Item | Value |
---|---|
geneid | 5158 |
ensemblid | ENSG00000133256.13 |
hgncid | 8786 |
symbol | PDE6B |
name | phosphodiesterase 6B |
refseq_nuc | NM_000283.4 |
refseq_prot | NP_000274.3 |
ensembl_nuc | ENST00000496514.6 |
ensembl_prot | ENSP00000420295.1 |
mane_status | MANE Select |
chr | chr4 |
start | 625573 |
end | 670782 |
strand | + |
ver | v1.2 |
region | chr4:625573-670782 |
region5000 | chr4:620573-675782 |
regionname0 | PDE6B_chr4_625573_670782 |
regionname5000 | PDE6B_chr4_620573_675782 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 854 | 272 | 75 | 47 | 116 | 8 | 25 | 82 | PDE6B_chr4_620573_675782 | PDE6B | MSLSE others(849): Show |
chr4 | 620573 | 675782 |
a0002 | 0/0 | 854 | 10 | 8 | 2 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | MSLSE others(849): Show |
chr4 | 620573 | 675782 |
a0003 | 0/0 | 854 | 7 | 0 | 0 | 7 | 0 | 0 | 6 | PDE6B_chr4_620573_675782 | PDE6B | MSLSE others(849): Show |
chr4 | 620573 | 675782 |
a0004 | 0/0 | 854 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | PDE6B_chr4_620573_675782 | PDE6B | MSLSE others(849): Show |
chr4 | 620573 | 675782 |
a0005 | 0/0 | 854 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | MSLSE others(849): Show |
chr4 | 620573 | 675782 |
a0006 | 0/0 | 854 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | MSLSE others(849): Show |
chr4 | 620573 | 675782 |
a0007 | 0/0 | 854 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | MSLSE others(849): Show |
chr4 | 620573 | 675782 |
a0008 | 0/0 | 854 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | MSLSE others(849): Show |
chr4 | 620573 | 675782 |
a0009 | 0/0 | 854 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | MSLSE others(849): Show |
chr4 | 620573 | 675782 |
a0010 | 0/0 | 854 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | MSLSE others(849): Show |
chr4 | 620573 | 675782 |
a0011 | 0/0 | 854 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | MSLSE others(849): Show |
chr4 | 620573 | 675782 |
a0012 | 0/0 | 854 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PDE6B_chr4_620573_675782 | PDE6B | MSLSE others(849): Show |
chr4 | 620573 | 675782 |
a0013 | 0/0 | 854 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PDE6B_chr4_620573_675782 | PDE6B | MSLSE others(849): Show |
chr4 | 620573 | 675782 |
a0014 | 0/0 | 854 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | MSLSE others(849): Show |
chr4 | 620573 | 675782 |
a0015 | 0/0 | 854 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | MSLSE others(849): Show |
chr4 | 620573 | 675782 |
a0016 | 0/0 | 854 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | MSLSE others(849): Show |
chr4 | 620573 | 675782 |
a0017 | 0/0 | 854 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | MSLSE others(849): Show |
chr4 | 620573 | 675782 |
a0018 | 0/1 | 854 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | MSLSE others(849): Show |
chr4 | 620573 | 675782 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2562 | 234 | 43 | 44 | 115 | 6 | 25 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0001c0002 | 0/0 | 2562 | 13 | 9 | 2 | 0 | 2 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0001c0004 | 0/0 | 2562 | 7 | 7 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0001c0005 | 0/0 | 2562 | 4 | 4 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0001c0008 | 0/0 | 2562 | 3 | 3 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0001c0009 | 0/0 | 2562 | 3 | 3 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0001c0012 | 0/0 | 2562 | 2 | 2 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0001c0015 | 0/0 | 2562 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0001c0017 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0001c0022 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0001c0024 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0001c0026 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0001c0029 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0002c0003 | 0/0 | 2562 | 10 | 8 | 2 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0003c0006 | 0/0 | 2562 | 4 | 0 | 0 | 4 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0003c0010 | 0/0 | 2562 | 3 | 0 | 0 | 3 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0004c0007 | 0/0 | 2562 | 3 | 0 | 2 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0005c0011 | 0/0 | 2562 | 2 | 2 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0006c0013 | 0/0 | 2562 | 2 | 2 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0007c0027 | 0/0 | 2562 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0008c0028 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0009c0025 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0010c0021 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0011c0020 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0012c0031 | 0/0 | 2562 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0013c0016 | 0/0 | 2562 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0014c0023 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0015c0019 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0016c0014 | 0/0 | 2562 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0017c0030 | 0/0 | 2562 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 | ||
a0018c0018 | 0/1 | 2562 | 1 | 0 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | ATGAG others(2557): Show |
chr4 | 620573 | 675782 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3294 | 90 | 7 | 28 | 40 | 4 | 11 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0001c0001t0002 | 1/0 | 3294 | 81 | 29 | 11 | 31 | 2 | 7 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0001c0001t0003 | 0/0 | 3293 | 44 | 1 | 1 | 38 | 0 | 4 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3288): Show |
chr4 | 620573 | 675782 |
a0001c0001t0004 | 0/0 | 3295 | 5 | 1 | 2 | 2 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3290): Show |
chr4 | 620573 | 675782 |
a0001c0001t0005 | 0/0 | 3296 | 2 | 2 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3291): Show |
chr4 | 620573 | 675782 |
a0001c0001t0006 | 0/0 | 3293 | 6 | 0 | 2 | 2 | 0 | 2 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3288): Show |
chr4 | 620573 | 675782 |
a0001c0001t0007 | 0/0 | 3295 | 2 | 1 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3290): Show |
chr4 | 620573 | 675782 |
a0001c0001t0011 | 0/0 | 3296 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3291): Show |
chr4 | 620573 | 675782 |
a0001c0001t0012 | 0/0 | 3295 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3290): Show |
chr4 | 620573 | 675782 |
a0001c0001t0013 | 0/0 | 3294 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0001c0001t0014 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0001c0002t0001 | 0/0 | 3294 | 4 | 3 | 0 | 0 | 1 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0001c0002t0002 | 0/0 | 3294 | 2 | 2 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0001c0002t0004 | 0/0 | 3295 | 7 | 4 | 2 | 0 | 1 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3290): Show |
chr4 | 620573 | 675782 |
a0001c0004t0001 | 0/0 | 3294 | 7 | 7 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0001c0005t0001 | 0/0 | 3294 | 4 | 4 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0001c0008t0002 | 0/0 | 3294 | 3 | 3 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0001c0009t0009 | 0/0 | 3295 | 3 | 3 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3290): Show |
chr4 | 620573 | 675782 |
a0001c0012t0003 | 0/0 | 3293 | 2 | 2 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3288): Show |
chr4 | 620573 | 675782 |
a0001c0015t0002 | 0/0 | 3294 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0001c0017t0004 | 0/0 | 3295 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3290): Show |
chr4 | 620573 | 675782 |
a0001c0022t0002 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0001c0024t0002 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0001c0026t0001 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0001c0029t0001 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0002c0003t0005 | 0/0 | 3296 | 10 | 8 | 2 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3291): Show |
chr4 | 620573 | 675782 |
a0003c0006t0001 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0003c0006t0002 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0003c0006t0007 | 0/0 | 3295 | 2 | 0 | 0 | 2 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3290): Show |
chr4 | 620573 | 675782 |
a0003c0010t0002 | 0/0 | 3294 | 2 | 0 | 0 | 2 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0003c0010t0003 | 0/0 | 3293 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3288): Show |
chr4 | 620573 | 675782 |
a0004c0007t0008 | 0/0 | 3294 | 3 | 0 | 2 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0005c0011t0001 | 0/0 | 3294 | 2 | 2 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0006c0013t0010 | 0/0 | 3295 | 2 | 2 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3290): Show |
chr4 | 620573 | 675782 |
a0007c0027t0002 | 0/0 | 3294 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0008c0028t0008 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0009c0025t0002 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0010c0021t0002 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0011c0020t0001 | 0/0 | 3294 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0012c0031t0003 | 0/0 | 3293 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3288): Show |
chr4 | 620573 | 675782 |
a0013c0016t0001 | 0/0 | 3294 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0014c0023t0003 | 0/0 | 3293 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3288): Show |
chr4 | 620573 | 675782 |
a0015c0019t0003 | 0/0 | 3293 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3288): Show |
chr4 | 620573 | 675782 |
a0016c0014t0002 | 0/0 | 3294 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
a0017c0030t0007 | 0/0 | 3295 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3290): Show |
chr4 | 620573 | 675782 |
a0018c0018t0001 | 0/1 | 3294 | 1 | 0 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | CTGGG others(3289): Show |
chr4 | 620573 | 675782 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0002 | 0/0 | 6 | 1 | 1 | 3 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0001 | 0/0 | 8 | 4 | 2 | 1 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0206 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0006g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0006g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0006g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0007g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0007g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0011g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0012g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0013g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0001t0014g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0002t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0002t0004g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0002t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0002t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0002t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0002t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0004t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0004t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0004t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0004t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0004t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0005t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0005t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0005t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0005t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0008t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0008t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0008t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0009t0009g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0009t0009g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0009t0009g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0012t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0012t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0015t0002g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0017t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0022t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0024t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0026t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0001c0029t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0002c0003t0005g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0002c0003t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0002c0003t0005g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0002c0003t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0002c0003t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0002c0003t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0002c0003t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0002c0003t0005g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0002c0003t0005g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0002c0003t0005g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0003c0006t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0003c0006t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0003c0006t0007g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0003c0006t0007g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0003c0010t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0003c0010t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0003c0010t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0004c0007t0008g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0004c0007t0008g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0004c0007t0008g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0005c0011t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0005c0011t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0006c0013t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0006c0013t0010g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0007c0027t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0008c0028t0008g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0009c0025t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0010c0021t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0011c0020t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0012c0031t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0013c0016t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0014c0023t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0015c0019t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0016c0014t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0017c0030t0007g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
a0018c0018t0001g0170 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0023 | EUR | GBR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0187 | EUR | FIN | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0131 | EUR | FIN | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | CHS | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | CHS | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | CHS | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | CHS | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00558 | hp2 | a0001 | c0001 | t0007 | g0143 | EAS | CHS | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | CHS | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | CHS | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00621 | hp2 | a0003 | c0006 | t0007 | g0195 | EAS | CHS | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00642 | hp2 | a0004 | c0007 | t0008 | g0237 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00733 | hp2 | a0007 | c0027 | t0002 | g0019 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01070 | hp2 | a0001 | c0001 | t0006 | g0022 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0093 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01167 | hp2 | a0001 | c0001 | t0006 | g0167 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | CLM | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01255 | hp2 | a0002 | c0003 | t0005 | g0261 | AMR | CLM | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01258 | hp2 | a0001 | c0015 | t0002 | g0005 | AMR | CLM | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0110 | AMR | CLM | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01358 | hp2 | a0004 | c0007 | t0008 | g0238 | AMR | CLM | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01433 | hp1 | a0001 | c0002 | t0004 | g0013 | AMR | CLM | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0144 | EUR | IBS | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01517 | hp2 | a0001 | c0002 | t0004 | g0013 | EUR | IBS | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01884 | hp1 | a0001 | c0008 | t0002 | g0121 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0058 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01891 | hp1 | a0001 | c0009 | t0009 | g0248 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0134 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PEL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01975 | hp2 | a0002 | c0003 | t0005 | g0255 | AMR | PEL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0127 | AMR | PEL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0210 | AMR | PEL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02004 | hp2 | a0001 | c0002 | t0004 | g0036 | AMR | PEL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | KHV | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02055 | hp2 | a0001 | c0004 | t0001 | g0096 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | KHV | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | KHV | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | KHV | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | KHV | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | KHV | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | CDX | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02257 | hp2 | a0001 | c0005 | t0001 | g0245 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02280 | hp1 | a0001 | c0008 | t0002 | g0118 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0117 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0181 | EAS | KHV | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | KHV | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0217 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02572 | hp2 | a0001 | c0005 | t0001 | g0204 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02602 | hp1 | a0001 | c0001 | t0013 | g0002 | SAS | PJL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02615 | hp1 | a0001 | c0002 | t0004 | g0094 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02622 | hp1 | a0001 | c0009 | t0009 | g0249 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02622 | hp2 | a0008 | c0028 | t0008 | g0241 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02630 | hp1 | a0001 | c0026 | t0001 | g0007 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02630 | hp2 | a0005 | c0011 | t0001 | g0251 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02647 | hp1 | a0002 | c0003 | t0005 | g0262 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02683 | hp1 | a0004 | c0007 | t0008 | g0239 | SAS | PJL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02717 | hp1 | a0002 | c0003 | t0005 | g0259 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02723 | hp2 | a0001 | c0002 | t0004 | g0062 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0128 | SAS | PJL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0111 | SAS | PJL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02809 | hp1 | a0001 | c0029 | t0001 | g0033 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02818 | hp1 | a0001 | c0001 | t0011 | g0046 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02818 | hp2 | a0009 | c0025 | t0002 | g0205 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02886 | hp1 | a0001 | c0004 | t0001 | g0055 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02895 | hp1 | a0001 | c0001 | t0012 | g0034 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02895 | hp2 | a0001 | c0002 | t0001 | g0063 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02922 | hp2 | a0001 | c0012 | t0003 | g0031 | AFR | ESN | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | ESN | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02965 | hp2 | a0001 | c0004 | t0001 | g0038 | AFR | ESN | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | ESN | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02970 | hp2 | a0002 | c0003 | t0005 | g0257 | AFR | ESN | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03041 | hp1 | a0010 | c0021 | t0002 | g0129 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03098 | hp1 | a0001 | c0001 | t0007 | g0263 | AFR | MSL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | MSL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03130 | hp2 | a0001 | c0005 | t0001 | g0246 | AFR | ESN | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | ESN | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03195 | hp1 | a0001 | c0012 | t0003 | g0032 | AFR | ESN | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | ESN | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0068 | AFR | MSL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03209 | hp2 | a0001 | c0004 | t0001 | g0067 | AFR | MSL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03225 | hp1 | a0002 | c0003 | t0005 | g0260 | AFR | MSL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0188 | AFR | MSL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03453 | hp1 | a0001 | c0004 | t0001 | g0056 | AFR | MSL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03453 | hp2 | a0006 | c0013 | t0010 | g0045 | AFR | MSL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0152 | AFR | MSL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03486 | hp2 | a0002 | c0003 | t0005 | g0258 | AFR | MSL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03490 | hp2 | a0001 | c0001 | t0006 | g0240 | SAS | PJL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03516 | hp1 | a0001 | c0008 | t0002 | g0120 | AFR | ESN | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03516 | hp2 | a0001 | c0004 | t0001 | g0069 | AFR | ESN | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03579 | hp1 | a0002 | c0003 | t0005 | g0254 | AFR | MSL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03579 | hp2 | a0011 | c0020 | t0001 | g0064 | AFR | MSL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0066 | SAS | PJL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | PJL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0233 | SAS | BEB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | BEB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03942 | hp2 | a0012 | c0031 | t0003 | g0073 | SAS | BEB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG04115 | hp1 | a0013 | c0016 | t0001 | g0197 | SAS | STU | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | STU | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0176 | SAS | BEB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | STU | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG04199 | hp2 | a0001 | c0001 | t0006 | g0049 | SAS | STU | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | STU | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | STU | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0250 | AFR | YRI | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18522 | hp2 | a0001 | c0002 | t0004 | g0014 | AFR | YRI | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18612 | hp1 | a0014 | c0023 | t0003 | g0082 | EAS | CHB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18906 | hp1 | a0001 | c0005 | t0001 | g0247 | AFR | YRI | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | YRI | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18943 | hp2 | a0003 | c0006 | t0001 | g0194 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18959 | hp2 | a0003 | c0010 | t0002 | g0191 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18970 | hp2 | a0001 | c0022 | t0002 | g0150 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18980 | hp1 | a0001 | c0001 | t0006 | g0125 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18982 | hp1 | a0003 | c0010 | t0002 | g0192 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18984 | hp1 | a0003 | c0010 | t0003 | g0190 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18989 | hp2 | a0001 | c0001 | t0006 | g0223 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18991 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18999 | hp1 | a0003 | c0006 | t0007 | g0193 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19004 | hp1 | a0015 | c0019 | t0003 | g0074 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19010 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19011 | hp2 | a0003 | c0006 | t0002 | g0104 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19030 | hp1 | a0006 | c0013 | t0010 | g0044 | AFR | LWK | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | LWK | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0141 | AFR | LWK | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19056 | hp2 | a0001 | c0001 | t0014 | g0123 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19080 | hp2 | a0016 | c0014 | t0002 | g0010 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19240 | hp1 | a0005 | c0011 | t0001 | g0252 | AFR | YRI | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | YRI | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA20129 | hp1 | a0001 | c0002 | t0004 | g0014 | AFR | ASW | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0060 | EUR | TSI | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0169 | EUR | TSI | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0244 | SAS | GIH | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | GIH | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02109 | hp1 | a0001 | c0009 | t0009 | g0053 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02486 | hp1 | a0001 | c0024 | t0002 | g0047 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02486 | hp2 | a0001 | c0017 | t0004 | g0037 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02559 | hp1 | a0001 | c0004 | t0001 | g0091 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0065 | AFR | ACB | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | MSL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | MSL | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0057 | AFR | USA | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA20300 | hp2 | a0002 | c0003 | t0005 | g0253 | AFR | USA | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA21309 | hp1 | a0002 | c0003 | t0005 | g0256 | AFR | LWK | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
NA21309 | hp2 | a0017 | c0030 | t0007 | g0137 | AFR | LWK | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
homoSapiens | chm13v2 | a0018 | c0018 | t0001 | g0170 | REF | REF | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0206 | REF | REF | PDE6B_chr4_620573_675782 | PDE6B | chr4 | 620573 | 675782 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:625652 | G | A | 1 | a0005 | 2 | HG02630.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.26G>A | p.Arg9Gln | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/22 | 80/3294 | 26/2565 | 9/854 | chr4 | 625652 | |||
chr4:625727 | C | T | 1 | a0006 | 2 | HG03453.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.101C>T | p.Ala34Val | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/22 | 155/3294 | 101/2565 | 34/854 | chr4 | 625727 | |||
chr4:625758 | C | G | 1 | a0012 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.132C>G | p.Cys44Trp | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/22 | 186/3294 | 132/2565 | 44/854 | chr4 | 625758 | |||
chr4:625769 | G | A | 1 | a0002 | 10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
missense_variant | MODERATE | c.143G>A | p.Arg48Gln | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/22 | 197/3294 | 143/2565 | 48/854 | chr4 | 625769 | |||
chr4:625771 | G | T | 1 | a0003 | 7 | HG00621.hp2 NA18943.hp2 NA18959.hp2 others(4): Show |
missense_variant | MODERATE | c.145G>T | p.Asp49Tyr | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/22 | 199/3294 | 145/2565 | 49/854 | chr4 | 625771 | |||
chr4:625799 | C | T | 1 | a0017 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.173C>T | p.Ala58Val | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/22 | 227/3294 | 173/2565 | 58/854 | chr4 | 625799 | |||
chr4:625969 | C | G | 1 | a0008 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.343C>G | p.Pro115Ala | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/22 | 397/3294 | 343/2565 | 115/854 | chr4 | 625969 | |||
chr4:625999 | C | G | 1 | a0002 | 10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
missense_variant | MODERATE | c.373C>G | p.Pro125Ala | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/22 | 427/3294 | 373/2565 | 125/854 | chr4 | 625999 | |||
chr4:634704 | G | A | 1 | a0004 | 3 | HG00642.hp2 HG01358.hp2 HG02683.hp1 |
missense_variant | MODERATE | c.496G>A | p.Glu166Lys | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/22 | 550/3294 | 496/2565 | 166/854 | chr4 | 634704 | |||
chr4:634800 | G | A | 1 | a0016 | 1 | NA19080.hp2 | missense_variant | MODERATE | c.592G>A | p.Gly198Ser | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/22 | 646/3294 | 592/2565 | 198/854 | chr4 | 634800 | |||
