.-37-7743dupT | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98362173 | ||||||
| chr2:98362173 | CT | C | 20 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(17): Show |
21 | HG00140.hp1 HG00140.hp2 HG00544.hp1 others(18): Show |
intron_variant | MODIFIER | c.-37-7743delT | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98362173 | ||||||
| chr2:98362173 | CTT | C | 23 | a0001c0001t0001g0014 a0001c0001t0001g0058 a0001c0001t0001g0061 others(20): Show |
24 | HG01358.hp2 HG01891.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.-37-7744_-37-7743d others(4): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98362173 | ||||||
| chr2:98362199 | G | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-7740G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98362199 | |||||||
| chr2:98362265 | T | C | 70 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0014 others(67): Show |
76 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.-37-7674T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98362265 | |||||||
| chr2:98362398 | A | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-7541A>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98362398 | |||||||
| chr2:98362428 | G | C | 1 | a0001c0001t0001g0176 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-37-7511G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98362428 | |||||||
| chr2:98362438 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-37-7501C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98362438 | |||||||
| chr2:98362468 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0002g0116 |
2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-37-7471A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98362468 | |||||||
| chr2:98362476 | C | T | 3 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 |
3 | HG00597.hp2 HG01952.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.-37-7463C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98362476 | |||||||
| chr2:98362477 | G | A | 15 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0058 others(12): Show |
15 | HG01358.hp2 HG01891.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.-37-7462G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98362477 | |||||||
| chr2:98362497 | T | G | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-7442T>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98362497 | |||||||
| chr2:98362499 | G | T | 30 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0067 others(27): Show |
35 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.-37-7440G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98362499 | |||||||
| chr2:98362622 | G | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-7317G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98362622 | |||||||
| chr2:98362642 | GCA | G | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-7293_-37-7292d others(4): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98362642 | ||||||
| chr2:98362715 | T | C | 4 | a0001c0001t0001g0069 a0001c0001t0001g0121 a0004c0007t0001g0070 others(1): Show |
4 | HG02809.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-7224T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98362715 | |||||||
| chr2:98362751 | C | T | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-7188C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98362751 | |||||||
| chr2:98362817 | T | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-7122T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98362817 | |||||||
| chr2:98362831 | A | G | 18 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(15): Show |
19 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-37-7108A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98362831 | |||||||
| chr2:98362851 | G | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-7088G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98362851 | |||||||
| chr2:98362936 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 |
4 | HG01257.hp2 HG01258.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-7003A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98362936 | |||||||
| chr2:98362968 | G | A | 6 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0155 others(3): Show |
6 | HG02027.hp1 NA18967.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-6971G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98362968 | |||||||
| chr2:98363051 | A | G | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-6888A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98363051 | |||||||
| chr2:98363101 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 |
4 | HG01257.hp2 HG01258.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-6838G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98363101 | |||||||
| chr2:98363210 | G | A | 1 | a0001c0002t0001g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-37-6729G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98363210 | |||||||
| chr2:98363332 | T | C | 3 | a0001c0001t0001g0069 a0004c0007t0001g0070 a0004c0007t0001g0071 |
3 | HG02809.hp1 HG02895.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-37-6607T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98363332 | |||||||
| chr2:98363572 | A | G | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-6367A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98363572 | |||||||
| chr2:98363677 | A | G | 6 | a0001c0002t0001g0002 a0001c0002t0001g0022 a0001c0002t0001g0023 others(3): Show |
8 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-6262A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98363677 | |||||||
| chr2:98363720 | C | T | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-6219C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98363720 | |||||||
| chr2:98363776 | C | G | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-6163C>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98363776 | |||||||
| chr2:98363806 | A | G | 239 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(236): Show |
259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.-37-6133A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98363806 | |||||||
| chr2:98363864 | G | A | 1 | a0001c0002t0001g0073 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-37-6075G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98363864 | |||||||
| chr2:98363906 | G | A | 36 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0001t0001g0061 others(33): Show |
40 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(37): Show |
intron_variant | MODIFIER | c.-37-6033G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98363906 | |||||||
| chr2:98363983 | G | T | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-5956G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98363983 | |||||||
| chr2:98363988 | C | A | 1 | a0001c0001t0001g0081 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-37-5951C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98363988 | |||||||
| chr2:98364021 | G | T | 1 | a0001c0001t0001g0138 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-37-5918G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98364021 | |||||||
| chr2:98364054 | C | CTG | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-5881_-37-5880d others(4): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98364054 | ||||||
| chr2:98364258 | A | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02155.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.-37-5681A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98364258 | |||||||
| chr2:98364265 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 |
4 | HG01257.hp2 HG01258.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-5674C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98364265 | |||||||
| chr2:98364282 | C | G | 70 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0014 others(67): Show |
76 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.-37-5657C>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98364282 | |||||||
| chr2:98364379 | A | AAAAT | 27 | a0001c0001t0001g0061 a0001c0001t0001g0152 a0001c0001t0003g0060 others(24): Show |
30 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.-37-5536_-37-5533d others(6): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98364379 | ||||||
| chr2:98364443 | T | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-5496T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98364443 | |||||||
| chr2:98364484 | G | T | 1 | a0001c0002t0001g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-37-5455G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98364484 | |||||||
| chr2:98364490 | T | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-5449T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98364490 | |||||||
| chr2:98364561 | C | T | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-5378C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98364561 | |||||||
| chr2:98364567 | G | T | 1 | a0001c0001t0001g0256 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-37-5372G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98364567 | |||||||
| chr2:98364801 | T | G | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-5138T>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98364801 | |||||||
| chr2:98365043 | A | AT | 48 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0042 others(45): Show |
50 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(47): Show |
intron_variant | MODIFIER | c.-37-4884dupT | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98365043 | ||||||
| chr2:98365043 | AT | A | 48 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(45): Show |
52 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.-37-4884delT | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98365043 | ||||||
| chr2:98365085 | T | A | 1 | a0001c0001t0001g0138 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-37-4854T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98365085 | |||||||
| chr2:98365087 | A | G | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-4852A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98365087 | |||||||
| chr2:98365131 | C | G | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-4808C>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98365131 | |||||||
| chr2:98365131 | C | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0065 a0001c0001t0001g0066 others(10): Show |
14 | HG02027.hp1 HG02109.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.-37-4808C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98365131 | |||||||
| chr2:98365170 | A | G | 71 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0014 others(68): Show |
77 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.-37-4769A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98365170 | |||||||
