geneid | 55615 |
---|---|
ensemblid | ENSG00000186654.21 |
hgncid | 31682 |
symbol | PRR5 |
name | proline rich 5 |
refseq_nuc | NM_181333.4 |
refseq_prot | NP_851850.1 |
ensembl_nuc | ENST00000336985.11 |
ensembl_prot | ENSP00000337464.6 |
mane_status | MANE Select |
chr | chr22 |
start | 44702204 |
end | 44737681 |
strand | + |
ver | v1.2 |
region | chr22:44702204-44737681 |
region5000 | chr22:44697204-44742681 |
regionname0 | PRR5_chr22_44702204_44737681 |
regionname5000 | PRR5_chr22_44697204_44742681 |
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 | 1/1 | 388 | 385 | 90 | 76 | 158 | 13 | 46 | 121 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0002 | 0/0 | 388 | 51 | 4 | 1 | 42 | 0 | 4 | 33 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0003 | 0/0 | 388 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0004 | 0/0 | 388 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0005 | 0/0 | 388 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0006 | 0/0 | 324 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0007 | 0/0 | 388 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
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 | 1/1 | 1167 | 225 | 36 | 50 | 100 | 9 | 28 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
c0002 | 0/0 | 1167 | 103 | 47 | 13 | 27 | 3 | 13 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
c0003 | 0/0 | 1167 | 51 | 4 | 1 | 42 | 0 | 4 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
c0004 | 0/0 | 1167 | 40 | 7 | 13 | 15 | 1 | 4 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
c0005 | 0/0 | 1167 | 8 | 0 | 0 | 8 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
c0006 | 0/0 | 1167 | 3 | 0 | 0 | 3 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
c0007 | 0/0 | 1167 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
c0008 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
c0009 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
c0010 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
c0011 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
c0012 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
c0013 | 0/0 | 1153 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
c0014 | 0/0 | 1167 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
c0015 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
c0016 | 0/0 | 1167 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
c0017 | 0/0 | 1167 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
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 | 706 | 200 | 10 | 48 | 91 | 12 | 37 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0002 | 0/0 | 706 | 50 | 3 | 1 | 43 | 0 | 3 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0003 | 0/0 | 706 | 46 | 13 | 5 | 28 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0004 | 0/0 | 706 | 40 | 7 | 13 | 16 | 0 | 4 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0005 | 0/0 | 706 | 32 | 11 | 5 | 15 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0006 | 0/0 | 706 | 13 | 7 | 3 | 1 | 0 | 2 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0007 | 0/0 | 706 | 7 | 6 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0008 | 0/0 | 706 | 7 | 7 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0009 | 0/0 | 706 | 5 | 5 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0010 | 0/0 | 706 | 4 | 4 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0011 | 0/0 | 706 | 3 | 1 | 0 | 1 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0012 | 0/0 | 706 | 3 | 3 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0013 | 0/0 | 706 | 3 | 0 | 0 | 3 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0014 | 0/0 | 706 | 3 | 3 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0015 | 0/0 | 706 | 3 | 3 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0016 | 0/0 | 706 | 2 | 1 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0017 | 0/0 | 706 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0018 | 0/0 | 706 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0019 | 0/0 | 706 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0020 | 0/0 | 706 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0021 | 0/0 | 706 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0022 | 0/0 | 706 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0023 | 0/0 | 706 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0024 | 0/0 | 690 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0025 | 0/0 | 690 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0026 | 0/0 | 690 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0027 | 0/0 | 706 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0028 | 0/0 | 706 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0029 | 0/0 | 706 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0030 | 0/0 | 706 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0031 | 0/0 | 706 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0032 | 0/0 | 706 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
t0033 | 0/0 | 706 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
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 | 6 | 0 | 6 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0200 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0392 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0395 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0396 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0398 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0399 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0400 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0406 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0407 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0408 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0409 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0410 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0411 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0412 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0413 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0414 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0415 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0416 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0417 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
g0418 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
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 | 1/1 | 1167 | 225 | 36 | 50 | 100 | 9 | 28 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002 | 0/0 | 1167 | 103 | 47 | 13 | 27 | 3 | 13 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0004 | 0/0 | 1167 | 40 | 7 | 13 | 15 | 1 | 4 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0005 | 0/0 | 1167 | 8 | 0 | 0 | 8 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0006 | 0/0 | 1167 | 3 | 0 | 0 | 3 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0008 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0009 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0011 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0012 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0015 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0017 | 0/0 | 1167 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0002c0003 | 0/0 | 1167 | 51 | 4 | 1 | 42 | 0 | 4 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0003c0007 | 0/0 | 1167 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0004c0010 | 0/0 | 1167 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0005c0014 | 0/0 | 1167 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0006c0013 | 0/0 | 1153 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0007c0016 | 0/0 | 1167 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1872 | 157 | 8 | 43 | 70 | 9 | 25 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0001t0003 | 0/0 | 1872 | 35 | 6 | 3 | 26 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0001t0006 | 0/0 | 1872 | 11 | 6 | 3 | 1 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0001t0007 | 0/0 | 1872 | 5 | 4 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0001t0009 | 0/0 | 1872 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0001t0012 | 0/0 | 1872 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0001t0014 | 0/0 | 1872 | 3 | 3 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0001t0015 | 0/0 | 1872 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0001t0018 | 0/0 | 1872 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0001t0020 | 0/0 | 1872 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0001t0024 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0001t0027 | 0/0 | 1872 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0001t0029 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0001t0030 | 0/0 | 1872 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0001t0032 | 0/0 | 1872 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0001 | 0/0 | 1872 | 25 | 2 | 4 | 6 | 2 | 11 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0003 | 0/0 | 1872 | 10 | 6 | 2 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0005 | 0/0 | 1872 | 32 | 11 | 5 | 15 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0006 | 0/0 | 1872 | 2 | 1 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0007 | 0/0 | 1872 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0008 | 0/0 | 1872 | 7 | 7 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0009 | 0/0 | 1872 | 3 | 3 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0010 | 0/0 | 1872 | 4 | 4 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0011 | 0/0 | 1872 | 3 | 1 | 0 | 1 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0012 | 0/0 | 1872 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0013 | 0/0 | 1872 | 3 | 0 | 0 | 3 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0015 | 0/0 | 1872 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0017 | 0/0 | 1872 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0019 | 0/0 | 1872 | 2 | 2 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0022 | 0/0 | 1872 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0023 | 0/0 | 1872 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0026 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0028 | 0/0 | 1872 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0002t0033 | 0/0 | 1872 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0004t0004 | 0/0 | 1872 | 38 | 6 | 13 | 15 | 0 | 4 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0004t0016 | 0/0 | 1872 | 2 | 1 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0005t0001 | 0/0 | 1872 | 8 | 0 | 0 | 8 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0006t0001 | 0/0 | 1872 | 3 | 0 | 0 | 3 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0008t0001 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0009t0001 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0011t0001 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0012t0004 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0015t0031 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0001c0017t0001 | 0/0 | 1872 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0002c0003t0002 | 0/0 | 1872 | 49 | 3 | 1 | 42 | 0 | 3 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0002c0003t0003 | 0/0 | 1872 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0002c0003t0021 | 0/0 | 1872 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0003c0007t0004 | 0/0 | 1872 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0003c0007t0025 | 0/0 | 1856 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0004c0010t0002 | 0/0 | 1872 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0005c0014t0001 | 0/0 | 1872 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0006c0013t0001 | 0/0 | 1858 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
a0007c0016t0001 | 0/0 | 1872 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | copy fasta | chr22 | 44697204 | 44742681 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0162 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0200 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0387 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0388 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0392 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0399 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0001g0416 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0400 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0407 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0003g0418 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0006g0414 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0007g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0007g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0009g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0009g0412 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0012g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0014g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0014g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0014g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0015g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0015g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0018g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0018g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0020g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0020g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0024g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0027g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0029g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0030g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0001t0032g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0395 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0396 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0001g0408 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0003g0409 