chr4:634809 | T | C | 1 | a0017 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.601T>C | p.Phe201Leu | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/22 | 655/3294 | 601/2565 | 201/854 | chr4 | 634809 | |||
chr4:654125 | T | C | 1 | a0013 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.898T>C | p.Tyr300His | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 5/22 | 952/3294 | 898/2565 | 300/854 | chr4 | 654125 | |||
chr4:654806 | G | GTGTCTTC others(15): Show |
1 | a0001 | 1 | HG02004.hp2 | frameshift_variant | HIGH | c.928-9_940dupGCTTCT others(16): Show |
p.Tyr314fs | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 6/22 | 995/3294 | 941/2565 | 314/854 | INFO_REALIGN_3_PRIME | chr4 | 654806 | ||
chr4:654863 | G | A | 1 | a0015 | 1 | NA19004.hp1 | missense_variant | MODERATE | c.967G>A | p.Gly323Ser | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 6/22 | 1021/3294 | 967/2565 | 323/854 | chr4 | 654863 | |||
chr4:656961 | G | A | 1 | a0011 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.1195G>A | p.Ala399Thr | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 9/22 | 1249/3294 | 1195/2565 | 399/854 | chr4 | 656961 | |||
chr4:657459 | G | A | 1 | a0010 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.1366G>A | p.Val456Met | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/22 | 1420/3294 | 1366/2565 | 456/854 | chr4 | 657459 | |||
chr4:658962 | C | T | 1 | a0007 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.1412C>T | p.Ala471Val | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/22 | 1466/3294 | 1412/2565 | 471/854 | chr4 | 658962 | |||
chr4:664190 | T | A | 1 | a0014 | 1 | NA18612.hp1 | missense_variant | MODERATE | c.2098T>A | p.Ser700Thr | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 17/22 | 2152/3294 | 2098/2565 | 700/854 | chr4 | 664190 | |||
chr4:667973 | A | G | 1 | a0009 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.2470A>G | p.Lys824Glu | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/22 | 2524/3294 | 2470/2565 | 824/854 | chr4 | 667973 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:625749 | G | A | 1 | a0002c0003 | 10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
synonymous_variant | LOW | c.123G>A | p.Pro41Pro | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/22 | 177/3294 | 123/2565 | 41/854 | chr4 | 625749 | |||
chr4:625896 | C | T | 2 | a0001c0012 a0001c0029 |
3 | HG02809.hp1 HG02922.hp2 HG03195.hp1 |
synonymous_variant | LOW | c.270C>T | p.Asp90Asp | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/22 | 324/3294 | 270/2565 | 90/854 | chr4 | 625896 | |||
chr4:626010 | C | T | 1 | a0002c0003 | 10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
synonymous_variant | LOW | c.384C>T | p.Ser128Ser | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/22 | 438/3294 | 384/2565 | 128/854 | chr4 | 626010 | |||
chr4:635909 | G | A | 1 | a0001c0015 | 1 | HG01258.hp2 | synonymous_variant | LOW | c.651G>A | p.Thr217Thr | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/22 | 705/3294 | 651/2565 | 217/854 | chr4 | 635909 | |||
chr4:635957 | G | A | 1 | a0003c0010 | 3 | NA18959.hp2 NA18982.hp1 NA18984.hp1 |
synonymous_variant | LOW | c.699G>A | p.Thr233Thr | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/22 | 753/3294 | 699/2565 | 233/854 | chr4 | 635957 | |||
chr4:654100 | T | C | 1 | a0001c0008 | 3 | HG01884.hp1 HG02280.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.873T>C | p.Ser291Ser | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 5/22 | 927/3294 | 873/2565 | 291/854 | chr4 | 654100 | |||
chr4:654142 | G | A | 4 | a0001c0002 a0001c0004 a0001c0017 others(1): Show |
22 | HG01433.hp1 HG01517.hp2 HG01884.hp2 others(19): Show |
synonymous_variant | LOW | c.915G>A | p.Thr305Thr | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 5/22 | 969/3294 | 915/2565 | 305/854 | chr4 | 654142 | |||
chr4:658996 | G | A | 1 | a0001c0022 | 1 | NA18970.hp2 | synonymous_variant | LOW | c.1446G>A | p.Glu482Glu | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/22 | 1500/3294 | 1446/2565 | 482/854 | chr4 | 658996 | |||
chr4:662154 | C | T | 1 | a0001c0004 | 7 | HG02055.hp2 HG02559.hp1 HG02886.hp1 others(4): Show |
synonymous_variant | LOW | c.1635C>T | p.Phe545Phe | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 13/22 | 1689/3294 | 1635/2565 | 545/854 | chr4 | 662154 | |||
chr4:663791 | C | T | 1 | a0001c0026 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.1942C>T | p.Leu648Leu | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 16/22 | 1996/3294 | 1942/2565 | 648/854 | chr4 | 663791 | |||
chr4:665257 | C | T | 1 | a0001c0017 | 1 | HG02486.hp2 | splice_region_variant&synonymous_variant | LOW | c.2196C>T | p.Val732Val | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 19/22 | 2250/3294 | 2196/2565 | 732/854 | chr4 | 665257 | |||
chr4:666551 | G | A | 1 | a0001c0009 | 3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
synonymous_variant | LOW | c.2289G>A | p.Lys763Lys | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/22 | 2343/3294 | 2289/2565 | 763/854 | chr4 | 666551 | |||
chr4:666593 | C | T | 3 | a0001c0005 a0005c0011 a0011c0020 |
7 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(4): Show |
synonymous_variant | LOW | c.2331C>T | p.Phe777Phe | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/22 | 2385/3294 | 2331/2565 | 777/854 | chr4 | 666593 | |||
chr4:670047 | A | G | 3 | a0001c0005 a0005c0011 a0011c0020 |
7 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(4): Show |
splice_region_variant&synonymous_variant | LOW | c.2505A>G | p.Val835Val | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 22/22 | 2559/3294 | 2505/2565 | 835/854 | chr4 | 670047 | |||
chr4:670068 | C | T | 1 | a0001c0024 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.2526C>T | p.Gly842Gly | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 22/22 | 2580/3294 | 2526/2565 | 842/854 | chr4 | 670068 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:670119 | A | G | 23 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(20): Show |
155 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(152): Show |
3_prime_UTR_variant | MODIFIER | c.*12A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 22/22 | 12 | chr4 | 670119 | ||||||
chr4:670127 | C | A | 4 | a0001c0001t0012 a0001c0009t0009 a0004c0007t0008 others(1): Show |
8 | HG00642.hp2 HG01358.hp2 HG01891.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*20C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 22/22 | 20 | chr4 | 670127 | ||||||
chr4:670239 | A | AT | 9 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0012 others(6): Show |
24 | HG00558.hp2 HG00621.hp2 HG01099.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*153dupT | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 22/22 | 154 | INFO_REALIGN_3_PRIME | chr4 | 670239 | |||||
chr4:670239 | A | ATT | 3 | a0001c0001t0005 a0001c0001t0011 a0002c0003t0005 |
13 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*152_*153dupTT | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 22/22 | 154 | INFO_REALIGN_3_PRIME | chr4 | 670239 | |||||
chr4:670239 | AT | A | 7 | a0001c0001t0003 a0001c0001t0006 a0001c0012t0003 others(4): Show |
56 | HG00423.hp1 HG00621.hp1 HG01070.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*153delT | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 22/22 | 153 | INFO_REALIGN_3_PRIME | chr4 | 670239 | |||||
chr4:670282 | A | G | 1 | a0001c0001t0014 | 1 | NA19056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*175A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 22/22 | 175 | chr4 | 670282 | ||||||
chr4:670298 | C | A | 4 | a0001c0001t0005 a0001c0001t0011 a0002c0003t0005 others(1): Show |
15 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*191C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 22/22 | 191 | chr4 | 670298 | ||||||
chr4:670298 | C | T | 1 | a0001c0001t0013 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*191C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 22/22 | 191 | chr4 | 670298 | ||||||
chr4:670521 | C | T | 1 | a0001c0009t0009 | 3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*414C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 22/22 | 414 | chr4 | 670521 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:626155 | G | T | 1 | a0001c0001t0007g0263 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.468+61G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 626155 | |||||||
chr4:626207 | C | T | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+113C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 626207 | |||||||
chr4:626261 | T | C | 1 | a0001c0001t0001g0030 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.468+167T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 626261 | |||||||
chr4:626420 | A | G | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+326A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 626420 | |||||||
chr4:626551 | C | T | 8 | a0001c0001t0005g0250 a0001c0005t0001g0245 a0001c0005t0001g0246 others(5): Show |
8 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+457C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 626551 | |||||||
chr4:626559 | G | C | 3 | a0001c0005t0001g0245 a0001c0005t0001g0246 a0001c0005t0001g0247 |
3 | HG02257.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.468+465G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 626559 | |||||||
chr4:626627 | C | T | 1 | a0001c0001t0002g0244 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.468+533C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 626627 | |||||||
chr4:626747 | G | A | 4 | a0001c0001t0003g0006 a0001c0012t0003g0031 a0001c0012t0003g0032 others(1): Show |
5 | HG01167.hp1 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+653G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 626747 | |||||||
chr4:626786 | G | A | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.468+692G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 626786 | |||||||
chr4:626829 | G | A | 2 | a0001c0001t0001g0007 a0001c0026t0001g0007 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.468+735G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 626829 | |||||||
chr4:626830 | A | C | 23 | a0001c0001t0001g0007 a0001c0001t0002g0242 a0001c0001t0002g0243 others(20): Show |
23 | HG00642.hp2 HG01255.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.468+736A>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 626830 | |||||||
chr4:626930 | G | A | 1 | a0001c0001t0002g0035 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.468+836G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 626930 | |||||||
chr4:626966 | G | A | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+872G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 626966 | |||||||
chr4:627072 | T | C | 109 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(106): Show |
116 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(113): Show |
intron_variant | MODIFIER | c.468+978T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 627072 | |||||||
chr4:627085 | G | A | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+991G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 627085 | |||||||
chr4:627138 | T | C | 1 | a0001c0002t0004g0036 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.468+1044T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 627138 | |||||||
chr4:627150 | G | GT | 20 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0224 others(17): Show |
20 | HG00621.hp1 HG00741.hp1 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.468+1070dupT | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 627150 | ||||||
chr4:627150 | G | GTTTT | 8 | a0002c0003t0005g0255 a0002c0003t0005g0256 a0002c0003t0005g0257 others(5): Show |
8 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+1067_468+1070d others(6): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 627150 | ||||||
chr4:627248 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.468+1154C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 627248 | |||||||
chr4:627268 | C | T | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+1174C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 627268 | |||||||
chr4:627291 | G | T | 19 | a0001c0001t0001g0007 a0001c0001t0002g0218 a0001c0001t0002g0219 others(16): Show |
19 | HG00642.hp2 HG01358.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.468+1197G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 627291 | |||||||
chr4:627296 | C | T | 11 | a0001c0001t0002g0217 a0002c0003t0005g0253 a0002c0003t0005g0254 others(8): Show |
11 | HG01255.hp2 HG01975.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.468+1202C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 627296 | |||||||
chr4:627326 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.468+1232A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 627326 | |||||||
chr4:627331 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.468+1237A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 627331 | |||||||
chr4:627342 | C | T | 1 | a0001c0001t0003g0102 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.468+1248C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 627342 | |||||||
chr4:627401 | T | C | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+1307T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 627401 | |||||||
chr4:627412 | C | G | 7 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(4): Show |
10 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.468+1318C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 627412 | |||||||
chr4:627447 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.468+1353G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 627447 | |||||||
chr4:627579 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.468+1485C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 627579 | |||||||
chr4:627727 | G | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(187): Show |
219 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.468+1633G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 627727 | |||||||
chr4:627894 | G | A | 2 | a0001c0001t0003g0054 a0003c0006t0002g0104 |
2 | NA18952.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.468+1800G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 627894 | |||||||
chr4:628083 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.468+1989C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 628083 | |||||||
chr4:628119 | A | G | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+2025A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 628119 | |||||||
chr4:628156 | A | AGCAAATC others(9): Show |
10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+2062_468+2063i others(18): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 628156 | |||||||
chr4:628157 | A | T | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+2063A>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 628157 | |||||||
chr4:628165 | T | C | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+2071T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 628165 | |||||||
chr4:628180 | T | G | 6 | a0001c0001t0005g0250 a0001c0005t0001g0245 a0001c0005t0001g0246 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+2086T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 628180 | |||||||
chr4:628195 | A | T | 6 | a0001c0001t0005g0250 a0001c0005t0001g0245 a0001c0005t0001g0246 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+2101A>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 628195 | |||||||
chr4:628196 | A | AGCCTCAT others(10): Show |
5 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+2103_468+2119d others(19): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 628196 | ||||||
chr4:628196 | A | C | 6 | a0001c0001t0005g0250 a0001c0005t0001g0245 a0001c0005t0001g0246 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.468+2102A>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 628196 | |||||||
chr4:628325 | C | T | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.468+2231C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 628325 | |||||||
chr4:628455 | G | A | 5 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+2361G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 628455 | |||||||
chr4:628558 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG00673.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.468+2464G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 628558 | |||||||
chr4:628560 | G | A | 1 | a0001c0001t0003g0006 | 2 | HG01167.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.468+2466G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 628560 | |||||||
chr4:628599 | C | A | 95 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0059 others(92): Show |
102 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.468+2505C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 628599 | |||||||
chr4:628670 | A | G | 1 | a0001c0002t0004g0014 | 2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.468+2576A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 628670 | |||||||
chr4:628864 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.468+2770C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 628864 | |||||||
chr4:628907 | C | T | 1 | a0013c0016t0001g0197 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.468+2813C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 628907 | |||||||
chr4:629033 | T | TCCCAGAA others(19): Show |
1 | a0001c0001t0002g0242 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.468+2940_468+2965d others(28): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 629033 | ||||||
chr4:629044 | G | A | 1 | a0001c0001t0007g0263 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.468+2950G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629044 | |||||||
chr4:629120 | T | C | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+3026T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629120 | |||||||
chr4:629137 | T | C | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+3043T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629137 | |||||||
chr4:629271 | T | A | 5 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+3177T>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629271 | |||||||
chr4:629302 | C | G | 1 | a0001c0001t0002g0196 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.468+3208C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629302 | |||||||
chr4:629338 | G | A | 1 | a0001c0001t0002g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.468+3244G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629338 | |||||||
chr4:629372 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | NA18948.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.468+3278G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629372 | |||||||
chr4:629381 | G | A | 2 | a0001c0004t0001g0055 a0001c0004t0001g0056 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.468+3287G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629381 | |||||||
chr4:629416 | C | A | 1 | a0001c0001t0002g0244 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.468+3322C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629416 | |||||||
chr4:629420 | A | G | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+3326A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629420 | |||||||
chr4:629459 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.468+3365C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629459 | |||||||
chr4:629477 | G | A | 2 | a0001c0002t0002g0057 a0001c0002t0002g0058 |
2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.468+3383G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629477 | |||||||
chr4:629487 | G | A | 2 | a0001c0001t0002g0110 a0001c0001t0002g0111 |
2 | HG01358.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.468+3393G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629487 | |||||||
chr4:629587 | C | A | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+3493C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629587 | |||||||
chr4:629704 | C | T | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+3610C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629704 | |||||||
chr4:629709 | T | G | 68 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0081 others(65): Show |
75 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.468+3615T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629709 | |||||||
chr4:629751 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.468+3657G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629751 | |||||||
chr4:629840 | G | T | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+3746G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629840 | |||||||
chr4:629891 | A | T | 105 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0059 others(102): Show |
113 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(110): Show |
intron_variant | MODIFIER | c.468+3797A>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629891 | |||||||
chr4:629897 | G | T | 7 | a0003c0006t0001g0194 a0003c0006t0002g0104 a0003c0006t0007g0193 others(4): Show |
7 | HG00621.hp2 NA18943.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.468+3803G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629897 | |||||||
chr4:629953 | A | G | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+3859A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 629953 | |||||||
chr4:630010 | G | A | 5 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+3916G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 630010 | |||||||
chr4:630050 | C | A | 1 | a0001c0001t0002g0244 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.468+3956C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 630050 | |||||||
chr4:630170 | T | C | 86 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0059 others(83): Show |
93 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.468+4076T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 630170 | |||||||
chr4:630215 | AGGCCGAG others(14): Show |
A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.468+4131_468+4151d others(23): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 630215 | ||||||
chr4:630233 | C | T | 3 | a0001c0005t0001g0245 a0001c0005t0001g0246 a0001c0005t0001g0247 |
3 | HG02257.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.468+4139C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 630233 | |||||||
chr4:630243 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.468+4149G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 630243 | |||||||
chr4:630260 | G | C | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.468+4166G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 630260 | |||||||
chr4:630292 | C | T | 1 | a0001c0001t0002g0189 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.468+4198C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 630292 | |||||||
chr4:630509 | C | T | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-4168C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 630509 | |||||||
chr4:630676 | A | G | 1 | a0001c0001t0002g0188 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.469-4001A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 630676 | |||||||
chr4:630730 | C | G | 1 | a0001c0001t0002g0189 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.469-3947C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 630730 | |||||||
chr4:630745 | G | A | 1 | a0001c0012t0003g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.469-3932G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 630745 | |||||||
chr4:630783 | G | A | 8 | a0001c0001t0005g0250 a0001c0005t0001g0245 a0001c0005t0001g0246 others(5): Show |
8 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.469-3894G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 630783 | |||||||
chr4:630795 | G | A | 3 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 |
3 | HG00642.hp2 HG01358.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.469-3882G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 630795 | |||||||
chr4:630842 | G | C | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.469-3835G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 630842 | |||||||
chr4:630868 | G | A | 2 | a0001c0002t0001g0060 a0001c0002t0004g0036 |
2 | HG02004.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.469-3809G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 630868 | |||||||
chr4:631012 | A | G | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-3665A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 631012 | |||||||
chr4:631108 | G | A | 96 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0059 others(93): Show |
103 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.469-3569G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 631108 | |||||||
chr4:631138 | A | T | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-3539A>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 631138 | |||||||
chr4:631160 | G | C | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-3517G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 631160 | |||||||
chr4:631241 | CAA | C | 3 | a0001c0012t0003g0031 a0001c0012t0003g0032 a0001c0029t0001g0033 |
3 | HG02809.hp1 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.469-3435_469-3434d others(4): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 631241 | |||||||
chr4:631321 | G | A | 2 | a0001c0001t0002g0114 a0001c0001t0002g0115 |
2 | NA18983.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.469-3356G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 631321 | |||||||
chr4:631349 | G | C | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-3328G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 631349 | |||||||
chr4:631579 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.469-3098G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 631579 | |||||||
chr4:631666 | A | G | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-3011A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 631666 | |||||||
chr4:631803 | C | G | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.469-2874C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 631803 | |||||||
chr4:631822 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-2855C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 631822 | |||||||
chr4:631902 | A | G | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-2775A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 631902 | |||||||
chr4:631915 | A | G | 1 | a0001c0002t0004g0036 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.469-2762A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 631915 | |||||||
chr4:632026 | A | G | 1 | a0001c0001t0002g0230 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.469-2651A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 632026 | |||||||
chr4:632065 | A | G | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-2612A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 632065 | |||||||
chr4:632070 | A | G | 96 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0059 others(93): Show |
103 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.469-2607A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 632070 | |||||||
chr4:632151 | T | A | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-2526T>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 632151 | |||||||
chr4:632173 | C | T | 96 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0059 others(93): Show |
103 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.469-2504C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 632173 | |||||||
chr4:632239 | T | A | 4 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-2438T>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 632239 | |||||||
chr4:632270 | G | T | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.469-2407G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 632270 | |||||||
chr4:632279 | G | A | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.469-2398G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 632279 | |||||||
chr4:632362 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.469-2315C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 632362 | |||||||
chr4:632363 | G | A | 5 | a0001c0001t0005g0250 a0001c0009t0009g0248 a0001c0009t0009g0249 others(2): Show |
5 | HG01891.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-2314G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 632363 | |||||||
chr4:632367 | G | A | 2 | a0005c0011t0001g0251 a0005c0011t0001g0252 |
2 | HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.469-2310G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 632367 | |||||||
chr4:632407 | G | T | 2 | a0001c0002t0002g0057 a0001c0002t0002g0058 |
2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.469-2270G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 632407 | |||||||
chr4:632432 | C | T | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-2245C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 632432 | |||||||
chr4:632518 | C | G | 1 | a0001c0001t0003g0101 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.469-2159C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 632518 | |||||||
chr4:632567 | GGTGGGGA others(98): Show |
G | 2 | a0001c0001t0001g0185 a0001c0001t0004g0186 |
2 | NA18612.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.469-2067_469-1963d others(2): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr4 | 632567 | ||||||
