Item | Value |
---|---|
geneid | 1258 |
ensemblid | ENSG00000070729.14 |
hgncid | 2151 |
symbol | CNGB1 |
name | cyclic nucleotide gated channel subunit beta 1 |
refseq_nuc | NM_001297.5 |
refseq_prot | NP_001288.3 |
ensembl_nuc | ENST00000251102.13 |
ensembl_prot | ENSP00000251102.8 |
mane_status | MANE Select |
chr | chr16 |
start | 57882340 |
end | 57971128 |
strand | - |
ver | v1.2 |
region | chr16:57882340-57971128 |
region5000 | chr16:57877340-57976128 |
regionname0 | CNGB1_chr16_57882340_57971128 |
regionname5000 | CNGB1_chr16_57877340_57976128 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1251 | 183 | 26 | 30 | 99 | 9 | 19 | 72 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0002 | 1/1 | 1251 | 56 | 14 | 6 | 27 | 1 | 6 | 20 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0003 | 0/0 | 1251 | 21 | 1 | 9 | 8 | 0 | 3 | 4 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0004 | 0/0 | 1251 | 12 | 5 | 3 | 1 | 2 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0005 | 0/0 | 1251 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0006 | 0/0 | 1252 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1247): Show |
chr16 | 57877340 | 57976128 |
a0007 | 0/0 | 1251 | 6 | 3 | 1 | 0 | 1 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0008 | 0/0 | 1251 | 6 | 1 | 1 | 4 | 0 | 0 | 4 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0009 | 0/0 | 1251 | 5 | 2 | 0 | 1 | 1 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0010 | 0/0 | 1251 | 5 | 3 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0011 | 0/0 | 1251 | 4 | 1 | 2 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0012 | 0/0 | 1251 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0013 | 0/0 | 1251 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0014 | 0/0 | 1251 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0015 | 0/0 | 1251 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0016 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0017 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0018 | 0/0 | 1251 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0019 | 0/0 | 1251 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0020 | 0/0 | 1251 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0021 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0022 | 0/0 | 1251 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0023 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0024 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0025 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0026 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0027 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0028 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0029 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0030 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0031 | 0/0 | 1251 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0032 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0033 | 0/0 | 122 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(117): Show |
chr16 | 57877340 | 57976128 |
a0034 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0035 | 0/0 | 1247 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1242): Show |
chr16 | 57877340 | 57976128 |
a0036 | 0/0 | 1252 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1247): Show |
chr16 | 57877340 | 57976128 |
a0037 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0038 | 0/0 | 1251 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0039 | 0/0 | 1251 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0040 | 0/0 | 1251 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0041 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0042 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0043 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0044 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0045 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0046 | 0/0 | 1251 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0047 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
a0048 | 0/0 | 1251 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | MLGWV others(1246): Show |
chr16 | 57877340 | 57976128 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3753 | 40 | 1 | 3 | 28 | 3 | 5 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0002 | 0/0 | 3753 | 36 | 3 | 10 | 16 | 1 | 6 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0003 | 0/0 | 3753 | 33 | 0 | 7 | 18 | 2 | 6 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0004 | 0/0 | 3753 | 30 | 3 | 2 | 23 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0007 | 0/0 | 3753 | 6 | 5 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0013 | 0/0 | 3753 | 4 | 1 | 3 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0015 | 0/0 | 3753 | 3 | 3 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0016 | 0/0 | 3753 | 3 | 3 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0017 | 0/0 | 3753 | 3 | 0 | 0 | 3 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0018 | 0/0 | 3753 | 3 | 0 | 0 | 3 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0019 | 0/0 | 3753 | 3 | 0 | 3 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0027 | 0/0 | 3753 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0028 | 0/0 | 3753 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0029 | 0/0 | 3753 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0035 | 0/0 | 3753 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0041 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0042 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0053 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0066 | 0/0 | 3753 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0068 | 0/0 | 3753 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0070 | 0/0 | 3753 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0073 | 0/0 | 3753 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0096 | 0/0 | 3753 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0097 | 0/0 | 3753 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0099 | 0/0 | 3753 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0001c0103 | 0/0 | 3753 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0002c0005 | 0/0 | 3753 | 25 | 3 | 3 | 16 | 0 | 3 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0002c0006 | 0/1 | 3753 | 16 | 2 | 2 | 9 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0002c0011 | 1/0 | 3753 | 5 | 4 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0002c0022 | 0/0 | 3753 | 3 | 2 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0002c0037 | 0/0 | 3753 | 2 | 0 | 0 | 0 | 0 | 2 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0002c0038 | 0/0 | 3753 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0002c0109 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0002c0113 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0002c0114 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0003c0008 | 0/0 | 3753 | 6 | 0 | 2 | 4 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0003c0009 | 0/0 | 3753 | 5 | 0 | 3 | 1 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0003c0012 | 0/0 | 3753 | 4 | 1 | 2 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0003c0040 | 0/0 | 3753 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0003c0064 | 0/0 | 3753 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0003c0074 | 0/0 | 3753 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0003c0101 | 0/0 | 3753 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0003c0104 | 0/0 | 3753 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0003c0105 | 0/0 | 3753 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0004c0026 | 0/0 | 3753 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0004c0030 | 0/0 | 3753 | 2 | 0 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0004c0034 | 0/0 | 3753 | 2 | 0 | 0 | 0 | 2 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0004c0036 | 0/0 | 3753 | 2 | 0 | 1 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0004c0061 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0004c0077 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0004c0098 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0004c0100 | 0/0 | 3753 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0005c0014 | 0/0 | 3753 | 3 | 3 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0005c0044 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0005c0045 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0005c0046 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0005c0048 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0005c0049 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0006c0081 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3751): Show |
chr16 | 57877340 | 57976128 | ||
a0006c0082 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3751): Show |
chr16 | 57877340 | 57976128 | ||
a0006c0083 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3751): Show |
chr16 | 57877340 | 57976128 | ||
a0006c0084 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3751): Show |
chr16 | 57877340 | 57976128 | ||
a0006c0085 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3751): Show |
chr16 | 57877340 | 57976128 | ||
a0006c0086 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3751): Show |
chr16 | 57877340 | 57976128 | ||
a0006c0087 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3751): Show |
chr16 | 57877340 | 57976128 | ||
a0007c0039 | 0/0 | 3753 | 2 | 0 | 0 | 0 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0007c0115 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0007c0119 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0007c0120 | 0/0 | 3753 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0007c0122 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0008c0020 | 0/0 | 3753 | 3 | 1 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0008c0021 | 0/0 | 3753 | 3 | 0 | 1 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0009c0025 | 0/0 | 3753 | 2 | 1 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0009c0032 | 0/0 | 3753 | 2 | 0 | 0 | 0 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0009c0054 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0010c0010 | 0/0 | 3753 | 5 | 3 | 0 | 0 | 2 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0011c0033 | 0/0 | 3753 | 2 | 0 | 1 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0011c0058 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0011c0059 | 0/0 | 3753 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0012c0024 | 0/0 | 3753 | 2 | 0 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0012c0091 | 0/0 | 3753 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0013c0031 | 0/0 | 3753 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0013c0078 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0014c0116 | 0/0 | 3753 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0014c0118 | 0/0 | 3753 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0015c0055 | 0/0 | 3753 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0015c0102 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0016c0023 | 0/0 | 3753 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0017c0110 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0017c0112 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0018c0060 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0018c0062 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0019c0052 | 0/0 | 3753 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0019c0090 | 0/0 | 3753 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0020c0095 | 0/0 | 3753 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0021c0117 | 0/0 | 3753 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0022c0079 | 0/0 | 3753 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0023c0069 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0024c0123 | 0/0 | 3753 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0025c0108 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0026c0121 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0027c0092 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0028c0080 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0029c0076 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0030c0111 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0031c0094 | 0/0 | 3753 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0032c0065 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0033c0051 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0034c0043 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0035c0057 | 0/0 | 3741 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3736): Show |
chr16 | 57877340 | 57976128 | ||
a0036c0088 | 0/0 | 3756 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3751): Show |
chr16 | 57877340 | 57976128 | ||
a0037c0063 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0038c0093 | 0/0 | 3753 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0039c0072 | 0/0 | 3753 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0040c0067 | 0/0 | 3753 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0041c0047 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0042c0089 | 0/0 | 3753 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0043c0075 | 0/0 | 3753 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0044c0071 | 0/0 | 3753 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0045c0106 | 0/0 | 3753 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0046c0107 | 0/0 | 3753 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0047c0056 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 | ||
a0048c0050 | 0/0 | 3753 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | ATGTT others(3748): Show |
chr16 | 57877340 | 57976128 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5653 | 20 | 0 | 1 | 14 | 1 | 4 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0001t0002 | 0/0 | 5656 | 7 | 1 | 0 | 5 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0001c0001t0003 | 0/0 | 5657 | 3 | 0 | 0 | 3 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0001t0005 | 0/0 | 5657 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0001t0006 | 0/0 | 5654 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5649): Show |
chr16 | 57877340 | 57976128 |
a0001c0001t0007 | 0/0 | 5657 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0001t0012 | 0/0 | 5656 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0001c0001t0013 | 0/0 | 5658 | 2 | 0 | 1 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0001c0001t0017 | 0/0 | 5654 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5649): Show |
chr16 | 57877340 | 57976128 |
a0001c0001t0037 | 0/0 | 5643 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5638): Show |
chr16 | 57877340 | 57976128 |
a0001c0002t0001 | 0/0 | 5653 | 14 | 1 | 3 | 7 | 0 | 3 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0002t0002 | 0/0 | 5656 | 7 | 0 | 3 | 3 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0001c0002t0003 | 0/0 | 5657 | 5 | 1 | 1 | 1 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0002t0005 | 0/0 | 5657 | 6 | 0 | 2 | 4 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0002t0007 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0002t0013 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0001c0002t0022 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0001c0002t0033 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0003t0001 | 0/0 | 5653 | 12 | 0 | 2 | 7 | 1 | 2 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0003t0002 | 0/0 | 5656 | 7 | 0 | 2 | 5 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0001c0003t0003 | 0/0 | 5657 | 6 | 0 | 2 | 2 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0003t0005 | 0/0 | 5657 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0003t0006 | 0/0 | 5654 | 3 | 0 | 0 | 2 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5649): Show |
chr16 | 57877340 | 57976128 |
a0001c0003t0012 | 0/0 | 5656 | 2 | 0 | 1 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0001c0003t0032 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0004t0001 | 0/0 | 5653 | 14 | 0 | 0 | 13 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0004t0002 | 0/0 | 5656 | 4 | 0 | 0 | 4 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0001c0004t0003 | 0/0 | 5657 | 4 | 0 | 0 | 4 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0004t0005 | 0/0 | 5657 | 2 | 0 | 1 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0004t0006 | 0/0 | 5654 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5649): Show |
chr16 | 57877340 | 57976128 |
a0001c0004t0008 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0004t0014 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0001c0004t0022 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0001c0004t0031 | 0/0 | 5652 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5647): Show |
chr16 | 57877340 | 57976128 |
a0001c0004t0035 | 0/0 | 5659 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5654): Show |
chr16 | 57877340 | 57976128 |
a0001c0007t0002 | 0/0 | 5656 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0001c0007t0003 | 0/0 | 5657 | 3 | 3 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0007t0004 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0007t0008 | 0/0 | 5653 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0013t0001 | 0/0 | 5653 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0013t0004 | 0/0 | 5653 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0013t0018 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0001c0013t0019 | 0/0 | 5653 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0015t0001 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0015t0002 | 0/0 | 5656 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0001c0015t0020 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0016t0004 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0016t0010 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0016t0046 | 0/0 | 5652 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5647): Show |
chr16 | 57877340 | 57976128 |
a0001c0017t0001 | 0/0 | 5653 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0017t0017 | 0/0 | 5654 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5649): Show |
chr16 | 57877340 | 57976128 |
a0001c0018t0001 | 0/0 | 5653 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0018t0002 | 0/0 | 5656 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0001c0019t0008 | 0/0 | 5653 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0019t0019 | 0/0 | 5653 | 2 | 0 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0027t0003 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0027t0040 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0001c0028t0042 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0028t0044 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0001c0029t0002 | 0/0 | 5656 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0001c0035t0010 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0035t0028 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0041t0005 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0042t0011 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0053t0004 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0066t0001 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0068t0005 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0070t0007 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0073t0002 | 0/0 | 5656 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0001c0096t0002 | 0/0 | 5656 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0001c0097t0003 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0001c0099t0001 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0001c0103t0029 | 0/0 | 5656 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0002c0005t0001 | 0/0 | 5653 | 16 | 2 | 3 | 9 | 0 | 2 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0002c0005t0002 | 0/0 | 5656 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0002c0005t0003 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0002c0005t0005 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0002c0005t0006 | 0/0 | 5654 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5649): Show |
chr16 | 57877340 | 57976128 |
a0002c0005t0008 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0002c0005t0009 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0002c0005t0041 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0002c0006t0001 | 0/1 | 5653 | 7 | 0 | 1 | 5 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0002c0006t0002 | 0/0 | 5656 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0002c0006t0003 | 0/0 | 5657 | 3 | 0 | 1 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0002c0006t0006 | 0/0 | 5654 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5649): Show |
chr16 | 57877340 | 57976128 |
a0002c0006t0008 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0002c0006t0013 | 0/0 | 5658 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0002c0006t0016 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0002c0006t0021 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0002c0011t0003 | 1/0 | 5657 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0002c0011t0004 | 0/0 | 5653 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0002c0011t0016 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0002c0011t0018 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0002c0022t0002 | 0/0 | 5656 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0002c0022t0008 | 0/0 | 5653 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0002c0022t0018 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0002c0037t0003 | 0/0 | 5657 | 2 | 0 | 0 | 0 | 0 | 2 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0002c0038t0003 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0002c0038t0010 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0002c0109t0004 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0002c0113t0003 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0002c0114t0010 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0003c0008t0002 | 0/0 | 5656 | 4 | 0 | 2 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0003c0008t0003 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0003c0008t0009 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0003c0009t0006 | 0/0 | 5654 | 2 | 0 | 1 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5649): Show |
chr16 | 57877340 | 57976128 |
a0003c0009t0007 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0003c0009t0009 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0003c0009t0039 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0003c0012t0003 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0003c0012t0007 | 0/0 | 5657 | 2 | 1 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0003c0012t0014 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0003c0040t0038 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0003c0064t0017 | 0/0 | 5654 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5649): Show |
chr16 | 57877340 | 57976128 |
a0003c0074t0009 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0003c0101t0030 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0003c0104t0007 | 0/0 | 5657 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0003c0105t0014 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0004c0026t0004 | 0/0 | 5653 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0004c0030t0003 | 0/0 | 5657 | 2 | 0 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0004c0034t0012 | 0/0 | 5656 | 2 | 0 | 0 | 0 | 2 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0004c0036t0001 | 0/0 | 5653 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0004c0036t0002 | 0/0 | 5656 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0004c0061t0004 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0004c0077t0004 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0004c0098t0003 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0004c0100t0002 | 0/0 | 5656 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0005c0014t0001 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0005c0014t0005 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0005c0014t0016 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0005c0044t0004 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0005c0045t0003 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0005c0046t0036 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0005c0048t0016 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0005c0049t0015 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0006c0081t0021 | 0/0 | 5661 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5656): Show |
chr16 | 57877340 | 57976128 |
a0006c0082t0010 | 0/0 | 5660 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5655): Show |
chr16 | 57877340 | 57976128 |
a0006c0083t0043 | 0/0 | 5662 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5657): Show |
chr16 | 57877340 | 57976128 |
a0006c0084t0003 | 0/0 | 5660 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5655): Show |
chr16 | 57877340 | 57976128 |
a0006c0085t0024 | 0/0 | 5656 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0006c0086t0003 | 0/0 | 5660 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5655): Show |
chr16 | 57877340 | 57976128 |
a0006c0087t0001 | 0/0 | 5656 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0007c0039t0002 | 0/0 | 5656 | 2 | 0 | 0 | 0 | 1 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0007c0115t0045 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0007c0119t0023 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0007c0120t0003 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0007c0122t0003 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0008c0020t0007 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0008c0020t0009 | 0/0 | 5657 | 2 | 0 | 0 | 2 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0008c0021t0003 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0008c0021t0009 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0008c0021t0014 | 0/0 | 5658 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0009c0025t0001 | 0/0 | 5653 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0009c0025t0023 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0009c0032t0002 | 0/0 | 5656 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0009c0032t0006 | 0/0 | 5654 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5649): Show |
chr16 | 57877340 | 57976128 |
a0009c0054t0002 | 0/0 | 5656 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0010c0010t0003 | 0/0 | 5657 | 3 | 3 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0010c0010t0008 | 0/0 | 5653 | 2 | 0 | 0 | 0 | 2 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0011c0033t0001 | 0/0 | 5653 | 2 | 0 | 1 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0011c0058t0004 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0011c0059t0001 | 0/0 | 5653 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0012c0024t0002 | 0/0 | 5656 | 2 | 0 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0012c0091t0007 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0013c0031t0004 | 0/0 | 5653 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0013c0078t0011 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0014c0116t0004 | 0/0 | 5653 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0014c0118t0001 | 0/0 | 5653 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0015c0055t0025 | 0/0 | 5657 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0015c0102t0003 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0016c0023t0002 | 0/0 | 5656 | 2 | 2 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0017c0110t0011 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0017c0112t0024 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0018c0060t0015 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0018c0062t0027 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0019c0052t0003 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0019c0090t0010 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0020c0095t0001 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0021c0117t0026 | 0/0 | 5658 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0022c0079t0006 | 0/0 | 5654 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5649): Show |
chr16 | 57877340 | 57976128 |
a0023c0069t0001 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0024c0123t0003 | 0/0 | 5657 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0025c0108t0004 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0026c0121t0011 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0027c0092t0001 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0028c0080t0015 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0029c0076t0003 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0030c0111t0003 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0031c0094t0002 | 0/0 | 5656 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0032c0065t0015 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0033c0051t0001 | 0/0 | 5653 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0034c0043t0011 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0035c0057t0002 | 0/0 | 5644 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5639): Show |
chr16 | 57877340 | 57976128 |
a0036c0088t0007 | 0/0 | 5660 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5655): Show |
chr16 | 57877340 | 57976128 |
a0037c0063t0020 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0038c0093t0001 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0039c0072t0001 | 0/0 | 5653 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0040c0067t0002 | 0/0 | 5656 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0041c0047t0034 | 0/0 | 5658 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5653): Show |
chr16 | 57877340 | 57976128 |
a0042c0089t0001 | 0/0 | 5653 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0043c0075t0001 | 0/0 | 5653 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5648): Show |
chr16 | 57877340 | 57976128 |
a0044c0071t0006 | 0/0 | 5654 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5649): Show |
chr16 | 57877340 | 57976128 |
a0045c0106t0002 | 0/0 | 5656 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5651): Show |
chr16 | 57877340 | 57976128 |
a0046c0107t0006 | 0/0 | 5654 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5649): Show |
chr16 | 57877340 | 57976128 |
a0047c0056t0011 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
a0048c0050t0003 | 0/0 | 5657 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | GTGTC others(5652): Show |
chr16 | 57877340 | 57976128 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0005g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0005g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0006g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0007g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0012g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0013g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0013g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0017g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0001t0037g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0005g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0005g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0005g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0005g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0007g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0013g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0022g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0002t0033g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0006g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0006g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0006g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0012g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0012g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0003t0032g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0005g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0008g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0014g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0022g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0031g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0004t0035g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0007t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0007t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0007t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0007t0003g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0007t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0007t0008g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0013t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0013t0004g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0013t0018g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0013t0019g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0015t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0015t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0015t0020g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0016t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0016t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0016t0046g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0017t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0017t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0017t0017g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0018t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0018t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0018t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0019t0008g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0019t0019g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0019t0019g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0027t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0027t0040g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0028t0042g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0028t0044g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0029t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0029t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0035t0010g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0035t0028g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0041t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0042t0011g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0053t0004g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0066t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0068t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0070t0007g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0073t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0096t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0097t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0099t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0001c0103t0029g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0005g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0008g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0009g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0005t0041g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0006t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0006t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0006t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0006t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0006t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0006t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0006t0001g0303 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0006t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0006t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0006t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0006t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0006t0006g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0006t0008g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0006t0013g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0006t0016g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0006t0021g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0011t0003g0072 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0011t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0011t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0011t0016g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0011t0018g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0022t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0022t0008g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0022t0018g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0037t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0037t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0038t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0038t0010g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0109t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0113t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0002c0114t0010g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0008t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0008t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0008t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0008t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0008t0009g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0009t0006g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0009t0006g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0009t0007g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0009t0009g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0009t0039g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0012t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0012t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0012t0007g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0012t0014g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0040t0038g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0064t0017g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0074t0009g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0101t0030g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0104t0007g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0003c0105t0014g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0004c0026t0004g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0004c0026t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0004c0030t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0004c0034t0012g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0004c0034t0012g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0004c0036t0001g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0004c0036t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0004c0061t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0004c0077t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0004c0098t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0004c0100t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0005c0014t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0005c0014t0005g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0005c0014t0016g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0005c0044t0004g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0005c0045t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0005c0046t0036g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0005c0048t0016g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0005c0049t0015g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0006c0081t0021g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0006c0082t0010g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0006c0083t0043g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0006c0084t0003g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0006c0085t0024g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0006c0086t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0006c0087t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0007c0039t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0007c0039t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0007c0115t0045g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0007c0119t0023g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0007c0120t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0007c0122t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0008c0020t0007g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0008c0020t0009g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0008c0020t0009g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0008c0021t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0008c0021t0009g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0008c0021t0014g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0009c0025t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0009c0025t0023g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0009c0032t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0009c0032t0006g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0009c0054t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0010c0010t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0010c0010t0003g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0010c0010t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0010c0010t0008g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0010c0010t0008g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0011c0033t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0011c0033t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0011c0058t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0011c0059t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0012c0024t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0012c0024t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0012c0091t0007g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0013c0031t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0013c0031t0004g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0013c0078t0011g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0014c0116t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0014c0118t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0015c0055t0025g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0015c0102t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0016c0023t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0016c0023t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0017c0110t0011g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0017c0112t0024g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0018c0060t0015g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0018c0062t0027g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0019c0052t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0019c0090t0010g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0020c0095t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0021c0117t0026g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0022c0079t0006g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0023c0069t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0024c0123t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0025c0108t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0026c0121t0011g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0027c0092t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0028c0080t0015g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0029c0076t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0030c0111t0003g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0031c0094t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0032c0065t0015g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0033c0051t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0034c0043t0011g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0035c0057t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0036c0088t0007g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0037c0063t0020g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0038c0093t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0039c0072t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0040c0067t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0041c0047t0034g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0042c0089t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0043c0075t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0044c0071t0006g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0045c0106t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0046c0107t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0047c0056t0011g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
