Item | Value |
---|---|
geneid | 57223 |
ensemblid | ENSG00000275052.5 |
hgncid | 29267 |
symbol | PPP4R3B |
name | protein phosphatase 4 regulatory subunit 3B |
refseq_nuc | NM_001122964.3 |
refseq_prot | NP_001116436.3 |
ensembl_nuc | ENST00000616407.2 |
ensembl_prot | ENSP00000483228.1 |
mane_status | MANE Select |
chr | chr2 |
start | 55547292 |
end | 55617622 |
strand | - |
ver | v1.2 |
region | chr2:55547292-55617622 |
region5000 | chr2:55542292-55622622 |
regionname0 | PPP4R3B_chr2_55547292_55617622 |
regionname5000 | PPP4R3B_chr2_55542292_55622622 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 849 | 379 | 96 | 64 | 166 | 10 | 42 | 138 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | MSDTR others(844): Show |
chr2 | 55542292 | 55622622 |
a0002 | 0/0 | 849 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | MSDTR others(844): Show |
chr2 | 55542292 | 55622622 |
a0003 | 0/0 | 849 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | MSDTR others(844): Show |
chr2 | 55542292 | 55622622 |
a0004 | 0/1 | 849 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | MSDTR others(844): Show |
chr2 | 55542292 | 55622622 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2547 | 354 | 86 | 61 | 161 | 10 | 35 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | ATGTC others(2542): Show |
chr2 | 55542292 | 55622622 | ||
a0001c0002 | 0/0 | 2547 | 17 | 3 | 2 | 5 | 0 | 7 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | ATGTC others(2542): Show |
chr2 | 55542292 | 55622622 | ||
a0001c0003 | 0/0 | 2547 | 7 | 6 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | ATGTC others(2542): Show |
chr2 | 55542292 | 55622622 | ||
a0001c0007 | 0/0 | 2547 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | ATGTC others(2542): Show |
chr2 | 55542292 | 55622622 | ||
a0002c0005 | 0/0 | 2547 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | ATGTC others(2542): Show |
chr2 | 55542292 | 55622622 | ||
a0003c0006 | 0/0 | 2547 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | ATGTC others(2542): Show |
chr2 | 55542292 | 55622622 | ||
a0004c0004 | 0/1 | 2547 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | ATGTC others(2542): Show |
chr2 | 55542292 | 55622622 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 5506 | 121 | 25 | 15 | 64 | 1 | 15 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0002 | 0/0 | 5506 | 93 | 14 | 14 | 59 | 3 | 3 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0003 | 0/0 | 5506 | 87 | 31 | 16 | 29 | 5 | 6 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0004 | 0/0 | 5506 | 10 | 0 | 5 | 0 | 0 | 5 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0005 | 0/0 | 5506 | 9 | 8 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0006 | 0/0 | 5506 | 4 | 0 | 3 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0007 | 0/0 | 5506 | 4 | 0 | 4 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0008 | 0/0 | 5506 | 4 | 0 | 0 | 2 | 0 | 2 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0009 | 0/0 | 5506 | 3 | 3 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0010 | 0/0 | 5506 | 3 | 1 | 2 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0012 | 0/0 | 5506 | 2 | 0 | 0 | 1 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0013 | 0/0 | 5506 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0014 | 0/0 | 5506 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0015 | 0/0 | 5506 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0016 | 0/0 | 5506 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0017 | 0/0 | 5506 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0018 | 0/0 | 5506 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0019 | 0/0 | 5506 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0020 | 0/0 | 5506 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0021 | 0/0 | 5506 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0022 | 0/0 | 5506 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0023 | 0/0 | 5506 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0024 | 0/0 | 5506 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0026 | 0/0 | 5506 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0001t0027 | 0/0 | 5506 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0002t0002 | 0/0 | 5506 | 15 | 3 | 2 | 5 | 0 | 5 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0002t0011 | 0/0 | 5506 | 2 | 0 | 0 | 0 | 0 | 2 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0003t0002 | 0/0 | 5506 | 6 | 5 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0003t0025 | 0/0 | 5506 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0001c0007t0002 | 0/0 | 5506 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0002c0005t0006 | 0/0 | 5506 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0003c0006t0004 | 0/0 | 5506 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
a0004c0004t0001 | 0/1 | 5506 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | GAAGA others(5501): Show |
chr2 | 55542292 | 55622622 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0009 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0004g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0005g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0005g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0005g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0005g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0006g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0006g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0006g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0006g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0007g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0008g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0008g0353 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0008g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0008g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0009g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0009g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0009g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0010g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0010g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0010g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0012g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0012g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0013g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0014g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0015g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0016g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0017g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0018g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0019g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0020g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0021g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0022g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0023g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0024g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0026g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0027g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0011g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0003t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0003t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0003t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0003t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0003t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0003t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0003t0025g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0007t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0002c0005t0006g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0003c0006t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0004c0004t0001g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0096 | EUR | GBR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0287 | EUR | GBR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | GBR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0324 | EUR | GBR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | CHS | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0280 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0296 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0351 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0143 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0350 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0283 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01074 | hp2 | a0001 | c0001 | t0006 | g0316 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01081 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01081 | hp2 | a0001 | c0001 | t0010 | g0321 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0291 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01168 | hp1 | a0001 | c0001 | t0006 | g0310 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01175 | hp2 | a0001 | c0001 | t0015 | g0146 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0104 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0144 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0102 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01255 | hp2 | a0001 | c0001 | t0005 | g0179 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01257 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01258 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0295 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0297 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01346 | hp1 | a0001 | c0003 | t0002 | g0265 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01361 | hp2 | a0001 | c0001 | t0010 | g0290 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0141 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01496 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0298 | EUR | IBS | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0018 | EUR | IBS | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01516 | hp2 | a0001 | c0001 | t0006 | g0315 | EUR | IBS | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01884 | hp2 | a0001 | c0001 | t0023 | g0135 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0294 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0326 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01952 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02027 | hp2 | a0001 | c0001 | t0024 | g0050 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0309 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02055 | hp2 | a0001 | c0002 | t0002 | g0099 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0327 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02129 | hp2 | a0001 | c0001 | t0014 | g0193 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02145 | hp2 | a0001 | c0001 | t0010 | g0325 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02155 | hp1 | a0001 | c0001 | t0021 | g0046 | EAS | CDX | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | CDX | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | CDX | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CDX | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0344 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02280 | hp1 | a0001 | c0003 | t0002 | g0266 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0337 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02300 | hp1 | a0001 | c0001 | t0006 | g0318 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0098 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02572 | hp1 | a0001 | c0003 | t0002 | g0267 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0274 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0278 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0336 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0277 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02647 | hp2 | a0001 | c0003 | t0002 | g0264 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0115 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0335 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0311 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0284 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02735 | hp2 | a0001 | c0001 | t0018 | g0231 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02738 | hp2 | a0002 | c0005 | t0006 | g0273 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02809 | hp1 | a0001 | c0001 | t0022 | g0037 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02818 | hp2 | a0001 | c0003 | t0002 | g0263 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0334 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0276 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0174 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0177 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0275 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0181 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0130 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0320 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0175 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03017 | hp1 | a0003 | c0006 | t0004 | g0140 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0035 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0312 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03130 | hp1 | a0001 | c0001 | t0026 | g0347 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0319 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0343 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0346 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0345 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0136 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0317 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03490 | hp2 | a0001 | c0002 | t0011 | g0011 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0137 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03491 | hp2 | a0001 | c0001 | t0016 | g0262 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0138 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03492 | hp2 | a0001 | c0002 | t0011 | g0011 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0183 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03516 | hp2 | a0001 | c0003 | t0025 | g0268 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03540 | hp2 | a0001 | c0003 | t0002 | g0269 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0314 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0279 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03669 | hp1 | a0001 | c0001 | t0012 | g0340 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0103 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0333 | SAS | STU | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | STU | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03704 | hp1 | a0001 | c0001 | t0008 | g0354 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0114 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0139 | SAS | BEB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0109 | SAS | BEB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | BEB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0123 | SAS | BEB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | STU | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0142 | SAS | STU | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG04184 | hp1 | a0001 | c0001 | t0027 | g0292 | SAS | BEB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG04184 | hp2 | a0001 | c0001 | t0008 | g0353 | SAS | BEB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | STU | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0293 | SAS | STU | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0286 | SAS | STU | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18522 | hp1 | a0001 | c0007 | t0002 | g0270 | AFR | YRI | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0313 | AFR | YRI | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0342 | AFR | YRI | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0329 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0328 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18964 | hp1 | a0001 | c0001 | t0012 | g0331 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0323 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18975 | hp2 | a0001 | c0001 | t0020 | g0049 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18979 | hp1 | a0001 | c0001 | t0008 | g0355 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18987 | hp1 | a0001 | c0001 | t0017 | g0205 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19001 | hp2 | a0001 | c0001 | t0019 | g0070 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19002 | hp1 | a0001 | c0001 | t0008 | g0352 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0124 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19030 | hp1 | a0001 | c0001 | t0009 | g0026 | AFR | LWK | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0176 | AFR | LWK | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | LWK | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19043 | hp2 | a0001 | c0001 | t0009 | g0025 | AFR | LWK | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0330 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | YRI | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | YRI | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0349 | AFR | ASW | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ASW | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | TSI | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0017 | EUR | TSI | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | GIH | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | GIH | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0100 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0182 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0348 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0178 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0339 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG06807 | hp1 | a0001 | c0001 | t0013 | g0023 | AFR | USA | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | USA | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0111 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | USA | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | USA | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | LWK | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0341 | AFR | LWK | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
homoSapiens | chm13v2 | a0004 | c0004 | t0001 | g0150 | REF | REF | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0238 | REF | REF | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55585065 | G | C | 1 | a0002 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.1219C>G | p.Gln407Glu | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/17 | 1556/5506 | 1219/2550 | 407/849 | chr2 | 55585065 | |||
chr2:55598923 | T | G | 1 | a0003 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.414A>C | p.Glu138Asp | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/17 | 751/5506 | 414/2550 | 138/849 | chr2 | 55598923 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55573728 | T | C | 1 | a0001c0003 | 7 | HG01346.hp1 HG02280.hp1 HG02572.hp1 others(4): Show |
synonymous_variant | LOW | c.1656A>G | p.Thr552Thr | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/17 | 1993/5506 | 1656/2550 | 552/849 | chr2 | 55573728 | |||
chr2:55579776 | G | A | 1 | a0001c0002 | 17 | HG01192.hp1 HG01243.hp1 HG02055.hp2 others(14): Show |
synonymous_variant | LOW | c.1371C>T | p.Thr457Thr | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 9/17 | 1708/5506 | 1371/2550 | 457/849 | chr2 | 55579776 | |||
chr2:55617202 | G | A | 2 | a0001c0003 a0001c0007 |
8 | HG01346.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
synonymous_variant | LOW | c.84C>T | p.Ser28Ser | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/17 | 421/5506 | 84/2550 | 28/849 | chr2 | 55617202 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55547418 | G | C | 1 | a0001c0002t0011 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2493C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 2493 | chr2 | 55547418 | ||||||
chr2:55547831 | T | C | 1 | a0001c0001t0022 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2080A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 2080 | chr2 | 55547831 | ||||||
chr2:55547849 | C | T | 1 | a0001c0001t0021 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2062G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 2062 | chr2 | 55547849 | ||||||
chr2:55547933 | C | T | 7 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0010 others(4): Show |
98 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1978G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 1978 | chr2 | 55547933 | ||||||
chr2:55548107 | A | G | 1 | a0001c0001t0005 | 9 | HG01255.hp2 HG02109.hp2 HG02895.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1804T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 1804 | chr2 | 55548107 | ||||||
chr2:55548247 | G | A | 1 | a0001c0001t0017 | 1 | NA18987.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1664C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 1664 | chr2 | 55548247 | ||||||
chr2:55548259 | C | T | 1 | a0001c0001t0009 | 3 | HG03098.hp1 NA19030.hp1 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1652G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 1652 | chr2 | 55548259 | ||||||
chr2:55548588 | A | G | 14 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0013 others(11): Show |
128 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1323T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 1323 | chr2 | 55548588 | ||||||
chr2:55548859 | T | C | 1 | a0001c0001t0024 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1052A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 1052 | chr2 | 55548859 | ||||||
chr2:55548927 | A | G | 1 | a0001c0001t0007 | 4 | HG01257.hp2 HG01258.hp1 HG01496.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*984T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 984 | chr2 | 55548927 | ||||||
chr2:55548993 | A | G | 1 | a0001c0001t0015 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*918T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 918 | chr2 | 55548993 | ||||||
chr2:55549088 | G | T | 1 | a0001c0001t0014 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*823C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 823 | chr2 | 55549088 | ||||||
chr2:55549126 | T | A | 1 | a0001c0003t0025 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*785A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 785 | chr2 | 55549126 | ||||||