chr4:632708 | T | G | 78 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0081 others(75): Show |
85 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(82): Show |
intron_variant | MODIFIER | c.469-1969T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 632708 | |||||||
chr4:632801 | G | T | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1876G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 632801 | |||||||
chr4:632832 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.469-1845C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 632832 | |||||||
chr4:632997 | C | T | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-1680C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 632997 | |||||||
chr4:633014 | T | G | 96 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0059 others(93): Show |
103 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.469-1663T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 633014 | |||||||
chr4:633170 | C | T | 1 | a0001c0002t0004g0094 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.469-1507C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 633170 | |||||||
chr4:633203 | G | T | 1 | a0001c0001t0002g0184 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.469-1474G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 633203 | |||||||
chr4:633449 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.469-1228C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 633449 | |||||||
chr4:633506 | T | C | 2 | a0006c0013t0010g0044 a0006c0013t0010g0045 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.469-1171T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 633506 | |||||||
chr4:633599 | A | G | 96 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0059 others(93): Show |
103 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.469-1078A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 633599 | |||||||
chr4:633687 | A | G | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-990A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 633687 | |||||||
chr4:633725 | G | A | 68 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0081 others(65): Show |
75 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.469-952G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 633725 | |||||||
chr4:633733 | T | C | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-944T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 633733 | |||||||
chr4:633791 | G | A | 10 | a0001c0001t0002g0117 a0001c0001t0002g0119 a0001c0001t0002g0122 others(7): Show |
10 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-886G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 633791 | |||||||
chr4:633862 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.469-815G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 633862 | |||||||
chr4:633889 | G | A | 96 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0059 others(93): Show |
103 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.469-788G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 633889 | |||||||
chr4:633936 | G | A | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-741G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 633936 | |||||||
chr4:633939 | G | A | 2 | a0001c0009t0009g0248 a0001c0009t0009g0249 |
2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.469-738G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 633939 | |||||||
chr4:633964 | G | A | 1 | a0001c0001t0003g0234 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.469-713G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 633964 | |||||||
chr4:634005 | T | G | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-672T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 634005 | |||||||
chr4:634012 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0124 a0001c0001t0001g0224 others(2): Show |
6 | NA18945.hp2 NA18966.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-665G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 634012 | |||||||
chr4:634051 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-626C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 634051 | |||||||
chr4:634151 | G | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.469-526G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 634151 | |||||||
chr4:634203 | A | G | 1 | a0008c0028t0008g0241 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.469-474A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 634203 | |||||||
chr4:634386 | T | G | 96 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0059 others(93): Show |
103 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(100): Show |
intron_variant | MODIFIER | c.469-291T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 634386 | |||||||
chr4:634452 | G | T | 1 | a0001c0001t0002g0183 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.469-225G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 634452 | |||||||
chr4:634467 | C | T | 11 | a0001c0029t0001g0033 a0002c0003t0005g0253 a0002c0003t0005g0254 others(8): Show |
11 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.469-210C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 634467 | |||||||
chr4:634498 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-179C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 1/21 | chr4 | 634498 | |||||||
chr4:634904 | C | T | 68 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0081 others(65): Show |
75 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.621+75C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 634904 | |||||||
chr4:634905 | G | A | 1 | a0001c0001t0006g0125 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.621+76G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 634905 | |||||||
chr4:634916 | TTTACCTG others(127): Show |
T | 1 | a0001c0001t0003g0061 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.621+245_621+378del | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 634916 | ||||||
chr4:634939 | G | A | 1 | a0001c0001t0003g0102 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.621+110G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 634939 | |||||||
chr4:634980 | CGCGTGTT others(161): Show |
C | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+154_621+321del | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 634980 | ||||||
chr4:635061 | G | C | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.621+232G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635061 | |||||||
chr4:635064 | CGCCTGCC others(77): Show |
C | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.621+245_621+328del others(84): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 635064 | ||||||
chr4:635072 | C | T | 3 | a0001c0005t0001g0245 a0001c0005t0001g0246 a0001c0005t0001g0247 |
3 | HG02257.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.621+243C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635072 | |||||||
chr4:635082 | CTGCTGCG others(35): Show |
C | 1 | a0001c0001t0002g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.621+303_621+344del others(42): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 635082 | ||||||
chr4:635145 | A | ACCTGCCT others(3): Show |
1 | a0001c0001t0002g0189 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.621+323_621+324ins others(10): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 635145 | ||||||
chr4:635157 | G | A | 20 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(17): Show |
20 | HG00642.hp2 HG01255.hp2 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.621+328G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635157 | |||||||
chr4:635159 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.621+330G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635159 | |||||||
chr4:635174 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.621+345C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635174 | |||||||
chr4:635174 | CGTCCACC others(43): Show |
C | 20 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0116 others(17): Show |
22 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(19): Show |
intron_variant | MODIFIER | c.621+377_621+426del others(50): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 635174 | ||||||
chr4:635178 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.621+349C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635178 | |||||||
chr4:635179 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.621+350A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635179 | |||||||
chr4:635198 | C | CGCCTGCC others(169): Show |
1 | a0001c0022t0002g0150 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.621+376_621+377ins others(176): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 635198 | ||||||
chr4:635199 | G | A | 2 | a0001c0001t0001g0227 a0001c0001t0001g0232 |
2 | HG01099.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.621+370G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635199 | |||||||
chr4:635206 | C | T | 1 | a0001c0001t0002g0035 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.621+377C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635206 | |||||||
chr4:635208 | CGTGTTCT others(281): Show |
C | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.621+393_622-371del | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 635208 | ||||||
chr4:635222 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | NA18964.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.621+393C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635222 | |||||||
chr4:635224 | T | C | 5 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0182 others(2): Show |
5 | HG02683.hp2 NA18964.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.621+395T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635224 | |||||||
chr4:635256 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.621+427T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635256 | |||||||
chr4:635274 | C | T | 1 | a0001c0005t0001g0247 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.621+445C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635274 | |||||||
chr4:635278 | T | C | 1 | a0001c0005t0001g0247 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.621+449T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635278 | |||||||
chr4:635279 | G | A | 1 | a0001c0005t0001g0247 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.621+450G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635279 | |||||||
chr4:635285 | C | T | 1 | a0001c0005t0001g0247 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.621+456C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635285 | |||||||
chr4:635287 | G | A | 1 | a0001c0005t0001g0247 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.621+458G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635287 | |||||||
chr4:635302 | CGCCTGCC others(85): Show |
C | 9 | a0002c0003t0005g0254 a0002c0003t0005g0255 a0002c0003t0005g0256 others(6): Show |
9 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.621+483_622-477del others(92): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 635302 | ||||||
chr4:635310 | C | T | 1 | a0001c0005t0001g0247 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.621+481C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635310 | |||||||
chr4:635312 | C | CGTGTTCT others(85): Show |
3 | a0001c0001t0001g0130 a0001c0001t0001g0158 a0001c0001t0001g0201 |
3 | HG02056.hp2 NA18960.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.622-520_622-429dup others(92): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 635312 | ||||||
chr4:635312 | CGTGTTCT others(85): Show |
C | 5 | a0001c0001t0005g0250 a0001c0009t0009g0248 a0001c0009t0009g0249 others(2): Show |
5 | HG01891.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.622-520_622-429del others(92): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 635312 | ||||||
chr4:635326 | T | C | 2 | a0001c0002t0004g0062 a0001c0005t0001g0247 |
2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.621+497T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635326 | |||||||
chr4:635332 | C | T | 2 | a0001c0002t0004g0062 a0001c0005t0001g0247 |
2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.621+503C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635332 | |||||||
chr4:635333 | A | G | 2 | a0001c0002t0004g0062 a0001c0005t0001g0247 |
2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.621+504A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635333 | |||||||
chr4:635339 | T | C | 2 | a0001c0002t0004g0062 a0001c0005t0001g0247 |
2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.621+510T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635339 | |||||||
chr4:635340 | TACCTGCC others(31): Show |
T | 2 | a0001c0002t0004g0062 a0001c0005t0001g0247 |
2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.621+512_622-502del others(38): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635340 | |||||||
chr4:635345 | G | GCCTGCCT others(35): Show |
3 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0225 |
3 | NA18939.hp1 NA18973.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.622-518_622-477dup others(42): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 635345 | ||||||
chr4:635352 | T | C | 1 | a0002c0003t0005g0253 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.621+523T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635352 | |||||||
chr4:635360 | C | T | 1 | a0002c0003t0005g0253 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.622-520C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635360 | |||||||
chr4:635360 | CGCGTGTT others(85): Show |
C | 1 | a0001c0008t0002g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.622-428_622-337del others(92): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 635360 | ||||||
chr4:635374 | C | T | 1 | a0002c0003t0005g0253 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.622-506C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635374 | |||||||
chr4:635375 | A | G | 1 | a0002c0003t0005g0253 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.622-505A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635375 | |||||||
chr4:635380 | T | C | 2 | a0001c0002t0004g0062 a0001c0005t0001g0247 |
2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.622-500T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635380 | |||||||
chr4:635387 | CCCTGCCT others(135): Show |
C | 69 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0081 others(66): Show |
76 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.622-476_622-335del | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 635387 | ||||||
chr4:635394 | T | C | 2 | a0001c0002t0004g0062 a0001c0005t0001g0247 |
2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.622-486T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635394 | |||||||
chr4:635394 | T | TGCCTCCC others(5): Show |
1 | a0002c0003t0005g0253 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.622-482_622-481ins others(12): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 635394 | ||||||
chr4:635404 | T | C | 2 | a0001c0002t0004g0062 a0001c0005t0001g0247 |
2 | HG02723.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.622-476T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635404 | |||||||
chr4:635452 | T | C | 1 | a0001c0002t0004g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.622-428T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635452 | |||||||
chr4:635452 | TGCGTGTT others(85): Show |
T | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.622-384_622-293del others(92): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 635452 | ||||||
chr4:635479 | CCCTGCCT others(43): Show |
C | 1 | a0001c0002t0004g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.622-384_622-335del others(50): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 635479 | ||||||
chr4:635529 | G | GCCTGCCT others(35): Show |
1 | a0001c0001t0001g0164 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.622-322_622-281dup others(42): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr4 | 635529 | ||||||
chr4:635544 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.622-336C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635544 | |||||||
chr4:635606 | T | G | 1 | a0001c0024t0002g0047 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.622-274T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635606 | |||||||
chr4:635648 | T | G | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.622-232T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635648 | |||||||
chr4:635693 | G | C | 3 | a0001c0005t0001g0245 a0001c0005t0001g0246 a0001c0005t0001g0247 |
3 | HG02257.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.622-187G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635693 | |||||||
chr4:635704 | C | T | 5 | a0001c0001t0002g0242 a0001c0001t0003g0233 a0001c0001t0003g0234 others(2): Show |
5 | HG03831.hp1 NA18948.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.622-176C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635704 | |||||||
chr4:635821 | C | T | 1 | a0005c0011t0001g0252 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.622-59C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 2/21 | chr4 | 635821 | |||||||
chr4:635980 | G | A | 2 | a0001c0009t0009g0248 a0001c0009t0009g0249 |
2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.711+11G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 635980 | |||||||
chr4:636040 | G | C | 1 | a0001c0001t0002g0127 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.711+71G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 636040 | |||||||
chr4:636403 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+434C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 636403 | |||||||
chr4:636409 | C | T | 1 | a0005c0011t0001g0252 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.711+440C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 636409 | |||||||
chr4:636430 | C | T | 1 | a0001c0002t0004g0013 | 2 | HG01433.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.711+461C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 636430 | |||||||
chr4:636609 | G | A | 4 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0097 others(1): Show |
4 | HG02055.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+640G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 636609 | |||||||
chr4:636658 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+689G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 636658 | |||||||
chr4:636660 | C | T | 1 | a0001c0001t0004g0093 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.711+691C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 636660 | |||||||
chr4:636680 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.711+711C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 636680 | |||||||
chr4:636681 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.711+712G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 636681 | |||||||
chr4:636728 | C | T | 1 | a0001c0005t0001g0247 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.711+759C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 636728 | |||||||
chr4:636860 | C | T | 1 | a0001c0001t0003g0043 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.711+891C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 636860 | |||||||
chr4:636881 | G | T | 5 | a0001c0001t0001g0007 a0001c0001t0012g0034 a0001c0026t0001g0007 others(2): Show |
5 | HG02630.hp1 HG02895.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.711+912G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 636881 | |||||||
chr4:636907 | G | A | 8 | a0001c0001t0005g0250 a0001c0005t0001g0245 a0001c0005t0001g0246 others(5): Show |
8 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.711+938G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 636907 | |||||||
chr4:636924 | T | C | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+955T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 636924 | |||||||
chr4:636995 | G | C | 3 | a0001c0005t0001g0245 a0001c0005t0001g0246 a0001c0005t0001g0247 |
3 | HG02257.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.711+1026G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 636995 | |||||||
chr4:637101 | T | C | 5 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.711+1132T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 637101 | |||||||
chr4:637189 | C | T | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.711+1220C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 637189 | |||||||
chr4:637232 | T | G | 1 | a0004c0007t0008g0237 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.711+1263T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 637232 | |||||||
chr4:637295 | C | T | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.711+1326C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 637295 | |||||||
chr4:637309 | C | T | 2 | a0001c0002t0002g0057 a0001c0002t0002g0058 |
2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.711+1340C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 637309 | |||||||
chr4:637313 | C | G | 8 | a0001c0001t0005g0250 a0001c0005t0001g0245 a0001c0005t0001g0246 others(5): Show |
8 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.711+1344C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 637313 | |||||||
chr4:637315 | C | T | 2 | a0001c0001t0002g0220 a0001c0001t0002g0221 |
2 | HG02258.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.711+1346C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 637315 | |||||||
chr4:637412 | G | T | 5 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.711+1443G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 637412 | |||||||
chr4:637446 | T | C | 20 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(17): Show |
20 | HG00642.hp2 HG01255.hp2 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.711+1477T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 637446 | |||||||
chr4:637537 | T | C | 3 | a0001c0001t0001g0004 a0001c0001t0001g0105 a0001c0001t0001g0106 |
5 | HG00673.hp2 HG02129.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.711+1568T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 637537 | |||||||
chr4:637639 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(10): Show |
18 | HG00597.hp1 HG00673.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.711+1670C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 637639 | |||||||
chr4:637766 | G | A | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.711+1797G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 637766 | |||||||
chr4:637798 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.711+1829C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 637798 | |||||||
chr4:637823 | C | T | 1 | a0001c0001t0002g0173 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.711+1854C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 637823 | |||||||
chr4:637845 | C | T | 5 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.711+1876C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 637845 | |||||||
chr4:637900 | C | T | 1 | a0002c0003t0005g0262 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.711+1931C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 637900 | |||||||
chr4:637935 | G | A | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.711+1966G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 637935 | |||||||
chr4:637953 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+1984C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 637953 | |||||||
chr4:638051 | G | A | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.711+2082G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638051 | |||||||
chr4:638071 | C | G | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+2102C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638071 | |||||||
chr4:638086 | C | T | 3 | a0001c0001t0005g0250 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.711+2117C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638086 | |||||||
chr4:638093 | G | C | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.711+2124G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638093 | |||||||
chr4:638192 | T | C | 1 | a0001c0001t0003g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.711+2223T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638192 | |||||||
chr4:638289 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+2320G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638289 | |||||||
chr4:638423 | A | G | 1 | a0001c0001t0002g0172 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.711+2454A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638423 | |||||||
chr4:638437 | C | A | 3 | a0001c0005t0001g0245 a0001c0005t0001g0246 a0001c0005t0001g0247 |
3 | HG02257.hp2 HG03130.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.711+2468C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638437 | |||||||
chr4:638467 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+2498C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638467 | |||||||
chr4:638525 | G | A | 5 | a0001c0002t0001g0063 a0001c0002t0001g0065 a0001c0004t0001g0055 others(2): Show |
5 | HG02559.hp2 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.711+2556G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638525 | |||||||
chr4:638543 | G | A | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.711+2574G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638543 | |||||||
chr4:638543 | G | C | 1 | a0001c0001t0003g0176 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.711+2574G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638543 | |||||||
chr4:638600 | A | C | 2 | a0002c0003t0005g0260 a0002c0003t0005g0261 |
2 | HG01255.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.711+2631A>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638600 | |||||||
chr4:638642 | T | G | 2 | a0001c0002t0004g0062 a0001c0017t0004g0037 |
2 | HG02486.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.711+2673T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638642 | |||||||
chr4:638696 | G | T | 5 | a0001c0001t0005g0250 a0001c0009t0009g0248 a0001c0009t0009g0249 others(2): Show |
5 | HG01891.hp1 HG02622.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.711+2727G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638696 | |||||||
chr4:638766 | G | A | 2 | a0006c0013t0010g0044 a0006c0013t0010g0045 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.711+2797G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638766 | |||||||
chr4:638774 | G | T | 1 | a0001c0001t0001g0215 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.711+2805G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638774 | |||||||
chr4:638890 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+2921G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638890 | |||||||
chr4:638941 | G | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0092 |
3 | HG00099.hp1 HG01346.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.711+2972G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638941 | |||||||
chr4:638985 | G | C | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+3016G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 638985 | |||||||
chr4:639016 | C | G | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+3047C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 639016 | |||||||
chr4:639069 | C | T | 2 | a0005c0011t0001g0251 a0005c0011t0001g0252 |
2 | HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.711+3100C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 639069 | |||||||
chr4:639106 | G | A | 3 | a0003c0010t0002g0191 a0003c0010t0002g0192 a0003c0010t0003g0190 |
3 | NA18959.hp2 NA18982.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.711+3137G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 639106 | |||||||
chr4:639148 | GT | G | 13 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(10): Show |
13 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.711+3190delT | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 639148 | ||||||
chr4:639314 | A | T | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+3345A>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 639314 | |||||||
chr4:639340 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+3371C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 639340 | |||||||
chr4:639504 | C | T | 3 | a0001c0001t0005g0250 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02622.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.711+3535C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 639504 | |||||||
chr4:639590 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+3621G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 639590 | |||||||
chr4:639644 | C | T | 1 | a0001c0004t0001g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.711+3675C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 639644 | |||||||
chr4:639693 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.711+3724G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 639693 | |||||||
chr4:639782 | G | A | 67 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0081 others(64): Show |
74 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.711+3813G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 639782 | |||||||
chr4:639947 | G | A | 4 | a0001c0001t0001g0007 a0001c0026t0001g0007 a0006c0013t0010g0044 others(1): Show |
4 | HG02630.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+3978G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 639947 | |||||||
