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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 849 | 379 | 96 | 64 | 166 | 10 | 42 | 138 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0002 | 0/0 | 849 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0003 | 0/0 | 849 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0004 | 1/0 | 849 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 2550 | 354 | 86 | 61 | 161 | 10 | 35 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
c0002 | 0/0 | 2550 | 17 | 3 | 2 | 5 | 0 | 7 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
c0003 | 0/0 | 2550 | 7 | 6 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
c0004 | 1/0 | 2550 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
c0005 | 0/0 | 2550 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
c0006 | 0/0 | 2550 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
c0007 | 0/0 | 2550 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2957 | 122 | 25 | 15 | 64 | 1 | 15 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0002 | 0/0 | 2957 | 115 | 23 | 17 | 64 | 3 | 8 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0003 | 0/0 | 2957 | 87 | 31 | 16 | 29 | 5 | 6 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0004 | 0/0 | 2957 | 11 | 0 | 5 | 0 | 0 | 6 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0005 | 0/0 | 2957 | 9 | 8 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0006 | 0/0 | 2957 | 5 | 0 | 3 | 0 | 1 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0007 | 0/0 | 2957 | 4 | 0 | 4 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0008 | 0/0 | 2957 | 4 | 0 | 0 | 2 | 0 | 2 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0009 | 0/0 | 2957 | 3 | 3 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0010 | 0/0 | 2957 | 3 | 1 | 2 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0011 | 0/0 | 2957 | 2 | 0 | 0 | 0 | 0 | 2 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0012 | 0/0 | 2957 | 2 | 0 | 0 | 1 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0013 | 0/0 | 2957 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0014 | 0/0 | 2957 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0015 | 0/0 | 2957 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0016 | 0/0 | 2957 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0017 | 0/0 | 2957 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0018 | 0/0 | 2957 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0019 | 0/0 | 2957 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0020 | 0/0 | 2957 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0021 | 0/0 | 2957 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0022 | 0/0 | 2957 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0023 | 0/0 | 2957 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0024 | 0/0 | 2957 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0025 | 0/0 | 2957 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0026 | 0/0 | 2957 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
t0027 | 0/0 | 2957 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0003 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0008 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0148 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0236 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2550 | 354 | 86 | 61 | 161 | 10 | 35 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0002 | 0/0 | 2550 | 17 | 3 | 2 | 5 | 0 | 7 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0003 | 0/0 | 2550 | 7 | 6 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0007 | 0/0 | 2550 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0002c0006 | 0/0 | 2550 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0003c0005 | 0/0 | 2550 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0004c0004 | 1/0 | 2550 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5506 | 121 | 25 | 15 | 64 | 1 | 15 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0002 | 0/0 | 5506 | 93 | 14 | 14 | 59 | 3 | 3 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0003 | 0/0 | 5506 | 87 | 31 | 16 | 29 | 5 | 6 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0004 | 0/0 | 5506 | 10 | 0 | 5 | 0 | 0 | 5 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0005 | 0/0 | 5506 | 9 | 8 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0006 | 0/0 | 5506 | 4 | 0 | 3 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0007 | 0/0 | 5506 | 4 | 0 | 4 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0008 | 0/0 | 5506 | 4 | 0 | 0 | 2 | 0 | 2 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0009 | 0/0 | 5506 | 3 | 3 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0010 | 0/0 | 5506 | 3 | 1 | 2 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0012 | 0/0 | 5506 | 2 | 0 | 0 | 1 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0013 | 0/0 | 5506 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0014 | 0/0 | 5506 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0015 | 0/0 | 5506 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0016 | 0/0 | 5506 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0017 | 0/0 | 5506 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0018 | 0/0 | 5506 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0019 | 0/0 | 5506 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0020 | 0/0 | 5506 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0021 | 0/0 | 5506 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0022 | 0/0 | 5506 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0023 | 0/0 | 5506 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0024 | 0/0 | 5506 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0026 | 0/0 | 5506 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0001t0027 | 0/0 | 5506 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0002t0002 | 0/0 | 5506 | 15 | 3 | 2 | 5 | 0 | 5 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0002t0011 | 0/0 | 5506 | 2 | 0 | 0 | 0 | 0 | 2 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0003t0002 | 0/0 | 5506 | 6 | 5 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0003t0025 | 0/0 | 5506 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0001c0007t0002 | 0/0 | 5506 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0002c0006t0004 | 0/0 | 5506 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0003c0005t0006 | 0/0 | 5506 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
a0004c0004t0001 | 1/0 | 5506 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | copy fasta | chr2 | 55542292 | 55622622 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0148 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 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 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 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 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0216 | 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 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 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 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 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 | 0 | 1 | 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 | 0 | 0 | 1 | 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 |
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 | 2 | 0 | 0 | 2 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | 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 | 1 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 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 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0026 | 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 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 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 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 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 |
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 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0050 | 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 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 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 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0118 | 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 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0002g0214 | 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 | 0 | 0 | 2 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0316 | 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 |
a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0326 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0331 | 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 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0001t0003g0340 | 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 | 0 | 0 | 1 | 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 |
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 |
a0001c0001t0003g0347 | 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 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0003g0355 | 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 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0004g0140 | 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 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0005g0173 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0005g0180 | 0/0 | 1 | 1 | 0 | 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 |
a0001c0001t0006g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0006g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0006g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0006g0322 | 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 |
a0001c0001t0008g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0008g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0008g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0008g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0009g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0010g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0010g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0010g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0012g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0012g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0013g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0014g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0015g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0016g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0017g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0018g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0019g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0020g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0021g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0022g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0023g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0024g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0026g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0001t0027g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0002t0002g0122 | 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 |
a0001c0003t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0003t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0003t0002g0263 | 0/0 | 1 | 0 | 1 | 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 | 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 |