a0048c0050t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0003 | g0221 | EUR | GBR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00099 | hp2 | a0001 | c0004 | t0008 | g0135 | EUR | GBR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | GBR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00140 | hp2 | a0001 | c0001 | t0012 | g0212 | EUR | GBR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00280 | hp1 | a0009 | c0032 | t0006 | g0220 | EUR | FIN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00280 | hp2 | a0020 | c0095 | t0001 | g0193 | EUR | FIN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00323 | hp1 | a0001 | c0096 | t0002 | g0293 | EUR | FIN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00323 | hp2 | a0007 | c0039 | t0002 | g0305 | EUR | FIN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00408 | hp1 | a0001 | c0003 | t0002 | g0201 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00408 | hp2 | a0001 | c0003 | t0006 | g0284 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00423 | hp1 | a0002 | c0005 | t0001 | g0027 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00423 | hp2 | a0002 | c0006 | t0006 | g0323 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00438 | hp1 | a0001 | c0097 | t0003 | g0230 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00438 | hp2 | a0001 | c0002 | t0005 | g0143 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00544 | hp1 | a0001 | c0002 | t0003 | g0031 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00544 | hp2 | a0001 | c0004 | t0001 | g0119 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00558 | hp1 | a0003 | c0008 | t0003 | g0145 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00558 | hp2 | a0001 | c0103 | t0029 | g0272 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00597 | hp2 | a0003 | c0105 | t0014 | g0298 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0040 | EAS | CHS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00639 | hp1 | a0014 | c0118 | t0001 | g0302 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00642 | hp1 | a0002 | c0006 | t0001 | g0071 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00642 | hp2 | a0003 | c0009 | t0007 | g0080 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00733 | hp1 | a0001 | c0003 | t0002 | g0191 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00733 | hp2 | a0001 | c0003 | t0012 | g0266 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00735 | hp1 | a0003 | c0009 | t0006 | g0217 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00735 | hp2 | a0001 | c0001 | t0037 | g0246 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00738 | hp1 | a0001 | c0013 | t0001 | g0306 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00738 | hp2 | a0001 | c0070 | t0007 | g0134 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00741 | hp1 | a0021 | c0117 | t0026 | g0186 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG00741 | hp2 | a0011 | c0059 | t0001 | g0123 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01069 | hp1 | a0004 | c0036 | t0002 | g0256 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01069 | hp2 | a0012 | c0024 | t0002 | g0170 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01070 | hp1 | a0014 | c0116 | t0004 | g0070 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01070 | hp2 | a0004 | c0030 | t0003 | g0001 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01071 | hp1 | a0004 | c0030 | t0003 | g0001 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01071 | hp2 | a0012 | c0024 | t0002 | g0169 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01074 | hp1 | a0001 | c0002 | t0007 | g0126 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01074 | hp2 | a0012 | c0091 | t0007 | g0268 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01081 | hp1 | a0001 | c0019 | t0008 | g0247 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0329 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01109 | hp1 | a0002 | c0006 | t0003 | g0022 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01109 | hp2 | a0007 | c0120 | t0003 | g0065 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01168 | hp1 | a0001 | c0007 | t0008 | g0356 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01168 | hp2 | a0001 | c0019 | t0019 | g0286 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01169 | hp1 | a0001 | c0019 | t0019 | g0299 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0032 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01175 | hp1 | a0022 | c0079 | t0006 | g0194 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01175 | hp2 | a0001 | c0004 | t0005 | g0127 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01243 | hp1 | a0011 | c0033 | t0001 | g0267 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0168 | AMR | PUR | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01255 | hp1 | a0003 | c0012 | t0007 | g0167 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01255 | hp2 | a0001 | c0002 | t0005 | g0184 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01256 | hp1 | a0003 | c0008 | t0002 | g0002 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01256 | hp2 | a0001 | c0003 | t0001 | g0214 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01258 | hp1 | a0003 | c0008 | t0002 | g0002 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01258 | hp2 | a0001 | c0003 | t0001 | g0248 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01261 | hp1 | a0002 | c0005 | t0001 | g0016 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01261 | hp2 | a0001 | c0002 | t0002 | g0183 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01346 | hp1 | a0001 | c0003 | t0002 | g0244 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0124 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01358 | hp1 | a0002 | c0022 | t0008 | g0011 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01358 | hp2 | a0001 | c0013 | t0004 | g0308 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01361 | hp1 | a0003 | c0009 | t0039 | g0307 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01361 | hp2 | a0001 | c0001 | t0013 | g0251 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01433 | hp1 | a0001 | c0002 | t0005 | g0142 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01433 | hp2 | a0001 | c0013 | t0019 | g0213 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01496 | hp1 | a0002 | c0005 | t0001 | g0015 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01496 | hp2 | a0001 | c0003 | t0003 | g0296 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01515 | hp1 | a0001 | c0003 | t0001 | g0199 | EUR | IBS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01515 | hp2 | a0010 | c0010 | t0008 | g0090 | EUR | IBS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01516 | hp1 | a0001 | c0002 | t0003 | g0038 | EUR | IBS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01516 | hp2 | a0004 | c0034 | t0012 | g0255 | EUR | IBS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01517 | hp1 | a0010 | c0010 | t0008 | g0102 | EUR | IBS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01517 | hp2 | a0004 | c0034 | t0012 | g0292 | EUR | IBS | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01884 | hp1 | a0023 | c0069 | t0001 | g0045 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01884 | hp2 | a0016 | c0023 | t0002 | g0347 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01891 | hp1 | a0004 | c0026 | t0004 | g0059 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01891 | hp2 | a0008 | c0020 | t0007 | g0007 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01934 | hp1 | a0003 | c0064 | t0017 | g0179 | AMR | PEL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01934 | hp2 | a0008 | c0021 | t0003 | g0105 | AMR | PEL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01978 | hp1 | a0003 | c0012 | t0003 | g0176 | AMR | PEL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01978 | hp2 | a0003 | c0074 | t0009 | g0177 | AMR | PEL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02015 | hp1 | a0001 | c0004 | t0001 | g0138 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02027 | hp1 | a0001 | c0018 | t0001 | g0263 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02027 | hp2 | a0001 | c0004 | t0001 | g0172 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02040 | hp2 | a0002 | c0005 | t0001 | g0319 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02055 | hp1 | a0002 | c0011 | t0004 | g0185 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02055 | hp2 | a0001 | c0041 | t0005 | g0028 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02056 | hp1 | a0001 | c0002 | t0005 | g0154 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02056 | hp2 | a0001 | c0004 | t0001 | g0174 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02071 | hp1 | a0001 | c0002 | t0013 | g0041 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02071 | hp2 | a0001 | c0073 | t0002 | g0132 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02074 | hp2 | a0002 | c0005 | t0006 | g0089 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02080 | hp1 | a0001 | c0018 | t0001 | g0297 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02080 | hp2 | a0001 | c0068 | t0005 | g0175 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02083 | hp1 | a0004 | c0036 | t0001 | g0355 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02083 | hp2 | a0002 | c0005 | t0001 | g0013 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02129 | hp2 | a0003 | c0008 | t0002 | g0131 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02132 | hp1 | a0002 | c0005 | t0001 | g0024 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02132 | hp2 | a0024 | c0123 | t0003 | g0085 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02135 | hp1 | a0001 | c0004 | t0003 | g0136 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02135 | hp2 | a0001 | c0003 | t0001 | g0259 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02145 | hp1 | a0004 | c0098 | t0003 | g0241 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02145 | hp2 | a0005 | c0014 | t0005 | g0346 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02148 | hp1 | a0002 | c0005 | t0001 | g0304 | AMR | PEL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02148 | hp2 | a0001 | c0002 | t0003 | g0113 | AMR | PEL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02257 | hp1 | a0025 | c0108 | t0004 | g0061 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02257 | hp2 | a0001 | c0015 | t0001 | g0335 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02258 | hp1 | a0026 | c0121 | t0011 | g0315 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02258 | hp2 | a0027 | c0092 | t0001 | g0285 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02280 | hp1 | a0028 | c0080 | t0015 | g0188 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02280 | hp2 | a0006 | c0086 | t0003 | g0067 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02300 | hp1 | a0001 | c0003 | t0003 | g0215 | AMR | PEL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0159 | AMR | PEL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02451 | hp1 | a0011 | c0058 | t0004 | g0140 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02451 | hp2 | a0007 | c0122 | t0003 | g0317 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02523 | hp1 | a0003 | c0040 | t0038 | g0203 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02572 | hp1 | a0005 | c0048 | t0016 | g0354 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02572 | hp2 | a0001 | c0016 | t0004 | g0313 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02615 | hp1 | a0017 | c0110 | t0011 | g0321 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02615 | hp2 | a0006 | c0083 | t0043 | g0063 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02622 | hp1 | a0001 | c0027 | t0040 | g0078 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02622 | hp2 | a0029 | c0076 | t0003 | g0055 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02630 | hp1 | a0002 | c0113 | t0003 | g0318 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02630 | hp2 | a0003 | c0012 | t0007 | g0048 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02647 | hp1 | a0001 | c0004 | t0022 | g0107 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02647 | hp2 | a0002 | c0011 | t0004 | g0066 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02698 | hp1 | a0001 | c0002 | t0003 | g0050 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02698 | hp2 | a0001 | c0004 | t0001 | g0153 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02717 | hp1 | a0030 | c0111 | t0003 | g0327 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02717 | hp2 | a0006 | c0082 | t0010 | g0337 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02723 | hp1 | a0001 | c0007 | t0003 | g0189 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02723 | hp2 | a0013 | c0078 | t0011 | g0353 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02735 | hp1 | a0002 | c0005 | t0001 | g0101 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02735 | hp2 | a0031 | c0094 | t0002 | g0295 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02738 | hp1 | a0001 | c0003 | t0006 | g0288 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02738 | hp2 | a0001 | c0002 | t0002 | g0157 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02809 | hp1 | a0001 | c0016 | t0010 | g0057 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02809 | hp2 | a0002 | c0005 | t0001 | g0314 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02818 | hp1 | a0005 | c0014 | t0016 | g0326 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02818 | hp2 | a0006 | c0087 | t0001 | g0211 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02886 | hp1 | a0002 | c0005 | t0041 | g0068 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02886 | hp2 | a0009 | c0025 | t0023 | g0077 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02895 | hp1 | a0001 | c0007 | t0003 | g0004 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02895 | hp2 | a0010 | c0010 | t0003 | g0328 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02896 | hp1 | a0013 | c0031 | t0004 | g0333 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02896 | hp2 | a0001 | c0028 | t0044 | g0064 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02897 | hp1 | a0013 | c0031 | t0004 | g0334 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02897 | hp2 | a0010 | c0010 | t0003 | g0325 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02922 | hp1 | a0001 | c0053 | t0004 | g0200 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02922 | hp2 | a0001 | c0042 | t0011 | g0029 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02965 | hp1 | a0002 | c0006 | t0021 | g0187 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02965 | hp2 | a0001 | c0015 | t0002 | g0006 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02970 | hp1 | a0032 | c0065 | t0015 | g0043 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02970 | hp2 | a0005 | c0046 | t0036 | g0348 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02976 | hp1 | a0002 | c0022 | t0018 | g0112 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02976 | hp2 | a0001 | c0007 | t0002 | g0073 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03017 | hp1 | a0002 | c0037 | t0003 | g0023 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03017 | hp2 | a0003 | c0104 | t0007 | g0232 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03041 | hp1 | a0001 | c0015 | t0020 | g0336 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03041 | hp2 | a0001 | c0013 | t0018 | g0294 | AFR | GWD | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03098 | hp1 | a0007 | c0115 | t0045 | g0111 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03098 | hp2 | a0004 | c0026 | t0004 | g0310 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03130 | hp1 | a0001 | c0007 | t0004 | g0046 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03130 | hp2 | a0006 | c0084 | t0003 | g0330 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03139 | hp1 | a0005 | c0049 | t0015 | g0344 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03139 | hp2 | a0033 | c0051 | t0001 | g0339 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03195 | hp1 | a0002 | c0109 | t0004 | g0108 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03195 | hp2 | a0034 | c0043 | t0011 | g0351 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0056 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03209 | hp2 | a0002 | c0006 | t0016 | g0110 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03225 | hp1 | a0005 | c0045 | t0003 | g0342 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03225 | hp2 | a0004 | c0061 | t0004 | g0049 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03239 | hp1 | a0035 | c0057 | t0002 | g0147 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03239 | hp2 | a0002 | c0005 | t0008 | g0025 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03453 | hp1 | a0036 | c0088 | t0007 | g0210 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03453 | hp2 | a0037 | c0063 | t0020 | g0009 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03486 | hp1 | a0001 | c0007 | t0003 | g0340 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03486 | hp2 | a0018 | c0062 | t0027 | g0324 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0052 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03492 | hp2 | a0001 | c0003 | t0003 | g0265 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03516 | hp1 | a0006 | c0081 | t0021 | g0331 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03516 | hp2 | a0007 | c0119 | t0023 | g0091 | AFR | ESN | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03579 | hp1 | a0004 | c0077 | t0004 | g0060 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03579 | hp2 | a0005 | c0014 | t0001 | g0345 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03654 | hp1 | a0038 | c0093 | t0001 | g0258 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03654 | hp2 | a0001 | c0002 | t0033 | g0053 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03669 | hp1 | a0004 | c0100 | t0002 | g0231 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03669 | hp2 | a0001 | c0003 | t0001 | g0270 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03704 | hp1 | a0001 | c0003 | t0032 | g0109 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0039 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03710 | hp1 | a0001 | c0003 | t0012 | g0204 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03710 | hp2 | a0001 | c0003 | t0001 | g0253 | SAS | PJL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0312 | SAS | BEB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03831 | hp2 | a0002 | c0005 | t0001 | g0332 | SAS | BEB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03834 | hp1 | a0002 | c0006 | t0013 | g0083 | SAS | BEB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03942 | hp1 | a0039 | c0072 | t0001 | g0137 | SAS | BEB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03942 | hp2 | a0002 | c0037 | t0003 | g0092 | SAS | BEB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG04115 | hp1 | a0003 | c0009 | t0006 | g0289 | SAS | STU | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG04115 | hp2 | a0007 | c0039 | t0002 | g0086 | SAS | STU | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG04204 | hp1 | a0001 | c0066 | t0001 | g0130 | SAS | STU | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG04204 | hp2 | a0009 | c0032 | t0002 | g0269 | SAS | STU | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG04228 | hp2 | a0040 | c0067 | t0002 | g0051 | SAS | STU | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18747 | hp2 | a0002 | c0038 | t0010 | g0103 | EAS | CHB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18906 | hp1 | a0001 | c0027 | t0003 | g0058 | AFR | YRI | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18906 | hp2 | a0041 | c0047 | t0034 | g0350 | AFR | YRI | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18939 | hp1 | a0001 | c0017 | t0001 | g0114 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18939 | hp2 | a0001 | c0003 | t0002 | g0196 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18940 | hp1 | a0001 | c0004 | t0002 | g0156 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18940 | hp2 | a0008 | c0020 | t0009 | g0081 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0338 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18942 | hp2 | a0001 | c0003 | t0001 | g0202 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18943 | hp1 | a0001 | c0004 | t0001 | g0164 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18943 | hp2 | a0001 | c0003 | t0002 | g0228 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18944 | hp1 | a0001 | c0001 | t0013 | g0206 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0036 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18945 | hp1 | a0001 | c0004 | t0001 | g0133 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18945 | hp2 | a0002 | c0006 | t0002 | g0096 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18948 | hp1 | a0001 | c0017 | t0001 | g0139 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18954 | hp1 | a0002 | c0005 | t0002 | g0320 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18954 | hp2 | a0001 | c0001 | t0005 | g0274 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18956 | hp1 | a0001 | c0003 | t0005 | g0300 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18956 | hp2 | a0001 | c0004 | t0001 | g0150 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18957 | hp1 | a0001 | c0004 | t0001 | g0115 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18957 | hp2 | a0001 | c0003 | t0001 | g0278 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18959 | hp1 | a0002 | c0038 | t0003 | g0094 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18960 | hp1 | a0002 | c0005 | t0001 | g0014 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18962 | hp1 | a0001 | c0004 | t0031 | g0152 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18962 | hp2 | a0001 | c0018 | t0002 | g0254 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18966 | hp2 | a0002 | c0006 | t0001 | g0017 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18967 | hp1 | a0002 | c0005 | t0006 | g0097 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0161 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18970 | hp2 | a0019 | c0052 | t0003 | g0180 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18972 | hp2 | a0001 | c0004 | t0001 | g0117 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18974 | hp1 | a0001 | c0003 | t0001 | g0227 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18974 | hp2 | a0001 | c0004 | t0001 | g0166 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18977 | hp1 | a0001 | c0002 | t0005 | g0160 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18977 | hp2 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18980 | hp1 | a0008 | c0021 | t0014 | g0088 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18981 | hp1 | a0002 | c0005 | t0009 | g0104 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18981 | hp2 | a0001 | c0001 | t0005 | g0277 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18982 | hp1 | a0001 | c0029 | t0002 | g0163 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18982 | hp2 | a0001 | c0003 | t0006 | g0218 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18983 | hp1 | a0001 | c0004 | t0003 | g0037 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18983 | hp2 | a0001 | c0003 | t0001 | g0282 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18984 | hp1 | a0002 | c0006 | t0001 | g0095 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18984 | hp2 | a0001 | c0004 | t0003 | g0151 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18986 | hp2 | a0001 | c0001 | t0006 | g0225 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18989 | hp1 | a0008 | c0021 | t0009 | g0093 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18989 | hp2 | a0043 | c0075 | t0001 | g0144 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18994 | hp1 | a0001 | c0003 | t0002 | g0239 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18994 | hp2 | a0002 | c0005 | t0001 | g0026 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18998 | hp1 | a0001 | c0035 | t0028 | g0291 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18998 | hp2 | a0001 | c0002 | t0005 | g0129 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18999 | hp1 | a0001 | c0035 | t0010 | g0229 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19000 | hp2 | a0001 | c0029 | t0002 | g0034 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19002 | hp2 | a0044 | c0071 | t0006 | g0148 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19003 | hp1 | a0001 | c0004 | t0002 | g0178 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19003 | hp2 | a0001 | c0003 | t0001 | g0301 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19004 | hp1 | a0002 | c0005 | t0001 | g0021 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19004 | hp2 | a0001 | c0004 | t0003 | g0128 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19005 | hp1 | a0002 | c0005 | t0001 | g0098 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19005 | hp2 | a0003 | c0009 | t0009 | g0287 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19007 | hp1 | a0001 | c0004 | t0001 | g0118 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19007 | hp2 | a0009 | c0025 | t0001 | g0122 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19030 | hp1 | a0002 | c0022 | t0002 | g0074 | AFR | LWK | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19030 | hp2 | a0001 | c0002 | t0022 | g0062 | AFR | LWK | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19043 | hp1 | a0009 | c0054 | t0002 | g0044 | AFR | LWK | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19043 | hp2 | a0006 | c0085 | t0024 | g0209 | AFR | LWK | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19054 | hp2 | a0002 | c0005 | t0005 | g0322 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19056 | hp1 | a0019 | c0090 | t0010 | g0219 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19056 | hp2 | a0045 | c0106 | t0002 | g0075 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19057 | hp1 | a0002 | c0006 | t0001 | g0100 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19063 | hp1 | a0001 | c0003 | t0003 | g0198 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19064 | hp1 | a0001 | c0004 | t0002 | g0171 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19064 | hp2 | a0001 | c0002 | t0001 | g0162 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19065 | hp2 | a0001 | c0004 | t0001 | g0165 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19066 | hp1 | a0001 | c0004 | t0001 | g0173 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19066 | hp2 | a0002 | c0005 | t0003 | g0106 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19067 | hp1 | a0001 | c0001 | t0017 | g0224 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19067 | hp2 | a0001 | c0017 | t0017 | g0033 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19068 | hp1 | a0046 | c0107 | t0006 | g0099 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19068 | hp2 | a0001 | c0001 | t0006 | g0242 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19074 | hp1 | a0001 | c0004 | t0002 | g0116 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19074 | hp2 | a0002 | c0006 | t0003 | g0076 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19077 | hp2 | a0002 | c0006 | t0001 | g0019 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19079 | hp1 | a0003 | c0012 | t0014 | g0158 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19079 | hp2 | a0002 | c0005 | t0002 | g0082 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19081 | hp1 | a0002 | c0006 | t0001 | g0020 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19081 | hp2 | a0001 | c0003 | t0005 | g0240 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19084 | hp1 | a0002 | c0006 | t0003 | g0012 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19087 | hp1 | a0001 | c0003 | t0002 | g0245 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19087 | hp2 | a0003 | c0008 | t0009 | g0146 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19088 | hp1 | a0001 | c0003 | t0003 | g0283 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19088 | hp2 | a0003 | c0008 | t0002 | g0120 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19090 | hp1 | a0001 | c0004 | t0005 | g0182 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19090 | hp2 | a0008 | c0020 | t0009 | g0018 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19240 | hp1 | a0002 | c0011 | t0016 | g0190 | AFR | YRI | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA19240 | hp2 | a0047 | c0056 | t0011 | g0047 | AFR | YRI | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | ASW | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA20129 | hp2 | a0001 | c0016 | t0046 | g0054 | AFR | ASW | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA20752 | hp1 | a0002 | c0006 | t0008 | g0084 | EUR | TSI | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA20752 | hp2 | a0001 | c0099 | t0001 | g0216 | EUR | TSI | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA20805 | hp1 | a0011 | c0033 | t0001 | g0249 | EUR | TSI | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA20805 | hp2 | a0001 | c0001 | t0007 | g0290 | EUR | TSI | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA20905 | hp1 | a0003 | c0101 | t0030 | g0264 | SAS | GIH | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0125 | SAS | GIH | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01123 | hp1 | a0001 | c0004 | t0014 | g0192 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG01123 | hp2 | a0015 | c0055 | t0025 | g0042 | AMR | CLM | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02109 | hp1 | a0002 | c0005 | t0001 | g0316 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02109 | hp2 | a0002 | c0114 | t0010 | g0357 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02486 | hp1 | a0005 | c0044 | t0004 | g0343 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02486 | hp2 | a0017 | c0112 | t0024 | g0010 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02559 | hp1 | a0016 | c0023 | t0002 | g0349 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG02559 | hp2 | a0018 | c0060 | t0015 | g0005 | AFR | ACB | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03471 | hp1 | a0010 | c0010 | t0003 | g0030 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG03471 | hp2 | a0001 | c0028 | t0042 | g0069 | AFR | MSL | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG06807 | hp1 | a0002 | c0011 | t0018 | g0341 | AFR | USA | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
HG06807 | hp2 | a0015 | c0102 | t0003 | g0271 | AFR | USA | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18955 | hp1 | a0002 | c0005 | t0001 | g0087 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA18955 | hp2 | a0042 | c0089 | t0001 | g0257 | EAS | JPT | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA20300 | hp1 | a0001 | c0004 | t0006 | g0149 | AFR | USA | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA20300 | hp2 | a0048 | c0050 | t0003 | g0352 | AFR | USA | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA21309 | hp1 | a0001 | c0002 | t0003 | g0008 | AFR | LWK | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
NA21309 | hp2 | a0001 | c0004 | t0035 | g0079 | AFR | LWK | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
homoSapiens | chm13v2 | a0002 | c0006 | t0001 | g0303 | REF | REF | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
homoSapiens | grch38p0 | a0002 | c0011 | t0003 | g0072 | REF | REF | CNGB1_chr16_57877340_57976128 | CNGB1 | chr16 | 57877340 | 57976128 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:57882340 | A | T | 1 | a0003 | 1 | NA20905.hp1 | splice_region_variant | LOW | c.*1824T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | chr16 | 57882340 | |||||||
chr16:57884336 | G | C | 1 | a0039 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.3584C>G | p.Ser1195Cys | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 3661/5657 | 3584/3756 | 1195/1251 | chr16 | 57884336 | |||
chr16:57884364 | G | A | 4 | a0006 a0015 a0030 others(1): Show |
5 | HG01123.hp2 HG02717.hp1 HG03130.hp2 others(2): Show |
missense_variant | MODERATE | c.3556C>T | p.Pro1186Ser | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 3633/5657 | 3556/3756 | 1186/1251 | chr16 | 57884364 | |||
chr16:57884393 | G | A | 3 | a0026 a0034 a0047 |
3 | HG02258.hp1 HG03195.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.3527C>T | p.Pro1176Leu | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 3604/5657 | 3527/3756 | 1176/1251 | chr16 | 57884393 | |||
chr16:57884432 | C | T | 1 | a0044 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.3488G>A | p.Gly1163Glu | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 3565/5657 | 3488/3756 | 1163/1251 | chr16 | 57884432 | |||
chr16:57887977 | C | T | 2 | a0037 a0041 |
2 | HG03453.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.3340G>A | p.Ala1114Thr | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/33 | 3417/5657 | 3340/3756 | 1114/1251 | chr16 | 57887977 | |||
chr16:57901538 | G | A | 3 | a0004 a0007 a0020 |
10 | HG00280.hp2 HG00323.hp2 HG01069.hp1 others(7): Show |
missense_variant | MODERATE | c.2882C>T | p.Ala961Val | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 28/33 | 2959/5657 | 2882/3756 | 961/1251 | chr16 | 57901538 | |||
chr16:57901539 | C | A | 5 | a0004 a0007 a0010 others(2): Show |
17 | HG01109.hp2 HG01515.hp2 HG01517.hp1 others(14): Show |
missense_variant | MODERATE | c.2881G>T | p.Ala961Ser | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 28/33 | 2958/5657 | 2881/3756 | 961/1251 | chr16 | 57901539 | |||
chr16:57901566 | C | T | 5 | a0018 a0021 a0025 others(2): Show |
6 | HG00741.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
missense_variant | MODERATE | c.2854G>A | p.Val952Met | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 28/33 | 2931/5657 | 2854/3756 | 952/1251 | chr16 | 57901566 | |||
chr16:57901567 | G | T | 2 | a0023 a0033 |
2 | HG01884.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.2853C>A | p.Asp951Glu | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 28/33 | 2930/5657 | 2853/3756 | 951/1251 | chr16 | 57901567 | |||
chr16:57903884 | T | C | 5 | a0003 a0008 a0012 others(2): Show |
32 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(29): Show |
missense_variant | MODERATE | c.2732A>G | p.Lys911Arg | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/33 | 2809/5657 | 2732/3756 | 911/1251 | chr16 | 57903884 | |||
chr16:57903971 | A | G | 1 | a0040 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.2645T>C | p.Val882Ala | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/33 | 2722/5657 | 2645/3756 | 882/1251 | chr16 | 57903971 | |||
chr16:57915320 | G | T | 13 | a0009 a0010 a0011 others(10): Show |
28 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(25): Show |
missense_variant | MODERATE | c.2233C>A | p.Leu745Ile | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/33 | 2310/5657 | 2233/3756 | 745/1251 | chr16 | 57915320 | |||
chr16:57916139 | C | T | 1 | a0032 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.2207G>A | p.Arg736His | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/33 | 2284/5657 | 2207/3756 | 736/1251 | chr16 | 57916139 | |||
chr16:57920489 | G | A | 1 | a0024 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.1699C>T | p.Arg567Trp | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/33 | 1776/5657 | 1699/3756 | 567/1251 | chr16 | 57920489 | |||
chr16:57920517 | GGCCGTGG others(5): Show |
G | 1 | a0035 | 1 | HG03239.hp1 | disruptive_inframe_deletion | MODERATE | c.1659_1670delGGCCTC others(6): Show |
p.Ala554_Ala557del | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/33 | 1747/5657 | 1659/3756 | 553/1251 | chr16 | 57920517 | |||
chr16:57923285 | G | A | 1 | a0043 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.1631C>T | p.Pro544Leu | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/33 | 1708/5657 | 1631/3756 | 544/1251 | chr16 | 57923285 | |||
chr16:57923312 | A | G | 10 | a0009 a0010 a0012 others(7): Show |
21 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(18): Show |
missense_variant | MODERATE | c.1604T>C | p.Val535Ala | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/33 | 1681/5657 | 1604/3756 | 535/1251 | chr16 | 57923312 | |||
chr16:57923336 | G | A | 2 | a0029 a0036 |
2 | HG02622.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.1580C>T | p.Ala527Val | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/33 | 1657/5657 | 1580/3756 | 527/1251 | chr16 | 57923336 | |||
chr16:57931816 | G | T | 2 | a0019 a0046 |
3 | NA18970.hp2 NA19056.hp1 NA19068.hp1 |
missense_variant | MODERATE | c.1435C>A | p.Leu479Ile | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/33 | 1512/5657 | 1435/3756 | 479/1251 | chr16 | 57931816 | |||
chr16:57940239 | C | T | 2 | a0042 a0045 |
2 | NA18955.hp2 NA19056.hp2 |
missense_variant | MODERATE | c.1204G>A | p.Asp402Asn | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 15/33 | 1281/5657 | 1204/3756 | 402/1251 | chr16 | 57940239 | |||
chr16:57949370 | T | TTCC | 2 | a0006 a0036 |
8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
disruptive_inframe_insertion | MODERATE | c.1101_1103dupGGA | p.Glu368dup | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/33 | 1180/5657 | 1103/3756 | 368/1251 | chr16 | 57949370 | |||
chr16:57959937 | C | T | 1 | a0022 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.712G>A | p.Gly238Ser | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/33 | 789/5657 | 712/3756 | 238/1251 | chr16 | 57959937 | |||
chr16:57960014 | G | A | 1 | a0013 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.635C>T | p.Thr212Ile | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/33 | 712/5657 | 635/3756 | 212/1251 | chr16 | 57960014 | |||
chr16:57960015 | T | A | 2 | a0013 a0028 |
3 | HG02280.hp1 HG02896.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.634A>T | p.Thr212Ser | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/33 | 711/5657 | 634/3756 | 212/1251 | chr16 | 57960015 | |||
chr16:57960054 | G | A | 1 | a0028 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.595C>T | p.Arg199Cys | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/33 | 672/5657 | 595/3756 | 199/1251 | chr16 | 57960054 | |||
chr16:57962583 | A | C | 5 | a0005 a0016 a0033 others(2): Show |
13 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(10): Show |
missense_variant | MODERATE | c.440T>G | p.Leu147Arg | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/33 | 517/5657 | 440/3756 | 147/1251 | chr16 | 57962583 | |||
chr16:57962988 | C | A | 1 | a0033 | 1 | HG03139.hp2 | stop_gained | HIGH | c.367G>T | p.Glu123* | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/33 | 444/5657 | 367/3756 | 123/1251 | chr16 | 57962988 | |||
chr16:57963017 | A | T | 1 | a0033 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.338T>A | p.Val113Glu | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/33 | 415/5657 | 338/3756 | 113/1251 | chr16 | 57963017 | |||
chr16:57963056 | C | T | 35 | a0001 a0003 a0004 others(32): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
missense_variant | MODERATE | c.299G>A | p.Arg100His | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/33 | 376/5657 | 299/3756 | 100/1251 | chr16 | 57963056 | |||
chr16:57964163 | C | T | 5 | a0005 a0016 a0034 others(2): Show |
13 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(10): Show |
missense_variant | MODERATE | c.257G>A | p.Arg86Gln | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/33 | 334/5657 | 257/3756 | 86/1251 | chr16 | 57964163 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:57887939 | G | A | 8 | a0001c0029 a0001c0035 a0001c0073 others(5): Show |
11 | HG02071.hp2 HG03239.hp1 HG04228.hp2 others(8): Show |
synonymous_variant | LOW | c.3378C>T | p.Gly1126Gly | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/33 | 3455/5657 | 3378/3756 | 1126/1251 | chr16 | 57887939 | |||
chr16:57887987 | G | A | 1 | a0001c0103 | 1 | HG00558.hp2 | synonymous_variant | LOW | c.3330C>T | p.Asn1110Asn | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/33 | 3407/5657 | 3330/3756 | 1110/1251 | chr16 | 57887987 | |||
chr16:57903853 | G | A | 1 | a0005c0046 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.2763C>T | p.Tyr921Tyr | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/33 | 2840/5657 | 2763/3756 | 921/1251 | chr16 | 57903853 | |||
chr16:57903952 | G | C | 58 | a0001c0001 a0001c0002 a0001c0003 others(55): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
synonymous_variant | LOW | c.2664C>G | p.Ala888Ala | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/33 | 2741/5657 | 2664/3756 | 888/1251 | chr16 | 57903952 | |||
chr16:57903952 | G | T | 34 | a0001c0015 a0001c0028 a0001c0053 others(31): Show |
54 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(51): Show |
synonymous_variant | LOW | c.2664C>A | p.Ala888Ala | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/33 | 2741/5657 | 2664/3756 | 888/1251 | chr16 | 57903952 | |||
chr16:57904851 | A | G | 2 | a0001c0096 a0004c0034 |
3 | HG00323.hp1 HG01516.hp2 HG01517.hp2 |
synonymous_variant | LOW | c.2517T>C | p.Ala839Ala | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/33 | 2594/5657 | 2517/3756 | 839/1251 | chr16 | 57904851 | |||
chr16:57904854 | A | G | 2 | a0001c0066 a0002c0037 |
3 | HG03017.hp1 HG03942.hp2 HG04204.hp1 |
synonymous_variant | LOW | c.2514T>C | p.Phe838Phe | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/33 | 2591/5657 | 2514/3756 | 838/1251 | chr16 | 57904854 | |||
chr16:57911764 | G | A | 5 | a0001c0017 a0001c0018 a0003c0064 others(2): Show |
9 | HG01934.hp1 HG01978.hp2 HG02027.hp1 others(6): Show |
synonymous_variant | LOW | c.2481C>T | p.Gly827Gly | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/33 | 2558/5657 | 2481/3756 | 827/1251 | chr16 | 57911764 | |||
chr16:57916153 | G | A | 36 | a0001c0001 a0001c0004 a0001c0019 others(33): Show |
144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
synonymous_variant | LOW | c.2193C>T | p.Asn731Asn | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/33 | 2270/5657 | 2193/3756 | 731/1251 | chr16 | 57916153 | |||
chr16:57916165 | G | A | 1 | a0003c0105 | 1 | HG00597.hp2 | synonymous_variant | LOW | c.2181C>T | p.Asp727Asp | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/33 | 2258/5657 | 2181/3756 | 727/1251 | chr16 | 57916165 | |||
chr16:57919106 | C | G | 13 | a0009c0025 a0009c0032 a0009c0054 others(10): Show |
20 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
synonymous_variant | LOW | c.1950G>C | p.Pro650Pro | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/33 | 2027/5657 | 1950/3756 | 650/1251 | chr16 | 57919106 | |||
chr16:57920544 | A | G | 26 | a0001c0015 a0001c0016 a0001c0027 others(23): Show |
35 | HG01123.hp2 HG01891.hp1 HG02055.hp2 others(32): Show |
splice_region_variant&synonymous_variant | LOW | c.1644T>C | p.Asp548Asp | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/33 | 1721/5657 | 1644/3756 | 548/1251 | chr16 | 57920544 | |||
chr16:57931778 | C | T | 3 | a0001c0053 a0002c0109 a0025c0108 |
3 | HG02257.hp1 HG02922.hp1 HG03195.hp1 |
synonymous_variant | LOW | c.1473G>A | p.Pro491Pro | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/33 | 1550/5657 | 1473/3756 | 491/1251 | chr16 | 57931778 | |||
chr16:57939527 | G | A | 1 | a0004c0077 | 1 | HG03579.hp1 | synonymous_variant | LOW | c.1275C>T | p.Ala425Ala | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/33 | 1352/5657 | 1275/3756 | 425/1251 | chr16 | 57939527 | |||
chr16:57960043 | T | C | 1 | a0022c0079 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.606A>G | p.Glu202Glu | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/33 | 683/5657 | 606/3756 | 202/1251 | chr16 | 57960043 | |||
chr16:57962570 | G | A | 8 | a0006c0081 a0006c0082 a0006c0083 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
synonymous_variant | LOW | c.453C>T | p.Asp151Asp | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/33 | 530/5657 | 453/3756 | 151/1251 | chr16 | 57962570 | |||
chr16:57962864 | C | A | 1 | a0033c0051 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.390G>T | p.Gly130Gly | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/33 | 467/5657 | 390/3756 | 130/1251 | chr16 | 57962864 | |||
chr16:57962980 | C | A | 1 | a0033c0051 | 1 | HG03139.hp2 | synonymous_variant | LOW | c.375G>T | p.Pro125Pro | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/33 | 452/5657 | 375/3756 | 125/1251 | chr16 | 57962980 | |||
chr16:57963028 | G | A | 29 | a0001c0001 a0001c0003 a0001c0013 others(26): Show |
116 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(113): Show |
synonymous_variant | LOW | c.327C>T | p.Gly109Gly | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/33 | 404/5657 | 327/3756 | 109/1251 | chr16 | 57963028 | |||
chr16:57967164 | C | T | 2 | a0001c0041 a0001c0042 |
2 | HG02055.hp2 HG02922.hp2 |
synonymous_variant | LOW | c.123G>A | p.Pro41Pro | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/33 | 200/5657 | 123/3756 | 41/1251 | chr16 | 57967164 | |||
chr16:57967197 | C | T | 1 | a0003c0040 | 1 | HG02523.hp1 | synonymous_variant | LOW | c.90G>A | p.Glu30Glu | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/33 | 167/5657 | 90/3756 | 30/1251 | chr16 | 57967197 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:57882384 | A | G | 1 | a0005c0046t0036 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1780T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1780 | chr16 | 57882384 | ||||||
chr16:57882484 | A | G | 1 | a0001c0003t0032 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1680T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1680 | chr16 | 57882484 | ||||||
chr16:57882493 | T | C | 2 | a0001c0013t0019 a0001c0019t0019 |
3 | HG01168.hp2 HG01169.hp1 HG01433.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1671A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1671 | chr16 | 57882493 | ||||||
chr16:57882646 | A | C | 3 | a0001c0015t0020 a0037c0063t0020 a0041c0047t0034 |
3 | HG03041.hp1 HG03453.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1518T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1518 | chr16 | 57882646 | ||||||
chr16:57882702 | T | C | 10 | a0001c0004t0014 a0002c0005t0009 a0003c0008t0009 others(7): Show |
11 | HG00597.hp2 HG01123.hp1 HG01978.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1462A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1462 | chr16 | 57882702 | ||||||
chr16:57882735 | A | G | 1 | a0018c0062t0027 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1429T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1429 | chr16 | 57882735 | ||||||
chr16:57882782 | C | CT | 35 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0013 others(32): Show |
49 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1381dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1381 | chr16 | 57882782 | ||||||
chr16:57882784 | T | C | 1 | a0015c0055t0025 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1380A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1380 | chr16 | 57882784 | ||||||
chr16:57882799 | C | CT | 11 | a0001c0001t0017 a0001c0004t0035 a0001c0013t0018 others(8): Show |
11 | HG01934.hp1 HG02615.hp2 HG02896.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1364dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1364 | chr16 | 57882799 | ||||||
chr16:57882799 | CT | C | 40 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0012 others(37): Show |
79 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*1364delA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1364 | chr16 | 57882799 | ||||||
chr16:57882833 | A | G | 1 | a0003c0040t0038 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1331T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1331 | chr16 | 57882833 | ||||||
chr16:57882872 | T | G | 24 | a0001c0007t0004 a0001c0013t0004 a0001c0013t0019 others(21): Show |
28 | HG01070.hp1 HG01168.hp2 HG01169.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1292A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1292 | chr16 | 57882872 | ||||||
chr16:57882923 | A | G | 1 | a0007c0115t0045 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1241T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1241 | chr16 | 57882923 | ||||||
chr16:57882931 | A | G | 32 | a0001c0007t0004 a0001c0013t0004 a0001c0013t0019 others(29): Show |
36 | HG01070.hp1 HG01168.hp2 HG01169.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1233T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1233 | chr16 | 57882931 | ||||||
chr16:57882936 | G | C | 8 | a0001c0003t0032 a0001c0004t0008 a0001c0007t0008 others(5): Show |
9 | HG00099.hp2 HG01081.hp1 HG01168.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1228C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1228 | chr16 | 57882936 | ||||||
chr16:57882973 | C | T | 2 | a0006c0085t0024 a0017c0112t0024 |
2 | HG02486.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1191G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1191 | chr16 | 57882973 | ||||||
chr16:57883022 | T | C | 1 | a0001c0002t0033 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1142A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1142 | chr16 | 57883022 | ||||||
chr16:57883108 | T | C | 7 | a0001c0002t0022 a0001c0004t0022 a0001c0013t0018 others(4): Show |
7 | HG02647.hp1 HG02886.hp2 HG02976.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1056A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 1056 | chr16 | 57883108 | ||||||
chr16:57883210 | A | G | 3 | a0001c0015t0020 a0037c0063t0020 a0041c0047t0034 |
3 | HG03041.hp1 HG03453.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*954T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 954 | chr16 | 57883210 | ||||||
chr16:57883245 | C | T | 52 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0017 others(49): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*919G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 919 | chr16 | 57883245 | ||||||
chr16:57883246 | G | T | 4 | a0002c0006t0016 a0002c0011t0016 a0005c0014t0016 others(1): Show |
4 | HG02572.hp1 HG02818.hp1 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*918C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 918 | chr16 | 57883246 | ||||||