chr4:639970 | C | A | 1 | a0001c0001t0003g0066 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.711+4001C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 639970 | |||||||
chr4:640023 | A | G | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+4054A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 640023 | |||||||
chr4:640432 | A | G | 1 | a0001c0002t0001g0065 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.711+4463A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 640432 | |||||||
chr4:640493 | C | T | 1 | a0001c0001t0004g0181 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.711+4524C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 640493 | |||||||
chr4:640541 | G | A | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+4572G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 640541 | |||||||
chr4:640541 | G | GA | 6 | a0001c0001t0004g0068 a0001c0004t0001g0038 a0001c0004t0001g0067 others(3): Show |
6 | HG02055.hp2 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.711+4582dupA | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 640541 | ||||||
chr4:640655 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.711+4686G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 640655 | |||||||
chr4:640669 | T | G | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+4700T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 640669 | |||||||
chr4:640718 | A | T | 10 | a0001c0001t0001g0007 a0001c0001t0006g0240 a0001c0001t0012g0034 others(7): Show |
10 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+4749A>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 640718 | |||||||
chr4:640809 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG00323.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.711+4840G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 640809 | |||||||
chr4:640812 | G | A | 66 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0081 others(63): Show |
73 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.711+4843G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 640812 | |||||||
chr4:640849 | C | G | 2 | a0001c0001t0001g0007 a0001c0026t0001g0007 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.711+4880C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 640849 | |||||||
chr4:641109 | C | T | 1 | a0001c0001t0002g0244 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.711+5140C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 641109 | |||||||
chr4:641186 | T | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0177 |
3 | NA19002.hp1 NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.711+5217T>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 641186 | |||||||
chr4:641376 | T | G | 4 | a0001c0005t0001g0245 a0001c0005t0001g0246 a0001c0005t0001g0247 others(1): Show |
4 | HG02257.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+5407T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 641376 | |||||||
chr4:641416 | C | T | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.711+5447C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 641416 | |||||||
chr4:641417 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.711+5448G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 641417 | |||||||
chr4:641506 | C | T | 4 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+5537C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 641506 | |||||||
chr4:641537 | A | G | 110 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0059 others(107): Show |
118 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.711+5568A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 641537 | |||||||
chr4:641571 | G | A | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.711+5602G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 641571 | |||||||
chr4:641637 | G | GT | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.711+5674dupT | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 641637 | ||||||
chr4:641699 | T | G | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.711+5730T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 641699 | |||||||
chr4:641756 | C | G | 1 | a0001c0001t0001g0023 | 2 | HG00099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.711+5787C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 641756 | |||||||
chr4:641759 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.711+5790G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 641759 | |||||||
chr4:641835 | T | C | 90 | a0001c0001t0001g0012 a0001c0001t0001g0048 a0001c0001t0001g0050 others(87): Show |
98 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.711+5866T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 641835 | |||||||
chr4:641835 | T | G | 1 | a0001c0001t0003g0100 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.711+5866T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 641835 | |||||||
chr4:641898 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.711+5929C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 641898 | |||||||
chr4:641899 | A | T | 4 | a0001c0001t0001g0007 a0001c0026t0001g0007 a0006c0013t0010g0044 others(1): Show |
4 | HG02630.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+5930A>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 641899 | |||||||
chr4:642084 | A | G | 3 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0003g0171 |
3 | NA18983.hp1 NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.711+6115A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 642084 | |||||||
chr4:642116 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.711+6147G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 642116 | |||||||
chr4:642116 | G | C | 5 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.711+6147G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 642116 | |||||||
chr4:642189 | C | CAGCT | 5 | a0001c0001t0002g0242 a0001c0001t0003g0233 a0001c0001t0003g0234 others(2): Show |
5 | HG03831.hp1 NA18948.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.711+6221_711+6224d others(6): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 642189 | ||||||
chr4:642551 | C | T | 1 | a0004c0007t0008g0239 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.711+6582C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 642551 | |||||||
chr4:642725 | C | CA | 19 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0201 others(16): Show |
19 | HG01358.hp1 HG01891.hp2 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.711+6781dupA | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 642725 | ||||||
chr4:642725 | C | CAAAAAAA others(3): Show |
30 | a0001c0001t0001g0012 a0001c0001t0001g0081 a0001c0001t0001g0084 others(27): Show |
33 | HG00099.hp1 HG01346.hp2 HG02004.hp2 others(30): Show |
intron_variant | MODIFIER | c.711+6772_711+6781d others(12): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 642725 | ||||||
chr4:642725 | C | CAAAAAAA others(4): Show |
25 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0059 others(22): Show |
28 | HG00423.hp1 HG00735.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.711+6771_711+6781d others(13): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 642725 | ||||||
chr4:642725 | C | CAAAAAAA others(5): Show |
13 | a0001c0001t0001g0097 a0001c0001t0002g0070 a0001c0001t0002g0072 others(10): Show |
14 | HG01433.hp1 HG01517.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.711+6770_711+6781d others(14): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 642725 | ||||||
chr4:642725 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0003g0043 a0001c0001t0003g0098 a0001c0002t0004g0094 |
3 | HG00621.hp1 HG02615.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.711+6769_711+6781d others(15): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 642725 | ||||||
chr4:642725 | C | CAAAAAAA others(7): Show |
1 | a0001c0005t0001g0245 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.711+6768_711+6781d others(16): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 642725 | ||||||
chr4:642725 | C | CAAAAAAA others(8): Show |
2 | a0005c0011t0001g0251 a0005c0011t0001g0252 |
2 | HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.711+6767_711+6781d others(17): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 642725 | ||||||
chr4:642725 | C | CAAAAAAA others(11): Show |
4 | a0002c0003t0005g0254 a0002c0003t0005g0255 a0002c0003t0005g0259 others(1): Show |
4 | HG01255.hp2 HG01975.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+6764_711+6781d others(20): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 642725 | ||||||
chr4:642725 | C | CAAAAAAA others(12): Show |
4 | a0002c0003t0005g0257 a0002c0003t0005g0258 a0002c0003t0005g0260 others(1): Show |
4 | HG02647.hp1 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+6763_711+6781d others(21): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 642725 | ||||||
chr4:642725 | C | CAAAAAAA others(14): Show |
1 | a0002c0003t0005g0256 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.711+6761_711+6781d others(23): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 642725 | ||||||
chr4:642725 | C | CAAAAAAA others(22): Show |
1 | a0011c0020t0001g0064 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.711+6781_711+6782i others(31): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 642725 | ||||||
chr4:642725 | C | CAAAAAAA others(24): Show |
1 | a0001c0005t0001g0247 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.711+6781_711+6782i others(33): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 642725 | ||||||
chr4:642725 | C | CAGAAAAA others(4): Show |
4 | a0001c0001t0001g0007 a0001c0026t0001g0007 a0006c0013t0010g0044 others(1): Show |
4 | HG02630.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+6757_711+6758i others(13): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 642725 | ||||||
chr4:642730 | A | C | 4 | a0001c0001t0001g0007 a0001c0026t0001g0007 a0006c0013t0010g0044 others(1): Show |
4 | HG02630.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+6761A>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 642730 | |||||||
chr4:642814 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.711+6845T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 642814 | |||||||
chr4:642845 | T | C | 2 | a0001c0002t0002g0057 a0001c0002t0002g0058 |
2 | HG01884.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.711+6876T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 642845 | |||||||
chr4:642990 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.711+7021G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 642990 | |||||||
chr4:643032 | G | A | 1 | a0017c0030t0007g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.711+7063G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 643032 | |||||||
chr4:643113 | T | A | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.711+7144T>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 643113 | |||||||
chr4:643158 | A | C | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.711+7189A>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 643158 | |||||||
chr4:643305 | C | A | 1 | a0001c0002t0004g0014 | 2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.711+7336C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 643305 | |||||||
chr4:643474 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.711+7505G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 643474 | |||||||
chr4:643724 | T | G | 10 | a0001c0001t0002g0017 a0001c0001t0002g0127 a0001c0001t0002g0138 others(7): Show |
11 | HG00438.hp1 HG00609.hp1 HG00639.hp2 others(8): Show |
intron_variant | MODIFIER | c.711+7755T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 643724 | |||||||
chr4:643743 | TTAGGCTT others(4725): Show |
T | 2 | a0005c0011t0001g0251 a0005c0011t0001g0252 |
2 | HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.711+7776_712-5376d others(2): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 643743 | ||||||
chr4:643747 | G | A | 1 | a0002c0003t0005g0253 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.711+7778G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 643747 | |||||||
chr4:643789 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.711+7820G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 643789 | |||||||
chr4:643863 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.711+7894T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 643863 | |||||||
chr4:643905 | T | C | 2 | a0006c0013t0010g0044 a0006c0013t0010g0045 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.711+7936T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 643905 | |||||||
chr4:643918 | C | CT | 61 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0018 others(58): Show |
65 | HG00099.hp1 HG00423.hp1 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.711+7970dupT | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 643918 | ||||||
chr4:643918 | C | CTT | 13 | a0001c0001t0001g0092 a0001c0001t0011g0046 a0001c0004t0001g0038 others(10): Show |
13 | HG01975.hp2 HG02486.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.711+7969_711+7970d others(4): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 643918 | ||||||
chr4:644108 | G | A | 4 | a0001c0005t0001g0245 a0001c0005t0001g0246 a0001c0005t0001g0247 others(1): Show |
4 | HG02257.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+8139G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 644108 | |||||||
chr4:644139 | G | A | 4 | a0001c0005t0001g0245 a0001c0005t0001g0246 a0001c0005t0001g0247 others(1): Show |
4 | HG02257.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+8170G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 644139 | |||||||
chr4:644163 | C | T | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.711+8194C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 644163 | |||||||
chr4:644197 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.711+8228G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 644197 | |||||||
chr4:644392 | G | A | 2 | a0001c0001t0001g0007 a0001c0026t0001g0007 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.711+8423G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 644392 | |||||||
chr4:644531 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.711+8562T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 644531 | |||||||
chr4:644641 | C | T | 2 | a0001c0001t0002g0051 a0001c0001t0011g0046 |
2 | HG02818.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.711+8672C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 644641 | |||||||
chr4:644654 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.711+8685C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 644654 | |||||||
chr4:644667 | C | T | 3 | a0001c0001t0002g0016 a0001c0001t0002g0132 a0001c0001t0002g0188 |
4 | HG01243.hp2 HG02717.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+8698C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 644667 | |||||||
chr4:644678 | C | T | 4 | a0001c0001t0005g0250 a0001c0009t0009g0053 a0001c0009t0009g0248 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+8709C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 644678 | |||||||
chr4:644687 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.711+8718G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 644687 | |||||||
chr4:644772 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.711+8803C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 644772 | |||||||
chr4:644913 | C | T | 1 | a0006c0013t0010g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.712-8939C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 644913 | |||||||
chr4:644959 | T | C | 1 | a0001c0002t0004g0094 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.712-8893T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 644959 | |||||||
chr4:644960 | G | C | 1 | a0001c0001t0003g0043 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.712-8892G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 644960 | |||||||
chr4:645290 | A | AT | 21 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0028 others(18): Show |
23 | HG00408.hp2 HG00438.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.712-8539dupT | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 645290 | ||||||
chr4:645290 | AT | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0113 a0001c0001t0001g0130 others(8): Show |
11 | HG00639.hp1 HG01433.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.712-8539delT | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 645290 | ||||||
chr4:645290 | ATTT | A | 12 | a0001c0001t0003g0003 a0001c0001t0003g0100 a0001c0001t0003g0101 others(9): Show |
12 | HG01433.hp1 HG02055.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.712-8541_712-8539d others(5): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 645290 | ||||||
chr4:645290 | ATTTT | A | 63 | a0001c0001t0001g0012 a0001c0001t0001g0048 a0001c0001t0001g0050 others(60): Show |
68 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.712-8542_712-8539d others(6): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 645290 | ||||||
chr4:645316 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.712-8536G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 645316 | |||||||
chr4:645319 | G | A | 1 | a0001c0001t0006g0049 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.712-8533G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 645319 | |||||||
chr4:645334 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-8518C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 645334 | |||||||
chr4:645335 | G | A | 1 | a0001c0001t0003g0080 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.712-8517G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 645335 | |||||||
chr4:645397 | G | A | 1 | a0001c0004t0001g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.712-8455G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 645397 | |||||||
chr4:645420 | C | T | 1 | a0001c0001t0007g0263 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.712-8432C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 645420 | |||||||
chr4:645440 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-8412C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 645440 | |||||||
chr4:645519 | T | A | 1 | a0001c0001t0007g0263 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.712-8333T>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 645519 | |||||||
chr4:645575 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-8277G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 645575 | |||||||
chr4:645594 | C | T | 2 | a0006c0013t0010g0044 a0006c0013t0010g0045 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.712-8258C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 645594 | |||||||
chr4:645640 | T | G | 1 | a0001c0001t0002g0147 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.712-8212T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 645640 | |||||||
chr4:645804 | C | T | 1 | a0001c0024t0002g0047 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.712-8048C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 645804 | |||||||
chr4:645881 | T | C | 100 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(97): Show |
107 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.712-7971T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 645881 | |||||||
chr4:645893 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-7959C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 645893 | |||||||
chr4:646035 | G | C | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-7817G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 646035 | |||||||
chr4:646319 | C | G | 2 | a0001c0009t0009g0248 a0001c0009t0009g0249 |
2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.712-7533C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 646319 | |||||||
chr4:646376 | C | T | 10 | a0002c0003t0005g0253 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.712-7476C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 646376 | |||||||
chr4:646396 | T | G | 1 | a0001c0001t0001g0222 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.712-7456T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 646396 | |||||||
chr4:646624 | G | A | 8 | a0001c0001t0001g0007 a0001c0005t0001g0245 a0001c0005t0001g0246 others(5): Show |
8 | HG02257.hp2 HG02630.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.712-7228G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 646624 | |||||||
chr4:646853 | C | G | 1 | a0001c0001t0001g0002 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.712-6999C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 646853 | |||||||
chr4:646915 | T | G | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.712-6937T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 646915 | |||||||
chr4:646978 | C | G | 73 | a0001c0001t0001g0012 a0001c0001t0001g0048 a0001c0001t0001g0050 others(70): Show |
80 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.712-6874C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 646978 | |||||||
chr4:647015 | G | A | 1 | a0001c0008t0002g0121 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.712-6837G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 647015 | |||||||
chr4:647019 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.712-6833C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 647019 | |||||||
chr4:647209 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-6643C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 647209 | |||||||
chr4:647495 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-6357C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 647495 | |||||||
chr4:647528 | T | A | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.712-6324T>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 647528 | |||||||
chr4:647596 | G | T | 1 | a0001c0001t0001g0023 | 2 | HG00099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.712-6256G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 647596 | |||||||
chr4:647632 | C | T | 73 | a0001c0001t0001g0012 a0001c0001t0001g0048 a0001c0001t0001g0050 others(70): Show |
80 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.712-6220C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 647632 | |||||||
chr4:647730 | G | A | 5 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.712-6122G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 647730 | |||||||
chr4:647747 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-6105G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 647747 | |||||||
chr4:647799 | G | C | 6 | a0001c0001t0001g0007 a0001c0005t0001g0245 a0001c0005t0001g0246 others(3): Show |
6 | HG02257.hp2 HG02630.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.712-6053G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 647799 | |||||||
chr4:647882 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-5970G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 647882 | |||||||
chr4:647942 | G | C | 4 | a0001c0001t0003g0075 a0001c0001t0003g0076 a0001c0001t0003g0077 others(1): Show |
4 | HG02523.hp2 NA18950.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.712-5910G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 647942 | |||||||
chr4:647952 | A | G | 98 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(95): Show |
105 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.712-5900A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 647952 | |||||||
chr4:648000 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-5852G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648000 | |||||||
chr4:648071 | A | G | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-5781A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648071 | |||||||
chr4:648076 | G | GA | 11 | a0001c0001t0005g0141 a0002c0003t0005g0253 a0002c0003t0005g0254 others(8): Show |
11 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.712-5766dupA | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 648076 | ||||||
chr4:648084 | A | G | 1 | a0001c0002t0004g0036 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.712-5768A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648084 | |||||||
chr4:648113 | A | G | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-5739A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648113 | |||||||
chr4:648176 | C | T | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.712-5676C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648176 | |||||||
chr4:648238 | C | T | 1 | a0001c0001t0007g0263 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.712-5614C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648238 | |||||||
chr4:648259 | C | G | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.712-5593C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648259 | |||||||
chr4:648264 | T | C | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-5588T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648264 | |||||||
chr4:648375 | T | C | 4 | a0001c0001t0001g0026 a0001c0001t0001g0208 a0001c0001t0001g0209 others(1): Show |
5 | NA18747.hp1 NA18943.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.712-5477T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648375 | |||||||
chr4:648437 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-5415G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648437 | |||||||
chr4:648454 | C | T | 1 | a0001c0001t0007g0263 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.712-5398C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648454 | |||||||
chr4:648476 | T | A | 2 | a0005c0011t0001g0251 a0005c0011t0001g0252 |
2 | HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.712-5376T>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648476 | |||||||
chr4:648524 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.712-5328C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648524 | |||||||
chr4:648525 | C | A | 1 | a0001c0001t0002g0244 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.712-5327C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648525 | |||||||
chr4:648600 | C | T | 65 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0015 others(62): Show |
79 | HG00323.hp2 HG00408.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.712-5252C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648600 | |||||||
chr4:648677 | G | C | 1 | a0014c0023t0003g0082 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.712-5175G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648677 | |||||||
chr4:648713 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.712-5139C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648713 | |||||||
chr4:648716 | C | T | 1 | a0014c0023t0003g0082 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.712-5136C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648716 | |||||||
chr4:648780 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.712-5072G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648780 | |||||||
chr4:648782 | A | G | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-5070A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648782 | |||||||
chr4:648833 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.712-5019G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648833 | |||||||
chr4:648834 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.712-5018C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648834 | |||||||
chr4:648878 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-4974G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648878 | |||||||
chr4:648903 | G | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | NA18964.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.712-4949G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648903 | |||||||
chr4:648935 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-4917C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648935 | |||||||
chr4:648989 | C | T | 8 | a0001c0001t0002g0242 a0001c0001t0003g0006 a0001c0001t0003g0233 others(5): Show |
9 | HG01167.hp1 HG02922.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.712-4863C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648989 | |||||||
chr4:648992 | G | A | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.712-4860G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 648992 | |||||||
chr4:649045 | C | T | 5 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.712-4807C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 649045 | |||||||
chr4:649110 | T | C | 92 | a0001c0001t0001g0012 a0001c0001t0001g0048 a0001c0001t0001g0050 others(89): Show |
99 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.712-4742T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 649110 | |||||||
chr4:649139 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-4713G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 649139 | |||||||
chr4:649164 | G | A | 1 | a0001c0001t0005g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.712-4688G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 649164 | |||||||
chr4:649460 | C | G | 5 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0169 others(2): Show |
5 | HG00642.hp1 HG00741.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.712-4392C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 649460 | |||||||
chr4:649526 | G | A | 9 | a0002c0003t0005g0254 a0002c0003t0005g0255 a0002c0003t0005g0256 others(6): Show |
9 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.712-4326G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 649526 | |||||||
chr4:649552 | G | A | 2 | a0006c0013t0010g0044 a0006c0013t0010g0045 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.712-4300G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 649552 | |||||||