chr2:55549425 | T | A | 2 | a0001c0001t0006 a0002c0005t0006 |
5 | HG01074.hp2 HG01168.hp1 HG01516.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*486A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 486 | chr2 | 55549425 | ||||||
chr2:55549436 | G | A | 1 | a0001c0001t0018 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*475C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 475 | chr2 | 55549436 | ||||||
chr2:55549487 | A | T | 1 | a0001c0001t0020 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*424T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 424 | chr2 | 55549487 | ||||||
chr2:55549505 | A | G | 3 | a0001c0001t0004 a0001c0001t0007 a0003c0006t0004 |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*406T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 406 | chr2 | 55549505 | ||||||
chr2:55549614 | C | G | 1 | a0001c0001t0019 | 1 | NA19001.hp2 | 3_prime_UTR_variant | MODIFIER | c.*297G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 297 | chr2 | 55549614 | ||||||
chr2:55549657 | G | A | 22 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(19): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
3_prime_UTR_variant | MODIFIER | c.*254C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 254 | chr2 | 55549657 | ||||||
chr2:55549802 | T | C | 1 | a0001c0001t0026 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*109A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 109 | chr2 | 55549802 | ||||||
chr2:55549862 | C | A | 1 | a0001c0001t0027 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*49G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 17/17 | 49 | chr2 | 55549862 | ||||||
chr2:55617309 | T | C | 7 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0010 others(4): Show |
99 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(96): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-24A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/17 | chr2 | 55617309 | |||||||
chr2:55617440 | G | A | 1 | a0001c0001t0008 | 4 | HG03704.hp1 HG04184.hp2 NA18979.hp1 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-155C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/17 | chr2 | 55617440 | |||||||
chr2:55617609 | C | T | 1 | a0001c0001t0013 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-324G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/17 | 324 | chr2 | 55617609 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55550070 | A | C | 1 | a0001c0001t0001g0239 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2455-64T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55550070 | |||||||
chr2:55550083 | T | TA | 9 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(6): Show |
9 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2455-78dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55550083 | |||||||
chr2:55550188 | C | T | 1 | a0001c0001t0003g0272 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2455-182G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55550188 | |||||||
chr2:55550523 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2455-517C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55550523 | |||||||
chr2:55551034 | C | T | 2 | a0001c0001t0002g0057 a0001c0001t0002g0084 |
2 | HG00642.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.2455-1028G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55551034 | |||||||
chr2:55551053 | A | G | 1 | a0001c0001t0005g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2455-1047T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55551053 | |||||||
chr2:55551117 | C | T | 2 | a0001c0001t0002g0043 a0001c0001t0002g0075 |
2 | HG02451.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.2455-1111G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55551117 | |||||||
chr2:55551214 | C | T | 90 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(87): Show |
99 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.2455-1208G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55551214 | |||||||
chr2:55551753 | A | AAAAT | 117 | a0001c0001t0001g0169 a0001c0001t0001g0172 a0001c0001t0002g0002 others(114): Show |
130 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.2455-1751_2455-174 others(8): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55551753 | |||||||
chr2:55551821 | GTAGT | G | 4 | a0001c0002t0002g0104 a0001c0002t0002g0109 a0001c0002t0002g0123 others(1): Show |
5 | HG01192.hp1 HG03490.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.2455-1819_2455-181 others(8): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55551821 | |||||||
chr2:55551990 | A | G | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.2455-1984T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55551990 | |||||||
chr2:55552157 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2455-2151G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55552157 | |||||||
chr2:55552326 | TA | T | 229 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(226): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2455-2321delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55552326 | |||||||
chr2:55552340 | C | T | 214 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0004 others(211): Show |
240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.2455-2334G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55552340 | |||||||
chr2:55552411 | T | A | 4 | a0001c0001t0003g0346 a0001c0001t0003g0348 a0001c0001t0003g0349 others(1): Show |
4 | HG02559.hp2 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2455-2405A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55552411 | |||||||
chr2:55552496 | C | T | 1 | a0001c0001t0003g0336 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2455-2490G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55552496 | |||||||
chr2:55552658 | C | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2455-2652G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55552658 | |||||||
chr2:55552903 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2455-2897G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55552903 | |||||||
chr2:55552981 | A | G | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.2455-2975T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55552981 | |||||||
chr2:55553019 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2455-3013A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55553019 | |||||||
chr2:55553089 | T | G | 274 | a0001c0001t0001g0013 a0001c0001t0001g0086 a0001c0001t0001g0087 others(271): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.2455-3083A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55553089 | |||||||
chr2:55553115 | T | C | 259 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(256): Show |
286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.2455-3109A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55553115 | |||||||
chr2:55553198 | C | G | 5 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0302 others(2): Show |
5 | NA18952.hp1 NA18979.hp2 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.2455-3192G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55553198 | |||||||
chr2:55553398 | G | A | 1 | a0001c0001t0006g0316 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2455-3392C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55553398 | |||||||
chr2:55553454 | G | T | 1 | a0001c0001t0003g0305 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2455-3448C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55553454 | |||||||
chr2:55553460 | T | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2455-3454A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55553460 | |||||||
chr2:55553938 | CAT | C | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0235 |
3 | HG02145.hp1 HG03139.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2455-3934_2455-393 others(6): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55553938 | |||||||
chr2:55553997 | A | G | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(8): Show |
11 | HG00099.hp1 HG01106.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.2455-3991T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55553997 | |||||||
chr2:55553997 | A | T | 57 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0007 others(54): Show |
65 | HG00140.hp1 HG00621.hp1 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.2455-3991T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55553997 | |||||||
chr2:55554014 | T | C | 14 | a0001c0001t0001g0192 a0001c0001t0001g0194 a0001c0001t0001g0208 others(11): Show |
14 | HG02129.hp2 NA18612.hp1 NA18943.hp1 others(11): Show |
intron_variant | MODIFIER | c.2455-4008A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55554014 | |||||||
chr2:55554243 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.2455-4237C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55554243 | |||||||
chr2:55554433 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2454+4342A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55554433 | |||||||
chr2:55554619 | G | C | 1 | a0001c0001t0003g0327 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2454+4156C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55554619 | |||||||
chr2:55554740 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2454+4035C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55554740 | |||||||
chr2:55554881 | C | G | 1 | a0001c0001t0003g0327 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2454+3894G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55554881 | |||||||
chr2:55554978 | A | G | 1 | a0001c0001t0003g0319 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2454+3797T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55554978 | |||||||
chr2:55555002 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2454+3773G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55555002 | |||||||
chr2:55555253 | C | T | 2 | a0001c0001t0003g0330 a0001c0001t0003g0338 |
2 | NA19009.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.2454+3522G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55555253 | |||||||
chr2:55555278 | T | TA | 26 | a0001c0001t0001g0246 a0001c0001t0002g0127 a0001c0001t0002g0128 others(23): Show |
30 | HG01081.hp1 HG01099.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.2454+3496dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55555278 | |||||||
chr2:55555278 | T | TAA | 90 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(87): Show |
99 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.2454+3495_2454+349 others(6): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55555278 | |||||||
chr2:55555537 | A | G | 1 | a0001c0001t0003g0283 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.2454+3238T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55555537 | |||||||
chr2:55555583 | G | A | 1 | a0001c0001t0002g0069 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2454+3192C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55555583 | |||||||
chr2:55555737 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2454+3038C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55555737 | |||||||
chr2:55555784 | A | C | 1 | a0001c0001t0003g0293 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2454+2991T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55555784 | |||||||
chr2:55555912 | T | C | 1 | a0001c0001t0002g0079 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2454+2863A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55555912 | |||||||
chr2:55556097 | T | C | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.2454+2678A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55556097 | |||||||
chr2:55556620 | A | G | 3 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0035 |
3 | HG03098.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2454+2155T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55556620 | |||||||
chr2:55556632 | T | TA | 47 | a0001c0001t0001g0013 a0001c0001t0001g0095 a0001c0001t0001g0133 others(44): Show |
48 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(45): Show |
intron_variant | MODIFIER | c.2454+2142dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55556632 | |||||||
chr2:55556632 | TA | T | 6 | a0001c0001t0001g0189 a0001c0001t0001g0239 a0001c0001t0002g0068 others(3): Show |
6 | HG01070.hp1 HG01169.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2454+2142delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55556632 | |||||||
chr2:55556699 | C | A | 1 | a0001c0001t0024g0050 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2454+2076G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55556699 | |||||||
chr2:55556765 | T | A | 1 | a0001c0001t0003g0287 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2454+2010A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55556765 | |||||||
chr2:55557032 | C | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0230 |
2 | NA19000.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.2454+1743G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55557032 | |||||||
chr2:55557053 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2454+1722T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55557053 | |||||||
chr2:55557066 | A | AACG | 101 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(98): Show |
112 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.2454+1706_2454+170 others(7): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55557066 | |||||||
chr2:55557318 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0156 |
2 | NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.2454+1457C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55557318 | |||||||
chr2:55557379 | G | A | 1 | a0001c0001t0024g0050 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2454+1396C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55557379 | |||||||
chr2:55557472 | C | A | 102 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(99): Show |
113 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.2454+1303G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55557472 | |||||||
chr2:55557616 | G | A | 3 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0035 |
3 | HG03098.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.2454+1159C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55557616 | |||||||
chr2:55557638 | G | C | 54 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(51): Show |
61 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.2454+1137C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55557638 | |||||||
chr2:55557938 | CT | C | 3 | a0001c0001t0003g0309 a0001c0001t0003g0311 a0001c0001t0003g0312 |
3 | HG02055.hp1 HG02723.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2454+836delA | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55557938 | |||||||
chr2:55558155 | T | A | 2 | a0001c0001t0002g0055 a0001c0001t0002g0083 |
2 | NA18992.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.2454+620A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55558155 | |||||||
chr2:55558165 | T | C | 48 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(45): Show |
49 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.2454+610A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55558165 | |||||||
chr2:55558215 | T | TA | 13 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(10): Show |
15 | HG00423.hp2 HG02027.hp1 HG02129.hp1 others(12): Show |
intron_variant | MODIFIER | c.2454+559dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55558215 | |||||||
chr2:55558272 | T | C | 1 | a0001c0001t0003g0018 | 2 | HG01433.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2454+503A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55558272 | |||||||
chr2:55558360 | TTC | T | 101 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(98): Show |
112 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.2454+413_2454+414d others(4): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55558360 | |||||||
chr2:55558388 | A | T | 88 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(85): Show |
97 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(94): Show |
intron_variant | MODIFIER | c.2454+387T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55558388 | |||||||
chr2:55558480 | C | T | 1 | a0001c0001t0001g0255 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2454+295G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55558480 | |||||||
chr2:55558496 | T | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0029 a0001c0001t0002g0030 others(1): Show |
5 | NA18951.hp2 NA18961.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.2454+279A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55558496 | |||||||
chr2:55558556 | T | C | 261 | a0001c0001t0001g0013 a0001c0001t0001g0086 a0001c0001t0001g0087 others(258): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.2454+219A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55558556 | |||||||
chr2:55558585 | C | T | 1 | a0001c0001t0002g0119 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2454+190G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55558585 | |||||||
chr2:55558590 | G | C | 1 | a0001c0001t0001g0245 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2454+185C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55558590 | |||||||
chr2:55558692 | A | G | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.2454+83T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55558692 | |||||||
chr2:55558703 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2454+72A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55558703 | |||||||
chr2:55559085 | C | T | 1 | a0001c0001t0002g0032 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2261-117G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55559085 | |||||||
chr2:55559175 | C | T | 85 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(82): Show |
94 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.2261-207G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55559175 | |||||||
chr2:55559182 | G | A | 258 | a0001c0001t0001g0013 a0001c0001t0001g0086 a0001c0001t0001g0087 others(255): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.2261-214C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55559182 | |||||||
chr2:55559224 | T | C | 1 | a0001c0001t0012g0340 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2261-256A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55559224 | |||||||
chr2:55559329 | A | G | 78 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(75): Show |
87 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.2261-361T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55559329 | |||||||
chr2:55559359 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2261-391T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55559359 | |||||||
chr2:55559380 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2261-412G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55559380 | |||||||
chr2:55559397 | G | A | 66 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(63): Show |
76 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.2261-429C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55559397 | |||||||
chr2:55559458 | T | G | 1 | a0001c0001t0001g0233 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2261-490A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55559458 | |||||||
chr2:55559494 | CACAT | C | 13 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(10): Show |
16 | HG00438.hp2 HG03710.hp1 HG04199.hp1 others(13): Show |
intron_variant | MODIFIER | c.2261-530_2261-527d others(6): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55559494 | |||||||
chr2:55559603 | G | A | 53 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0008 others(50): Show |
60 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.2261-635C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55559603 | |||||||
chr2:55559847 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0190 |
2 | HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.2261-879G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55559847 | |||||||
chr2:55560080 | C | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2261-1112G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55560080 | |||||||
chr2:55560238 | C | G | 1 | a0001c0001t0002g0056 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2261-1270G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55560238 | |||||||
chr2:55560250 | T | C | 1 | a0001c0001t0002g0063 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2261-1282A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55560250 | |||||||
chr2:55560778 | G | GA | 9 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0213 others(6): Show |
9 | HG02027.hp1 HG02074.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.2261-1811dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55560778 | |||||||
chr2:55560778 | GA | G | 45 | a0001c0001t0001g0054 a0001c0001t0001g0118 a0001c0001t0001g0121 others(42): Show |
45 | HG00621.hp2 HG01255.hp1 HG02080.hp1 others(42): Show |
intron_variant | MODIFIER | c.2261-1811delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55560778 | |||||||
chr2:55560778 | GAA | G | 25 | a0001c0001t0001g0149 a0001c0001t0001g0191 a0001c0001t0001g0195 others(22): Show |
25 | HG01346.hp1 HG01433.hp2 HG01928.hp2 others(22): Show |
intron_variant | MODIFIER | c.2261-1812_2261-181 others(6): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55560778 | |||||||
chr2:55560778 | GAAA | G | 22 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0161 others(19): Show |
22 | HG01361.hp1 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.2261-1813_2261-181 others(7): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55560778 | |||||||
chr2:55560778 | GAAAA | G | 109 | a0001c0001t0001g0013 a0001c0001t0001g0145 a0001c0001t0001g0151 others(106): Show |
125 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2261-1814_2261-181 others(8): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55560778 | |||||||
chr2:55560778 | GAAAAA | G | 21 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(18): Show |
21 | HG00099.hp1 HG01070.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.2261-1815_2261-181 others(9): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55560778 | |||||||
chr2:55560778 | GAAAAAAA others(4): Show |
G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0154 |
2 | NA18612.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.2261-1821_2261-181 others(15): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55560778 | |||||||
chr2:55560778 | GAAAAAAA others(5): Show |
G | 2 | a0001c0001t0001g0148 a0001c0001t0001g0156 |