chr16:57883256 | CCTTT | C | 24 | a0001c0007t0004 a0001c0013t0004 a0001c0013t0019 others(21): Show |
28 | HG01070.hp1 HG01168.hp2 HG01169.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*904_*907delAAAG | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 904 | chr16 | 57883256 | ||||||
chr16:57883269 | TTTTG | T | 52 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0017 others(49): Show |
137 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(134): Show |
3_prime_UTR_variant | MODIFIER | c.*891_*894delCAAA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 891 | chr16 | 57883269 | ||||||
chr16:57883328 | G | A | 51 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0012 others(48): Show |
90 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*836C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 836 | chr16 | 57883328 | ||||||
chr16:57883416 | ATGTGAAC others(3): Show |
A | 1 | a0001c0001t0037 | 1 | HG00735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*738_*747delGTGGTT others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 738 | chr16 | 57883416 | ||||||
chr16:57883489 | C | T | 3 | a0001c0001t0012 a0001c0003t0012 a0004c0034t0012 |
5 | HG00140.hp2 HG00733.hp2 HG01516.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*675G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 675 | chr16 | 57883489 | ||||||
chr16:57883569 | G | C | 21 | a0001c0001t0007 a0001c0002t0007 a0001c0004t0014 others(18): Show |
23 | HG00597.hp2 HG00642.hp2 HG00738.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*595C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 595 | chr16 | 57883569 | ||||||
chr16:57883671 | G | A | 7 | a0001c0027t0040 a0001c0042t0011 a0013c0078t0011 others(4): Show |
7 | HG02258.hp1 HG02615.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*493C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 493 | chr16 | 57883671 | ||||||
chr16:57883843 | C | G | 2 | a0001c0035t0028 a0001c0103t0029 |
2 | HG00558.hp2 NA18998.hp1 |
3_prime_UTR_variant | MODIFIER | c.*321G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 321 | chr16 | 57883843 | ||||||
chr16:57883854 | A | G | 26 | a0001c0007t0004 a0001c0013t0004 a0001c0013t0019 others(23): Show |
30 | HG01070.hp1 HG01168.hp2 HG01169.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*310T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 310 | chr16 | 57883854 | ||||||
chr16:57883883 | A | G | 2 | a0018c0062t0027 a0021c0117t0026 |
2 | HG00741.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*281T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 281 | chr16 | 57883883 | ||||||
chr16:57883920 | T | C | 8 | a0001c0028t0042 a0001c0028t0044 a0002c0005t0041 others(5): Show |
8 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*244A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 244 | chr16 | 57883920 | ||||||
chr16:57883995 | G | T | 1 | a0015c0055t0025 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*169C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 169 | chr16 | 57883995 | ||||||
chr16:57884131 | T | C | 24 | a0001c0007t0004 a0001c0013t0004 a0001c0013t0019 others(21): Show |
28 | HG01070.hp1 HG01168.hp2 HG01169.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*33A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 33/33 | 33 | chr16 | 57884131 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:57884580 | G | T | 5 | a0001c0004t0003g0151 a0001c0097t0003g0230 a0002c0006t0003g0022 others(2): Show |
5 | HG00438.hp1 HG00558.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.3463-123C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57884580 | |||||||
chr16:57884643 | G | A | 1 | a0032c0065t0015g0043 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3463-186C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57884643 | |||||||
chr16:57884665 | T | A | 12 | a0001c0007t0002g0073 a0001c0096t0002g0293 a0004c0036t0002g0256 others(9): Show |
12 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.3463-208A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57884665 | |||||||
chr16:57884705 | T | A | 1 | a0001c0001t0001g0279 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3463-248A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57884705 | |||||||
chr16:57884863 | C | T | 14 | a0001c0007t0002g0073 a0001c0041t0005g0028 a0001c0096t0002g0293 others(11): Show |
14 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.3463-406G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57884863 | |||||||
chr16:57884869 | T | C | 28 | a0001c0007t0004g0046 a0001c0013t0004g0308 a0001c0013t0019g0213 others(25): Show |
28 | HG01070.hp1 HG01168.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.3463-412A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57884869 | |||||||
chr16:57884963 | G | C | 15 | a0001c0007t0002g0073 a0001c0041t0005g0028 a0001c0096t0002g0293 others(12): Show |
15 | HG00323.hp1 HG00323.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.3463-506C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57884963 | |||||||
chr16:57885130 | C | T | 224 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(221): Show |
225 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.3463-673G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885130 | |||||||
chr16:57885137 | C | T | 22 | a0001c0001t0007g0290 a0001c0002t0007g0126 a0001c0004t0014g0192 others(19): Show |
22 | HG00597.hp2 HG00642.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.3463-680G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885137 | |||||||
chr16:57885212 | G | A | 1 | a0021c0117t0026g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3463-755C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885212 | |||||||
chr16:57885224 | C | T | 1 | a0003c0009t0006g0217 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3463-767G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885224 | |||||||
chr16:57885505 | CTTTCCTT others(13): Show |
C | 2 | a0006c0084t0003g0330 a0030c0111t0003g0327 |
2 | HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3463-1068_3463-104 others(24): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885505 | |||||||
chr16:57885525 | T | C | 1 | a0001c0003t0001g0197 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.3463-1068A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885525 | |||||||
chr16:57885543 | TTCTTTCC others(7): Show |
T | 2 | a0001c0007t0004g0046 a0002c0011t0004g0185 |
2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3463-1100_3463-108 others(18): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885543 | |||||||
chr16:57885557 | C | CCT | 7 | a0001c0015t0002g0006 a0001c0016t0010g0057 a0001c0073t0002g0132 others(4): Show |
7 | HG00323.hp1 HG01069.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.3463-1102_3463-110 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | |||||||
chr16:57885557 | C | CCTCT | 14 | a0001c0001t0002g0250 a0001c0001t0005g0274 a0001c0001t0012g0212 others(11): Show |
14 | HG00140.hp2 HG00733.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.3463-1104_3463-110 others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | |||||||
chr16:57885557 | C | CCTCTCT | 27 | a0001c0001t0002g0252 a0001c0001t0002g0273 a0001c0001t0002g0309 others(24): Show |
27 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.3463-1106_3463-110 others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | |||||||
chr16:57885557 | C | CCTCTCTC others(1): Show |
13 | a0001c0001t0002g0222 a0001c0001t0002g0312 a0001c0002t0005g0143 others(10): Show |
13 | HG00438.hp2 HG00558.hp2 HG00597.hp1 others(10): Show |
intron_variant | MODIFIER | c.3463-1108_3463-110 others(12): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | |||||||
chr16:57885557 | C | CCTCTCTC others(3): Show |
10 | a0001c0001t0002g0238 a0001c0002t0002g0183 a0001c0004t0005g0127 others(7): Show |
11 | HG01175.hp2 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.3463-1110_3463-110 others(14): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | |||||||
chr16:57885557 | C | CCTCTCTC others(5): Show |
7 | a0001c0001t0003g0223 a0001c0002t0002g0124 a0001c0003t0002g0196 others(4): Show |
7 | HG01346.hp1 HG01346.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.3463-1112_3463-110 others(16): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | |||||||
chr16:57885557 | C | CCTCTCTC others(7): Show |
13 | a0001c0002t0003g0031 a0001c0002t0003g0038 a0001c0002t0005g0184 others(10): Show |
14 | HG00544.hp1 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.3463-1114_3463-110 others(18): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | |||||||
chr16:57885557 | C | CCTCTCTC others(9): Show |
7 | a0001c0001t0013g0206 a0001c0002t0003g0050 a0001c0002t0005g0142 others(4): Show |
7 | HG00099.hp1 HG01433.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.3463-1116_3463-110 others(20): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | |||||||
chr16:57885557 | C | CCTCTCTC others(11): Show |
3 | a0001c0003t0003g0198 a0002c0006t0013g0083 a0002c0038t0003g0094 |
3 | HG03834.hp1 NA18959.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.3463-1118_3463-110 others(22): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | |||||||
chr16:57885557 | C | CCTCTCTC others(13): Show |
10 | a0001c0001t0001g0262 a0001c0001t0003g0208 a0001c0002t0002g0157 others(7): Show |
10 | HG02145.hp1 HG02738.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.3463-1120_3463-110 others(24): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | |||||||
chr16:57885557 | C | CCTCTCTC others(15): Show |
3 | a0001c0002t0003g0113 a0001c0002t0013g0041 a0010c0010t0003g0030 |
3 | HG02071.hp1 HG02148.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3463-1122_3463-110 others(26): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | |||||||
chr16:57885557 | C | CCTCTCTC others(17): Show |
2 | a0001c0001t0013g0251 a0007c0122t0003g0317 |
2 | HG01361.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.3463-1101_3463-110 others(28): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | |||||||
chr16:57885557 | C | CCTCTCTC others(21): Show |
2 | a0006c0086t0003g0067 a0007c0120t0003g0065 |
2 | HG01109.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.3463-1101_3463-110 others(32): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | |||||||
chr16:57885557 | C | CCTCTCTC others(23): Show |
1 | a0009c0032t0002g0269 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3463-1101_3463-110 others(34): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | |||||||
chr16:57885557 | C | CTCTCTCT others(8): Show |
1 | a0001c0003t0002g0201 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3463-1101_3463-110 others(19): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885557 | |||||||
chr16:57885576 | C | CTCTT | 3 | a0002c0005t0001g0024 a0013c0078t0011g0353 a0017c0110t0011g0321 |
3 | HG02132.hp1 HG02615.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3463-1123_3463-112 others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885576 | |||||||
chr16:57885576 | CTCTT | C | 122 | a0001c0001t0001g0195 a0001c0001t0001g0205 a0001c0001t0001g0207 others(119): Show |
122 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.3463-1123_3463-112 others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885576 | |||||||
chr16:57885576 | CTCTTTCT others(1): Show |
C | 34 | a0001c0002t0003g0008 a0001c0007t0003g0004 a0001c0007t0003g0340 others(31): Show |
34 | HG01070.hp1 HG01123.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.3463-1127_3463-112 others(12): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885576 | |||||||
chr16:57885576 | CTCTTTCT others(5): Show |
C | 10 | a0001c0028t0044g0064 a0005c0049t0015g0344 a0006c0083t0043g0063 others(7): Show |
10 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.3463-1131_3463-112 others(16): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885576 | |||||||
chr16:57885576 | CTCTTTCT others(9): Show |
C | 3 | a0022c0079t0006g0194 a0037c0063t0020g0009 a0041c0047t0034g0350 |
3 | HG01175.hp1 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3463-1135_3463-112 others(20): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885576 | |||||||
chr16:57885578 | CTT | C | 4 | a0001c0001t0037g0246 a0001c0013t0018g0294 a0002c0011t0018g0341 others(1): Show |
4 | HG00735.hp2 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.3463-1123_3463-112 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885578 | |||||||
chr16:57885578 | CTTTCTT | C | 4 | a0002c0011t0016g0190 a0003c0008t0009g0146 a0008c0021t0014g0088 others(1): Show |
4 | HG02257.hp1 NA18980.hp1 NA19087.hp2 others(1): Show |
intron_variant | MODIFIER | c.3463-1127_3463-112 others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885578 | |||||||
chr16:57885578 | CTTTCTTT others(3): Show |
C | 23 | a0001c0001t0007g0290 a0001c0002t0007g0126 a0001c0004t0014g0192 others(20): Show |
23 | HG00597.hp2 HG00642.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.3463-1131_3463-112 others(14): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885578 | |||||||
chr16:57885578 | CTTTCTTT others(7): Show |
C | 7 | a0001c0004t0003g0151 a0001c0097t0003g0230 a0002c0006t0003g0022 others(4): Show |
7 | HG00438.hp1 HG00558.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.3463-1135_3463-112 others(18): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885578 | |||||||
chr16:57885580 | T | C | 126 | a0001c0001t0001g0262 a0001c0001t0002g0222 a0001c0001t0002g0238 others(123): Show |
128 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.3463-1123A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885580 | |||||||
chr16:57885584 | T | C | 128 | a0001c0001t0001g0262 a0001c0001t0002g0222 a0001c0001t0002g0238 others(125): Show |
130 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.3463-1127A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885584 | |||||||
chr16:57885584 | TTC | T | 3 | a0001c0004t0001g0166 a0002c0005t0001g0087 a0046c0107t0006g0099 |
3 | NA18955.hp1 NA18974.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.3463-1129_3463-112 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885584 | |||||||
chr16:57885588 | T | C | 157 | a0001c0001t0001g0262 a0001c0001t0002g0222 a0001c0001t0002g0238 others(154): Show |
159 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.3463-1131A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885588 | |||||||
chr16:57885592 | T | C | 133 | a0001c0001t0001g0262 a0001c0001t0002g0222 a0001c0001t0002g0238 others(130): Show |
135 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.3463-1135A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885592 | |||||||
chr16:57885595 | T | TCTCTCTC others(8): Show |
1 | a0002c0006t0003g0012 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.3463-1139_3463-113 others(19): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885595 | |||||||
chr16:57885607 | T | C | 11 | a0001c0028t0044g0064 a0005c0049t0015g0344 a0006c0083t0043g0063 others(8): Show |
11 | HG01123.hp2 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.3463-1150A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885607 | |||||||
chr16:57885696 | C | G | 3 | a0001c0013t0018g0294 a0002c0011t0018g0341 a0002c0022t0018g0112 |
3 | HG02976.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3463-1239G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885696 | |||||||
chr16:57885750 | T | C | 6 | a0001c0028t0044g0064 a0005c0049t0015g0344 a0006c0083t0043g0063 others(3): Show |
6 | HG02280.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.3463-1293A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885750 | |||||||
chr16:57885805 | G | A | 5 | a0001c0004t0003g0151 a0001c0097t0003g0230 a0002c0006t0003g0022 others(2): Show |
5 | HG00438.hp1 HG00558.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.3463-1348C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885805 | |||||||
chr16:57885814 | A | G | 41 | a0001c0007t0004g0046 a0001c0013t0004g0308 a0001c0013t0019g0213 others(38): Show |
41 | HG01070.hp1 HG01123.hp2 HG01168.hp2 others(38): Show |
intron_variant | MODIFIER | c.3463-1357T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885814 | |||||||
chr16:57885830 | G | A | 5 | a0001c0002t0001g0056 a0002c0005t0001g0314 a0002c0005t0001g0316 others(2): Show |
5 | HG02109.hp1 HG02809.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.3463-1373C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57885830 | |||||||
chr16:57886002 | A | G | 11 | a0001c0028t0044g0064 a0005c0049t0015g0344 a0006c0083t0043g0063 others(8): Show |
11 | HG01123.hp2 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.3463-1545T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886002 | |||||||
chr16:57886173 | T | C | 5 | a0001c0002t0003g0008 a0001c0007t0003g0004 a0001c0007t0003g0340 others(2): Show |
5 | HG02622.hp2 HG02895.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.3462+1682A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886173 | |||||||
chr16:57886212 | G | A | 1 | a0002c0006t0003g0076 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3462+1643C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886212 | |||||||
chr16:57886265 | A | C | 1 | a0006c0081t0021g0331 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3462+1590T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886265 | |||||||
chr16:57886485 | T | C | 2 | a0001c0001t0001g0205 a0002c0005t0006g0089 |
2 | HG02015.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.3462+1370A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886485 | |||||||
chr16:57886557 | C | T | 39 | a0001c0001t0001g0262 a0001c0001t0003g0208 a0001c0001t0003g0223 others(36): Show |
40 | HG00544.hp1 HG01070.hp2 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.3462+1298G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886557 | |||||||
chr16:57886707 | TCCTAAAG others(5): Show |
T | 28 | a0001c0007t0004g0046 a0001c0013t0004g0308 a0001c0013t0019g0213 others(25): Show |
28 | HG01070.hp1 HG01168.hp2 HG01169.hp1 others(25): Show |
intron_variant | MODIFIER | c.3462+1136_3462+114 others(16): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886707 | |||||||
chr16:57886798 | T | C | 1 | a0046c0107t0006g0099 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3462+1057A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886798 | |||||||
chr16:57886864 | C | T | 341 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(338): Show |
343 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.3462+991G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886864 | |||||||
chr16:57886998 | C | T | 1 | a0001c0003t0003g0296 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3462+857G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57886998 | |||||||
chr16:57887062 | A | C | 83 | a0001c0001t0007g0290 a0001c0002t0001g0125 a0001c0002t0007g0126 others(80): Show |
83 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.3462+793T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887062 | |||||||
chr16:57887212 | A | G | 236 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(233): Show |
237 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.3462+643T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887212 | |||||||
chr16:57887542 | A | G | 1 | a0008c0021t0009g0093 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.3462+313T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887542 | |||||||
chr16:57887588 | G | A | 203 | a0001c0001t0001g0003 a0001c0001t0001g0207 a0001c0001t0001g0226 others(200): Show |
204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.3462+267C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887588 | |||||||
chr16:57887600 | C | T | 1 | a0004c0098t0003g0241 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3462+255G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887600 | |||||||
chr16:57887652 | G | A | 115 | a0001c0001t0001g0003 a0001c0001t0001g0207 a0001c0001t0001g0226 others(112): Show |
116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.3462+203C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887652 | |||||||
chr16:57887718 | C | A | 1 | a0015c0102t0003g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3462+137G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887718 | |||||||
chr16:57887729 | T | C | 12 | a0001c0007t0003g0189 a0001c0013t0018g0294 a0002c0005t0041g0068 others(9): Show |
12 | HG00741.hp2 HG01109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.3462+126A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887729 | |||||||
chr16:57887748 | G | C | 1 | a0001c0001t0001g0280 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.3462+107C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887748 | |||||||
chr16:57887848 | A | G | 132 | a0001c0001t0001g0195 a0001c0001t0001g0205 a0001c0001t0001g0236 others(129): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
splice_region_variant&intron_variant | LOW | c.3462+7T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 32/32 | chr16 | 57887848 | |||||||
chr16:57888097 | G | T | 4 | a0001c0002t0003g0008 a0001c0007t0003g0340 a0005c0046t0036g0348 others(1): Show |
4 | HG02622.hp2 HG02970.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.3243-23C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888097 | |||||||
chr16:57888180 | T | G | 41 | a0001c0001t0012g0212 a0001c0002t0001g0052 a0001c0002t0002g0157 others(38): Show |
41 | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.3243-106A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888180 | |||||||
chr16:57888362 | C | T | 1 | a0001c0053t0004g0200 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3243-288G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888362 | |||||||
chr16:57888363 | G | A | 1 | a0017c0110t0011g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3243-289C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888363 | |||||||
chr16:57888467 | GTC | G | 55 | a0001c0007t0003g0189 a0001c0013t0018g0294 a0001c0015t0001g0335 others(52): Show |
56 | HG00597.hp2 HG00642.hp2 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.3243-395_3243-394d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888467 | |||||||
chr16:57888562 | T | C | 3 | a0002c0109t0004g0108 a0037c0063t0020g0009 a0041c0047t0034g0350 |
3 | HG03195.hp1 HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3243-488A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888562 | |||||||
chr16:57888625 | A | G | 1 | a0001c0001t0001g0275 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3243-551T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888625 | |||||||
chr16:57888653 | T | C | 3 | a0001c0013t0018g0294 a0002c0011t0018g0341 a0002c0022t0018g0112 |
3 | HG02976.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3243-579A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888653 | |||||||
chr16:57888690 | G | A | 5 | a0001c0001t0001g0234 a0002c0005t0001g0015 a0002c0005t0001g0016 others(2): Show |
5 | HG00639.hp2 HG00642.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.3243-616C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888690 | |||||||
chr16:57888757 | C | CT | 76 | a0001c0001t0007g0290 a0001c0001t0012g0212 a0001c0002t0001g0052 others(73): Show |
77 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.3243-684dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888757 | |||||||
chr16:57888918 | C | T | 4 | a0001c0007t0003g0189 a0001c0042t0011g0029 a0037c0063t0020g0009 others(1): Show |
4 | HG02723.hp1 HG02922.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3243-844G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57888918 | |||||||
chr16:57889044 | C | T | 249 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(246): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.3243-970G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889044 | |||||||
chr16:57889209 | C | T | 1 | a0001c0002t0001g0052 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3243-1135G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889209 | |||||||
chr16:57889210 | T | C | 15 | a0001c0004t0035g0079 a0001c0015t0020g0336 a0001c0028t0044g0064 others(12): Show |
15 | HG00438.hp1 HG00741.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.3243-1136A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889210 | |||||||
chr16:57889487 | T | C | 13 | a0001c0004t0035g0079 a0001c0015t0020g0336 a0001c0028t0044g0064 others(10): Show |
13 | HG01884.hp1 HG02451.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.3243-1413A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889487 | |||||||
chr16:57889546 | A | G | 1 | a0017c0110t0011g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3243-1472T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889546 | |||||||
chr16:57889556 | C | T | 2 | a0001c0041t0005g0028 a0002c0022t0002g0074 |
2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.3243-1482G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889556 | |||||||
chr16:57889557 | G | A | 1 | a0001c0002t0001g0162 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3243-1483C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889557 | |||||||
chr16:57889573 | G | C | 12 | a0001c0015t0001g0335 a0001c0016t0046g0054 a0001c0028t0042g0069 others(9): Show |
12 | HG02257.hp1 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.3243-1499C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889573 | |||||||
chr16:57889613 | T | C | 1 | a0001c0003t0001g0199 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3243-1539A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889613 | |||||||
chr16:57889755 | C | G | 51 | a0001c0001t0002g0238 a0001c0001t0002g0252 a0001c0001t0002g0273 others(48): Show |
51 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.3243-1681G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889755 | |||||||
chr16:57889894 | A | G | 1 | a0001c0027t0040g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3243-1820T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889894 | |||||||
chr16:57889987 | C | T | 1 | a0003c0008t0002g0131 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.3243-1913G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889987 | |||||||
chr16:57889998 | A | G | 2 | a0018c0062t0027g0324 a0021c0117t0026g0186 |
2 | HG00741.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3243-1924T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57889998 | |||||||
chr16:57890141 | C | G | 1 | a0011c0059t0001g0123 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3243-2067G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890141 | |||||||
chr16:57890247 | G | A | 1 | a0015c0102t0003g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3243-2173C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890247 | |||||||
chr16:57890339 | C | T | 2 | a0005c0049t0015g0344 a0028c0080t0015g0188 |
2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.3243-2265G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890339 | |||||||
chr16:57890360 | C | A | 2 | a0037c0063t0020g0009 a0041c0047t0034g0350 |
2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3243-2286G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890360 | |||||||
chr16:57890471 | T | C | 1 | a0001c0002t0001g0039 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.3243-2397A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890471 | |||||||
chr16:57890496 | C | A | 55 | a0001c0001t0012g0212 a0001c0003t0012g0266 a0001c0007t0002g0073 others(52): Show |
55 | HG00140.hp2 HG00438.hp1 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.3243-2422G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890496 | |||||||
chr16:57890528 | C | T | 1 | a0001c0001t0005g0277 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3243-2454G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890528 | |||||||
chr16:57890653 | T | C | 96 | a0001c0001t0007g0290 a0001c0001t0012g0212 a0001c0002t0001g0052 others(93): Show |
97 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.3243-2579A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890653 | |||||||
chr16:57890798 | T | C | 2 | a0018c0062t0027g0324 a0021c0117t0026g0186 |
2 | HG00741.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3243-2724A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890798 | |||||||
chr16:57890917 | A | G | 1 | a0003c0012t0014g0158 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3243-2843T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890917 | |||||||
chr16:57890946 | C | T | 12 | a0001c0015t0001g0335 a0001c0016t0046g0054 a0001c0028t0042g0069 others(9): Show |
12 | HG02257.hp1 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.3243-2872G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890946 | |||||||
chr16:57890976 | C | T | 1 | a0001c0029t0002g0163 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3243-2902G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57890976 | |||||||
chr16:57891025 | G | A | 3 | a0006c0084t0003g0330 a0011c0058t0004g0140 a0030c0111t0003g0327 |
3 | HG02451.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3243-2951C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57891025 | |||||||
chr16:57891089 | C | A | 1 | a0001c0002t0001g0052 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.3243-3015G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57891089 | |||||||
chr16:57891250 | C | T | 1 | a0001c0003t0001g0227 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.3243-3176G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57891250 | |||||||
chr16:57891351 | T | C | 6 | a0001c0001t0001g0237 a0001c0002t0001g0329 a0001c0002t0033g0053 others(3): Show |
6 | HG00280.hp1 HG00639.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.3243-3277A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57891351 | |||||||
chr16:57891356 | G | A | 26 | a0001c0013t0018g0294 a0001c0015t0001g0335 a0001c0016t0010g0057 others(23): Show |
26 | HG00438.hp1 HG02109.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.3243-3282C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57891356 | |||||||
chr16:57891625 | T | C | 67 | a0001c0001t0012g0212 a0001c0002t0001g0052 a0001c0002t0002g0157 others(64): Show |
67 | HG00140.hp2 HG00438.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.3243-3551A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57891625 | |||||||
chr16:57891800 | A | G | 97 | a0001c0001t0007g0290 a0001c0001t0012g0212 a0001c0002t0001g0052 others(94): Show |
98 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.3243-3726T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57891800 | |||||||
chr16:57891842 | C | T | 12 | a0001c0015t0001g0335 a0001c0016t0046g0054 a0001c0028t0042g0069 others(9): Show |
12 | HG02257.hp1 HG02257.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.3243-3768G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57891842 | |||||||
chr16:57891901 | C | T | 2 | a0001c0007t0004g0046 a0002c0011t0004g0185 |
2 | HG02055.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.3243-3827G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57891901 | |||||||
chr16:57892072 | C | CA | 38 | a0001c0001t0012g0212 a0001c0002t0001g0039 a0001c0002t0002g0157 others(35): Show |
38 | HG00140.hp2 HG00438.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.3243-3999dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892072 | |||||||
chr16:57892072 | C | CAA | 33 | a0001c0001t0007g0290 a0001c0002t0001g0052 a0001c0035t0010g0229 others(30): Show |
34 | HG00558.hp1 HG00558.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.3243-4000_3243-399 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892072 | |||||||
chr16:57892072 | CA | C | 150 | a0001c0001t0001g0003 a0001c0001t0001g0205 a0001c0001t0001g0260 others(147): Show |
151 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.3243-3999delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892072 | |||||||
chr16:57892072 | CAA | C | 6 | a0018c0060t0015g0005 a0025c0108t0004g0061 a0028c0080t0015g0188 others(3): Show |
6 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3243-4000_3243-399 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892072 | |||||||
chr16:57892128 | G | T | 1 | a0015c0055t0025g0042 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3243-4054C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892128 | |||||||
chr16:57892160 | A | T | 198 | a0001c0001t0001g0262 a0001c0001t0001g0279 a0001c0001t0002g0238 others(195): Show |
199 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.3243-4086T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892160 | |||||||
chr16:57892178 | C | T | 1 | a0001c0004t0003g0037 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3243-4104G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892178 | |||||||
chr16:57892262 | G | A | 2 | a0001c0027t0003g0058 a0006c0086t0003g0067 |
2 | HG02280.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3243-4188C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892262 | |||||||
chr16:57892265 | G | A | 97 | a0001c0001t0007g0290 a0001c0001t0012g0212 a0001c0002t0001g0052 others(94): Show |
98 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.3243-4191C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892265 | |||||||
chr16:57892267 | A | G | 97 | a0001c0001t0007g0290 a0001c0001t0012g0212 a0001c0002t0001g0052 others(94): Show |
98 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.3243-4193T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892267 | |||||||
chr16:57892288 | C | T | 5 | a0005c0049t0015g0344 a0018c0060t0015g0005 a0025c0108t0004g0061 others(2): Show |
5 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.3243-4214G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892288 | |||||||
chr16:57892314 | A | G | 16 | a0001c0004t0035g0079 a0001c0016t0010g0057 a0002c0005t0041g0068 others(13): Show |
16 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.3243-4240T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892314 | |||||||
chr16:57892336 | C | T | 19 | a0001c0001t0001g0262 a0001c0001t0001g0279 a0001c0001t0003g0223 others(16): Show |
19 | HG00544.hp1 HG00609.hp1 HG01978.hp1 others(16): Show |
intron_variant | MODIFIER | c.3243-4262G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892336 | |||||||
chr16:57892423 | C | T | 1 | a0002c0113t0003g0318 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3243-4349G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892423 | |||||||
chr16:57892466 | G | A | 3 | a0001c0013t0018g0294 a0002c0011t0018g0341 a0002c0022t0018g0112 |
3 | HG02976.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3243-4392C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892466 | |||||||
chr16:57892526 | T | C | 3 | a0001c0016t0010g0057 a0002c0114t0010g0357 a0006c0082t0010g0337 |
3 | HG02109.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3243-4452A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892526 | |||||||
chr16:57892631 | T | C | 1 | a0001c0001t0013g0251 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3243-4557A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892631 | |||||||
chr16:57892637 | C | T | 3 | a0001c0013t0018g0294 a0002c0011t0018g0341 a0002c0022t0018g0112 |
3 | HG02976.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3243-4563G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892637 | |||||||
chr16:57892656 | CA | C | 40 | a0001c0001t0012g0212 a0001c0002t0001g0052 a0001c0002t0002g0157 others(37): Show |
40 | HG00140.hp2 HG00733.hp2 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.3243-4583delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892656 | |||||||
chr16:57892665 | C | A | 62 | a0001c0001t0012g0212 a0001c0002t0001g0052 a0001c0002t0002g0157 others(59): Show |
62 | HG00140.hp2 HG00438.hp1 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.3243-4591G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892665 | |||||||
chr16:57892769 | C | G | 67 | a0001c0001t0012g0212 a0001c0002t0001g0052 a0001c0002t0002g0157 others(64): Show |
67 | HG00140.hp2 HG00438.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.3242+4628G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892769 | |||||||
chr16:57892855 | C | A | 1 | a0001c0007t0003g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3242+4542G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892855 | |||||||
chr16:57892915 | G | A | 1 | a0039c0072t0001g0137 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.3242+4482C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892915 | |||||||
chr16:57892943 | G | A | 16 | a0001c0013t0018g0294 a0001c0016t0010g0057 a0002c0005t0041g0068 others(13): Show |
16 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.3242+4454C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892943 | |||||||
chr16:57892955 | C | T | 1 | a0006c0081t0021g0331 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3242+4442G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57892955 | |||||||
chr16:57893010 | T | C | 3 | a0001c0013t0018g0294 a0002c0011t0018g0341 a0002c0022t0018g0112 |
3 | HG02976.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3242+4387A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893010 | |||||||
chr16:57893053 | T | G | 49 | a0001c0001t0012g0212 a0001c0002t0001g0052 a0001c0002t0002g0157 others(46): Show |
49 | HG00140.hp2 HG00438.hp1 HG00733.hp2 others(46): Show |
intron_variant | MODIFIER | c.3242+4344A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893053 | |||||||
chr16:57893217 | C | T | 18 | a0001c0004t0035g0079 a0001c0013t0018g0294 a0001c0016t0010g0057 others(15): Show |
18 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.3242+4180G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893217 | |||||||
chr16:57893264 | T | C | 2 | a0023c0069t0001g0045 a0033c0051t0001g0339 |
2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3242+4133A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893264 | |||||||
chr16:57893317 | C | A | 1 | a0001c0003t0032g0109 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3242+4080G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893317 | |||||||
chr16:57893369 | G | A | 2 | a0001c0042t0011g0029 a0001c0068t0005g0175 |
2 | HG02080.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.3242+4028C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893369 | |||||||
chr16:57893387 | G | T | 1 | a0001c0003t0001g0282 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3242+4010C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893387 | |||||||
chr16:57893413 | C | T | 3 | a0001c0002t0001g0052 a0001c0002t0002g0157 a0039c0072t0001g0137 |
3 | HG02738.hp2 HG03491.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.3242+3984G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893413 | |||||||
chr16:57893414 | G | A | 3 | a0001c0016t0010g0057 a0002c0114t0010g0357 a0006c0082t0010g0337 |
3 | HG02109.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3242+3983C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893414 | |||||||
chr16:57893432 | C | A | 18 | a0001c0004t0035g0079 a0001c0013t0018g0294 a0001c0016t0010g0057 others(15): Show |
18 | HG02109.hp2 HG02257.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.3242+3965G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893432 | |||||||
chr16:57893475 | C | T | 1 | a0005c0014t0001g0345 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3242+3922G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893475 | |||||||
chr16:57893614 | A | G | 2 | a0001c0001t0001g0205 a0002c0005t0006g0089 |
2 | HG02015.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.3242+3783T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893614 | |||||||
chr16:57893630 | T | C | 47 | a0001c0001t0012g0212 a0001c0002t0001g0052 a0001c0002t0002g0157 others(44): Show |
47 | HG00140.hp2 HG00733.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.3242+3767A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893630 | |||||||
chr16:57893671 | G | T | 5 | a0001c0013t0018g0294 a0002c0011t0018g0341 a0002c0022t0018g0112 others(2): Show |
5 | HG02976.hp1 HG03041.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3242+3726C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893671 | |||||||
chr16:57893763 | G | A | 3 | a0001c0001t0001g0261 a0001c0004t0001g0150 a0009c0025t0001g0122 |
3 | NA18956.hp2 NA19007.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.3242+3634C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893763 | |||||||
chr16:57893822 | T | A | 2 | a0037c0063t0020g0009 a0041c0047t0034g0350 |
2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3242+3575A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893822 | |||||||
chr16:57893830 | A | C | 1 | a0002c0005t0041g0068 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3242+3567T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893830 | |||||||
chr16:57893850 | C | A | 3 | a0010c0010t0008g0090 a0010c0010t0008g0102 a0027c0092t0001g0285 |
3 | HG01515.hp2 HG01517.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.3242+3547G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893850 | |||||||
chr16:57893879 | C | G | 5 | a0001c0013t0018g0294 a0002c0011t0018g0341 a0002c0022t0018g0112 others(2): Show |
5 | HG02976.hp1 HG03041.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3242+3518G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893879 | |||||||
chr16:57893895 | C | A | 1 | a0002c0005t0001g0332 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.3242+3502G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57893895 | |||||||
chr16:57894027 | G | A | 47 | a0001c0001t0012g0212 a0001c0002t0001g0052 a0001c0002t0002g0157 others(44): Show |
47 | HG00140.hp2 HG00733.hp2 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.3242+3370C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894027 | |||||||
chr16:57894040 | G | A | 1 | a0001c0007t0003g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3242+3357C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894040 | |||||||
chr16:57894225 | G | A | 2 | a0015c0102t0003g0271 a0048c0050t0003g0352 |
2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3242+3172C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894225 | |||||||
chr16:57894252 | C | A | 5 | a0001c0004t0035g0079 a0002c0005t0041g0068 a0002c0006t0021g0187 others(2): Show |
5 | HG02886.hp1 HG02965.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.3242+3145G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894252 | |||||||
chr16:57894310 | A | C | 1 | a0008c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3087T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894310 | |||||||
chr16:57894311 | A | T | 1 | a0008c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3086T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894311 | |||||||
chr16:57894314 | G | A | 1 | a0008c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3083C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894314 | |||||||
chr16:57894315 | T | C | 1 | a0008c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3082A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894315 | |||||||
chr16:57894316 | T | A | 1 | a0008c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3081A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894316 | |||||||
chr16:57894318 | G | A | 1 | a0008c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3079C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894318 | |||||||
chr16:57894320 | G | T | 1 | a0008c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3077C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894320 | |||||||
chr16:57894321 | C | G | 1 | a0008c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3076G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894321 | |||||||
chr16:57894322 | T | A | 1 | a0008c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3075A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894322 | |||||||
chr16:57894323 | G | T | 1 | a0008c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3074C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894323 | |||||||
chr16:57894325 | G | T | 1 | a0008c0020t0009g0081 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.3242+3072C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894325 | |||||||
chr16:57894384 | T | C | 2 | a0015c0102t0003g0271 a0048c0050t0003g0352 |
2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.3242+3013A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894384 | |||||||
chr16:57894417 | G | A | 90 | a0001c0001t0007g0290 a0001c0001t0012g0212 a0001c0002t0001g0052 others(87): Show |
91 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.3242+2980C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894417 | |||||||
chr16:57894497 | A | ATGCCTGT others(6): Show |
2 | a0037c0063t0020g0009 a0041c0047t0034g0350 |
2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3242+2899_3242+290 others(17): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894497 | |||||||
chr16:57894498 | G | A | 2 | a0037c0063t0020g0009 a0041c0047t0034g0350 |
2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3242+2899C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894498 | |||||||
chr16:57894516 | A | G | 67 | a0001c0001t0012g0212 a0001c0002t0001g0052 a0001c0002t0002g0157 others(64): Show |
67 | HG00140.hp2 HG00438.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.3242+2881T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894516 | |||||||
chr16:57894559 | C | A | 1 | a0001c0097t0003g0230 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.3242+2838G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894559 | |||||||
chr16:57894643 | G | A | 27 | a0001c0001t0007g0290 a0003c0008t0002g0002 a0003c0008t0003g0145 others(24): Show |
28 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.3242+2754C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894643 | |||||||
chr16:57894823 | A | G | 1 | a0002c0005t0001g0101 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3242+2574T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894823 | |||||||
chr16:57894875 | A | G | 2 | a0018c0062t0027g0324 a0021c0117t0026g0186 |
2 | HG00741.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3242+2522T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57894875 | |||||||
chr16:57895021 | T | C | 1 | a0015c0102t0003g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.3242+2376A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895021 | |||||||
chr16:57895028 | AG | A | 23 | a0001c0007t0004g0046 a0001c0007t0008g0356 a0001c0013t0004g0308 others(20): Show |
23 | HG00738.hp2 HG01070.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.3242+2368delC | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895028 | |||||||
chr16:57895033 | C | A | 1 | a0001c0007t0003g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3242+2364G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895033 | |||||||
chr16:57895221 | A | G | 2 | a0001c0097t0003g0230 a0002c0037t0003g0023 |
2 | HG00438.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.3242+2176T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895221 | |||||||
chr16:57895272 | C | A | 8 | a0001c0002t0022g0062 a0001c0004t0022g0107 a0001c0027t0040g0078 others(5): Show |
8 | HG02258.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.3242+2125G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895272 | |||||||
chr16:57895368 | C | T | 1 | a0002c0005t0041g0068 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3242+2029G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895368 | |||||||
chr16:57895398 | G | A | 1 | a0001c0015t0020g0336 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3242+1999C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895398 | |||||||