| chr2:98365328 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-37-4611G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98365328 | |||||||
| chr2:98365416 | GA | G | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-4522delA | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98365416 | |||||||
| chr2:98365418 | G | T | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-4521G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98365418 | |||||||
| chr2:98365487 | C | T | 71 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0014 others(68): Show |
77 | HG00140.hp1 HG00323.hp1 HG00735.hp2 others(74): Show |
intron_variant | MODIFIER | c.-37-4452C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98365487 | |||||||
| chr2:98365491 | G | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-4448G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98365491 | |||||||
| chr2:98365586 | CA | C | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-4352delA | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98365586 | |||||||
| chr2:98365610 | AT | A | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-4320delT | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98365610 | ||||||
| chr2:98365823 | C | T | 22 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0022 others(19): Show |
25 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-37-4116C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98365823 | |||||||
| chr2:98365916 | C | A | 7 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(4): Show |
7 | HG01358.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-4023C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98365916 | |||||||
| chr2:98365949 | T | C | 1 | a0001c0001t0001g0254 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-37-3990T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98365949 | |||||||
| chr2:98366004 | T | G | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-3935T>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366004 | |||||||
| chr2:98366023 | T | G | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-3916T>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366023 | |||||||
| chr2:98366089 | CTT | C | 22 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0022 others(19): Show |
25 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-37-3846_-37-3845d others(4): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98366089 | ||||||
| chr2:98366090 | T | A | 1 | a0001c0001t0002g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-37-3849T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366090 | |||||||
| chr2:98366242 | C | A | 2 | a0001c0001t0004g0219 a0001c0001t0004g0220 |
2 | HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-37-3697C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366242 | |||||||
| chr2:98366250 | C | CAA | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-3687_-37-3686d others(4): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98366250 | ||||||
| chr2:98366276 | C | T | 148 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(145): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.-37-3663C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366276 | |||||||
| chr2:98366278 | G | A | 1 | a0009c0011t0001g0035 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-37-3661G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366278 | |||||||
| chr2:98366298 | C | T | 148 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(145): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.-37-3641C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366298 | |||||||
| chr2:98366313 | G | A | 147 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(144): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.-37-3626G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366313 | |||||||
| chr2:98366335 | A | G | 25 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): Show |
29 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.-37-3604A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366335 | |||||||
| chr2:98366447 | C | T | 4 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
4 | HG02071.hp1 HG02135.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-3492C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366447 | |||||||
| chr2:98366448 | G | A | 6 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0155 others(3): Show |
6 | HG02027.hp1 NA18967.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-3491G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366448 | |||||||
| chr2:98366548 | G | A | 21 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0043 others(18): Show |
22 | HG02027.hp1 HG02109.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-37-3391G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366548 | |||||||
| chr2:98366584 | G | A | 148 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(145): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.-37-3355G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366584 | |||||||
| chr2:98366630 | G | A | 1 | a0001c0002t0005g0068 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-37-3309G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366630 | |||||||
| chr2:98366683 | A | G | 148 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(145): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.-37-3256A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366683 | |||||||
| chr2:98366712 | C | T | 1 | a0009c0011t0001g0035 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-37-3227C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366712 | |||||||
| chr2:98366745 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-37-3194G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366745 | |||||||
| chr2:98366912 | G | A | 22 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0022 others(19): Show |
25 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.-37-3027G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366912 | |||||||
| chr2:98366912 | G | T | 144 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(141): Show |
152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.-37-3027G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366912 | |||||||
| chr2:98366970 | C | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0117 |
3 | HG02922.hp2 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-37-2969C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98366970 | |||||||
| chr2:98367046 | G | T | 145 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(142): Show |
153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-37-2893G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367046 | |||||||
| chr2:98367167 | G | A | 1 | a0001c0001t0003g0239 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-37-2772G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367167 | |||||||
| chr2:98367167 | G | GTTTATTT others(2): Show |
11 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(8): Show |
14 | HG00642.hp1 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.-37-2769_-37-2768i others(11): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98367167 | ||||||
| chr2:98367167 | G | GTTTATTT others(3): Show |
6 | a0001c0001t0001g0132 a0001c0001t0001g0151 a0001c0001t0001g0156 others(3): Show |
6 | HG01358.hp2 HG01981.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-2769_-37-2768i others(12): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98367167 | ||||||
| chr2:98367167 | G | GTTTATTT others(4): Show |
5 | a0001c0001t0001g0061 a0001c0001t0001g0131 a0001c0001t0001g0158 others(2): Show |
5 | HG02027.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.-37-2769_-37-2768i others(13): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98367167 | ||||||
| chr2:98367167 | G | GTTTATTT others(15): Show |
1 | a0001c0001t0001g0121 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-37-2769_-37-2768i others(24): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98367167 | ||||||
| chr2:98367167 | G | GTTTATTT others(18): Show |
1 | a0001c0001t0001g0069 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-37-2769_-37-2768i others(27): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98367167 | ||||||
| chr2:98367167 | G | GTTTATTT others(20): Show |
1 | a0004c0007t0001g0070 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-37-2769_-37-2768i others(29): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98367167 | ||||||
| chr2:98367167 | G | GTTTATTT others(21): Show |
1 | a0004c0007t0001g0071 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-37-2769_-37-2768i others(30): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98367167 | ||||||
| chr2:98367168 | T | TTTATTTT others(1): Show |
11 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0067 others(8): Show |
11 | HG00741.hp1 HG01515.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.-37-2769_-37-2768i others(10): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98367168 | ||||||
| chr2:98367169 | T | TTATTTTC | 22 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(19): Show |
24 | HG00597.hp1 HG00621.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.-37-2769_-37-2768i others(9): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr2 | 98367169 | ||||||
| chr2:98367170 | T | TATTTTC | 6 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0104 others(3): Show |
6 | HG00558.hp2 HG01243.hp1 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.-37-2769_-37-2768i others(8): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367170 | |||||||
| chr2:98367170 | T | TATTTTCC | 15 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(12): Show |
16 | HG00140.hp1 HG00323.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-37-2769_-37-2768i others(9): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367170 | |||||||
| chr2:98367171 | T | A | 66 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0027 others(63): Show |
69 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.-37-2768T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367171 | |||||||
| chr2:98367176 | C | T | 82 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(79): Show |
88 | HG00140.hp1 HG00323.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.-37-2763C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367176 | |||||||
| chr2:98367184 | TC | T | 50 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0040 others(47): Show |
53 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.-37-2754delC | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367184 | |||||||
| chr2:98367185 | C | T | 93 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(90): Show |
99 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-37-2754C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367185 | |||||||