2 | NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.2261-1822_2261-181 others(16): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55560778 | |||||||
chr2:55560778 | GAAAAAAA others(8): Show |
G | 1 | a0001c0001t0003g0018 | 2 | HG01433.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.2261-1825_2261-181 others(19): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55560778 | |||||||
chr2:55560778 | GAAAAAAA others(9): Show |
G | 88 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0001c0001t0001g0190 others(85): Show |
95 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.2261-1826_2261-181 others(20): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55560778 | |||||||
chr2:55560778 | GAAAAAAA others(10): Show |
G | 3 | a0001c0001t0003g0021 a0001c0001t0003g0307 a0001c0001t0003g0351 |
4 | HG01070.hp1 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.2261-1827_2261-181 others(21): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55560778 | |||||||
chr2:55560825 | G | A | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.2261-1857C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55560825 | |||||||
chr2:55560932 | C | G | 1 | a0001c0001t0003g0327 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2261-1964G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55560932 | |||||||
chr2:55561117 | G | C | 92 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(89): Show |
101 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.2261-2149C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55561117 | |||||||
chr2:55561181 | G | A | 1 | a0001c0001t0005g0179 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2261-2213C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55561181 | |||||||
chr2:55561371 | C | T | 1 | a0001c0001t0003g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2261-2403G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55561371 | |||||||
chr2:55561398 | C | T | 8 | a0001c0003t0002g0263 a0001c0003t0002g0264 a0001c0003t0002g0265 others(5): Show |
8 | HG01346.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.2261-2430G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55561398 | |||||||
chr2:55561414 | C | A | 1 | a0001c0001t0001g0258 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2261-2446G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55561414 | |||||||
chr2:55561530 | T | C | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(8): Show |
11 | HG00099.hp1 HG01106.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.2261-2562A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55561530 | |||||||
chr2:55561689 | G | T | 3 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0005g0174 |
3 | HG02895.hp2 HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2260+2624C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55561689 | |||||||
chr2:55561748 | T | G | 45 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(42): Show |
46 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.2260+2565A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55561748 | |||||||
chr2:55561785 | T | C | 92 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(89): Show |
101 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.2260+2528A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55561785 | |||||||
chr2:55561949 | G | T | 1 | a0001c0001t0001g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2260+2364C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55561949 | |||||||
chr2:55562077 | C | T | 1 | a0001c0001t0003g0304 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2260+2236G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55562077 | |||||||
chr2:55562107 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2260+2206C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55562107 | |||||||
chr2:55562278 | T | C | 159 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0133 others(156): Show |
175 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.2260+2035A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55562278 | |||||||
chr2:55562302 | A | T | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.2260+2011T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55562302 | |||||||
chr2:55562339 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0166 |
3 | HG01167.hp2 HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2260+1974A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55562339 | |||||||
chr2:55562519 | G | A | 102 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(99): Show |
113 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.2260+1794C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55562519 | |||||||
chr2:55562540 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2260+1773C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55562540 | |||||||
chr2:55562545 | C | T | 9 | a0001c0001t0003g0341 a0001c0001t0003g0342 a0001c0001t0003g0343 others(6): Show |
9 | HG02257.hp2 HG02559.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.2260+1768G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55562545 | |||||||
chr2:55562546 | G | C | 1 | a0001c0001t0001g0201 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2260+1767C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55562546 | |||||||
chr2:55562627 | T | G | 9 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(6): Show |
9 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2260+1686A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55562627 | |||||||
chr2:55562656 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2260+1657C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55562656 | |||||||
chr2:55562687 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2260+1626A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55562687 | |||||||
chr2:55562735 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2260+1578T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55562735 | |||||||
chr2:55563008 | C | T | 1 | a0001c0001t0003g0327 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2260+1305G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55563008 | |||||||
chr2:55563026 | T | C | 1 | a0001c0001t0003g0279 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2260+1287A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55563026 | |||||||
chr2:55563158 | G | T | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.2260+1155C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55563158 | |||||||
chr2:55563177 | A | G | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.2260+1136T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55563177 | |||||||
chr2:55563193 | G | A | 1 | a0001c0001t0003g0279 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2260+1120C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55563193 | |||||||
chr2:55563457 | C | T | 8 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(5): Show |
8 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.2260+856G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55563457 | |||||||
chr2:55563492 | C | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2260+821G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55563492 | |||||||
chr2:55563660 | C | T | 1 | a0001c0001t0002g0034 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2260+653G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55563660 | |||||||
chr2:55563690 | T | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.2260+623A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55563690 | |||||||
chr2:55564076 | T | G | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.2260+237A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55564076 | |||||||
chr2:55564303 | A | G | 2 | a0001c0001t0003g0297 a0001c0001t0003g0298 |
2 | HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.2260+10T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55564303 | |||||||
chr2:55564552 | T | C | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.2076-55A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 14/16 | chr2 | 55564552 | |||||||
chr2:55564760 | G | A | 1 | a0001c0001t0013g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2075+142C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 14/16 | chr2 | 55564760 | |||||||
chr2:55565310 | G | GTA | 72 | a0001c0001t0001g0209 a0001c0001t0001g0212 a0001c0001t0001g0259 others(69): Show |
81 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1936-271_1936-270d others(4): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55565310 | |||||||
chr2:55565310 | G | GTATA | 3 | a0001c0001t0001g0054 a0001c0001t0002g0076 a0001c0001t0024g0050 |
3 | HG02027.hp2 NA18941.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1936-273_1936-270d others(6): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55565310 | |||||||
chr2:55565310 | G | T | 8 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0128 others(5): Show |
8 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1936-269C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55565310 | |||||||
chr2:55565310 | GTA | G | 67 | a0001c0001t0001g0013 a0001c0001t0001g0086 a0001c0001t0001g0087 others(64): Show |
72 | HG00099.hp1 HG01070.hp2 HG01081.hp1 others(69): Show |
intron_variant | MODIFIER | c.1936-271_1936-270d others(4): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55565310 | |||||||
chr2:55565314 | A | G | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1936-273T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55565314 | |||||||
chr2:55565368 | T | C | 5 | a0001c0001t0003g0014 a0001c0001t0003g0271 a0001c0001t0003g0272 others(2): Show |
6 | NA18939.hp1 NA19004.hp2 NA19012.hp2 others(3): Show |
intron_variant | MODIFIER | c.1936-327A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55565368 | |||||||
chr2:55565603 | C | T | 13 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(10): Show |
16 | HG00438.hp2 HG03710.hp1 HG04199.hp1 others(13): Show |
intron_variant | MODIFIER | c.1936-562G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55565603 | |||||||
chr2:55565834 | G | A | 1 | a0001c0001t0003g0313 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1936-793C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55565834 | |||||||
chr2:55565834 | G | C | 1 | a0001c0001t0002g0079 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1936-793C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55565834 | |||||||
chr2:55565965 | T | C | 2 | a0001c0001t0002g0055 a0001c0001t0002g0083 |
2 | NA18992.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1936-924A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55565965 | |||||||
chr2:55566079 | A | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1936-1038T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55566079 | |||||||
chr2:55566115 | A | T | 1 | a0001c0002t0002g0124 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1936-1074T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55566115 | |||||||
chr2:55566151 | T | G | 1 | a0001c0001t0018g0231 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1936-1110A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55566151 | |||||||
chr2:55566162 | T | C | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1936-1121A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55566162 | |||||||
chr2:55566242 | A | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1936-1201T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55566242 | |||||||
chr2:55566340 | G | A | 111 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(108): Show |
126 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.1936-1299C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55566340 | |||||||
chr2:55566500 | G | A | 2 | a0001c0001t0002g0055 a0001c0001t0002g0083 |
2 | NA18992.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1936-1459C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55566500 | |||||||
chr2:55566637 | T | C | 1 | a0001c0002t0002g0112 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1935+1557A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55566637 | |||||||
chr2:55566785 | C | T | 5 | a0001c0001t0006g0310 a0001c0001t0006g0315 a0001c0001t0006g0316 others(2): Show |
5 | HG01074.hp2 HG01168.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1935+1409G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55566785 | |||||||
chr2:55566801 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1935+1393C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55566801 | |||||||
chr2:55566834 | C | G | 1 | a0001c0001t0001g0191 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1935+1360G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55566834 | |||||||
chr2:55567142 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1935+1052G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55567142 | |||||||
chr2:55567384 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1935+810G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55567384 | |||||||
chr2:55567466 | G | GA | 5 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
5 | HG01928.hp2 HG01934.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1935+727dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55567466 | |||||||
chr2:55567560 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1935+634G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55567560 | |||||||
chr2:55567707 | C | T | 8 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(5): Show |
8 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1935+487G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55567707 | |||||||
chr2:55567760 | A | T | 1 | a0001c0001t0001g0250 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1935+434T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55567760 | |||||||
chr2:55568156 | T | C | 9 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(6): Show |
9 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1935+38A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 13/16 | chr2 | 55568156 | |||||||
chr2:55568421 | C | T | 13 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(10): Show |
13 | HG00099.hp1 HG01106.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1766-58G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55568421 | |||||||
chr2:55568959 | G | A | 16 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(13): Show |
17 | HG01192.hp1 HG01243.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1766-596C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55568959 | |||||||
chr2:55569084 | A | C | 57 | a0001c0001t0001g0054 a0001c0001t0001g0223 a0001c0001t0002g0002 others(54): Show |
64 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(61): Show |
intron_variant | MODIFIER | c.1766-721T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55569084 | |||||||
chr2:55569208 | C | T | 4 | a0001c0002t0002g0104 a0001c0002t0002g0109 a0001c0002t0002g0123 others(1): Show |
5 | HG01192.hp1 HG03490.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.1766-845G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55569208 | |||||||
chr2:55569273 | T | C | 103 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(100): Show |
114 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1766-910A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55569273 | |||||||
chr2:55569391 | C | G | 90 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(87): Show |
99 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.1766-1028G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55569391 | |||||||
chr2:55569408 | A | G | 193 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(190): Show |
213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1766-1045T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55569408 | |||||||
chr2:55569451 | C | T | 44 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(41): Show |
45 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(42): Show |
intron_variant | MODIFIER | c.1766-1088G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55569451 | |||||||
chr2:55569616 | A | T | 103 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(100): Show |
114 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1766-1253T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55569616 | |||||||
chr2:55569702 | G | A | 84 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(81): Show |
95 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1766-1339C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55569702 | |||||||
chr2:55569754 | G | T | 1 | a0001c0001t0020g0049 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1766-1391C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55569754 | |||||||
chr2:55569848 | C | T | 129 | a0001c0001t0001g0054 a0001c0001t0001g0086 a0001c0001t0001g0087 others(126): Show |
144 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(141): Show |
intron_variant | MODIFIER | c.1766-1485G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55569848 | |||||||
chr2:55569897 | G | T | 128 | a0001c0001t0001g0054 a0001c0001t0001g0086 a0001c0001t0001g0087 others(125): Show |
143 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.1766-1534C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55569897 | |||||||
chr2:55569941 | T | C | 1 | a0001c0001t0013g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1766-1578A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55569941 | |||||||
chr2:55570047 | C | T | 3 | a0001c0001t0002g0127 a0001c0001t0002g0128 a0001c0001t0002g0131 |
3 | HG02258.hp2 NA19240.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1766-1684G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55570047 | |||||||
chr2:55570095 | A | G | 93 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(90): Show |
102 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.1766-1732T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55570095 | |||||||
chr2:55570167 | T | C | 94 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(91): Show |
103 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.1766-1804A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55570167 | |||||||
chr2:55570251 | A | G | 3 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0001g0242 |
3 | HG01358.hp1 HG02738.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1766-1888T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55570251 | |||||||
chr2:55570371 | T | C | 94 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(91): Show |
103 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.1766-2008A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55570371 | |||||||
chr2:55570550 | T | G | 1 | a0001c0001t0001g0235 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1766-2187A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55570550 | |||||||
chr2:55570562 | A | T | 1 | a0001c0001t0001g0157 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1766-2199T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55570562 | |||||||
chr2:55570701 | A | G | 43 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(40): Show |
44 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(41): Show |
intron_variant | MODIFIER | c.1766-2338T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55570701 | |||||||
chr2:55570881 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1766-2518C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55570881 | |||||||
chr2:55570967 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1766-2604G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55570967 | |||||||
chr2:55570972 | C | T | 93 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(90): Show |
102 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.1766-2609G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55570972 | |||||||
chr2:55571114 | G | C | 1 | a0001c0001t0001g0153 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1765+2505C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55571114 | |||||||
chr2:55571232 | A | C | 224 | a0001c0001t0001g0054 a0001c0001t0001g0086 a0001c0001t0001g0087 others(221): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1765+2387T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55571232 | |||||||
chr2:55571273 | A | G | 209 | a0001c0001t0001g0054 a0001c0001t0001g0201 a0001c0001t0001g0212 others(206): Show |
233 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(230): Show |
intron_variant | MODIFIER | c.1765+2346T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55571273 | |||||||
chr2:55571309 | CA | C | 93 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(90): Show |
102 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.1765+2309delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55571309 | |||||||
chr2:55571336 | T | C | 13 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(10): Show |
16 | HG00438.hp2 HG03710.hp1 HG04199.hp1 others(13): Show |
intron_variant | MODIFIER | c.1765+2283A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55571336 | |||||||
chr2:55571574 | T | A | 1 | a0001c0001t0002g0066 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1765+2045A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55571574 | |||||||
chr2:55571586 | C | A | 1 | a0001c0001t0002g0085 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1765+2033G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55571586 | |||||||
chr2:55571621 | TTTTG | T | 9 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(6): Show |
9 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1765+1994_1765+199 others(8): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55571621 | |||||||
chr2:55571712 | G | A | 13 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(10): Show |
13 | HG00099.hp1 HG01106.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1765+1907C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55571712 | |||||||
chr2:55571719 | G | A | 1 | a0001c0001t0003g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1765+1900C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55571719 | |||||||
chr2:55571768 | G | A | 3 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0035 |
3 | HG03098.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1765+1851C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55571768 | |||||||
chr2:55571801 | G | T | 202 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(199): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.1765+1818C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55571801 | |||||||
chr2:55572119 | T | G | 1 | a0001c0001t0001g0164 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1765+1500A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55572119 | |||||||