chr16:57895438 | G | T | 4 | a0001c0001t0003g0208 a0001c0001t0005g0277 a0001c0001t0013g0206 others(1): Show |
4 | NA18944.hp1 NA18962.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.3242+1959C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895438 | |||||||
chr16:57895540 | A | C | 2 | a0001c0002t0001g0125 a0001c0003t0001g0270 |
2 | HG03669.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.3242+1857T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895540 | |||||||
chr16:57895549 | T | TTA | 18 | a0001c0015t0020g0336 a0001c0028t0044g0064 a0001c0097t0003g0230 others(15): Show |
18 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.3242+1847_3242+184 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895549 | |||||||
chr16:57895551 | T | A | 30 | a0001c0004t0035g0079 a0001c0015t0020g0336 a0001c0028t0044g0064 others(27): Show |
30 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.3242+1846A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895551 | |||||||
chr16:57895551 | T | TTA | 18 | a0001c0001t0007g0290 a0003c0008t0002g0002 a0003c0009t0006g0289 others(15): Show |
19 | HG00642.hp2 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.3242+1844_3242+184 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895551 | |||||||
chr16:57895553 | A | T | 2 | a0001c0015t0001g0335 a0001c0028t0042g0069 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3242+1844T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895553 | |||||||
chr16:57895959 | A | G | 2 | a0002c0011t0016g0190 a0005c0048t0016g0354 |
2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3242+1438T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57895959 | |||||||
chr16:57896041 | G | A | 27 | a0001c0001t0007g0290 a0003c0008t0002g0002 a0003c0008t0003g0145 others(24): Show |
28 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.3242+1356C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896041 | |||||||
chr16:57896110 | A | G | 3 | a0006c0084t0003g0330 a0011c0058t0004g0140 a0030c0111t0003g0327 |
3 | HG02451.hp1 HG02717.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.3242+1287T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896110 | |||||||
chr16:57896291 | G | A | 23 | a0001c0007t0004g0046 a0001c0007t0008g0356 a0001c0013t0004g0308 others(20): Show |
23 | HG00738.hp2 HG01070.hp1 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.3242+1106C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896291 | |||||||
chr16:57896429 | T | C | 1 | a0001c0013t0001g0306 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.3242+968A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896429 | |||||||
chr16:57896485 | G | T | 1 | a0002c0005t0001g0013 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.3242+912C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896485 | |||||||
chr16:57896497 | G | A | 3 | a0001c0016t0010g0057 a0002c0114t0010g0357 a0006c0082t0010g0337 |
3 | HG02109.hp2 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3242+900C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896497 | |||||||
chr16:57896503 | A | G | 33 | a0001c0007t0002g0073 a0001c0007t0003g0189 a0001c0015t0001g0335 others(30): Show |
33 | HG00438.hp1 HG00741.hp2 HG01515.hp2 others(30): Show |
intron_variant | MODIFIER | c.3242+894T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896503 | |||||||
chr16:57896574 | G | A | 2 | a0003c0012t0007g0048 a0008c0020t0007g0007 |
2 | HG01891.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.3242+823C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896574 | |||||||
chr16:57896593 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3242+804T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896593 | |||||||
chr16:57896621 | G | A | 31 | a0001c0007t0002g0073 a0001c0007t0003g0189 a0001c0015t0001g0335 others(28): Show |
31 | HG00741.hp2 HG01515.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.3242+776C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896621 | |||||||
chr16:57896641 | A | G | 5 | a0005c0049t0015g0344 a0018c0060t0015g0005 a0025c0108t0004g0061 others(2): Show |
5 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.3242+756T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896641 | |||||||
chr16:57896713 | A | AAAAT | 61 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0207 others(58): Show |
62 | HG00099.hp2 HG00140.hp2 HG01074.hp2 others(59): Show |
intron_variant | MODIFIER | c.3242+680_3242+683d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896713 | |||||||
chr16:57896713 | A | AAAATAAA others(1): Show |
3 | a0003c0104t0007g0232 a0007c0115t0045g0111 a0010c0010t0003g0030 |
3 | HG03017.hp2 HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3242+676_3242+683d others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896713 | |||||||
chr16:57896713 | A | AAAATAAA others(5): Show |
1 | a0001c0007t0003g0004 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3242+672_3242+683d others(14): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896713 | |||||||
chr16:57896713 | AAAAT | A | 137 | a0001c0001t0001g0205 a0001c0001t0001g0226 a0001c0001t0001g0234 others(134): Show |
138 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.3242+680_3242+683d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896713 | |||||||
chr16:57896713 | AAAATAAA others(1): Show |
A | 19 | a0001c0001t0003g0223 a0001c0001t0013g0206 a0001c0002t0001g0125 others(16): Show |
19 | HG00733.hp1 HG01255.hp2 HG01261.hp2 others(16): Show |
intron_variant | MODIFIER | c.3242+676_3242+683d others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896713 | |||||||
chr16:57896713 | AAAATAAA others(5): Show |
A | 5 | a0001c0003t0001g0278 a0001c0007t0003g0189 a0001c0097t0003g0230 others(2): Show |
5 | HG00438.hp1 HG02723.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.3242+672_3242+683d others(14): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896713 | |||||||
chr16:57896713 | AAAATAAA others(13): Show |
A | 1 | a0005c0014t0005g0346 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3242+664_3242+683d others(22): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896713 | |||||||
chr16:57896713 | AAAATAAA others(17): Show |
A | 2 | a0018c0062t0027g0324 a0021c0117t0026g0186 |
2 | HG00741.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3242+660_3242+683d others(26): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896713 | |||||||
chr16:57896761 | T | A | 4 | a0001c0002t0007g0126 a0001c0003t0003g0296 a0001c0017t0001g0139 others(1): Show |
4 | HG00280.hp2 HG01074.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.3242+636A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896761 | |||||||
chr16:57896778 | A | G | 1 | a0011c0059t0001g0123 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.3242+619T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896778 | |||||||
chr16:57896993 | G | A | 1 | a0009c0054t0002g0044 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3242+404C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57896993 | |||||||
chr16:57897032 | A | T | 31 | a0001c0007t0002g0073 a0001c0007t0003g0189 a0001c0015t0001g0335 others(28): Show |
31 | HG00741.hp2 HG01515.hp2 HG01517.hp1 others(28): Show |
intron_variant | MODIFIER | c.3242+365T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57897032 | |||||||
chr16:57897039 | C | G | 2 | a0001c0028t0044g0064 a0006c0083t0043g0063 |
2 | HG02615.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.3242+358G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57897039 | |||||||
chr16:57897050 | C | T | 51 | a0001c0004t0035g0079 a0001c0007t0002g0073 a0001c0007t0003g0189 others(48): Show |
51 | HG00438.hp1 HG00741.hp2 HG01515.hp2 others(48): Show |
intron_variant | MODIFIER | c.3242+347G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57897050 | |||||||
chr16:57897117 | T | C | 13 | a0001c0001t0012g0212 a0001c0002t0001g0052 a0001c0002t0002g0157 others(10): Show |
13 | HG00140.hp2 HG00733.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.3242+280A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57897117 | |||||||
chr16:57897145 | T | A | 6 | a0001c0015t0020g0336 a0001c0028t0044g0064 a0006c0083t0043g0063 others(3): Show |
6 | HG02451.hp1 HG02615.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3242+252A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57897145 | |||||||
chr16:57897294 | G | C | 3 | a0001c0013t0018g0294 a0002c0011t0018g0341 a0002c0022t0018g0112 |
3 | HG02976.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3242+103C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57897294 | |||||||
chr16:57897301 | C | CA | 27 | a0001c0004t0003g0151 a0001c0007t0002g0073 a0001c0015t0001g0335 others(24): Show |
27 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.3242+95dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57897301 | |||||||
chr16:57897301 | CA | C | 37 | a0001c0001t0007g0290 a0001c0002t0003g0008 a0001c0016t0010g0057 others(34): Show |
38 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.3242+95delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57897301 | |||||||
chr16:57897329 | C | G | 50 | a0001c0001t0002g0238 a0001c0001t0002g0252 a0001c0001t0002g0309 others(47): Show |
50 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.3242+68G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 31/32 | chr16 | 57897329 | |||||||
chr16:57898001 | C | T | 1 | a0001c0002t0001g0039 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2977-87G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898001 | |||||||
chr16:57898154 | A | G | 24 | a0001c0007t0004g0046 a0001c0007t0008g0356 a0001c0013t0004g0308 others(21): Show |
24 | HG00738.hp2 HG01070.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.2977-240T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898154 | |||||||
chr16:57898383 | C | T | 1 | a0003c0012t0007g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2977-469G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898383 | |||||||
chr16:57898384 | CT | C | 44 | a0001c0007t0002g0073 a0001c0013t0018g0294 a0001c0015t0001g0335 others(41): Show |
44 | HG00438.hp1 HG00741.hp2 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.2977-471delA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898384 | |||||||
chr16:57898504 | A | G | 5 | a0005c0049t0015g0344 a0018c0060t0015g0005 a0025c0108t0004g0061 others(2): Show |
5 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.2977-590T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898504 | |||||||
chr16:57898521 | G | A | 2 | a0001c0097t0003g0230 a0002c0037t0003g0023 |
2 | HG00438.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.2977-607C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898521 | |||||||
chr16:57898540 | C | T | 1 | a0002c0005t0001g0098 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2977-626G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898540 | |||||||
chr16:57898577 | G | A | 2 | a0037c0063t0020g0009 a0041c0047t0034g0350 |
2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2977-663C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898577 | |||||||
chr16:57898636 | G | A | 24 | a0001c0007t0002g0073 a0001c0015t0001g0335 a0001c0015t0020g0336 others(21): Show |
24 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.2977-722C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898636 | |||||||
chr16:57898838 | G | A | 1 | a0003c0101t0030g0264 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2977-924C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898838 | |||||||
chr16:57898879 | C | T | 1 | a0002c0006t0003g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2977-965G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898879 | |||||||
chr16:57898887 | C | T | 1 | a0001c0001t0037g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2977-973G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898887 | |||||||
chr16:57898930 | A | G | 1 | a0003c0012t0003g0176 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2977-1016T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57898930 | |||||||
chr16:57899049 | A | C | 1 | a0019c0052t0003g0180 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2977-1135T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899049 | |||||||
chr16:57899050 | A | G | 26 | a0001c0007t0002g0073 a0001c0015t0001g0335 a0001c0015t0020g0336 others(23): Show |
26 | HG00741.hp2 HG01884.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.2977-1136T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899050 | |||||||
chr16:57899162 | G | A | 8 | a0001c0004t0035g0079 a0001c0016t0010g0057 a0002c0005t0041g0068 others(5): Show |
8 | HG02109.hp2 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2977-1248C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899162 | |||||||
chr16:57899221 | A | C | 1 | a0002c0038t0003g0094 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2977-1307T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899221 | |||||||
chr16:57899232 | C | T | 5 | a0003c0009t0006g0289 a0003c0009t0007g0080 a0003c0009t0039g0307 others(2): Show |
5 | HG00642.hp2 HG01074.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.2977-1318G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899232 | |||||||
chr16:57899241 | A | G | 1 | a0019c0052t0003g0180 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2977-1327T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899241 | |||||||
chr16:57899282 | G | C | 2 | a0037c0063t0020g0009 a0041c0047t0034g0350 |
2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2977-1368C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899282 | |||||||
chr16:57899322 | GAAA | G | 74 | a0001c0001t0007g0290 a0001c0001t0012g0212 a0001c0003t0012g0266 others(71): Show |
75 | HG00140.hp2 HG00438.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.2977-1411_2977-140 others(7): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899322 | |||||||
chr16:57899330 | A | T | 261 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(258): Show |
263 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.2977-1416T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899330 | |||||||
chr16:57899330 | AAAT | A | 9 | a0001c0007t0002g0073 a0001c0015t0001g0335 a0001c0028t0042g0069 others(6): Show |
9 | HG01884.hp2 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.2977-1419_2977-141 others(7): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899330 | |||||||
chr16:57899333 | T | A | 1 | a0018c0060t0015g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2977-1419A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899333 | |||||||
chr16:57899351 | A | G | 1 | a0001c0027t0040g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2977-1437T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899351 | |||||||
chr16:57899362 | G | A | 150 | a0001c0001t0001g0195 a0001c0001t0001g0205 a0001c0001t0001g0236 others(147): Show |
151 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.2977-1448C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899362 | |||||||
chr16:57899497 | G | A | 3 | a0001c0013t0018g0294 a0002c0011t0018g0341 a0002c0022t0018g0112 |
3 | HG02976.hp1 HG03041.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2977-1583C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899497 | |||||||
chr16:57899572 | G | A | 1 | a0001c0004t0022g0107 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2977-1658C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899572 | |||||||
chr16:57899588 | C | T | 3 | a0001c0068t0005g0175 a0001c0097t0003g0230 a0002c0037t0003g0023 |
3 | HG00438.hp1 HG02080.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.2977-1674G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899588 | |||||||
chr16:57899612 | C | G | 2 | a0010c0010t0008g0090 a0010c0010t0008g0102 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2977-1698G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899612 | |||||||
chr16:57899616 | GGA | G | 8 | a0001c0004t0035g0079 a0001c0016t0010g0057 a0002c0005t0041g0068 others(5): Show |
8 | HG02109.hp2 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2977-1704_2977-170 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899616 | |||||||
chr16:57899627 | G | A | 1 | a0002c0006t0003g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2977-1713C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899627 | |||||||
chr16:57899643 | T | TAAAC | 32 | a0001c0001t0007g0290 a0001c0068t0005g0175 a0001c0097t0003g0230 others(29): Show |
33 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.2976+1705_2976+170 others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899643 | |||||||
chr16:57899643 | TAAAC | T | 8 | a0001c0004t0035g0079 a0001c0016t0010g0057 a0002c0005t0041g0068 others(5): Show |
8 | HG02109.hp2 HG02717.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2976+1705_2976+170 others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899643 | |||||||
chr16:57899683 | G | A | 21 | a0001c0007t0002g0073 a0001c0015t0001g0335 a0001c0028t0042g0069 others(18): Show |
21 | HG00741.hp2 HG02055.hp2 HG02083.hp2 others(18): Show |
intron_variant | MODIFIER | c.2976+1669C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899683 | |||||||
chr16:57899722 | T | C | 1 | a0001c0001t0002g0238 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2976+1630A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899722 | |||||||
chr16:57899839 | C | T | 19 | a0001c0001t0001g0262 a0001c0001t0001g0279 a0001c0001t0003g0223 others(16): Show |
19 | HG00544.hp1 HG00609.hp1 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.2976+1513G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899839 | |||||||
chr16:57899867 | T | C | 34 | a0001c0001t0007g0290 a0001c0068t0005g0175 a0001c0097t0003g0230 others(31): Show |
35 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.2976+1485A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899867 | |||||||
chr16:57899892 | C | T | 2 | a0001c0018t0001g0263 a0002c0005t0003g0106 |
2 | HG02027.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2976+1460G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899892 | |||||||
chr16:57899895 | G | T | 1 | a0001c0001t0006g0225 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2976+1457C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899895 | |||||||
chr16:57899919 | G | A | 15 | a0004c0026t0004g0059 a0004c0026t0004g0310 a0004c0061t0004g0049 others(12): Show |
15 | HG01109.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2976+1433C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57899919 | |||||||
chr16:57900043 | G | A | 1 | a0039c0072t0001g0137 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2976+1309C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57900043 | |||||||
chr16:57900176 | C | T | 1 | a0001c0003t0003g0265 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2976+1176G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57900176 | |||||||
chr16:57900346 | C | G | 2 | a0015c0102t0003g0271 a0048c0050t0003g0352 |
2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2976+1006G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57900346 | |||||||
chr16:57900499 | G | A | 1 | a0004c0036t0002g0256 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2976+853C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57900499 | |||||||
chr16:57900594 | A | G | 1 | a0001c0042t0011g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2976+758T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57900594 | |||||||
chr16:57900859 | G | GA | 11 | a0001c0003t0005g0300 a0001c0003t0006g0288 a0001c0004t0001g0117 others(8): Show |
11 | HG00438.hp1 HG00741.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.2976+492dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57900859 | |||||||
chr16:57900870 | A | C | 2 | a0001c0041t0005g0028 a0002c0022t0002g0074 |
2 | HG02055.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2976+482T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57900870 | |||||||
chr16:57900921 | A | C | 6 | a0018c0060t0015g0005 a0018c0062t0027g0324 a0021c0117t0026g0186 others(3): Show |
6 | HG00741.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2976+431T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57900921 | |||||||
chr16:57901059 | TG | T | 302 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(299): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.2976+292delC | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57901059 | |||||||
chr16:57901066 | G | T | 2 | a0001c0001t0003g0208 a0001c0001t0013g0206 |
2 | NA18944.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.2976+286C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57901066 | |||||||
chr16:57901067 | G | A | 2 | a0001c0003t0001g0202 a0001c0004t0001g0173 |
2 | NA18942.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.2976+285C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57901067 | |||||||
chr16:57901181 | T | C | 314 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(311): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.2976+171A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57901181 | |||||||
chr16:57901251 | T | A | 3 | a0001c0042t0011g0029 a0015c0102t0003g0271 a0048c0050t0003g0352 |
3 | HG02922.hp2 HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2976+101A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57901251 | |||||||
chr16:57901252 | C | A | 3 | a0001c0042t0011g0029 a0015c0102t0003g0271 a0048c0050t0003g0352 |
3 | HG02922.hp2 HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2976+100G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57901252 | |||||||
chr16:57901307 | G | A | 1 | a0001c0013t0019g0213 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2976+45C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57901307 | |||||||
chr16:57901327 | C | T | 17 | a0004c0026t0004g0059 a0004c0026t0004g0310 a0004c0061t0004g0049 others(14): Show |
17 | HG01109.hp2 HG01515.hp2 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.2976+25G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57901327 | |||||||
chr16:57901344 | C | G | 1 | a0001c0003t0002g0201 | 1 | HG00408.hp1 | splice_region_variant&intron_variant | LOW | c.2976+8G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 29/32 | chr16 | 57901344 | |||||||
chr16:57901462 | C | A | 1 | a0001c0004t0022g0107 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2893-27G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 28/32 | chr16 | 57901462 | |||||||
chr16:57901473 | A | C | 1 | a0001c0002t0022g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2893-38T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 28/32 | chr16 | 57901473 | |||||||
chr16:57901476 | T | C | 2 | a0002c0006t0016g0110 a0005c0014t0016g0326 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2893-41A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 28/32 | chr16 | 57901476 | |||||||
chr16:57901479 | G | T | 1 | a0001c0002t0022g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2893-44C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 28/32 | chr16 | 57901479 | |||||||
chr16:57901522 | G | A | 15 | a0004c0026t0004g0059 a0004c0026t0004g0310 a0004c0061t0004g0049 others(12): Show |
15 | HG01109.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.2892+6C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 28/32 | chr16 | 57901522 | |||||||
chr16:57901662 | C | T | 1 | a0002c0005t0001g0014 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2795-37G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57901662 | |||||||
chr16:57901680 | T | A | 5 | a0001c0004t0035g0079 a0002c0005t0041g0068 a0002c0006t0013g0083 others(2): Show |
5 | HG02886.hp1 HG02965.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.2795-55A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57901680 | |||||||
chr16:57901722 | A | G | 1 | a0040c0067t0002g0051 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2795-97T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57901722 | |||||||
chr16:57901940 | C | T | 1 | a0002c0006t0008g0084 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2795-315G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57901940 | |||||||
chr16:57901975 | T | G | 6 | a0018c0060t0015g0005 a0018c0062t0027g0324 a0021c0117t0026g0186 others(3): Show |
6 | HG00741.hp1 HG02257.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2795-350A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57901975 | |||||||
chr16:57902066 | T | TTTG | 15 | a0004c0026t0004g0059 a0004c0026t0004g0310 a0004c0061t0004g0049 others(12): Show |
15 | HG01109.hp2 HG01515.hp2 HG01517.hp1 others(12): Show |
intron_variant | MODIFIER | c.2795-444_2795-442d others(5): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902066 | |||||||
chr16:57902066 | TTTG | T | 4 | a0001c0004t0022g0107 a0001c0013t0018g0294 a0002c0011t0018g0341 others(1): Show |
4 | HG02647.hp1 HG02976.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.2795-444_2795-442d others(5): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902066 | |||||||
chr16:57902186 | T | C | 5 | a0001c0004t0035g0079 a0002c0005t0041g0068 a0002c0006t0013g0083 others(2): Show |
5 | HG02886.hp1 HG02965.hp1 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.2795-561A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902186 | |||||||
chr16:57902230 | G | T | 306 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.2795-605C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902230 | |||||||
chr16:57902259 | C | T | 2 | a0015c0102t0003g0271 a0048c0050t0003g0352 |
2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2795-634G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902259 | |||||||
chr16:57902263 | G | T | 1 | a0001c0003t0032g0109 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2795-638C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902263 | |||||||
chr16:57902308 | T | G | 3 | a0026c0121t0011g0315 a0034c0043t0011g0351 a0047c0056t0011g0047 |
3 | HG02258.hp1 HG03195.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2795-683A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902308 | |||||||
chr16:57902346 | C | T | 302 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(299): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.2795-721G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902346 | |||||||
chr16:57902461 | G | A | 1 | a0001c0002t0003g0050 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2795-836C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902461 | |||||||
chr16:57902477 | T | A | 1 | a0008c0021t0003g0105 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2795-852A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902477 | |||||||
chr16:57902691 | C | T | 2 | a0001c0001t0002g0312 a0002c0037t0003g0092 |
2 | HG03831.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.2795-1066G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902691 | |||||||
chr16:57902712 | G | A | 12 | a0001c0068t0005g0175 a0001c0097t0003g0230 a0002c0037t0003g0023 others(9): Show |
12 | HG00438.hp1 HG01515.hp2 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.2795-1087C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902712 | |||||||
chr16:57902714 | G | A | 12 | a0001c0068t0005g0175 a0001c0097t0003g0230 a0002c0037t0003g0023 others(9): Show |
12 | HG00438.hp1 HG01515.hp2 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.2795-1089C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902714 | |||||||
chr16:57902888 | C | A | 11 | a0001c0068t0005g0175 a0001c0097t0003g0230 a0002c0037t0003g0023 others(8): Show |
11 | HG00438.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.2794+934G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902888 | |||||||
chr16:57902928 | A | T | 1 | a0001c0001t0012g0212 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2794+894T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902928 | |||||||
chr16:57902948 | G | A | 1 | a0001c0042t0011g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2794+874C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902948 | |||||||
chr16:57902978 | T | A | 1 | a0001c0070t0007g0134 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2794+844A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902978 | |||||||
chr16:57902983 | G | A | 1 | a0001c0002t0001g0162 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2794+839C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902983 | |||||||
chr16:57902998 | G | A | 1 | a0002c0006t0003g0022 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2794+824C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57902998 | |||||||
chr16:57903089 | G | A | 12 | a0001c0068t0005g0175 a0001c0097t0003g0230 a0002c0037t0003g0023 others(9): Show |
12 | HG00438.hp1 HG01123.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.2794+733C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903089 | |||||||
chr16:57903133 | G | A | 1 | a0001c0002t0001g0155 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2794+689C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903133 | |||||||
chr16:57903185 | C | CT | 14 | a0001c0001t0002g0222 a0001c0001t0002g0312 a0001c0004t0001g0174 others(11): Show |
14 | HG00423.hp1 HG00597.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.2794+636dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903185 | |||||||
chr16:57903185 | C | CTT | 14 | a0001c0002t0001g0052 a0001c0004t0035g0079 a0002c0006t0013g0083 others(11): Show |
14 | HG00741.hp2 HG01123.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2794+635_2794+636d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903185 | |||||||
chr16:57903185 | C | CTTT | 9 | a0001c0013t0018g0294 a0001c0068t0005g0175 a0001c0097t0003g0230 others(6): Show |
9 | HG00438.hp1 HG02080.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.2794+634_2794+636d others(5): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903185 | |||||||
chr16:57903187 | T | C | 1 | a0001c0003t0001g0278 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2794+635A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903187 | |||||||
chr16:57903246 | C | T | 8 | a0004c0030t0003g0001 a0004c0034t0012g0255 a0004c0034t0012g0292 others(5): Show |
9 | HG00280.hp2 HG00323.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.2794+576G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903246 | |||||||
chr16:57903289 | C | T | 4 | a0001c0068t0005g0175 a0001c0097t0003g0230 a0002c0037t0003g0023 others(1): Show |
4 | HG00438.hp1 HG02080.hp2 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.2794+533G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903289 | |||||||
chr16:57903349 | A | T | 2 | a0002c0006t0016g0110 a0005c0014t0016g0326 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2794+473T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903349 | |||||||
chr16:57903537 | C | T | 56 | a0001c0001t0001g0260 a0001c0001t0002g0238 a0001c0001t0002g0273 others(53): Show |
56 | HG00408.hp1 HG00408.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.2794+285G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903537 | |||||||
chr16:57903551 | T | C | 4 | a0001c0015t0002g0006 a0002c0109t0004g0108 a0005c0014t0005g0346 others(1): Show |
4 | HG02145.hp2 HG02965.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2794+271A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903551 | |||||||
chr16:57903589 | C | G | 2 | a0016c0023t0002g0347 a0016c0023t0002g0349 |
2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2794+233G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903589 | |||||||
chr16:57903705 | G | A | 1 | a0001c0002t0002g0157 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2794+117C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903705 | |||||||
chr16:57903711 | G | A | 2 | a0018c0062t0027g0324 a0021c0117t0026g0186 |
2 | HG00741.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2794+111C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903711 | |||||||
chr16:57903755 | T | G | 12 | a0001c0003t0001g0227 a0001c0004t0035g0079 a0001c0017t0001g0114 others(9): Show |
12 | HG00438.hp1 HG02080.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.2794+67A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 27/32 | chr16 | 57903755 | |||||||
chr16:57903991 | G | A | 256 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(253): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2635-10C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57903991 | |||||||
chr16:57904035 | C | T | 5 | a0001c0015t0001g0335 a0001c0015t0002g0006 a0001c0028t0042g0069 others(2): Show |
5 | HG02257.hp2 HG02486.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2635-54G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904035 | |||||||
chr16:57904098 | G | C | 1 | a0001c0004t0001g0117 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2635-117C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904098 | |||||||
chr16:57904099 | C | G | 1 | a0001c0004t0001g0117 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2635-118G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904099 | |||||||
chr16:57904099 | C | T | 1 | a0001c0004t0001g0115 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2635-118G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904099 | |||||||
chr16:57904296 | C | T | 1 | a0007c0115t0045g0111 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2635-315G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904296 | |||||||
chr16:57904305 | T | C | 283 | a0001c0001t0001g0003 a0001c0001t0001g0205 a0001c0001t0001g0207 others(280): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.2635-324A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904305 | |||||||
chr16:57904333 | A | G | 6 | a0001c0035t0010g0229 a0001c0103t0029g0272 a0002c0038t0003g0094 others(3): Show |
6 | HG00558.hp2 NA18747.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.2635-352T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904333 | |||||||
chr16:57904360 | C | T | 1 | a0001c0016t0004g0313 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2634+374G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904360 | |||||||
chr16:57904361 | G | A | 2 | a0001c0097t0003g0230 a0040c0067t0002g0051 |
2 | HG00438.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2634+373C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904361 | |||||||
chr16:57904503 | G | A | 66 | a0001c0001t0001g0207 a0001c0001t0001g0261 a0001c0001t0001g0275 others(63): Show |
66 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(63): Show |
intron_variant | MODIFIER | c.2634+231C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904503 | |||||||
chr16:57904568 | C | G | 2 | a0004c0026t0004g0059 a0004c0077t0004g0060 |
2 | HG01891.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2634+166G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904568 | |||||||
chr16:57904577 | G | A | 1 | a0001c0004t0005g0127 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2634+157C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904577 | |||||||
chr16:57904600 | T | C | 2 | a0001c0015t0020g0336 a0001c0027t0040g0078 |
2 | HG02622.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.2634+134A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904600 | |||||||
chr16:57904724 | G | C | 1 | a0001c0003t0003g0198 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2634+10C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904724 | |||||||
chr16:57904729 | G | A | 1 | a0002c0005t0006g0089 | 1 | HG02074.hp2 | splice_region_variant&intron_variant | LOW | c.2634+5C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 26/32 | chr16 | 57904729 | |||||||
chr16:57905094 | G | A | 2 | a0001c0002t0001g0125 a0001c0066t0001g0130 |
2 | HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2493-219C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905094 | |||||||
chr16:57905270 | G | A | 1 | a0001c0002t0001g0125 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2493-395C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905270 | |||||||
chr16:57905305 | G | A | 3 | a0001c0001t0001g0234 a0002c0005t0001g0015 a0002c0005t0001g0016 |
3 | HG00639.hp2 HG01261.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2493-430C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905305 | |||||||
chr16:57905361 | GA | G | 37 | a0001c0001t0001g0243 a0001c0001t0037g0246 a0001c0002t0001g0052 others(34): Show |
37 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.2493-487delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905361 | |||||||
chr16:57905394 | C | T | 41 | a0001c0001t0001g0207 a0001c0001t0001g0279 a0001c0001t0001g0280 others(38): Show |
41 | HG00099.hp2 HG00408.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.2493-519G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905394 | |||||||
chr16:57905400 | C | T | 6 | a0001c0015t0001g0335 a0001c0016t0046g0054 a0002c0109t0004g0108 others(3): Show |
6 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2493-525G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905400 | |||||||
chr16:57905434 | G | A | 1 | a0003c0101t0030g0264 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2493-559C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905434 | |||||||
chr16:57905484 | G | A | 4 | a0005c0046t0036g0348 a0010c0010t0003g0325 a0010c0010t0003g0328 others(1): Show |
4 | HG02717.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2493-609C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905484 | |||||||
chr16:57905644 | C | T | 1 | a0001c0018t0001g0263 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2493-769G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905644 | |||||||
chr16:57905645 | G | A | 1 | a0001c0002t0001g0039 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2493-770C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905645 | |||||||
chr16:57905680 | G | T | 1 | a0015c0055t0025g0042 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2493-805C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905680 | |||||||
chr16:57905829 | C | T | 39 | a0001c0002t0002g0161 a0001c0002t0002g0183 a0001c0002t0005g0184 others(36): Show |
39 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.2493-954G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905829 | |||||||
chr16:57905845 | C | G | 10 | a0001c0004t0001g0164 a0001c0017t0001g0114 a0001c0017t0001g0139 others(7): Show |
10 | HG01934.hp1 HG02027.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.2493-970G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905845 | |||||||
chr16:57905998 | G | A | 1 | a0001c0004t0001g0166 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2493-1123C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57905998 | |||||||
chr16:57906000 | C | T | 1 | a0011c0033t0001g0249 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2493-1125G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906000 | |||||||
chr16:57906066 | C | G | 159 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.2493-1191G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906066 | |||||||
chr16:57906184 | G | A | 3 | a0002c0006t0021g0187 a0002c0109t0004g0108 a0002c0114t0010g0357 |
3 | HG02109.hp2 HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2493-1309C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906184 | |||||||
chr16:57906213 | C | T | 1 | a0005c0014t0005g0346 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2493-1338G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906213 | |||||||
chr16:57906215 | C | T | 3 | a0001c0002t0003g0038 a0001c0002t0003g0050 a0001c0003t0003g0221 |
3 | HG00099.hp1 HG01516.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.2493-1340G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906215 | |||||||
chr16:57906264 | T | C | 1 | a0001c0053t0004g0200 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2493-1389A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906264 | |||||||
chr16:57906277 | A | C | 1 | a0001c0053t0004g0200 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2493-1402T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906277 | |||||||
chr16:57906284 | A | G | 45 | a0001c0001t0001g0207 a0001c0001t0001g0279 a0001c0001t0001g0280 others(42): Show |
45 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.2493-1409T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906284 | |||||||
chr16:57906317 | G | A | 24 | a0001c0002t0002g0183 a0001c0002t0005g0184 a0001c0013t0019g0213 others(21): Show |
24 | HG00280.hp1 HG00639.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.2493-1442C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906317 | |||||||
chr16:57906323 | G | A | 1 | a0001c0002t0001g0329 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2493-1448C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906323 | |||||||
chr16:57906381 | C | T | 32 | a0001c0002t0001g0056 a0001c0002t0003g0008 a0001c0004t0022g0107 others(29): Show |
32 | HG01123.hp2 HG01884.hp2 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.2493-1506G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906381 | |||||||
chr16:57906440 | G | A | 7 | a0001c0017t0001g0114 a0001c0017t0001g0139 a0001c0018t0001g0263 others(4): Show |
7 | HG01934.hp1 HG01978.hp2 HG02027.hp1 others(4): Show |
intron_variant | MODIFIER | c.2493-1565C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906440 | |||||||
chr16:57906442 | C | T | 2 | a0003c0104t0007g0232 a0040c0067t0002g0051 |
2 | HG03017.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2493-1567G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906442 | |||||||
chr16:57906443 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2493-1568C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906443 | |||||||
chr16:57906449 | T | C | 2 | a0002c0006t0021g0187 a0002c0114t0010g0357 |
2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2493-1574A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57906449 | |||||||
chr16:57907059 | C | T | 1 | a0015c0102t0003g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2493-2184G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907059 | |||||||
chr16:57907123 | G | A | 257 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(254): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.2493-2248C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907123 | |||||||
chr16:57907148 | C | T | 1 | a0001c0002t0001g0125 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2493-2273G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907148 | |||||||
chr16:57907166 | G | A | 19 | a0001c0001t0001g0207 a0001c0001t0002g0250 a0001c0001t0003g0208 others(16): Show |
19 | HG00099.hp2 HG00738.hp2 HG02015.hp1 others(16): Show |
intron_variant | MODIFIER | c.2493-2291C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907166 | |||||||
chr16:57907190 | T | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(216): Show |
222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.2493-2315A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907190 | |||||||
chr16:57907197 | C | A | 1 | a0015c0055t0025g0042 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2493-2322G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907197 | |||||||
chr16:57907264 | C | T | 2 | a0001c0016t0004g0313 a0001c0016t0010g0057 |
2 | HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2493-2389G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907264 | |||||||
chr16:57907373 | A | T | 1 | a0004c0036t0001g0355 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2493-2498T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907373 | |||||||
chr16:57907390 | T | TG | 29 | a0001c0042t0011g0029 a0009c0025t0001g0122 a0009c0025t0023g0077 others(26): Show |
29 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.2493-2516dupC | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907390 | |||||||
chr16:57907433 | T | A | 1 | a0001c0003t0003g0221 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2493-2558A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907433 | |||||||
chr16:57907434 | A | T | 1 | a0001c0003t0003g0221 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2493-2559T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907434 | |||||||
chr16:57907493 | C | T | 126 | a0001c0001t0001g0233 a0001c0002t0001g0032 a0001c0002t0001g0035 others(123): Show |
126 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.2493-2618G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907493 | |||||||
chr16:57907524 | T | A | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2493-2649A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57907524 | |||||||
chr16:57908034 | G | A | 2 | a0002c0005t0001g0024 a0002c0011t0018g0341 |
2 | HG02132.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2493-3159C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908034 | |||||||
chr16:57908068 | TTTTGTAG others(4): Show |
T | 7 | a0001c0002t0003g0008 a0001c0028t0044g0064 a0004c0061t0004g0049 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2493-3204_2493-319 others(15): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908068 | |||||||
chr16:57908088 | C | G | 220 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(217): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2493-3213G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908088 | |||||||
chr16:57908089 | C | T | 1 | a0037c0063t0020g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2493-3214G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908089 | |||||||
chr16:57908090 | C | T | 1 | a0004c0026t0004g0310 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2493-3215G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908090 | |||||||
chr16:57908211 | G | A | 1 | a0001c0003t0005g0240 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.2493-3336C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908211 | |||||||
chr16:57908228 | C | A | 37 | a0001c0002t0022g0062 a0001c0015t0002g0006 a0001c0027t0003g0058 others(34): Show |
37 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.2493-3353G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908228 | |||||||
chr16:57908329 | C | T | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2492+3424G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908329 | |||||||
chr16:57908505 | A | G | 5 | a0001c0007t0003g0004 a0001c0007t0004g0046 a0001c0028t0042g0069 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2492+3248T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908505 | |||||||
chr16:57908573 | T | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(217): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2492+3180A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908573 | |||||||
chr16:57908695 | C | T | 212 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(209): Show |
215 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(212): Show |
intron_variant | MODIFIER | c.2492+3058G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908695 | |||||||
chr16:57908721 | G | A | 4 | a0001c0002t0022g0062 a0003c0012t0007g0048 a0007c0119t0023g0091 others(1): Show |
4 | HG02280.hp1 HG02630.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2492+3032C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908721 | |||||||
chr16:57908808 | G | A | 165 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(162): Show |
168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.2492+2945C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908808 | |||||||
chr16:57908833 | G | A | 6 | a0001c0002t0003g0008 a0001c0028t0044g0064 a0004c0061t0004g0049 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2492+2920C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908833 | |||||||