a0001c0003t0025g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0001c0007t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0002c0006t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0003c0005t0006g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
a0004c0004t0001g0236 | 1/0 | 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 | g0093 | EUR | GBR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00099 | hp2 | a0001 | c0001 | t0003 | g0286 | 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 | g0328 | EUR | GBR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | CHS | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | CHS | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | CHS | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0009 | 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 | g0019 | 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 | g0081 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0278 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0300 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0355 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0141 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0354 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0281 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01074 | hp2 | a0001 | c0001 | t0006 | g0320 | 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 | g0325 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0292 | 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 | g0295 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01168 | hp1 | a0001 | c0001 | t0006 | g0314 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01175 | hp2 | a0001 | c0001 | t0015 | g0144 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01192 | hp1 | a0001 | c0002 | t0002 | g0101 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0142 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0099 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01255 | hp2 | a0001 | c0001 | t0005 | g0177 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0019 | 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 | g0299 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0302 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01346 | hp1 | a0001 | c0003 | t0002 | g0263 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0285 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01361 | hp2 | a0001 | c0001 | t0010 | g0294 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0291 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0139 | 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 | g0084 | AMR | CLM | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0301 | EUR | IBS | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0289 | 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 | g0319 | EUR | IBS | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01884 | hp2 | a0001 | c0001 | t0023 | g0133 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0298 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0330 | 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 | g0063 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02027 | hp2 | a0001 | c0001 | t0024 | g0046 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0313 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02055 | hp2 | a0001 | c0002 | t0002 | g0096 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0331 | 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 | g0244 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02129 | hp2 | a0001 | c0001 | t0014 | g0191 | EAS | KHV | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02145 | hp2 | a0001 | c0001 | t0010 | g0329 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02155 | hp1 | a0001 | c0001 | t0021 | g0042 | EAS | CDX | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CDX | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | CDX | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0348 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0129 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02280 | hp1 | a0001 | c0003 | t0002 | g0264 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0341 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02300 | hp1 | a0001 | c0001 | t0006 | g0322 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02451 | hp1 | a0001 | c0002 | t0002 | g0095 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0102 | 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 | g0265 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0272 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0276 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0340 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0275 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02647 | hp2 | a0001 | c0003 | t0002 | g0262 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02683 | hp2 | a0001 | c0002 | t0002 | g0113 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0339 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0315 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0282 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02735 | hp2 | a0001 | c0001 | t0018 | g0229 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02738 | hp2 | a0003 | c0005 | t0006 | g0271 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02809 | hp1 | a0001 | c0001 | t0022 | g0034 | 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 | g0085 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02818 | hp2 | a0001 | c0003 | t0002 | g0261 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0338 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0273 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0172 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0175 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0274 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0179 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0130 | 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 | g0128 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0324 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0173 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03017 | hp1 | a0002 | c0006 | t0004 | g0138 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0032 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0316 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03130 | hp1 | a0001 | c0001 | t0026 | g0351 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0323 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0347 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0350 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0349 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0134 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0321 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0240 | 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 | g0136 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03491 | hp2 | a0001 | c0001 | t0016 | g0260 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0135 | 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 | g0181 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03516 | hp2 | a0001 | c0003 | t0025 | g0266 | AFR | ESN | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0287 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03540 | hp2 | a0001 | c0003 | t0002 | g0267 | AFR | GWD | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0318 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0277 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03669 | hp1 | a0001 | c0001 | t0012 | g0344 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03669 | hp2 | a0001 | c0002 | t0002 | g0100 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0337 | SAS | STU | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | STU | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03704 | hp1 | a0001 | c0001 | t0008 | g0358 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0112 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0137 | SAS | BEB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03834 | hp2 | a0001 | c0002 | t0002 | g0107 | SAS | BEB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | BEB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0121 | SAS | BEB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | STU | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0140 | SAS | STU | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG04184 | hp1 | a0001 | c0001 | t0027 | g0296 | SAS | BEB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG04184 | hp2 | a0001 | c0001 | t0008 | g0356 | SAS | BEB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | STU | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0297 | SAS | STU | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0284 | SAS | STU | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18522 | hp1 | a0001 | c0007 | t0002 | g0268 | AFR | YRI | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0317 | AFR | YRI | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0187 | 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 | g0346 | AFR | YRI | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | YRI | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0110 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0333 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0326 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0219 | 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 | g0223 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18964 | hp1 | a0001 | c0001 | t0012 | g0335 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18975 | hp2 | a0001 | c0001 | t0020 | g0045 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18979 | hp1 | a0001 | c0001 | t0008 | g0359 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18987 | hp1 | a0001 | c0001 | t0017 | g0203 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19001 | hp1 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19001 | hp2 | a0001 | c0001 | t0019 | g0067 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19002 | hp1 | a0001 | c0001 | t0008 | g0357 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0189 | 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 | g0259 | 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 | g0193 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0342 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19010 | hp1 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0010 | 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 | g0023 | AFR | LWK | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0174 | AFR | LWK | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | LWK | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19043 | hp2 | a0001 | c0001 | t0009 | g0022 | AFR | LWK | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0334 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19057 | hp1 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19090 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0125 | AFR | YRI | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | YRI | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0353 | AFR | ASW | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | ASW | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | TSI | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0290 | EUR | TSI | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | GIH | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | GIH | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0097 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0180 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0352 | AFR | ACB | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0176 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0343 | AFR | MSL | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