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0005g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0006g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0008g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0008g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0008g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0008g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0008g0410 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0009g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0009g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0009g0413 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0010g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0010g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0010g0406 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0011g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0011g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0011g0415 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0012g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0012g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0013g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0013g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0015g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0017g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0017g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0019g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0019g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0022g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0023g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0026g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0028g0398 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0002t0033g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0004g0411 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0016g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0004t0016g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0005t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0005t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0005t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0005t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0005t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0005t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0005t0001g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0006t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0006t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0006t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0008t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0009t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0011t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0012t0004g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0015t0031g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0001c0017t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0002g0417 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0002c0003t0021g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0003c0007t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0003c0007t0025g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0004c0010t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0005c0014t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0006c0013t0001g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
a0007c0016t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | GBR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0315 | EUR | GBR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00140 | hp1 | a0001 | c0004 | t0016 | g0039 | EUR | GBR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00140 | hp2 | a0005 | c0014 | t0001 | g0201 | EUR | GBR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | FIN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0108 | EUR | FIN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00323 | hp1 | a0001 | c0002 | t0005 | g0106 | EUR | FIN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | FIN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00408 | hp1 | a0002 | c0003 | t0002 | g0354 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00408 | hp2 | a0002 | c0003 | t0002 | g0148 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00423 | hp1 | a0002 | c0003 | t0002 | g0150 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00423 | hp2 | a0001 | c0004 | t0004 | g0250 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00438 | hp2 | a0002 | c0003 | t0002 | g0307 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0373 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00609 | hp1 | a0001 | c0011 | t0001 | g0282 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00609 | hp2 | a0001 | c0002 | t0005 | g0222 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00621 | hp1 | a0001 | c0002 | t0005 | g0375 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0361 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00639 | hp1 | a0001 | c0004 | t0004 | g0364 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0367 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00642 | hp2 | a0001 | c0004 | t0004 | g0010 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00673 | hp1 | a0002 | c0003 | t0002 | g0255 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0109 | EAS | CHS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0387 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0046 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00738 | hp1 | a0001 | c0002 | t0028 | g0398 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0389 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01069 | hp2 | a0001 | c0004 | t0004 | g0017 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01070 | hp1 | a0001 | c0002 | t0005 | g0173 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01070 | hp2 | a0001 | c0002 | t0005 | g0380 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01071 | hp1 | a0001 | c0004 | t0004 | g0017 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01071 | hp2 | a0001 | c0002 | t0005 | g0339 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01099 | hp1 | a0002 | c0003 | t0002 | g0145 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0299 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0058 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01109 | hp2 | a0001 | c0001 | t0007 | g0024 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0186 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01168 | hp2 | a0001 | c0001 | t0006 | g0041 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01175 | hp2 | a0001 | c0004 | t0004 | g0010 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0399 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01243 | hp1 | a0001 | c0002 | t0003 | g0409 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01243 | hp2 | a0001 | c0002 | t0003 | g0071 | AMR | PUR | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01255 | hp2 | a0001 | c0004 | t0004 | g0345 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01256 | hp1 | a0001 | c0004 | t0004 | g0135 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0391 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0346 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0390 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01433 | hp2 | a0001 | c0001 | t0006 | g0035 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01496 | hp2 | a0001 | c0002 | t0005 | g0085 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | IBS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0363 | EUR | IBS | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01884 | hp1 | a0001 | c0002 | t0003 | g0253 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01884 | hp2 | a0001 | c0002 | t0003 | g0193 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01891 | hp1 | a0001 | c0002 | t0007 | g0022 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01928 | hp1 | a0001 | c0004 | t0004 | g0355 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01934 | hp1 | a0001 | c0002 | t0022 | g0004 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01943 | hp1 | a0001 | c0002 | t0005 | g0252 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01943 | hp2 | a0001 | c0004 | t0004 | g0411 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0388 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01975 | hp1 | a0001 | c0004 | t0004 | g0393 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0400 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0366 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0392 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0358 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01993 | hp2 | a0001 | c0004 | t0004 | g0235 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02015 | hp1 | a0001 | c0004 | t0004 | g0287 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02015 | hp2 | a0002 | c0003 | t0002 | g0123 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0335 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02027 | hp2 | a0001 | c0002 | t0005 | g0334 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02055 | hp1 | a0001 | c0004 | t0004 | g0277 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02055 | hp2 | a0001 | c0001 | t0018 | g0057 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02056 | hp1 | a0002 | c0003 | t0002 | g0362 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0336 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0294 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02071 | hp2 | a0001 | c0004 | t0004 | g0308 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02080 | hp2 | a0001 | c0015 | t0031 | g0359 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0383 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02129 | hp2 | a0001 | c0002 | t0005 | g0165 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02132 | hp1 | a0001 | c0002 | t0005 | g0365 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02135 | hp2 | a0002 | c0003 | t0002 | g0327 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02145 | hp1 | a0002 | c0003 | t0002 | g0094 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02145 | hp2 | a0001 | c0002 | t0005 | g0021 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02165 | hp1 | a0001 | c0002 | t0005 | g0105 | EAS | CDX | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02257 | hp1 | a0001 | c0002 | t0010 | g0405 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02258 | hp1 | a0001 | c0001 | t0024 | g0062 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02258 | hp2 | a0001 | c0001 | t0015 | g0267 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02273 | hp1 | a0001 | c0004 | t0004 | g0368 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02273 | hp2 | a0001 | c0004 | t0004 | g0240 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02280 | hp1 | a0001 | c0002 | t0008 | g0091 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02280 | hp2 | a0002 | c0003 | t0003 | g0115 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0360 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0394 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02451 | hp1 | a0001 | c0002 | t0026 | g0061 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0045 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02523 | hp1 | a0002 | c0003 | t0002 | g0351 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02572 | hp1 | a0001 | c0002 | t0019 | g0020 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0404 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0352 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0414 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02615 | hp2 | a0001 | c0002 | t0007 | g0023 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02622 | hp1 | a0001 | c0004 | t0016 | g0028 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02622 | hp2 | a0001 | c0002 | t0010 | g0089 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02630 | hp1 | a0001 | c0002 | t0019 | g0208 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02630 | hp2 | a0001 | c0002 | t0003 | g0202 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02647 | hp1 | a0001 | c0004 | t0004 | g0206 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02647 | hp2 | a0001 | c0002 | t0023 | g0134 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02683 | hp2 | a0001 | c0004 | t0004 | g0137 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02717 | hp1 | a0001 | c0001 | t0014 | g0266 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02717 | hp2 | a0001 | c0001 | t0027 | g0275 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02723 | hp1 | a0001 | c0002 | t0005 | g0067 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0077 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02738 | hp1 | a0001 | c0004 | t0004 | g0305 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0396 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02809 | hp1 | a0001 | c0002 | t0001 | g0320 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02809 | hp2 | a0001 | c0004 | t0004 | g0263 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02818 | hp1 | a0001 | c0001 | t0014 | g0265 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02818 | hp2 | a0001 | c0002 | t0005 | g0129 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02886 | hp1 | a0001 | c0002 | t0017 | g0038 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02895 | hp1 | a0001 | c0002 | t0005 | g0251 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02895 | hp2 | a0001 | c0004 | t0004 | g0340 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0034 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02897 | hp2 | a0001 | c0004 | t0004 | g0381 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02922 | hp1 | a0001 | c0001 | t0009 | g0412 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02922 | hp2 | a0001 | c0002 | t0005 | g0254 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02965 | hp1 | a0001 | c0002 | t0003 | g0302 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0408 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02970 | hp1 | a0001 | c0002 | t0009 | g0032 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02970 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02976 | hp1 | a0001 | c0002 | t0006 | g0031 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02976 | hp2 | a0001 | c0002 | t0010 | g0406 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03017 | hp1 | a0001 | c0002 | t0006 | g0049 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03017 | hp2 | a0001 | c0002 | t0001 | g0143 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03041 | hp1 | a0001 | c0002 | t0005 | g0184 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03041 | hp2 | a0001 | c0001 | t0015 | g0268 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03098 | hp1 | a0001 | c0001 | t0018 | g0132 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03098 | hp2 | a0001 | c0002 | t0008 | g0410 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0033 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03130 | hp2 | a0001 | c0001 | t0007 | g0036 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03139 | hp1 | a0001 | c0002 | t0005 | g0276 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03195 | hp1 | a0001 | c0002 | t0003 | g0070 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03195 | hp2 | a0001 | c0002 | t0008 | g0183 | AFR | ESN | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03209 | hp2 | a0001 | c0002 | t0033 | g0059 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0026 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03225 | hp2 | a0001 | c0001 | t0009 | g0025 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03239 | hp1 | a0001 | c0002 | t0001 | g0207 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03453 | hp1 | a0001 | c0001 | t0006 | g0027 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03453 | hp2 | a0001 | c0002 | t0005 | g0185 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03486 | hp1 | a0003 | c0007 | t0025 | g0063 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03486 | hp2 | a0001 | c0002 | t0008 | g0086 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03490 | hp1 | a0001 | c0004 | t0004 | g0356 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0210 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0211 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03540 | hp1 | a0001 | c0002 | t0008 | g0301 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03540 | hp2 | a0001 | c0004 | t0004 | g0204 | AFR | GWD | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0030 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03579 | hp2 | a0001 | c0002 | t0011 | g0415 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0300 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03669 | hp1 | a0002 | c0003 | t0002 | g0248 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03669 | hp2 | a0001 | c0001 | t0032 | g0221 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03688 | hp1 | a0001 | c0001 | t0006 | g0042 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03704 | hp2 | a0001 | c0001 | t0030 | g0112 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03710 | hp2 | a0002 | c0003 | t0021 | g0048 | SAS | PJL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03831 | hp1 | a0001 | c0002 | t0011 | g0044 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03831 | hp2 | a0002 | c0003 | t0002 | g0311 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0395 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0246 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0122 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0271 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04115 | hp1 | a0001 | c0004 | t0004 | g0110 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04199 | hp1 | a0002 | c0003 | t0002 | g0093 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0312 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0198 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04204 | hp2 | a0001 | c0017 | t0001 | g0215 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | YRI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18522 | hp2 | a0001 | c0002 | t0015 | g0270 | AFR | YRI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0374 | EAS | CHB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0190 | EAS | CHB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0378 | EAS | CHB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18906 | hp1 | a0001 | c0002 | t0012 | g0269 | AFR | YRI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0407 | AFR | YRI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0097 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18941 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18942 | hp1 | a0001 | c0002 | t0005 | g0249 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18942 | hp2 | a0002 | c0003 | t0002 | g0376 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18943 | hp1 | a0001 | c0002 | t0013 | g0008 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18943 | hp2 | a0002 | c0003 | t0002 | g0149 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18944 | hp1 | a0001 | c0002 | t0005 | g0231 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18945 | hp1 | a0001 | c0004 | t0004 | g0236 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18945 | hp2 | a0001 | c0002 | t0003 | g0018 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18946 | hp2 | a0001 | c0001 | t0020 | g0232 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18947 | hp1 | a0001 | c0002 | t0005 | g0369 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18947 | hp2 | a0001 | c0004 | t0004 | g0234 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18948 | hp1 | a0002 | c0003 | t0002 | g0136 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18948 | hp2 | a0006 | c0013 | t0001 | g0379 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18950 | hp1 | a0002 | c0003 | t0002 | g0121 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18951 | hp2 | a0001 | c0005 | t0001 | g0386 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18953 | hp1 | a0001 | c0002 | t0005 | g0126 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18954 | hp2 | a0002 | c0003 | t0002 | g0002 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18957 | hp2 | a0001 | c0004 | t0004 | g0012 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18960 | hp2 | a0002 | c0003 | t0002 | g0257 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18961 | hp1 | a0001 | c0004 | t0004 | g0083 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18961 | hp2 | a0001 | c0002 | t0013 | g0008 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18962 | hp1 | a0002 | c0003 | t0002 | g0333 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18962 | hp2 | a0001 | c0006 | t0001 | g0130 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0397 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18963 | hp2 | a0002 | c0003 | t0002 | g0154 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18964 | hp1 | a0001 | c0005 | t0001 | g0096 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18964 | hp2 | a0001 | c0001 | t0006 | g0047 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18965 | hp1 | a0001 | c0002 | t0003 | g0337 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18965 | hp2 | a0001 | c0002 | t0005 | g0213 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18966 | hp1 | a0002 | c0003 | t0002 | g0384 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18969 | hp2 | a0002 | c0003 | t0002 | g0171 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18970 | hp1 | a0002 | c0003 | t0002 | g0002 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18971 | hp2 | a0002 | c0003 | t0002 | g0125 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18973 | hp1 | a0002 | c0003 | t0002 | g0119 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0382 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18974 | hp1 | a0002 | c0003 | t0002 | g0417 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18974 | hp2 | a0002 | c0003 | t0002 | g0286 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18978 | hp1 | a0002 | c0003 | t0002 | g0100 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18978 | hp2 | a0001 | c0002 | t0005 | g0102 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18979 | hp2 | a0001 | c0002 | t0001 | g0080 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18980 | hp2 | a0002 | c0003 | t0002 | g0303 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18981 | hp1 | a0004 | c0010 | t0002 | g0002 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18981 | hp2 | a0001 | c0001 | t0020 | g0239 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18982 | hp1 | a0001 | c0002 | t0005 | g0285 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18982 | hp2 | a0001 | c0002 | t0013 | g0169 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18983 | hp1 | a0002 | c0003 | t0002 | g0328 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18983 | hp2 | a0001 | c0004 | t0004 | g0344 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18984 | hp1 | a0001 | c0005 | t0001 | g0015 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18986 | hp1 | a0001 | c0005 | t0001 | g0172 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18986 | hp2 | a0002 | c0003 | t0002 | g0209 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18987 | hp1 | a0002 | c0003 | t0002 | g0332 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18987 | hp2 | a0001 | c0002 | t0005 | g0092 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18989 | hp2 | a0002 | c0003 | t0002 | g0117 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18990 | hp1 | a0001 | c0002 | t0005 | g0331 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18992 | hp1 | a0001 | c0004 | t0004 | g0012 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18992 | hp2 | a0001 | c0006 | t0001 | g0167 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0416 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18997 | hp1 | a0001 | c0005 | t0001 | g0226 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18997 | hp2 | a0002 | c0003 | t0002 | g0325 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18998 | hp1 | a0001 | c0004 | t0004 | g0322 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0418 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA18999 | hp2 | a0001 | c0005 | t0001 | g0349 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19001 | hp1 | a0001 | c0002 | t0011 | g0043 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19003 | hp1 | a0002 | c0003 | t0002 | g0256 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19005 | hp1 | a0002 | c0003 | t0002 | g0291 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19007 | hp1 | a0002 | c0003 | t0002 | g0156 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0290 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19010 | hp1 | a0001 | c0001 | t0029 | g0013 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19012 | hp1 | a0001 | c0004 | t0004 | g0230 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19030 | hp1 | a0001 | c0001 | t0014 | g0264 | AFR | LWK | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19030 | hp2 | a0001 | c0002 | t0012 | g0133 | AFR | LWK | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19043 | hp1 | a0003 | c0007 | t0004 | g0069 | AFR | LWK | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19043 | hp2 | a0002 | c0003 | t0002 | g0259 | AFR | LWK | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0385 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19054 | hp2 | a0002 | c0003 | t0002 | g0155 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0401 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19056 | hp2 | a0001 | c0006 | t0001 | g0274 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0377 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19060 | hp2 | a0002 | c0003 | t0002 | g0306 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0370 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19063 | hp2 | a0002 | c0003 | t0002 | g0298 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19066 | hp1 | a0001 | c0004 | t0004 | g0212 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19068 | hp2 | a0001 | c0004 | t0004 | g0220 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19074 | hp1 | a0002 | c0003 | t0002 | g0120 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0347 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19079 | hp2 | a0001 | c0012 | t0004 | g0372 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19080 | hp2 | a0001 | c0004 | t0004 | g0214 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19081 | hp1 | a0001 | c0009 | t0001 | g0111 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19082 | hp1 | a0002 | c0003 | t0002 | g0321 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19084 | hp2 | a0001 | c0005 | t0001 | g0227 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19087 | hp1 | a0002 | c0003 | t0002 | g0338 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19087 | hp2 | a0001 | c0008 | t0001 | g0279 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19088 | hp1 | a0002 | c0003 | t0002 | g0064 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19088 | hp2 | a0001 | c0005 | t0001 | g0015 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19089 | hp1 | a0002 | c0003 | t0002 | g0319 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19089 | hp2 | a0001 | c0004 | t0004 | g0371 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19240 | hp1 | a0002 | c0003 | t0002 | g0402 | AFR | YRI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA19240 | hp2 | a0001 | c0002 | t0008 | g0090 | AFR | YRI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20129 | hp1 | a0001 | c0002 | t0005 | g0261 | AFR | ASW | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20129 | hp2 | a0001 | c0002 | t0005 | g0403 | AFR | ASW | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0219 | EUR | TSI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0273 | EUR | TSI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0353 | EUR | TSI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | TSI | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | GIH | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0329 | SAS | GIH | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01123 | hp1 | a0007 | c0016 | t0001 | g0138 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | CLM | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0040 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02109 | hp2 | a0001 | c0002 | t0009 | g0004 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02486 | hp1 | a0001 | c0002 | t0010 | g0019 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02486 | hp2 | a0001 | c0002 | t0005 | g0068 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02559 | hp1 | a0001 | c0001 | t0012 | g0084 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG02559 | hp2 | a0001 | c0002 | t0008 | g0087 | AFR | ACB | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03471 | hp1 | a0001 | c0002 | t0009 | g0413 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG03471 | hp2 | a0001 | c0002 | t0003 | g0258 | AFR | MSL | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | USA | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | USA | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | USA | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA20300 | hp2 | a0001 | c0002 | t0017 | g0037 | AFR | USA | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0182 | AFR | LWK | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0200 | REF | REF | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0162 | REF | REF | PRR5_chr22_44697204_44742681 | PRR5 | chr22 | 44697204 | 44742681 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:44732330
|
C | T | 1 | a0007 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.494C>T | p.Ala165Val | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/8 | 765/1872 | 494/1167 | 165/388 | chr22 | 44732330 | ||
chr22:44735067
|
G | A | 1 | a0004 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.596G>A | p.Arg199His | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/8 | 867/1872 | 596/1167 | 199/388 | chr22 | 44735067 | ||
chr22:44735117
|
G | A | 1 | a0003 | 2 | HG03486.hp1 NA19043.hp1 |
missense_variant | MODERATE | c.646G>A | p.Gly216Ser | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/8 | 917/1872 | 646/1167 | 216/388 | chr22 | 44735117 | ||
chr22:44736807
|
G | A | 2 | a0002a0004 | 52 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
missense_variant | MODERATE | c.727G>A | p.Val243Met | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 998/1872 | 727/1167 | 243/388 | chr22 | 44736807 | ||
chr22:44736872
|
GGAGCACG others(7): Show |
G | 1 | a0006 | 1 | NA18948.hp2 | frameshift_variant | HIGH | c.794_807delAGCACGAG others(6): Show |
p.Glu265fs | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 1065/1872 | 794/1167 | 265/388 | INFO_REALIGN_3_PRIME | chr22 | 44736872 | |
chr22:44736951
|
G | A | 1 | a0005 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.871G>A | p.Glu291Lys | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 1142/1872 | 871/1167 | 291/388 | chr22 | 44736951 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:44725280
|
G | A | 1 | a0001c0008 | 1 | NA19087.hp2 | synonymous_variant | LOW | c.252G>A | p.Thr84Thr | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/8 | 523/1872 | 252/1167 | 84/388 | chr22 | 44725280 | ||
chr22:44726603
|
G | C | 2 | a0001c0006a0001c0009 | 4 | NA18962.hp2 NA18992.hp2 NA19056.hp2 others(1): Show |
synonymous_variant | LOW | c.291G>C | p.Val97Val | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/8 | 562/1872 | 291/1167 | 97/388 | chr22 | 44726603 | ||
chr22:44731782
|
C | T | 1 | a0001c0017 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.375C>T | p.Asp125Asp | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/8 | 646/1872 | 375/1167 | 125/388 | chr22 | 44731782 | ||
chr22:44732352
|
T | C | 7 | a0001c0002a0001c0004a0001c0006others(4): Show | 201 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(198): Show |
synonymous_variant | LOW | c.516T>C | p.Arg172Arg | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/8 | 787/1872 | 516/1167 | 172/388 | chr22 | 44732352 | ||
chr22:44735077
|
G | A | 1 | a0001c0005 | 8 | NA18951.hp2 NA18964.hp1 NA18984.hp1 others(5): Show |
synonymous_variant | LOW | c.606G>A | p.Thr202Thr | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/8 | 877/1872 | 606/1167 | 202/388 | chr22 | 44735077 | ||
chr22:44736824
|
T | C | 4 | a0001c0004a0001c0011a0001c0012others(1): Show | 44 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(41): Show |
synonymous_variant | LOW | c.744T>C | p.Pro248Pro | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 1015/1872 | 744/1167 | 248/388 | chr22 | 44736824 | ||
chr22:44736845
|
C | T | 1 | a0001c0015 | 1 | HG02080.hp2 | synonymous_variant | LOW | c.765C>T | p.Tyr255Tyr | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 1036/1872 | 765/1167 | 255/388 | chr22 | 44736845 | ||
chr22:44736887
|
G | A | 1 | a0006c0013 | 1 | NA18948.hp2 | synonymous_variant | LOW | c.807G>A | p.Glu269Glu | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 1078/1872 | 807/1167 | 269/388 | chr22 | 44736887 | ||
chr22:44736905
|
T | C | 3 | a0001c0004a0001c0012a0003c0007 | 43 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(40): Show |
synonymous_variant | LOW | c.825T>C | p.Gly275Gly | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 1096/1872 | 825/1167 | 275/388 | chr22 | 44736905 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:44702227
|
T | G | 11 | a0001c0001t0006a0001c0001t0007a0001c0001t0009others(8): Show | 34 | HG00140.hp1 HG00735.hp2 HG01109.hp2 others(31): Show |
5_prime_UTR_variant | MODIFIER | c.-248T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/8 | 248 | chr22 | 44702227 | |||||
chr22:44702231
|
G | T | 3 | a0001c0001t0014a0001c0001t0015a0001c0002t0015 | 6 | HG02258.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-244G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/8 | chr22 | 44702231 | ||||||
chr22:44702255
|
T | C | 4 | a0001c0001t0012a0001c0001t0018a0001c0002t0012others(1): Show | 6 | HG02055.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-220T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/8 | 220 | chr22 | 44702255 | |||||
chr22:44702263
|
TCCGTGCA others(9): Show |
T | 3 | a0001c0001t0024a0001c0002t0026a0003c0007t0025 | 3 | HG02258.hp1 HG02451.hp1 HG03486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-208_-193delTGCAAT others(10): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/8 | 193 | INFO_REALIGN_3_PRIME | chr22 | 44702263 | ||||
chr22:44702307
|
A | G | 4 | a0001c0001t0012a0001c0001t0018a0001c0002t0012others(1): Show | 6 | HG02055.hp2 HG02559.hp1 HG02647.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-168A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/8 | 168 | chr22 | 44702307 | |||||
chr22:44702391
|
C | A | 1 | a0001c0001t0027 | 1 | HG02717.hp2 | 5_prime_UTR_variant | MODIFIER | c.-84C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/8 | 84 | chr22 | 44702391 | |||||
chr22:44702427
|
G | T | 1 | a0001c0002t0033 | 1 | HG03209.hp2 | 5_prime_UTR_variant | MODIFIER | c.-48G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/8 | 48 | chr22 | 44702427 | |||||
chr22:44737287
|
T | C | 1 | a0001c0002t0019 | 2 | HG02572.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*40T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 40 | chr22 | 44737287 | |||||
chr22:44737343
|
C | T | 3 | a0001c0001t0032a0001c0002t0010a0001c0002t0017 | 7 | HG02257.hp1 HG02486.hp1 HG02622.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*96C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 96 | chr22 | 44737343 | |||||
chr22:44737349
|
G | A | 2 | a0001c0001t0029a0001c0002t0028 | 2 | HG00738.hp1 NA19010.hp1 |
3_prime_UTR_variant | MODIFIER | c.*102G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 102 | chr22 | 44737349 | |||||
chr22:44737358
|
A | G | 32 | a0001c0001t0003a0001c0001t0007a0001c0001t0009others(29): Show | 215 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*111A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 111 | chr22 | 44737358 | |||||
chr22:44737378
|
T | C | 5 | a0001c0004t0004a0001c0004t0016a0001c0012t0004others(2): Show | 43 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*131T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 131 | chr22 | 44737378 | |||||
chr22:44737414
|
A | G | 6 | a0001c0001t0009a0001c0002t0008a0001c0002t0009others(3): Show | 15 | HG01934.hp1 HG02109.hp2 HG02280.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*167A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 167 | chr22 | 44737414 | |||||
chr22:44737453
|
C | G | 6 | a0001c0001t0009a0001c0002t0008a0001c0002t0009others(3): Show | 15 | HG01934.hp1 HG02109.hp2 HG02280.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*206C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 206 | chr22 | 44737453 | |||||
chr22:44737460
|
G | A | 9 | a0001c0002t0005a0001c0002t0010a0001c0002t0011others(6): Show | 95 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*213G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 213 | chr22 | 44737460 | |||||
chr22:44737530
|
C | T | 1 | a0001c0015t0031 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*283C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 283 | chr22 | 44737530 | |||||
chr22:44737574
|
C | A | 1 | a0001c0002t0022 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*327C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 327 | chr22 | 44737574 | |||||
chr22:44737577
|
T | C | 1 | a0001c0001t0030 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*330T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 330 | chr22 | 44737577 | |||||
chr22:44737587
|
G | A | 3 | a0002c0003t0002a0002c0003t0021a0004c0010t0002 | 51 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*340G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 340 | chr22 | 44737587 | |||||
chr22:44737595
|
A | G | 1 | a0001c0001t0020 | 2 | NA18946.hp2 NA18981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*348A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 348 | chr22 | 44737595 | |||||
chr22:44737655
|
G | T | 6 | a0001c0002t0013a0001c0004t0004a0001c0004t0016others(3): Show | 46 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*408G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 8/8 | 408 | chr22 | 44737655 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr22:44702745
|
C | G | 5 | a0001c0001t0001g0416a0001c0001t0003g0018a0001c0001t0003g0418others(2): Show | 5 | NA18945.hp2 NA18974.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.134+137C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44702745 | ||||||
chr22:44702990
|
C | T | 4 | a0001c0001t0006g0414a0001c0001t0009g0412a0001c0002t0009g0413others(1): Show | 4 | HG02615.hp1 HG02922.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.134+382C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44702990 | ||||||
chr22:44703028
|
G | T | 1 | a0001c0004t0004g0411 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.134+420G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44703028 | ||||||
chr22:44703107
|
G | A | 3 | a0001c0002t0005g0021a0001c0002t0010g0019a0001c0002t0019g0020 | 3 | HG02145.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.134+499G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44703107 | ||||||
chr22:44703211
|
T | G | 34 | a0001c0001t0006g0027a0001c0001t0006g0030a0001c0001t0006g0034others(31): Show | 34 | HG00140.hp1 HG00735.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.134+603T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44703211 | ||||||
chr22:44703310
|
CGGGAGGC others(39): Show |
C | 11 | a0001c0001t0006g0040a0001c0001t0006g0041a0001c0001t0006g0042others(8): Show | 11 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.134+710_134+755del others(46): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44703310 | |||||
chr22:44703318
|
AGTGGACA others(16): Show |
A | 23 | a0001c0001t0006g0027a0001c0001t0006g0030a0001c0001t0006g0034others(20): Show | 23 | HG01109.hp2 HG01433.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.134+740_134+762del others(23): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44703318 | |||||
chr22:44703586
|
T | G | 34 | a0001c0001t0006g0027a0001c0001t0006g0030a0001c0001t0006g0034others(31): Show | 34 | HG00140.hp1 HG00735.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.134+978T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44703586 | ||||||
chr22:44703674
|
G | T | 1 | a0001c0002t0008g0410 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.134+1066G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44703674 | ||||||
chr22:44703678
|
C | G | 1 | a0001c0002t0003g0409 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.134+1070C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44703678 | ||||||
chr22:44703891
|
A | G | 7 | a0001c0001t0001g0404a0001c0001t0003g0407a0001c0002t0001g0408others(4): Show | 7 | HG02257.hp1 HG02572.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.134+1283A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44703891 | ||||||
chr22:44703946
|
A | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0278others(167): Show | 181 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.134+1338A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44703946 | ||||||
chr22:44703974
|
T | C | 6 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0052others(3): Show | 6 | HG00323.hp2 HG01081.hp1 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.134+1366T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44703974 | ||||||
chr22:44704309
|
G | A | 1 | a0001c0001t0003g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.134+1701G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44704309 | ||||||
chr22:44704312
|
G | C | 34 | a0001c0001t0006g0027a0001c0001t0006g0030a0001c0001t0006g0034others(31): Show | 34 | HG00140.hp1 HG00735.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.134+1704G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44704312 | ||||||
chr22:44704339
|
A | T | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+1731A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44704339 | ||||||
chr22:44704475
|
C | G | 14 | a0001c0001t0001g0001a0001c0001t0001g0388a0001c0001t0001g0389others(11): Show | 19 | HG00738.hp1 HG00738.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.134+1867C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44704475 | ||||||
chr22:44704610
|
C | A | 1 | a0001c0001t0018g0057 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.134+2002C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44704610 | ||||||
chr22:44704747
|
A | G | 3 | a0001c0002t0005g0021a0001c0002t0010g0019a0001c0002t0019g0020 | 3 | HG02145.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.134+2139A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44704747 | ||||||
chr22:44704794
|
G | A | 1 | a0001c0002t0001g0058 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.134+2186G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44704794 | ||||||
chr22:44705049
|
C | T | 1 | a0001c0001t0001g0387 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.134+2441C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705049 | ||||||
chr22:44705085
|
G | A | 1 | a0001c0002t0033g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.134+2477G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705085 | ||||||
chr22:44705117
|
A | G | 109 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0304others(106): Show | 118 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.134+2509A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705117 | ||||||
chr22:44705134
|
A | C | 1 | a0001c0001t0001g0273 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.134+2526A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705134 | ||||||
chr22:44705204
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.134+2596T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705204 | ||||||
chr22:44705283
|
C | CT | 16 | a0001c0001t0001g0288a0001c0001t0001g0292a0001c0001t0001g0293others(13): Show | 18 | HG00558.hp1 HG02015.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.134+2678dupT | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44705283 | |||||
chr22:44705315
|
TTC | T | 3 | a0001c0001t0024g0062a0001c0002t0026g0061a0003c0007t0025g0063 | 3 | HG02258.hp1 HG02451.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.134+2717_134+2718d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44705315 | |||||
chr22:44705328
|
T | C | 2 | a0001c0002t0007g0022a0001c0002t0007g0023 | 2 | HG01891.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.134+2720T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705328 | ||||||
chr22:44705348
|
C | T | 1 | a0001c0001t0001g0272 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.134+2740C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705348 | ||||||
chr22:44705349
|
G | A | 1 | a0002c0003t0002g0064 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.134+2741G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705349 | ||||||
chr22:44705362
|
T | C | 2 | a0001c0001t0027g0275a0001c0002t0033g0059 | 2 | HG02717.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.134+2754T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705362 | ||||||
chr22:44705364
|
T | G | 16 | a0001c0001t0001g0288a0001c0001t0001g0292a0001c0001t0001g0293others(13): Show | 18 | HG00558.hp1 HG02015.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.134+2756T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705364 | ||||||
chr22:44705447
|
T | A | 1 | a0001c0001t0001g0065 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.134+2839T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705447 | ||||||
chr22:44705490
|
A | T | 1 | a0001c0005t0001g0386 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.134+2882A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705490 | ||||||
chr22:44705501
|
T | G | 1 | a0001c0001t0001g0066 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.134+2893T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705501 | ||||||
chr22:44705569
|
C | T | 3 | a0001c0001t0007g0036a0001c0002t0017g0037a0001c0002t0017g0038 | 3 | HG02886.hp1 HG03130.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.134+2961C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705569 | ||||||
chr22:44705614
|
C | T | 34 | a0001c0001t0006g0027a0001c0001t0006g0030a0001c0001t0006g0034others(31): Show | 34 | HG00140.hp1 HG00735.hp2 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.134+3006C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705614 | ||||||
chr22:44705615
|
G | A | 2 | a0001c0002t0005g0067a0001c0002t0005g0068 | 2 | HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.134+3007G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705615 | ||||||
chr22:44705717
|
C | T | 1 | a0001c0002t0001g0408 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.134+3109C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705717 | ||||||
chr22:44705767
|
G | T | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3159G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705767 | ||||||
chr22:44705768
|
G | C | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3160G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705768 | ||||||
chr22:44705775
|
C | T | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3167C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705775 | ||||||
chr22:44705778
|
C | T | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3170C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705778 | ||||||
chr22:44705780
|
A | T | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3172A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705780 | ||||||
chr22:44705783
|
C | T | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3175C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705783 | ||||||
chr22:44705784
|
C | A | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3176C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705784 | ||||||
chr22:44705792
|
T | G | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3184T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705792 | ||||||
chr22:44705794
|
T | A | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3186T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705794 | ||||||
chr22:44705795
|
T | A | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3187T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705795 | ||||||
chr22:44705797
|
G | C | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3189G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705797 | ||||||
chr22:44705798
|
T | A | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3190T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705798 | ||||||
chr22:44705799
|
T | C | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3191T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705799 | ||||||
chr22:44705805
|
T | C | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3197T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705805 | ||||||
chr22:44705806
|
T | A | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3198T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705806 | ||||||
chr22:44705811
|
G | C | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3203G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705811 | ||||||
chr22:44705812
|
G | C | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3204G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705812 | ||||||
chr22:44705814
|
G | C | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3206G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705814 | ||||||
chr22:44705817
|
G | C | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3209G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705817 | ||||||
chr22:44705818
|
T | C | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3210T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705818 | ||||||
chr22:44705820
|
T | C | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3212T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705820 | ||||||
chr22:44705822
|
A | G | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3214A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705822 | ||||||
chr22:44705832
|
C | G | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3224C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705832 | ||||||
chr22:44705836
|
G | C | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3228G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705836 | ||||||
chr22:44705839
|
G | T | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3231G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705839 | ||||||
chr22:44705858
|
T | C | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3250T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705858 | ||||||
chr22:44705859
|
C | G | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3251C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705859 | ||||||
chr22:44705860
|
A | T | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3252A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705860 | ||||||
chr22:44705865
|
A | T | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3257A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705865 | ||||||
chr22:44705866
|
T | A | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3258T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705866 | ||||||
chr22:44705869
|
C | T | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3261C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705869 | ||||||
chr22:44705870
|
A | C | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3262A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705870 | ||||||
chr22:44705874
|
T | A | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3266T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705874 | ||||||
chr22:44705878
|
C | G | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3270C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705878 | ||||||
chr22:44705880
|
C | T | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3272C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705880 | ||||||
chr22:44705881
|
C | G | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3273C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705881 | ||||||
chr22:44705884
|
C | CGGCTCAG others(8): Show |
1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3276_134+3277i others(17): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705884 | ||||||
chr22:44705910
|
G | C | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3302G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705910 | ||||||
chr22:44705911
|
C | G | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+3303C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705911 | ||||||
chr22:44705931
|
G | A | 35 | a0001c0001t0006g0027a0001c0001t0006g0030a0001c0001t0006g0034others(32): Show | 35 | HG00140.hp1 HG00735.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.134+3323G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705931 | ||||||
chr22:44705936
|
C | T | 1 | a0001c0002t0001g0058 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.134+3328C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44705936 | ||||||
chr22:44706055
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.134+3447C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706055 | ||||||
chr22:44706171
|
G | C | 1 | a0001c0001t0027g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.134+3563G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706171 | ||||||
chr22:44706246
|
CATTG | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0082 | 3 | NA18969.hp1 NA18999.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.134+3654_134+3657d others(6): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44706246 | |||||
chr22:44706262
|
G | C | 21 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(18): Show | 21 | HG00733.hp1 HG00735.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.134+3654G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706262 | ||||||
chr22:44706266
|
C | G | 2 | a0001c0001t0001g0385a0002c0003t0002g0384 | 2 | NA18966.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.134+3658C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706266 | ||||||
chr22:44706682
|
C | T | 30 | a0001c0001t0006g0030a0001c0001t0006g0034a0001c0001t0006g0035others(27): Show | 30 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.134+4074C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706682 | ||||||
chr22:44706700
|
G | C | 1 | a0001c0002t0033g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.134+4092G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706700 | ||||||
chr22:44706845
|
GGAGCTAT others(12): Show |
G | 138 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0278others(135): Show | 149 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.134+4239_134+4257d others(21): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44706845 | |||||