| chr2:98367189 | T | C | 1 | a0001c0001t0001g0016 | 2 | HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.-37-2750T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367189 | |||||||
| chr2:98367210 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-37-2729A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367210 | |||||||
| chr2:98367218 | A | G | 151 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(148): Show |
160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.-37-2721A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367218 | |||||||
| chr2:98367250 | A | C | 145 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(142): Show |
153 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.-37-2689A>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367250 | |||||||
| chr2:98367272 | G | A | 4 | a0001c0001t0001g0069 a0001c0001t0001g0121 a0004c0007t0001g0070 others(1): Show |
4 | HG02809.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-2667G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367272 | |||||||
| chr2:98367288 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-37-2651G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367288 | |||||||
| chr2:98367355 | C | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(15): Show |
19 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-37-2584C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367355 | |||||||
| chr2:98367389 | T | C | 1 | a0001c0012t0001g0122 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-37-2550T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367389 | |||||||
| chr2:98367419 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | NA19067.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-37-2520C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367419 | |||||||
| chr2:98367490 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-37-2449G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367490 | |||||||
| chr2:98367527 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-37-2412C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367527 | |||||||
| chr2:98367640 | C | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0117 |
3 | HG02922.hp2 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-37-2299C>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367640 | |||||||
| chr2:98367650 | A | G | 1 | a0001c0001t0008g0101 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.-37-2289A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367650 | |||||||
| chr2:98367714 | C | T | 4 | a0001c0001t0001g0141 a0001c0001t0001g0270 a0001c0001t0001g0271 others(1): Show |
4 | HG00438.hp2 HG00735.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-2225C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98367714 | |||||||
| chr2:98368016 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 |
4 | HG01257.hp2 HG01258.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-1923C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98368016 | |||||||
| chr2:98368031 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-37-1908T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98368031 | |||||||
| chr2:98368033 | T | C | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0069 others(4): Show |
7 | HG02809.hp1 HG02895.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.-37-1906T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98368033 | |||||||
| chr2:98368062 | C | G | 8 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(5): Show |
8 | HG00597.hp2 HG01952.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.-37-1877C>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98368062 | |||||||
| chr2:98368138 | C | G | 5 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG02071.hp1 HG02135.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.-37-1801C>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98368138 | |||||||
| chr2:98368191 | G | C | 146 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(143): Show |
154 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.-37-1748G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98368191 | |||||||
| chr2:98368229 | A | T | 1 | a0001c0001t0001g0123 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-37-1710A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98368229 | |||||||
| chr2:98368339 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-37-1600C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98368339 | |||||||
| chr2:98368354 | T | A | 1 | a0001c0002t0001g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-37-1585T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98368354 | |||||||
| chr2:98368424 | C | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0121 a0004c0007t0001g0070 others(1): Show |
4 | HG02809.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-37-1515C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98368424 | |||||||
| chr2:98368905 | C | A | 1 | a0001c0013t0001g0180 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-37-1034C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98368905 | |||||||
| chr2:98368991 | C | A | 1 | a0001c0001t0001g0051 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-37-948C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98368991 | |||||||
| chr2:98369000 | T | C | 1 | a0001c0003t0001g0106 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-37-939T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98369000 | |||||||
| chr2:98369176 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 |
4 | HG01257.hp2 HG01258.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-763G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98369176 | |||||||
| chr2:98369176 | G | C | 18 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(15): Show |
19 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-37-763G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98369176 | |||||||
| chr2:98369270 | T | C | 4 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
4 | HG02080.hp2 NA18939.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.-37-669T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98369270 | |||||||
| chr2:98369327 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-37-612T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98369327 | |||||||
| chr2:98369354 | G | A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(15): Show |
19 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-37-585G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98369354 | |||||||
| chr2:98369434 | G | A | 6 | a0001c0001t0001g0040 a0001c0001t0001g0166 a0001c0001t0001g0167 others(3): Show |
6 | HG02647.hp1 HG02717.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.-37-505G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98369434 | |||||||
| chr2:98369435 | TG | T | 7 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(4): Show |
7 | HG01358.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-37-503delG | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98369435 | |||||||
| chr2:98369653 | G | A | 21 | a0001c0001t0001g0014 a0001c0001t0001g0042 a0001c0001t0001g0043 others(18): Show |
22 | HG02027.hp1 HG02109.hp2 HG02559.hp2 others(19): Show |
intron_variant | MODIFIER | c.-37-286G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98369653 | |||||||
| chr2:98369735 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-37-204A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98369735 | |||||||
| chr2:98369771 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0166 |
2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.-37-168G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98369771 | |||||||
| chr2:98369888 | G | A | 2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-37-51G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 1/7 | chr2 | 98369888 | |||||||
| chr2:98370193 | G | A | 3 | a0001c0002t0001g0047 a0001c0002t0002g0046 a0001c0002t0002g0048 |
3 | HG02965.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.101+117G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98370193 | |||||||
| chr2:98370322 | A | C | 1 | a0001c0001t0001g0238 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.101+246A>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98370322 | |||||||
| chr2:98370650 | A | G | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | NA18971.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.101+574A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98370650 | |||||||
| chr2:98370736 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0118 a0001c0001t0001g0119 |
4 | HG01257.hp2 HG01258.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.101+660C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98370736 | |||||||
| chr2:98370938 | C | A | 59 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0027 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.101+862C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98370938 | |||||||
| chr2:98371298 | C | T | 22 | a0001c0002t0001g0002 a0001c0002t0001g0008 a0001c0002t0001g0022 others(19): Show |
25 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(22): Show |
intron_variant | MODIFIER | c.101+1222C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98371298 | |||||||
| chr2:98371403 | C | T | 9 | a0001c0001t0001g0021 a0001c0001t0001g0034 a0001c0001t0001g0036 others(6): Show |
9 | HG02055.hp1 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.101+1327C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98371403 | |||||||
| chr2:98371415 | C | A | 14 | a0001c0001t0001g0014 a0001c0001t0001g0065 a0001c0001t0001g0066 others(11): Show |
15 | HG02027.hp1 HG02109.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.101+1339C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98371415 | |||||||
| chr2:98371470 | A | G | 6 | a0001c0002t0001g0002 a0001c0002t0001g0022 a0001c0002t0001g0023 others(3): Show |
8 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+1394A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98371470 | |||||||
| chr2:98371572 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.101+1496T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98371572 | |||||||
| chr2:98371755 | C | T | 144 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(141): Show |
152 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.101+1679C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98371755 | |||||||
| chr2:98371939 | G | C | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0117 |
3 | HG02922.hp2 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.101+1863G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98371939 | |||||||
| chr2:98371940 | G | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0117 |