HG06807 | hp1 | a0001 | c0001 | t0013 | g0020 | 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 | g0209 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0108 | EAS | JPT | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0149 | 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 | g0126 | AFR | LWK | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0345 | AFR | LWK | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0148 | REF | REF | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
homoSapiens_grch38 | hp1 | a0004 | c0004 | t0001 | g0236 | REF | REF | PPP4R3B_chr2_55542292_55622622 | PPP4R3B | chr2 | 55542292 | 55622622 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:55578304
|
T | C | 3 | a0001a0002a0003 | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
missense_variant | MODERATE | c.1507A>G | p.Ile503Val | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 10/17 | 1844/5506 | 1507/2550 | 503/849 | chr2 | 55578304 | ||
chr2:55585065
|
G | C | 1 | a0003 | 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 | a0002 | 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 |
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 | a0001c0003a0001c0007 | 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 |
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 | a0001c0001t0003a0001c0001t0006a0001c0001t0010others(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 | a0001c0001t0002a0001c0001t0009a0001c0001t0013others(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 | a0001c0001t0006a0003c0005t0006 | 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 | a0001c0001t0004a0001c0001t0007a0002c0006t0004 | 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 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(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 | a0001c0001t0003a0001c0001t0006a0001c0001t0010others(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 |
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 | a0001c0001t0001g0237 | 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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0001t0003g0270 | 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0002g0054a0001c0001t0002g0081 | 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 | a0001c0001t0005g0174 | 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 | a0001c0001t0002g0040a0001c0001t0002g0072 | 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 | 93 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(90): 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 | 118 | a0001c0001t0001g0167a0001c0001t0001g0170a0001c0001t0002g0002others(115): 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 | a0001c0002t0002g0101a0001c0002t0002g0107a0001c0002t0002g0121others(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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0001g0153 | 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 | 233 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(230): 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 | 218 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(215): 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 | a0001c0001t0003g0350a0001c0001t0003g0352a0001c0001t0003g0353others(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 | a0001c0001t0003g0340 | 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 | a0001c0001t0001g0085a0001c0001t0001g0086 | 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 | a0001c0001t0001g0159a0001c0001t0001g0160 | 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0001g0205 | 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 | 279 | a0001c0001t0001g0013a0001c0001t0001g0083a0001c0001t0001g0084others(276): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.2455-3083A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55553089 | ||||||
chr2:55553115
|
T | C | 264 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(261): Show | 287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): 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 | a0001c0001t0003g0304a0001c0001t0003g0305a0001c0001t0003g0306others(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 | a0001c0001t0006g0320 | 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 | a0001c0001t0003g0309 | 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 | a0001c0001t0001g0159a0001c0001t0001g0160 | 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 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0233 | 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 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0087others(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 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0006others(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 | a0001c0001t0001g0190a0001c0001t0001g0192a0001c0001t0001g0206others(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 | a0001c0001t0001g0157a0001c0001t0001g0158 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0003g0331 | 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 | a0001c0001t0001g0090 | 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 | a0001c0001t0003g0331 | 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 | a0001c0001t0003g0323 | 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 | a0001c0001t0002g0072 | 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 | a0001c0001t0003g0334a0001c0001t0003g0342 | 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 | a0001c0001t0001g0244a0001c0001t0002g0125a0001c0001t0002g0126others(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 | 93 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(90): 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 | a0001c0001t0003g0281 | 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 | a0001c0001t0002g0066 | 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 | a0001c0001t0001g0256 | 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 | a0001c0001t0003g0297 | 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 | a0001c0001t0002g0075 | 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0032 | 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 | 48 | a0001c0001t0001g0013a0001c0001t0001g0092a0001c0001t0001g0131others(45): Show | 49 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(46): Show |
intron_variant | MODIFIER | c.2454+2142dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55556632 | ||||||
chr2:55556632
|
TA | T | 6 | a0001c0001t0001g0187a0001c0001t0001g0237a0001c0001t0002g0065others(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 | a0001c0001t0024g0046 | 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 | a0001c0001t0003g0286 | 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 | a0001c0001t0001g0200a0001c0001t0001g0228 | 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0001c0001t0001g0146a0001c0001t0001g0154 | 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 | a0001c0001t0024g0046 | 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 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0032 | 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 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(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 | a0001c0001t0003g0313a0001c0001t0003g0315a0001c0001t0003g0316 | 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 | a0001c0001t0002g0052a0001c0001t0002g0080 | 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 | 49 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(46): Show | 50 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(47): Show |
intron_variant | MODIFIER | c.2454+610A>G | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 16/16 | chr2 | 55558165 | ||||||
chr2:55558215
|
T | TA | 14 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(11): 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 | 2 | a0001c0001t0003g0289a0001c0001t0003g0291 | 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 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(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 | 91 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(88): 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 | a0001c0001t0001g0253 | 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 | a0001c0001t0002g0006a0001c0001t0002g0026a0001c0001t0002g0027others(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 | 265 | a0001c0001t0001g0013a0001c0001t0001g0083a0001c0001t0001g0084others(262): Show | 287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): 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 | a0001c0001t0002g0117 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0001g0091 | 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 | a0001c0001t0002g0029 | 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 | 88 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(85): 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 | 261 | a0001c0001t0001g0013a0001c0001t0001g0083a0001c0001t0001g0084others(258): 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 | a0001c0001t0012g0344 | 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 | 81 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(78): 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0001c0001t0001g0231 | 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 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(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 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0007others(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 | a0001c0001t0001g0157a0001c0001t0001g0188 | 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 | a0001c0001t0001g0085a0001c0001t0001g0086 | 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 | a0001c0001t0002g0053 | 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 | a0001c0001t0002g0060 | 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 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0211others(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 | 46 | a0001c0001t0001g0051a0001c0001t0001g0116a0001c0001t0001g0119others(43): Show | 46 | HG00621.hp2 HG01255.hp1 HG02080.hp1 others(43): Show |
intron_variant | MODIFIER | c.2261-1811delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55560778 | ||||||
chr2:55560778
|
GAA | G | 25 | a0001c0001t0001g0147a0001c0001t0001g0189a0001c0001t0001g0193others(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 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0159others(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 | a0001c0001t0001g0013a0001c0001t0001g0143a0001c0001t0001g0149others(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 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(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 | a0001c0001t0001g0151a0001c0001t0001g0152 | 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 | a0001c0001t0001g0146a0001c0001t0001g0154 | 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 | 2 | a0001c0001t0003g0289a0001c0001t0003g0291 | 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 | 90 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0188others(87): 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 | a0001c0001t0003g0018a0001c0001t0003g0311a0001c0001t0003g0355 | 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0003g0331 | 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 | 95 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(92): 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 | a0001c0001t0005g0177 | 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 | a0001c0001t0003g0284 | 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 | a0001c0003t0002g0261a0001c0003t0002g0262a0001c0003t0002g0263others(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 | a0001c0001t0001g0256 | 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 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0087others(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 | a0001c0001t0001g0145a0001c0001t0001g0149a0001c0001t0005g0172 | 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 | 46 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(43): Show | 47 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(44): Show |