chr16:57908886 | A | C | 1 | a0001c0002t0022g0062 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2492+2867T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908886 | |||||||
chr16:57908962 | C | A | 220 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(217): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2492+2791G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57908962 | |||||||
chr16:57909001 | T | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(217): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2492+2752A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909001 | |||||||
chr16:57909002 | G | A | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2492+2751C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909002 | |||||||
chr16:57909126 | G | A | 1 | a0029c0076t0003g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2492+2627C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909126 | |||||||
chr16:57909212 | G | A | 4 | a0002c0005t0005g0322 a0003c0008t0003g0145 a0003c0008t0009g0146 others(1): Show |
4 | HG00558.hp1 NA18980.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.2492+2541C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909212 | |||||||
chr16:57909216 | T | C | 220 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(217): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2492+2537A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909216 | |||||||
chr16:57909244 | A | G | 220 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(217): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2492+2509T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909244 | |||||||
chr16:57909372 | TTAAG | T | 14 | a0001c0007t0003g0004 a0001c0007t0004g0046 a0001c0016t0046g0054 others(11): Show |
14 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2492+2377_2492+238 others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909372 | |||||||
chr16:57909403 | CT | C | 11 | a0001c0002t0001g0035 a0001c0002t0002g0036 a0001c0002t0003g0031 others(8): Show |
11 | HG00438.hp1 HG00544.hp1 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.2492+2349delA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909403 | |||||||
chr16:57909413 | C | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(217): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2492+2340G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909413 | |||||||
chr16:57909462 | T | C | 16 | a0001c0001t0001g0207 a0001c0001t0001g0279 a0001c0001t0001g0280 others(13): Show |
16 | HG00099.hp2 HG00609.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.2492+2291A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909462 | |||||||
chr16:57909478 | C | T | 2 | a0006c0083t0043g0063 a0006c0085t0024g0209 |
2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2492+2275G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909478 | |||||||
chr16:57909491 | T | C | 1 | a0029c0076t0003g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2492+2262A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909491 | |||||||
chr16:57909494 | T | C | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2492+2259A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909494 | |||||||
chr16:57909576 | A | G | 6 | a0001c0016t0046g0054 a0002c0109t0004g0108 a0005c0014t0005g0346 others(3): Show |
6 | HG02145.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2492+2177T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909576 | |||||||
chr16:57909586 | G | A | 6 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0002g0273 others(3): Show |
6 | NA18947.hp1 NA18948.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.2492+2167C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909586 | |||||||
chr16:57909614 | C | A | 1 | a0029c0076t0003g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2492+2139G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909614 | |||||||
chr16:57909624 | T | A | 220 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(217): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2492+2129A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909624 | |||||||
chr16:57909760 | C | T | 6 | a0001c0002t0003g0008 a0001c0028t0044g0064 a0004c0061t0004g0049 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2492+1993G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909760 | |||||||
chr16:57909772 | T | C | 1 | a0001c0003t0012g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2492+1981A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909772 | |||||||
chr16:57909803 | C | T | 220 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(217): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.2492+1950G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909803 | |||||||
chr16:57909834 | C | A | 1 | a0001c0001t0002g0222 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2492+1919G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909834 | |||||||
chr16:57909923 | G | A | 205 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(202): Show |
208 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.2492+1830C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909923 | |||||||
chr16:57909942 | G | A | 1 | a0002c0006t0021g0187 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2492+1811C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57909942 | |||||||
chr16:57910038 | C | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(216): Show |
222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.2492+1715G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910038 | |||||||
chr16:57910252 | G | A | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2492+1501C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910252 | |||||||
chr16:57910313 | C | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(216): Show |
222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.2492+1440G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910313 | |||||||
chr16:57910318 | A | C | 188 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(185): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.2492+1435T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910318 | |||||||
chr16:57910411 | A | G | 228 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(225): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.2492+1342T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910411 | |||||||
chr16:57910462 | C | T | 188 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(185): Show |
191 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.2492+1291G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910462 | |||||||
chr16:57910519 | C | T | 8 | a0001c0001t0001g0234 a0001c0001t0007g0290 a0001c0001t0013g0251 others(5): Show |
8 | HG00639.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.2492+1234G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910519 | |||||||
chr16:57910555 | T | G | 216 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(213): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.2492+1198A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910555 | |||||||
chr16:57910561 | A | G | 1 | a0002c0022t0018g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2492+1192T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910561 | |||||||
chr16:57910571 | G | A | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2492+1182C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910571 | |||||||
chr16:57910601 | T | G | 2 | a0009c0032t0002g0269 a0012c0091t0007g0268 |
2 | HG01074.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.2492+1152A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910601 | |||||||
chr16:57910644 | G | A | 1 | a0001c0004t0001g0138 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2492+1109C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910644 | |||||||
chr16:57910667 | C | T | 35 | a0001c0002t0022g0062 a0001c0042t0011g0029 a0003c0012t0007g0048 others(32): Show |
35 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.2492+1086G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910667 | |||||||
chr16:57910672 | C | A | 1 | a0002c0114t0010g0357 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2492+1081G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910672 | |||||||
chr16:57910673 | C | CT | 164 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(161): Show |
167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.2492+1079dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910673 | |||||||
chr16:57910673 | C | CTT | 13 | a0001c0001t0001g0207 a0001c0001t0001g0279 a0001c0004t0001g0150 others(10): Show |
13 | HG00609.hp1 HG01175.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.2492+1078_2492+107 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910673 | |||||||
chr16:57910673 | C | CTTT | 6 | a0001c0016t0046g0054 a0002c0109t0004g0108 a0005c0014t0005g0346 others(3): Show |
6 | HG02145.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2492+1077_2492+107 others(7): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910673 | |||||||
chr16:57910673 | C | T | 1 | a0002c0006t0021g0187 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2492+1080G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910673 | |||||||
chr16:57910673 | CTTTT | C | 30 | a0001c0042t0011g0029 a0009c0025t0001g0122 a0009c0025t0023g0077 others(27): Show |
30 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.2492+1076_2492+107 others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910673 | |||||||
chr16:57910695 | T | C | 31 | a0001c0042t0011g0029 a0009c0025t0001g0122 a0009c0025t0023g0077 others(28): Show |
31 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2492+1058A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910695 | |||||||
chr16:57910707 | A | AT | 31 | a0001c0042t0011g0029 a0009c0025t0001g0122 a0009c0025t0023g0077 others(28): Show |
31 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2492+1045dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910707 | |||||||
chr16:57910709 | T | G | 1 | a0007c0039t0002g0086 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2492+1044A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910709 | |||||||
chr16:57910752 | A | T | 2 | a0002c0006t0021g0187 a0002c0114t0010g0357 |
2 | HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2492+1001T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910752 | |||||||
chr16:57910794 | T | A | 31 | a0001c0042t0011g0029 a0009c0025t0001g0122 a0009c0025t0023g0077 others(28): Show |
31 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2492+959A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910794 | |||||||
chr16:57910860 | A | G | 31 | a0001c0042t0011g0029 a0009c0025t0001g0122 a0009c0025t0023g0077 others(28): Show |
31 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.2492+893T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57910860 | |||||||
chr16:57911119 | A | G | 207 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(204): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.2492+634T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911119 | |||||||
chr16:57911131 | G | A | 9 | a0001c0017t0001g0114 a0001c0017t0001g0139 a0001c0017t0017g0033 others(6): Show |
9 | HG01934.hp1 HG01978.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.2492+622C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911131 | |||||||
chr16:57911177 | G | C | 206 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(203): Show |
209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.2492+576C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911177 | |||||||
chr16:57911186 | C | A | 1 | a0001c0003t0001g0278 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.2492+567G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911186 | |||||||
chr16:57911226 | C | T | 27 | a0001c0002t0001g0056 a0001c0004t0022g0107 a0001c0015t0001g0335 others(24): Show |
27 | HG01123.hp2 HG02055.hp2 HG02257.hp2 others(24): Show |
intron_variant | MODIFIER | c.2492+527G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911226 | |||||||
chr16:57911251 | G | A | 1 | a0001c0007t0008g0356 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2492+502C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911251 | |||||||
chr16:57911275 | A | G | 206 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(203): Show |
209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.2492+478T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911275 | |||||||
chr16:57911287 | C | T | 1 | a0001c0001t0001g0279 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2492+466G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911287 | |||||||
chr16:57911311 | A | G | 236 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(233): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.2492+442T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911311 | |||||||
chr16:57911364 | T | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(233): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.2492+389A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911364 | |||||||
chr16:57911374 | C | T | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2492+379G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911374 | |||||||
chr16:57911433 | T | C | 236 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(233): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.2492+320A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911433 | |||||||
chr16:57911455 | A | G | 1 | a0001c0003t0001g0199 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2492+298T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911455 | |||||||
chr16:57911456 | G | GTTTTTTT others(184): Show |
1 | a0001c0001t0001g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2492+296_2492+297i others(193): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911456 | |||||||
chr16:57911477 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2492+276A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911477 | |||||||
chr16:57911494 | G | A | 1 | a0001c0001t0001g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2492+259C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911494 | |||||||
chr16:57911509 | T | G | 1 | a0001c0001t0001g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2492+244A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911509 | |||||||
chr16:57911634 | G | A | 2 | a0001c0003t0002g0196 a0001c0003t0002g0228 |
2 | NA18939.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.2492+119C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911634 | |||||||
chr16:57911692 | C | T | 1 | a0001c0004t0002g0116 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2492+61G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911692 | |||||||
chr16:57911734 | G | C | 1 | a0001c0003t0002g0244 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2492+19C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 25/32 | chr16 | 57911734 | |||||||
chr16:57911909 | C | T | 1 | a0006c0083t0043g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2370-34G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57911909 | |||||||
chr16:57911973 | G | A | 2 | a0001c0004t0001g0166 a0002c0005t0001g0026 |
2 | NA18974.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.2370-98C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57911973 | |||||||
chr16:57912029 | G | A | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2370-154C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912029 | |||||||
chr16:57912056 | A | C | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2370-181T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912056 | |||||||
chr16:57912110 | ATG | A | 50 | a0001c0002t0001g0056 a0001c0002t0003g0008 a0001c0004t0022g0107 others(47): Show |
50 | HG01123.hp2 HG01884.hp2 HG01934.hp1 others(47): Show |
intron_variant | MODIFIER | c.2370-237_2370-236d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912110 | |||||||
chr16:57912174 | G | A | 49 | a0001c0002t0001g0056 a0001c0002t0003g0008 a0001c0004t0022g0107 others(46): Show |
49 | HG01123.hp2 HG01884.hp2 HG01934.hp1 others(46): Show |
intron_variant | MODIFIER | c.2370-299C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912174 | |||||||
chr16:57912410 | A | G | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2369+520T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912410 | |||||||
chr16:57912478 | C | T | 6 | a0001c0002t0003g0008 a0001c0028t0044g0064 a0004c0061t0004g0049 others(3): Show |
6 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2369+452G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912478 | |||||||
chr16:57912493 | C | T | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2369+437G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912493 | |||||||
chr16:57912571 | G | GTT | 4 | a0002c0109t0004g0108 a0002c0113t0003g0318 a0004c0026t0004g0310 others(1): Show |
4 | HG02630.hp1 HG03098.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.2369+357_2369+358d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912571 | |||||||
chr16:57912572 | T | TTG | 10 | a0002c0005t0001g0314 a0002c0005t0001g0316 a0002c0006t0001g0071 others(7): Show |
10 | HG00642.hp1 HG01109.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.2369+356_2369+357d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912572 | |||||||
chr16:57912572 | TTGTGTGT others(3): Show |
T | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2369+348_2369+357d others(12): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912572 | |||||||
chr16:57912574 | G | T | 46 | a0001c0002t0001g0056 a0001c0002t0003g0008 a0001c0004t0022g0107 others(43): Show |
46 | HG01123.hp2 HG01884.hp2 HG01934.hp1 others(43): Show |
intron_variant | MODIFIER | c.2369+356C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912574 | |||||||
chr16:57912584 | G | T | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2369+346C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912584 | |||||||
chr16:57912657 | T | C | 6 | a0001c0003t0005g0300 a0001c0004t0001g0174 a0001c0004t0003g0037 others(3): Show |
6 | HG02056.hp2 HG02071.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.2369+273A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912657 | |||||||
chr16:57912677 | G | C | 2 | a0001c0001t0012g0212 a0002c0022t0008g0011 |
2 | HG00140.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2369+253C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912677 | |||||||
chr16:57912680 | T | G | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2369+250A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912680 | |||||||
chr16:57912715 | G | A | 1 | a0001c0001t0001g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2369+215C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 24/32 | chr16 | 57912715 | |||||||
chr16:57913033 | A | T | 60 | a0001c0002t0001g0056 a0001c0002t0003g0008 a0001c0002t0022g0062 others(57): Show |
60 | HG01123.hp2 HG01884.hp2 HG01934.hp1 others(57): Show |
intron_variant | MODIFIER | c.2305-39T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913033 | |||||||
chr16:57913055 | G | A | 1 | a0001c0096t0002g0293 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2305-61C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913055 | |||||||
chr16:57913068 | G | A | 8 | a0001c0002t0001g0162 a0001c0002t0005g0160 a0001c0003t0001g0197 others(5): Show |
8 | NA18942.hp2 NA18957.hp2 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.2305-74C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913068 | |||||||
chr16:57913069 | A | G | 237 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(234): Show |
240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.2305-75T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913069 | |||||||
chr16:57913110 | C | T | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2305-116G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913110 | |||||||
chr16:57913276 | T | C | 61 | a0001c0002t0001g0056 a0001c0002t0003g0008 a0001c0002t0022g0062 others(58): Show |
61 | HG01123.hp2 HG01884.hp2 HG01934.hp1 others(58): Show |
intron_variant | MODIFIER | c.2305-282A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913276 | |||||||
chr16:57913402 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2305-408C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913402 | |||||||
chr16:57913474 | T | A | 60 | a0001c0002t0001g0056 a0001c0002t0003g0008 a0001c0002t0022g0062 others(57): Show |
60 | HG01123.hp2 HG01884.hp2 HG01934.hp1 others(57): Show |
intron_variant | MODIFIER | c.2305-480A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913474 | |||||||
chr16:57913619 | T | G | 49 | a0001c0002t0003g0008 a0001c0002t0022g0062 a0001c0004t0022g0107 others(46): Show |
49 | HG01123.hp2 HG01884.hp2 HG02055.hp1 others(46): Show |
intron_variant | MODIFIER | c.2305-625A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913619 | |||||||
chr16:57913640 | A | T | 59 | a0001c0002t0003g0008 a0001c0002t0022g0062 a0001c0004t0022g0107 others(56): Show |
59 | HG01123.hp2 HG01884.hp2 HG01934.hp1 others(56): Show |
intron_variant | MODIFIER | c.2305-646T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913640 | |||||||
chr16:57913828 | G | A | 1 | a0004c0030t0003g0001 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2305-834C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913828 | |||||||
chr16:57913853 | A | G | 1 | a0001c0003t0002g0191 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2305-859T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57913853 | |||||||
chr16:57914012 | T | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(174): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.2305-1018A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914012 | |||||||
chr16:57914070 | G | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(174): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.2305-1076C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914070 | |||||||
chr16:57914146 | A | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(174): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.2304+1103T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914146 | |||||||
chr16:57914154 | C | T | 1 | a0020c0095t0001g0193 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2304+1095G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914154 | |||||||
chr16:57914332 | T | C | 11 | a0001c0002t0003g0008 a0001c0007t0003g0004 a0001c0007t0004g0046 others(8): Show |
11 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2304+917A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914332 | |||||||
chr16:57914409 | G | A | 14 | a0001c0002t0003g0008 a0001c0007t0003g0004 a0001c0007t0004g0046 others(11): Show |
14 | HG01884.hp2 HG02055.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.2304+840C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914409 | |||||||
chr16:57914467 | C | T | 1 | a0001c0013t0001g0306 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2304+782G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914467 | |||||||
chr16:57914519 | C | T | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2304+730G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914519 | |||||||
chr16:57914639 | G | T | 47 | a0001c0002t0003g0008 a0001c0004t0022g0107 a0001c0007t0003g0004 others(44): Show |
47 | HG01123.hp2 HG01884.hp2 HG01934.hp1 others(44): Show |
intron_variant | MODIFIER | c.2304+610C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914639 | |||||||
chr16:57914708 | A | G | 1 | a0002c0006t0008g0084 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2304+541T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914708 | |||||||
chr16:57914917 | A | C | 1 | a0018c0060t0015g0005 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2304+332T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914917 | |||||||
chr16:57914933 | T | TG | 178 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(175): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.2304+315dupC | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914933 | |||||||
chr16:57914939 | G | A | 178 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(175): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.2304+310C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57914939 | |||||||
chr16:57915169 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2304+80C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 23/32 | chr16 | 57915169 | |||||||
chr16:57915347 | G | A | 182 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(179): Show |
185 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(182): Show |
intron_variant | MODIFIER | c.2218-12C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915347 | |||||||
chr16:57915370 | G | A | 1 | a0007c0039t0002g0305 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2218-35C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915370 | |||||||
chr16:57915456 | G | A | 2 | a0003c0009t0009g0287 a0045c0106t0002g0075 |
2 | NA19005.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2218-121C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915456 | |||||||
chr16:57915487 | C | T | 4 | a0001c0015t0002g0006 a0001c0027t0003g0058 a0004c0077t0004g0060 others(1): Show |
4 | HG02965.hp2 HG03579.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2218-152G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915487 | |||||||
chr16:57915552 | A | G | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2218-217T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915552 | |||||||
chr16:57915724 | C | T | 3 | a0001c0053t0004g0200 a0002c0109t0004g0108 a0013c0078t0011g0353 |
3 | HG02723.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2218-389G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915724 | |||||||
chr16:57915730 | C | G | 1 | a0001c0041t0005g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2218-395G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915730 | |||||||
chr16:57915770 | A | G | 1 | a0001c0001t0003g0223 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2217+359T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915770 | |||||||
chr16:57915779 | A | G | 276 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(273): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.2217+350T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915779 | |||||||
chr16:57915897 | C | CA | 79 | a0001c0001t0001g0003 a0001c0002t0001g0035 a0001c0002t0001g0039 others(76): Show |
80 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.2217+231dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915897 | |||||||
chr16:57915897 | C | CAA | 32 | a0001c0007t0003g0004 a0001c0007t0004g0046 a0001c0015t0002g0006 others(29): Show |
32 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.2217+230_2217+231d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915897 | |||||||
chr16:57915909 | A | AG | 5 | a0001c0002t0003g0008 a0001c0028t0044g0064 a0004c0061t0004g0049 others(2): Show |
5 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.2217+219_2217+220i others(3): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57915909 | |||||||
chr16:57916000 | C | T | 9 | a0002c0005t0001g0314 a0002c0005t0001g0316 a0007c0120t0003g0065 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.2217+129G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57916000 | |||||||
chr16:57916039 | A | G | 2 | a0009c0032t0006g0220 a0027c0092t0001g0285 |
2 | HG00280.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.2217+90T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57916039 | |||||||
chr16:57916101 | C | T | 1 | a0001c0007t0003g0340 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2217+28G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57916101 | |||||||
chr16:57916118 | C | T | 1 | a0011c0033t0001g0267 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2217+11G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 22/32 | chr16 | 57916118 | |||||||
chr16:57916220 | C | T | 1 | a0006c0086t0003g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2167-41G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57916220 | |||||||
chr16:57916274 | G | C | 275 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(272): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.2167-95C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57916274 | |||||||
chr16:57916366 | C | T | 126 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(123): Show |
126 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.2167-187G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57916366 | |||||||
chr16:57916590 | C | T | 5 | a0005c0045t0003g0342 a0005c0046t0036g0348 a0013c0031t0004g0333 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2167-411G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57916590 | |||||||
chr16:57916732 | G | A | 1 | a0002c0005t0001g0024 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2166+536C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57916732 | |||||||
chr16:57916748 | G | A | 1 | a0001c0013t0001g0306 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2166+520C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57916748 | |||||||
chr16:57916855 | C | T | 101 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(98): Show |
101 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.2166+413G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57916855 | |||||||
chr16:57916884 | G | T | 1 | a0001c0002t0002g0159 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2166+384C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57916884 | |||||||
chr16:57917081 | G | A | 100 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(97): Show |
100 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.2166+187C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57917081 | |||||||
chr16:57917202 | T | C | 4 | a0001c0003t0001g0253 a0001c0013t0004g0308 a0003c0009t0007g0080 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.2166+66A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57917202 | |||||||
chr16:57917212 | G | T | 1 | a0002c0006t0021g0187 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2166+56C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 21/32 | chr16 | 57917212 | |||||||
chr16:57917490 | T | G | 101 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(98): Show |
101 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.1958-14A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917490 | |||||||
chr16:57917514 | C | T | 13 | a0001c0002t0003g0008 a0001c0028t0044g0064 a0002c0005t0001g0314 others(10): Show |
13 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1958-38G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917514 | |||||||
chr16:57917517 | G | A | 135 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(132): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1958-41C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917517 | |||||||
chr16:57917597 | A | AGT | 144 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(141): Show |
147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.1958-123_1958-122d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917597 | |||||||
chr16:57917604 | G | GTGTA | 4 | a0001c0001t0005g0277 a0002c0005t0001g0314 a0002c0005t0001g0316 others(1): Show |
4 | HG02109.hp1 HG02809.hp2 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1958-129_1958-128i others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917604 | |||||||
chr16:57917606 | A | G | 109 | a0001c0001t0005g0277 a0001c0002t0001g0035 a0001c0002t0001g0039 others(106): Show |
109 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.1958-130T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917606 | |||||||
chr16:57917608 | G | A | 103 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(100): Show |
103 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1958-132C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917608 | |||||||
chr16:57917620 | G | A | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1958-144C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917620 | |||||||
chr16:57917620 | G | GTGTA | 9 | a0001c0002t0003g0008 a0001c0028t0044g0064 a0004c0061t0004g0049 others(6): Show |
9 | HG01109.hp2 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1958-145_1958-144i others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917620 | |||||||
chr16:57917620 | GTA | G | 3 | a0001c0053t0004g0200 a0002c0109t0004g0108 a0013c0078t0011g0353 |
3 | HG02723.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1958-146_1958-145d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917620 | |||||||
chr16:57917622 | A | G | 4 | a0001c0007t0003g0004 a0001c0028t0042g0069 a0002c0011t0004g0185 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1958-146T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917622 | |||||||
chr16:57917627 | T | C | 10 | a0001c0002t0003g0008 a0001c0028t0044g0064 a0002c0006t0021g0187 others(7): Show |
10 | HG01109.hp2 HG01884.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1958-151A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917627 | |||||||
chr16:57917627 | T | TACAC | 4 | a0002c0005t0001g0314 a0002c0005t0001g0316 a0023c0069t0001g0045 others(1): Show |
4 | HG01884.hp1 HG02109.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1958-155_1958-152d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917627 | |||||||
chr16:57917627 | TAC | T | 68 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(65): Show |
68 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1958-153_1958-152d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917627 | |||||||
chr16:57917627 | TACAC | T | 21 | a0001c0001t0002g0252 a0001c0001t0037g0246 a0001c0004t0001g0117 others(18): Show |
21 | HG00280.hp1 HG00735.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.1958-155_1958-152d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917627 | |||||||
chr16:57917627 | TACACACA others(3): Show |
T | 5 | a0005c0045t0003g0342 a0005c0046t0036g0348 a0013c0031t0004g0333 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1958-161_1958-152d others(12): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917627 | |||||||
chr16:57917629 | C | T | 14 | a0001c0003t0005g0300 a0001c0007t0003g0004 a0001c0017t0001g0114 others(11): Show |
14 | HG01934.hp1 HG02055.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.1958-153G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917629 | |||||||
chr16:57917631 | C | T | 36 | a0001c0003t0005g0300 a0001c0007t0003g0004 a0001c0015t0001g0335 others(33): Show |
36 | HG01123.hp2 HG01891.hp1 HG01934.hp1 others(33): Show |
intron_variant | MODIFIER | c.1958-155G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917631 | |||||||
chr16:57917633 | C | T | 18 | a0009c0025t0001g0122 a0009c0025t0023g0077 a0009c0032t0002g0269 others(15): Show |
18 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1958-157G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917633 | |||||||
chr16:57917635 | C | T | 18 | a0009c0025t0001g0122 a0009c0025t0023g0077 a0009c0032t0002g0269 others(15): Show |
18 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1958-159G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917635 | |||||||
chr16:57917639 | C | T | 5 | a0005c0045t0003g0342 a0005c0046t0036g0348 a0013c0031t0004g0333 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1958-163G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917639 | |||||||
chr16:57917742 | G | T | 2 | a0006c0083t0043g0063 a0006c0085t0024g0209 |
2 | HG02615.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1958-266C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917742 | |||||||
chr16:57917801 | TA | T | 154 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(151): Show |
157 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1958-326delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917801 | |||||||
chr16:57917955 | A | G | 2 | a0014c0118t0001g0302 a0022c0079t0006g0194 |
2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1958-479T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57917955 | |||||||
chr16:57918038 | C | CATGG | 29 | a0001c0001t0001g0003 a0001c0002t0001g0056 a0001c0002t0003g0008 others(26): Show |
30 | HG00280.hp1 HG00639.hp1 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.1958-566_1958-563d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918038 | |||||||
chr16:57918038 | C | CATGGATG others(1): Show |
6 | a0009c0054t0002g0044 a0010c0010t0008g0090 a0010c0010t0008g0102 others(3): Show |
6 | HG01515.hp2 HG01517.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1958-570_1958-563d others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918038 | |||||||
chr16:57918038 | CATGG | C | 40 | a0001c0002t0003g0038 a0001c0002t0003g0050 a0001c0002t0003g0113 others(37): Show |
40 | HG00099.hp1 HG00597.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.1958-566_1958-563d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918038 | |||||||
chr16:57918038 | CATGGATG others(5): Show |
C | 1 | a0001c0096t0002g0293 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1958-574_1958-563d others(14): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918038 | |||||||
chr16:57918038 | CATGGATG others(9): Show |
C | 1 | a0001c0003t0003g0198 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1958-578_1958-563d others(18): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918038 | |||||||
chr16:57918108 | G | GTTAT | 226 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(223): Show |
229 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.1958-636_1958-633d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918108 | |||||||
chr16:57918108 | G | GTTATTTA others(1): Show |
5 | a0001c0001t0005g0277 a0002c0005t0001g0101 a0002c0005t0009g0104 others(2): Show |
5 | HG01884.hp2 HG02735.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.1958-640_1958-633d others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918108 | |||||||
chr16:57918108 | GTTATTTA others(1): Show |
G | 44 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(41): Show |
44 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.1958-640_1958-633d others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918108 | |||||||
chr16:57918108 | GTTATTTA others(5): Show |
G | 1 | a0006c0085t0024g0209 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1958-644_1958-633d others(14): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918108 | |||||||
chr16:57918148 | C | T | 5 | a0005c0045t0003g0342 a0005c0046t0036g0348 a0013c0031t0004g0333 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1958-672G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918148 | |||||||
chr16:57918178 | T | G | 4 | a0001c0007t0003g0004 a0001c0028t0042g0069 a0002c0011t0004g0185 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1958-702A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918178 | |||||||
chr16:57918348 | G | A | 1 | a0013c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1957+751C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918348 | |||||||
chr16:57918368 | C | T | 1 | a0017c0110t0011g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1957+731G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918368 | |||||||
chr16:57918426 | C | T | 1 | a0002c0006t0021g0187 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1957+673G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918426 | |||||||
chr16:57918443 | C | A | 1 | a0001c0003t0012g0266 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1957+656G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918443 | |||||||
chr16:57918458 | A | C | 1 | a0011c0058t0004g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1957+641T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918458 | |||||||
chr16:57918520 | T | C | 1 | a0001c0001t0003g0311 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1957+579A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918520 | |||||||
chr16:57918557 | C | T | 1 | a0003c0074t0009g0177 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1957+542G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918557 | |||||||
chr16:57918601 | G | T | 1 | a0001c0003t0003g0265 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1957+498C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918601 | |||||||
chr16:57918652 | G | A | 1 | a0003c0064t0017g0179 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1957+447C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918652 | |||||||
chr16:57918773 | C | G | 2 | a0005c0014t0005g0346 a0005c0044t0004g0343 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1957+326G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918773 | |||||||
chr16:57918779 | A | G | 6 | a0001c0004t0002g0116 a0001c0004t0002g0156 a0001c0004t0005g0182 others(3): Show |
6 | NA18940.hp1 NA18955.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.1957+320T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918779 | |||||||
chr16:57918966 | A | G | 135 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(132): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1957+133T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57918966 | |||||||
chr16:57919031 | C | T | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1957+68G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 20/32 | chr16 | 57919031 | |||||||
chr16:57919410 | T | C | 170 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(167): Show |
173 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1802-156A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919410 | |||||||
chr16:57919476 | G | A | 34 | a0001c0003t0005g0300 a0001c0015t0001g0335 a0001c0015t0002g0006 others(31): Show |
34 | HG01123.hp2 HG01891.hp1 HG01934.hp1 others(31): Show |
intron_variant | MODIFIER | c.1802-222C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919476 | |||||||
chr16:57919549 | G | A | 7 | a0001c0002t0003g0008 a0001c0007t0003g0189 a0001c0028t0044g0064 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1802-295C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919549 | |||||||
chr16:57919581 | C | A | 18 | a0001c0002t0003g0008 a0001c0007t0003g0004 a0001c0007t0003g0189 others(15): Show |
18 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.1802-327G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919581 | |||||||
chr16:57919709 | A | T | 20 | a0009c0025t0001g0122 a0009c0025t0023g0077 a0009c0032t0002g0269 others(17): Show |
20 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1802-455T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919709 | |||||||
chr16:57919718 | T | A | 1 | a0003c0008t0002g0131 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1802-464A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919718 | |||||||
chr16:57919811 | G | T | 20 | a0009c0025t0001g0122 a0009c0025t0023g0077 a0009c0032t0002g0269 others(17): Show |
20 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1802-557C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919811 | |||||||
chr16:57919815 | A | G | 5 | a0001c0002t0003g0008 a0001c0028t0044g0064 a0004c0061t0004g0049 others(2): Show |
5 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1802-561T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919815 | |||||||
chr16:57919819 | T | C | 46 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(43): Show |
46 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1802-565A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919819 | |||||||
chr16:57919868 | C | T | 1 | a0015c0102t0003g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1801+519G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57919868 | |||||||
chr16:57920161 | G | C | 34 | a0001c0004t0035g0079 a0001c0015t0001g0335 a0001c0015t0002g0006 others(31): Show |
34 | HG01123.hp2 HG01891.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.1801+226C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57920161 | |||||||
chr16:57920218 | C | T | 4 | a0001c0007t0003g0004 a0001c0028t0042g0069 a0002c0011t0004g0185 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1801+169G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57920218 | |||||||
chr16:57920364 | A | G | 247 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(244): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.1801+23T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 19/32 | chr16 | 57920364 | |||||||
chr16:57920585 | A | C | 1 | a0003c0008t0002g0131 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1644-41T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57920585 | |||||||
chr16:57920621 | G | A | 10 | a0011c0033t0001g0249 a0011c0033t0001g0267 a0011c0058t0004g0140 others(7): Show |
10 | HG00280.hp2 HG00639.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.1644-77C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57920621 | |||||||
chr16:57920693 | C | T | 1 | a0001c0013t0018g0294 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1644-149G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57920693 | |||||||
chr16:57920892 | A | T | 1 | a0001c0001t0002g0309 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1644-348T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57920892 | |||||||
chr16:57920910 | G | A | 1 | a0020c0095t0001g0193 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1644-366C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57920910 | |||||||
chr16:57921082 | A | G | 42 | a0001c0002t0022g0062 a0001c0007t0004g0046 a0001c0015t0001g0335 others(39): Show |
42 | HG01123.hp2 HG01891.hp1 HG02055.hp2 others(39): Show |
intron_variant | MODIFIER | c.1644-538T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921082 | |||||||
chr16:57921125 | C | CT | 47 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(44): Show |
47 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(44): Show |
intron_variant | MODIFIER | c.1644-582dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921125 | |||||||
chr16:57921125 | CT | C | 7 | a0001c0016t0046g0054 a0001c0053t0004g0200 a0002c0109t0004g0108 others(4): Show |
7 | HG02145.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1644-582delA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921125 | |||||||
chr16:57921177 | T | G | 100 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(97): Show |
103 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.1644-633A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921177 | |||||||
chr16:57921196 | C | A | 30 | a0001c0002t0022g0062 a0001c0007t0004g0046 a0001c0015t0001g0335 others(27): Show |
30 | HG01123.hp2 HG01891.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1644-652G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921196 | |||||||
chr16:57921198 | G | A | 2 | a0001c0004t0022g0107 a0002c0022t0018g0112 |
2 | HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1644-654C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921198 | |||||||
chr16:57921217 | C | CT | 36 | a0001c0001t0002g0250 a0001c0002t0001g0181 a0001c0002t0002g0161 others(33): Show |
36 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(33): Show |
intron_variant | MODIFIER | c.1644-674dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921217 | |||||||
chr16:57921217 | CT | C | 78 | a0001c0001t0001g0226 a0001c0001t0006g0225 a0001c0001t0012g0212 others(75): Show |
78 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.1644-674delA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921217 | |||||||
chr16:57921317 | G | A | 20 | a0009c0025t0001g0122 a0009c0025t0023g0077 a0009c0032t0002g0269 others(17): Show |
20 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1644-773C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921317 | |||||||