3 | HG02922.hp2 HG03098.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.101+1864G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98371940 | |||||||
| chr2:98372075 | C | T | 1 | a0002c0005t0003g0306 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.101+1999C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98372075 | |||||||
| chr2:98372086 | G | A | 7 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(4): Show |
7 | HG01358.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+2010G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98372086 | |||||||
| chr2:98372146 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.101+2070C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98372146 | |||||||
| chr2:98372202 | C | T | 1 | a0001c0001t0001g0284 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.101+2126C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98372202 | |||||||
| chr2:98372218 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.101+2142G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98372218 | |||||||
| chr2:98372239 | C | A | 1 | a0001c0001t0001g0305 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.101+2163C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98372239 | |||||||
| chr2:98372287 | A | G | 7 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(4): Show |
7 | HG01358.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+2211A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98372287 | |||||||
| chr2:98372308 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.101+2232C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98372308 | |||||||
| chr2:98372599 | A | G | 102 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(99): Show |
108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.101+2523A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98372599 | |||||||
| chr2:98372695 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02155.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.101+2619C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98372695 | |||||||
| chr2:98372747 | C | G | 61 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0027 others(58): Show |
64 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(61): Show |
intron_variant | MODIFIER | c.101+2671C>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98372747 | |||||||
| chr2:98372768 | C | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.101+2692C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98372768 | |||||||
| chr2:98372841 | G | A | 99 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(96): Show |
105 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.101+2765G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98372841 | |||||||
| chr2:98372895 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.101+2819C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98372895 | |||||||
| chr2:98372955 | C | T | 38 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(35): Show |
41 | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.101+2879C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98372955 | |||||||
| chr2:98372956 | G | A | 7 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(4): Show |
7 | HG01358.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+2880G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98372956 | |||||||
| chr2:98373039 | G | A | 1 | a0008c0010t0001g0145 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.101+2963G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98373039 | |||||||
| chr2:98373196 | C | A | 1 | a0001c0003t0001g0291 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.101+3120C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98373196 | |||||||
| chr2:98373237 | A | C | 147 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(144): Show |
155 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.101+3161A>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98373237 | |||||||
| chr2:98373249 | C | T | 7 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(4): Show |
7 | HG01358.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+3173C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98373249 | |||||||
| chr2:98373303 | T | C | 1 | a0001c0002t0001g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.101+3227T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98373303 | |||||||
| chr2:98373396 | C | T | 7 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(4): Show |
7 | HG01358.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.101+3320C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98373396 | |||||||
| chr2:98373493 | G | A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(15): Show |
19 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.101+3417G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98373493 | |||||||
| chr2:98373592 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.101+3516G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98373592 | |||||||
| chr2:98373646 | C | CA | 7 | a0001c0001t0001g0013 a0001c0001t0001g0148 a0001c0001t0001g0149 others(4): Show |
8 | HG00642.hp1 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+3575dupA | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr2 | 98373646 | ||||||
| chr2:98373754 | C | A | 1 | a0001c0001t0001g0298 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.101+3678C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98373754 | |||||||
| chr2:98373847 | G | A | 7 | a0001c0002t0001g0008 a0001c0002t0001g0072 a0001c0002t0001g0073 others(4): Show |
8 | HG00735.hp2 HG01069.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.101+3771G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98373847 | |||||||
| chr2:98373864 | G | C | 4 | a0001c0001t0001g0069 a0001c0001t0001g0121 a0004c0007t0001g0070 others(1): Show |
4 | HG02809.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.101+3788G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98373864 | |||||||
| chr2:98373961 | A | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | NA18967.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.102-3726A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98373961 | |||||||
| chr2:98373970 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.102-3717T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98373970 | |||||||
| chr2:98374372 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG00639.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.102-3315G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98374372 | |||||||
| chr2:98374442 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.102-3245C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98374442 | |||||||
| chr2:98374701 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0275 |
2 | HG02735.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.102-2986A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98374701 | |||||||
| chr2:98374801 | G | C | 18 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0049 others(15): Show |
19 | HG00140.hp1 HG00323.hp1 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.102-2886G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98374801 | |||||||
| chr2:98374870 | A | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0236 a0001c0001t0001g0237 |
3 | NA18942.hp2 NA18988.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.102-2817A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98374870 | |||||||
| chr2:98375089 | A | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0069 others(4): Show |
7 | HG02809.hp1 HG02895.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.102-2598A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98375089 | |||||||
| chr2:98375213 | G | A | 2 | a0001c0003t0001g0181 a0001c0013t0001g0180 |
2 | HG00408.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.102-2474G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98375213 | |||||||
| chr2:98375217 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.102-2470G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98375217 | |||||||
| chr2:98375331 | G | A | 59 | a0001c0001t0001g0005 a0001c0001t0001g0018 a0001c0001t0001g0027 others(56): Show |
62 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.102-2356G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98375331 | |||||||
| chr2:98375374 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0062 a0001c0001t0002g0063 |
3 | HG01891.hp1 HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.102-2313G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98375374 | |||||||
| chr2:98375588 | T | C | 1 | a0001c0002t0001g0114 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.102-2099T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98375588 | |||||||
| chr2:98375650 | G | A | 126 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0010 others(123): Show |
133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.102-2037G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98375650 | |||||||
| chr2:98375953 | T | A | 1 | a0001c0001t0003g0060 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.102-1734T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98375953 | |||||||
| chr2:98375967 | A | C | 1 | a0001c0001t0001g0158 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.102-1720A>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98375967 | |||||||
| chr2:98375989 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.102-1698T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98375989 | |||||||
| chr2:98376025 | T | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0142 a0001c0001t0001g0154 |
3 | HG00280.hp2 HG01261.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.102-1662T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98376025 | |||||||
| chr2:98376060 | A | G | 1 | a0001c0001t0001g0289 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.102-1627A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98376060 | |||||||
| chr2:98376094 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.102-1593G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98376094 | |||||||
| chr2:98376363 | T | A | 1 | a0001c0001t0001g0102 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.102-1324T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98376363 | |||||||
| chr2:98376366 | T | C | 8 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(5): Show |
8 | HG01358.hp2 HG01891.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.102-1321T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98376366 | |||||||
| chr2:98376503 | C | T | 5 | a0001c0001t0001g0027 a0001c0001t0001g0045 a0001c0001t0001g0300 others(2): Show |
5 | HG00639.hp1 HG01175.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.102-1184C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98376503 | |||||||