intron_variant | MODIFIER | c.2260+2565A>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 15/16 | chr2 | 55561748 | ||||||
chr2:55561785
|
T | C | 95 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(92): 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0003g0308 | 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 | a0001c0001t0001g0197 | 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 | 160 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0131others(157): Show | 176 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(173): 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0001g0013a0001c0001t0001g0164 | 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 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0001c0001t0001g0153 | 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 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(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 | a0001c0001t0001g0199 | 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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0003g0331 | 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 | a0001c0001t0003g0277 | 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0003g0277 | 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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0001t0001g0085a0001c0001t0001g0086 | 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 | a0001c0001t0002g0031 | 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 | a0001c0001t0001g0085a0001c0001t0001g0086 | 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0003g0301a0001c0001t0003g0302 | 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0013g0020 | 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 | a0001c0001t0001g0207a0001c0001t0001g0210a0001c0001t0001g0257others(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 | a0001c0001t0001g0051a0001c0001t0002g0074a0001c0001t0024g0046 | 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 | a0001c0001t0002g0124a0001c0001t0002g0125a0001c0001t0002g0126others(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 | a0001c0001t0001g0013a0001c0001t0001g0083a0001c0001t0001g0084others(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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0003g0014a0001c0001t0003g0269a0001c0001t0003g0270others(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 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(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 | a0001c0001t0003g0317 | 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 | a0001c0001t0002g0075 | 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 | a0001c0001t0002g0052a0001c0001t0002g0080 | 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 | a0001c0001t0001g0157a0001c0001t0001g0158 | 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 | a0001c0002t0002g0122 | 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 | a0001c0001t0018g0229 | 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0001g0159a0001c0001t0001g0160 | 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 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0001c0001t0002g0052a0001c0001t0002g0080 | 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 | a0001c0002t0002g0110 | 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 | a0001c0001t0006g0314a0001c0001t0006g0319a0001c0001t0006g0320others(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 | a0001c0001t0001g0085a0001c0001t0001g0086 | 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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(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 | a0001c0001t0001g0205 | 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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(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 | a0001c0002t0002g0095a0001c0002t0002g0096a0001c0002t0002g0097others(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 | a0001c0001t0001g0051a0001c0001t0001g0221a0001c0001t0002g0002others(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 | a0001c0002t0002g0101a0001c0002t0002g0107a0001c0002t0002g0121others(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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | 93 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(90): 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 | 196 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(193): 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 | 45 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(42): Show | 46 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(43): 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0020g0045 | 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 | a0001c0001t0001g0051a0001c0001t0001g0083a0001c0001t0001g0084others(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 | a0001c0001t0001g0051a0001c0001t0001g0083a0001c0001t0001g0084others(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 | a0001c0001t0013g0020 | 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 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0129 | 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 | 96 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(93): 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 | 97 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(94): 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 | a0001c0001t0001g0234a0001c0001t0001g0239a0001c0001t0001g0240 | 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 | 97 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(94): 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0155 | 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 | 44 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(41): Show | 45 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(42): 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 | a0001c0001t0001g0212 | 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 | a0001c0001t0001g0157a0001c0001t0001g0158 | 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 | 96 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(93): 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 | a0001c0001t0001g0151 | 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 | 227 | a0001c0001t0001g0051a0001c0001t0001g0083a0001c0001t0001g0084others(224): 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 | 212 | a0001c0001t0001g0051a0001c0001t0001g0199a0001c0001t0001g0210others(209): 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 | 96 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(93): 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 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(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 | a0001c0001t0002g0063 | 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 | a0001c0001t0002g0082 | 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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(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 | a0001c0001t0003g0284 | 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 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0032 | 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 | 205 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(202): 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0001g0256 | 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 | a0001c0001t0002g0004a0001c0001t0002g0021 | 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 | a0001c0001t0001g0222 | 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 | 95 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(92): 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 | a0001c0001t0003g0301 | 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 | a0001c0001t0002g0040 | 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 | a0001c0001t0003g0293 | 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 | a0001c0001t0001g0143a0001c0001t0001g0150 | 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0003g0336 | 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 | 16 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0146others(13): Show | 16 | HG01168.hp2 HG01169.hp2 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.1765+839C>T | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 12/16 | chr2 | 55572780 | ||||||
chr2:55572855
|
C | G | 96 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(93): 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 | a0001c0001t0003g0279a0001c0001t0003g0280a0001c0001t0003g0308others(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 | a0001c0001t0015g0144 | 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 | a0001c0001t0001g0215 | 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 | a0001c0001t0008g0356a0001c0001t0008g0358 | 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 | a0001c0001t0008g0357 | 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 | a0001c0001t0001g0189a0001c0001t0001g0193a0001c0001t0001g0195others(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 | a0001c0001t0002g0124a0001c0001t0002g0128 | 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 | a0001c0001t0002g0043 | 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 | 209 | a0001c0001t0001g0051a0001c0001t0001g0199a0001c0001t0001g0210others(206): 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 | a0001c0001t0001g0231a0001c0001t0001g0232 | 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 | a0001c0001t0001g0163a0001c0001t0001g0209a0001c0001t0001g0257others(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 | 93 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(90): 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 | a0001c0003t0002g0261a0001c0003t0002g0262a0001c0003t0002g0263others(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 | a0001c0001t0003g0333a0001c0001t0003g0334a0001c0001t0003g0342 | 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 | 13 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(10): 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 | a0001c0001t0023g0133 | 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 | a0001c0002t0002g0115 | 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 | a0001c0001t0003g0313 | 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 | a0001c0001t0002g0057 | 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 | 95 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(92): 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0087others(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 | 95 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(92): 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 | a0001c0001t0001g0157 | 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 | 6 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(3): Show | 6 | NA18612.hp2 NA18946.hp1 NA18984.hp2 others(3): 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 | a0001c0001t0001g0232 | 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 | 117 | a0001c0001t0001g0154a0001c0001t0001g0199a0001c0001t0001g0210others(114): 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 | a0001c0001t0001g0051a0001c0001t0002g0003a0001c0001t0002g0004others(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 | a0001c0001t0001g0167a0001c0001t0001g0170 | 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0001g0205 | 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 | 46 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(43): Show | 47 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(44): Show |