chr2:55572154 | A | T | 1 | a0001c0001t0001g0258 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1765+1465T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55572154 | |||||||
chr2:55572208 | T | A | 2 | a0001c0001t0002g0005 a0001c0001t0002g0024 |
3 | NA18945.hp1 NA18953.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1765+1411A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55572208 | |||||||
chr2:55572220 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1765+1399T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55572220 | |||||||
chr2:55572221 | TA | T | 92 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(89): Show |
101 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.1765+1397delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55572221 | |||||||
chr2:55572321 | T | C | 1 | a0001c0001t0003g0298 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1765+1298A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55572321 | |||||||
chr2:55572332 | A | C | 1 | a0001c0001t0002g0043 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1765+1287T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55572332 | |||||||
chr2:55572464 | C | T | 1 | a0001c0001t0003g0289 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1765+1155G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55572464 | |||||||
chr2:55572470 | T | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0152 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1765+1149A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55572470 | |||||||
chr2:55572664 | A | G | 104 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(101): Show |
115 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.1765+955T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55572664 | |||||||
chr2:55572700 | T | C | 1 | a0001c0001t0003g0332 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1765+919A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55572700 | |||||||
chr2:55572780 | G | A | 15 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0148 others(12): Show |
15 | HG01168.hp2 HG01169.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1765+839C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55572780 | |||||||
chr2:55572855 | C | G | 93 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(90): Show |
102 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.1765+764G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55572855 | |||||||
chr2:55572955 | T | C | 5 | a0001c0001t0003g0281 a0001c0001t0003g0282 a0001c0001t0003g0304 others(2): Show |
5 | NA18940.hp1 NA18949.hp2 NA18960.hp2 others(2): Show |
intron_variant | MODIFIER | c.1765+664A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55572955 | |||||||
chr2:55573071 | C | T | 1 | a0001c0001t0015g0146 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1765+548G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55573071 | |||||||
chr2:55573129 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1765+490T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55573129 | |||||||
chr2:55573320 | C | G | 2 | a0001c0001t0008g0353 a0001c0001t0008g0354 |
2 | HG03704.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1765+299G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55573320 | |||||||
chr2:55573528 | A | T | 1 | a0001c0001t0008g0352 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1765+91T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55573528 | |||||||
chr2:55573565 | A | G | 14 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(11): Show |
14 | HG01928.hp2 HG01934.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.1765+54T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55573565 | |||||||
chr2:55573819 | A | C | 2 | a0001c0001t0002g0126 a0001c0001t0002g0130 |
2 | HG01884.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1607-42T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55573819 | |||||||
chr2:55573854 | A | G | 1 | a0001c0001t0002g0047 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1607-77T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55573854 | |||||||
chr2:55573856 | G | T | 206 | a0001c0001t0001g0054 a0001c0001t0001g0201 a0001c0001t0001g0212 others(203): Show |
230 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.1607-79C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55573856 | |||||||
chr2:55573863 | C | T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | NA18960.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1607-86G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55573863 | |||||||
chr2:55573886 | C | CT | 19 | a0001c0001t0001g0165 a0001c0001t0001g0211 a0001c0001t0001g0259 others(16): Show |
23 | HG00642.hp1 HG01070.hp2 HG01081.hp1 others(20): Show |
intron_variant | MODIFIER | c.1607-110dupA | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55573886 | |||||||
chr2:55573886 | C | CTT | 90 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(87): Show |
99 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(96): Show |
intron_variant | MODIFIER | c.1607-111_1607-110d others(4): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55573886 | |||||||
chr2:55573886 | CTTT | C | 8 | a0001c0003t0002g0263 a0001c0003t0002g0264 a0001c0003t0002g0265 others(5): Show |
8 | HG01346.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1607-112_1607-110d others(5): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55573886 | |||||||
chr2:55573911 | CAAA | C | 3 | a0001c0001t0003g0329 a0001c0001t0003g0330 a0001c0001t0003g0338 |
3 | NA18946.hp2 NA19009.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1607-137_1607-135d others(5): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55573911 | |||||||
chr2:55573922 | T | C | 12 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(9): Show |
14 | HG00423.hp2 HG02027.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.1607-145A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55573922 | |||||||
chr2:55574017 | T | C | 1 | a0001c0001t0023g0135 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1607-240A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55574017 | |||||||
chr2:55574045 | T | C | 1 | a0001c0002t0002g0117 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1607-268A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55574045 | |||||||
chr2:55574180 | C | T | 1 | a0001c0001t0003g0309 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1607-403G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55574180 | |||||||
chr2:55574520 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1607-743C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55574520 | |||||||
chr2:55574655 | G | A | 92 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(89): Show |
101 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.1607-878C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55574655 | |||||||
chr2:55574657 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1607-880C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55574657 | |||||||
chr2:55574664 | G | GCT | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(8): Show |
11 | HG00099.hp1 HG01106.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.1607-889_1607-888d others(4): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55574664 | |||||||
chr2:55574676 | C | T | 92 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(89): Show |
101 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.1607-899G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55574676 | |||||||
chr2:55574830 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1607-1053C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55574830 | |||||||
chr2:55574873 | C | T | 5 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0153 others(2): Show |
5 | NA18612.hp2 NA18946.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.1607-1096G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55574873 | |||||||
chr2:55574914 | A | G | 1 | a0001c0001t0001g0234 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1607-1137T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55574914 | |||||||
chr2:55574935 | CT | C | 114 | a0001c0001t0001g0156 a0001c0001t0001g0201 a0001c0001t0001g0212 others(111): Show |
129 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.1607-1159delA | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55574935 | |||||||
chr2:55574935 | CTT | C | 86 | a0001c0001t0001g0054 a0001c0001t0002g0003 a0001c0001t0002g0005 others(83): Show |
95 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1607-1160_1607-115 others(6): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55574935 | |||||||
chr2:55574961 | G | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0172 |
2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1607-1184C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55574961 | |||||||
chr2:55575082 | C | T | 102 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(99): Show |
113 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1607-1305G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55575082 | |||||||
chr2:55575119 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1607-1342A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55575119 | |||||||
chr2:55575305 | A | AT | 45 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(42): Show |
46 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.1607-1529dupA | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55575305 | |||||||
chr2:55575330 | T | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1607-1553A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55575330 | |||||||
chr2:55575411 | T | C | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1607-1634A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55575411 | |||||||
chr2:55575832 | G | C | 3 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0033 |
3 | NA18988.hp1 NA18998.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1606+1483C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55575832 | |||||||
chr2:55575834 | G | C | 45 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(42): Show |
46 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.1606+1481C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55575834 | |||||||
chr2:55576010 | A | C | 103 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(100): Show |
114 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.1606+1305T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55576010 | |||||||
chr2:55576025 | C | CAA | 9 | a0001c0001t0003g0341 a0001c0001t0003g0342 a0001c0001t0003g0343 others(6): Show |
9 | HG02257.hp2 HG02559.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.1606+1288_1606+128 others(6): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55576025 | |||||||
chr2:55576031 | T | A | 92 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(89): Show |
101 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.1606+1284A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55576031 | |||||||
chr2:55576083 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1606+1232T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55576083 | |||||||
chr2:55576126 | C | T | 4 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1606+1189G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55576126 | |||||||
chr2:55576284 | G | A | 1 | a0001c0001t0020g0049 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1606+1031C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55576284 | |||||||
chr2:55576300 | A | G | 1 | a0001c0001t0004g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1606+1015T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55576300 | |||||||
chr2:55576355 | C | CAAA | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1606+959_1606+960i others(5): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55576355 | |||||||
chr2:55576356 | G | A | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1606+959C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55576356 | |||||||
chr2:55576446 | A | C | 102 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(99): Show |
113 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1606+869T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55576446 | |||||||
chr2:55576452 | AC | A | 102 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(99): Show |
113 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1606+862delG | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55576452 | |||||||
chr2:55576465 | G | A | 1 | a0001c0001t0002g0116 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1606+850C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55576465 | |||||||
chr2:55576470 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1606+845G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55576470 | |||||||
chr2:55576473 | T | G | 1 | a0001c0001t0001g0180 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1606+842A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55576473 | |||||||
chr2:55576531 | A | T | 1 | a0001c0001t0003g0326 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1606+784T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55576531 | |||||||
chr2:55576539 | G | A | 5 | a0001c0001t0001g0208 a0001c0001t0001g0210 a0001c0001t0001g0218 others(2): Show |
5 | HG00423.hp1 NA18994.hp2 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.1606+776C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55576539 | |||||||
chr2:55576680 | C | T | 1 | a0001c0001t0003g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1606+635G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55576680 | |||||||
chr2:55577145 | G | A | 102 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(99): Show |
113 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1606+170C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55577145 | |||||||
chr2:55577357 | C | G | 1 | a0001c0001t0003g0348 | 1 | HG02559.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1565-1G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 10/16 | chr2 | 55577357 | |||||||
chr2:55577414 | C | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0230 |
2 | NA19000.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1565-58G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 10/16 | chr2 | 55577414 | |||||||
chr2:55577465 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1565-109G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 10/16 | chr2 | 55577465 | |||||||
chr2:55577522 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1565-166T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 10/16 | chr2 | 55577522 | |||||||
chr2:55577742 | A | G | 1 | a0001c0001t0010g0321 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1565-386T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 10/16 | chr2 | 55577742 | |||||||
chr2:55577941 | T | C | 1 | a0003c0006t0004g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1564+306A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 10/16 | chr2 | 55577941 | |||||||
chr2:55578036 | A | C | 93 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(90): Show |
102 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.1564+211T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 10/16 | chr2 | 55578036 | |||||||
chr2:55578448 | A | G | 1 | a0001c0001t0003g0283 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1469-106T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 9/16 | chr2 | 55578448 | |||||||
chr2:55578545 | T | C | 1 | a0001c0001t0021g0046 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1469-203A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 9/16 | chr2 | 55578545 | |||||||
chr2:55578873 | C | A | 4 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1469-531G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 9/16 | chr2 | 55578873 | |||||||
chr2:55579017 | T | C | 1 | a0001c0001t0012g0340 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1468+662A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 9/16 | chr2 | 55579017 | |||||||
chr2:55579018 | T | C | 1 | a0001c0001t0003g0312 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1468+661A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 9/16 | chr2 | 55579018 | |||||||
chr2:55579148 | T | G | 102 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(99): Show |
113 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1468+531A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 9/16 | chr2 | 55579148 | |||||||
chr2:55579172 | G | C | 8 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(5): Show |
8 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1468+507C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 9/16 | chr2 | 55579172 | |||||||
chr2:55579177 | C | T | 94 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(91): Show |
103 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.1468+502G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 9/16 | chr2 | 55579177 | |||||||
chr2:55579219 | G | T | 265 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0086 others(262): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.1468+460C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 9/16 | chr2 | 55579219 | |||||||
chr2:55579324 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1468+355G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 9/16 | chr2 | 55579324 | |||||||
chr2:55579326 | C | T | 102 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(99): Show |
113 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1468+353G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 9/16 | chr2 | 55579326 | |||||||
chr2:55579355 | A | G | 1 | a0001c0003t0025g0268 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1468+324T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 9/16 | chr2 | 55579355 | |||||||
chr2:55579367 | A | G | 94 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(91): Show |
103 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.1468+312T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 9/16 | chr2 | 55579367 | |||||||
chr2:55579508 | A | AC | 94 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(91): Show |
103 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.1468+170dupG | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 9/16 | chr2 | 55579508 | |||||||
chr2:55579571 | G | A | 1 | a0001c0002t0002g0123 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1468+108C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 9/16 | chr2 | 55579571 | |||||||
chr2:55579788 | CAT | C | 102 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(99): Show |
113 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(110): Show |
splice_region_variant&intron_variant | LOW | c.1366-9_1366-8delAT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 8/16 | chr2 | 55579788 | |||||||
chr2:55579790 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1366-9A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 8/16 | chr2 | 55579790 | |||||||
chr2:55579920 | TA | T | 102 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(99): Show |
113 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.1366-140delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 8/16 | chr2 | 55579920 | |||||||
chr2:55579963 | A | T | 2 | a0001c0001t0002g0005 a0001c0001t0002g0024 |
3 | NA18945.hp1 NA18953.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1366-182T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 8/16 | chr2 | 55579963 | |||||||
chr2:55580038 | G | A | 207 | a0001c0001t0001g0054 a0001c0001t0001g0201 a0001c0001t0001g0212 others(204): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.1366-257C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 8/16 | chr2 | 55580038 | |||||||
chr2:55580152 | C | T | 207 | a0001c0001t0001g0054 a0001c0001t0001g0201 a0001c0001t0001g0212 others(204): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.1366-371G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 8/16 | chr2 | 55580152 | |||||||
chr2:55580277 | TAAAACAG others(4): Show |
T | 8 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(5): Show |
8 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1366-507_1366-497d others(13): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 8/16 | chr2 | 55580277 | |||||||
chr2:55580319 | A | T | 207 | a0001c0001t0001g0054 a0001c0001t0001g0201 a0001c0001t0001g0212 others(204): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.1366-538T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 8/16 | chr2 | 55580319 | |||||||
chr2:55580374 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1366-593A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 8/16 | chr2 | 55580374 | |||||||
chr2:55580491 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1366-710T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 8/16 | chr2 | 55580491 | |||||||
chr2:55580749 | T | C | 1 | a0001c0001t0001g0218 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1365+818A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 8/16 | chr2 | 55580749 | |||||||
chr2:55580790 | C | G | 1 | a0001c0001t0004g0139 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1365+777G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 8/16 | chr2 | 55580790 | |||||||
chr2:55581070 | T | G | 1 | a0001c0001t0003g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1365+497A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 8/16 | chr2 | 55581070 | |||||||
chr2:55581096 | T | C | 1 | a0001c0001t0001g0194 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1365+471A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 8/16 | chr2 | 55581096 | |||||||
chr2:55581442 | G | C | 13 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(10): Show |
13 | HG00099.hp1 HG01106.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.1365+125C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 8/16 | chr2 | 55581442 | |||||||
chr2:55581819 | T | TAAGCTAT others(15): Show |
1 | a0001c0001t0001g0189 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1234-122_1234-121i others(24): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55581819 | |||||||
chr2:55581833 | C | T | 278 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0086 others(275): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.1234-135G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55581833 | |||||||
chr2:55581873 | A | C | 1 | a0001c0001t0004g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1234-175T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55581873 | |||||||
chr2:55581879 | G | A | 44 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(41): Show |
45 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(42): Show |
intron_variant | MODIFIER | c.1234-181C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55581879 | |||||||