| chr2:98376504 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.102-1183G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98376504 | |||||||
| chr2:98376516 | C | T | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.102-1171C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98376516 | |||||||
| chr2:98376536 | A | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.102-1151A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98376536 | |||||||
| chr2:98376572 | A | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0065 a0001c0001t0001g0066 others(10): Show |
14 | HG02027.hp1 HG02109.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.102-1115A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98376572 | |||||||
| chr2:98376654 | G | T | 7 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(4): Show |
7 | HG01358.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.102-1033G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98376654 | |||||||
| chr2:98376712 | G | A | 1 | a0001c0003t0001g0140 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.102-975G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98376712 | |||||||
| chr2:98376821 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.102-866G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98376821 | |||||||
| chr2:98376873 | A | T | 2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.102-814A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98376873 | |||||||
| chr2:98376879 | T | A | 1 | a0001c0001t0001g0118 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.102-808T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98376879 | |||||||
| chr2:98376944 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0062 a0001c0001t0002g0063 |
3 | HG01891.hp1 HG02572.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.102-743C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98376944 | |||||||
| chr2:98376992 | A | G | 7 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0062 others(4): Show |
7 | HG01358.hp2 HG01891.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.102-695A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98376992 | |||||||
| chr2:98377053 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.102-634G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98377053 | |||||||
| chr2:98377077 | T | G | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(2): Show |
5 | HG02155.hp2 NA18612.hp2 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.102-610T>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98377077 | |||||||
| chr2:98377133 | G | A | 1 | a0001c0003t0001g0291 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.102-554G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98377133 | |||||||
| chr2:98377163 | C | T | 4 | a0001c0001t0001g0069 a0001c0001t0001g0121 a0004c0007t0001g0070 others(1): Show |
4 | HG02809.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.102-524C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98377163 | |||||||
| chr2:98377164 | G | A | 1 | a0001c0003t0001g0181 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.102-523G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98377164 | |||||||
| chr2:98377172 | A | G | 106 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(103): Show |
114 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(111): Show |
intron_variant | MODIFIER | c.102-515A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98377172 | |||||||
| chr2:98377230 | G | A | 1 | a0001c0001t0001g0289 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.102-457G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98377230 | |||||||
| chr2:98377230 | G | C | 1 | a0001c0001t0001g0263 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.102-457G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98377230 | |||||||
| chr2:98377391 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.102-296C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98377391 | |||||||
| chr2:98377446 | C | T | 2 | a0001c0001t0001g0043 a0001c0001t0001g0253 |
2 | HG02922.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.102-241C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98377446 | |||||||
| chr2:98377667 | C | T | 2 | a0001c0002t0001g0029 a0001c0012t0001g0122 |
2 | HG01243.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.102-20C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98377667 | |||||||
| chr2:98377671 | A | G | 30 | a0001c0001t0001g0005 a0001c0001t0001g0078 a0001c0001t0001g0112 others(27): Show |
32 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.102-16A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98377671 | |||||||
| chr2:98377673 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.102-14A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 2/7 | chr2 | 98377673 | |||||||
| chr2:98377846 | T | A | 4 | a0001c0002t0001g0047 a0001c0002t0002g0028 a0002c0006t0003g0030 others(1): Show |
4 | HG02647.hp2 HG02976.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.215+46T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98377846 | |||||||
| chr2:98377846 | T | G | 18 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0017 others(15): Show |
21 | HG01106.hp2 HG01243.hp1 HG01257.hp2 others(18): Show |
intron_variant | MODIFIER | c.215+46T>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98377846 | |||||||
| chr2:98377936 | C | T | 3 | a0001c0001t0001g0061 a0001c0001t0003g0060 a0001c0001t0003g0064 |
3 | HG02280.hp1 HG02559.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.215+136C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98377936 | |||||||
| chr2:98377951 | T | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(181): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.215+151T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98377951 | |||||||
| chr2:98378113 | C | A | 3 | a0001c0001t0001g0062 a0001c0001t0001g0066 a0001c0002t0001g0025 |
3 | HG02622.hp2 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.215+313C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98378113 | |||||||
| chr2:98378178 | G | A | 107 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0011 others(104): Show |
115 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.215+378G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98378178 | |||||||
| chr2:98378422 | C | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0173 |
2 | HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.215+622C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98378422 | |||||||
| chr2:98378510 | C | T | 255 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(252): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.215+710C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98378510 | |||||||
| chr2:98378573 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.215+773T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98378573 | |||||||
| chr2:98378585 | T | A | 1 | a0001c0001t0001g0227 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.215+785T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98378585 | |||||||
| chr2:98378613 | T | G | 3 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0002t0001g0025 |
3 | HG02622.hp2 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.215+813T>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98378613 | |||||||
| chr2:98378738 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.215+938G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98378738 | |||||||
| chr2:98379057 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.216-1118G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98379057 | |||||||
| chr2:98379088 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.216-1087G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98379088 | |||||||
| chr2:98379140 | G | C | 98 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0013 others(95): Show |
107 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.216-1035G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98379140 | |||||||
| chr2:98379173 | G | A | 1 | a0001c0001t0001g0007 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.216-1002G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98379173 | |||||||
| chr2:98379295 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.216-880C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98379295 | |||||||
| chr2:98379372 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.216-803C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98379372 | |||||||
| chr2:98379404 | C | CCTGTTCC others(3): Show |
91 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0015 others(88): Show |
100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.216-761_216-752dup others(10): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr2 | 98379404 | ||||||
| chr2:98379519 | C | T | 8 | a0001c0001t0001g0232 a0001c0002t0002g0046 a0001c0002t0002g0048 others(5): Show |
8 | HG02647.hp2 HG02896.hp2 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.216-656C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98379519 | |||||||
| chr2:98379537 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0066 a0004c0007t0001g0070 others(1): Show |
4 | HG02723.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-638C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98379537 | |||||||
| chr2:98379557 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.216-618C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98379557 | |||||||
| chr2:98379623 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.216-552G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98379623 | |||||||
| chr2:98379706 | T | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0204 |
2 | HG02135.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.216-469T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98379706 | |||||||
| chr2:98379909 | T | C | 11 | a0001c0001t0001g0119 a0001c0001t0001g0187 a0001c0001t0001g0244 others(8): Show |
11 | HG00558.hp1 HG03669.hp2 HG03704.hp1 others(8): Show |
intron_variant | MODIFIER | c.216-266T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98379909 | |||||||
| chr2:98380132 | G | T | 1 | a0001c0001t0001g0248 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.216-43G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 3/7 | chr2 | 98380132 | |||||||
| chr2:98380506 | G | T | 1 | a0001c0002t0001g0077 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.395+152G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98380506 | |||||||
| chr2:98380522 | A | T | 157 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(154): Show |
166 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.395+168A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98380522 | |||||||
| chr2:98380775 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.395+421G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98380775 | |||||||