chr4:649555 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.712-4297G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 649555 | |||||||
chr4:649561 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.712-4291C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 649561 | |||||||
chr4:649609 | A | AAGGCCTG others(28): Show |
2 | a0001c0001t0002g0243 a0001c0001t0003g0180 |
2 | NA18969.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.712-4208_712-4174d others(37): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 649609 | ||||||
chr4:649644 | GAGGCCTG others(28): Show |
G | 4 | a0001c0001t0005g0250 a0001c0009t0009g0053 a0001c0009t0009g0248 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.712-4198_712-4164d others(37): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 649644 | ||||||
chr4:649695 | A | AC | 3 | a0001c0001t0001g0232 a0001c0001t0002g0052 a0001c0001t0003g0075 |
3 | HG01099.hp2 HG01175.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.712-4155dupC | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 649695 | ||||||
chr4:649835 | C | T | 71 | a0001c0001t0001g0012 a0001c0001t0001g0048 a0001c0001t0001g0050 others(68): Show |
78 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.712-4017C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 649835 | |||||||
chr4:649898 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-3954G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 649898 | |||||||
chr4:649950 | C | T | 4 | a0001c0001t0005g0250 a0001c0009t0009g0053 a0001c0009t0009g0248 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.712-3902C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 649950 | |||||||
chr4:649951 | G | A | 1 | a0001c0001t0007g0143 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.712-3901G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 649951 | |||||||
chr4:649955 | T | C | 105 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(102): Show |
112 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.712-3897T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 649955 | |||||||
chr4:650053 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-3799C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650053 | |||||||
chr4:650074 | C | T | 2 | a0001c0001t0001g0007 a0001c0026t0001g0007 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.712-3778C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650074 | |||||||
chr4:650109 | C | T | 1 | a0001c0001t0001g0023 | 2 | HG00099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.712-3743C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650109 | |||||||
chr4:650137 | T | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(265): Show |
303 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.712-3715T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650137 | |||||||
chr4:650179 | T | C | 105 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(102): Show |
112 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.712-3673T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650179 | |||||||
chr4:650194 | C | T | 67 | a0001c0001t0001g0012 a0001c0001t0001g0048 a0001c0001t0001g0050 others(64): Show |
74 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.712-3658C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650194 | |||||||
chr4:650260 | G | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-3592G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650260 | |||||||
chr4:650277 | G | A | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.712-3575G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650277 | |||||||
chr4:650396 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-3456C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650396 | |||||||
chr4:650621 | C | T | 67 | a0001c0001t0001g0012 a0001c0001t0001g0048 a0001c0001t0001g0050 others(64): Show |
74 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.712-3231C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650621 | |||||||
chr4:650647 | C | T | 4 | a0001c0001t0005g0250 a0001c0009t0009g0053 a0001c0009t0009g0248 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.712-3205C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650647 | |||||||
chr4:650649 | A | G | 105 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(102): Show |
112 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.712-3203A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650649 | |||||||
chr4:650677 | A | AGGGAGGG others(222): Show |
1 | a0001c0001t0003g0061 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.712-3174_712-2946d others(231): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 650677 | ||||||
chr4:650708 | C | T | 4 | a0001c0001t0005g0250 a0001c0009t0009g0053 a0001c0009t0009g0248 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.712-3144C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650708 | |||||||
chr4:650733 | G | A | 11 | a0001c0001t0006g0240 a0001c0002t0001g0083 a0001c0004t0001g0038 others(8): Show |
11 | HG00642.hp2 HG01358.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.712-3119G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650733 | |||||||
chr4:650789 | G | C | 2 | a0001c0001t0011g0046 a0001c0001t0012g0034 |
2 | HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.712-3063G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650789 | |||||||
chr4:650831 | G | A | 1 | a0001c0001t0003g0039 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.712-3021G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650831 | |||||||
chr4:650835 | C | T | 4 | a0001c0001t0005g0250 a0001c0009t0009g0053 a0001c0009t0009g0248 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.712-3017C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650835 | |||||||
chr4:650842 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0097 |
3 | HG02055.hp1 HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.712-3010G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650842 | |||||||
chr4:650844 | A | C | 2 | a0001c0001t0011g0046 a0001c0001t0012g0034 |
2 | HG02818.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.712-3008A>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650844 | |||||||
chr4:650915 | C | T | 113 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(110): Show |
121 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.712-2937C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 650915 | |||||||
chr4:651026 | G | A | 103 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(100): Show |
110 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.712-2826G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651026 | |||||||
chr4:651026 | GGCAGTGG others(91): Show |
G | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-2815_712-2718d others(100): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 651026 | ||||||
chr4:651085 | T | TGTCACAG others(43): Show |
8 | a0001c0001t0002g0019 a0001c0001t0002g0152 a0001c0001t0002g0244 others(5): Show |
8 | HG00733.hp2 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.712-2757_712-2708d others(52): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 651085 | ||||||
chr4:651145 | A | G | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-2707A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651145 | |||||||
chr4:651148 | A | G | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-2704A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651148 | |||||||
chr4:651162 | C | G | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-2690C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651162 | |||||||
chr4:651173 | A | AGCAGTGG others(42): Show |
2 | a0005c0011t0001g0251 a0005c0011t0001g0252 |
2 | HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.712-2659_712-2658i others(51): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 651173 | ||||||
chr4:651173 | A | AGCAGTGG others(43): Show |
6 | a0001c0001t0001g0007 a0001c0001t0003g0066 a0001c0001t0003g0076 others(3): Show |
6 | HG02630.hp1 HG02922.hp1 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.712-2629_712-2580d others(52): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 651173 | ||||||
chr4:651173 | A | AGCAGTGG others(242): Show |
1 | a0001c0001t0002g0154 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.712-2559_712-2558i others(251): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 651173 | ||||||
chr4:651173 | A | AGCAGTGG others(93): Show |
60 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0070 others(57): Show |
65 | HG00423.hp1 HG00621.hp1 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.712-2580_712-2579i others(102): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 651173 | ||||||
chr4:651173 | A | AGCAGTGG others(143): Show |
3 | a0001c0002t0004g0013 a0001c0004t0001g0069 a0015c0019t0003g0074 |
4 | HG01433.hp1 HG01517.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.712-2580_712-2579i others(152): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 651173 | ||||||
chr4:651173 | A | AGCAGTGG others(193): Show |
1 | a0001c0001t0006g0049 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.712-2580_712-2579i others(202): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 651173 | ||||||
chr4:651173 | A | AGCAGTGG others(243): Show |
3 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0097 |
3 | HG02055.hp1 HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.712-2580_712-2579i others(252): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 651173 | ||||||
chr4:651173 | A | G | 2 | a0001c0001t0001g0231 a0001c0001t0011g0046 |
2 | HG01243.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.712-2679A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651173 | |||||||
chr4:651210 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-2642C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651210 | |||||||
chr4:651211 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.712-2641G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651211 | |||||||
chr4:651223 | G | A | 1 | a0001c0001t0002g0184 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.712-2629G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651223 | |||||||
chr4:651223 | GGCAGTGG others(43): Show |
G | 6 | a0001c0001t0002g0144 a0001c0001t0006g0240 a0004c0007t0008g0237 others(3): Show |
6 | HG00642.hp2 HG01358.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.712-2594_712-2545d others(52): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 651223 | ||||||
chr4:651235 | G | GTCACAGG others(93): Show |
6 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0081 others(3): Show |
7 | HG00099.hp1 HG00735.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.712-2580_712-2579i others(102): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 651235 | ||||||
chr4:651260 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-2592C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651260 | |||||||
chr4:651273 | A | G | 18 | a0001c0001t0001g0231 a0001c0001t0002g0051 a0001c0001t0002g0147 others(15): Show |
18 | HG01243.hp1 HG01884.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.712-2579A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651273 | |||||||
chr4:651394 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-2458G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651394 | |||||||
chr4:651490 | G | C | 102 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(99): Show |
109 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.712-2362G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651490 | |||||||
chr4:651507 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0158 |
2 | NA18960.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.712-2345G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651507 | |||||||
chr4:651511 | A | G | 105 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(102): Show |
112 | HG00099.hp1 HG00423.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.712-2341A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651511 | |||||||
chr4:651531 | C | T | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.712-2321C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651531 | |||||||
chr4:651619 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-2233G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651619 | |||||||
chr4:651629 | AGAGCCGT others(29): Show |
A | 2 | a0001c0001t0004g0210 a0001c0001t0011g0046 |
2 | HG01978.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.712-2200_712-2165d others(38): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 651629 | ||||||
chr4:651665 | GGAGCCGT others(29): Show |
G | 2 | a0001c0001t0002g0152 a0007c0027t0002g0019 |
2 | HG00733.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.712-2164_712-2129d others(38): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 651665 | ||||||
chr4:651670 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.712-2182C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651670 | |||||||
chr4:651687 | CTCTGGAG others(65): Show |
C | 2 | a0005c0011t0001g0251 a0005c0011t0001g0252 |
2 | HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.712-2164_712-2093d others(74): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651687 | |||||||
chr4:651707 | G | A | 1 | a0001c0004t0001g0069 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.712-2145G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651707 | |||||||
chr4:651733 | A | G | 20 | a0001c0001t0005g0141 a0001c0001t0006g0240 a0001c0001t0011g0046 others(17): Show |
20 | HG00642.hp2 HG01255.hp2 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.712-2119A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651733 | |||||||
chr4:651737 | G | A | 20 | a0001c0001t0005g0141 a0001c0001t0006g0240 a0001c0001t0011g0046 others(17): Show |
20 | HG00642.hp2 HG01255.hp2 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.712-2115G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651737 | |||||||
chr4:651737 | G | GGAGCCGT others(29): Show |
4 | a0001c0005t0001g0245 a0001c0005t0001g0246 a0001c0005t0001g0247 others(1): Show |
4 | HG02257.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.712-2094_712-2093i others(38): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 651737 | ||||||
chr4:651759 | T | C | 103 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(100): Show |
110 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(107): Show |
intron_variant | MODIFIER | c.712-2093T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651759 | |||||||
chr4:651779 | C | G | 20 | a0001c0001t0005g0141 a0001c0001t0006g0240 a0001c0001t0011g0046 others(17): Show |
20 | HG00642.hp2 HG01255.hp2 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.712-2073C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651779 | |||||||
chr4:651891 | A | G | 90 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0059 others(87): Show |
98 | HG00099.hp1 HG00423.hp1 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.712-1961A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651891 | |||||||
chr4:651904 | G | A | 1 | a0001c0009t0009g0248 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.712-1948G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651904 | |||||||
chr4:651958 | G | A | 1 | a0001c0001t0003g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.712-1894G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 651958 | |||||||
chr4:651973 | A | AGCTCCAT others(22): Show |
1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.712-1872_712-1844d others(31): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 651973 | ||||||
chr4:651984 | T | TGTGACTG others(22): Show |
5 | a0001c0001t0001g0022 a0001c0001t0001g0030 a0001c0001t0001g0169 others(2): Show |
5 | HG00642.hp1 HG00741.hp2 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.712-1860_712-1859i others(31): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 651984 | ||||||
chr4:651984 | T | TGTGACTG others(22): Show |
209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(206): Show |
241 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.712-1860_712-1832d others(31): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 651984 | ||||||
chr4:651984 | T | TGTGACTG others(51): Show |
28 | a0001c0001t0001g0105 a0001c0001t0002g0003 a0001c0001t0002g0070 others(25): Show |
30 | HG00621.hp1 HG00673.hp2 HG02074.hp2 others(27): Show |
intron_variant | MODIFIER | c.712-1832_712-1831i others(60): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 651984 | ||||||
chr4:652218 | G | C | 1 | a0001c0001t0003g0086 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.712-1634G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 652218 | |||||||
chr4:652220 | C | G | 1 | a0001c0001t0003g0086 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.712-1632C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 652220 | |||||||
chr4:652301 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.712-1551G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 652301 | |||||||
chr4:652388 | G | A | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.712-1464G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 652388 | |||||||
chr4:652515 | G | A | 1 | a0001c0001t0006g0125 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.712-1337G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 652515 | |||||||
chr4:652620 | G | T | 53 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(50): Show |
56 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.712-1232G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 652620 | |||||||
chr4:652714 | G | A | 59 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(56): Show |
62 | HG00099.hp1 HG00735.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.712-1138G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 652714 | |||||||
chr4:652714 | G | C | 5 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.712-1138G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 652714 | |||||||
chr4:652845 | A | G | 4 | a0001c0001t0002g0242 a0001c0001t0003g0234 a0001c0001t0003g0235 others(1): Show |
4 | NA18948.hp1 NA19054.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.712-1007A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 652845 | |||||||
chr4:652880 | CA | C | 54 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(51): Show |
57 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.712-964delA | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr4 | 652880 | ||||||
chr4:653132 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.712-720G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 653132 | |||||||
chr4:653210 | G | A | 4 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0097 others(1): Show |
4 | HG02055.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.712-642G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 653210 | |||||||
chr4:653211 | G | A | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.712-641G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 653211 | |||||||
chr4:653225 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.712-627G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 653225 | |||||||
chr4:653228 | C | T | 1 | a0001c0001t0003g0042 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.712-624C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 653228 | |||||||
chr4:653343 | G | A | 2 | a0001c0001t0002g0243 a0001c0001t0003g0180 |
2 | NA18969.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.712-509G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 653343 | |||||||
chr4:653394 | G | C | 2 | a0001c0005t0001g0204 a0005c0011t0001g0251 |
2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.712-458G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 653394 | |||||||
chr4:653439 | G | A | 1 | a0001c0017t0004g0037 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.712-413G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 653439 | |||||||
chr4:653458 | C | G | 47 | a0001c0001t0001g0012 a0001c0001t0001g0048 a0001c0001t0001g0050 others(44): Show |
50 | HG00099.hp1 HG00642.hp2 HG01071.hp1 others(47): Show |
intron_variant | MODIFIER | c.712-394C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 653458 | |||||||
chr4:653480 | G | A | 3 | a0001c0005t0001g0245 a0001c0005t0001g0247 a0011c0020t0001g0064 |
3 | HG02257.hp2 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.712-372G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 653480 | |||||||
chr4:653534 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.712-318G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 653534 | |||||||
chr4:653547 | G | A | 12 | a0001c0001t0005g0141 a0001c0001t0005g0250 a0002c0003t0005g0253 others(9): Show |
12 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.712-305G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 653547 | |||||||
chr4:653626 | C | T | 1 | a0012c0031t0003g0073 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.712-226C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 653626 | |||||||
chr4:653627 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.712-225G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 653627 | |||||||
chr4:653714 | G | C | 32 | a0001c0001t0001g0012 a0001c0001t0001g0048 a0001c0001t0001g0050 others(29): Show |
34 | HG00099.hp1 HG00735.hp2 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.712-138G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 653714 | |||||||
chr4:653717 | A | G | 65 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0048 others(62): Show |
67 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.712-135A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 653717 | |||||||
chr4:653793 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0158 |
2 | NA18960.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.712-59G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 653793 | |||||||
chr4:653813 | G | A | 23 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0097 others(20): Show |
24 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.712-39G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 3/21 | chr4 | 653813 | |||||||
chr4:654003 | C | T | 1 | a0008c0028t0008g0241 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.852+11C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 4/21 | chr4 | 654003 | |||||||
chr4:654359 | T | C | 4 | a0001c0005t0001g0245 a0001c0005t0001g0246 a0001c0005t0001g0247 others(1): Show |
4 | HG02257.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.927+205T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 5/21 | chr4 | 654359 | |||||||
chr4:654367 | G | A | 3 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0003g0171 |
3 | NA18983.hp1 NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.927+213G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 5/21 | chr4 | 654367 | |||||||
chr4:654462 | C | CGT | 7 | a0001c0001t0003g0041 a0001c0004t0001g0038 a0001c0004t0001g0067 others(4): Show |
7 | HG01975.hp2 HG02055.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.927+326_927+327dup others(2): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 5/21 | INFO_REALIGN_3_PRIME | chr4 | 654462 | ||||||
chr4:654649 | G | A | 1 | a0001c0001t0003g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.928-175G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 5/21 | chr4 | 654649 | |||||||
chr4:654662 | G | A | 3 | a0001c0005t0001g0204 a0005c0011t0001g0251 a0005c0011t0001g0252 |
3 | HG02572.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.928-162G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 5/21 | chr4 | 654662 | |||||||
chr4:654700 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.928-124C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 5/21 | chr4 | 654700 | |||||||
chr4:654920 | G | C | 60 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(57): Show |
64 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.992+32G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 6/21 | chr4 | 654920 | |||||||
chr4:654931 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.992+43C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 6/21 | chr4 | 654931 | |||||||
chr4:654964 | G | A | 1 | a0001c0001t0006g0049 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.992+76G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 6/21 | chr4 | 654964 | |||||||
chr4:655187 | C | T | 1 | a0001c0001t0003g0140 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.992+299C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 6/21 | chr4 | 655187 | |||||||
chr4:655195 | A | G | 14 | a0001c0001t0001g0007 a0001c0001t0005g0141 a0001c0001t0005g0250 others(11): Show |
14 | HG01255.hp2 HG01975.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.992+307A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 6/21 | chr4 | 655195 | |||||||
chr4:655340 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.992+452C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 6/21 | chr4 | 655340 | |||||||
chr4:655462 | G | A | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.993-478G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 6/21 | chr4 | 655462 | |||||||
chr4:655488 | G | A | 1 | a0001c0001t0004g0181 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.993-452G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 6/21 | chr4 | 655488 | |||||||
chr4:655609 | A | G | 7 | a0001c0001t0011g0046 a0001c0005t0001g0204 a0001c0009t0009g0053 others(4): Show |
7 | HG01891.hp1 HG02109.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.993-331A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 6/21 | chr4 | 655609 | |||||||
chr4:655691 | A | G | 3 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0225 |
3 | NA18939.hp1 NA18973.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.993-249A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 6/21 | chr4 | 655691 | |||||||
chr4:655747 | C | G | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.993-193C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 6/21 | chr4 | 655747 | |||||||
chr4:655759 | GGCCCCTC others(33): Show |
G | 5 | a0001c0001t0001g0007 a0001c0001t0011g0046 a0001c0026t0001g0007 others(2): Show |
5 | HG02630.hp1 HG02818.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.993-147_993-108del others(40): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr4 | 655759 | ||||||
chr4:655808 | G | C | 25 | a0001c0001t0002g0070 a0001c0001t0005g0141 a0001c0001t0005g0250 others(22): Show |
25 | HG01255.hp2 HG01891.hp1 HG01975.hp2 others(22): Show |
intron_variant | MODIFIER | c.993-132G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 6/21 | chr4 | 655808 | |||||||
chr4:655850 | C | A | 54 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(51): Show |
58 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.993-90C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 6/21 | chr4 | 655850 | |||||||
chr4:655891 | G | C | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.993-49G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 6/21 | chr4 | 655891 | |||||||
chr4:656015 | C | G | 3 | a0001c0005t0001g0204 a0005c0011t0001g0251 a0005c0011t0001g0252 |
3 | HG02572.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1059+9C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 7/21 | chr4 | 656015 | |||||||
chr4:656031 | C | A | 2 | a0001c0001t0001g0007 a0001c0026t0001g0007 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1059+25C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 7/21 | chr4 | 656031 | |||||||
chr4:656057 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1059+51G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 7/21 | chr4 | 656057 | |||||||
chr4:656082 | TGCCACGT others(3): Show |
T | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1059+80_1059+89del others(10): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr4 | 656082 | ||||||
chr4:656087 | C | T | 68 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(65): Show |
72 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.1059+81C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 7/21 | chr4 | 656087 | |||||||
chr4:656180 | C | A | 1 | a0001c0001t0002g0146 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1060-65C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 7/21 | chr4 | 656180 | |||||||
chr4:656201 | C | T | 1 | a0001c0001t0003g0140 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1060-44C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 7/21 | chr4 | 656201 | |||||||
chr4:656223 | C | T | 1 | a0001c0002t0004g0094 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1060-22C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 7/21 | chr4 | 656223 | |||||||
chr4:656224 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0226 |
2 | HG04184.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1060-21G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 7/21 | chr4 | 656224 | |||||||
chr4:656404 | G | T | 43 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0070 others(40): Show |
47 | HG00423.hp1 HG00621.hp1 HG02056.hp1 others(44): Show |
intron_variant | MODIFIER | c.1107+112G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 8/21 | chr4 | 656404 | |||||||
chr4:656451 | G | C | 1 | a0002c0003t0005g0253 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1107+159G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 8/21 | chr4 | 656451 | |||||||
chr4:656497 | A | AAGGCCGT others(26): Show |