intron_variant | MODIFIER | c.1607-1529dupA | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 11/16 | chr2 | 55575305 | ||||||
chr2:55575330
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0001g0158 | 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0030 | 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 | 46 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(43): Show | 47 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(44): 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(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 | 95 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(92): 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 | a0001c0001t0001g0085a0001c0001t0001g0086 | 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 | a0001c0002t0002g0095a0001c0002t0002g0096a0001c0002t0002g0097others(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 | a0001c0001t0020g0045 | 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 | a0001c0001t0004g0134 | 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0002g0114 | 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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0003g0330 | 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 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0216others(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 | a0001c0001t0003g0284 | 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0003g0352 | 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 | a0001c0001t0001g0200a0001c0001t0001g0228 | 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 | a0001c0001t0001g0207 | 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 | a0001c0001t0001g0149 | 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 | a0001c0001t0010g0325 | 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 | a0002c0006t0004g0138 | 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 | 96 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(93): 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 | a0001c0001t0003g0281 | 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 | a0001c0001t0021g0042 | 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 | a0001c0002t0002g0095a0001c0002t0002g0096a0001c0002t0002g0097others(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 | a0001c0001t0012g0344 | 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 | a0001c0001t0003g0316 | 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | 97 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(94): 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 | 269 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0083others(266): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): 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 | a0001c0001t0001g0159 | 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0003t0025g0266 | 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 | 97 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(94): 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 | ||||||
chr2:55579407
|
C | CT | 358 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0083others(355): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1468+271dupA | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 9/16 | chr2 | 55579407 | ||||||
chr2:55579508
|
A | AC | 97 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(94): 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 | a0001c0002t0002g0121 | 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0002g0004a0001c0001t0002g0021 | 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 | 210 | a0001c0001t0001g0051a0001c0001t0001g0199a0001c0001t0001g0210others(207): 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 | 210 | a0001c0001t0001g0051a0001c0001t0001g0199a0001c0001t0001g0210others(207): 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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | 210 | a0001c0001t0001g0051a0001c0001t0001g0199a0001c0001t0001g0210others(207): 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0001g0093 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1366-710T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 8/16 | chr2 | 55580491 | ||||||
chr2:55580721
|
A | G | 1 | a0001c0001t0001g0148 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1365+846T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 8/16 | chr2 | 55580721 | ||||||
chr2:55580749
|
T | C | 1 | a0001c0001t0001g0216 | 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 | a0001c0001t0004g0137 | 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 | a0001c0001t0003g0284 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(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 | a0001c0001t0001g0187 | 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 | 283 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0083others(280): Show | 306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): 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 | a0001c0001t0004g0134 | 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 | 45 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(42): Show | 46 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(43): 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 | a0001c0002t0002g0095a0001c0002t0002g0096a0001c0002t0002g0097others(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 | 96 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(93): 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 | a0001c0001t0003g0279a0001c0001t0003g0308a0001c0001t0003g0327 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0004g0134 | 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 | a0001c0001t0001g0157a0001c0001t0001g0158 | 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 | a0001c0001t0001g0151 | 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 | a0001c0001t0003g0015a0001c0001t0003g0272a0001c0001t0003g0273others(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 | a0001c0001t0013g0020 | 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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0001t0004g0012a0001c0001t0004g0135a0001c0001t0004g0136others(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 | 118 | a0001c0001t0001g0051a0001c0001t0001g0116a0001c0001t0001g0119others(115): 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 | 118 | a0001c0001t0001g0051a0001c0001t0001g0116a0001c0001t0001g0119others(115): 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 | a0001c0001t0002g0024a0001c0001t0002g0025 | 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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0007t0002g0268 | 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 | a0001c0001t0001g0159a0001c0001t0001g0160 | 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 | a0001c0001t0018g0229 | 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 | a0001c0001t0004g0012a0001c0001t0004g0135a0001c0001t0004g0136others(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 | a0001c0002t0002g0095a0001c0002t0002g0096a0001c0002t0002g0097others(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 | a0001c0001t0002g0052a0001c0001t0002g0080 | 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 | a0001c0001t0022g0034 | 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0003t0002g0261a0001c0003t0002g0262a0001c0003t0002g0263others(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 | a0001c0001t0001g0208a0001c0001t0001g0218 | 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 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0217others(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 | 188 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0083others(185): Show | 205 | HG00099.hp1 HG00140.hp1 HG00423.hp2 others(202): Show |
intron_variant | MODIFIER | c.1233+126T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 7/16 | chr2 | 55584925 | ||||||
chr2:55584937
|
T | G | 96 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219others(93): 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 | a0001c0001t0001g0199a0001c0001t0001g0210a0001c0001t0001g0219 | 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 | 29 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(26): 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 | a0001c0001t0014g0191 | 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 | a0001c0001t0002g0214 | 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 | a0001c0001t0003g0323 | 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 | a0001c0003t0002g0261a0001c0003t0002g0262a0001c0003t0002g0263others(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 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(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 | 44 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(41): Show | 45 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(42): 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 | 29 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(26): 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 | a0001c0001t0001g0209 | 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 | 118 | a0001c0001t0001g0051a0001c0001t0001g0116a0001c0001t0001g0119others(115): 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 | a0001c0001t0002g0029 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0002g0037 | 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 | a0001c0001t0001g0085a0001c0001t0001g0086 | 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 | a0001c0001t0001g0238a0001c0001t0001g0245a0001c0001t0003g0279 | 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 | a0001c0001t0002g0003a0001c0001t0002g0054a0001c0001t0002g0055others(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 | a0001c0001t0003g0017a0001c0001t0003g0275a0001c0001t0003g0317others(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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0002t0002g0095a0001c0002t0002g0096a0001c0002t0002g0097others(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 | a0001c0001t0002g0125 | 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 | a0001c0001t0001g0168 | 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0001g0157a0001c0001t0001g0158 | 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 | 219 | a0001c0001t0001g0051a0001c0001t0001g0116a0001c0001t0001g0119others(216): 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 | a0001c0001t0001g0153a0001c0001t0001g0155 | 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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0002g0114 | 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 | a0001c0001t0001g0210 | 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 | a0001c0001t0001g0051a0001c0001t0001g0188a0001c0001t0002g0002others(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 | 45 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(42): Show | 46 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(43): 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 | a0001c0001t0001g0189a0001c0001t0001g0193a0001c0001t0001g0195others(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 | a0001c0001t0003g0016a0001c0001t0003g0309 | 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 | a0001c0001t0003g0350a0001c0001t0026g0351 | 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 | 58 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(55): Show | 63 | HG01070.hp2 HG01081.hp1 HG01099.hp2 others(60): 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0001g0183a0001c0001t0001g0222a0001c0001t0001g0225others(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 | 265 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0116others(262): Show | 288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0002t0002g0095a0001c0002t0002g0096a0001c0002t0002g0097others(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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0003g0284a0001c0001t0012g0344 | 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 | a0001c0001t0003g0339 | 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 | 48 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(45): Show | 49 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(46): 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | 119 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(116): 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0002t0002g0095a0001c0002t0002g0096a0001c0002t0002g0097others(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 | 280 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0083others(277): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.922-1206G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55590162 | ||||||
chr2:55590364
|
T | A | 13 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(10): 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 | a0001c0001t0001g0219 | 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0002t0002g0113 | 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 | a0001c0001t0001g0215 | 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 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(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 | 117 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(114): 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 | a0001c0001t0003g0282 | 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 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(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 | a0001c0001t0002g0039 | 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 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0032 | 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 | a0001c0001t0001g0220a0001c0001t0001g0250 | 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0001g0093a0001c0001t0001g0098 | 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | 117 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(114): 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 | a0001c0001t0005g0174 | 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 | 281 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0083others(278): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): 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 | a0001c0001t0003g0333a0001c0001t0003g0334a0001c0001t0003g0342others(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 | a0001c0002t0002g0122 | 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 | a0001c0001t0002g0058 | 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 | a0001c0001t0002g0062a0001c0001t0002g0065 | 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 | a0001c0001t0002g0120 | 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 | a0001c0001t0001g0216a0001c0001t0001g0252 | 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 | a0001c0001t0020g0045 | 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 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(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 | 59 | a0001c0001t0001g0013a0001c0001t0001g0083a0001c0001t0001g0084others(56): Show | 60 | HG00099.hp1 HG01106.hp2 HG01167.hp2 others(57): 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 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(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 | a0001c0001t0001g0209 | 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 | a0001c0001t0001g0225a0001c0001t0001g0255 | 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 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(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 | a0001c0001t0001g0184a0001c0001t0001g0208a0001c0001t0001g0209others(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 | 187 | a0001c0001t0001g0051a0001c0001t0001g0116a0001c0001t0001g0119others(184): 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 | a0001c0001t0001g0145a0001c0001t0002g0030a0001c0001t0002g0049others(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 | 46 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(43): Show | 47 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(44): 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 | a0001c0001t0003g0014a0001c0001t0003g0269a0001c0001t0003g0270others(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 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(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 | 48 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(45): Show | 49 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(46): 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 | a0001c0003t0002g0261a0001c0003t0002g0262a0001c0003t0002g0263others(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 | a0001c0001t0001g0247a0001c0001t0001g0257a0001c0001t0003g0014others(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 | a0001c0001t0001g0147a0001c0001t0001g0183a0001c0001t0001g0198others(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 | 46 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(43): Show | 47 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(44): 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 | a0001c0001t0001g0145a0001c0001t0001g0149 | 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 | a0001c0001t0001g0215 | 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 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0032 | 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 | a0001c0001t0012g0335 | 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0003t0002g0263 | 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 | a0001c0001t0002g0068a0001c0001t0002g0078 | 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 | a0001c0001t0001g0051a0001c0001t0001g0188a0001c0001t0001g0210others(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 | 120 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(117): 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 | a0001c0001t0001g0199 | 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 | 280 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0083others(277): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): 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 | a0001c0001t0003g0318a0001c0001t0004g0135a0001c0001t0004g0136 | 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 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0187others(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 | 264 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0083others(261): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.921+2069delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55596346 | ||||||
chr2:55596355
|
A | T | 1 | a0001c0001t0001g0151 | 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 | a0001c0002t0002g0101 | 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 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0001g0146a0001c0001t0001g0152a0001c0001t0001g0154 | 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 | a0001c0001t0004g0134 | 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 | a0001c0001t0001g0212 | 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 | 46 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(43): Show | 47 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(44): 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 | a0001c0001t0003g0018 | 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 | 46 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(43): Show | 47 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(44): 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0003g0331 | 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 | 119 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(116): 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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0001t0004g0139a0001c0001t0004g0140 | 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 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 |
177 | a0001c0001t0001g0013a0001c0001t0001g0083a0001c0001t0001g0084others(174): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(187): 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 | a0001c0001t0001g0156 | 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 | 222 | a0001c0001t0001g0051a0001c0001t0001g0116a0001c0001t0001g0119others(219): 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 | 46 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(43): Show | 47 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(44): 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 | a0001c0001t0002g0033 | 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 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(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 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(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 | 13 | a0001c0001t0001g0143a0001c0001t0001g0146a0001c0001t0001g0147others(10): Show | 13 | HG01168.hp2 HG01169.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.921+428G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55597988 | ||||||
chr2:55598150
|
G | T | 1 | a0001c0001t0001g0148 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.921+266C>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 4/16 | chr2 | 55598150 | ||||||
chr2:55598176
|
C | T | 2 | a0001c0001t0003g0284a0001c0001t0012g0344 | 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0003g0339 | 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 | 119 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(116): 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 | a0001c0002t0002g0095a0001c0002t0002g0096a0001c0002t0002g0097others(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 | a0001c0002t0002g0100 | 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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | 281 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0083others(278): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): 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 | a0001c0002t0002g0110 | 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0002t0002g0122 | 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 | a0001c0001t0001g0159a0001c0001t0001g0160 | 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 | 119 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(116): 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 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0032 | 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 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | 45 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(42): Show | 46 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(43): Show |