| chr2:98381100 | AGTCTCCC others(9): Show |
A | 1 | a0001c0001t0001g0199 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.395+751_395+766del others(16): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr2 | 98381100 | ||||||
| chr2:98381191 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.395+837C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98381191 | |||||||
| chr2:98381219 | C | T | 251 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(248): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.395+865C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98381219 | |||||||
| chr2:98381268 | C | A | 167 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(164): Show |
179 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.395+914C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98381268 | |||||||
| chr2:98381345 | C | T | 75 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0020 others(72): Show |
81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.395+991C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98381345 | |||||||
| chr2:98381494 | G | A | 2 | a0001c0001t0002g0079 a0001c0002t0002g0028 |
2 | HG02896.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.395+1140G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98381494 | |||||||
| chr2:98381546 | C | A | 73 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(70): Show |
77 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.395+1192C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98381546 | |||||||
| chr2:98381776 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.395+1422T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98381776 | |||||||
| chr2:98381779 | A | G | 15 | a0001c0001t0001g0040 a0001c0001t0001g0058 a0001c0001t0001g0069 others(12): Show |
15 | HG01243.hp1 HG01358.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.395+1425A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98381779 | |||||||
| chr2:98381860 | A | T | 3 | a0001c0003t0001g0181 a0001c0003t0001g0194 a0001c0013t0001g0180 |
3 | HG00408.hp2 HG02129.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.395+1506A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98381860 | |||||||
| chr2:98381881 | G | A | 263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(260): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.396-1507G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98381881 | |||||||
| chr2:98382140 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.396-1248G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98382140 | |||||||
| chr2:98382168 | T | G | 1 | a0001c0001t0001g0150 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.396-1220T>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98382168 | |||||||
| chr2:98382169 | G | C | 8 | a0001c0001t0001g0176 a0001c0001t0001g0227 a0001c0001t0002g0063 others(5): Show |
8 | HG01891.hp1 HG02486.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.396-1219G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98382169 | |||||||
| chr2:98382426 | C | G | 1 | a0001c0001t0001g0305 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.396-962C>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98382426 | |||||||
| chr2:98382431 | G | T | 1 | a0001c0001t0001g0305 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.396-957G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98382431 | |||||||
| chr2:98382520 | G | C | 4 | a0001c0001t0001g0078 a0001c0001t0001g0118 a0001c0001t0001g0310 others(1): Show |
5 | HG00099.hp2 HG00280.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.396-868G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98382520 | |||||||
| chr2:98382583 | C | T | 1 | a0001c0001t0003g0041 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.396-805C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98382583 | |||||||
| chr2:98382760 | C | T | 7 | a0002c0004t0002g0088 a0002c0004t0002g0098 a0002c0004t0002g0126 others(4): Show |
7 | HG00558.hp1 NA18944.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-628C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98382760 | |||||||
| chr2:98382770 | A | T | 1 | a0002c0005t0003g0233 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.396-618A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98382770 | |||||||
| chr2:98382910 | C | T | 30 | a0001c0001t0001g0034 a0001c0001t0001g0176 a0001c0001t0001g0227 others(27): Show |
30 | HG00558.hp1 HG01261.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.396-478C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98382910 | |||||||
| chr2:98383023 | G | A | 1 | a0010c0014t0002g0260 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.396-365G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98383023 | |||||||
| chr2:98383185 | C | T | 7 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0043 others(4): Show |
7 | HG02109.hp2 HG02723.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.396-203C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98383185 | |||||||
| chr2:98383297 | G | C | 1 | a0001c0003t0001g0095 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.396-91G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98383297 | |||||||
| chr2:98383304 | G | T | 23 | a0001c0001t0001g0176 a0001c0001t0001g0227 a0001c0001t0001g0232 others(20): Show |
23 | HG00558.hp1 HG01891.hp1 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.396-84G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 4/7 | chr2 | 98383304 | |||||||
| chr2:98383598 | C | A | 1 | a0001c0001t0001g0227 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.449+157C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98383598 | |||||||
| chr2:98383739 | C | T | 2 | a0001c0001t0001g0195 a0001c0002t0001g0114 |
2 | NA18962.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.449+298C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98383739 | |||||||
| chr2:98383912 | A | T | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(226): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.449+471A>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98383912 | |||||||
| chr2:98383951 | A | G | 2 | a0001c0001t0001g0221 a0001c0001t0001g0268 |
2 | HG01106.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.449+510A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98383951 | |||||||
| chr2:98384077 | G | C | 7 | a0001c0001t0001g0104 a0001c0001t0001g0131 a0001c0001t0001g0132 others(4): Show |
7 | HG02071.hp2 NA18949.hp2 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.449+636G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98384077 | |||||||
| chr2:98384348 | A | C | 8 | a0001c0001t0001g0232 a0001c0001t0001g0305 a0002c0005t0003g0164 others(5): Show |
8 | HG02559.hp2 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.449+907A>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98384348 | |||||||
| chr2:98384351 | G | A | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(226): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.449+910G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98384351 | |||||||
| chr2:98384371 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.449+930G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98384371 | |||||||
| chr2:98384385 | G | C | 229 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(226): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.449+944G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98384385 | |||||||
| chr2:98384416 | G | C | 6 | a0001c0001t0001g0232 a0002c0005t0003g0164 a0002c0005t0003g0165 others(3): Show |
6 | HG02647.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.449+975G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98384416 | |||||||
| chr2:98384469 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.449+1028C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98384469 | |||||||
| chr2:98384470 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.449+1029T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98384470 | |||||||
| chr2:98384487 | G | T | 1 | a0001c0002t0001g0022 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.449+1046G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98384487 | |||||||
| chr2:98384570 | G | A | 1 | a0001c0002t0001g0023 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.449+1129G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98384570 | |||||||
| chr2:98384782 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.449+1341G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98384782 | |||||||
| chr2:98384805 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.449+1364G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98384805 | |||||||
| chr2:98384818 | G | A | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG00741.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.449+1377G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98384818 | |||||||
| chr2:98384824 | T | G | 1 | a0001c0001t0001g0305 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.449+1383T>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98384824 | |||||||
| chr2:98384940 | C | T | 96 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0015 others(93): Show |
104 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.449+1499C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98384940 | |||||||
| chr2:98385052 | A | G | 8 | a0001c0001t0001g0176 a0001c0001t0001g0227 a0001c0001t0002g0063 others(5): Show |
8 | HG01891.hp1 HG02486.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.449+1611A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98385052 | |||||||
| chr2:98385274 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.449+1833G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98385274 | |||||||
| chr2:98385287 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.449+1846T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98385287 | |||||||
| chr2:98385288 | G | C | 1 | a0001c0001t0001g0211 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.449+1847G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98385288 | |||||||
| chr2:98385314 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.449+1873C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98385314 | |||||||
| chr2:98385378 | T | C | 1 | a0002c0005t0003g0306 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.449+1937T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98385378 | |||||||
| chr2:98385453 | ACACAAAA others(4): Show |
A | 1 | a0001c0001t0001g0297 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.449+2016_449+2026d others(13): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr2 | 98385453 | ||||||
| chr2:98385667 | G | C | 1 | a0001c0001t0001g0123 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.449+2226G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98385667 | |||||||