chr16:57921370 | C | T | 29 | a0001c0002t0022g0062 a0001c0007t0004g0046 a0001c0015t0001g0335 others(26): Show |
29 | HG01123.hp2 HG01891.hp1 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.1644-826G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921370 | |||||||
chr16:57921452 | C | G | 1 | a0006c0086t0003g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1644-908G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921452 | |||||||
chr16:57921489 | T | C | 11 | a0001c0002t0001g0181 a0001c0003t0005g0300 a0001c0017t0001g0114 others(8): Show |
11 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1644-945A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921489 | |||||||
chr16:57921682 | A | G | 11 | a0001c0002t0001g0181 a0001c0003t0005g0300 a0001c0017t0001g0114 others(8): Show |
11 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1644-1138T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921682 | |||||||
chr16:57921709 | A | G | 36 | a0001c0002t0022g0062 a0001c0007t0004g0046 a0001c0015t0001g0335 others(33): Show |
36 | HG01123.hp2 HG01891.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1644-1165T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921709 | |||||||
chr16:57921788 | C | G | 36 | a0001c0002t0022g0062 a0001c0007t0004g0046 a0001c0015t0001g0335 others(33): Show |
36 | HG01123.hp2 HG01891.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.1644-1244G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921788 | |||||||
chr16:57921799 | G | A | 10 | a0001c0001t0001g0195 a0001c0001t0001g0275 a0001c0001t0001g0276 others(7): Show |
10 | HG00099.hp2 HG00738.hp2 NA18947.hp1 others(7): Show |
intron_variant | MODIFIER | c.1644-1255C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921799 | |||||||
chr16:57921850 | C | A | 1 | a0023c0069t0001g0045 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1644-1306G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921850 | |||||||
chr16:57921912 | A | G | 46 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(43): Show |
46 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1643+1361T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921912 | |||||||
chr16:57921986 | A | G | 1 | a0007c0115t0045g0111 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1643+1287T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57921986 | |||||||
chr16:57922021 | G | A | 1 | a0001c0004t0005g0182 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1643+1252C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922021 | |||||||
chr16:57922107 | G | A | 46 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(43): Show |
46 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.1643+1166C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922107 | |||||||
chr16:57922279 | G | T | 1 | a0001c0007t0003g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1643+994C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922279 | |||||||
chr16:57922289 | C | G | 258 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(255): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1643+984G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922289 | |||||||
chr16:57922327 | G | A | 34 | a0001c0002t0022g0062 a0001c0007t0004g0046 a0001c0015t0001g0335 others(31): Show |
34 | HG01123.hp2 HG01891.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.1643+946C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922327 | |||||||
chr16:57922413 | C | CTCTT | 118 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(115): Show |
121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.1643+856_1643+859d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922413 | |||||||
chr16:57922413 | CTCTT | C | 6 | a0001c0007t0003g0340 a0003c0040t0038g0203 a0005c0048t0016g0354 others(3): Show |
6 | HG02523.hp1 HG02572.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1643+856_1643+859d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922413 | |||||||
chr16:57922427 | C | CT | 4 | a0001c0007t0003g0189 a0001c0053t0004g0200 a0002c0109t0004g0108 others(1): Show |
4 | HG02723.hp1 HG02723.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1643+845dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922427 | |||||||
chr16:57922427 | C | CTTT | 12 | a0001c0002t0022g0062 a0001c0007t0004g0046 a0001c0042t0011g0029 others(9): Show |
12 | HG02145.hp2 HG02257.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1643+843_1643+845d others(5): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922427 | |||||||
chr16:57922427 | C | CTTTTT | 16 | a0001c0015t0001g0335 a0001c0015t0002g0006 a0001c0015t0020g0336 others(13): Show |
16 | HG01123.hp2 HG02055.hp2 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1643+845_1643+846i others(7): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922427 | |||||||
chr16:57922431 | C | CT | 7 | a0001c0003t0001g0199 a0001c0003t0001g0282 a0001c0003t0003g0283 others(4): Show |
7 | HG01515.hp1 HG02895.hp1 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.1643+841dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922431 | |||||||
chr16:57922431 | C | CTTTTT | 11 | a0001c0002t0001g0181 a0001c0003t0005g0300 a0001c0017t0001g0114 others(8): Show |
11 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1643+837_1643+841d others(7): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922431 | |||||||
chr16:57922431 | C | T | 38 | a0001c0002t0022g0062 a0001c0007t0003g0189 a0001c0007t0004g0046 others(35): Show |
38 | HG01123.hp2 HG01891.hp1 HG02055.hp2 others(35): Show |
intron_variant | MODIFIER | c.1643+842G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922431 | |||||||
chr16:57922709 | A | G | 39 | a0001c0002t0022g0062 a0001c0004t0035g0079 a0001c0007t0004g0046 others(36): Show |
39 | HG01123.hp2 HG01891.hp1 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.1643+564T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922709 | |||||||
chr16:57922711 | G | A | 3 | a0001c0053t0004g0200 a0002c0109t0004g0108 a0013c0078t0011g0353 |
3 | HG02723.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1643+562C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922711 | |||||||
chr16:57922771 | C | T | 1 | a0004c0030t0003g0001 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1643+502G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922771 | |||||||
chr16:57922839 | C | T | 4 | a0001c0007t0002g0073 a0002c0006t0021g0187 a0002c0011t0016g0190 others(1): Show |
4 | HG02965.hp1 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1643+434G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922839 | |||||||
chr16:57922863 | C | CT | 47 | a0001c0001t0002g0309 a0001c0002t0001g0181 a0001c0002t0022g0062 others(44): Show |
47 | HG01123.hp2 HG01891.hp1 HG01934.hp1 others(44): Show |
intron_variant | MODIFIER | c.1643+409dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57922863 | |||||||
chr16:57923050 | G | A | 7 | a0001c0002t0003g0008 a0001c0007t0003g0189 a0001c0028t0044g0064 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1643+223C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57923050 | |||||||
chr16:57923090 | A | T | 37 | a0001c0002t0022g0062 a0001c0007t0004g0046 a0001c0015t0001g0335 others(34): Show |
37 | HG01123.hp2 HG01891.hp1 HG02055.hp2 others(34): Show |
intron_variant | MODIFIER | c.1643+183T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57923090 | |||||||
chr16:57923165 | A | C | 1 | a0002c0005t0001g0087 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1643+108T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57923165 | |||||||
chr16:57923214 | C | T | 20 | a0009c0025t0001g0122 a0009c0025t0023g0077 a0009c0032t0002g0269 others(17): Show |
20 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.1643+59G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57923214 | |||||||
chr16:57923218 | A | G | 2 | a0014c0118t0001g0302 a0022c0079t0006g0194 |
2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1643+55T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57923218 | |||||||
chr16:57923229 | T | TC | 11 | a0001c0002t0001g0181 a0001c0003t0005g0300 a0001c0017t0001g0114 others(8): Show |
11 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1643+43dupG | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57923229 | |||||||
chr16:57923234 | G | C | 258 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(255): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1643+39C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57923234 | |||||||
chr16:57923235 | C | T | 7 | a0001c0002t0003g0008 a0001c0007t0003g0189 a0001c0028t0044g0064 others(4): Show |
7 | HG01884.hp2 HG02559.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1643+38G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57923235 | |||||||
chr16:57923259 | CA | C | 22 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(19): Show |
22 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.1643+13delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 18/32 | chr16 | 57923259 | |||||||
chr16:57923545 | C | T | 11 | a0001c0002t0001g0181 a0001c0003t0005g0300 a0001c0017t0001g0114 others(8): Show |
11 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1536-165G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57923545 | |||||||
chr16:57923882 | C | T | 1 | a0001c0042t0011g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1536-502G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57923882 | |||||||
chr16:57923897 | C | A | 1 | a0001c0001t0013g0251 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1536-517G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57923897 | |||||||
chr16:57924027 | A | G | 2 | a0014c0118t0001g0302 a0022c0079t0006g0194 |
2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1536-647T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57924027 | |||||||
chr16:57924255 | C | T | 57 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(54): Show |
57 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.1536-875G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57924255 | |||||||
chr16:57924540 | A | G | 5 | a0005c0045t0003g0342 a0005c0046t0036g0348 a0013c0031t0004g0333 others(2): Show |
5 | HG02896.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.1536-1160T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57924540 | |||||||
chr16:57924620 | A | G | 1 | a0015c0055t0025g0042 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1536-1240T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57924620 | |||||||
chr16:57924660 | AC | A | 5 | a0001c0002t0003g0008 a0001c0028t0044g0064 a0004c0061t0004g0049 others(2): Show |
5 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1536-1281delG | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57924660 | |||||||
chr16:57924683 | T | C | 2 | a0001c0004t0022g0107 a0002c0022t0018g0112 |
2 | HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1536-1303A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57924683 | |||||||
chr16:57924693 | C | T | 7 | a0001c0016t0046g0054 a0001c0053t0004g0200 a0002c0109t0004g0108 others(4): Show |
7 | HG02145.hp2 HG02257.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1536-1313G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57924693 | |||||||
chr16:57924952 | G | C | 1 | a0037c0063t0020g0009 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1536-1572C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57924952 | |||||||
chr16:57924966 | G | A | 1 | a0001c0002t0001g0155 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1536-1586C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57924966 | |||||||
chr16:57925079 | T | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(216): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1536-1699A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925079 | |||||||
chr16:57925146 | G | T | 1 | a0001c0002t0001g0125 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1536-1766C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925146 | |||||||
chr16:57925191 | T | C | 58 | a0001c0002t0022g0062 a0001c0007t0004g0046 a0001c0015t0001g0335 others(55): Show |
58 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(55): Show |
intron_variant | MODIFIER | c.1536-1811A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925191 | |||||||
chr16:57925196 | T | A | 1 | a0001c0001t0001g0205 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1536-1816A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925196 | |||||||
chr16:57925223 | A | G | 60 | a0001c0002t0022g0062 a0001c0004t0035g0079 a0001c0007t0003g0004 others(57): Show |
60 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(57): Show |
intron_variant | MODIFIER | c.1536-1843T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925223 | |||||||
chr16:57925334 | G | A | 66 | a0001c0002t0001g0181 a0001c0002t0003g0008 a0001c0002t0022g0062 others(63): Show |
66 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(63): Show |
intron_variant | MODIFIER | c.1536-1954C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925334 | |||||||
chr16:57925433 | G | A | 4 | a0001c0028t0044g0064 a0004c0061t0004g0049 a0016c0023t0002g0347 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536-2053C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925433 | |||||||
chr16:57925471 | G | A | 2 | a0001c0004t0035g0079 a0002c0022t0002g0074 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1536-2091C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925471 | |||||||
chr16:57925499 | C | T | 1 | a0001c0013t0019g0213 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1536-2119G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925499 | |||||||
chr16:57925500 | G | A | 1 | a0002c0037t0003g0023 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1536-2120C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925500 | |||||||
chr16:57925689 | A | T | 4 | a0001c0007t0002g0073 a0002c0006t0021g0187 a0002c0011t0016g0190 others(1): Show |
4 | HG02965.hp1 HG02976.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536-2309T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925689 | |||||||
chr16:57925700 | T | TC | 87 | a0001c0001t0001g0003 a0001c0001t0001g0226 a0001c0001t0001g0237 others(84): Show |
90 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.1536-2321_1536-232 others(5): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925700 | |||||||
chr16:57925765 | G | A | 1 | a0004c0077t0004g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1536-2385C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925765 | |||||||
chr16:57925915 | T | A | 4 | a0001c0028t0044g0064 a0004c0061t0004g0049 a0016c0023t0002g0347 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536-2535A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925915 | |||||||
chr16:57925964 | C | A | 249 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(246): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.1536-2584G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925964 | |||||||
chr16:57925978 | G | A | 1 | a0025c0108t0004g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1536-2598C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57925978 | |||||||
chr16:57926253 | C | A | 1 | a0001c0004t0022g0107 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1536-2873G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926253 | |||||||
chr16:57926324 | C | T | 24 | a0001c0002t0022g0062 a0001c0007t0003g0004 a0001c0007t0004g0046 others(21): Show |
24 | HG02055.hp1 HG02280.hp1 HG02559.hp2 others(21): Show |
intron_variant | MODIFIER | c.1536-2944G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926324 | |||||||
chr16:57926341 | T | G | 4 | a0001c0002t0001g0181 a0001c0018t0002g0254 a0002c0006t0002g0096 others(1): Show |
4 | HG02074.hp1 NA18945.hp2 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536-2961A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926341 | |||||||
chr16:57926351 | G | A | 8 | a0001c0053t0004g0200 a0002c0113t0003g0318 a0004c0026t0004g0310 others(5): Show |
8 | HG02280.hp2 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1536-2971C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926351 | |||||||
chr16:57926380 | G | T | 95 | a0001c0001t0001g0003 a0001c0001t0001g0226 a0001c0001t0001g0237 others(92): Show |
98 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1536-3000C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926380 | |||||||
chr16:57926595 | C | T | 92 | a0001c0001t0001g0195 a0001c0001t0001g0205 a0001c0001t0001g0207 others(89): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(89): Show |
intron_variant | MODIFIER | c.1536-3215G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926595 | |||||||
chr16:57926633 | A | G | 34 | a0001c0002t0003g0008 a0001c0015t0001g0335 a0001c0015t0020g0336 others(31): Show |
34 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1536-3253T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926633 | |||||||
chr16:57926715 | T | C | 42 | a0001c0002t0003g0008 a0001c0002t0007g0126 a0001c0015t0001g0335 others(39): Show |
42 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.1536-3335A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926715 | |||||||
chr16:57926737 | T | C | 1 | a0001c0002t0001g0162 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1536-3357A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926737 | |||||||
chr16:57926910 | G | A | 1 | a0002c0005t0009g0104 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1536-3530C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926910 | |||||||
chr16:57926921 | A | G | 1 | a0003c0012t0007g0048 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1536-3541T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926921 | |||||||
chr16:57926932 | A | ACCATTG | 6 | a0001c0053t0004g0200 a0002c0109t0004g0108 a0005c0014t0005g0346 others(3): Show |
6 | HG02145.hp2 HG02257.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1536-3558_1536-355 others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926932 | |||||||
chr16:57926971 | C | T | 1 | a0001c0002t0002g0157 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1536-3591G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57926971 | |||||||
chr16:57927154 | A | G | 1 | a0001c0004t0001g0117 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1536-3774T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927154 | |||||||
chr16:57927189 | G | A | 2 | a0001c0007t0003g0340 a0009c0032t0002g0269 |
2 | HG03486.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1536-3809C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927189 | |||||||
chr16:57927368 | C | T | 1 | a0003c0009t0039g0307 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1536-3988G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927368 | |||||||
chr16:57927403 | C | A | 2 | a0011c0033t0001g0267 a0021c0117t0026g0186 |
2 | HG00741.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1536-4023G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927403 | |||||||
chr16:57927411 | T | A | 4 | a0001c0028t0044g0064 a0004c0061t0004g0049 a0016c0023t0002g0347 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1536-4031A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927411 | |||||||
chr16:57927522 | T | C | 3 | a0001c0028t0044g0064 a0016c0023t0002g0347 a0016c0023t0002g0349 |
3 | HG01884.hp2 HG02559.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1536-4142A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927522 | |||||||
chr16:57927746 | C | A | 32 | a0001c0002t0003g0008 a0001c0015t0001g0335 a0001c0015t0020g0336 others(29): Show |
32 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1535+3970G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927746 | |||||||
chr16:57927777 | C | T | 3 | a0001c0002t0001g0056 a0001c0027t0003g0058 a0004c0077t0004g0060 |
3 | HG03209.hp1 HG03579.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1535+3939G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927777 | |||||||
chr16:57927842 | C | T | 32 | a0001c0002t0003g0008 a0001c0015t0001g0335 a0001c0015t0020g0336 others(29): Show |
32 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.1535+3874G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927842 | |||||||
chr16:57927867 | G | C | 1 | a0003c0074t0009g0177 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1535+3849C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927867 | |||||||
chr16:57927903 | G | A | 8 | a0001c0027t0040g0078 a0001c0028t0044g0064 a0001c0053t0004g0200 others(5): Show |
8 | HG01884.hp2 HG02559.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1535+3813C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57927903 | |||||||
chr16:57928158 | C | T | 88 | a0001c0001t0001g0195 a0001c0001t0001g0205 a0001c0001t0001g0234 others(85): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.1535+3558G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57928158 | |||||||
chr16:57928583 | G | C | 2 | a0001c0007t0003g0340 a0033c0051t0001g0339 |
2 | HG03139.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1535+3133C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57928583 | |||||||
chr16:57928647 | T | G | 115 | a0001c0001t0001g0195 a0001c0001t0001g0205 a0001c0001t0001g0207 others(112): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.1535+3069A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57928647 | |||||||
chr16:57928729 | G | C | 15 | a0001c0001t0001g0226 a0001c0001t0006g0225 a0001c0004t0005g0127 others(12): Show |
16 | HG00423.hp1 HG00558.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.1535+2987C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57928729 | |||||||
chr16:57928905 | C | A | 8 | a0002c0005t0001g0314 a0002c0005t0001g0316 a0007c0120t0003g0065 others(5): Show |
8 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1535+2811G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57928905 | |||||||
chr16:57928919 | A | G | 1 | a0001c0053t0004g0200 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1535+2797T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57928919 | |||||||
chr16:57928989 | G | A | 1 | a0011c0033t0001g0249 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1535+2727C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57928989 | |||||||
chr16:57929178 | G | A | 15 | a0001c0002t0022g0062 a0001c0004t0022g0107 a0001c0007t0004g0046 others(12): Show |
15 | HG02280.hp1 HG02630.hp2 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.1535+2538C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929178 | |||||||
chr16:57929262 | G | A | 5 | a0001c0007t0003g0004 a0001c0015t0002g0006 a0001c0028t0042g0069 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1535+2454C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929262 | |||||||
chr16:57929268 | T | G | 11 | a0001c0002t0001g0181 a0001c0003t0005g0300 a0001c0004t0005g0182 others(8): Show |
11 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1535+2448A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929268 | |||||||
chr16:57929277 | C | A | 2 | a0001c0053t0004g0200 a0002c0109t0004g0108 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1535+2439G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929277 | |||||||
chr16:57929308 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1535+2408T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929308 | |||||||
chr16:57929337 | T | A | 1 | a0001c0018t0001g0263 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1535+2379A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929337 | |||||||
chr16:57929476 | G | GGAGAGAG others(1): Show |
216 | a0001c0001t0001g0195 a0001c0001t0001g0205 a0001c0001t0001g0207 others(213): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.1535+2232_1535+223 others(12): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929476 | |||||||
chr16:57929476 | G | GGAGAGAG others(3): Show |
5 | a0001c0007t0003g0004 a0001c0015t0002g0006 a0001c0028t0042g0069 others(2): Show |
5 | HG02055.hp2 HG02559.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1535+2230_1535+223 others(14): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929476 | |||||||
chr16:57929476 | G | GGAGAGAG others(5): Show |
4 | a0001c0015t0001g0335 a0001c0015t0020g0336 a0002c0011t0004g0185 others(1): Show |
4 | HG02055.hp1 HG02257.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1535+2228_1535+223 others(16): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929476 | |||||||
chr16:57929514 | A | G | 109 | a0001c0001t0001g0195 a0001c0001t0001g0205 a0001c0001t0001g0207 others(106): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.1535+2202T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929514 | |||||||
chr16:57929654 | C | A | 1 | a0001c0002t0001g0052 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1535+2062G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929654 | |||||||
chr16:57929710 | T | C | 6 | a0001c0007t0003g0189 a0002c0113t0003g0318 a0004c0026t0004g0310 others(3): Show |
6 | HG02630.hp1 HG02723.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1535+2006A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929710 | |||||||
chr16:57929818 | C | T | 1 | a0001c0002t0001g0162 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1535+1898G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929818 | |||||||
chr16:57929932 | T | A | 109 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(106): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.1535+1784A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929932 | |||||||
chr16:57929935 | A | G | 5 | a0001c0053t0004g0200 a0002c0109t0004g0108 a0005c0014t0005g0346 others(2): Show |
5 | HG02145.hp2 HG02257.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1535+1781T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57929935 | |||||||
chr16:57930074 | G | C | 143 | a0001c0001t0005g0277 a0001c0002t0001g0035 a0001c0002t0001g0039 others(140): Show |
143 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(140): Show |
intron_variant | MODIFIER | c.1535+1642C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930074 | |||||||
chr16:57930184 | A | T | 11 | a0001c0002t0022g0062 a0001c0004t0022g0107 a0001c0007t0004g0046 others(8): Show |
11 | HG02280.hp1 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1535+1532T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930184 | |||||||
chr16:57930185 | T | A | 5 | a0001c0007t0003g0004 a0001c0015t0002g0006 a0001c0028t0042g0069 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1535+1531A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930185 | |||||||
chr16:57930194 | A | C | 1 | a0001c0001t0001g0207 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1535+1522T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930194 | |||||||
chr16:57930247 | G | A | 1 | a0048c0050t0003g0352 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1535+1469C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930247 | |||||||
chr16:57930388 | G | A | 1 | a0001c0027t0040g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1535+1328C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930388 | |||||||
chr16:57930403 | G | A | 3 | a0001c0003t0003g0265 a0001c0003t0003g0296 a0001c0003t0012g0266 |
3 | HG00733.hp2 HG01496.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1535+1313C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930403 | |||||||
chr16:57930457 | G | A | 11 | a0001c0002t0001g0181 a0001c0003t0005g0300 a0001c0004t0005g0182 others(8): Show |
11 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1535+1259C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930457 | |||||||
chr16:57930496 | A | G | 1 | a0004c0100t0002g0231 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1535+1220T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930496 | |||||||
chr16:57930525 | A | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0207 a0001c0001t0001g0279 others(175): Show |
179 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(176): Show |
intron_variant | MODIFIER | c.1535+1191T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930525 | |||||||
chr16:57930538 | G | A | 11 | a0001c0002t0001g0181 a0001c0003t0005g0300 a0001c0004t0005g0182 others(8): Show |
11 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1535+1178C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930538 | |||||||
chr16:57930575 | G | C | 1 | a0001c0029t0002g0034 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1535+1141C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930575 | |||||||
chr16:57930582 | G | A | 1 | a0001c0001t0002g0250 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1535+1134C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930582 | |||||||
chr16:57930611 | T | G | 1 | a0044c0071t0006g0148 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1535+1105A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930611 | |||||||
chr16:57930702 | A | G | 2 | a0011c0058t0004g0140 a0011c0059t0001g0123 |
2 | HG00741.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.1535+1014T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930702 | |||||||
chr16:57930941 | G | A | 4 | a0001c0015t0002g0006 a0001c0028t0042g0069 a0002c0011t0004g0185 others(1): Show |
4 | HG02055.hp1 HG02559.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1535+775C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930941 | |||||||
chr16:57930999 | A | G | 11 | a0001c0002t0001g0181 a0001c0003t0005g0300 a0001c0004t0005g0182 others(8): Show |
11 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1535+717T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57930999 | |||||||
chr16:57931010 | T | A | 1 | a0001c0003t0005g0240 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1535+706A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57931010 | |||||||
chr16:57931011 | A | T | 1 | a0019c0090t0010g0219 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1535+705T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57931011 | |||||||
chr16:57931253 | A | C | 10 | a0001c0002t0001g0181 a0001c0003t0005g0300 a0001c0004t0005g0182 others(7): Show |
10 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.1535+463T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57931253 | |||||||
chr16:57931261 | T | C | 1 | a0011c0058t0004g0140 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1535+455A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57931261 | |||||||
chr16:57931264 | T | C | 1 | a0002c0022t0002g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1535+452A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57931264 | |||||||
chr16:57931351 | C | T | 2 | a0014c0118t0001g0302 a0022c0079t0006g0194 |
2 | HG00639.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1535+365G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57931351 | |||||||
chr16:57931392 | C | T | 3 | a0001c0001t0001g0226 a0001c0001t0006g0225 a0003c0008t0002g0120 |
3 | NA18959.hp2 NA18986.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1535+324G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57931392 | |||||||
chr16:57931541 | G | T | 4 | a0001c0001t0001g0236 a0001c0001t0001g0262 a0001c0001t0002g0252 others(1): Show |
4 | NA18972.hp1 NA18980.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1535+175C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 17/32 | chr16 | 57931541 | |||||||
chr16:57931881 | G | T | 2 | a0003c0104t0007g0232 a0040c0067t0002g0051 |
2 | HG03017.hp2 HG04228.hp2 |
splice_region_variant&intron_variant | LOW | c.1373-3C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57931881 | |||||||
chr16:57931889 | G | T | 10 | a0001c0002t0001g0181 a0001c0003t0005g0300 a0001c0004t0005g0182 others(7): Show |
10 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.1373-11C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57931889 | |||||||
chr16:57931938 | C | T | 7 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0002g0273 others(4): Show |
7 | NA18947.hp1 NA18948.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.1373-60G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57931938 | |||||||
chr16:57932014 | C | A | 3 | a0001c0053t0004g0200 a0002c0109t0004g0108 a0025c0108t0004g0061 |
3 | HG02257.hp1 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1373-136G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932014 | |||||||
chr16:57932036 | G | T | 13 | a0001c0015t0001g0335 a0001c0015t0020g0336 a0001c0016t0046g0054 others(10): Show |
13 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1373-158C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932036 | |||||||
chr16:57932219 | A | G | 2 | a0001c0007t0003g0189 a0018c0062t0027g0324 |
2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1373-341T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932219 | |||||||
chr16:57932250 | C | A | 51 | a0001c0001t0001g0237 a0001c0001t0005g0277 a0001c0002t0001g0035 others(48): Show |
52 | HG00544.hp1 HG00609.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.1373-372G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932250 | |||||||
chr16:57932262 | C | T | 1 | a0001c0013t0019g0213 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1373-384G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932262 | |||||||
chr16:57932400 | C | CT | 36 | a0001c0002t0003g0008 a0001c0004t0001g0117 a0001c0004t0001g0150 others(33): Show |
36 | HG00280.hp1 HG00642.hp2 HG01069.hp2 others(33): Show |
intron_variant | MODIFIER | c.1373-523dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932400 | |||||||
chr16:57932400 | CT | C | 13 | a0001c0003t0005g0300 a0001c0003t0006g0288 a0001c0004t0005g0182 others(10): Show |
13 | HG01934.hp1 HG02080.hp1 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.1373-523delA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932400 | |||||||
chr16:57932400 | CTT | C | 55 | a0001c0001t0001g0237 a0001c0001t0005g0277 a0001c0002t0001g0035 others(52): Show |
56 | HG00544.hp1 HG00609.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1373-524_1373-523d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932400 | |||||||
chr16:57932400 | CTTTTTTT others(3): Show |
C | 1 | a0002c0006t0008g0084 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1373-532_1373-523d others(12): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932400 | |||||||
chr16:57932551 | C | T | 1 | a0003c0105t0014g0298 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1373-673G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932551 | |||||||
chr16:57932684 | C | A | 4 | a0001c0001t0001g0236 a0001c0001t0001g0262 a0001c0001t0002g0252 others(1): Show |
4 | NA18972.hp1 NA18980.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1373-806G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932684 | |||||||
chr16:57932723 | G | A | 5 | a0001c0004t0035g0079 a0002c0005t0001g0101 a0002c0022t0002g0074 others(2): Show |
5 | HG02109.hp2 HG02735.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1373-845C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932723 | |||||||
chr16:57932772 | G | A | 13 | a0001c0015t0001g0335 a0001c0015t0020g0336 a0001c0016t0046g0054 others(10): Show |
13 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1373-894C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932772 | |||||||
chr16:57932832 | G | A | 4 | a0001c0002t0003g0008 a0009c0054t0002g0044 a0017c0112t0024g0010 others(1): Show |
4 | HG02486.hp2 HG03195.hp2 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1373-954C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932832 | |||||||
chr16:57932909 | T | C | 5 | a0001c0004t0035g0079 a0002c0005t0001g0101 a0002c0022t0002g0074 others(2): Show |
5 | HG02109.hp2 HG02735.hp1 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1373-1031A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932909 | |||||||
chr16:57932932 | G | T | 10 | a0001c0002t0001g0181 a0001c0003t0005g0300 a0001c0004t0005g0182 others(7): Show |
10 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.1373-1054C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932932 | |||||||
chr16:57932935 | G | A | 49 | a0001c0001t0001g0237 a0001c0001t0005g0277 a0001c0002t0001g0035 others(46): Show |
50 | HG00544.hp1 HG00609.hp2 HG00733.hp1 others(47): Show |
intron_variant | MODIFIER | c.1373-1057C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932935 | |||||||
chr16:57932939 | G | A | 1 | a0001c0003t0001g0248 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1373-1061C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932939 | |||||||
chr16:57932980 | T | C | 1 | a0027c0092t0001g0285 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1373-1102A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57932980 | |||||||
chr16:57933224 | G | A | 1 | a0007c0120t0003g0065 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1373-1346C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933224 | |||||||
chr16:57933288 | T | C | 73 | a0001c0002t0001g0056 a0001c0002t0001g0181 a0001c0002t0003g0008 others(70): Show |
73 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(70): Show |
intron_variant | MODIFIER | c.1373-1410A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933288 | |||||||
chr16:57933314 | T | C | 290 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(287): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1373-1436A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933314 | |||||||
chr16:57933315 | C | T | 4 | a0002c0113t0003g0318 a0004c0026t0004g0310 a0006c0081t0021g0331 others(1): Show |
4 | HG02630.hp1 HG03098.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1373-1437G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933315 | |||||||
chr16:57933682 | A | G | 13 | a0001c0015t0001g0335 a0001c0015t0020g0336 a0001c0016t0046g0054 others(10): Show |
13 | HG02145.hp2 HG02257.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1373-1804T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933682 | |||||||
chr16:57933724 | C | CT | 14 | a0001c0016t0004g0313 a0002c0005t0001g0101 a0002c0005t0001g0314 others(11): Show |
14 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1373-1847dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933724 | |||||||
chr16:57933724 | C | CTT | 9 | a0001c0002t0001g0181 a0001c0004t0005g0182 a0001c0017t0001g0114 others(6): Show |
9 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.1373-1848_1373-184 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933724 | |||||||
chr16:57933724 | CT | C | 246 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(243): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1373-1847delA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933724 | |||||||
chr16:57933754 | G | A | 3 | a0001c0007t0003g0189 a0013c0078t0011g0353 a0018c0062t0027g0324 |
3 | HG02723.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1373-1876C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933754 | |||||||
chr16:57933795 | T | A | 3 | a0006c0082t0010g0337 a0015c0055t0025g0042 a0047c0056t0011g0047 |
3 | HG01123.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1373-1917A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57933795 | |||||||
chr16:57934004 | T | C | 2 | a0002c0006t0003g0022 a0031c0094t0002g0295 |
2 | HG01109.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.1373-2126A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934004 | |||||||
chr16:57934028 | G | A | 4 | a0002c0113t0003g0318 a0004c0026t0004g0310 a0006c0081t0021g0331 others(1): Show |
4 | HG02630.hp1 HG03098.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1373-2150C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934028 | |||||||
chr16:57934389 | G | A | 3 | a0001c0017t0001g0114 a0001c0017t0001g0139 a0003c0064t0017g0179 |
3 | HG01934.hp1 NA18939.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.1373-2511C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934389 | |||||||
chr16:57934413 | C | T | 1 | a0038c0093t0001g0258 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1373-2535G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934413 | |||||||
chr16:57934576 | T | C | 1 | a0017c0110t0011g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1373-2698A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934576 | |||||||
chr16:57934695 | G | A | 1 | a0013c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1373-2817C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934695 | |||||||
chr16:57934788 | C | G | 1 | a0001c0002t0007g0126 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1373-2910G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934788 | |||||||
chr16:57934854 | G | A | 2 | a0001c0003t0003g0296 a0001c0003t0012g0266 |
2 | HG00733.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1373-2976C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934854 | |||||||
chr16:57934881 | C | T | 10 | a0001c0002t0001g0181 a0001c0003t0005g0300 a0001c0004t0005g0182 others(7): Show |
10 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.1373-3003G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934881 | |||||||
chr16:57934913 | C | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0279 a0001c0001t0001g0280 others(22): Show |
26 | HG00609.hp1 HG02015.hp1 HG02027.hp2 others(23): Show |
intron_variant | MODIFIER | c.1373-3035G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934913 | |||||||
chr16:57934956 | C | A | 1 | a0002c0011t0018g0341 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1373-3078G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934956 | |||||||
chr16:57934956 | C | CA | 79 | a0001c0001t0002g0252 a0001c0002t0001g0056 a0001c0002t0002g0157 others(76): Show |
79 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(76): Show |
intron_variant | MODIFIER | c.1373-3079dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57934956 | |||||||
chr16:57935036 | A | T | 10 | a0001c0002t0001g0181 a0001c0003t0005g0300 a0001c0004t0005g0182 others(7): Show |
10 | HG01934.hp1 HG02074.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.1373-3158T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935036 | |||||||
chr16:57935062 | A | G | 1 | a0038c0093t0001g0258 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1373-3184T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935062 | |||||||
chr16:57935103 | G | A | 3 | a0001c0016t0004g0313 a0001c0016t0010g0057 a0004c0026t0004g0059 |
3 | HG01891.hp1 HG02572.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1373-3225C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935103 | |||||||
chr16:57935112 | C | A | 5 | a0001c0007t0003g0004 a0001c0015t0002g0006 a0001c0028t0042g0069 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1373-3234G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935112 | |||||||
chr16:57935402 | G | A | 1 | a0011c0033t0001g0267 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1373-3524C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935402 | |||||||
chr16:57935572 | C | T | 1 | a0015c0102t0003g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1373-3694G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935572 | |||||||
chr16:57935605 | G | A | 1 | a0015c0102t0003g0271 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1373-3727C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935605 | |||||||
chr16:57935642 | C | T | 5 | a0001c0007t0003g0189 a0001c0019t0019g0286 a0001c0019t0019g0299 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1373-3764G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935642 | |||||||
chr16:57935652 | C | A | 2 | a0001c0004t0001g0118 a0001c0029t0002g0163 |
2 | NA18982.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.1373-3774G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935652 | |||||||
chr16:57935653 | A | C | 88 | a0001c0001t0001g0237 a0001c0001t0005g0277 a0001c0002t0001g0035 others(85): Show |
89 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.1373-3775T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935653 | |||||||
chr16:57935756 | C | CT | 70 | a0001c0002t0001g0181 a0001c0002t0003g0008 a0001c0002t0022g0062 others(67): Show |
70 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(67): Show |
intron_variant | MODIFIER | c.1372+3673dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935756 | |||||||
chr16:57935756 | C | CTT | 11 | a0001c0002t0001g0056 a0001c0007t0003g0340 a0001c0016t0004g0313 others(8): Show |
11 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.1372+3672_1372+367 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57935756 | |||||||
chr16:57936014 | A | G | 1 | a0001c0004t0001g0117 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1372+3416T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936014 | |||||||
chr16:57936047 | G | A | 13 | a0001c0004t0035g0079 a0001c0053t0004g0200 a0002c0005t0001g0314 others(10): Show |
13 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1372+3383C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936047 | |||||||
chr16:57936168 | G | A | 3 | a0001c0004t0035g0079 a0002c0022t0002g0074 a0002c0114t0010g0357 |
3 | HG02109.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1372+3262C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936168 | |||||||
chr16:57936367 | G | A | 9 | a0002c0005t0001g0314 a0002c0005t0001g0316 a0002c0109t0004g0108 others(6): Show |
9 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1372+3063C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936367 | |||||||
chr16:57936610 | T | G | 2 | a0001c0003t0003g0198 a0001c0003t0006g0284 |
2 | HG00408.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.1372+2820A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936610 | |||||||
chr16:57936652 | C | T | 1 | a0001c0027t0040g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1372+2778G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936652 | |||||||
chr16:57936653 | G | A | 8 | a0001c0001t0001g0234 a0001c0001t0007g0290 a0001c0001t0013g0251 others(5): Show |
8 | HG00639.hp2 HG00735.hp2 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.1372+2777C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936653 | |||||||
chr16:57936675 | C | T | 1 | a0001c0027t0040g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1372+2755G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936675 | |||||||
chr16:57936799 | C | A | 3 | a0001c0007t0003g0189 a0015c0102t0003g0271 a0018c0062t0027g0324 |
3 | HG02723.hp1 HG03486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1372+2631G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936799 | |||||||
chr16:57936799 | C | CA | 65 | a0001c0001t0001g0237 a0001c0001t0005g0277 a0001c0002t0001g0035 others(62): Show |
66 | HG00544.hp1 HG00609.hp2 HG00733.hp1 others(63): Show |
intron_variant | MODIFIER | c.1372+2630dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936799 | |||||||
chr16:57936799 | C | CAA | 23 | a0001c0002t0003g0008 a0001c0015t0001g0335 a0001c0015t0020g0336 others(20): Show |
23 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.1372+2629_1372+263 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936799 | |||||||
chr16:57936801 | A | AAC | 37 | a0001c0002t0001g0056 a0001c0002t0022g0062 a0001c0004t0022g0107 others(34): Show |
37 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1372+2628_1372+262 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936801 | |||||||
chr16:57936961 | A | G | 133 | a0001c0001t0001g0237 a0001c0001t0005g0277 a0001c0002t0001g0035 others(130): Show |
134 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.1372+2469T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57936961 | |||||||
chr16:57937154 | C | T | 1 | a0001c0001t0002g0312 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1372+2276G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57937154 | |||||||