chr22:44706860
|
C | T | 30 | a0001c0001t0006g0030a0001c0001t0006g0034a0001c0001t0006g0035others(27): Show | 30 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.134+4252C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706860 | ||||||
chr22:44706864
|
T | A | 1 | a0001c0004t0004g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.134+4256T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706864 | ||||||
chr22:44706866
|
G | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0278others(135): Show | 149 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.134+4258G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706866 | ||||||
chr22:44706877
|
G | A | 128 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0278others(125): Show | 139 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.134+4269G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706877 | ||||||
chr22:44706879
|
G | C | 1 | a0001c0001t0003g0296 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.134+4271G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706879 | ||||||
chr22:44706946
|
G | T | 1 | a0001c0001t0001g0295 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.134+4338G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706946 | ||||||
chr22:44706951
|
G | C | 2 | a0001c0002t0003g0302a0001c0002t0008g0301 | 2 | HG02965.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.134+4343G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706951 | ||||||
chr22:44706958
|
C | T | 4 | a0001c0001t0006g0027a0001c0002t0005g0021a0001c0002t0010g0019others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.134+4350C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44706958 | ||||||
chr22:44707060
|
C | T | 1 | a0001c0004t0004g0083 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.134+4452C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707060 | ||||||
chr22:44707139
|
C | G | 1 | a0001c0001t0006g0035 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.134+4531C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707139 | ||||||
chr22:44707155
|
G | A | 1 | a0001c0004t0016g0039 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.134+4547G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707155 | ||||||
chr22:44707193
|
G | A | 1 | a0001c0002t0007g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.134+4585G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707193 | ||||||
chr22:44707199
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.134+4591A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707199 | ||||||
chr22:44707386
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.134+4778C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707386 | ||||||
chr22:44707437
|
C | T | 1 | a0001c0002t0001g0383 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.134+4829C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707437 | ||||||
chr22:44707528
|
C | T | 3 | a0001c0001t0006g0034a0001c0002t0009g0004a0001c0002t0022g0004 | 3 | HG01934.hp1 HG02109.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.134+4920C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707528 | ||||||
chr22:44707606
|
C | T | 293 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(290): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.134+4998C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707606 | ||||||
chr22:44707671
|
C | T | 3 | a0001c0001t0001g0260a0001c0002t0005g0261a0002c0003t0002g0259 | 3 | NA18522.hp1 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.134+5063C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707671 | ||||||
chr22:44707755
|
C | A | 106 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0304others(103): Show | 115 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.134+5147C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707755 | ||||||
chr22:44707932
|
T | C | 1 | a0001c0002t0033g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.134+5324T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707932 | ||||||
chr22:44707935
|
G | A | 2 | a0001c0001t0003g0182a0001c0002t0008g0183 | 2 | HG03195.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.134+5327G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44707935 | ||||||
chr22:44708059
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.134+5451C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708059 | ||||||
chr22:44708132
|
G | A | 1 | a0001c0002t0008g0410 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.134+5524G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708132 | ||||||
chr22:44708153
|
A | G | 2 | a0001c0002t0005g0276a0001c0004t0004g0277 | 2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.134+5545A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708153 | ||||||
chr22:44708161
|
C | G | 7 | a0001c0001t0014g0264a0001c0001t0014g0265a0001c0001t0014g0266others(4): Show | 7 | HG02258.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.134+5553C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708161 | ||||||
chr22:44708186
|
C | G | 1 | a0001c0002t0003g0409 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.134+5578C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708186 | ||||||
chr22:44708363
|
G | A | 1 | a0001c0001t0012g0084 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.134+5755G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708363 | ||||||
chr22:44708445
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.134+5837C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708445 | ||||||
chr22:44708468
|
C | T | 30 | a0001c0001t0006g0030a0001c0001t0006g0034a0001c0001t0006g0035others(27): Show | 30 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.134+5860C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708468 | ||||||
chr22:44708486
|
A | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0278others(166): Show | 180 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.134+5878A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708486 | ||||||
chr22:44708491
|
A | T | 1 | a0001c0001t0001g0401 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.134+5883A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708491 | ||||||
chr22:44708670
|
G | A | 3 | a0001c0002t0003g0070a0001c0002t0003g0071a0003c0007t0004g0069 | 3 | HG01243.hp2 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.135-5921G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708670 | ||||||
chr22:44708761
|
G | C | 1 | a0001c0002t0005g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.135-5830G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708761 | ||||||
chr22:44708792
|
C | T | 32 | a0001c0001t0006g0030a0001c0001t0006g0034a0001c0001t0006g0035others(29): Show | 32 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(29): Show |
intron_variant | MODIFIER | c.135-5799C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708792 | ||||||
chr22:44708843
|
T | C | 44 | a0001c0001t0001g0088a0001c0001t0006g0030a0001c0001t0006g0034others(41): Show | 44 | HG00140.hp1 HG00735.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.135-5748T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44708843 | ||||||
chr22:44708966
|
C | CA | 111 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0072others(108): Show | 120 | HG00099.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.135-5598dupA | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44708966 | |||||
chr22:44708966
|
C | CAA | 35 | a0001c0001t0001g0088a0001c0001t0001g0288a0001c0001t0001g0292others(32): Show | 36 | HG00438.hp2 HG00558.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.135-5599_135-5598d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44708966 | |||||
chr22:44708966
|
CA | C | 14 | a0001c0001t0001g0082a0001c0001t0001g0166a0001c0001t0001g0168others(11): Show | 14 | HG01069.hp1 HG01070.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.135-5598delA | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44708966 | |||||
chr22:44708966
|
CAA | C | 7 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0015g0267others(4): Show | 7 | HG02055.hp1 HG02258.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.135-5599_135-5598d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44708966 | |||||
chr22:44708966
|
CAAAAAA | C | 11 | a0001c0001t0006g0040a0001c0001t0006g0041a0001c0001t0006g0042others(8): Show | 11 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.135-5603_135-5598d others(8): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44708966 | |||||
chr22:44708966
|
CAAAAAAA | C | 22 | a0001c0001t0006g0030a0001c0001t0006g0034a0001c0001t0006g0035others(19): Show | 22 | HG01433.hp2 HG01891.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.135-5604_135-5598d others(9): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44708966 | |||||
chr22:44708966
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0416 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.135-5607_135-5598d others(12): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44708966 | |||||
chr22:44708966
|
CAAAAAAA others(4): Show |
C | 111 | a0001c0001t0001g0011a0001c0001t0001g0078a0001c0001t0001g0079others(108): Show | 114 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.135-5608_135-5598d others(13): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44708966 | |||||
chr22:44709036
|
G | A | 1 | a0001c0002t0005g0184 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.135-5555G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709036 | ||||||
chr22:44709079
|
A | AC | 43 | a0001c0001t0001g0088a0001c0001t0006g0030a0001c0001t0006g0034others(40): Show | 43 | HG00140.hp1 HG00735.hp2 HG01168.hp2 others(40): Show |
intron_variant | MODIFIER | c.135-5512_135-5511i others(3): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709079 | ||||||
chr22:44709096
|
C | A | 1 | a0001c0001t0001g0166 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.135-5495C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709096 | ||||||
chr22:44709136
|
C | T | 1 | a0001c0002t0003g0258 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.135-5455C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709136 | ||||||
chr22:44709229
|
C | T | 87 | a0001c0001t0001g0011a0001c0001t0001g0078a0001c0001t0001g0079others(84): Show | 90 | HG00140.hp2 HG00423.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.135-5362C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709229 | ||||||
chr22:44709230
|
G | A | 10 | a0001c0001t0001g0088a0001c0001t0027g0275a0001c0002t0003g0070others(7): Show | 10 | HG01243.hp2 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.135-5361G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709230 | ||||||
chr22:44709403
|
C | T | 2 | a0001c0002t0005g0105a0001c0002t0005g0165 | 2 | HG02129.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.135-5188C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709403 | ||||||
chr22:44709432
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.135-5159G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709432 | ||||||
chr22:44709491
|
C | T | 1 | a0001c0002t0033g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.135-5100C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709491 | ||||||
chr22:44709492
|
T | G | 1 | a0002c0003t0002g0311 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.135-5099T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709492 | ||||||
chr22:44709498
|
C | G | 1 | a0001c0001t0001g0377 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.135-5093C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709498 | ||||||
chr22:44709503
|
G | A | 1 | a0001c0002t0005g0106 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.135-5088G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709503 | ||||||
chr22:44709534
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.135-5057G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709534 | ||||||
chr22:44709622
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.135-4969C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709622 | ||||||
chr22:44709627
|
G | A | 23 | a0001c0001t0001g0066a0001c0001t0001g0187a0001c0001t0001g0195others(20): Show | 23 | HG01168.hp2 HG01433.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.135-4964G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709627 | ||||||
chr22:44709816
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.135-4775C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709816 | ||||||
chr22:44709827
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.135-4764A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709827 | ||||||
chr22:44709838
|
C | T | 2 | a0001c0002t0001g0281a0001c0011t0001g0282 | 2 | HG00609.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.135-4753C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709838 | ||||||
chr22:44709851
|
C | CA | 21 | a0001c0001t0001g0288a0001c0001t0001g0292a0001c0001t0001g0293others(18): Show | 23 | HG00558.hp1 HG01109.hp1 HG02015.hp1 others(20): Show |
intron_variant | MODIFIER | c.135-4733dupA | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44709851 | |||||
chr22:44709881
|
G | A | 1 | a0001c0002t0003g0193 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.135-4710G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44709881 | ||||||
chr22:44710027
|
G | A | 1 | a0001c0002t0001g0108 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.135-4564G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710027 | ||||||
chr22:44710137
|
T | C | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(236): Show | 252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.135-4454T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710137 | ||||||
chr22:44710285
|