1 | a0001c0002t0002g0058 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1107+285_1108-265d others(35): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr4 | 656497 | ||||||
chr4:656497 | A | AAGGCCGT others(59): Show |
1 | a0001c0002t0002g0057 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1107+252_1108-265d others(68): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr4 | 656497 | ||||||
chr4:656559 | CT | C | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1107+268delT | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 8/21 | chr4 | 656559 | |||||||
chr4:656563 | G | GAGGCCGT others(26): Show |
1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1108-279_1108-278i others(35): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr4 | 656563 | ||||||
chr4:656596 | G | A | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1108-278G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 8/21 | chr4 | 656596 | |||||||
chr4:656608 | G | A | 1 | a0001c0001t0002g0218 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1108-266G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 8/21 | chr4 | 656608 | |||||||
chr4:656669 | G | A | 9 | a0001c0001t0006g0240 a0001c0001t0011g0046 a0001c0009t0009g0053 others(6): Show |
9 | HG00642.hp2 HG01358.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1108-205G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 8/21 | chr4 | 656669 | |||||||
chr4:656865 | C | T | 4 | a0001c0005t0001g0245 a0001c0005t0001g0246 a0001c0005t0001g0247 others(1): Show |
4 | HG02257.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1108-9C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 8/21 | chr4 | 656865 | |||||||
chr4:657073 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1257+50G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 9/21 | chr4 | 657073 | |||||||
chr4:657119 | T | C | 1 | a0001c0001t0002g0242 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1257+96T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 9/21 | chr4 | 657119 | |||||||
chr4:657134 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1257+111G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 9/21 | chr4 | 657134 | |||||||
chr4:657184 | G | C | 1 | a0001c0009t0009g0053 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1257+161G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 9/21 | chr4 | 657184 | |||||||
chr4:657209 | G | A | 7 | a0001c0005t0001g0204 a0001c0005t0001g0245 a0001c0005t0001g0246 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1258-142G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 9/21 | chr4 | 657209 | |||||||
chr4:657227 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1258-124G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 9/21 | chr4 | 657227 | |||||||
chr4:657494 | GGTGCGGC others(38): Show |
G | 1 | a0001c0001t0001g0169 | 1 | NA20805.hp2 | splice_region_variant&intron_variant | LOW | c.1401+4_1401+48delC others(44): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 657494 | ||||||
chr4:657519 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1401+25G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 657519 | |||||||
chr4:657580 | T | A | 60 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(57): Show |
64 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.1401+86T>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 657580 | |||||||
chr4:657604 | ATCCAGGG others(85): Show |
A | 1 | a0001c0004t0001g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1401+134_1401+225d others(94): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 657604 | ||||||
chr4:657684 | T | C | 4 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1401+190T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 657684 | |||||||
chr4:657704 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1401+210G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 657704 | |||||||
chr4:657718 | A | ATGGCTGT others(129): Show |
4 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1401+224_1401+225i others(138): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 657718 | |||||||
chr4:657720 | A | ATG | 4 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1401+226_1401+227i others(4): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 657720 | |||||||
chr4:657720 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1401+226A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 657720 | |||||||
chr4:657731 | G | A | 4 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1401+237G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 657731 | |||||||
chr4:657740 | G | T | 4 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1401+246G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 657740 | |||||||
chr4:657742 | A | G | 4 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1401+248A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 657742 | |||||||
chr4:657820 | G | A | 10 | a0001c0001t0005g0141 a0002c0003t0005g0254 a0002c0003t0005g0255 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1401+326G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 657820 | |||||||
chr4:657823 | GGGGGCAG others(39): Show |
G | 1 | a0001c0001t0002g0051 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1401+363_1401+408d others(48): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 657823 | ||||||
chr4:657831 | G | A | 1 | a0001c0001t0002g0001 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1401+337G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 657831 | |||||||
chr4:657834 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1401+340G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 657834 | |||||||
chr4:657887 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0097 |
3 | HG02055.hp1 HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1401+393G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 657887 | |||||||
chr4:657890 | C | T | 36 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0048 others(33): Show |
40 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1401+396C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 657890 | |||||||
chr4:657964 | G | A | 1 | a0003c0006t0007g0193 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1401+470G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 657964 | |||||||
chr4:658026 | T | A | 4 | a0001c0005t0001g0245 a0001c0005t0001g0246 a0001c0005t0001g0247 others(1): Show |
4 | HG02257.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1401+532T>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658026 | |||||||
chr4:658028 | ATCCAGGG others(28): Show |
A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0097 |
3 | HG02055.hp1 HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1401+545_1401+579d others(37): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 658028 | ||||||
chr4:658037 | T | C | 5 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1401+543T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658037 | |||||||
chr4:658041 | G | A | 56 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(53): Show |
60 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.1401+547G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658041 | |||||||
chr4:658057 | C | A | 1 | a0001c0001t0002g0151 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1401+563C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658057 | |||||||
chr4:658114 | GCAGGTCA others(27): Show |
G | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1401+638_1401+671d others(36): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | INFO_REALIGN_3_PRIME | chr4 | 658114 | ||||||
chr4:658140 | C | A | 1 | a0001c0001t0001g0142 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1401+646C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658140 | |||||||
chr4:658179 | G | T | 3 | a0001c0001t0002g0122 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1401+685G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658179 | |||||||
chr4:658212 | G | A | 2 | a0001c0001t0003g0010 a0016c0014t0002g0010 |
2 | NA19010.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1401+718G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658212 | |||||||
chr4:658250 | G | A | 60 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(57): Show |
64 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.1402-702G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658250 | |||||||
chr4:658280 | C | T | 4 | a0001c0001t0004g0093 a0001c0002t0001g0060 a0001c0002t0004g0013 others(1): Show |
5 | HG01099.hp1 HG01433.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402-672C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658280 | |||||||
chr4:658439 | C | A | 1 | a0001c0004t0001g0055 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1402-513C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658439 | |||||||
chr4:658441 | G | C | 1 | a0001c0004t0001g0055 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1402-511G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658441 | |||||||
chr4:658444 | C | T | 1 | a0001c0004t0001g0055 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1402-508C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658444 | |||||||
chr4:658447 | T | C | 1 | a0001c0004t0001g0055 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1402-505T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658447 | |||||||
chr4:658448 | G | A | 1 | a0001c0004t0001g0055 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1402-504G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658448 | |||||||
chr4:658451 | G | A | 1 | a0001c0004t0001g0055 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1402-501G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658451 | |||||||
chr4:658452 | G | A | 1 | a0001c0004t0001g0055 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1402-500G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658452 | |||||||
chr4:658472 | A | G | 1 | a0001c0004t0001g0055 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1402-480A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658472 | |||||||
chr4:658479 | T | G | 1 | a0001c0004t0001g0055 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1402-473T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658479 | |||||||
chr4:658490 | A | G | 1 | a0001c0004t0001g0055 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1402-462A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658490 | |||||||
chr4:658491 | C | T | 1 | a0001c0004t0001g0055 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1402-461C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658491 | |||||||
chr4:658541 | G | A | 2 | a0001c0009t0009g0248 a0001c0009t0009g0249 |
2 | HG01891.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1402-411G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 10/21 | chr4 | 658541 | |||||||
chr4:659035 | G | A | 1 | a0001c0001t0002g0147 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1467+18G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659035 | |||||||
chr4:659037 | C | T | 8 | a0001c0001t0004g0093 a0001c0002t0001g0060 a0001c0002t0004g0013 others(5): Show |
10 | HG01099.hp1 HG01433.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1467+20C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659037 | |||||||
chr4:659058 | C | T | 4 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1467+41C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659058 | |||||||
chr4:659094 | G | A | 16 | a0001c0001t0001g0007 a0001c0001t0005g0141 a0001c0001t0005g0250 others(13): Show |
16 | HG01255.hp2 HG01975.hp2 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.1467+77G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659094 | |||||||
chr4:659137 | T | C | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1467+120T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659137 | |||||||
chr4:659252 | C | CT | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1467+238dupT | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr4 | 659252 | ||||||
chr4:659277 | A | G | 1 | a0001c0002t0004g0013 | 2 | HG01433.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1467+260A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659277 | |||||||
chr4:659466 | T | C | 1 | a0001c0001t0002g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1467+449T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659466 | |||||||
chr4:659501 | A | G | 1 | a0001c0001t0003g0080 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1467+484A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659501 | |||||||
chr4:659538 | C | T | 69 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(66): Show |
73 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.1467+521C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659538 | |||||||
chr4:659541 | C | CTGTG | 32 | a0001c0001t0001g0007 a0001c0001t0005g0141 a0001c0001t0005g0250 others(29): Show |
32 | HG00642.hp2 HG01255.hp2 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.1467+526_1467+527i others(6): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr4 | 659541 | ||||||
chr4:659557 | ATGTGTGC others(13): Show |
A | 1 | a0001c0029t0001g0033 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1467+558_1467+577d others(22): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr4 | 659557 | ||||||
chr4:659575 | G | A | 64 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(61): Show |
68 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.1467+558G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659575 | |||||||
chr4:659595 | A | G | 2 | a0001c0008t0002g0120 a0001c0008t0002g0121 |
2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1467+578A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659595 | |||||||
chr4:659605 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1467+588G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659605 | |||||||
chr4:659615 | TG | T | 59 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(56): Show |
63 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1467+599delG | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659615 | |||||||
chr4:659621 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1467+604A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659621 | |||||||
chr4:659622 | A | ATGTGCAC others(15): Show |
1 | a0001c0001t0004g0210 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1467+619_1467+640d others(24): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr4 | 659622 | ||||||
chr4:659624 | G | A | 60 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(57): Show |
64 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.1467+607G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659624 | |||||||
chr4:659639 | CAT | C | 10 | a0001c0001t0001g0026 a0001c0001t0001g0130 a0001c0001t0001g0158 others(7): Show |
11 | HG00408.hp2 HG02056.hp2 NA18612.hp2 others(8): Show |
intron_variant | MODIFIER | c.1467+623_1467+624d others(4): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659639 | |||||||
chr4:659668 | ATG | A | 4 | a0001c0001t0012g0034 a0001c0005t0001g0204 a0005c0011t0001g0251 others(1): Show |
4 | HG02572.hp2 HG02630.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1467+658_1467+659d others(4): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr4 | 659668 | ||||||
chr4:659698 | TTGTG | T | 36 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0048 others(33): Show |
40 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1467+690_1467+693d others(6): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr4 | 659698 | ||||||
chr4:659708 | G | T | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1467+691G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659708 | |||||||
chr4:659714 | G | A | 57 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0048 others(54): Show |
61 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.1467+697G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659714 | |||||||
chr4:659735 | T | C | 4 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0097 others(1): Show |
4 | HG02055.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1467+718T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659735 | |||||||
chr4:659749 | C | G | 59 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(56): Show |
63 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1468-718C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659749 | |||||||
chr4:659764 | G | T | 1 | a0003c0006t0002g0104 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1468-703G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659764 | |||||||
chr4:659860 | C | T | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1468-607C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659860 | |||||||
chr4:659944 | G | A | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1468-523G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659944 | |||||||
chr4:659972 | C | T | 1 | a0001c0001t0006g0240 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1468-495C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 659972 | |||||||
chr4:660055 | G | A | 4 | a0001c0001t0002g0019 a0001c0001t0002g0152 a0001c0001t0002g0244 others(1): Show |
4 | HG00733.hp2 HG03486.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-412G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 660055 | |||||||
chr4:660092 | C | T | 4 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468-375C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 660092 | |||||||
chr4:660108 | C | G | 15 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0035 others(12): Show |
17 | HG00408.hp1 HG00423.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.1468-359C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 660108 | |||||||
chr4:660296 | G | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0092 |
3 | HG00099.hp1 HG01346.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.1468-171G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 660296 | |||||||
chr4:660302 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1468-165G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 11/21 | chr4 | 660302 | |||||||
chr4:660758 | G | A | 4 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0097 others(1): Show |
4 | HG02055.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1614+145G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | chr4 | 660758 | |||||||
chr4:660816 | TTGGATGG others(5): Show |
T | 2 | a0006c0013t0010g0044 a0006c0013t0010g0045 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1614+215_1614+226d others(14): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660816 | ||||||
chr4:660856 | A | G | 65 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(62): Show |
69 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.1614+243A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | chr4 | 660856 | |||||||
chr4:660975 | A | AAATGGAT others(180): Show |
3 | a0001c0005t0001g0204 a0005c0011t0001g0251 a0005c0011t0001g0252 |
3 | HG02572.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1614+362_1614+363i others(189): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | chr4 | 660975 | |||||||
chr4:660975 | A | AGTTGGAT others(879): Show |
1 | a0001c0001t0005g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1614+379_1614+380i others(888): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(282): Show |
1 | a0001c0001t0001g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1614+379_1614+380i others(291): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(283): Show |
1 | a0001c0001t0002g0203 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1614+379_1614+380i others(292): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(383): Show |
1 | a0002c0003t0005g0259 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1614+379_1614+380i others(392): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(282): Show |
4 | a0001c0005t0001g0245 a0001c0005t0001g0246 a0001c0005t0001g0247 others(1): Show |
4 | HG02257.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1614+379_1614+380i others(291): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(282): Show |
181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(178): Show |
212 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.1614+379_1614+380i others(291): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(376): Show |
1 | a0001c0001t0002g0149 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1614+379_1614+380i others(385): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(282): Show |
5 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+379_1614+380i others(291): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(235): Show |
1 | a0001c0001t0001g0224 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1614+379_1614+380i others(244): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(380): Show |
4 | a0001c0001t0004g0093 a0001c0002t0001g0060 a0001c0002t0004g0013 others(1): Show |
5 | HG01099.hp1 HG01433.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+379_1614+380i others(389): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(235): Show |
4 | a0001c0001t0001g0103 a0001c0009t0009g0053 a0001c0009t0009g0248 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1614+379_1614+380i others(244): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(188): Show |
23 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0048 others(20): Show |
25 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.1614+379_1614+380i others(197): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(333): Show |
4 | a0001c0002t0004g0014 a0001c0002t0004g0062 a0001c0002t0004g0094 others(1): Show |
5 | HG02486.hp2 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+379_1614+380i others(342): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(239): Show |
2 | a0001c0004t0001g0069 a0001c0004t0001g0091 |
2 | HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1614+379_1614+380i others(248): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(282): Show |
1 | a0001c0001t0001g0232 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1614+379_1614+380i others(291): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(387): Show |
4 | a0002c0003t0005g0254 a0002c0003t0005g0255 a0002c0003t0005g0257 others(1): Show |
4 | HG01975.hp2 HG02970.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1614+379_1614+380i others(396): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(438): Show |
9 | a0001c0001t0001g0007 a0001c0001t0005g0141 a0001c0026t0001g0007 others(6): Show |
9 | HG01255.hp2 HG02630.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.1614+379_1614+380i others(447): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(282): Show |
1 | a0001c0001t0002g0051 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1614+379_1614+380i others(291): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(284): Show |
1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1614+379_1614+380i others(293): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(235): Show |
14 | a0001c0001t0002g0117 a0001c0001t0002g0119 a0001c0001t0002g0122 others(11): Show |
14 | HG01884.hp1 HG02258.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1614+379_1614+380i others(244): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660975 | A | AGTTGGAT others(391): Show |
1 | a0006c0013t0010g0045 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1614+379_1614+380i others(400): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660975 | ||||||
chr4:660984 | A | AATGGATG others(192): Show |
3 | a0001c0002t0001g0063 a0001c0002t0001g0065 a0001c0029t0001g0033 |
3 | HG02559.hp2 HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1614+379_1614+380i others(201): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660984 | ||||||
chr4:660993 | G | A | 1 | a0001c0001t0002g0095 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1614+380G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | chr4 | 660993 | |||||||
chr4:660995 | G | GGGTGGGT others(281): Show |
1 | a0001c0001t0002g0095 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1614+388_1614+389i others(290): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr4 | 660995 | ||||||
chr4:661043 | A | G | 36 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0048 others(33): Show |
40 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1614+430A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | chr4 | 661043 | |||||||
chr4:661199 | G | A | 5 | a0001c0001t0006g0240 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1614+586G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | chr4 | 661199 | |||||||
chr4:661900 | C | G | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1615-234C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | chr4 | 661900 | |||||||
chr4:661993 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0228 |
3 | HG00741.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1615-141G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | chr4 | 661993 | |||||||
chr4:662092 | C | G | 59 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(56): Show |
63 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.1615-42C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 12/21 | chr4 | 662092 | |||||||
chr4:662246 | G | A | 1 | a0005c0011t0001g0252 | 1 | NA19240.hp1 | splice_region_variant&intron_variant | LOW | c.1722+5G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 13/21 | chr4 | 662246 | |||||||
chr4:662426 | G | T | 4 | a0002c0003t0005g0254 a0002c0003t0005g0255 a0002c0003t0005g0257 others(1): Show |
4 | HG01975.hp2 HG02970.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1723-83G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 13/21 | chr4 | 662426 | |||||||
chr4:662702 | A | G | 1 | a0001c0001t0007g0263 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1832+84A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 14/21 | chr4 | 662702 | |||||||
chr4:662761 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1832+143G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 14/21 | chr4 | 662761 | |||||||
chr4:662815 | G | T | 66 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(63): Show |
70 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.1832+197G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 14/21 | chr4 | 662815 | |||||||
chr4:662834 | T | TA | 22 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0105 others(19): Show |
24 | HG00673.hp2 HG01167.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.1832+238dupA | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr4 | 662834 | ||||||
chr4:662834 | TA | T | 51 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(48): Show |
56 | HG00099.hp1 HG00621.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1832+238delA | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr4 | 662834 | ||||||
chr4:662834 | TAA | T | 6 | a0001c0001t0001g0084 a0001c0001t0006g0240 a0001c0002t0001g0060 others(3): Show |
6 | HG00642.hp2 HG01358.hp2 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.1832+237_1832+238d others(4): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr4 | 662834 | ||||||
chr4:662865 | T | C | 2 | a0001c0001t0001g0007 a0001c0026t0001g0007 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1833-235T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 14/21 | chr4 | 662865 | |||||||
chr4:662871 | C | T | 1 | a0001c0001t0007g0263 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1833-229C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 14/21 | chr4 | 662871 | |||||||
chr4:662877 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1833-223C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 14/21 | chr4 | 662877 | |||||||
chr4:663012 | A | G | 5 | a0001c0001t0002g0242 a0001c0001t0003g0233 a0001c0001t0003g0234 others(2): Show |
5 | HG03831.hp1 NA18948.hp1 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.1833-88A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 14/21 | chr4 | 663012 | |||||||
chr4:663047 | G | T | 3 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 |
3 | HG00642.hp2 HG01358.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1833-53G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 14/21 | chr4 | 663047 | |||||||
chr4:663242 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1920+55A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 15/21 | chr4 | 663242 | |||||||
chr4:663244 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1920+57G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 15/21 | chr4 | 663244 | |||||||
chr4:663271 | G | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0097 |
3 | HG02055.hp1 HG03041.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1920+84G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 15/21 | chr4 | 663271 | |||||||
chr4:663339 | G | T | 2 | a0001c0001t0002g0117 a0001c0001t0002g0119 |
2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1920+152G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 15/21 | chr4 | 663339 | |||||||
chr4:663341 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1920+154C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 15/21 | chr4 | 663341 | |||||||
chr4:663423 | G | A | 1 | a0001c0002t0004g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1920+236G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 15/21 | chr4 | 663423 | |||||||
chr4:663432 | G | A | 1 | a0001c0001t0002g0148 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1920+245G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 15/21 | chr4 | 663432 | |||||||