chr2:55581911 | AAAG | A | 16 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(13): Show |
17 | HG01192.hp1 HG01243.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1234-216_1234-214d others(5): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55581911 | |||||||
chr2:55581918 | A | G | 93 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(90): Show |
102 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.1234-220T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55581918 | |||||||
chr2:55581932 | A | G | 3 | a0001c0001t0003g0281 a0001c0001t0003g0304 a0001c0001t0003g0323 |
3 | NA18960.hp2 NA18966.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1234-234T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55581932 | |||||||
chr2:55582088 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1234-390G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55582088 | |||||||
chr2:55582408 | C | T | 1 | a0001c0001t0004g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1234-710G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55582408 | |||||||
chr2:55582469 | A | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1234-771T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55582469 | |||||||
chr2:55582498 | C | A | 1 | a0001c0001t0001g0153 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1234-800G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55582498 | |||||||
chr2:55582612 | T | C | 4 | a0001c0001t0003g0015 a0001c0001t0003g0274 a0001c0001t0003g0275 others(1): Show |
5 | HG02572.hp2 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1234-914A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55582612 | |||||||
chr2:55582793 | C | A | 1 | a0001c0001t0013g0023 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1234-1095G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55582793 | |||||||
chr2:55582807 | A | C | 9 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(6): Show |
9 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1234-1109T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55582807 | |||||||
chr2:55582853 | A | G | 9 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(6): Show |
9 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1234-1155T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55582853 | |||||||
chr2:55582909 | A | G | 10 | a0001c0001t0004g0012 a0001c0001t0004g0137 a0001c0001t0004g0138 others(7): Show |
14 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.1234-1211T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55582909 | |||||||
chr2:55583286 | T | C | 117 | a0001c0001t0001g0054 a0001c0001t0001g0118 a0001c0001t0001g0121 others(114): Show |
130 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1234-1588A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55583286 | |||||||
chr2:55583302 | T | G | 117 | a0001c0001t0001g0054 a0001c0001t0001g0118 a0001c0001t0001g0121 others(114): Show |
130 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1234-1604A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55583302 | |||||||
chr2:55583331 | A | G | 2 | a0001c0001t0002g0027 a0001c0001t0002g0028 |
2 | NA18988.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1234-1633T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55583331 | |||||||
chr2:55583370 | A | G | 9 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(6): Show |
9 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1234-1672T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55583370 | |||||||
chr2:55583426 | C | G | 1 | a0001c0007t0002g0270 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1233+1625G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55583426 | |||||||
chr2:55583534 | G | C | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1233+1517C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55583534 | |||||||
chr2:55583542 | T | C | 1 | a0001c0001t0018g0231 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1233+1509A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55583542 | |||||||
chr2:55583972 | G | A | 10 | a0001c0001t0004g0012 a0001c0001t0004g0137 a0001c0001t0004g0138 others(7): Show |
14 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.1233+1079C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55583972 | |||||||
chr2:55584074 | G | A | 4 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1233+977C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55584074 | |||||||
chr2:55584089 | T | C | 2 | a0001c0001t0002g0055 a0001c0001t0002g0083 |
2 | NA18992.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1233+962A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55584089 | |||||||
chr2:55584168 | G | A | 1 | a0001c0001t0022g0037 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1233+883C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55584168 | |||||||
chr2:55584536 | C | T | 93 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(90): Show |
103 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.1233+515G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55584536 | |||||||
chr2:55584544 | T | C | 8 | a0001c0003t0002g0263 a0001c0003t0002g0264 a0001c0003t0002g0265 others(5): Show |
8 | HG01346.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1233+507A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55584544 | |||||||
chr2:55584578 | T | C | 2 | a0001c0001t0001g0210 a0001c0001t0001g0221 |
2 | HG00423.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.1233+473A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55584578 | |||||||
chr2:55584750 | C | T | 4 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0219 others(1): Show |
4 | NA18945.hp2 NA18957.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1233+301G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55584750 | |||||||
chr2:55584925 | A | G | 186 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0086 others(183): Show |
204 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.1233+126T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55584925 | |||||||
chr2:55584937 | T | G | 93 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 others(90): Show |
102 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(99): Show |
intron_variant | MODIFIER | c.1233+114A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55584937 | |||||||
chr2:55584955 | A | G | 3 | a0001c0001t0001g0201 a0001c0001t0001g0212 a0001c0001t0001g0222 |
3 | HG02083.hp1 NA18950.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1233+96T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55584955 | |||||||
chr2:55585591 | T | C | 28 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(25): Show |
31 | HG00423.hp2 HG01192.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1117-424A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 6/16 | chr2 | 55585591 | |||||||
chr2:55585642 | T | C | 1 | a0001c0001t0014g0193 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1117-475A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 6/16 | chr2 | 55585642 | |||||||
chr2:55585668 | T | A | 1 | a0001c0001t0002g0216 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1117-501A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 6/16 | chr2 | 55585668 | |||||||
chr2:55585874 | A | G | 1 | a0001c0001t0003g0319 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1117-707T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 6/16 | chr2 | 55585874 | |||||||
chr2:55585885 | C | G | 8 | a0001c0003t0002g0263 a0001c0003t0002g0264 a0001c0003t0002g0265 others(5): Show |
8 | HG01346.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1117-718G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 6/16 | chr2 | 55585885 | |||||||
chr2:55585920 | C | T | 25 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(22): Show |
26 | HG01167.hp2 HG01243.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.1116+698G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 6/16 | chr2 | 55585920 | |||||||
chr2:55585947 | CATG | C | 43 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(40): Show |
44 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(41): Show |
intron_variant | MODIFIER | c.1116+668_1116+670d others(5): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 6/16 | chr2 | 55585947 | |||||||
chr2:55585992 | A | G | 28 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(25): Show |
31 | HG00423.hp2 HG01192.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1116+626T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 6/16 | chr2 | 55585992 | |||||||
chr2:55586145 | C | A | 1 | a0001c0001t0001g0211 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1116+473G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 6/16 | chr2 | 55586145 | |||||||
chr2:55586197 | A | G | 117 | a0001c0001t0001g0054 a0001c0001t0001g0118 a0001c0001t0001g0121 others(114): Show |
130 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1116+421T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 6/16 | chr2 | 55586197 | |||||||
chr2:55586398 | G | A | 1 | a0001c0001t0002g0032 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1116+220C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 6/16 | chr2 | 55586398 | |||||||
chr2:55586520 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1116+98A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 6/16 | chr2 | 55586520 | |||||||
chr2:55586542 | T | C | 1 | a0001c0001t0002g0040 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1116+76A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 6/16 | chr2 | 55586542 | |||||||
chr2:55586898 | C | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1000-164G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55586898 | |||||||
chr2:55586938 | CA | C | 3 | a0001c0001t0001g0240 a0001c0001t0001g0247 a0001c0001t0003g0281 |
3 | HG03654.hp1 NA18960.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.1000-205delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55586938 | |||||||
chr2:55587041 | G | C | 13 | a0001c0001t0002g0003 a0001c0001t0002g0057 a0001c0001t0002g0058 others(10): Show |
15 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.1000-307C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55587041 | |||||||
chr2:55587295 | G | C | 6 | a0001c0001t0003g0020 a0001c0001t0003g0277 a0001c0001t0003g0313 others(3): Show |
7 | HG00738.hp1 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1000-561C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55587295 | |||||||
chr2:55587304 | C | T | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.1000-570G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55587304 | |||||||
chr2:55587316 | G | A | 4 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.1000-582C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55587316 | |||||||
chr2:55587325 | T | C | 1 | a0001c0001t0002g0127 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1000-591A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55587325 | |||||||
chr2:55587358 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1000-624G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55587358 | |||||||
chr2:55587464 | A | C | 1 | a0001c0001t0001g0219 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1000-730T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55587464 | |||||||
chr2:55587725 | C | T | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1000-991G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55587725 | |||||||
chr2:55588018 | C | T | 215 | a0001c0001t0001g0054 a0001c0001t0001g0118 a0001c0001t0001g0121 others(212): Show |
241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.999+861G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55588018 | |||||||
chr2:55588067 | T | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0157 |
2 | HG02622.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.999+812A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55588067 | |||||||
chr2:55588369 | C | T | 8 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(5): Show |
8 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.999+510G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55588369 | |||||||
chr2:55588440 | G | A | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.999+439C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55588440 | |||||||
chr2:55588461 | C | T | 90 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(87): Show |
100 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.999+418G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55588461 | |||||||
chr2:55588468 | G | A | 1 | a0001c0001t0002g0116 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.999+411C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55588468 | |||||||
chr2:55588501 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.999+378C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55588501 | |||||||
chr2:55588515 | G | GA | 68 | a0001c0001t0001g0054 a0001c0001t0001g0190 a0001c0001t0002g0002 others(65): Show |
78 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.999+363dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55588515 | |||||||
chr2:55588756 | C | T | 44 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(41): Show |
45 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(42): Show |
intron_variant | MODIFIER | c.999+123G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55588756 | |||||||
chr2:55588766 | ATC | A | 12 | a0001c0001t0001g0191 a0001c0001t0001g0195 a0001c0001t0001g0197 others(9): Show |
12 | HG01928.hp2 HG01934.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.999+111_999+112del others(2): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55588766 | |||||||
chr2:55588799 | CAA | C | 2 | a0001c0001t0003g0019 a0001c0001t0003g0305 |
3 | NA18947.hp2 NA18983.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.999+78_999+79delTT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55588799 | |||||||
chr2:55588844 | A | C | 2 | a0001c0001t0003g0346 a0001c0001t0026g0347 |
2 | HG03130.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.999+35T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55588844 | |||||||
chr2:55588861 | T | C | 57 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(54): Show |
62 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(59): Show |
intron_variant | MODIFIER | c.999+18A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 5/16 | chr2 | 55588861 | |||||||
chr2:55589029 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.922-73T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55589029 | |||||||
chr2:55589162 | TTAAC | T | 71 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(68): Show |
81 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.922-210_922-207del others(4): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55589162 | |||||||
chr2:55589205 | A | C | 91 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(88): Show |
101 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.922-249T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55589205 | |||||||
chr2:55589257 | GCC | G | 6 | a0001c0001t0001g0185 a0001c0001t0001g0224 a0001c0001t0001g0227 others(3): Show |
6 | HG02080.hp1 NA18947.hp1 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.922-303_922-302del others(2): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55589257 | |||||||
chr2:55589347 | C | CAAG | 260 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0118 others(257): Show |
287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.922-394_922-392dup others(3): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55589347 | |||||||
chr2:55589558 | G | A | 90 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(87): Show |
100 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.922-602C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55589558 | |||||||
chr2:55589670 | C | T | 4 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.922-714G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55589670 | |||||||
chr2:55589711 | C | T | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.922-755G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55589711 | |||||||
chr2:55589832 | C | T | 2 | a0001c0001t0003g0286 a0001c0001t0012g0340 |
2 | HG03669.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.922-876G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55589832 | |||||||
chr2:55589853 | T | C | 1 | a0001c0001t0003g0335 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.922-897A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55589853 | |||||||
chr2:55589915 | CA | C | 47 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(44): Show |
48 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(45): Show |
intron_variant | MODIFIER | c.922-960delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55589915 | |||||||
chr2:55589927 | AAATTATA others(20): Show |
A | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.922-998_922-972del others(27): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55589927 | |||||||
chr2:55589970 | T | C | 115 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(112): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.922-1014A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55589970 | |||||||
chr2:55589983 | A | C | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.922-1027T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55589983 | |||||||
chr2:55590029 | T | A | 4 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.922-1073A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55590029 | |||||||
chr2:55590162 | C | T | 275 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0086 others(272): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.922-1206G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55590162 | |||||||
chr2:55590364 | T | A | 12 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(9): Show |
14 | HG00423.hp2 HG02027.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.922-1408A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55590364 | |||||||
chr2:55590711 | G | C | 1 | a0001c0001t0001g0222 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.922-1755C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55590711 | |||||||
chr2:55590881 | C | G | 54 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(51): Show |
61 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.922-1925G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55590881 | |||||||
chr2:55591033 | C | T | 1 | a0001c0002t0002g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.922-2077G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55591033 | |||||||
chr2:55591063 | G | A | 1 | a0001c0001t0001g0217 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.922-2107C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55591063 | |||||||
chr2:55591179 | C | T | 28 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(25): Show |
29 | HG01167.hp2 HG01243.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.922-2223G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55591179 | |||||||
chr2:55591283 | C | T | 113 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(110): Show |
125 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.922-2327G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55591283 | |||||||
chr2:55591302 | A | T | 1 | a0001c0001t0003g0284 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.922-2346T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55591302 | |||||||
chr2:55591328 | T | TG | 29 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(26): Show |
30 | HG01167.hp2 HG01243.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.922-2373dupC | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55591328 | |||||||
chr2:55591376 | C | G | 1 | a0001c0001t0002g0042 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.922-2420G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55591376 | |||||||
chr2:55591752 | T | C | 3 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0035 |
3 | HG03098.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.922-2796A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55591752 | |||||||
chr2:55591890 | T | C | 2 | a0001c0001t0001g0220 a0001c0001t0001g0250 |
2 | HG00621.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.922-2934A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55591890 | |||||||
chr2:55591905 | C | A | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.922-2949G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55591905 | |||||||
chr2:55592530 | T | A | 2 | a0001c0001t0001g0096 a0001c0001t0001g0101 |
2 | HG00099.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.922-3574A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55592530 | |||||||
chr2:55592616 | C | T | 102 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(99): Show |
116 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.922-3660G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55592616 | |||||||
chr2:55592908 | C | A | 1 | a0001c0001t0007g0001 | 4 | HG01257.hp2 HG01258.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.922-3952G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55592908 | |||||||
chr2:55593145 | G | A | 113 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(110): Show |
125 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.922-4189C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55593145 | |||||||
chr2:55593310 | C | T | 1 | a0001c0001t0005g0176 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.922-4354G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55593310 | |||||||
chr2:55593346 | C | T | 276 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0086 others(273): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.922-4390G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55593346 | |||||||
chr2:55593632 | G | A | 4 | a0001c0001t0003g0329 a0001c0001t0003g0330 a0001c0001t0003g0338 others(1): Show |
4 | NA18946.hp2 NA18964.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.922-4676C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55593632 | |||||||
chr2:55593643 | C | T | 1 | a0001c0002t0002g0124 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.922-4687G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55593643 | |||||||
chr2:55593957 | T | C | 1 | a0001c0001t0002g0061 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.921+4459A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55593957 | |||||||
chr2:55593966 | T | C | 2 | a0001c0001t0002g0065 a0001c0001t0002g0068 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.921+4450A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55593966 | |||||||