chr16:57937281 | A | G | 309 | a0001c0001t0001g0195 a0001c0001t0001g0205 a0001c0001t0001g0207 others(306): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.1372+2149T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57937281 | |||||||
chr16:57937709 | T | C | 1 | a0001c0013t0001g0306 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1372+1721A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57937709 | |||||||
chr16:57937716 | G | A | 1 | a0001c0001t0001g0236 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1372+1714C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57937716 | |||||||
chr16:57938017 | C | T | 124 | a0001c0001t0001g0237 a0001c0001t0002g0312 a0001c0001t0005g0277 others(121): Show |
125 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.1372+1413G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938017 | |||||||
chr16:57938042 | G | C | 1 | a0002c0022t0002g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1372+1388C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938042 | |||||||
chr16:57938045 | C | T | 14 | a0001c0004t0022g0107 a0001c0007t0003g0189 a0001c0053t0004g0200 others(11): Show |
14 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1372+1385G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938045 | |||||||
chr16:57938254 | T | C | 73 | a0001c0001t0001g0237 a0001c0001t0002g0312 a0001c0001t0005g0277 others(70): Show |
74 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1372+1176A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938254 | |||||||
chr16:57938382 | G | C | 7 | a0001c0002t0001g0056 a0001c0007t0003g0189 a0001c0027t0003g0058 others(4): Show |
7 | HG01891.hp1 HG02723.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1372+1048C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938382 | |||||||
chr16:57938388 | T | C | 1 | a0043c0075t0001g0144 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1372+1042A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938388 | |||||||
chr16:57938416 | C | T | 1 | a0013c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1372+1014G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938416 | |||||||
chr16:57938596 | G | A | 1 | a0006c0083t0043g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1372+834C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938596 | |||||||
chr16:57938643 | TG | T | 10 | a0001c0004t0022g0107 a0002c0005t0001g0314 a0002c0005t0001g0316 others(7): Show |
10 | HG01109.hp2 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1372+786delC | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938643 | |||||||
chr16:57938736 | G | A | 4 | a0009c0032t0002g0269 a0009c0032t0006g0220 a0012c0091t0007g0268 others(1): Show |
4 | HG00280.hp1 HG01074.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1372+694C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57938736 | |||||||
chr16:57939013 | C | T | 1 | a0001c0001t0037g0246 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1372+417G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57939013 | |||||||
chr16:57939099 | A | T | 2 | a0004c0061t0004g0049 a0016c0023t0002g0347 |
2 | HG01884.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1372+331T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57939099 | |||||||
chr16:57939164 | T | C | 87 | a0001c0001t0001g0003 a0001c0001t0001g0207 a0001c0001t0001g0237 others(84): Show |
89 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.1372+266A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57939164 | |||||||
chr16:57939173 | G | C | 1 | a0006c0086t0003g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1372+257C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57939173 | |||||||
chr16:57939237 | T | A | 1 | a0002c0114t0010g0357 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1372+193A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57939237 | |||||||
chr16:57939315 | G | C | 1 | a0001c0066t0001g0130 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1372+115C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 16/32 | chr16 | 57939315 | |||||||
chr16:57940020 | C | T | 4 | a0002c0006t0001g0095 a0002c0006t0001g0100 a0002c0038t0003g0094 others(1): Show |
4 | NA18959.hp1 NA18984.hp1 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.1209+214G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 15/32 | chr16 | 57940020 | |||||||
chr16:57940085 | G | A | 108 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(105): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(106): Show |
intron_variant | MODIFIER | c.1209+149C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 15/32 | chr16 | 57940085 | |||||||
chr16:57940173 | C | T | 1 | a0002c0005t0001g0101 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1209+61G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 15/32 | chr16 | 57940173 | |||||||
chr16:57940336 | G | A | 143 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(140): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1122-15C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940336 | |||||||
chr16:57940339 | G | A | 2 | a0001c0007t0003g0189 a0018c0062t0027g0324 |
2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1122-18C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940339 | |||||||
chr16:57940371 | TA | T | 4 | a0001c0007t0003g0340 a0001c0007t0008g0356 a0002c0011t0004g0185 others(1): Show |
4 | HG01168.hp1 HG02055.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-51delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940371 | |||||||
chr16:57940418 | G | A | 4 | a0001c0007t0003g0340 a0001c0007t0008g0356 a0002c0011t0004g0185 others(1): Show |
4 | HG01168.hp1 HG02055.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1122-97C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940418 | |||||||
chr16:57940490 | C | A | 1 | a0001c0002t0002g0121 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1122-169G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940490 | |||||||
chr16:57940534 | C | A | 3 | a0001c0007t0002g0073 a0005c0014t0005g0346 a0005c0044t0004g0343 |
3 | HG02145.hp2 HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1122-213G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940534 | |||||||
chr16:57940711 | A | G | 1 | a0002c0006t0008g0084 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1122-390T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940711 | |||||||
chr16:57940775 | A | G | 12 | a0001c0001t0007g0290 a0001c0001t0012g0212 a0001c0002t0001g0329 others(9): Show |
12 | HG00140.hp2 HG00642.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1122-454T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940775 | |||||||
chr16:57940781 | C | A | 10 | a0001c0002t0001g0056 a0001c0007t0003g0340 a0001c0007t0008g0356 others(7): Show |
10 | HG01168.hp1 HG01891.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1122-460G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940781 | |||||||
chr16:57940838 | C | T | 2 | a0002c0005t0001g0101 a0002c0037t0003g0092 |
2 | HG02735.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1122-517G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940838 | |||||||
chr16:57940895 | G | C | 1 | a0005c0045t0003g0342 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1122-574C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940895 | |||||||
chr16:57940937 | G | A | 26 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(23): Show |
26 | HG00544.hp1 HG00609.hp2 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.1122-616C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940937 | |||||||
chr16:57940972 | C | T | 3 | a0001c0013t0018g0294 a0004c0098t0003g0241 a0015c0102t0003g0271 |
3 | HG02145.hp1 HG03041.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1122-651G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57940972 | |||||||
chr16:57941035 | G | T | 1 | a0013c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1122-714C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941035 | |||||||
chr16:57941274 | C | T | 1 | a0013c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1122-953G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941274 | |||||||
chr16:57941276 | A | C | 1 | a0001c0003t0006g0218 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1122-955T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941276 | |||||||
chr16:57941311 | G | A | 40 | a0001c0001t0001g0207 a0001c0001t0002g0250 a0001c0001t0003g0208 others(37): Show |
40 | HG00099.hp2 HG00423.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1122-990C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941311 | |||||||
chr16:57941493 | C | T | 1 | a0001c0066t0001g0130 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1122-1172G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941493 | |||||||
chr16:57941598 | T | C | 1 | a0001c0003t0001g0197 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1122-1277A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941598 | |||||||
chr16:57941657 | T | C | 17 | a0001c0007t0003g0004 a0001c0015t0002g0006 a0002c0006t0006g0323 others(14): Show |
17 | HG00423.hp2 HG02559.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1122-1336A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941657 | |||||||
chr16:57941661 | C | T | 13 | a0002c0006t0006g0323 a0005c0014t0001g0345 a0005c0014t0016g0326 others(10): Show |
13 | HG00423.hp2 HG02559.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1122-1340G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941661 | |||||||
chr16:57941674 | C | A | 31 | a0001c0002t0001g0056 a0001c0007t0003g0004 a0001c0007t0003g0189 others(28): Show |
31 | HG00423.hp2 HG01891.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.1122-1353G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941674 | |||||||
chr16:57941713 | G | T | 7 | a0002c0005t0001g0314 a0002c0005t0001g0316 a0002c0006t0016g0110 others(4): Show |
7 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1122-1392C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941713 | |||||||
chr16:57941720 | G | A | 36 | a0001c0002t0001g0056 a0001c0007t0003g0004 a0001c0007t0003g0189 others(33): Show |
36 | HG00423.hp2 HG01168.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.1122-1399C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941720 | |||||||
chr16:57941819 | T | C | 3 | a0001c0041t0005g0028 a0002c0109t0004g0108 a0028c0080t0015g0188 |
3 | HG02055.hp2 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1122-1498A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941819 | |||||||
chr16:57941836 | TTTTA | T | 6 | a0001c0007t0004g0046 a0001c0028t0044g0064 a0001c0042t0011g0029 others(3): Show |
6 | HG01884.hp1 HG02896.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1122-1519_1122-151 others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941836 | |||||||
chr16:57941863 | T | C | 1 | a0001c0003t0002g0191 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1122-1542A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57941863 | |||||||
chr16:57942014 | G | T | 1 | a0002c0011t0004g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1122-1693C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942014 | |||||||
chr16:57942028 | T | TGTTTG | 3 | a0001c0041t0005g0028 a0002c0109t0004g0108 a0028c0080t0015g0188 |
3 | HG02055.hp2 HG02280.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1122-1712_1122-170 others(9): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942028 | |||||||
chr16:57942256 | G | A | 1 | a0006c0083t0043g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1122-1935C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942256 | |||||||
chr16:57942429 | T | C | 1 | a0001c0004t0001g0119 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1122-2108A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942429 | |||||||
chr16:57942561 | G | A | 14 | a0001c0002t0001g0032 a0002c0006t0006g0323 a0005c0014t0001g0345 others(11): Show |
14 | HG00423.hp2 HG01169.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.1122-2240C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942561 | |||||||
chr16:57942563 | C | T | 30 | a0001c0002t0001g0056 a0001c0007t0003g0340 a0001c0007t0008g0356 others(27): Show |
30 | HG00423.hp2 HG01168.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.1122-2242G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942563 | |||||||
chr16:57942653 | G | A | 6 | a0001c0002t0001g0056 a0001c0016t0010g0057 a0001c0027t0003g0058 others(3): Show |
6 | HG01891.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1122-2332C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942653 | |||||||
chr16:57942682 | C | T | 13 | a0002c0006t0006g0323 a0005c0014t0001g0345 a0005c0014t0016g0326 others(10): Show |
13 | HG00423.hp2 HG02559.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1122-2361G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942682 | |||||||
chr16:57942862 | C | CA | 28 | a0001c0001t0013g0251 a0001c0002t0005g0154 a0001c0004t0001g0117 others(25): Show |
28 | HG00423.hp2 HG00735.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.1122-2542dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942862 | |||||||
chr16:57942862 | CA | C | 7 | a0001c0004t0002g0178 a0001c0029t0002g0034 a0002c0005t0003g0106 others(4): Show |
7 | HG02055.hp1 HG02723.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.1122-2542delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942862 | |||||||
chr16:57942862 | CAA | C | 32 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(29): Show |
32 | HG00544.hp1 HG00609.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.1122-2543_1122-254 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942862 | |||||||
chr16:57942870 | A | G | 1 | a0001c0013t0001g0306 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1122-2549T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942870 | |||||||
chr16:57942893 | T | C | 2 | a0001c0028t0042g0069 a0041c0047t0034g0350 |
2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1122-2572A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942893 | |||||||
chr16:57942952 | A | G | 6 | a0001c0007t0003g0004 a0001c0015t0002g0006 a0001c0016t0046g0054 others(3): Show |
6 | HG02559.hp2 HG02622.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1122-2631T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57942952 | |||||||
chr16:57943123 | A | G | 1 | a0013c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1122-2802T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57943123 | |||||||
chr16:57943243 | G | A | 26 | a0001c0001t0012g0212 a0001c0003t0001g0214 a0001c0003t0003g0215 others(23): Show |
26 | HG00140.hp2 HG00423.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.1122-2922C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57943243 | |||||||
chr16:57943348 | C | CGT | 6 | a0001c0007t0003g0340 a0001c0007t0008g0356 a0001c0015t0001g0335 others(3): Show |
6 | HG01168.hp1 HG02257.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1122-3028_1122-302 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57943348 | |||||||
chr16:57943437 | C | T | 1 | a0001c0001t0017g0224 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1122-3116G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57943437 | |||||||
chr16:57943546 | T | C | 1 | a0001c0041t0005g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1122-3225A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57943546 | |||||||
chr16:57943854 | G | A | 12 | a0002c0005t0001g0098 a0002c0005t0003g0106 a0002c0005t0006g0097 others(9): Show |
12 | NA18940.hp2 NA18945.hp2 NA18959.hp1 others(9): Show |
intron_variant | MODIFIER | c.1122-3533C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57943854 | |||||||
chr16:57943921 | T | C | 1 | a0002c0038t0010g0103 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1122-3600A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57943921 | |||||||
chr16:57944036 | T | C | 3 | a0001c0002t0003g0008 a0002c0011t0004g0066 a0002c0022t0002g0074 |
3 | HG02647.hp2 NA19030.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1122-3715A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944036 | |||||||
chr16:57944077 | G | A | 63 | a0001c0002t0001g0039 a0001c0002t0001g0052 a0001c0002t0001g0056 others(60): Show |
63 | HG00423.hp2 HG00738.hp1 HG01168.hp1 others(60): Show |
intron_variant | MODIFIER | c.1122-3756C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944077 | |||||||
chr16:57944343 | AAGGAG | A | 3 | a0001c0007t0002g0073 a0005c0014t0005g0346 a0005c0044t0004g0343 |
3 | HG02145.hp2 HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1122-4027_1122-402 others(9): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944343 | |||||||
chr16:57944633 | C | T | 1 | a0001c0041t0005g0028 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1122-4312G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944633 | |||||||
chr16:57944737 | T | C | 17 | a0001c0002t0001g0056 a0001c0007t0003g0004 a0001c0007t0003g0189 others(14): Show |
17 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1122-4416A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944737 | |||||||
chr16:57944744 | C | T | 2 | a0001c0016t0046g0054 a0029c0076t0003g0055 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1122-4423G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944744 | |||||||
chr16:57944786 | T | A | 1 | a0001c0003t0003g0198 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1122-4465A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944786 | |||||||
chr16:57944825 | A | G | 21 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(18): Show |
21 | HG00544.hp1 HG00609.hp2 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.1122-4504T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944825 | |||||||
chr16:57944916 | T | G | 1 | a0002c0006t0006g0323 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1121+4437A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944916 | |||||||
chr16:57944951 | T | TA | 74 | a0001c0001t0001g0237 a0001c0001t0003g0208 a0001c0001t0006g0242 others(71): Show |
74 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.1121+4401dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944951 | |||||||
chr16:57944951 | T | TAA | 14 | a0001c0002t0001g0162 a0001c0002t0001g0329 a0001c0004t0005g0182 others(11): Show |
14 | HG01081.hp2 HG01175.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1121+4400_1121+440 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944951 | |||||||
chr16:57944951 | TA | T | 11 | a0001c0001t0002g0252 a0001c0003t0001g0278 a0001c0003t0003g0296 others(8): Show |
11 | HG01070.hp1 HG01496.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1121+4401delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944951 | |||||||
chr16:57944951 | TAAAAAAA | T | 36 | a0001c0004t0001g0153 a0002c0005t0001g0015 a0002c0005t0001g0016 others(33): Show |
36 | HG00323.hp2 HG00639.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.1121+4395_1121+440 others(11): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57944951 | |||||||
chr16:57945241 | A | G | 2 | a0001c0003t0005g0300 a0001c0018t0001g0297 |
2 | HG02080.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.1121+4112T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945241 | |||||||
chr16:57945316 | T | C | 1 | a0004c0061t0004g0049 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1121+4037A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945316 | |||||||
chr16:57945351 | G | C | 4 | a0001c0007t0003g0004 a0001c0015t0002g0006 a0018c0060t0015g0005 others(1): Show |
4 | HG02559.hp2 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1121+4002C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945351 | |||||||
chr16:57945428 | G | A | 1 | a0002c0011t0004g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1121+3925C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945428 | |||||||
chr16:57945508 | T | C | 1 | a0013c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1121+3845A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945508 | |||||||
chr16:57945615 | G | C | 30 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(27): Show |
30 | HG00544.hp1 HG00609.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.1121+3738C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945615 | |||||||
chr16:57945692 | A | G | 8 | a0002c0005t0001g0314 a0002c0005t0001g0316 a0002c0006t0016g0110 others(5): Show |
8 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1121+3661T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945692 | |||||||
chr16:57945733 | C | T | 16 | a0002c0011t0004g0185 a0002c0109t0004g0108 a0005c0014t0001g0345 others(13): Show |
16 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.1121+3620G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945733 | |||||||
chr16:57945789 | G | A | 1 | a0001c0003t0012g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1121+3564C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945789 | |||||||
chr16:57945877 | G | T | 17 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(14): Show |
17 | HG00544.hp1 HG00609.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1121+3476C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57945877 | |||||||
chr16:57946004 | A | T | 7 | a0001c0001t0001g0234 a0001c0001t0002g0250 a0001c0001t0013g0251 others(4): Show |
7 | HG00639.hp2 HG00735.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121+3349T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946004 | |||||||
chr16:57946006 | G | T | 3 | a0001c0001t0001g0205 a0001c0001t0001g0233 a0001c0003t0002g0245 |
3 | HG02015.hp2 NA18747.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1121+3347C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946006 | |||||||
chr16:57946106 | G | T | 1 | a0001c0007t0003g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1121+3247C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946106 | |||||||
chr16:57946260 | T | G | 8 | a0006c0081t0021g0331 a0006c0082t0010g0337 a0006c0083t0043g0063 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1121+3093A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946260 | |||||||
chr16:57946347 | G | A | 1 | a0001c0001t0002g0309 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1121+3006C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946347 | |||||||
chr16:57946387 | G | A | 1 | a0026c0121t0011g0315 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1121+2966C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946387 | |||||||
chr16:57946398 | C | T | 31 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(28): Show |
31 | HG00544.hp1 HG00609.hp2 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.1121+2955G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946398 | |||||||
chr16:57946424 | C | T | 1 | a0025c0108t0004g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1121+2929G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946424 | |||||||
chr16:57946449 | G | A | 2 | a0008c0020t0007g0007 a0025c0108t0004g0061 |
2 | HG01891.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1121+2904C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946449 | |||||||
chr16:57946680 | C | T | 1 | a0002c0006t0013g0083 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1121+2673G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946680 | |||||||
chr16:57946800 | G | T | 12 | a0001c0001t0007g0290 a0001c0001t0012g0212 a0001c0002t0001g0329 others(9): Show |
12 | HG00140.hp2 HG00642.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.1121+2553C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946800 | |||||||
chr16:57946876 | T | C | 8 | a0006c0081t0021g0331 a0006c0082t0010g0337 a0006c0083t0043g0063 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1121+2477A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946876 | |||||||
chr16:57946907 | G | A | 1 | a0001c0007t0003g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1121+2446C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946907 | |||||||
chr16:57946962 | C | T | 1 | a0021c0117t0026g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1121+2391G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57946962 | |||||||
chr16:57947101 | G | C | 3 | a0001c0004t0001g0166 a0002c0005t0001g0024 a0002c0005t0001g0026 |
3 | HG02132.hp1 NA18974.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1121+2252C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947101 | |||||||
chr16:57947123 | C | A | 1 | a0001c0029t0002g0163 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1121+2230G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947123 | |||||||
chr16:57947145 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1121+2208T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947145 | |||||||
chr16:57947162 | A | ATG | 8 | a0006c0081t0021g0331 a0006c0082t0010g0337 a0006c0083t0043g0063 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1121+2189_1121+219 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947162 | |||||||
chr16:57947314 | G | T | 1 | a0025c0108t0004g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1121+2039C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947314 | |||||||
chr16:57947331 | G | A | 1 | a0046c0107t0006g0099 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1121+2022C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947331 | |||||||
chr16:57947411 | T | G | 1 | a0002c0005t0006g0089 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1121+1942A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947411 | |||||||
chr16:57947452 | G | A | 3 | a0001c0004t0003g0136 a0001c0004t0008g0135 a0001c0070t0007g0134 |
3 | HG00099.hp2 HG00738.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1121+1901C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947452 | |||||||
chr16:57947488 | A | G | 1 | a0001c0004t0001g0119 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1121+1865T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947488 | |||||||
chr16:57947981 | T | G | 1 | a0039c0072t0001g0137 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1121+1372A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57947981 | |||||||
chr16:57948051 | C | T | 1 | a0001c0003t0001g0199 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1121+1302G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948051 | |||||||
chr16:57948053 | C | T | 1 | a0001c0004t0001g0117 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1121+1300G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948053 | |||||||
chr16:57948174 | A | C | 174 | a0001c0001t0001g0207 a0001c0001t0003g0208 a0001c0001t0013g0206 others(171): Show |
174 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.1121+1179T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948174 | |||||||
chr16:57948179 | A | G | 1 | a0001c0029t0002g0163 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1121+1174T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948179 | |||||||
chr16:57948220 | C | T | 1 | a0028c0080t0015g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1121+1133G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948220 | |||||||
chr16:57948252 | T | C | 12 | a0005c0014t0001g0345 a0005c0014t0005g0346 a0005c0014t0016g0326 others(9): Show |
12 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.1121+1101A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948252 | |||||||
chr16:57948256 | A | G | 1 | a0002c0006t0021g0187 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1121+1097T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948256 | |||||||
chr16:57948313 | CTTCTT | C | 30 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(27): Show |
30 | HG00544.hp1 HG00609.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.1121+1035_1121+103 others(9): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948313 | |||||||
chr16:57948316 | CTT | C | 250 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(247): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.1121+1035_1121+103 others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948316 | |||||||
chr16:57948319 | T | C | 2 | a0003c0008t0003g0145 a0003c0008t0009g0146 |
2 | HG00558.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1121+1034A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948319 | |||||||
chr16:57948321 | T | C | 7 | a0001c0001t0002g0238 a0001c0003t0001g0227 a0001c0003t0002g0196 others(4): Show |
7 | NA18939.hp2 NA18943.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.1121+1032A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948321 | |||||||
chr16:57948407 | G | A | 8 | a0001c0002t0001g0056 a0001c0016t0010g0057 a0001c0027t0003g0058 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1121+946C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948407 | |||||||
chr16:57948432 | G | A | 91 | a0001c0001t0001g0207 a0001c0001t0003g0208 a0001c0001t0013g0206 others(88): Show |
91 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1121+921C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948432 | |||||||
chr16:57948533 | C | G | 3 | a0001c0007t0003g0004 a0001c0015t0002g0006 a0018c0060t0015g0005 |
3 | HG02559.hp2 HG02895.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1121+820G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948533 | |||||||
chr16:57948562 | C | A | 1 | a0003c0008t0002g0002 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1121+791G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948562 | |||||||
chr16:57948693 | C | T | 1 | a0001c0001t0007g0290 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1121+660G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948693 | |||||||
chr16:57948740 | A | G | 138 | a0001c0001t0001g0207 a0001c0001t0003g0208 a0001c0001t0013g0206 others(135): Show |
138 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.1121+613T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948740 | |||||||
chr16:57948755 | G | A | 2 | a0010c0010t0008g0090 a0010c0010t0008g0102 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1121+598C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948755 | |||||||
chr16:57948833 | G | A | 1 | a0002c0011t0004g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1121+520C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57948833 | |||||||
chr16:57949054 | G | A | 1 | a0001c0002t0003g0031 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1121+299C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57949054 | |||||||
chr16:57949131 | T | TG | 5 | a0001c0003t0001g0270 a0001c0004t0001g0138 a0004c0026t0004g0310 others(2): Show |
5 | HG01891.hp2 HG02015.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1121+221dupC | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57949131 | |||||||
chr16:57949133 | T | A | 1 | a0008c0020t0007g0007 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1121+220A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57949133 | |||||||
chr16:57949133 | T | G | 277 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(274): Show |
278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.1121+220A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57949133 | |||||||
chr16:57949134 | G | C | 5 | a0001c0002t0001g0040 a0001c0003t0001g0199 a0001c0013t0018g0294 others(2): Show |
5 | HG00609.hp2 HG01515.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1121+219C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57949134 | |||||||
chr16:57949324 | G | A | 2 | a0001c0004t0001g0117 a0035c0057t0002g0147 |
2 | HG03239.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1121+29C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 14/32 | chr16 | 57949324 | |||||||
chr16:57949447 | G | A | 2 | a0013c0031t0004g0333 a0013c0031t0004g0334 |
2 | HG02896.hp1 HG02897.hp1 |
splice_region_variant&intron_variant | LOW | c.1035-8C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 13/32 | chr16 | 57949447 | |||||||
chr16:57949664 | T | C | 1 | a0004c0077t0004g0060 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1035-225A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 13/32 | chr16 | 57949664 | |||||||
chr16:57949778 | A | T | 5 | a0002c0005t0041g0068 a0002c0006t0016g0110 a0002c0114t0010g0357 others(2): Show |
5 | HG02109.hp2 HG02486.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1035-339T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 13/32 | chr16 | 57949778 | |||||||
chr16:57949807 | C | T | 111 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(108): Show |
112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1035-368G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 13/32 | chr16 | 57949807 | |||||||
chr16:57949808 | G | A | 1 | a0001c0002t0005g0154 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1035-369C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 13/32 | chr16 | 57949808 | |||||||
chr16:57949850 | T | C | 1 | a0001c0103t0029g0272 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1035-411A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 13/32 | chr16 | 57949850 | |||||||
chr16:57949859 | A | G | 1 | a0001c0002t0001g0329 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1035-420T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 13/32 | chr16 | 57949859 | |||||||
chr16:57949887 | G | A | 1 | a0001c0002t0005g0129 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1035-448C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 13/32 | chr16 | 57949887 | |||||||
chr16:57949999 | A | G | 104 | a0001c0001t0001g0207 a0001c0001t0003g0208 a0001c0001t0013g0206 others(101): Show |
104 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.1034+382T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 13/32 | chr16 | 57949999 | |||||||
chr16:57950575 | G | A | 1 | a0013c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.875-35C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950575 | |||||||
chr16:57950579 | G | A | 353 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(350): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.875-39C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950579 | |||||||
chr16:57950606 | C | CCAGGGAG others(4): Show |
36 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(33): Show |
36 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.875-77_875-67dupCA others(9): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950606 | |||||||
chr16:57950675 | TG | T | 8 | a0006c0081t0021g0331 a0006c0082t0010g0337 a0006c0083t0043g0063 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.875-136delC | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950675 | |||||||
chr16:57950785 | G | A | 9 | a0001c0001t0001g0195 a0001c0001t0001g0275 a0001c0001t0001g0276 others(6): Show |
9 | NA18947.hp1 NA18948.hp2 NA18954.hp2 others(6): Show |
intron_variant | MODIFIER | c.875-245C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950785 | |||||||
chr16:57950810 | G | T | 6 | a0001c0007t0003g0340 a0001c0007t0008g0356 a0001c0015t0001g0335 others(3): Show |
6 | HG01168.hp1 HG02257.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.875-270C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950810 | |||||||
chr16:57950818 | C | A | 1 | a0044c0071t0006g0148 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.875-278G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950818 | |||||||
chr16:57950818 | C | T | 1 | a0025c0108t0004g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.875-278G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950818 | |||||||
chr16:57950944 | TTGTCCTG others(3): Show |
T | 6 | a0001c0002t0001g0056 a0001c0016t0010g0057 a0001c0027t0003g0058 others(3): Show |
6 | HG01891.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.875-414_875-405del others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950944 | |||||||
chr16:57950986 | T | C | 10 | a0001c0007t0003g0189 a0001c0053t0004g0200 a0002c0005t0001g0314 others(7): Show |
10 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.875-446A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950986 | |||||||
chr16:57950991 | A | G | 100 | a0001c0001t0001g0207 a0001c0001t0003g0208 a0001c0001t0013g0206 others(97): Show |
100 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.875-451T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57950991 | |||||||
chr16:57951014 | G | T | 1 | a0001c0003t0032g0109 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.875-474C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57951014 | |||||||
chr16:57951194 | G | C | 1 | a0013c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.875-654C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57951194 | |||||||
chr16:57951436 | C | G | 1 | a0048c0050t0003g0352 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.875-896G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57951436 | |||||||
chr16:57951538 | T | G | 2 | a0002c0022t0018g0112 a0002c0113t0003g0318 |
2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.875-998A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57951538 | |||||||
chr16:57951938 | A | T | 8 | a0006c0081t0021g0331 a0006c0082t0010g0337 a0006c0083t0043g0063 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.875-1398T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57951938 | |||||||
chr16:57951957 | C | T | 27 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(24): Show |
27 | HG00544.hp1 HG00609.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.875-1417G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57951957 | |||||||
chr16:57951958 | T | C | 9 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 others(6): Show |
9 | HG00408.hp2 HG00609.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.875-1418A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57951958 | |||||||
chr16:57951981 | T | A | 1 | a0027c0092t0001g0285 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.875-1441A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57951981 | |||||||
chr16:57952060 | C | G | 144 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(141): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.875-1520G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952060 | |||||||
chr16:57952141 | G | A | 1 | a0009c0025t0001g0122 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.875-1601C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952141 | |||||||
chr16:57952230 | C | A | 5 | a0001c0002t0001g0056 a0001c0016t0010g0057 a0001c0027t0003g0058 others(2): Show |
5 | HG01891.hp1 HG02809.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.875-1690G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952230 | |||||||
chr16:57952301 | G | A | 1 | a0001c0028t0044g0064 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.875-1761C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952301 | |||||||
chr16:57952311 | T | C | 4 | a0001c0007t0003g0004 a0001c0015t0002g0006 a0018c0060t0015g0005 others(1): Show |
4 | HG02559.hp2 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.875-1771A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952311 | |||||||
chr16:57952333 | G | A | 5 | a0001c0004t0006g0149 a0003c0008t0002g0002 a0010c0010t0008g0090 others(2): Show |
6 | HG01256.hp1 HG01258.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.875-1793C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952333 | |||||||
chr16:57952493 | C | CT | 131 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(128): Show |
132 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.875-1954dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952493 | |||||||
chr16:57952493 | C | CTT | 30 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(27): Show |
30 | HG00140.hp2 HG00438.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.875-1955_875-1954d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952493 | |||||||
chr16:57952493 | CT | C | 21 | a0001c0002t0007g0126 a0001c0004t0001g0150 a0001c0004t0001g0153 others(18): Show |
21 | HG01069.hp2 HG01074.hp1 HG02027.hp2 others(18): Show |
intron_variant | MODIFIER | c.875-1954delA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952493 | |||||||
chr16:57952493 | CTT | C | 67 | a0001c0004t0001g0166 a0002c0005t0001g0013 a0002c0005t0001g0014 others(64): Show |
67 | HG00323.hp2 HG00423.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.875-1955_875-1954d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952493 | |||||||
chr16:57952493 | CTTT | C | 8 | a0002c0005t0001g0026 a0002c0006t0001g0100 a0002c0006t0006g0323 others(5): Show |
8 | HG00423.hp2 HG02257.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.875-1956_875-1954d others(5): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952493 | |||||||
chr16:57952660 | C | T | 1 | a0001c0002t0033g0053 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.875-2120G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952660 | |||||||
chr16:57952875 | T | TCTG | 11 | a0001c0007t0003g0189 a0001c0053t0004g0200 a0002c0005t0001g0314 others(8): Show |
11 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.875-2338_875-2336d others(5): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952875 | |||||||
chr16:57952880 | A | C | 11 | a0001c0007t0003g0189 a0001c0053t0004g0200 a0002c0005t0001g0314 others(8): Show |
11 | HG01109.hp2 HG01891.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.875-2340T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952880 | |||||||
chr16:57952958 | G | C | 8 | a0006c0081t0021g0331 a0006c0082t0010g0337 a0006c0083t0043g0063 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.875-2418C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952958 | |||||||
chr16:57952976 | G | A | 1 | a0002c0022t0008g0011 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.875-2436C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57952976 | |||||||
chr16:57953019 | C | T | 8 | a0001c0002t0001g0056 a0001c0016t0010g0057 a0001c0027t0003g0058 others(5): Show |
8 | HG01891.hp1 HG02055.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.875-2479G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953019 | |||||||
chr16:57953031 | C | G | 6 | a0001c0007t0003g0340 a0001c0007t0008g0356 a0001c0015t0001g0335 others(3): Show |
6 | HG01168.hp1 HG02257.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.875-2491G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953031 | |||||||
chr16:57953033 | G | T | 82 | a0001c0004t0001g0166 a0002c0005t0001g0013 a0002c0005t0001g0014 others(79): Show |
82 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.875-2493C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953033 | |||||||
chr16:57953061 | G | A | 2 | a0013c0031t0004g0333 a0013c0031t0004g0334 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.875-2521C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953061 | |||||||
chr16:57953100 | G | A | 8 | a0006c0081t0021g0331 a0006c0082t0010g0337 a0006c0083t0043g0063 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.875-2560C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953100 | |||||||
chr16:57953268 | C | T | 2 | a0002c0022t0018g0112 a0002c0113t0003g0318 |
2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.875-2728G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953268 | |||||||
chr16:57953306 | C | T | 2 | a0002c0022t0018g0112 a0002c0113t0003g0318 |
2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.875-2766G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953306 | |||||||
chr16:57953419 | C | T | 1 | a0001c0003t0012g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.875-2879G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953419 | |||||||
chr16:57953493 | T | TA | 90 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(87): Show |
90 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.875-2954dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953493 | |||||||
chr16:57953493 | T | TAA | 14 | a0001c0007t0003g0189 a0001c0007t0003g0340 a0001c0007t0008g0356 others(11): Show |
14 | HG00423.hp1 HG01168.hp1 HG02083.hp2 others(11): Show |
intron_variant | MODIFIER | c.875-2955_875-2954d others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953493 | |||||||
chr16:57953493 | TA | T | 32 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0002t0001g0056 others(29): Show |
32 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.875-2954delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953493 | |||||||
chr16:57953555 | G | A | 3 | a0001c0001t0007g0290 a0001c0013t0004g0308 a0003c0009t0039g0307 |
3 | HG01358.hp2 HG01361.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.875-3015C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953555 | |||||||
chr16:57953791 | C | T | 1 | a0001c0002t0005g0154 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.875-3251G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953791 | |||||||
chr16:57953793 | G | A | 12 | a0005c0014t0001g0345 a0005c0014t0005g0346 a0005c0014t0016g0326 others(9): Show |
12 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.875-3253C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953793 | |||||||
chr16:57953865 | C | A | 74 | a0001c0004t0001g0166 a0002c0005t0001g0013 a0002c0005t0001g0014 others(71): Show |
74 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.875-3325G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953865 | |||||||
chr16:57953888 | G | GA | 9 | a0002c0005t0001g0332 a0006c0081t0021g0331 a0006c0082t0010g0337 others(6): Show |
9 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.875-3349dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953888 | |||||||
chr16:57953892 | A | G | 24 | a0001c0002t0001g0056 a0001c0007t0003g0004 a0001c0015t0002g0006 others(21): Show |
24 | HG01884.hp2 HG01891.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.875-3352T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57953892 | |||||||
chr16:57954281 | C | T | 3 | a0002c0005t0001g0015 a0002c0005t0001g0016 a0015c0055t0025g0042 |
3 | HG01123.hp2 HG01261.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.874+3060G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57954281 | |||||||
chr16:57954429 | C | T | 258 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(255): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.874+2912G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57954429 | |||||||
chr16:57954447 | T | G | 1 | a0001c0002t0001g0329 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.874+2894A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57954447 | |||||||
chr16:57954560 | C | A | 3 | a0005c0048t0016g0354 a0016c0023t0002g0349 a0034c0043t0011g0351 |
3 | HG02559.hp1 HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.874+2781G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57954560 | |||||||
chr16:57954582 | C | T | 80 | a0001c0002t0001g0032 a0001c0002t0001g0125 a0001c0002t0001g0141 others(77): Show |
82 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.874+2759G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57954582 | |||||||
chr16:57954731 | TTGGTGTC others(24): Show |
T | 2 | a0002c0005t0001g0015 a0002c0005t0001g0016 |
2 | HG01261.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.874+2579_874+2609d others(33): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57954731 | |||||||
chr16:57954801 | T | C | 1 | a0007c0039t0002g0305 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.874+2540A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57954801 | |||||||
chr16:57954893 | A | G | 6 | a0002c0005t0001g0314 a0002c0005t0001g0316 a0002c0011t0018g0341 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.874+2448T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57954893 | |||||||
chr16:57954959 | C | T | 4 | a0001c0007t0003g0004 a0001c0015t0002g0006 a0018c0060t0015g0005 others(1): Show |