AC | A | 220 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(217): Show | 234 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.135-4296delC | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44710285 | |||||
chr22:44710285
|
ACC | A | 59 | a0001c0001t0001g0098a0001c0001t0001g0139a0001c0001t0001g0174others(56): Show | 62 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.135-4297_135-4296d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44710285 | |||||
chr22:44710293
|
C | A | 1 | a0001c0002t0001g0219 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.135-4298C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710293 | ||||||
chr22:44710293
|
C | G | 61 | a0001c0001t0001g0001a0001c0001t0001g0088a0001c0001t0001g0187others(58): Show | 67 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(64): Show |
intron_variant | MODIFIER | c.135-4298C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710293 | ||||||
chr22:44710353
|
C | T | 67 | a0001c0001t0001g0003a0001c0001t0001g0073a0001c0001t0001g0118others(64): Show | 69 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.135-4238C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710353 | ||||||
chr22:44710488
|
A | G | 9 | a0001c0001t0001g0065a0001c0001t0014g0265a0001c0001t0014g0266others(6): Show | 9 | HG01243.hp2 HG02258.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.135-4103A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710488 | ||||||
chr22:44710513
|
G | T | 4 | a0001c0002t0003g0253a0001c0002t0005g0251a0001c0002t0005g0252others(1): Show | 4 | HG01884.hp1 HG01943.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.135-4078G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710513 | ||||||
chr22:44710515
|
C | T | 4 | a0001c0002t0003g0253a0001c0002t0005g0251a0001c0002t0005g0252others(1): Show | 4 | HG01884.hp1 HG01943.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.135-4076C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710515 | ||||||
chr22:44710516
|
T | C | 4 | a0001c0002t0003g0253a0001c0002t0005g0251a0001c0002t0005g0252others(1): Show | 4 | HG01884.hp1 HG01943.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.135-4075T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710516 | ||||||
chr22:44710626
|
AGC | A | 40 | a0001c0001t0001g0001a0001c0001t0001g0191a0001c0001t0001g0278others(37): Show | 46 | HG00408.hp1 HG00609.hp1 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.135-3963_135-3962d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44710626 | |||||
chr22:44710656
|
T | C | 1 | a0002c0003t0002g0117 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.135-3935T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710656 | ||||||
chr22:44710731
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.135-3860G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710731 | ||||||
chr22:44710817
|
G | A | 1 | a0001c0002t0005g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.135-3774G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710817 | ||||||
chr22:44710906
|
G | A | 102 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0051others(99): Show | 105 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.135-3685G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710906 | ||||||
chr22:44710926
|
C | T | 3 | a0001c0001t0001g0342a0001c0001t0001g0343a0001c0004t0004g0344 | 3 | NA18957.hp1 NA18983.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.135-3665C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710926 | ||||||
chr22:44710927
|
G | A | 3 | a0001c0002t0003g0070a0001c0002t0003g0071a0003c0007t0004g0069 | 3 | HG01243.hp2 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.135-3664G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710927 | ||||||
chr22:44710930
|
C | T | 3 | a0001c0001t0001g0260a0001c0002t0005g0261a0002c0003t0002g0259 | 3 | NA18522.hp1 NA19043.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.135-3661C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44710930 | ||||||
chr22:44711101
|
A | C | 5 | a0001c0001t0001g0416a0001c0001t0003g0018a0001c0001t0003g0418others(2): Show | 5 | NA18945.hp2 NA18974.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.135-3490A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711101 | ||||||
chr22:44711102
|
G | C | 5 | a0001c0001t0001g0416a0001c0001t0003g0018a0001c0001t0003g0418others(2): Show | 5 | NA18945.hp2 NA18974.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.135-3489G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711102 | ||||||
chr22:44711114
|
G | C | 1 | a0002c0003t0002g0303 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.135-3477G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711114 | ||||||
chr22:44711140
|
T | C | 229 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(226): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.135-3451T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711140 | ||||||
chr22:44711159
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.135-3432T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711159 | ||||||
chr22:44711190
|
T | C | 1 | a0001c0001t0009g0412 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.135-3401T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711190 | ||||||
chr22:44711245
|
A | G | 234 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(231): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.135-3346A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711245 | ||||||
chr22:44711249
|
G | A | 91 | a0001c0001t0001g0065a0001c0001t0001g0073a0001c0001t0001g0118others(88): Show | 91 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.135-3342G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711249 | ||||||
chr22:44711262
|
C | T | 2 | a0001c0002t0005g0021a0001c0002t0005g0184 | 2 | HG02145.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.135-3329C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711262 | ||||||
chr22:44711357
|
G | T | 1 | a0001c0002t0001g0190 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.135-3234G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711357 | ||||||
chr22:44711380
|
T | C | 416 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(413): Show | 436 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(433): Show |
intron_variant | MODIFIER | c.135-3211T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711380 | ||||||
chr22:44711416
|
G | A | 10 | a0001c0001t0001g0066a0001c0001t0001g0187a0001c0001t0001g0216others(7): Show | 10 | HG01168.hp2 HG01255.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.135-3175G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711416 | ||||||
chr22:44711486
|
A | AG | 11 | a0001c0001t0001g0247a0001c0001t0001g0309a0001c0001t0001g0370others(8): Show | 11 | HG00735.hp2 HG02451.hp2 HG02683.hp1 others(8): Show |
intron_variant | MODIFIER | c.135-3102dupG | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44711486 | |||||
chr22:44711598
|
A | C | 1 | a0001c0002t0003g0071 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.135-2993A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711598 | ||||||
chr22:44711686
|
C | T | 2 | a0001c0002t0001g0058a0001c0002t0005g0129 | 2 | HG01109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.135-2905C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711686 | ||||||
chr22:44711797
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.135-2794C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711797 | ||||||
chr22:44711808
|
C | G | 2 | a0001c0001t0006g0045a0001c0001t0006g0046 | 2 | HG00735.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.135-2783C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711808 | ||||||
chr22:44711846
|
C | G | 1 | a0001c0004t0004g0277 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.135-2745C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711846 | ||||||
chr22:44711928
|
G | A | 4 | a0001c0001t0007g0036a0001c0002t0017g0037a0001c0002t0019g0208others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.135-2663G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711928 | ||||||
chr22:44711979
|
T | C | 4 | a0001c0001t0001g0192a0001c0001t0001g0218a0001c0001t0001g0385others(1): Show | 4 | NA18960.hp2 NA18967.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.135-2612T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711979 | ||||||
chr22:44711998
|
G | C | 1 | a0002c0003t0002g0259 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.135-2593G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44711998 | ||||||
chr22:44712045
|
C | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(167): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.135-2546C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712045 | ||||||
chr22:44712081
|
A | AGG | 6 | a0001c0001t0006g0034a0001c0001t0014g0265a0001c0001t0014g0266others(3): Show | 6 | HG02258.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.135-2507_135-2506d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44712081 | |||||
chr22:44712106
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.135-2485C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712106 | ||||||
chr22:44712135
|
C | T | 5 | a0001c0001t0001g0060a0001c0001t0001g0314a0001c0001t0001g0360others(2): Show | 5 | HG01981.hp2 HG02293.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.135-2456C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712135 | ||||||
chr22:44712204
|
G | T | 1 | a0001c0005t0001g0386 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.135-2387G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712204 | ||||||
chr22:44712312
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(167): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.135-2279A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712312 | ||||||
chr22:44712377
|
C | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(166): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.135-2214C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712377 | ||||||
chr22:44712404
|
T | C | 56 | a0001c0001t0001g0073a0001c0001t0001g0118a0001c0001t0001g0142others(53): Show | 56 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.135-2187T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712404 | ||||||
chr22:44712465
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(165): Show | 180 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.135-2126G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712465 | ||||||
chr22:44712484
|
C | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(62): Show | 73 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.135-2107C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712484 | ||||||
chr22:44712523
|
G | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(166): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.135-2068G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712523 | ||||||
chr22:44712706
|
GCAGCATC others(20): Show |
G | 1 | a0002c0003t0002g0417 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.135-1882_135-1856d others(29): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44712706 | |||||
chr22:44712709
|
G | A | 4 | a0001c0002t0005g0173a0001c0002t0005g0339a0001c0002t0005g0380others(1): Show | 4 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.135-1882G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712709 | ||||||
chr22:44712800
|
C | T | 3 | a0001c0001t0001g0003a0002c0003t0002g0338a0006c0013t0001g0379 | 5 | NA18948.hp2 NA18952.hp1 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.135-1791C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712800 | ||||||
chr22:44712975
|
A | G | 1 | a0001c0001t0001g0377 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.135-1616A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44712975 | ||||||
chr22:44713147
|
C | T | 189 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(186): Show | 193 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.135-1444C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713147 | ||||||
chr22:44713223
|
G | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(147): Show | 162 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.135-1368G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713223 | ||||||
chr22:44713225
|
G | A | 1 | a0001c0004t0004g0345 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.135-1366G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713225 | ||||||
chr22:44713331
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(167): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.135-1260A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713331 | ||||||
chr22:44713413
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(167): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.135-1178G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713413 | ||||||
chr22:44713553
|
G | T | 1 | a0001c0002t0003g0193 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.135-1038G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713553 | ||||||
chr22:44713661
|
C | T | 5 | a0001c0001t0014g0265a0001c0001t0014g0266a0001c0001t0015g0267others(2): Show | 5 | HG02258.hp2 HG02717.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.135-930C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713661 | ||||||
chr22:44713682
|
C | T | 1 | a0001c0002t0006g0049 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.135-909C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713682 | ||||||
chr22:44713690
|
C | T | 10 | a0001c0001t0001g0066a0001c0001t0001g0187a0001c0001t0001g0216others(7): Show | 10 | HG01168.hp2 HG01255.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.135-901C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713690 | ||||||
chr22:44713786
|
C | T | 170 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(167): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.135-805C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713786 | ||||||