chr4:663443 | G | C | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1920+256G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 15/21 | chr4 | 663443 | |||||||
chr4:663458 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1920+271A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 15/21 | chr4 | 663458 | |||||||
chr4:663503 | C | A | 1 | a0001c0001t0002g0107 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1921-267C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 15/21 | chr4 | 663503 | |||||||
chr4:663567 | C | T | 3 | a0001c0005t0001g0204 a0005c0011t0001g0251 a0005c0011t0001g0252 |
3 | HG02572.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1921-203C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 15/21 | chr4 | 663567 | |||||||
chr4:663577 | A | G | 57 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(54): Show |
61 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.1921-193A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 15/21 | chr4 | 663577 | |||||||
chr4:663585 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1921-185G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 15/21 | chr4 | 663585 | |||||||
chr4:663983 | G | A | 2 | a0001c0001t0001g0007 a0001c0026t0001g0007 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2021+113G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 16/21 | chr4 | 663983 | |||||||
chr4:664021 | T | C | 1 | a0001c0002t0004g0062 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2022-93T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 16/21 | chr4 | 664021 | |||||||
chr4:664068 | CT | C | 28 | a0001c0001t0001g0007 a0001c0001t0005g0141 a0001c0001t0005g0250 others(25): Show |
28 | HG00642.hp2 HG01255.hp2 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.2022-45delT | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 16/21 | chr4 | 664068 | |||||||
chr4:664237 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2129+16G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 17/21 | chr4 | 664237 | |||||||
chr4:664300 | G | A | 56 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(53): Show |
60 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.2129+79G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 17/21 | chr4 | 664300 | |||||||
chr4:664372 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2129+151C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 17/21 | chr4 | 664372 | |||||||
chr4:664375 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2129+154C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 17/21 | chr4 | 664375 | |||||||
chr4:664376 | C | T | 2 | a0001c0001t0001g0007 a0001c0026t0001g0007 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2129+155C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 17/21 | chr4 | 664376 | |||||||
chr4:664415 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2129+194G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 17/21 | chr4 | 664415 | |||||||
chr4:664515 | G | T | 64 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(61): Show |
68 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.2129+294G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 17/21 | chr4 | 664515 | |||||||
chr4:664568 | G | A | 2 | a0001c0001t0001g0007 a0001c0026t0001g0007 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2130-313G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 17/21 | chr4 | 664568 | |||||||
chr4:664676 | C | G | 2 | a0006c0013t0010g0044 a0006c0013t0010g0045 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2130-205C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 17/21 | chr4 | 664676 | |||||||
chr4:664689 | G | A | 1 | a0001c0001t0003g0054 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2130-192G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 17/21 | chr4 | 664689 | |||||||
chr4:664743 | T | C | 1 | a0001c0001t0006g0125 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2130-138T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 17/21 | chr4 | 664743 | |||||||
chr4:664831 | C | T | 5 | a0001c0004t0001g0038 a0001c0004t0001g0067 a0001c0004t0001g0069 others(2): Show |
5 | HG02055.hp2 HG02559.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.2130-50C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 17/21 | chr4 | 664831 | |||||||
chr4:665007 | G | A | 1 | a0001c0001t0006g0049 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2193+63G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 18/21 | chr4 | 665007 | |||||||
chr4:665017 | C | G | 1 | a0001c0001t0006g0223 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2193+73C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 18/21 | chr4 | 665017 | |||||||
chr4:665124 | G | A | 4 | a0001c0001t0002g0072 a0001c0001t0003g0071 a0001c0001t0003g0098 others(1): Show |
4 | HG00621.hp1 HG02074.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.2194-131G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 18/21 | chr4 | 665124 | |||||||
chr4:665147 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2194-108C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 18/21 | chr4 | 665147 | |||||||
chr4:665175 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2194-80C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 18/21 | chr4 | 665175 | |||||||
chr4:665242 | C | A | 2 | a0006c0013t0010g0044 a0006c0013t0010g0045 |
2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.2194-13C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 18/21 | chr4 | 665242 | |||||||
chr4:665355 | A | T | 3 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 |
3 | HG00642.hp2 HG01358.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.2268+26A>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 19/21 | chr4 | 665355 | |||||||
chr4:665539 | C | T | 4 | a0001c0005t0001g0245 a0001c0005t0001g0246 a0001c0005t0001g0247 others(1): Show |
4 | HG02257.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2268+210C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 19/21 | chr4 | 665539 | |||||||
chr4:665574 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2268+245C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 19/21 | chr4 | 665574 | |||||||
chr4:665582 | G | A | 70 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(67): Show |
75 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.2268+253G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 19/21 | chr4 | 665582 | |||||||
chr4:665596 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2268+267C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 19/21 | chr4 | 665596 | |||||||
chr4:665806 | G | A | 1 | a0001c0022t0002g0150 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2268+477G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 19/21 | chr4 | 665806 | |||||||
chr4:665842 | C | T | 10 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0059 others(7): Show |
12 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.2268+513C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 19/21 | chr4 | 665842 | |||||||
chr4:665899 | G | C | 1 | a0001c0001t0001g0103 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2268+570G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 19/21 | chr4 | 665899 | |||||||
chr4:666052 | C | T | 45 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0070 others(42): Show |
49 | HG00423.hp1 HG00621.hp1 HG02056.hp1 others(46): Show |
intron_variant | MODIFIER | c.2269-479C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 19/21 | chr4 | 666052 | |||||||
chr4:666143 | G | A | 3 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 |
3 | HG00642.hp2 HG01358.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.2269-388G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 19/21 | chr4 | 666143 | |||||||
chr4:666293 | G | A | 1 | a0001c0001t0002g0178 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2269-238G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 19/21 | chr4 | 666293 | |||||||
chr4:666347 | G | T | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2269-184G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 19/21 | chr4 | 666347 | |||||||
chr4:666441 | A | C | 2 | a0002c0003t0005g0260 a0002c0003t0005g0261 |
2 | HG01255.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2269-90A>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 19/21 | chr4 | 666441 | |||||||
chr4:666471 | C | T | 3 | a0001c0005t0001g0204 a0005c0011t0001g0251 a0005c0011t0001g0252 |
3 | HG02572.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2269-60C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 19/21 | chr4 | 666471 | |||||||
chr4:666520 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2269-11C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 19/21 | chr4 | 666520 | |||||||
chr4:666617 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG01070.hp1 HG01071.hp2 |
splice_region_variant&intron_variant | LOW | c.2352+3G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 666617 | |||||||
chr4:666915 | A | C | 2 | a0001c0001t0001g0007 a0001c0026t0001g0007 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2352+301A>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 666915 | |||||||
chr4:666928 | G | A | 48 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0048 others(45): Show |
52 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.2352+314G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 666928 | |||||||
chr4:666964 | C | G | 1 | a0001c0001t0004g0068 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2352+350C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 666964 | |||||||
chr4:667005 | C | T | 2 | a0002c0003t0005g0259 a0002c0003t0005g0262 |
2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2352+391C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667005 | |||||||
chr4:667042 | A | C | 1 | a0001c0001t0005g0141 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2352+428A>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667042 | |||||||
chr4:667050 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2352+436G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667050 | |||||||
chr4:667208 | C | T | 1 | a0001c0001t0002g0016 | 2 | HG01243.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2352+594C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667208 | |||||||
chr4:667209 | G | A | 3 | a0001c0005t0001g0204 a0005c0011t0001g0251 a0005c0011t0001g0252 |
3 | HG02572.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2352+595G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667209 | |||||||
chr4:667213 | A | G | 67 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(64): Show |
71 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.2352+599A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667213 | |||||||
chr4:667240 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2353-616C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667240 | |||||||
chr4:667256 | G | A | 1 | a0002c0003t0005g0260 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2353-600G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667256 | |||||||
chr4:667301 | G | T | 2 | a0001c0001t0001g0007 a0001c0026t0001g0007 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2353-555G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667301 | |||||||
chr4:667325 | G | A | 2 | a0001c0001t0002g0110 a0001c0001t0002g0111 |
2 | HG01358.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.2353-531G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667325 | |||||||
chr4:667388 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2353-468G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667388 | |||||||
chr4:667422 | A | C | 1 | a0001c0001t0004g0186 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2353-434A>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667422 | |||||||
chr4:667459 | C | T | 2 | a0001c0001t0002g0051 a0001c0001t0002g0147 |
2 | HG02647.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2353-397C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667459 | |||||||
chr4:667489 | G | A | 1 | a0014c0023t0003g0082 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2353-367G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667489 | |||||||
chr4:667552 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2353-304C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667552 | |||||||
chr4:667674 | C | T | 1 | a0001c0001t0002g0147 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2353-182C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667674 | |||||||
chr4:667723 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2353-133G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667723 | |||||||
chr4:667764 | C | T | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2353-92C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667764 | |||||||
chr4:667814 | C | T | 1 | a0001c0001t0002g0149 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2353-42C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 20/21 | chr4 | 667814 | |||||||
chr4:668142 | C | T | 67 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(64): Show |
71 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.2503+136C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668142 | |||||||
chr4:668166 | G | A | 57 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0048 others(54): Show |
61 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.2503+160G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668166 | |||||||
chr4:668193 | C | T | 11 | a0001c0002t0001g0063 a0001c0002t0001g0065 a0001c0002t0001g0083 others(8): Show |
11 | HG02055.hp2 HG02258.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2503+187C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668193 | |||||||
chr4:668206 | G | A | 4 | a0001c0005t0001g0245 a0001c0005t0001g0246 a0001c0005t0001g0247 others(1): Show |
4 | HG02257.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2503+200G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668206 | |||||||
chr4:668234 | C | T | 1 | a0011c0020t0001g0064 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2503+228C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668234 | |||||||
chr4:668341 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2503+335G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668341 | |||||||
chr4:668429 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2503+423C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668429 | |||||||
chr4:668430 | G | GCTACCCC others(12): Show |
3 | a0001c0001t0003g0006 a0001c0012t0003g0031 a0001c0012t0003g0032 |
4 | HG01167.hp1 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2503+475_2503+493d others(21): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 668430 | ||||||
chr4:668430 | GCTACCCC others(12): Show |
G | 3 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0003g0171 |
3 | NA18983.hp1 NA19005.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.2503+475_2503+493d others(21): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 668430 | ||||||
chr4:668472 | C | A | 60 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(57): Show |
64 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.2503+466C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668472 | |||||||
chr4:668481 | G | A | 64 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(61): Show |
68 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.2503+475G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668481 | |||||||
chr4:668482 | C | T | 64 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(61): Show |
68 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.2503+476C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668482 | |||||||
chr4:668486 | CA | C | 64 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(61): Show |
68 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.2503+481delA | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668486 | |||||||
chr4:668487 | ACTACCCC others(11): Show |
A | 1 | a0012c0031t0003g0073 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2503+495_2503+512d others(20): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 668487 | ||||||
chr4:668496 | T | C | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2503+490T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668496 | |||||||
chr4:668518 | A | G | 60 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(57): Show |
64 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.2503+512A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668518 | |||||||
chr4:668519 | G | C | 60 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(57): Show |
64 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.2503+513G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668519 | |||||||
chr4:668519 | G | T | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2503+513G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668519 | |||||||
chr4:668521 | A | C | 64 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(61): Show |
68 | HG00099.hp1 HG00642.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.2503+515A>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668521 | |||||||
chr4:668524 | A | G | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2503+518A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668524 | |||||||
chr4:668528 | C | T | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2503+522C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668528 | |||||||
chr4:668529 | C | G | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2503+523C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668529 | |||||||
chr4:668537 | A | G | 60 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(57): Show |
64 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.2503+531A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668537 | |||||||
chr4:668538 | T | C | 60 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(57): Show |
64 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.2503+532T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668538 | |||||||
chr4:668543 | G | A | 60 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(57): Show |
64 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.2503+537G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668543 | |||||||
chr4:668561 | CCTACCCC others(68): Show |
C | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2503+568_2503+642d others(77): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 668561 | ||||||
chr4:668575 | G | T | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2503+569G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668575 | |||||||
chr4:668577 | A | C | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2503+571A>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668577 | |||||||
chr4:668579 | C | T | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2503+573C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668579 | |||||||
chr4:668580 | A | ACTACCCC others(12): Show |
1 | a0001c0001t0002g0152 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2503+593_2503+611d others(21): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 668580 | ||||||
chr4:668580 | A | G | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2503+574A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668580 | |||||||
chr4:668598 | CG | C | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2503+593delG | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668598 | |||||||
chr4:668622 | CCCATGCT others(68): Show |
C | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2503+630_2503+704d others(77): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 668622 | ||||||
chr4:668633 | CCCGCTAC others(122): Show |
C | 2 | a0001c0001t0001g0007 a0001c0026t0001g0007 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2503+630_2503+758d others(2): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 668633 | ||||||
chr4:668636 | GCTACCCC others(122): Show |
G | 52 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0048 others(49): Show |
56 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.2503+680_2503+808d others(2): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 668636 | ||||||
chr4:668636 | GCTACCCC others(289): Show |
G | 4 | a0002c0003t0005g0254 a0002c0003t0005g0255 a0002c0003t0005g0257 others(1): Show |
4 | HG01975.hp2 HG02970.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2503+680_2503+975d others(2): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 668636 | ||||||
chr4:668674 | C | T | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2503+668C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668674 | |||||||
chr4:668686 | A | G | 5 | a0001c0001t0011g0046 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2503+680A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668686 | |||||||
chr4:668687 | T | C | 5 | a0001c0001t0011g0046 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2503+681T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668687 | |||||||
chr4:668692 | G | A | 5 | a0001c0001t0011g0046 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2503+686G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668692 | |||||||
chr4:668692 | GCTATGCC others(233): Show |
G | 1 | a0001c0001t0012g0034 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2503+690_2503+929d others(2): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 668692 | ||||||
chr4:668696 | T | C | 5 | a0001c0001t0011g0046 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2503+690T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668696 | |||||||
chr4:668697 | G | C | 5 | a0001c0001t0011g0046 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2503+691G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668697 | |||||||
chr4:668701 | T | C | 5 | a0001c0001t0011g0046 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2503+695T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668701 | |||||||
chr4:668728 | T | C | 8 | a0001c0001t0011g0046 a0001c0009t0009g0053 a0001c0009t0009g0248 others(5): Show |
8 | HG00642.hp2 HG01358.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2503+722T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668728 | |||||||
chr4:668734 | GCCATGCT others(11): Show |
G | 1 | a0001c0001t0001g0131 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2503+754_2503+771d others(20): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 668734 | ||||||
chr4:668747 | C | CG | 8 | a0001c0001t0011g0046 a0001c0009t0009g0053 a0001c0009t0009g0248 others(5): Show |
8 | HG00642.hp2 HG01358.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2503+741_2503+742i others(3): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668747 | |||||||
chr4:668765 | C | A | 2 | a0001c0001t0001g0007 a0001c0026t0001g0007 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2503+759C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668765 | |||||||
chr4:668852 | A | G | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2503+846A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668852 | |||||||
chr4:668853 | T | C | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2503+847T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668853 | |||||||
chr4:668858 | G | A | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2503+852G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668858 | |||||||
chr4:668862 | T | C | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2503+856T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668862 | |||||||
chr4:668863 | G | C | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2503+857G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668863 | |||||||
chr4:668877 | GCTACCCC others(30): Show |
G | 3 | a0001c0005t0001g0204 a0005c0011t0001g0251 a0005c0011t0001g0252 |
3 | HG02572.hp2 HG02630.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2503+880_2503+916d others(39): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 668877 | ||||||
chr4:668881 | C | T | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2503+875C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668881 | |||||||
chr4:668882 | C | G | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2503+876C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668882 | |||||||
chr4:668886 | TGCTATTC others(30): Show |
T | 51 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(48): Show |
55 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.2503+976_2503+1012 others(40): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 668886 | ||||||
chr4:668886 | TGCTATTC others(67): Show |
T | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2503+939_2503+1012 others(77): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 668886 | ||||||
chr4:668891 | TTCCCCTA others(11): Show |
T | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2503+890_2503+907d others(20): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 668891 | ||||||
chr4:668914 | A | ACTACCCC others(11): Show |
3 | a0001c0001t0003g0003 a0001c0001t0003g0054 a0001c0001t0003g0086 |
3 | NA18952.hp2 NA18979.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.2503+917_2503+934d others(20): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 668914 | ||||||
chr4:668914 | A | G | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2503+908A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668914 | |||||||
chr4:668923 | C | T | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2503+917C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668923 | |||||||
chr4:668960 | C | T | 1 | a0013c0016t0001g0197 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2503+954C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668960 | |||||||
chr4:668980 | C | CTATTCCC others(126): Show |
1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2503+975_2503+976i others(135): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 668980 | ||||||
chr4:668997 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2503+991C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 668997 | |||||||
chr4:669029 | T | C | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2504-1017T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669029 | |||||||
chr4:669030 | G | C | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2504-1016G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669030 | |||||||
chr4:669036 | C | CTATT | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2504-1009_2504-100 others(8): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669036 | ||||||
chr4:669044 | G | A | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2504-1002G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669044 | |||||||
chr4:669046 | T | G | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2504-1000T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669046 | |||||||
chr4:669053 | TGCTATTC others(67): Show |
T | 59 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(56): Show |
63 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.2504-934_2504-861d others(76): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669053 | ||||||
chr4:669069 | CATGCTGC others(160): Show |
C | 2 | a0001c0001t0002g0132 a0001c0001t0003g0006 |
3 | HG01167.hp1 HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2504-956_2504-790d others(2): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669069 | ||||||
chr4:669075 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2504-971G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669075 | |||||||
chr4:669076 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2504-970C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669076 | |||||||
chr4:669090 | C | T | 207 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(204): Show |
237 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.2504-956C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669090 | |||||||
chr4:669099 | C | CA | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(203): Show |
236 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.2504-947_2504-946i others(3): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669099 | |||||||
chr4:669099 | C | CG | 4 | a0001c0001t0011g0046 a0001c0009t0009g0053 a0001c0009t0009g0248 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2504-947_2504-946i others(3): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669099 | |||||||
chr4:669104 | C | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(203): Show |
236 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.2504-942C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669104 | |||||||
chr4:669110 | C | CTATTCCC others(9): Show |
3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-935_2504-934i others(18): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669110 | ||||||
chr4:669112 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2504-934G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669112 | |||||||
chr4:669113 | C | CTATTTAT | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-932_2504-931i others(9): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669113 | ||||||
chr4:669113 | C | CTGCCACT others(86): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0106 a0001c0001t0001g0124 |
4 | NA18944.hp1 NA18945.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.2504-932_2504-931i others(95): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669113 | ||||||
chr4:669113 | C | T | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2504-933C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669113 | |||||||