chr2:55594037 | C | T | 1 | a0001c0001t0002g0122 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.921+4379G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55594037 | |||||||
chr2:55594056 | A | G | 2 | a0001c0001t0001g0218 a0001c0001t0001g0254 |
2 | NA18994.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.921+4360T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55594056 | |||||||
chr2:55594075 | T | G | 1 | a0001c0001t0020g0049 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.921+4341A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55594075 | |||||||
chr2:55594088 | C | T | 13 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(10): Show |
16 | HG00438.hp2 HG03710.hp1 HG04199.hp1 others(13): Show |
intron_variant | MODIFIER | c.921+4328G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55594088 | |||||||
chr2:55594133 | C | A | 58 | a0001c0001t0001g0013 a0001c0001t0001g0086 a0001c0001t0001g0087 others(55): Show |
59 | HG00099.hp1 HG01106.hp2 HG01167.hp2 others(56): Show |
intron_variant | MODIFIER | c.921+4283G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55594133 | |||||||
chr2:55594159 | G | A | 27 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
28 | HG01167.hp2 HG01243.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.921+4257C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55594159 | |||||||
chr2:55594191 | T | G | 1 | a0001c0001t0001g0211 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.921+4225A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55594191 | |||||||
chr2:55594215 | T | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0257 |
2 | HG02080.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.921+4201A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55594215 | |||||||
chr2:55594301 | AT | A | 24 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(21): Show |
28 | HG00099.hp1 HG01070.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.921+4114delA | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55594301 | |||||||
chr2:55594302 | T | TA | 6 | a0001c0001t0001g0186 a0001c0001t0001g0210 a0001c0001t0001g0211 others(3): Show |
6 | HG03654.hp1 NA18955.hp1 NA19006.hp1 others(3): Show |
intron_variant | MODIFIER | c.921+4113dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55594302 | |||||||
chr2:55594302 | TA | T | 185 | a0001c0001t0001g0054 a0001c0001t0001g0118 a0001c0001t0001g0121 others(182): Show |
205 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(202): Show |
intron_variant | MODIFIER | c.921+4113delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55594302 | |||||||
chr2:55594302 | TAA | T | 18 | a0001c0001t0001g0147 a0001c0001t0002g0033 a0001c0001t0002g0052 others(15): Show |
18 | HG01346.hp1 HG01515.hp1 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.921+4112_921+4113d others(4): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55594302 | |||||||
chr2:55594365 | T | A | 45 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(42): Show |
46 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.921+4051A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55594365 | |||||||
chr2:55594377 | AACAG | A | 20 | a0001c0001t0003g0014 a0001c0001t0003g0271 a0001c0001t0003g0272 others(17): Show |
21 | HG02071.hp1 HG02602.hp1 HG03654.hp2 others(18): Show |
intron_variant | MODIFIER | c.921+4035_921+4038d others(6): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55594377 | |||||||
chr2:55594536 | A | G | 13 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(10): Show |
13 | HG00099.hp1 HG01106.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.921+3880T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55594536 | |||||||
chr2:55594710 | A | G | 47 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(44): Show |
48 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(45): Show |
intron_variant | MODIFIER | c.921+3706T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55594710 | |||||||
chr2:55594908 | AAATTAAA others(9): Show |
A | 8 | a0001c0003t0002g0263 a0001c0003t0002g0264 a0001c0003t0002g0265 others(5): Show |
8 | HG01346.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.921+3492_921+3507d others(18): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55594908 | |||||||
chr2:55595026 | C | CT | 30 | a0001c0001t0001g0249 a0001c0001t0001g0259 a0001c0001t0003g0014 others(27): Show |
31 | HG02071.hp1 HG02257.hp2 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.921+3389dupA | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55595026 | |||||||
chr2:55595026 | CT | C | 14 | a0001c0001t0001g0149 a0001c0001t0001g0185 a0001c0001t0001g0200 others(11): Show |
16 | HG01070.hp1 HG01891.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.921+3389delA | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55595026 | |||||||
chr2:55595170 | C | T | 45 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(42): Show |
46 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.921+3246G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55595170 | |||||||
chr2:55595216 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0151 |
2 | HG03041.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.921+3200C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55595216 | |||||||
chr2:55595229 | G | T | 1 | a0001c0001t0001g0217 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.921+3187C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55595229 | |||||||
chr2:55595239 | G | C | 3 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0035 |
3 | HG03098.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.921+3177C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55595239 | |||||||
chr2:55595436 | G | C | 1 | a0001c0001t0012g0331 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.921+2980C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55595436 | |||||||
chr2:55595452 | C | A | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.921+2964G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55595452 | |||||||
chr2:55595615 | A | C | 1 | a0001c0003t0002g0265 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.921+2801T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55595615 | |||||||
chr2:55595657 | C | T | 2 | a0001c0001t0002g0071 a0001c0001t0002g0081 |
2 | HG02896.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.921+2759G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55595657 | |||||||
chr2:55595738 | G | GA | 62 | a0001c0001t0001g0054 a0001c0001t0001g0190 a0001c0001t0001g0212 others(59): Show |
68 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.921+2677dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55595738 | |||||||
chr2:55595738 | GA | G | 116 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(113): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.921+2677delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55595738 | |||||||
chr2:55595775 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.921+2641T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55595775 | |||||||
chr2:55596169 | G | T | 275 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0086 others(272): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.921+2247C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55596169 | |||||||
chr2:55596345 | C | T | 3 | a0001c0001t0003g0314 a0001c0001t0004g0137 a0001c0001t0004g0138 |
3 | HG03491.hp1 HG03492.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.921+2071G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55596345 | |||||||
chr2:55596346 | G | GA | 12 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(9): Show |
12 | HG02074.hp1 HG04115.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.921+2069dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55596346 | |||||||
chr2:55596346 | GA | G | 259 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0086 others(256): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.921+2069delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55596346 | |||||||
chr2:55596355 | A | T | 1 | a0001c0001t0001g0153 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.921+2061T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55596355 | |||||||
chr2:55596435 | C | T | 1 | a0001c0002t0002g0104 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.921+1981G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55596435 | |||||||
chr2:55596594 | A | C | 13 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(10): Show |
13 | HG00099.hp1 HG01106.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.921+1822T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55596594 | |||||||
chr2:55596754 | G | A | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.921+1662C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55596754 | |||||||
chr2:55596799 | C | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0154 a0001c0001t0001g0156 |
3 | NA18612.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.921+1617G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55596799 | |||||||
chr2:55596806 | T | C | 1 | a0001c0001t0004g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.921+1610A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55596806 | |||||||
chr2:55597060 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.921+1356C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597060 | |||||||
chr2:55597100 | T | C | 45 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(42): Show |
46 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.921+1316A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597100 | |||||||
chr2:55597194 | T | C | 1 | a0001c0001t0003g0021 | 2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.921+1222A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597194 | |||||||
chr2:55597257 | C | A | 45 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(42): Show |
46 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.921+1159G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597257 | |||||||
chr2:55597296 | G | A | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.921+1120C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597296 | |||||||
chr2:55597338 | T | C | 1 | a0001c0001t0003g0327 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.921+1078A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597338 | |||||||
chr2:55597360 | C | T | 115 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(112): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.921+1056G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597360 | |||||||
chr2:55597483 | G | A | 9 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(6): Show |
9 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.921+933C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597483 | |||||||
chr2:55597560 | T | C | 2 | a0001c0001t0004g0141 a0001c0001t0004g0142 |
2 | HG01433.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.921+856A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597560 | |||||||
chr2:55597578 | C | T | 9 | a0001c0001t0003g0341 a0001c0001t0003g0342 a0001c0001t0003g0343 others(6): Show |
9 | HG02257.hp2 HG02559.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.921+838G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597578 | |||||||
chr2:55597623 | A | AAAAC | 102 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(99): Show |
112 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.921+789_921+792dup others(4): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597623 | |||||||
chr2:55597623 | A | AAAACAAA others(1): Show |
172 | a0001c0001t0001g0013 a0001c0001t0001g0086 a0001c0001t0001g0087 others(169): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.921+785_921+792dup others(8): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597623 | |||||||
chr2:55597623 | A | AAAACAAA others(5): Show |
1 | a0001c0001t0001g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.921+781_921+792dup others(12): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597623 | |||||||
chr2:55597657 | T | C | 218 | a0001c0001t0001g0054 a0001c0001t0001g0118 a0001c0001t0001g0121 others(215): Show |
244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.921+759A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597657 | |||||||
chr2:55597741 | C | T | 45 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(42): Show |
46 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.921+675G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597741 | |||||||
chr2:55597933 | C | A | 1 | a0001c0001t0002g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.921+483G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597933 | |||||||
chr2:55597936 | G | C | 13 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(10): Show |
13 | HG00099.hp1 HG01106.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.921+480C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597936 | |||||||
chr2:55597943 | C | T | 13 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(10): Show |
16 | HG00438.hp2 HG03710.hp1 HG04199.hp1 others(13): Show |
intron_variant | MODIFIER | c.921+473G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597943 | |||||||
chr2:55597988 | C | T | 12 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0149 others(9): Show |
12 | HG01168.hp2 HG01169.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.921+428G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597988 | |||||||
chr2:55598176 | C | T | 2 | a0001c0001t0003g0286 a0001c0001t0012g0340 |
2 | HG03669.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.921+240G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55598176 | |||||||
chr2:55598177 | G | A | 92 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(89): Show |
102 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.921+239C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55598177 | |||||||
chr2:55598215 | G | C | 1 | a0001c0001t0003g0335 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.921+201C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55598215 | |||||||
chr2:55598216 | A | G | 115 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(112): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.921+200T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55598216 | |||||||
chr2:55598331 | AAT | A | 4 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.921+83_921+84delAT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55598331 | |||||||
chr2:55599166 | G | A | 1 | a0001c0002t0002g0103 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.298-127C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55599166 | |||||||
chr2:55599175 | C | A | 8 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(5): Show |
8 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-136G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55599175 | |||||||
chr2:55599267 | A | G | 276 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0086 others(273): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.298-228T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55599267 | |||||||
chr2:55599308 | T | A | 1 | a0001c0002t0002g0112 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.298-269A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55599308 | |||||||
chr2:55599355 | T | A | 54 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(51): Show |
61 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.298-316A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55599355 | |||||||
chr2:55599458 | A | G | 83 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(80): Show |
93 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.298-419T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55599458 | |||||||
chr2:55599493 | C | T | 1 | a0001c0002t0002g0124 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.298-454G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55599493 | |||||||
chr2:55599555 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.298-516G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55599555 | |||||||
chr2:55599625 | C | G | 115 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(112): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.298-586G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55599625 | |||||||
chr2:55599671 | T | C | 3 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0035 |
3 | HG03098.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.298-632A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55599671 | |||||||
chr2:55599743 | C | G | 27 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(24): Show |
28 | HG01167.hp2 HG01243.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.298-704G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55599743 | |||||||
chr2:55599814 | GAAGAT | G | 54 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(51): Show |
61 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.298-780_298-776del others(5): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55599814 | |||||||
chr2:55599889 | T | G | 72 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(69): Show |
82 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.298-850A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55599889 | |||||||
chr2:55599979 | C | T | 44 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(41): Show |
45 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(42): Show |
intron_variant | MODIFIER | c.298-940G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55599979 | |||||||
chr2:55599989 | G | A | 12 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(9): Show |
14 | HG00423.hp2 HG02027.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.298-950C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55599989 | |||||||
chr2:55600151 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.298-1112C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600151 | |||||||
chr2:55600196 | T | G | 288 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0086 others(285): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.298-1157A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600196 | |||||||
chr2:55600309 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.298-1270G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600309 | |||||||
chr2:55600319 | G | A | 1 | a0001c0001t0003g0308 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.298-1280C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600319 | |||||||
chr2:55600358 | G | A | 1 | a0001c0001t0002g0062 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.298-1319C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600358 | |||||||
chr2:55600361 | G | T | 1 | a0001c0001t0003g0286 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.298-1322C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600361 | |||||||
chr2:55600375 | G | A | 3 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0035 |
3 | HG03098.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.298-1336C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600375 | |||||||
chr2:55600399 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.298-1360G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600399 | |||||||
chr2:55600412 | G | C | 115 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(112): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.298-1373C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600412 | |||||||
chr2:55600414 | G | T | 8 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(5): Show |
8 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-1375C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600414 | |||||||
chr2:55600415 | A | T | 8 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(5): Show |
8 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-1376T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600415 | |||||||
chr2:55600416 | A | C | 8 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(5): Show |
8 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-1377T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600416 | |||||||
chr2:55600426 | C | CA | 43 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0147 others(40): Show |
44 | HG00423.hp1 HG00621.hp2 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.298-1388dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600426 | |||||||
chr2:55600426 | C | CAA | 18 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(15): Show |
18 | HG00099.hp1 HG01167.hp2 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.298-1389_298-1388d others(4): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600426 | |||||||
chr2:55600426 | C | CAAA | 10 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0001g0097 others(7): Show |
10 | HG01106.hp2 HG01175.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.298-1390_298-1388d others(5): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600426 | |||||||
chr2:55600426 | C | CAAAA | 36 | a0001c0001t0001g0092 a0001c0001t0001g0148 a0001c0001t0001g0155 others(33): Show |
44 | HG00099.hp2 HG01070.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.298-1391_298-1388d others(6): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600426 | |||||||
chr2:55600426 | C | CAAAAA | 37 | a0001c0001t0001g0156 a0001c0001t0003g0017 a0001c0001t0003g0018 others(34): Show |
41 | HG00642.hp2 HG00735.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.298-1392_298-1388d others(7): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600426 | |||||||
chr2:55600426 | C | CAAAAAA | 23 | a0001c0001t0003g0277 a0001c0001t0003g0278 a0001c0001t0003g0285 others(20): Show |
23 | HG01074.hp2 HG01106.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.298-1393_298-1388d others(8): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600426 | |||||||
chr2:55600426 | C | CAAAAAAA | 16 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0003g0014 others(13): Show |
18 | HG00140.hp2 HG00639.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.298-1394_298-1388d others(9): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600426 | |||||||
chr2:55600426 | C | CAAAAAAA others(1): Show |
6 | a0001c0001t0003g0302 a0001c0001t0003g0332 a0001c0001t0003g0335 others(3): Show |
6 | HG02615.hp2 HG02683.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.298-1395_298-1388d others(10): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600426 | |||||||
chr2:55600426 | CA | C | 54 | a0001c0001t0001g0187 a0001c0001t0001g0189 a0001c0001t0001g0191 others(51): Show |
60 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.298-1388delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600426 | |||||||
chr2:55600426 | CAA | C | 28 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(25): Show |