| chr2:98385727 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.449+2286T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98385727 | |||||||
| chr2:98385944 | A | G | 6 | a0001c0001t0001g0037 a0001c0001t0001g0042 a0001c0001t0001g0043 others(3): Show |
6 | HG02723.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.449+2503A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98385944 | |||||||
| chr2:98385945 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.449+2504A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98385945 | |||||||
| chr2:98385985 | A | G | 17 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0027 others(14): Show |
18 | HG01255.hp2 HG01346.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.449+2544A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98385985 | |||||||
| chr2:98385997 | T | A | 30 | a0001c0001t0001g0034 a0001c0001t0001g0176 a0001c0001t0001g0227 others(27): Show |
30 | HG00558.hp1 HG01261.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.449+2556T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98385997 | |||||||
| chr2:98386358 | G | T | 7 | a0001c0003t0001g0095 a0001c0003t0001g0106 a0001c0003t0001g0140 others(4): Show |
7 | HG00408.hp1 HG00544.hp2 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.449+2917G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98386358 | |||||||
| chr2:98386481 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.449+3040G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98386481 | |||||||
| chr2:98386595 | C | T | 15 | a0001c0001t0001g0176 a0001c0001t0001g0227 a0001c0001t0002g0063 others(12): Show |
15 | HG00558.hp1 HG01891.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.450-3063C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98386595 | |||||||
| chr2:98386600 | A | G | 1 | a0001c0001t0011g0258 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.450-3058A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98386600 | |||||||
| chr2:98386818 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.450-2840C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98386818 | |||||||
| chr2:98386870 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.450-2788A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98386870 | |||||||
| chr2:98387006 | G | T | 1 | a0001c0003t0001g0095 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.450-2652G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98387006 | |||||||
| chr2:98387133 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.450-2525T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98387133 | |||||||
| chr2:98387202 | C | T | 1 | a0001c0001t0003g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.450-2456C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98387202 | |||||||
| chr2:98387245 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.450-2413A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98387245 | |||||||
| chr2:98387275 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.450-2383C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98387275 | |||||||
| chr2:98387643 | T | C | 30 | a0001c0001t0001g0034 a0001c0001t0001g0176 a0001c0001t0001g0227 others(27): Show |
30 | HG00558.hp1 HG01261.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.450-2015T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98387643 | |||||||
| chr2:98387710 | G | T | 233 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(230): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.450-1948G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98387710 | |||||||
| chr2:98387760 | C | T | 1 | a0001c0002t0001g0029 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.450-1898C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98387760 | |||||||
| chr2:98387788 | C | G | 7 | a0002c0004t0002g0088 a0002c0004t0002g0098 a0002c0004t0002g0126 others(4): Show |
7 | HG00558.hp1 NA18944.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.450-1870C>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98387788 | |||||||
| chr2:98387885 | C | T | 7 | a0001c0001t0001g0232 a0002c0005t0003g0164 a0002c0005t0003g0165 others(4): Show |
7 | HG02647.hp2 HG02896.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.450-1773C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98387885 | |||||||
| chr2:98387981 | A | G | 1 | a0001c0001t0003g0234 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.450-1677A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98387981 | |||||||
| chr2:98388138 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.450-1520G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98388138 | |||||||
| chr2:98388195 | A | C | 31 | a0001c0001t0001g0034 a0001c0001t0001g0176 a0001c0001t0001g0227 others(28): Show |
31 | HG00558.hp1 HG01261.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.450-1463A>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98388195 | |||||||
| chr2:98388334 | G | A | 1 | a0006c0015t0001g0120 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.450-1324G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98388334 | |||||||
| chr2:98388553 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.450-1105A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98388553 | |||||||
| chr2:98388632 | G | A | 9 | a0001c0001t0001g0176 a0001c0001t0001g0227 a0001c0001t0002g0063 others(6): Show |
9 | HG01891.hp1 HG02486.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.450-1026G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98388632 | |||||||
| chr2:98388670 | C | G | 2 | a0001c0001t0001g0266 a0001c0001t0001g0269 |
2 | HG01255.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.450-988C>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98388670 | |||||||
| chr2:98388837 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.450-821G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98388837 | |||||||
| chr2:98388846 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.450-812A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98388846 | |||||||
| chr2:98389033 | T | G | 8 | a0001c0001t0001g0110 a0002c0004t0002g0088 a0002c0004t0002g0098 others(5): Show |
8 | HG00558.hp1 NA18944.hp2 NA18950.hp1 others(5): Show |
intron_variant | MODIFIER | c.450-625T>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98389033 | |||||||
| chr2:98389049 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.450-609C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98389049 | |||||||
| chr2:98389138 | C | T | 138 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(135): Show |
148 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.450-520C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98389138 | |||||||
| chr2:98389174 | A | G | 2 | a0001c0001t0001g0264 a0001c0001t0008g0101 |
2 | NA18949.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.450-484A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98389174 | |||||||
| chr2:98389399 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.450-259A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98389399 | |||||||
| chr2:98389423 | C | T | 2 | a0005c0009t0001g0170 a0005c0009t0001g0240 |
2 | HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.450-235C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98389423 | |||||||
| chr2:98389451 | G | C | 1 | a0001c0001t0001g0034 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.450-207G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98389451 | |||||||
| chr2:98389475 | C | T | 2 | a0001c0001t0001g0105 a0008c0010t0001g0145 |
2 | HG00609.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.450-183C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 5/7 | chr2 | 98389475 | |||||||
| chr2:98389857 | G | A | 3 | a0001c0001t0001g0210 a0001c0001t0001g0236 a0001c0001t0001g0237 |
3 | NA18942.hp2 NA18988.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.566+83G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98389857 | |||||||
| chr2:98390049 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.566+275G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98390049 | |||||||
| chr2:98390056 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.566+282C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98390056 | |||||||
| chr2:98390080 | A | G | 7 | a0002c0004t0002g0088 a0002c0004t0002g0098 a0002c0004t0002g0126 others(4): Show |
7 | HG00558.hp1 NA18944.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.566+306A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98390080 | |||||||
| chr2:98390199 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.566+425G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98390199 | |||||||
| chr2:98390318 | A | AT | 19 | a0001c0001t0001g0012 a0001c0001t0001g0044 a0001c0001t0001g0051 others(16): Show |
20 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(17): Show |
intron_variant | MODIFIER | c.566+554dupT | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr2 | 98390318 | ||||||
| chr2:98390712 | A | G | 1 | a0001c0001t0007g0292 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.566+938A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98390712 | |||||||
| chr2:98390751 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.566+977T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98390751 | |||||||
| chr2:98390819 | T | C | 15 | a0001c0001t0001g0038 a0001c0001t0001g0167 a0001c0001t0001g0176 others(12): Show |
15 | HG01261.hp2 HG02280.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.566+1045T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98390819 | |||||||
| chr2:98390877 | A | C | 4 | a0001c0001t0002g0063 a0001c0001t0002g0080 a0001c0002t0002g0046 others(1): Show |
4 | HG01891.hp1 HG02818.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.567-987A>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98390877 | |||||||
| chr2:98390919 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.567-945C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98390919 | |||||||
| chr2:98391106 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.567-758G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98391106 | |||||||
| chr2:98391146 | G | A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0298 |
2 | NA18940.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.567-718G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98391146 | |||||||
| chr2:98391180 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.567-684G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98391180 | |||||||
| chr2:98391222 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.567-642C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98391222 | |||||||