intron_variant | MODIFIER | c.298-940G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55599979 | ||||||
chr2:55599989
|
G | A | 13 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(10): 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 | a0001c0001t0001g0085a0001c0001t0001g0086 | 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 | 293 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0083others(290): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0003g0312 | 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 | a0001c0001t0002g0059 | 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 | a0001c0001t0003g0284 | 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 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0032 | 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 | a0001c0001t0001g0157 | 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 | 119 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(116): 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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | 44 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0145others(41): Show | 45 | HG00423.hp1 HG00621.hp2 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.298-1388dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 3/16 | chr2 | 55600426 | ||||||
chr2:55600426
|
C | CAA | 18 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0087others(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 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0094others(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 | 37 | a0001c0001t0001g0089a0001c0001t0001g0146a0001c0001t0001g0153others(34): 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 | 39 | a0001c0001t0001g0154a0001c0001t0003g0017a0001c0001t0003g0018others(36): 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 | a0001c0001t0003g0275a0001c0001t0003g0276a0001c0001t0003g0283others(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 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0003g0014others(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 | a0001c0001t0003g0306a0001c0001t0003g0336a0001c0001t0003g0339others(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 | a0001c0001t0001g0185a0001c0001t0001g0187a0001c0001t0001g0189others(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 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(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 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0102others(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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0001t0001g0013a0001c0001t0001g0164 | 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 | 354 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0083others(351): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): 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 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0032 | 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 | a0001c0001t0004g0012a0001c0001t0004g0137a0001c0001t0004g0141others(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 | a0001c0001t0001g0051 | 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 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(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 | a0001c0001t0001g0085a0001c0001t0001g0086 | 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 | a0001c0001t0001g0183a0001c0001t0001g0222a0001c0001t0001g0223others(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 | a0001c0002t0002g0095a0001c0002t0002g0096a0001c0002t0002g0097others(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 | a0001c0001t0002g0066 | 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 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(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 | a0001c0001t0001g0234a0001c0001t0002g0060a0001c0001t0002g0061others(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 | a0001c0001t0001g0013a0001c0001t0001g0083a0001c0001t0001g0084others(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 | 102 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0146others(99): Show | 108 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(105): 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 | 25 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(22): 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 | a0001c0002t0002g0095a0001c0002t0002g0096a0001c0002t0002g0097others(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 | a0001c0001t0003g0347a0001c0001t0003g0348 | 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 | a0001c0001t0002g0040 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0002g0072 | 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 | a0001c0001t0003g0298 | 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 | a0001c0002t0002g0100 | 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0001g0230 | 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 | 119 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(116): 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 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0032 | 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 | a0001c0001t0003g0299 | 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0009g0022a0001c0001t0009g0023a0001c0001t0009g0032 | 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 | a0001c0001t0004g0137 | 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 | 119 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(116): 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | 119 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(116): 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 | a0001c0001t0012g0335 | 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 | a0001c0001t0002g0048a0001c0001t0003g0282a0001c0001t0004g0136 | 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 | 217 | a0001c0001t0001g0051a0001c0001t0001g0116a0001c0001t0001g0119others(214): 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 | a0001c0001t0003g0301a0001c0001t0003g0302 | 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 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(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 | a0001c0001t0001g0085a0001c0001t0001g0086 | 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 | a0001c0001t0003g0281 | 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 | a0001c0001t0003g0277 | 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 | a0001c0003t0002g0261a0001c0003t0002g0262a0001c0003t0002g0263others(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 | a0001c0001t0002g0049 | 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 | a0001c0001t0001g0231a0001c0001t0001g0232 | 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0002t0002g0100 | 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 | a0001c0001t0003g0272 | 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 | 281 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0083others(278): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): 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 | a0001c0001t0001g0161 | 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 | 280 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0083others(277): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): 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 | a0001c0001t0002g0080 | 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 | 46 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(43): Show | 47 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(44): 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 | a0001c0001t0002g0123a0001c0001t0002g0125a0001c0001t0002g0126others(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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0001g0163 | 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 | a0001c0001t0001g0192 | 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0001g0185a0001c0001t0001g0186 | 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0159a0001c0001t0001g0160 | 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 | a0001c0001t0003g0309 | 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | 45 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(42): Show | 46 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(43): 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 | a0001c0001t0001g0158 | 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 | a0001c0002t0002g0095a0001c0002t0002g0096a0001c0002t0002g0097others(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 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235others(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 | 142 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0131others(139): Show | 157 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.199-1829delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55605904 | ||||||
chr2:55605975
|
T | A | 4 | a0001c0001t0003g0015a0001c0001t0003g0272a0001c0001t0003g0273others(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 | a0001c0001t0003g0324a0001c0001t0003g0339a0001c0001t0003g0340others(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 | a0001c0001t0003g0324a0001c0001t0003g0339a0001c0001t0003g0340others(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 | a0001c0001t0001g0190 | 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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0001t0003g0313 | 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 | a0001c0001t0002g0068a0001c0001t0002g0078a0001c0001t0004g0012others(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 | a0001c0001t0002g0111a0001c0001t0003g0279a0001c0001t0003g0280others(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 | a0001c0001t0001g0187a0001c0001t0001g0239a0001c0001t0001g0257others(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 | 219 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0083others(216): Show | 230 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(227): 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 | a0001c0001t0002g0040 | 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0003g0333a0001c0001t0003g0334a0001c0001t0003g0342others(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 | 18 | a0001c0001t0001g0143a0001c0001t0001g0145a0001c0001t0001g0146others(15): Show | 18 | HG01168.hp2 HG01169.hp2 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.199-3385T>C | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55607461 | ||||||
chr2:55607591
|