chr4:669115 | C | A | 4 | a0001c0001t0002g0072 a0001c0001t0003g0071 a0001c0001t0003g0098 others(1): Show |
4 | HG00621.hp1 HG02074.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.2504-931C>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669115 | |||||||
chr4:669115 | C | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(196): Show |
228 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.2504-931C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669115 | |||||||
chr4:669118 | A | ACTACCCC others(86): Show |
134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
161 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.2504-920_2504-919i others(95): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669118 | ||||||
chr4:669118 | A | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0106 a0001c0001t0001g0124 |
4 | NA18944.hp1 NA18945.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.2504-928A>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669118 | |||||||
chr4:669120 | T | G | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-926T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669120 | |||||||
chr4:669123 | CCCACGCT others(67): Show |
C | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2504-919_2504-846d others(76): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669123 | ||||||
chr4:669127 | C | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(203): Show |
236 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.2504-919C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669127 | |||||||
chr4:669132 | T | G | 65 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0103 others(62): Show |
67 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.2504-914T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669132 | |||||||
chr4:669133 | T | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(134): Show |
165 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.2504-913T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669133 | |||||||
chr4:669136 | C | CA | 65 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0103 others(62): Show |
67 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.2504-910_2504-909i others(3): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669136 | |||||||
chr4:669149 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
232 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.2504-897G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669149 | |||||||
chr4:669150 | C | T | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
232 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.2504-896C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669150 | |||||||
chr4:669155 | A | G | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
232 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.2504-891A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669155 | |||||||
chr4:669164 | C | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(203): Show |
236 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.2504-882C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669164 | |||||||
chr4:669173 | C | CA | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-873_2504-872i others(3): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669173 | |||||||
chr4:669173 | C | CACTACTC others(367): Show |
1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2504-873_2504-872i others(376): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669173 | |||||||
chr4:669173 | C | CCTACCCC others(104): Show |
1 | a0001c0001t0001g0161 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2504-855_2504-854i others(113): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669173 | ||||||
chr4:669173 | C | CCTACCCC others(104): Show |
47 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0103 others(44): Show |
48 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.2504-855_2504-854i others(113): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669173 | ||||||
chr4:669178 | C | T | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-868C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669178 | |||||||
chr4:669186 | A | G | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-860A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669186 | |||||||
chr4:669187 | T | C | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-859T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669187 | |||||||
chr4:669188 | TC | T | 4 | a0001c0005t0001g0245 a0001c0005t0001g0246 a0001c0005t0001g0247 others(1): Show |
4 | HG02257.hp2 HG03130.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2504-855delC | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669188 | ||||||
chr4:669189 | C | G | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-857C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669189 | |||||||
chr4:669192 | G | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(202): Show |
235 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.2504-854G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669192 | |||||||
chr4:669196 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(203): Show |
236 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.2504-850T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669196 | |||||||
chr4:669197 | G | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(155): Show |
187 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.2504-849G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669197 | |||||||
chr4:669202 | G | A | 2 | a0001c0001t0001g0007 a0001c0026t0001g0007 |
2 | HG02630.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.2504-844G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669202 | |||||||
chr4:669203 | C | CTATT | 58 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(55): Show |
62 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.2504-842_2504-839d others(6): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669203 | ||||||
chr4:669206 | T | G | 7 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 others(4): Show |
7 | HG00642.hp2 HG01358.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.2504-840T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669206 | |||||||
chr4:669207 | TCCCGCTA others(8): Show |
T | 1 | a0002c0003t0005g0253 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2504-838_2504-824d others(17): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669207 | |||||||
chr4:669210 | CG | C | 17 | a0001c0001t0001g0158 a0001c0001t0001g0165 a0001c0001t0001g0185 others(14): Show |
18 | HG00408.hp2 HG01167.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.2504-835delG | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669210 | |||||||
chr4:669211 | G | A | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(199): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.2504-835G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669211 | |||||||
chr4:669213 | T | G | 58 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(55): Show |
62 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.2504-833T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669213 | |||||||
chr4:669216 | C | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(134): Show |
165 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.2504-830C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669216 | |||||||
chr4:669225 | TTCCCCTA others(11): Show |
T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0021 a0001c0001t0001g0103 others(44): Show |
48 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.2504-816_2504-799d others(20): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669225 | ||||||
chr4:669226 | T | C | 17 | a0001c0001t0001g0158 a0001c0001t0001g0165 a0001c0001t0001g0185 others(14): Show |
18 | HG00408.hp2 HG01167.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.2504-820T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669226 | |||||||
chr4:669229 | C | CG | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(134): Show |
165 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.2504-817_2504-816i others(3): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669229 | |||||||
chr4:669231 | T | G | 1 | a0002c0003t0005g0253 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2504-815T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669231 | |||||||
chr4:669236 | T | C | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(219): Show |
255 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(252): Show |
intron_variant | MODIFIER | c.2504-810T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669236 | |||||||
chr4:669240 | C | CTATTCCC others(84): Show |
2 | a0001c0001t0001g0216 a0001c0001t0006g0167 |
2 | HG01167.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.2504-805_2504-804i others(93): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669240 | ||||||
chr4:669240 | C | CTATTCCC others(84): Show |
12 | a0001c0001t0001g0158 a0001c0001t0001g0165 a0001c0001t0001g0185 others(9): Show |
12 | HG00408.hp2 HG03471.hp1 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.2504-805_2504-804i others(93): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669240 | ||||||
chr4:669240 | C | CTATTCCC others(103): Show |
1 | a0001c0001t0002g0133 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2504-805_2504-804i others(112): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669240 | ||||||
chr4:669242 | G | A | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(138): Show |
170 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.2504-804G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669242 | |||||||
chr4:669243 | C | CTAT | 15 | a0001c0001t0001g0158 a0001c0001t0001g0165 a0001c0001t0001g0185 others(12): Show |
15 | HG00408.hp2 HG01167.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.2504-802_2504-801i others(5): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669243 | ||||||
chr4:669243 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(138): Show |
170 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(167): Show |
intron_variant | MODIFIER | c.2504-803C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669243 | |||||||
chr4:669248 | A | G | 3 | a0001c0001t0002g0024 a0001c0001t0002g0051 a0001c0001t0002g0189 |
4 | HG03471.hp1 NA19002.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2504-798A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669248 | |||||||
chr4:669253 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2504-793C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669253 | |||||||
chr4:669261 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2504-785A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669261 | |||||||
chr4:669262 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2504-784T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669262 | |||||||
chr4:669264 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2504-782C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669264 | |||||||
chr4:669266 | CA | C | 2 | a0001c0001t0002g0024 a0001c0001t0002g0189 |
3 | NA19002.hp2 NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2504-779delA | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669266 | |||||||
chr4:669272 | T | C | 3 | a0001c0001t0001g0162 a0001c0001t0002g0024 a0001c0001t0002g0189 |
4 | HG01943.hp1 NA19002.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2504-774T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669272 | |||||||
chr4:669280 | G | A | 3 | a0001c0001t0001g0162 a0001c0001t0002g0024 a0001c0001t0002g0189 |
4 | HG01943.hp1 NA19002.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2504-766G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669280 | |||||||
chr4:669281 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2504-765C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669281 | |||||||
chr4:669281 | C | T | 2 | a0001c0001t0002g0024 a0001c0001t0002g0189 |
3 | NA19002.hp2 NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2504-765C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669281 | |||||||
chr4:669283 | G | C | 3 | a0001c0001t0001g0162 a0001c0001t0002g0024 a0001c0001t0002g0189 |
4 | HG01943.hp1 NA19002.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2504-763G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669283 | |||||||
chr4:669300 | G | T | 62 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(59): Show |
67 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.2504-746G>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669300 | |||||||
chr4:669304 | CACTACCC others(426): Show |
C | 59 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(56): Show |
63 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.2504-741_2504-309d others(2): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669304 | |||||||
chr4:669305 | A | G | 3 | a0001c0001t0001g0162 a0001c0001t0002g0147 a0001c0001t0011g0046 |
3 | HG01943.hp1 HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.2504-741A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669305 | |||||||
chr4:669310 | C | G | 2 | a0001c0001t0002g0024 a0001c0001t0002g0189 |
3 | NA19002.hp2 NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2504-736C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669310 | |||||||
chr4:669319 | T | G | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-727T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669319 | |||||||
chr4:669324 | G | A | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-722G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669324 | |||||||
chr4:669338 | TTCCCCTA others(47): Show |
T | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-702_2504-649d others(56): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669338 | ||||||
chr4:669342 | C | CACTACCC others(32): Show |
2 | a0001c0001t0002g0024 a0001c0001t0002g0189 |
3 | NA19002.hp2 NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2504-704_2504-703i others(41): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669342 | |||||||
chr4:669342 | C | CG | 5 | a0001c0001t0011g0046 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2504-704_2504-703i others(3): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669342 | |||||||
chr4:669356 | T | G | 2 | a0001c0001t0002g0024 a0001c0001t0002g0189 |
3 | NA19002.hp2 NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2504-690T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669356 | |||||||
chr4:669360 | CA | C | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2504-685delA | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669360 | |||||||
chr4:669361 | A | G | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2504-685A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669361 | |||||||
chr4:669376 | T | C | 1 | a0001c0001t0001g0004 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2504-670T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669376 | |||||||
chr4:669379 | C | CG | 6 | a0001c0001t0002g0024 a0001c0001t0002g0189 a0004c0007t0008g0237 others(3): Show |
7 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.2504-667_2504-666i others(3): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669379 | |||||||
chr4:669392 | A | AT | 5 | a0001c0001t0011g0046 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2504-653dupT | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669392 | ||||||
chr4:669394 | C | T | 2 | a0001c0001t0002g0024 a0001c0001t0002g0189 |
3 | NA19002.hp2 NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2504-652C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669394 | |||||||
chr4:669397 | C | G | 8 | a0001c0001t0011g0046 a0001c0009t0009g0053 a0001c0009t0009g0248 others(5): Show |
8 | HG00642.hp2 HG01358.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2504-649C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669397 | |||||||
chr4:669416 | G | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0189 |
3 | NA19002.hp2 NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2504-630G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669416 | |||||||
chr4:669432 | C | T | 1 | a0001c0001t0002g0149 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2504-614C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669432 | |||||||
chr4:669447 | AT | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0189 |
3 | NA19002.hp2 NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2504-597delT | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669447 | ||||||
chr4:669452 | CACTACCC others(32): Show |
C | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2504-593_2504-555d others(41): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669452 | |||||||
chr4:669453 | A | C | 2 | a0001c0001t0002g0024 a0001c0001t0002g0189 |
3 | NA19002.hp2 NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2504-593A>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669453 | |||||||
chr4:669453 | A | G | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-593A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669453 | |||||||
chr4:669472 | A | G | 5 | a0001c0001t0002g0024 a0001c0001t0002g0189 a0001c0009t0009g0053 others(2): Show |
6 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2504-574A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669472 | |||||||
chr4:669477 | G | C | 6 | a0001c0001t0002g0024 a0001c0001t0002g0189 a0001c0001t0011g0046 others(3): Show |
7 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2504-569G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669477 | |||||||
chr4:669477 | GCCATGCT others(88): Show |
G | 1 | a0001c0001t0003g0006 | 2 | HG01167.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2504-536_2504-442d others(97): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669477 | ||||||
chr4:669486 | T | TTCCCACT others(31): Show |
1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2504-556_2504-555i others(40): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669486 | ||||||
chr4:669490 | CG | C | 2 | a0001c0001t0002g0024 a0001c0001t0002g0189 |
3 | NA19002.hp2 NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2504-555delG | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669490 | |||||||
chr4:669491 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2504-555G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669491 | |||||||
chr4:669504 | A | G | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2504-542A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669504 | |||||||
chr4:669505 | T | C | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2504-541T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669505 | |||||||
chr4:669505 | T | G | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2504-541T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669505 | |||||||
chr4:669509 | CA | C | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-536delA | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669509 | |||||||
chr4:669510 | A | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0161 others(17): Show |
20 | HG00438.hp2 HG00639.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.2504-536A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669510 | |||||||
chr4:669528 | CG | C | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-517delG | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669528 | |||||||
chr4:669529 | G | A | 5 | a0001c0001t0002g0132 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2504-517G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669529 | |||||||
chr4:669534 | C | CCCATGCT others(12): Show |
1 | a0001c0001t0002g0011 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2504-498_2504-480d others(21): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669534 | ||||||
chr4:669534 | C | G | 2 | a0001c0001t0002g0024 a0001c0001t0002g0189 |
3 | NA19002.hp2 NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2504-512C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669534 | |||||||
chr4:669534 | C | T | 5 | a0001c0001t0002g0132 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2504-512C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669534 | |||||||
chr4:669542 | A | G | 8 | a0001c0001t0002g0132 a0001c0009t0009g0053 a0001c0009t0009g0248 others(5): Show |
8 | HG00642.hp2 HG01358.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2504-504A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669542 | |||||||
chr4:669543 | T | C | 8 | a0001c0001t0002g0132 a0001c0009t0009g0053 a0001c0009t0009g0248 others(5): Show |
8 | HG00642.hp2 HG01358.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2504-503T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669543 | |||||||
chr4:669545 | C | G | 5 | a0001c0001t0002g0132 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2504-501C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669545 | |||||||
chr4:669548 | G | A | 8 | a0001c0001t0002g0132 a0001c0009t0009g0053 a0001c0009t0009g0248 others(5): Show |
8 | HG00642.hp2 HG01358.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2504-498G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669548 | |||||||
chr4:669553 | G | C | 11 | a0001c0001t0002g0024 a0001c0001t0002g0132 a0001c0001t0002g0189 others(8): Show |
12 | HG00642.hp2 HG01358.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.2504-493G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669553 | |||||||
chr4:669553 | GCCATGCT others(12): Show |
G | 1 | a0001c0001t0002g0133 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2504-479_2504-461d others(21): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669553 | ||||||
chr4:669562 | T | G | 5 | a0001c0001t0002g0132 a0004c0007t0008g0237 a0004c0007t0008g0238 others(2): Show |
5 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2504-484T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669562 | |||||||
chr4:669566 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2504-480C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669566 | |||||||
chr4:669567 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(182): Show |
214 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(211): Show |
intron_variant | MODIFIER | c.2504-479A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669567 | |||||||
chr4:669572 | C | GCCATGCT others(12): Show |
1 | a0001c0001t0003g0078 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2504-475_2504-474i others(21): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669572 | |||||||
chr4:669572 | C | T | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-474C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669572 | |||||||
chr4:669580 | A | G | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-466A>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669580 | |||||||
chr4:669581 | T | C | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-465T>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669581 | |||||||
chr4:669581 | T | G | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2504-465T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669581 | |||||||
chr4:669583 | C | G | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-463C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669583 | |||||||
chr4:669586 | G | A | 7 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 others(4): Show |
7 | HG00642.hp2 HG01358.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.2504-460G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669586 | |||||||
chr4:669591 | C | T | 1 | a0001c0001t0003g0011 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2504-455C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669591 | |||||||
chr4:669600 | T | G | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-446T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669600 | |||||||
chr4:669605 | G | A | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-441G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669605 | |||||||
chr4:669610 | C | G | 2 | a0001c0001t0002g0024 a0001c0001t0002g0189 |
3 | NA19002.hp2 NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2504-436C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669610 | |||||||
chr4:669619 | T | G | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-427T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669619 | |||||||
chr4:669624 | G | A | 4 | a0001c0001t0002g0132 a0001c0009t0009g0053 a0001c0009t0009g0248 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.2504-422G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669624 | |||||||
chr4:669642 | C | CG | 5 | a0001c0001t0002g0024 a0001c0001t0002g0189 a0001c0009t0009g0053 others(2): Show |
6 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.2504-404_2504-403i others(3): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669642 | |||||||
chr4:669647 | CCCATGCT others(12): Show |
C | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2504-380_2504-362d others(21): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669647 | ||||||
chr4:669660 | CG | C | 3 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 |
3 | HG01891.hp1 HG02109.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2504-385delG | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669660 | |||||||
chr4:669661 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2504-385G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669661 | |||||||
chr4:669661 | G | C | 1 | a0001c0001t0002g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2504-385G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669661 | |||||||
chr4:669666 | G | C | 6 | a0001c0001t0002g0024 a0001c0001t0002g0189 a0001c0001t0011g0046 others(3): Show |
7 | HG01891.hp1 HG02109.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2504-380G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669666 | |||||||
chr4:669666 | GCCATGCT others(12): Show |
G | 2 | a0001c0001t0001g0015 a0001c0001t0003g0080 |
2 | NA18945.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2504-309_2504-291d others(21): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669666 | ||||||
chr4:669666 | GCCATGCT others(31): Show |
C | 1 | a0001c0001t0002g0132 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2504-380_2504-343d others(40): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669666 | |||||||
chr4:669675 | T | G | 7 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 others(4): Show |
7 | HG00642.hp2 HG01358.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.2504-371T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669675 | |||||||
chr4:669677 | C | CCCCTACC others(330): Show |
1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2504-367_2504-366i others(339): Show |
PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr4 | 669677 | ||||||
chr4:669679 | CG | C | 2 | a0001c0001t0002g0024 a0001c0001t0002g0189 |
3 | NA19002.hp2 NA19080.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.2504-366delG | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669679 | |||||||
chr4:669680 | G | A | 7 | a0001c0009t0009g0053 a0001c0009t0009g0248 a0001c0009t0009g0249 others(4): Show |
7 | HG00642.hp2 HG01358.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.2504-366G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669680 | |||||||
chr4:669680 | G | C | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2504-366G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669680 | |||||||
chr4:669694 | T | G | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2504-352T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669694 | |||||||
chr4:669699 | G | A | 8 | a0001c0001t0011g0046 a0001c0009t0009g0053 a0001c0009t0009g0248 others(5): Show |
8 | HG00642.hp2 HG01358.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.2504-347G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669699 | |||||||
chr4:669704 | C | G | 3 | a0001c0001t0002g0024 a0001c0001t0002g0189 a0001c0001t0003g0080 |
4 | NA19002.hp2 NA19009.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.2504-342C>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669704 | |||||||
chr4:669732 | T | G | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2504-314T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669732 | |||||||
chr4:669737 | G | A | 1 | a0001c0001t0011g0046 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2504-309G>A | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669737 | |||||||
chr4:669751 | T | G | 59 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0018 others(56): Show |
63 | HG00099.hp1 HG00735.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.2504-295T>G | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669751 | |||||||
chr4:669754 | C | T | 2 | a0001c0001t0003g0089 a0001c0001t0003g0090 |
2 | NA19074.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2504-292C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669754 | |||||||
chr4:669778 | C | T | 1 | a0001c0001t0007g0263 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2504-268C>T | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669778 | |||||||
chr4:669841 | G | C | 4 | a0004c0007t0008g0237 a0004c0007t0008g0238 a0004c0007t0008g0239 others(1): Show |
4 | HG00642.hp2 HG01358.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.2504-205G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669841 | |||||||
chr4:669863 | G | C | 7 | a0001c0005t0001g0204 a0001c0005t0001g0245 a0001c0005t0001g0246 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2504-183G>C | PDE6B | ENSG00000133256.13 | transcript | ENST00000496514.6 | protein_coding | 21/21 | chr4 | 669863 |