| chr2:98391283 | G | C | 1 | a0001c0001t0001g0176 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.567-581G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98391283 | |||||||
| chr2:98391387 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | NA18954.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.567-477C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98391387 | |||||||
| chr2:98391463 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.567-401A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98391463 | |||||||
| chr2:98391572 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.567-292G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98391572 | |||||||
| chr2:98391714 | G | A | 5 | a0002c0005t0003g0164 a0002c0005t0003g0165 a0002c0005t0003g0233 others(2): Show |
5 | HG02647.hp2 HG02896.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.567-150G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98391714 | |||||||
| chr2:98391791 | C | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0286 |
3 | NA18959.hp1 NA18967.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.567-73C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98391791 | |||||||
| chr2:98391811 | C | A | 2 | a0001c0002t0002g0046 a0001c0002t0002g0048 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.567-53C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 6/7 | chr2 | 98391811 | |||||||
| chr2:98392185 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.673+215T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98392185 | |||||||
| chr2:98392314 | C | A | 1 | a0001c0001t0001g0176 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.673+344C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98392314 | |||||||
| chr2:98392333 | A | G | 28 | a0001c0001t0002g0063 a0001c0001t0002g0079 a0001c0001t0002g0080 others(25): Show |
28 | HG00558.hp1 HG01261.hp2 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.673+363A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98392333 | |||||||
| chr2:98392412 | T | C | 6 | a0001c0001t0003g0041 a0001c0001t0003g0060 a0001c0001t0003g0064 others(3): Show |
6 | HG01261.hp2 HG02280.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.673+442T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98392412 | |||||||
| chr2:98392567 | A | G | 3 | a0001c0001t0001g0078 a0001c0001t0001g0118 a0001c0002t0001g0008 |
4 | HG00280.hp2 HG01099.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+597A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98392567 | |||||||
| chr2:98392574 | A | AAAAAG | 5 | a0001c0001t0002g0063 a0001c0001t0002g0079 a0001c0001t0002g0116 others(2): Show |
5 | HG01891.hp1 HG02896.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.673+624_673+628dup others(5): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 98392574 | ||||||
| chr2:98392574 | A | AAAAAGAA others(3): Show |
3 | a0001c0002t0002g0046 a0001c0002t0002g0048 a0010c0014t0002g0260 |
3 | HG02965.hp2 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.673+619_673+628dup others(10): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 98392574 | ||||||
| chr2:98392574 | AAAAAGAA others(3): Show |
A | 1 | a0002c0005t0003g0306 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.673+619_673+628del others(10): Show |
CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 98392574 | ||||||
| chr2:98392594 | G | GA | 11 | a0001c0001t0001g0027 a0001c0001t0001g0109 a0001c0001t0001g0131 others(8): Show |
11 | HG01261.hp2 HG02135.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.673+633dupA | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr2 | 98392594 | ||||||
| chr2:98392595 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0119 |
3 | HG01256.hp1 HG01258.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.673+625A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98392595 | |||||||
| chr2:98392599 | A | G | 15 | a0001c0001t0002g0063 a0001c0001t0002g0079 a0001c0001t0002g0116 others(12): Show |
15 | HG00558.hp1 HG01891.hp1 HG02896.hp1 others(12): Show |
intron_variant | MODIFIER | c.673+629A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98392599 | |||||||
| chr2:98392716 | T | C | 33 | a0001c0001t0001g0037 a0001c0001t0001g0065 a0001c0001t0001g0066 others(30): Show |
33 | HG00558.hp1 HG01261.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.673+746T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98392716 | |||||||
| chr2:98392739 | A | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0301 a0001c0002t0001g0075 |
3 | HG00140.hp1 HG01361.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.673+769A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98392739 | |||||||
| chr2:98392745 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.673+775C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98392745 | |||||||
| chr2:98392814 | G | C | 1 | a0006c0015t0001g0120 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.673+844G>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98392814 | |||||||
| chr2:98392819 | C | T | 2 | a0001c0001t0001g0288 a0001c0002t0001g0073 |
2 | HG02300.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.673+849C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98392819 | |||||||
| chr2:98392860 | C | A | 12 | a0001c0001t0003g0041 a0001c0001t0003g0060 a0001c0001t0003g0064 others(9): Show |
12 | HG01261.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.673+890C>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98392860 | |||||||
| chr2:98393125 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.673+1155G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98393125 | |||||||
| chr2:98393509 | C | T | 12 | a0001c0001t0003g0041 a0001c0001t0003g0060 a0001c0001t0003g0064 others(9): Show |
12 | HG01261.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.673+1539C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98393509 | |||||||
| chr2:98393620 | AC | A | 3 | a0001c0001t0001g0040 a0001c0001t0001g0160 a0001c0002t0005g0068 |
3 | HG02647.hp1 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.673+1651delC | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98393620 | |||||||
| chr2:98393830 | T | C | 1 | a0002c0005t0003g0233 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.673+1860T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98393830 | |||||||
| chr2:98394295 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.674-1549C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98394295 | |||||||
| chr2:98394298 | G | T | 3 | a0001c0001t0001g0294 a0001c0001t0001g0299 a0001c0001t0007g0292 |
3 | HG02056.hp1 NA18972.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.674-1546G>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98394298 | |||||||
| chr2:98394378 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.674-1466G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98394378 | |||||||
| chr2:98394446 | A | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0142 a0001c0001t0001g0173 |
3 | HG01516.hp1 HG02970.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.674-1398A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98394446 | |||||||
| chr2:98394491 | A | G | 4 | a0001c0003t0001g0100 a0001c0003t0001g0181 a0001c0003t0001g0194 others(1): Show |
4 | HG00408.hp2 HG02129.hp2 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-1353A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98394491 | |||||||
| chr2:98394652 | C | T | 7 | a0002c0004t0002g0088 a0002c0004t0002g0098 a0002c0004t0002g0126 others(4): Show |
7 | HG00558.hp1 NA18944.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.674-1192C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98394652 | |||||||
| chr2:98394654 | C | T | 16 | a0001c0001t0002g0063 a0001c0001t0002g0079 a0001c0001t0002g0080 others(13): Show |
16 | HG00558.hp1 HG01891.hp1 HG02818.hp2 others(13): Show |
intron_variant | MODIFIER | c.674-1190C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98394654 | |||||||
| chr2:98394708 | G | A | 76 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(73): Show |
84 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.674-1136G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98394708 | |||||||
| chr2:98394780 | G | A | 1 | a0001c0001t0003g0239 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.674-1064G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98394780 | |||||||
| chr2:98394928 | G | A | 6 | a0001c0001t0003g0041 a0001c0001t0003g0060 a0001c0001t0003g0064 others(3): Show |
6 | HG01261.hp2 HG02280.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.674-916G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98394928 | |||||||
| chr2:98395168 | G | A | 1 | a0010c0014t0002g0260 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.674-676G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98395168 | |||||||
| chr2:98395274 | G | A | 2 | a0001c0001t0001g0174 a0001c0001t0001g0229 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.674-570G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98395274 | |||||||
| chr2:98395357 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.674-487A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98395357 | |||||||
| chr2:98395413 | A | G | 104 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0013 others(101): Show |
112 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.674-431A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98395413 | |||||||
| chr2:98395416 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.674-428C>T | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98395416 | |||||||
| chr2:98395459 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.674-385G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98395459 | |||||||
| chr2:98395524 | T | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0111 |
2 | NA18954.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.674-320T>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98395524 | |||||||
| chr2:98395694 | T | C | 7 | a0002c0004t0002g0088 a0002c0004t0002g0098 a0002c0004t0002g0126 others(4): Show |
7 | HG00558.hp1 NA18944.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.674-150T>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98395694 | |||||||
| chr2:98395729 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.674-115A>G | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98395729 | |||||||
| chr2:98395761 | G | A | 1 | a0002c0005t0003g0306 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.674-83G>A | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98395761 | |||||||
| chr2:98395796 | A | C | 8 | a0001c0001t0002g0063 a0001c0001t0002g0079 a0001c0001t0002g0080 others(5): Show |
8 | HG01891.hp1 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.674-48A>C | CNGA3 | ENSG00000144191.12 | transcript | ENST00000272602.7 | protein_coding | 7/7 | chr2 | 98395796 |