T | A | 44 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(41): Show | 45 | HG01167.hp2 HG01168.hp2 HG01169.hp2 others(42): 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 | a0001c0002t0002g0112a0001c0002t0002g0113 | 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0001g0258 | 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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0003t0002g0261a0001c0003t0002g0262a0001c0003t0002g0263others(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 | a0001c0001t0005g0175a0001c0001t0005g0179 | 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0087others(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 | a0001c0001t0003g0018 | 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 | 95 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(92): 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 | a0001c0001t0003g0304a0001c0001t0003g0305a0001c0001t0003g0306others(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 | a0001c0001t0003g0337a0001c0001t0003g0354a0001c0001t0003g0355 | 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 | a0001c0001t0001g0246 | 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 | 219 | a0001c0001t0001g0051a0001c0001t0001g0116a0001c0001t0001g0119others(216): 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 | a0001c0001t0003g0281 | 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 | a0001c0003t0002g0261a0001c0003t0002g0265a0001c0003t0025g0266 | 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 | a0001c0001t0004g0135a0001c0001t0004g0136 | 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 | a0001c0001t0002g0124 | 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 | 179 | a0001c0001t0001g0051a0001c0001t0001g0116a0001c0001t0001g0119others(176): 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0259a0001c0001t0002g0064 | 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 | a0001c0001t0001g0166a0001c0001t0001g0259a0001c0001t0002g0064 | 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 | a0001c0003t0002g0261a0001c0003t0002g0262a0001c0003t0002g0263others(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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0001t0001g0189 | 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 | a0001c0001t0001g0237 | 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 | 253 | a0001c0001t0001g0013a0001c0001t0001g0083a0001c0001t0001g0084others(250): 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 | 13 | a0001c0001t0001g0116a0001c0001t0001g0148a0001c0001t0002g0024others(10): Show | 13 | HG00438.hp2 HG01175.hp1 HG02109.hp2 others(10): 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 | a0001c0001t0001g0085a0001c0001t0001g0086 | 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 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0238 | 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 | a0001c0001t0001g0146 | 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 | a0001c0002t0002g0115 | 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 | a0001c0001t0001g0157a0001c0001t0001g0158 | 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 | a0001c0001t0001g0187 | 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 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0243others(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 | a0001c0001t0003g0016a0001c0001t0003g0309a0001c0001t0003g0310others(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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0002g0026 | 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 | a0001c0001t0002g0039 | 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 | a0001c0001t0002g0069a0001c0001t0002g0070 | 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 | a0001c0001t0003g0278 | 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 | a0001c0001t0001g0167a0001c0001t0001g0170 | 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 | a0001c0001t0015g0144 | 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 | a0001c0001t0002g0052a0001c0001t0002g0080 | 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 | a0001c0001t0004g0134 | 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 | a0001c0001t0003g0276 | 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 | 100 | a0001c0001t0001g0013a0001c0001t0001g0164a0001c0001t0003g0014others(97): 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 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0029others(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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0002g0054others(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 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(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 | a0001c0001t0002g0039 | 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 | 58 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(55): Show | 58 | HG00099.hp1 HG01106.hp2 HG01168.hp2 others(55): Show |
intron_variant | MODIFIER | c.198+2096dupT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55613354 | ||||||
chr2:55613381
|
A | T | 11 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0001g0013a0001c0001t0001g0164a0001c0001t0003g0324others(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 | a0001c0001t0002g0053 | 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 | a0001c0001t0001g0090a0001c0001t0001g0239a0001c0001t0001g0240others(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 | a0001c0001t0001g0013a0001c0001t0001g0164a0001c0001t0003g0339others(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 | 125 | a0001c0001t0001g0051a0001c0001t0001g0085a0001c0001t0001g0086others(122): Show | 133 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.198+1641delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 2/16 | chr2 | 55613809 | ||||||
chr2:55613809
|
TAA | T | 13 | a0001c0001t0001g0146a0001c0001t0002g0030a0001c0001t0002g0036others(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 | a0001c0001t0001g0013a0001c0001t0001g0164a0001c0001t0003g0324others(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 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0087others(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 | a0001c0001t0001g0116a0001c0001t0002g0117a0001c0001t0002g0118 | 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 | a0001c0001t0003g0324a0001c0001t0003g0340a0001c0001t0003g0341others(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 | a0001c0001t0003g0326 | 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 | a0001c0001t0003g0273a0001c0001t0003g0274 | 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 | a0001c0001t0001g0145 | 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 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0087others(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 | 96 | a0001c0001t0001g0013a0001c0001t0001g0164a0001c0001t0003g0014others(93): 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 | a0001c0001t0003g0276 | 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 | 280 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0083others(277): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): 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 | a0001c0001t0003g0275 | 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 | a0001c0001t0002g0035 | 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 | a0001c0001t0010g0325 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0091 | 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0002g0066 | 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 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094others(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 | 67 | a0001c0001t0001g0051a0001c0001t0001g0098a0001c0001t0001g0116others(64): 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 | a0001c0001t0001g0119a0001c0001t0002g0009a0001c0001t0002g0068others(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 | a0001c0001t0001g0156a0001c0001t0001g0157 | 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 | a0001c0001t0001g0158a0001c0001t0001g0159 | 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 | a0001c0001t0001g0160 | 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 | a0001c0001t0001g0131a0001c0001t0001g0161a0001c0001t0001g0162others(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 | a0001c0001t0001g0013a0001c0001t0001g0132a0001c0001t0001g0165others(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 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170 | 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 | a0001c0001t0001g0171 | 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 | a0001c0001t0005g0172 | 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 | a0001c0001t0005g0173a0001c0001t0005g0174a0001c0001t0005g0175 | 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 | a0001c0001t0001g0178a0001c0001t0005g0176a0001c0001t0005g0177others(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 | a0001c0001t0005g0180 | 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 | a0001c0001t0005g0181 | 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 | 76 | a0001c0001t0001g0084a0001c0001t0001g0145a0001c0001t0001g0146others(73): Show | 80 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.143-352delT | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55615857 | ||||||
chr2:55615857
|
CAA | C | 6 | a0001c0001t0001g0143a0001c0001t0003g0015a0001c0001t0003g0272others(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 | a0001c0001t0004g0012a0001c0001t0004g0134a0001c0001t0004g0135others(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 | a0001c0001t0001g0083 | 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 | a0003c0005t0006g0271 | 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 | a0001c0001t0002g0021 | 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 | 94 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(91): 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 | a0001c0001t0012g0344 | 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 | a0001c0003t0002g0261a0001c0003t0002g0262a0001c0003t0002g0263others(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 | 94 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(91): 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 | a0001c0003t0002g0267 | 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 | a0001c0001t0016g0260 | 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 | a0001c0001t0002g0123 | 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 | 280 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0083others(277): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): 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 | a0001c0001t0003g0345a0001c0001t0003g0346a0001c0001t0003g0347others(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 | 25 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0002g0010others(22): 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 | a0001c0001t0001g0051a0001c0001t0002g0002a0001c0001t0002g0003others(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 | a0001c0001t0002g0123a0001c0001t0002g0124a0001c0001t0002g0125others(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 | a0001c0001t0001g0131a0001c0001t0001g0132 | 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 | a0001c0001t0003g0354a0001c0001t0003g0355 | 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 | 148 | a0001c0001t0001g0013a0001c0001t0001g0131a0001c0001t0001g0132others(145): Show | 158 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(155): 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 | a0001c0001t0003g0014a0001c0001t0003g0269a0001c0001t0003g0270 | 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 | a0001c0007t0002g0268 | 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 | 280 | a0001c0001t0001g0013a0001c0001t0001g0051a0001c0001t0001g0083others(277): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.142+175G>A | PPP4R3B | ENSG00000275052.5 | transcript | ENST00000616407.2 | protein_coding | 1/16 | chr2 | 55616969 |