31 | HG01243.hp1 HG01884.hp1 HG02155.hp1 others(28): Show |
intron_variant | MODIFIER | c.298-1389_298-1388d others(4): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600426 | |||||||
chr2:55600426 | CAAAAAA | C | 10 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0105 others(7): Show |
10 | HG02027.hp1 HG02129.hp1 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.298-1393_298-1388d others(8): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600426 | |||||||
chr2:55600456 | A | G | 8 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(5): Show |
8 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.298-1417T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600456 | |||||||
chr2:55600491 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0166 |
3 | HG01167.hp2 HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.298-1452A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600491 | |||||||
chr2:55600502 | C | T | 349 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0086 others(346): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.298-1463G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600502 | |||||||
chr2:55600536 | T | C | 3 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0035 |
3 | HG03098.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.298-1497A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600536 | |||||||
chr2:55600557 | G | C | 4 | a0001c0001t0004g0012 a0001c0001t0004g0139 a0001c0001t0004g0143 others(1): Show |
5 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.298-1518C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600557 | |||||||
chr2:55600592 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.298-1553G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600592 | |||||||
chr2:55600692 | C | G | 9 | a0001c0001t0003g0341 a0001c0001t0003g0342 a0001c0001t0003g0343 others(6): Show |
9 | HG02257.hp2 HG02559.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.298-1653G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600692 | |||||||
chr2:55600838 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.298-1799T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600838 | |||||||
chr2:55600941 | G | A | 11 | a0001c0001t0001g0185 a0001c0001t0001g0224 a0001c0001t0001g0225 others(8): Show |
11 | HG02080.hp1 NA18947.hp1 NA18951.hp1 others(8): Show |
intron_variant | MODIFIER | c.298-1902C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600941 | |||||||
chr2:55600976 | G | C | 4 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-1937C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600976 | |||||||
chr2:55601016 | G | A | 1 | a0001c0001t0002g0069 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.298-1977C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601016 | |||||||
chr2:55601068 | C | G | 13 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(10): Show |
13 | HG00099.hp1 HG01106.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.298-2029G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601068 | |||||||
chr2:55601141 | C | CA | 9 | a0001c0001t0001g0236 a0001c0001t0002g0063 a0001c0001t0002g0064 others(6): Show |
9 | HG01358.hp1 HG01978.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.298-2103dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601141 | |||||||
chr2:55601141 | CA | C | 140 | a0001c0001t0001g0013 a0001c0001t0001g0086 a0001c0001t0001g0087 others(137): Show |
145 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.298-2103delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601141 | |||||||
chr2:55601141 | CAA | C | 98 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0148 others(95): Show |
107 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.298-2104_298-2103d others(4): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601141 | |||||||
chr2:55601141 | CAAA | C | 24 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(21): Show |
27 | HG00423.hp2 HG01192.hp1 HG02129.hp1 others(24): Show |
intron_variant | MODIFIER | c.298-2105_298-2103d others(5): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601141 | |||||||
chr2:55601244 | A | G | 4 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.298-2205T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601244 | |||||||
chr2:55601295 | A | C | 2 | a0001c0001t0003g0343 a0001c0001t0003g0344 |
2 | HG02257.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.298-2256T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601295 | |||||||
chr2:55601446 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.298-2407A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601446 | |||||||
chr2:55601504 | C | A | 1 | a0001c0001t0001g0158 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.298-2465G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601504 | |||||||
chr2:55601506 | A | G | 1 | a0001c0001t0002g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.298-2467T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601506 | |||||||
chr2:55601508 | G | C | 1 | a0001c0001t0003g0294 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.298-2469C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601508 | |||||||
chr2:55601531 | C | G | 1 | a0001c0002t0002g0103 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.297+2447G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601531 | |||||||
chr2:55601570 | C | T | 90 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(87): Show |
100 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.297+2408G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601570 | |||||||
chr2:55601571 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.297+2407C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601571 | |||||||
chr2:55601582 | G | T | 115 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(112): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.297+2396C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601582 | |||||||
chr2:55601722 | C | T | 3 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0035 |
3 | HG03098.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.297+2256G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601722 | |||||||
chr2:55601787 | T | C | 1 | a0001c0001t0003g0295 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.297+2191A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601787 | |||||||
chr2:55601838 | T | C | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.297+2140A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601838 | |||||||
chr2:55601918 | G | A | 82 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(79): Show |
92 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.297+2060C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601918 | |||||||
chr2:55601995 | C | A | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.297+1983G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55601995 | |||||||
chr2:55602003 | G | GA | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.297+1974dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55602003 | |||||||
chr2:55602030 | G | T | 3 | a0001c0001t0009g0025 a0001c0001t0009g0026 a0001c0001t0009g0035 |
3 | HG03098.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.297+1948C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55602030 | |||||||
chr2:55602188 | A | G | 1 | a0001c0001t0004g0139 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.297+1790T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55602188 | |||||||
chr2:55602256 | G | C | 115 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(112): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.297+1722C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55602256 | |||||||
chr2:55602449 | G | A | 71 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(68): Show |
81 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.297+1529C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55602449 | |||||||
chr2:55602582 | T | C | 9 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(6): Show |
9 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.297+1396A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55602582 | |||||||
chr2:55602831 | A | G | 115 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(112): Show |
127 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.297+1147T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55602831 | |||||||
chr2:55602855 | T | C | 1 | a0001c0001t0012g0331 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.297+1123A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55602855 | |||||||
chr2:55602959 | TC | T | 3 | a0001c0001t0002g0044 a0001c0001t0003g0284 a0001c0001t0004g0137 |
3 | HG02735.hp1 HG03491.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.297+1018delG | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55602959 | |||||||
chr2:55602960 | C | T | 213 | a0001c0001t0001g0054 a0001c0001t0001g0118 a0001c0001t0001g0121 others(210): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.297+1018G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55602960 | |||||||
chr2:55603021 | C | T | 2 | a0001c0001t0003g0297 a0001c0001t0003g0298 |
2 | HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.297+957G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55603021 | |||||||
chr2:55603022 | T | C | 13 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0007 others(10): Show |
16 | HG00438.hp2 HG03710.hp1 HG04199.hp1 others(13): Show |
intron_variant | MODIFIER | c.297+956A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55603022 | |||||||
chr2:55603236 | A | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.297+742T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55603236 | |||||||
chr2:55603246 | T | C | 1 | a0001c0001t0003g0283 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.297+732A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55603246 | |||||||
chr2:55603254 | G | C | 1 | a0001c0001t0003g0279 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.297+724C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55603254 | |||||||
chr2:55603268 | T | A | 8 | a0001c0003t0002g0263 a0001c0003t0002g0264 a0001c0003t0002g0265 others(5): Show |
8 | HG01346.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.297+710A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55603268 | |||||||
chr2:55603512 | T | G | 1 | a0001c0001t0002g0052 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.297+466A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55603512 | |||||||
chr2:55603559 | T | C | 2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | NA18960.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.297+419A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55603559 | |||||||
chr2:55603560 | C | G | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.297+418G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55603560 | |||||||
chr2:55603827 | T | C | 1 | a0001c0002t0002g0103 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.297+151A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55603827 | |||||||
chr2:55603859 | T | C | 1 | a0001c0001t0003g0274 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.297+119A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55603859 | |||||||
chr2:55604279 | T | C | 276 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0086 others(273): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.199-203A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55604279 | |||||||
chr2:55604309 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.199-233T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55604309 | |||||||
chr2:55604533 | A | T | 275 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0086 others(272): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.199-457T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55604533 | |||||||
chr2:55604575 | C | G | 1 | a0001c0001t0002g0083 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.199-499G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55604575 | |||||||
chr2:55604795 | G | GAC | 45 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(42): Show |
46 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.199-721_199-720dup others(2): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55604795 | |||||||
chr2:55604795 | G | GACAC | 22 | a0001c0001t0002g0125 a0001c0001t0002g0127 a0001c0001t0002g0128 others(19): Show |
22 | HG01243.hp1 HG01346.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.199-723_199-720dup others(4): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55604795 | |||||||
chr2:55604795 | G | GACACAC | 70 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(67): Show |
80 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.199-725_199-720dup others(6): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55604795 | |||||||
chr2:55604817 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.199-741A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55604817 | |||||||
chr2:55604881 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.199-805G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55604881 | |||||||
chr2:55604965 | A | C | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.199-889T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55604965 | |||||||
chr2:55604968 | T | C | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.199-892A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55604968 | |||||||
chr2:55605206 | A | C | 1 | a0001c0001t0001g0163 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.199-1130T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55605206 | |||||||
chr2:55605466 | G | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.199-1390C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55605466 | |||||||
chr2:55605467 | C | T | 1 | a0001c0001t0003g0305 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.199-1391G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55605467 | |||||||
chr2:55605546 | T | C | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.199-1470A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55605546 | |||||||
chr2:55605741 | A | G | 44 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(41): Show |
45 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(42): Show |
intron_variant | MODIFIER | c.199-1665T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55605741 | |||||||
chr2:55605767 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.199-1691C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55605767 | |||||||
chr2:55605892 | G | A | 4 | a0001c0002t0002g0098 a0001c0002t0002g0099 a0001c0002t0002g0100 others(1): Show |
4 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-1816C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55605892 | |||||||
chr2:55605904 | C | CA | 14 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(11): Show |
14 | HG00735.hp2 HG01358.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.199-1829dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55605904 | |||||||
chr2:55605904 | CA | C | 141 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0133 others(138): Show |
156 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.199-1829delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55605904 | |||||||
chr2:55605975 | T | A | 4 | a0001c0001t0003g0015 a0001c0001t0003g0274 a0001c0001t0003g0275 others(1): Show |
5 | HG02572.hp2 HG02809.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-1899A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55605975 | |||||||
chr2:55606456 | AAGTGG | A | 5 | a0001c0001t0003g0320 a0001c0001t0003g0335 a0001c0001t0003g0336 others(2): Show |
5 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-2385_199-2381d others(7): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55606456 | |||||||
chr2:55606462 | A | C | 5 | a0001c0001t0003g0320 a0001c0001t0003g0335 a0001c0001t0003g0336 others(2): Show |
5 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-2386T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55606462 | |||||||
chr2:55606525 | A | T | 1 | a0001c0001t0001g0192 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.199-2449T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55606525 | |||||||
chr2:55606597 | G | A | 10 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(7): Show |
10 | HG01884.hp1 HG01952.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.199-2521C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55606597 | |||||||
chr2:55606735 | A | G | 1 | a0001c0001t0003g0309 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.199-2659T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55606735 | |||||||
chr2:55606775 | T | C | 13 | a0001c0001t0002g0071 a0001c0001t0002g0081 a0001c0001t0004g0012 others(10): Show |
17 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.199-2699A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55606775 | |||||||
chr2:55606822 | C | CA | 12 | a0001c0001t0002g0113 a0001c0001t0003g0281 a0001c0001t0003g0282 others(9): Show |
12 | HG01261.hp1 HG01515.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.199-2747dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55606822 | |||||||
chr2:55606822 | CA | C | 22 | a0001c0001t0001g0189 a0001c0001t0001g0241 a0001c0001t0001g0259 others(19): Show |
26 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.199-2747delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55606822 | |||||||
chr2:55606822 | CAA | C | 218 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0086 others(215): Show |
229 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.199-2748_199-2747d others(4): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55606822 | |||||||
chr2:55607287 | C | T | 1 | a0001c0001t0002g0043 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.199-3211G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55607287 | |||||||
chr2:55607288 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.199-3212C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55607288 | |||||||
chr2:55607368 | G | A | 4 | a0001c0001t0003g0329 a0001c0001t0003g0330 a0001c0001t0003g0338 others(1): Show |
4 | NA18946.hp2 NA18964.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-3292C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55607368 | |||||||
chr2:55607461 | A | G | 17 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0148 others(14): Show |
17 | HG01168.hp2 HG01169.hp2 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.199-3385T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55607461 | |||||||
chr2:55607591 | T | A | 43 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(40): Show |
44 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(41): Show |
intron_variant | MODIFIER | c.199-3515A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55607591 | |||||||
chr2:55607744 | T | A | 2 | a0001c0002t0002g0114 a0001c0002t0002g0115 |
2 | HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.199-3668A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55607744 | |||||||
chr2:55607934 | T | C | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.199-3858A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55607934 | |||||||
chr2:55608041 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.199-3965A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55608041 | |||||||
chr2:55608493 | T | A | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.199-4417A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55608493 | |||||||
chr2:55608514 | A | G | 9 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(6): Show |
9 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.199-4438T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55608514 | |||||||
chr2:55608638 | G | A | 7 | a0001c0003t0002g0263 a0001c0003t0002g0264 a0001c0003t0002g0265 others(4): Show |
7 | HG01346.hp1 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-4562C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55608638 | |||||||
chr2:55608712 | T | C | 2 | a0001c0001t0005g0177 a0001c0001t0005g0181 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.199-4636A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55608712 | |||||||
chr2:55608920 | G | T | 54 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(51): Show |
61 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.199-4844C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55608920 | |||||||
chr2:55608933 | T | A | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(8): Show |
11 | HG00099.hp1 HG01106.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.199-4857A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55608933 | |||||||
chr2:55609001 | T | C | 1 | a0001c0001t0003g0021 | 2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.199-4925A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55609001 | |||||||
chr2:55609029 | A | C | 92 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(89): Show |
101 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.199-4953T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55609029 | |||||||
chr2:55609061 | T | G | 5 | a0001c0001t0003g0300 a0001c0001t0003g0301 a0001c0001t0003g0302 others(2): Show |
5 | NA18952.hp1 NA18979.hp2 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-4985A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55609061 | |||||||
chr2:55609080 | C | A | 3 | a0001c0001t0003g0333 a0001c0001t0003g0350 a0001c0001t0003g0351 |
3 | HG01070.hp1 HG01071.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.199-5004G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55609080 | |||||||
chr2:55609187 | A | T | 1 | a0001c0001t0001g0248 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.199-5111T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55609187 | |||||||
chr2:55609230 | C | T | 215 | a0001c0001t0001g0054 a0001c0001t0001g0118 a0001c0001t0001g0121 others(212): Show |
241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.199-5154G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55609230 | |||||||
chr2:55609265 | C | T | 1 | a0001c0001t0003g0283 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.199-5189G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55609265 | |||||||
chr2:55609280 | C | A | 3 | a0001c0003t0002g0263 a0001c0003t0002g0267 a0001c0003t0025g0268 |
3 | HG02572.hp1 HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.199-5204G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55609280 | |||||||
chr2:55609308 | C | T | 2 | a0001c0001t0004g0137 a0001c0001t0004g0138 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.199-5232G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55609308 | |||||||