4 | HG02559.hp2 HG02895.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.874+2382G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57954959 | |||||||
chr16:57955077 | T | C | 1 | a0002c0011t0004g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.874+2264A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57955077 | |||||||
chr16:57955169 | A | C | 1 | a0002c0011t0004g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.874+2172T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57955169 | |||||||
chr16:57955259 | G | C | 1 | a0001c0001t0001g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.874+2082C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57955259 | |||||||
chr16:57955277 | G | A | 1 | a0002c0037t0003g0092 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.874+2064C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57955277 | |||||||
chr16:57955387 | C | T | 8 | a0006c0081t0021g0331 a0006c0082t0010g0337 a0006c0083t0043g0063 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.874+1954G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57955387 | |||||||
chr16:57955413 | G | T | 6 | a0001c0002t0001g0056 a0001c0016t0010g0057 a0001c0027t0003g0058 others(3): Show |
6 | HG01891.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.874+1928C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57955413 | |||||||
chr16:57955890 | T | G | 1 | a0031c0094t0002g0295 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.874+1451A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57955890 | |||||||
chr16:57956070 | A | G | 1 | a0002c0109t0004g0108 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.874+1271T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956070 | |||||||
chr16:57956173 | G | A | 1 | a0001c0003t0005g0300 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.874+1168C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956173 | |||||||
chr16:57956247 | T | C | 9 | a0002c0005t0001g0098 a0002c0005t0006g0097 a0002c0006t0001g0095 others(6): Show |
9 | NA18945.hp2 NA18959.hp1 NA18967.hp1 others(6): Show |
intron_variant | MODIFIER | c.874+1094A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956247 | |||||||
chr16:57956275 | G | A | 10 | a0001c0002t0001g0056 a0001c0016t0010g0057 a0001c0016t0046g0054 others(7): Show |
10 | HG01891.hp1 HG02055.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.874+1066C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956275 | |||||||
chr16:57956331 | A | G | 10 | a0001c0002t0001g0056 a0001c0016t0010g0057 a0001c0016t0046g0054 others(7): Show |
10 | HG01891.hp1 HG02055.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.874+1010T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956331 | |||||||
chr16:57956492 | C | T | 1 | a0013c0078t0011g0353 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.874+849G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956492 | |||||||
chr16:57956532 | G | A | 8 | a0006c0081t0021g0331 a0006c0082t0010g0337 a0006c0083t0043g0063 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.874+809C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956532 | |||||||
chr16:57956556 | G | T | 2 | a0002c0022t0018g0112 a0002c0113t0003g0318 |
2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.874+785C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956556 | |||||||
chr16:57956560 | A | G | 1 | a0001c0017t0001g0114 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.874+781T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956560 | |||||||
chr16:57956578 | A | G | 143 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(140): Show |
144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.874+763T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956578 | |||||||
chr16:57956630 | A | G | 12 | a0005c0014t0001g0345 a0005c0014t0005g0346 a0005c0014t0016g0326 others(9): Show |
12 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.874+711T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956630 | |||||||
chr16:57956746 | C | G | 1 | a0003c0074t0009g0177 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.874+595G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956746 | |||||||
chr16:57956837 | G | A | 10 | a0001c0002t0001g0056 a0001c0016t0010g0057 a0001c0016t0046g0054 others(7): Show |
10 | HG01891.hp1 HG02055.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.874+504C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956837 | |||||||
chr16:57956927 | G | A | 3 | a0002c0011t0004g0185 a0013c0078t0011g0353 a0018c0062t0027g0324 |
3 | HG02055.hp1 HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.874+414C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956927 | |||||||
chr16:57956956 | A | C | 114 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(111): Show |
115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.874+385T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57956956 | |||||||
chr16:57957113 | A | G | 115 | a0001c0002t0001g0056 a0001c0004t0001g0166 a0001c0007t0003g0189 others(112): Show |
115 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.874+228T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57957113 | |||||||
chr16:57957218 | TG | T | 6 | a0001c0002t0001g0056 a0001c0016t0010g0057 a0001c0027t0003g0058 others(3): Show |
6 | HG01891.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.874+122delC | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57957218 | |||||||
chr16:57957219 | GC | G | 262 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(259): Show |
263 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.874+121delG | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57957219 | |||||||
chr16:57957220 | C | T | 6 | a0001c0002t0001g0056 a0001c0016t0010g0057 a0001c0027t0003g0058 others(3): Show |
6 | HG01891.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.874+121G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57957220 | |||||||
chr16:57957224 | C | G | 1 | a0001c0002t0007g0126 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.874+117G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 12/32 | chr16 | 57957224 | |||||||
chr16:57957413 | C | T | 238 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(235): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.838-36G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57957413 | |||||||
chr16:57957456 | A | G | 1 | a0001c0004t0001g0164 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.838-79T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57957456 | |||||||
chr16:57957479 | G | A | 1 | a0001c0053t0004g0200 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.838-102C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57957479 | |||||||
chr16:57957550 | G | C | 3 | a0001c0004t0035g0079 a0001c0027t0040g0078 a0009c0025t0023g0077 |
3 | HG02622.hp1 HG02886.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.838-173C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57957550 | |||||||
chr16:57957555 | G | A | 4 | a0001c0016t0046g0054 a0001c0041t0005g0028 a0001c0042t0011g0029 others(1): Show |
4 | HG02055.hp2 HG02622.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.838-178C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57957555 | |||||||
chr16:57957598 | G | A | 3 | a0001c0004t0001g0115 a0001c0004t0001g0164 a0001c0004t0001g0165 |
3 | NA18943.hp1 NA18957.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.838-221C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57957598 | |||||||
chr16:57957631 | A | G | 1 | a0028c0080t0015g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.838-254T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57957631 | |||||||
chr16:57957777 | A | G | 1 | a0001c0007t0002g0073 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.838-400T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57957777 | |||||||
chr16:57958165 | C | A | 12 | a0005c0014t0001g0345 a0005c0014t0005g0346 a0005c0014t0016g0326 others(9): Show |
12 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.837+245G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57958165 | |||||||
chr16:57958198 | G | A | 1 | a0002c0011t0004g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.837+212C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57958198 | |||||||
chr16:57958215 | T | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(138): Show |
142 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.837+195A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57958215 | |||||||
chr16:57958325 | G | GGGTCCCT others(34): Show |
114 | a0001c0002t0001g0056 a0001c0004t0001g0166 a0001c0007t0003g0189 others(111): Show |
114 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.837+84_837+85insTG others(39): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 11/32 | chr16 | 57958325 | |||||||
chr16:57958508 | G | A | 1 | a0001c0035t0028g0291 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.762-23C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958508 | |||||||
chr16:57958520 | G | A | 17 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(14): Show |
17 | HG00544.hp1 HG00609.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.762-35C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958520 | |||||||
chr16:57958549 | G | A | 6 | a0002c0005t0001g0314 a0002c0005t0001g0316 a0002c0011t0018g0341 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.762-64C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958549 | |||||||
chr16:57958595 | C | G | 29 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(26): Show |
29 | HG00544.hp1 HG00609.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.762-110G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958595 | |||||||
chr16:57958627 | C | G | 1 | a0001c0097t0003g0230 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.762-142G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958627 | |||||||
chr16:57958650 | C | T | 7 | a0001c0007t0003g0189 a0001c0007t0003g0340 a0001c0007t0008g0356 others(4): Show |
7 | HG01168.hp1 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.762-165G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958650 | |||||||
chr16:57958677 | G | T | 1 | a0001c0035t0010g0229 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.762-192C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958677 | |||||||
chr16:57958699 | C | T | 1 | a0001c0003t0002g0201 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.762-214G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958699 | |||||||
chr16:57958712 | C | T | 1 | a0002c0011t0004g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.762-227G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958712 | |||||||
chr16:57958718 | C | T | 95 | a0001c0002t0001g0032 a0001c0002t0001g0125 a0001c0002t0001g0141 others(92): Show |
97 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.762-233G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958718 | |||||||
chr16:57958729 | G | A | 1 | a0001c0002t0001g0125 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.762-244C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958729 | |||||||
chr16:57958849 | A | G | 240 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(237): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.762-364T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958849 | |||||||
chr16:57958921 | C | CT | 79 | a0001c0002t0001g0141 a0001c0002t0001g0155 a0001c0002t0001g0162 others(76): Show |
81 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.762-437dupA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958921 | |||||||
chr16:57958921 | C | CTT | 7 | a0001c0002t0001g0125 a0001c0002t0002g0124 a0001c0007t0002g0073 others(4): Show |
7 | HG01255.hp1 HG01346.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.762-438_762-437dup others(2): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958921 | |||||||
chr16:57958921 | CT | C | 151 | a0001c0001t0001g0195 a0001c0001t0001g0207 a0001c0001t0001g0226 others(148): Show |
151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.762-437delA | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958921 | |||||||
chr16:57958921 | CTT | C | 13 | a0001c0001t0001g0003 a0001c0001t0001g0205 a0001c0002t0001g0052 others(10): Show |
14 | HG00323.hp1 HG01358.hp2 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.762-438_762-437del others(2): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57958921 | |||||||
chr16:57959004 | T | C | 3 | a0002c0011t0004g0066 a0002c0022t0002g0074 a0002c0109t0004g0108 |
3 | HG02647.hp2 HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.762-519A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959004 | |||||||
chr16:57959131 | C | T | 1 | a0002c0005t0001g0332 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.762-646G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959131 | |||||||
chr16:57959149 | T | C | 1 | a0002c0038t0010g0103 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.762-664A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959149 | |||||||
chr16:57959384 | C | T | 1 | a0003c0009t0007g0080 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.761+504G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959384 | |||||||
chr16:57959397 | T | C | 1 | a0002c0005t0001g0332 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.761+491A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959397 | |||||||
chr16:57959435 | G | T | 3 | a0013c0031t0004g0333 a0013c0031t0004g0334 a0028c0080t0015g0188 |
3 | HG02280.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.761+453C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959435 | |||||||
chr16:57959454 | A | G | 8 | a0006c0081t0021g0331 a0006c0082t0010g0337 a0006c0083t0043g0063 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.761+434T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959454 | |||||||
chr16:57959566 | C | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(139): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.761+322G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959566 | |||||||
chr16:57959588 | C | T | 1 | a0048c0050t0003g0352 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.761+300G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959588 | |||||||
chr16:57959605 | AAAAC | A | 179 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(176): Show |
180 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.761+279_761+282del others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959605 | |||||||
chr16:57959605 | AAAACAAA others(1): Show |
A | 85 | a0001c0002t0001g0032 a0001c0002t0001g0125 a0001c0002t0001g0141 others(82): Show |
87 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.761+275_761+282del others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959605 | |||||||
chr16:57959697 | C | T | 1 | a0008c0021t0003g0105 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.761+191G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959697 | |||||||
chr16:57959723 | T | C | 2 | a0001c0004t0001g0166 a0002c0005t0001g0026 |
2 | NA18974.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.761+165A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959723 | |||||||
chr16:57959866 | C | T | 1 | a0002c0109t0004g0108 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.761+22G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959866 | |||||||
chr16:57959873 | T | C | 2 | a0005c0046t0036g0348 a0016c0023t0002g0347 |
2 | HG01884.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.761+15A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 10/32 | chr16 | 57959873 | |||||||
chr16:57960148 | G | C | 1 | a0002c0006t0006g0323 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.584-83C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 9/32 | chr16 | 57960148 | |||||||
chr16:57960331 | C | A | 143 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(140): Show |
144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.583+151G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 9/32 | chr16 | 57960331 | |||||||
chr16:57960437 | C | T | 14 | a0002c0005t0001g0332 a0002c0006t0006g0323 a0005c0014t0001g0345 others(11): Show |
14 | HG00423.hp2 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.583+45G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 9/32 | chr16 | 57960437 | |||||||
chr16:57960438 | G | A | 1 | a0001c0015t0002g0006 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.583+44C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 9/32 | chr16 | 57960438 | |||||||
chr16:57960591 | C | T | 13 | a0002c0005t0001g0332 a0005c0014t0001g0345 a0005c0014t0005g0346 others(10): Show |
13 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.535-61G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 8/32 | chr16 | 57960591 | |||||||
chr16:57960711 | A | T | 3 | a0001c0001t0001g0226 a0001c0001t0006g0225 a0001c0003t0002g0191 |
3 | HG00733.hp1 NA18959.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.534+129T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 8/32 | chr16 | 57960711 | |||||||
chr16:57960764 | G | C | 1 | a0001c0003t0003g0296 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.534+76C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 8/32 | chr16 | 57960764 | |||||||
chr16:57960820 | C | T | 80 | a0001c0002t0001g0032 a0001c0002t0001g0125 a0001c0002t0001g0141 others(77): Show |
82 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.534+20G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 8/32 | chr16 | 57960820 | |||||||
chr16:57960833 | G | C | 8 | a0006c0081t0021g0331 a0006c0082t0010g0337 a0006c0083t0043g0063 others(5): Show |
8 | HG02280.hp2 HG02615.hp2 HG02717.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.534+7C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 8/32 | chr16 | 57960833 | |||||||
chr16:57961175 | C | T | 1 | a0048c0050t0003g0352 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.459-260G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961175 | |||||||
chr16:57961208 | C | T | 3 | a0001c0001t0002g0222 a0001c0001t0003g0223 a0001c0001t0017g0224 |
3 | HG00597.hp1 NA18960.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.459-293G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961208 | |||||||
chr16:57961394 | C | G | 1 | a0002c0011t0004g0185 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.459-479G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961394 | |||||||
chr16:57961422 | A | C | 1 | a0014c0118t0001g0302 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.459-507T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961422 | |||||||
chr16:57961497 | G | C | 12 | a0005c0014t0001g0345 a0005c0014t0005g0346 a0005c0014t0016g0326 others(9): Show |
12 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.459-582C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961497 | |||||||
chr16:57961518 | G | A | 21 | a0001c0007t0003g0189 a0001c0007t0003g0340 a0001c0007t0008g0356 others(18): Show |
21 | HG00423.hp2 HG01168.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.459-603C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961518 | |||||||
chr16:57961550 | C | T | 1 | a0001c0003t0003g0221 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.459-635G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961550 | |||||||
chr16:57961631 | G | GGAAT | 62 | a0001c0002t0001g0125 a0001c0002t0001g0141 a0001c0002t0001g0168 others(59): Show |
64 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.459-720_459-717dup others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961631 | |||||||
chr16:57961631 | G | GGAATGAA others(1): Show |
8 | a0001c0002t0002g0121 a0001c0004t0001g0115 a0001c0004t0001g0118 others(5): Show |
8 | HG00544.hp2 HG00741.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.459-724_459-717dup others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961631 | |||||||
chr16:57961631 | GGAAT | G | 132 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(129): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.459-720_459-717del others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961631 | |||||||
chr16:57961631 | GGAATGAA others(1): Show |
G | 33 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(30): Show |
33 | HG00423.hp2 HG00544.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.459-724_459-717del others(8): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961631 | |||||||
chr16:57961631 | GGAATGAA others(5): Show |
G | 2 | a0002c0011t0004g0185 a0006c0086t0003g0067 |
2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.459-728_459-717del others(12): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961631 | |||||||
chr16:57961666 | A | G | 1 | a0003c0104t0007g0232 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.459-751T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961666 | |||||||
chr16:57961670 | G | A | 1 | a0001c0004t0001g0165 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.459-755C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57961670 | |||||||
chr16:57962059 | G | A | 4 | a0001c0002t0001g0168 a0003c0012t0007g0167 a0012c0024t0002g0169 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.458+506C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57962059 | |||||||
chr16:57962266 | T | C | 2 | a0001c0004t0001g0172 a0001c0004t0002g0171 |
2 | HG02027.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.458+299A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57962266 | |||||||
chr16:57962366 | C | A | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.458+199G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57962366 | |||||||
chr16:57962367 | A | T | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.458+198T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57962367 | |||||||
chr16:57962487 | C | G | 1 | a0001c0001t0001g0195 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.458+78G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57962487 | |||||||
chr16:57962488 | C | T | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.458+77G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 7/32 | chr16 | 57962488 | |||||||
chr16:57962659 | C | A | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413-49G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962659 | |||||||
chr16:57962661 | C | A | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413-51G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962661 | |||||||
chr16:57962665 | C | A | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413-55G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962665 | |||||||
chr16:57962667 | C | T | 1 | a0001c0002t0003g0031 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.413-57G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962667 | |||||||
chr16:57962670 | G | T | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413-60C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962670 | |||||||
chr16:57962690 | C | T | 2 | a0002c0006t0006g0323 a0002c0011t0004g0185 |
2 | HG00423.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.413-80G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962690 | |||||||
chr16:57962707 | C | A | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413-97G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962707 | |||||||
chr16:57962711 | G | A | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413-101C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962711 | |||||||
chr16:57962717 | A | C | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413-107T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962717 | |||||||
chr16:57962744 | C | A | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.412+98G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962744 | |||||||
chr16:57962780 | C | G | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.412+62G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962780 | |||||||
chr16:57962790 | C | T | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.412+52G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962790 | |||||||
chr16:57962798 | C | A | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.412+44G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962798 | |||||||
chr16:57962808 | G | A | 1 | a0001c0028t0042g0069 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.412+34C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962808 | |||||||
chr16:57962834 | G | T | 2 | a0002c0006t0006g0323 a0033c0051t0001g0339 |
2 | HG00423.hp2 HG03139.hp2 |
splice_region_variant&intron_variant | LOW | c.412+8C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962834 | |||||||
chr16:57962835 | T | G | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | splice_region_variant&intron_variant | LOW | c.412+7A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 6/32 | chr16 | 57962835 | |||||||
chr16:57962931 | C | A | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.381+43G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/32 | chr16 | 57962931 | |||||||
chr16:57962941 | C | T | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.381+33G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/32 | chr16 | 57962941 | |||||||
chr16:57962943 | C | A | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.381+31G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/32 | chr16 | 57962943 | |||||||
chr16:57962944 | G | C | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.381+30C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/32 | chr16 | 57962944 | |||||||
chr16:57962946 | C | G | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.381+28G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/32 | chr16 | 57962946 | |||||||
chr16:57962948 | C | A | 2 | a0001c0003t0001g0301 a0033c0051t0001g0339 |
2 | HG03139.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.381+26G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/32 | chr16 | 57962948 | |||||||
chr16:57962963 | C | A | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.381+11G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/32 | chr16 | 57962963 | |||||||
chr16:57962964 | C | A | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.381+10G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/32 | chr16 | 57962964 | |||||||
chr16:57962969 | A | T | 1 | a0033c0051t0001g0339 | 1 | HG03139.hp2 | splice_region_variant&intron_variant | LOW | c.381+5T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 5/32 | chr16 | 57962969 | |||||||
chr16:57963122 | C | T | 13 | a0005c0014t0001g0345 a0005c0014t0005g0346 a0005c0014t0016g0326 others(10): Show |
13 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.291-58G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963122 | |||||||
chr16:57963373 | G | A | 1 | a0028c0080t0015g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.291-309C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963373 | |||||||
chr16:57963545 | A | T | 6 | a0001c0001t0012g0212 a0001c0003t0001g0214 a0001c0003t0003g0215 others(3): Show |
6 | HG00140.hp2 HG00735.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.291-481T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963545 | |||||||
chr16:57963596 | G | A | 1 | a0006c0083t0043g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.291-532C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963596 | |||||||
chr16:57963596 | G | C | 1 | a0002c0005t0005g0322 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.291-532C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963596 | |||||||
chr16:57963605 | G | T | 273 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(270): Show |
274 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.290+525C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963605 | |||||||
chr16:57963612 | T | C | 2 | a0001c0004t0001g0173 a0001c0004t0014g0192 |
2 | HG01123.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.290+518A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963612 | |||||||
chr16:57963615 | C | G | 1 | a0006c0083t0043g0063 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.290+515G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963615 | |||||||
chr16:57963689 | A | C | 259 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(256): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.290+441T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963689 | |||||||
chr16:57963725 | C | T | 7 | a0006c0081t0021g0331 a0006c0082t0010g0337 a0006c0083t0043g0063 others(4): Show |
7 | HG02615.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.290+405G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963725 | |||||||
chr16:57963752 | A | G | 29 | a0001c0002t0001g0032 a0001c0002t0001g0035 a0001c0002t0001g0039 others(26): Show |
29 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.290+378T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57963752 | |||||||
chr16:57964074 | G | T | 1 | a0001c0007t0002g0073 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.290+56C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57964074 | |||||||
chr16:57964075 | G | T | 1 | a0001c0007t0002g0073 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.290+55C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 4/32 | chr16 | 57964075 | |||||||
chr16:57964220 | A | G | 7 | a0006c0081t0021g0331 a0006c0082t0010g0337 a0006c0083t0043g0063 others(4): Show |
7 | HG02615.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.218-18T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 3/32 | chr16 | 57964220 | |||||||
chr16:57964441 | C | T | 255 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(252): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.217+46G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 3/32 | chr16 | 57964441 | |||||||
chr16:57964639 | A | G | 19 | a0001c0002t0001g0032 a0001c0002t0001g0035 a0001c0002t0001g0039 others(16): Show |
19 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.160-95T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57964639 | |||||||
chr16:57964734 | G | A | 7 | a0006c0081t0021g0331 a0006c0082t0010g0337 a0006c0083t0043g0063 others(4): Show |
7 | HG02615.hp2 HG02717.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-190C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57964734 | |||||||
chr16:57964742 | C | T | 6 | a0001c0007t0003g0340 a0001c0007t0008g0356 a0001c0015t0001g0335 others(3): Show |
6 | HG01168.hp1 HG02257.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.160-198G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57964742 | |||||||
chr16:57964856 | A | G | 1 | a0022c0079t0006g0194 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.160-312T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57964856 | |||||||
chr16:57964869 | A | G | 6 | a0001c0002t0001g0056 a0001c0016t0010g0057 a0001c0027t0003g0058 others(3): Show |
6 | HG01891.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.160-325T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57964869 | |||||||
chr16:57964884 | G | C | 1 | a0001c0004t0001g0174 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.160-340C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57964884 | |||||||
chr16:57964936 | T | C | 175 | a0001c0002t0001g0032 a0001c0002t0001g0035 a0001c0002t0001g0039 others(172): Show |
177 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.160-392A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57964936 | |||||||
chr16:57965123 | TACTC | T | 260 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(257): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.160-583_160-580del others(4): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965123 | |||||||
chr16:57965228 | TAC | T | 277 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(274): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.160-686_160-685del others(2): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965228 | |||||||
chr16:57965281 | A | T | 1 | a0001c0002t0001g0338 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.160-737T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965281 | |||||||
chr16:57965299 | A | G | 7 | a0001c0007t0003g0340 a0001c0007t0008g0356 a0001c0015t0001g0335 others(4): Show |
7 | HG01168.hp1 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.160-755T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965299 | |||||||
chr16:57965318 | C | T | 1 | a0002c0005t0001g0332 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.160-774G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965318 | |||||||
chr16:57965332 | C | T | 76 | a0001c0002t0001g0125 a0001c0002t0001g0141 a0001c0002t0001g0155 others(73): Show |
78 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.160-788G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965332 | |||||||
chr16:57965338 | T | G | 5 | a0001c0002t0001g0056 a0001c0016t0010g0057 a0001c0027t0003g0058 others(2): Show |
5 | HG01891.hp1 HG02809.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.160-794A>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965338 | |||||||
chr16:57965340 | T | A | 1 | a0001c0002t0003g0050 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.160-796A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965340 | |||||||
chr16:57965403 | G | A | 1 | a0001c0001t0002g0309 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.160-859C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965403 | |||||||
chr16:57965497 | G | A | 181 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(178): Show |
182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.160-953C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965497 | |||||||
chr16:57965616 | G | A | 119 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(116): Show |
120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.160-1072C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965616 | |||||||
chr16:57965657 | T | TACACATA others(6): Show |
171 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(168): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.160-1114_160-1113i others(15): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965657 | |||||||
chr16:57965718 | TCAGA | T | 28 | a0001c0002t0001g0032 a0001c0002t0001g0035 a0001c0002t0001g0039 others(25): Show |
28 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.160-1178_160-1175d others(6): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965718 | |||||||
chr16:57965867 | T | A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(168): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.159+1261A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965867 | |||||||
chr16:57965907 | G | A | 1 | a0001c0003t0032g0109 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.159+1221C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57965907 | |||||||
chr16:57966117 | C | T | 1 | a0001c0028t0042g0069 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.159+1011G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57966117 | |||||||
chr16:57966259 | A | G | 187 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(184): Show |
188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.159+869T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57966259 | |||||||
chr16:57966320 | A | G | 3 | a0001c0001t0001g0207 a0001c0001t0003g0208 a0001c0001t0013g0206 |
3 | NA18944.hp1 NA19002.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.159+808T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57966320 | |||||||
chr16:57966449 | T | C | 1 | a0006c0086t0003g0067 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.159+679A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57966449 | |||||||
chr16:57966623 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.159+505T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57966623 | |||||||
chr16:57966675 | A | G | 1 | a0001c0003t0012g0204 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.159+453T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57966675 | |||||||
chr16:57966810 | C | T | 76 | a0001c0002t0001g0125 a0001c0002t0001g0141 a0001c0002t0001g0155 others(73): Show |
78 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.159+318G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57966810 | |||||||
chr16:57967096 | C | T | 13 | a0005c0014t0001g0345 a0005c0014t0005g0346 a0005c0014t0016g0326 others(10): Show |
13 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.159+32G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 2/32 | chr16 | 57967096 | |||||||
chr16:57967412 | G | A | 1 | a0018c0062t0027g0324 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-8-118C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967412 | |||||||
chr16:57967485 | G | C | 1 | a0001c0068t0005g0175 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-8-191C>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967485 | |||||||
chr16:57967514 | C | T | 1 | a0016c0023t0002g0349 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-8-220G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967514 | |||||||
chr16:57967520 | C | T | 1 | a0001c0003t0001g0202 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-8-226G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967520 | |||||||
chr16:57967626 | G | T | 169 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(166): Show |
170 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.-8-332C>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967626 | |||||||
chr16:57967726 | T | C | 1 | a0007c0122t0003g0317 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-8-432A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967726 | |||||||
chr16:57967757 | T | C | 2 | a0008c0020t0007g0007 a0025c0108t0004g0061 |
2 | HG01891.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.-8-463A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967757 | |||||||
chr16:57967779 | G | A | 1 | a0004c0030t0003g0001 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-8-485C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967779 | |||||||
chr16:57967814 | G | A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(168): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.-8-520C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967814 | |||||||
chr16:57967924 | A | C | 2 | a0001c0015t0001g0335 a0001c0015t0020g0336 |
2 | HG02257.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-8-630T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57967924 | |||||||
chr16:57968006 | C | T | 1 | a0002c0022t0008g0011 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-8-712G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968006 | |||||||
chr16:57968025 | G | A | 171 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(168): Show |
172 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.-8-731C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968025 | |||||||
chr16:57968133 | G | A | 1 | a0008c0021t0003g0105 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-8-839C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968133 | |||||||
chr16:57968150 | A | G | 1 | a0001c0004t0001g0117 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-8-856T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968150 | |||||||
chr16:57968211 | A | T | 2 | a0013c0031t0004g0333 a0013c0031t0004g0334 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-8-917T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968211 | |||||||
chr16:57968228 | T | A | 1 | a0028c0080t0015g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-8-934A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968228 | |||||||
chr16:57968465 | C | G | 76 | a0001c0002t0001g0125 a0001c0002t0001g0141 a0001c0002t0001g0155 others(73): Show |
78 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.-8-1171G>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968465 | |||||||
chr16:57968499 | A | T | 1 | a0001c0003t0002g0201 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-8-1205T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968499 | |||||||
chr16:57968606 | ACTAATTG others(3): Show |
A | 143 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(140): Show |
144 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.-8-1322_-8-1313del others(10): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968606 | |||||||
chr16:57968633 | A | G | 3 | a0008c0020t0007g0007 a0018c0062t0027g0324 a0025c0108t0004g0061 |
3 | HG01891.hp2 HG02257.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-8-1339T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968633 | |||||||
chr16:57968865 | T | TA | 20 | a0001c0001t0002g0312 a0001c0001t0003g0311 a0001c0002t0001g0181 others(17): Show |
20 | HG00423.hp1 HG00423.hp2 HG01934.hp1 others(17): Show |
intron_variant | MODIFIER | c.-8-1572dupT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968865 | |||||||
chr16:57968865 | TA | T | 30 | a0001c0001t0001g0195 a0001c0003t0001g0197 a0001c0003t0001g0199 others(27): Show |
30 | HG01515.hp1 HG01891.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.-8-1572delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968865 | |||||||
chr16:57968865 | TAA | T | 32 | a0001c0002t0001g0032 a0001c0002t0001g0035 a0001c0002t0001g0039 others(29): Show |
32 | HG00544.hp1 HG00609.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.-8-1573_-8-1572del others(2): Show |
CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968865 | |||||||
chr16:57968866 | A | T | 2 | a0001c0016t0046g0054 a0029c0076t0003g0055 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-8-1572T>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968866 | |||||||
chr16:57968961 | T | C | 176 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(173): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.-8-1667A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57968961 | |||||||
chr16:57969017 | A | C | 1 | a0004c0030t0003g0001 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-8-1723T>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969017 | |||||||
chr16:57969200 | G | A | 168 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(165): Show |
169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.-9+1860C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969200 | |||||||
chr16:57969230 | C | T | 3 | a0002c0011t0004g0066 a0002c0022t0002g0074 a0006c0086t0003g0067 |
3 | HG02280.hp2 HG02647.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-9+1830G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969230 | |||||||
chr16:57969240 | A | G | 1 | a0001c0017t0001g0114 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-9+1820T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969240 | |||||||
chr16:57969288 | T | C | 281 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(278): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.-9+1772A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969288 | |||||||
chr16:57969327 | CA | C | 6 | a0002c0005t0001g0314 a0002c0005t0001g0316 a0002c0011t0018g0341 others(3): Show |
6 | HG01109.hp2 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+1732delT | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969327 | |||||||
chr16:57969478 | C | T | 1 | a0020c0095t0001g0193 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-9+1582G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969478 | |||||||
chr16:57969479 | G | A | 2 | a0001c0002t0002g0183 a0001c0002t0005g0184 |
2 | HG01255.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-9+1581C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969479 | |||||||
chr16:57969575 | C | A | 1 | a0002c0005t0001g0332 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-9+1485G>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969575 | |||||||
chr16:57969749 | C | T | 9 | a0001c0007t0003g0340 a0001c0007t0008g0356 a0001c0015t0001g0335 others(6): Show |
9 | HG01168.hp1 HG02257.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-9+1311G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969749 | |||||||
chr16:57969839 | T | C | 133 | a0001c0001t0001g0195 a0001c0001t0001g0205 a0001c0001t0001g0207 others(130): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.-9+1221A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969839 | |||||||
chr16:57969921 | A | G | 136 | a0001c0001t0001g0195 a0001c0001t0001g0205 a0001c0001t0001g0207 others(133): Show |
136 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.-9+1139T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57969921 | |||||||
chr16:57970152 | A | G | 1 | a0001c0007t0002g0073 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-9+908T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970152 | |||||||
chr16:57970177 | C | T | 6 | a0001c0002t0003g0008 a0001c0007t0003g0004 a0001c0015t0002g0006 others(3): Show |
6 | HG01891.hp2 HG02055.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+883G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970177 | |||||||
chr16:57970275 | C | T | 76 | a0001c0001t0001g0003 a0001c0002t0001g0125 a0001c0002t0001g0141 others(73): Show |
79 | HG00099.hp2 HG00438.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.-9+785G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970275 | |||||||
chr16:57970280 | C | T | 1 | a0002c0022t0018g0112 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-9+780G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970280 | |||||||
chr16:57970343 | T | C | 1 | a0001c0002t0001g0338 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-9+717A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970343 | |||||||
chr16:57970372 | C | T | 44 | a0001c0003t0032g0109 a0001c0004t0022g0107 a0001c0004t0035g0079 others(41): Show |
44 | HG00642.hp2 HG01109.hp2 HG01515.hp2 others(41): Show |
intron_variant | MODIFIER | c.-9+688G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970372 | |||||||
chr16:57970456 | G | A | 309 | a0001c0001t0001g0003 a0001c0001t0001g0195 a0001c0001t0001g0205 others(306): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.-9+604C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970456 | |||||||
chr16:57970621 | G | A | 16 | a0001c0007t0003g0340 a0002c0011t0018g0341 a0005c0014t0001g0345 others(13): Show |
16 | HG01884.hp2 HG02145.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9+439C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970621 | |||||||
chr16:57970765 | G | A | 1 | a0004c0036t0001g0355 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-9+295C>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970765 | |||||||
chr16:57970785 | A | G | 6 | a0001c0028t0042g0069 a0001c0028t0044g0064 a0002c0005t0041g0068 others(3): Show |
6 | HG01109.hp2 HG02280.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9+275T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970785 | |||||||
chr16:57970865 | T | A | 2 | a0001c0007t0008g0356 a0002c0114t0010g0357 |
2 | HG01168.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-9+195A>T | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970865 | |||||||
chr16:57970889 | T | C | 7 | a0001c0002t0003g0008 a0001c0007t0003g0004 a0001c0015t0002g0006 others(4): Show |
7 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+171A>G | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970889 | |||||||
chr16:57970928 | A | G | 53 | a0001c0002t0001g0032 a0001c0002t0001g0035 a0001c0002t0001g0039 others(50): Show |
53 | HG00423.hp1 HG00544.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.-9+132T>C | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57970928 | |||||||
chr16:57971023 | C | T | 7 | a0001c0002t0003g0008 a0001c0007t0003g0004 a0001c0015t0002g0006 others(4): Show |
7 | HG01891.hp2 HG02486.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+37G>A | CNGB1 | ENSG00000070729.14 | transcript | ENST00000251102.13 | protein_coding | 1/32 | chr16 | 57971023 |