chr2:55609361 | A | C | 1 | a0001c0001t0002g0126 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.199-5285T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55609361 | |||||||
chr2:55609667 | CA | C | 178 | a0001c0001t0001g0054 a0001c0001t0001g0118 a0001c0001t0001g0121 others(175): Show |
191 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.199-5592delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55609667 | |||||||
chr2:55609673 | A | C | 1 | a0001c0001t0001g0163 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.199-5597T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55609673 | |||||||
chr2:55609681 | A | C | 2 | a0001c0001t0001g0261 a0001c0001t0002g0067 |
2 | HG01346.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.199-5605T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55609681 | |||||||
chr2:55609682 | C | A | 3 | a0001c0001t0001g0168 a0001c0001t0001g0261 a0001c0001t0002g0067 |
3 | HG01346.hp2 HG02723.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.199-5606G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55609682 | |||||||
chr2:55609733 | A | C | 8 | a0001c0003t0002g0263 a0001c0003t0002g0264 a0001c0003t0002g0265 others(5): Show |
8 | HG01346.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.199-5657T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55609733 | |||||||
chr2:55609829 | T | A | 8 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(5): Show |
8 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.198+5622A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55609829 | |||||||
chr2:55609868 | A | G | 1 | a0001c0001t0001g0191 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.198+5583T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55609868 | |||||||
chr2:55609998 | T | A | 1 | a0001c0001t0001g0239 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+5453A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55609998 | |||||||
chr2:55610869 | G | GT | 249 | a0001c0001t0001g0013 a0001c0001t0001g0086 a0001c0001t0001g0087 others(246): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.198+4581dupA | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55610869 | |||||||
chr2:55610869 | G | GTT | 12 | a0001c0001t0001g0118 a0001c0001t0002g0027 a0001c0001t0002g0034 others(9): Show |
12 | HG00438.hp2 HG01175.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.198+4580_198+4581d others(4): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55610869 | |||||||
chr2:55610917 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.198+4534C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55610917 | |||||||
chr2:55611099 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.198+4352A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55611099 | |||||||
chr2:55611323 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.198+4128C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55611323 | |||||||
chr2:55611417 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.198+4034C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55611417 | |||||||
chr2:55611525 | G | C | 1 | a0001c0002t0002g0117 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.198+3926C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55611525 | |||||||
chr2:55611532 | G | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02970.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.198+3919C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55611532 | |||||||
chr2:55611634 | A | C | 1 | a0001c0001t0001g0189 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.198+3817T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55611634 | |||||||
chr2:55611648 | C | T | 4 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0245 others(1): Show |
4 | HG02074.hp1 NA18975.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+3803G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55611648 | |||||||
chr2:55611786 | T | C | 5 | a0001c0001t0003g0019 a0001c0001t0003g0305 a0001c0001t0003g0306 others(2): Show |
6 | NA18947.hp2 NA18973.hp2 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+3665A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55611786 | |||||||
chr2:55611820 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+3631G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55611820 | |||||||
chr2:55611850 | C | T | 1 | a0001c0001t0001g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.198+3601G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55611850 | |||||||
chr2:55611961 | C | T | 1 | a0001c0001t0002g0029 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.198+3490G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55611961 | |||||||
chr2:55612038 | A | G | 1 | a0001c0001t0002g0042 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.198+3413T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55612038 | |||||||
chr2:55612568 | A | G | 2 | a0001c0001t0002g0072 a0001c0001t0002g0073 |
2 | NA18989.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.198+2883T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55612568 | |||||||
chr2:55612719 | C | T | 1 | a0001c0001t0003g0280 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.198+2732G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55612719 | |||||||
chr2:55612763 | T | C | 2 | a0001c0001t0001g0169 a0001c0001t0001g0172 |
2 | HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.198+2688A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55612763 | |||||||
chr2:55612807 | G | A | 1 | a0001c0001t0015g0146 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.198+2644C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55612807 | |||||||
chr2:55612815 | G | A | 2 | a0001c0001t0002g0055 a0001c0001t0002g0083 |
2 | NA18992.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.198+2636C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55612815 | |||||||
chr2:55612818 | C | T | 1 | a0001c0001t0004g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.198+2633G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55612818 | |||||||
chr2:55612825 | A | T | 1 | a0001c0001t0003g0278 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.198+2626T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55612825 | |||||||
chr2:55612854 | G | A | 97 | a0001c0001t0001g0013 a0001c0001t0001g0166 a0001c0001t0003g0014 others(94): Show |
107 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(104): Show |
intron_variant | MODIFIER | c.198+2597C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55612854 | |||||||
chr2:55612945 | C | CA | 9 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0032 others(6): Show |
10 | NA18947.hp2 NA18973.hp2 NA18982.hp2 others(7): Show |
intron_variant | MODIFIER | c.198+2505dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55612945 | |||||||
chr2:55612945 | C | CAA | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.198+2504_198+2505d others(4): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55612945 | |||||||
chr2:55612945 | CA | C | 7 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0002g0057 others(4): Show |
7 | HG01074.hp1 HG02818.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+2505delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55612945 | |||||||
chr2:55612959 | A | C | 13 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(10): Show |
13 | HG00099.hp1 HG01106.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.198+2492T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55612959 | |||||||
chr2:55613035 | C | G | 1 | a0001c0001t0002g0042 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.198+2416G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55613035 | |||||||
chr2:55613354 | C | CA | 57 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(54): Show |
57 | HG00099.hp1 HG01106.hp2 HG01168.hp2 others(54): Show |
intron_variant | MODIFIER | c.198+2096dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55613354 | |||||||
chr2:55613381 | A | T | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.198+2070T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55613381 | |||||||
chr2:55613419 | G | C | 16 | a0001c0001t0001g0013 a0001c0001t0001g0166 a0001c0001t0003g0320 others(13): Show |
17 | HG01167.hp2 HG02257.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.198+2032C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55613419 | |||||||
chr2:55613605 | T | C | 1 | a0001c0001t0002g0056 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.198+1846A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55613605 | |||||||
chr2:55613809 | T | TA | 27 | a0001c0001t0001g0093 a0001c0001t0001g0241 a0001c0001t0001g0242 others(24): Show |
30 | HG00738.hp1 HG01074.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.198+1641dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55613809 | |||||||
chr2:55613809 | T | TAA | 23 | a0001c0001t0001g0013 a0001c0001t0001g0166 a0001c0001t0003g0335 others(20): Show |
28 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.198+1640_198+1641d others(4): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55613809 | |||||||
chr2:55613809 | TA | T | 123 | a0001c0001t0001g0054 a0001c0001t0001g0088 a0001c0001t0001g0089 others(120): Show |
132 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.198+1641delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55613809 | |||||||
chr2:55613809 | TAA | T | 13 | a0001c0001t0001g0148 a0001c0001t0002g0033 a0001c0001t0002g0039 others(10): Show |
13 | HG01346.hp1 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.198+1640_198+1641d others(4): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55613809 | |||||||
chr2:55613887 | G | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0166 a0001c0001t0003g0320 others(4): Show |
8 | HG01167.hp2 HG02280.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.198+1564C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55613887 | |||||||
chr2:55613897 | G | A | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(8): Show |
11 | HG00099.hp1 HG01106.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.198+1554C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55613897 | |||||||
chr2:55613971 | T | C | 3 | a0001c0001t0001g0118 a0001c0001t0002g0119 a0001c0001t0002g0120 |
3 | NA18962.hp1 NA18966.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.198+1480A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55613971 | |||||||
chr2:55614006 | C | A | 4 | a0001c0001t0003g0320 a0001c0001t0003g0336 a0001c0001t0003g0337 others(1): Show |
4 | HG02280.hp2 HG02615.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+1445G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55614006 | |||||||
chr2:55614061 | A | T | 1 | a0001c0001t0003g0322 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.198+1390T>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55614061 | |||||||
chr2:55614161 | T | C | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.198+1290A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55614161 | |||||||
chr2:55614230 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.198+1221G>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55614230 | |||||||
chr2:55614439 | T | G | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0090 others(8): Show |
11 | HG00099.hp1 HG01106.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.198+1012A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55614439 | |||||||
chr2:55614504 | T | C | 93 | a0001c0001t0001g0013 a0001c0001t0001g0166 a0001c0001t0003g0014 others(90): Show |
103 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.198+947A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55614504 | |||||||
chr2:55614537 | A | G | 1 | a0001c0001t0003g0278 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.198+914T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55614537 | |||||||
chr2:55614885 | G | A | 275 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0086 others(272): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.198+566C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55614885 | |||||||
chr2:55614900 | A | C | 1 | a0001c0001t0003g0277 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.198+551T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55614900 | |||||||
chr2:55614926 | A | G | 1 | a0001c0001t0002g0038 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.198+525T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55614926 | |||||||
chr2:55614935 | G | A | 1 | a0001c0001t0010g0321 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.198+516C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55614935 | |||||||
chr2:55615108 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.198+343T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55615108 | |||||||
chr2:55615134 | T | C | 1 | a0001c0001t0001g0243 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.198+317A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55615134 | |||||||
chr2:55615195 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.198+256C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55615195 | |||||||
chr2:55615288 | CTTTT | C | 54 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(51): Show |
61 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.198+159_198+162del others(4): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55615288 | |||||||
chr2:55615714 | T | C | 1 | a0001c0001t0002g0069 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.143-208A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615714 | |||||||
chr2:55615857 | C | CA | 45 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(42): Show |
48 | HG00099.hp1 HG01106.hp2 HG01884.hp1 others(45): Show |
intron_variant | MODIFIER | c.143-352dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | |||||||
chr2:55615857 | C | CAA | 66 | a0001c0001t0001g0054 a0001c0001t0001g0101 a0001c0001t0001g0118 others(63): Show |
75 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.143-353_143-352dup others(2): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | |||||||
chr2:55615857 | C | CAAA | 22 | a0001c0001t0001g0121 a0001c0001t0002g0010 a0001c0001t0002g0071 others(19): Show |
23 | HG00621.hp1 HG00642.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.143-354_143-352dup others(3): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | |||||||
chr2:55615857 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG03017.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.143-363_143-352dup others(12): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | |||||||
chr2:55615857 | C | CAAAAAAA others(6): Show |
2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG01891.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.143-364_143-352dup others(13): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | |||||||
chr2:55615857 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0162 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.143-365_143-352dup others(14): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | |||||||
chr2:55615857 | C | CAAAAAAA others(8): Show |
5 | a0001c0001t0001g0133 a0001c0001t0001g0163 a0001c0001t0001g0164 others(2): Show |
5 | HG01167.hp2 HG01243.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.143-366_143-352dup others(15): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | |||||||
chr2:55615857 | C | CAAAAAAA others(9): Show |
5 | a0001c0001t0001g0013 a0001c0001t0001g0134 a0001c0001t0001g0167 others(2): Show |
6 | HG02145.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.143-367_143-352dup others(16): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | |||||||
chr2:55615857 | C | CAAAAAAA others(10): Show |
3 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 |
3 | HG02630.hp1 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.143-368_143-352dup others(17): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | |||||||
chr2:55615857 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0173 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.143-369_143-352dup others(18): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | |||||||
chr2:55615857 | C | CAAAAAAA others(12): Show |
1 | a0001c0001t0005g0174 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.143-370_143-352dup others(19): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | |||||||
chr2:55615857 | C | CAAAAAAA others(15): Show |
3 | a0001c0001t0005g0175 a0001c0001t0005g0176 a0001c0001t0005g0177 |
3 | HG02896.hp1 HG02976.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.143-373_143-352dup others(22): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | |||||||
chr2:55615857 | C | CAAAAAAA others(16): Show |
4 | a0001c0001t0001g0180 a0001c0001t0005g0178 a0001c0001t0005g0179 others(1): Show |
4 | HG01255.hp2 HG02897.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.143-374_143-352dup others(23): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | |||||||
chr2:55615857 | C | CAAAAAAA others(21): Show |
1 | a0001c0001t0005g0182 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.143-352_143-351ins others(28): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | |||||||
chr2:55615857 | C | CAAAAAAA others(23): Show |
1 | a0001c0001t0005g0183 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.143-352_143-351ins others(30): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | |||||||
chr2:55615857 | CA | C | 72 | a0001c0001t0001g0087 a0001c0001t0001g0147 a0001c0001t0001g0148 others(69): Show |
79 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.143-352delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | |||||||
chr2:55615857 | CAA | C | 6 | a0001c0001t0001g0145 a0001c0001t0003g0015 a0001c0001t0003g0274 others(3): Show |
7 | HG01169.hp2 HG01175.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.143-353_143-352del others(2): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | |||||||
chr2:55615857 | CAAAAAAA | C | 11 | a0001c0001t0004g0012 a0001c0001t0004g0136 a0001c0001t0004g0137 others(8): Show |
15 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.143-358_143-352del others(7): Show |
PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | |||||||
chr2:55615905 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.143-399G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615905 | |||||||
chr2:55615916 | A | G | 1 | a0002c0005t0006g0273 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.143-410T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615916 | |||||||
chr2:55616031 | C | T | 1 | a0001c0001t0002g0024 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.143-525G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616031 | |||||||
chr2:55616158 | T | C | 91 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(88): Show |
100 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.143-652A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616158 | |||||||
chr2:55616175 | T | C | 1 | a0001c0001t0012g0340 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.143-669A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616175 | |||||||
chr2:55616249 | G | C | 8 | a0001c0003t0002g0263 a0001c0003t0002g0264 a0001c0003t0002g0265 others(5): Show |
8 | HG01346.hp1 HG02280.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.143-743C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616249 | |||||||
chr2:55616277 | C | T | 91 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(88): Show |
100 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.143-771G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616277 | |||||||
chr2:55616395 | T | C | 1 | a0001c0003t0002g0269 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.142+749A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616395 | |||||||
chr2:55616414 | G | C | 1 | a0001c0001t0016g0262 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.142+730C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616414 | |||||||
chr2:55616473 | A | C | 1 | a0001c0001t0002g0125 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.142+671T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616473 | |||||||
chr2:55616502 | C | T | 275 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0086 others(272): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.142+642G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616502 | |||||||
chr2:55616509 | G | C | 9 | a0001c0001t0003g0341 a0001c0001t0003g0342 a0001c0001t0003g0343 others(6): Show |
9 | HG02257.hp2 HG02559.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.142+635C>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616509 | |||||||
chr2:55616519 | T | C | 24 | a0001c0001t0001g0118 a0001c0001t0001g0121 a0001c0001t0002g0004 others(21): Show |
27 | HG00423.hp2 HG01192.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.142+625A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616519 | |||||||
chr2:55616610 | A | C | 87 | a0001c0001t0001g0054 a0001c0001t0002g0002 a0001c0001t0002g0003 others(84): Show |
97 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.142+534T>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616610 | |||||||
chr2:55616715 | C | A | 8 | a0001c0001t0002g0125 a0001c0001t0002g0126 a0001c0001t0002g0127 others(5): Show |
8 | HG01884.hp1 HG02258.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.142+429G>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616715 | |||||||
chr2:55616717 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG02145.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.142+427G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616717 | |||||||
chr2:55616738 | T | A | 2 | a0001c0001t0003g0350 a0001c0001t0003g0351 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.142+406A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616738 | |||||||
chr2:55616739 | T | A | 144 | a0001c0001t0001g0013 a0001c0001t0001g0133 a0001c0001t0001g0134 others(141): Show |
157 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(154): Show |
intron_variant | MODIFIER | c.142+405A>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616739 | |||||||
chr2:55616739 | T | TA | 3 | a0001c0001t0003g0014 a0001c0001t0003g0271 a0001c0001t0003g0272 |
4 | NA18939.hp1 NA19004.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.142+404dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616739 | |||||||
chr2:55616808 | G | A | 1 | a0001c0007t0002g0270 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.142+336C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616808 | |||||||
chr2:55616969 | C | T | 275 | a0001c0001t0001g0013 a0001c0001t0001g0054 a0001c0001t0001g0086 others(272): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.142+175G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616969 |