chr22:44713843
|
G | A | 1 | a0001c0002t0003g0409 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.135-748G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713843 | ||||||
chr22:44713889
|
T | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0082a0001c0001t0001g0161others(4): Show | 8 | HG00621.hp1 NA18612.hp2 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.135-702T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713889 | ||||||
chr22:44713948
|
C | T | 98 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0050others(95): Show | 102 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.135-643C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44713948 | ||||||
chr22:44714008
|
T | G | 1 | a0001c0002t0009g0413 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.135-583T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44714008 | ||||||
chr22:44714123
|
CAG | C | 175 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(172): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.135-467_135-466del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44714123 | ||||||
chr22:44714194
|
G | A | 4 | a0001c0001t0007g0036a0001c0002t0017g0037a0001c0002t0019g0208others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.135-397G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44714194 | ||||||
chr22:44714261
|
G | T | 1 | a0001c0001t0001g0200 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.135-330G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44714261 | ||||||
chr22:44714403
|
A | G | 6 | a0001c0001t0006g0034a0001c0001t0014g0265a0001c0001t0014g0266others(3): Show | 6 | HG02258.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.135-188A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44714403 | ||||||
chr22:44714483
|
T | TGGCTATC others(13): Show |
1 | a0001c0001t0003g0097 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.135-107_135-88dupG others(19): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr22 | 44714483 | |||||
chr22:44714541
|
G | C | 1 | a0001c0002t0001g0198 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.135-50G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44714541 | ||||||
chr22:44714584
|
C | A | 4 | a0001c0001t0007g0036a0001c0002t0017g0037a0001c0002t0019g0208others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.135-7C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 1/7 | chr22 | 44714584 | ||||||
chr22:44714705
|
T | C | 1 | a0001c0001t0012g0084 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.215+34T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44714705 | ||||||
chr22:44714852
|
T | C | 55 | a0001c0001t0001g0073a0001c0001t0001g0118a0001c0001t0001g0142others(52): Show | 55 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.215+181T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44714852 | ||||||
chr22:44714885
|
T | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(65): Show | 76 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.215+214T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44714885 | ||||||
chr22:44714971
|
G | A | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(59): Show | 70 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.215+300G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44714971 | ||||||
chr22:44714996
|
A | G | 111 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(108): Show | 115 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.215+325A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44714996 | ||||||
chr22:44715101
|
A | G | 1 | a0001c0001t0012g0084 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.215+430A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715101 | ||||||
chr22:44715169
|
G | A | 357 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(354): Show | 373 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(370): Show |
intron_variant | MODIFIER | c.215+498G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715169 | ||||||
chr22:44715225
|
A | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(140): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.215+554A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715225 | ||||||
chr22:44715354
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(140): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.215+683T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715354 | ||||||
chr22:44715397
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(140): Show | 155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.215+726G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715397 | ||||||
chr22:44715440
|
G | A | 55 | a0001c0001t0001g0073a0001c0001t0001g0118a0001c0001t0001g0142others(52): Show | 55 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.215+769G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715440 | ||||||
chr22:44715488
|
A | T | 1 | a0001c0001t0001g0295 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.215+817A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715488 | ||||||
chr22:44715518
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.215+847G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715518 | ||||||
chr22:44715529
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.215+858G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715529 | ||||||
chr22:44715533
|
C | T | 1 | a0002c0003t0002g0156 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.215+862C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715533 | ||||||
chr22:44715631
|
T | G | 2 | a0001c0002t0012g0269a0001c0002t0015g0270 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.215+960T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715631 | ||||||
chr22:44715901
|
A | G | 34 | a0001c0001t0001g0065a0001c0001t0001g0247a0001c0001t0001g0309others(31): Show | 34 | HG00735.hp2 HG02145.hp2 HG02257.hp1 others(31): Show |
intron_variant | MODIFIER | c.215+1230A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715901 | ||||||
chr22:44715959
|
T | A | 1 | a0002c0003t0002g0311 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.215+1288T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44715959 | ||||||
chr22:44716188
|
C | T | 1 | a0001c0001t0003g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.215+1517C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716188 | ||||||
chr22:44716268
|
A | G | 12 | a0001c0001t0001g0404a0001c0001t0018g0132a0001c0002t0005g0021others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.215+1597A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716268 | ||||||
chr22:44716308
|
C | T | 4 | a0001c0001t0001g0241a0001c0001t0003g0242a0001c0001t0003g0243others(1): Show | 4 | NA18960.hp1 NA18979.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.215+1637C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716308 | ||||||
chr22:44716337
|
C | G | 13 | a0001c0001t0001g0065a0001c0001t0006g0034a0001c0001t0007g0036others(10): Show | 13 | HG01109.hp1 HG02258.hp2 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.215+1666C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716337 | ||||||
chr22:44716396
|
T | C | 36 | a0001c0001t0001g0065a0001c0001t0001g0247a0001c0001t0001g0309others(33): Show | 36 | HG00735.hp2 HG01109.hp1 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.215+1725T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716396 | ||||||
chr22:44716426
|
A | G | 36 | a0001c0001t0001g0065a0001c0001t0001g0247a0001c0001t0001g0309others(33): Show | 36 | HG00735.hp2 HG01109.hp1 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.215+1755A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716426 | ||||||
chr22:44716434
|
G | A | 36 | a0001c0001t0001g0065a0001c0001t0001g0247a0001c0001t0001g0309others(33): Show | 36 | HG00735.hp2 HG01109.hp1 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.215+1763G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716434 | ||||||
chr22:44716463
|
G | C | 56 | a0001c0001t0001g0073a0001c0001t0001g0118a0001c0001t0001g0142others(53): Show | 56 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.215+1792G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716463 | ||||||
chr22:44716500
|
C | A | 36 | a0001c0001t0001g0065a0001c0001t0001g0247a0001c0001t0001g0309others(33): Show | 36 | HG00735.hp2 HG01109.hp1 HG02145.hp2 others(33): Show |
intron_variant | MODIFIER | c.215+1829C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716500 | ||||||
chr22:44716640
|
G | A | 1 | a0001c0002t0001g0229 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.215+1969G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716640 | ||||||
chr22:44716649
|
T | C | 1 | a0001c0001t0001g0316 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.215+1978T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716649 | ||||||
chr22:44716750
|
G | C | 2 | a0001c0001t0014g0265a0001c0001t0014g0266 | 2 | HG02717.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.215+2079G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716750 | ||||||
chr22:44716827
|
G | A | 1 | a0001c0001t0001g0317 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.215+2156G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716827 | ||||||
chr22:44716847
|
G | A | 1 | a0001c0005t0001g0226 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.215+2176G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716847 | ||||||
chr22:44716874
|
A | C | 1 | a0001c0001t0003g0056 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.215+2203A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716874 | ||||||
chr22:44716921
|
G | A | 1 | a0001c0004t0004g0220 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.215+2250G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716921 | ||||||
chr22:44716976
|
CAT | C | 7 | a0001c0001t0001g0066a0001c0001t0001g0187a0001c0001t0001g0216others(4): Show | 7 | HG01168.hp2 HG01433.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.215+2306_215+2307d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44716976 | ||||||
chr22:44717083
|
T | C | 92 | a0001c0001t0001g0065a0001c0001t0001g0073a0001c0001t0001g0118others(89): Show | 92 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.215+2412T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717083 | ||||||
chr22:44717189
|
C | CT | 253 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(250): Show | 269 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(266): Show |
intron_variant | MODIFIER | c.215+2537dupT | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44717189 | |||||
chr22:44717189
|
C | CTT | 25 | a0001c0001t0001g0065a0001c0001t0001g0116a0001c0001t0001g0341others(22): Show | 26 | HG01106.hp2 HG01243.hp2 HG02135.hp1 others(23): Show |
intron_variant | MODIFIER | c.215+2536_215+2537d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44717189 | |||||
chr22:44717189
|
C | CTTT | 9 | a0001c0001t0001g0309a0001c0001t0001g0370a0001c0001t0006g0046others(6): Show | 9 | HG00735.hp2 HG03453.hp2 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.215+2535_215+2537d others(5): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44717189 | |||||
chr22:44717193
|
TTTTTTTT others(517): Show |
T | 1 | a0001c0004t0004g0110 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.215+2538_215+3061d others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44717193 | |||||
chr22:44717206
|
T | TG | 3 | a0001c0001t0018g0132a0001c0002t0012g0133a0001c0002t0023g0134 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.215+2535_215+2536i others(3): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717206 | ||||||
chr22:44717271
|
G | A | 63 | a0001c0001t0001g0065a0001c0001t0001g0073a0001c0001t0001g0118others(60): Show | 63 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.215+2600G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717271 | ||||||
chr22:44717308
|
C | G | 1 | a0001c0001t0014g0264 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.215+2637C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717308 | ||||||
chr22:44717309
|
G | A | 1 | a0001c0001t0001g0373 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.215+2638G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717309 | ||||||
chr22:44717371
|
T | C | 2 | a0001c0002t0005g0173a0001c0004t0004g0135 | 2 | HG01070.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.215+2700T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717371 | ||||||
chr22:44717374
|
T | C | 1 | a0001c0001t0001g0318 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.215+2703T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717374 | ||||||
chr22:44717381
|
G | C | 1 | a0001c0001t0003g0097 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.215+2710G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717381 | ||||||
chr22:44717407
|
G | T | 1 | a0001c0001t0014g0264 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.215+2736G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717407 | ||||||
chr22:44717533
|
C | A | 5 | a0001c0001t0001g0088a0001c0002t0008g0086a0001c0002t0008g0090others(2): Show | 5 | HG02280.hp1 HG02622.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.215+2862C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717533 | ||||||
chr22:44717538
|
C | T | 30 | a0001c0001t0001g0065a0001c0001t0001g0247a0001c0001t0001g0309others(27): Show | 30 | HG00735.hp2 HG02145.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.215+2867C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717538 | ||||||
chr22:44717564
|
A | G | 30 | a0001c0001t0001g0065a0001c0001t0001g0247a0001c0001t0001g0309others(27): Show | 30 | HG00735.hp2 HG02145.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.215+2893A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717564 | ||||||
chr22:44717574
|
G | T | 30 | a0001c0001t0001g0065a0001c0001t0001g0247a0001c0001t0001g0309others(27): Show | 30 | HG00735.hp2 HG02145.hp2 HG02257.hp1 others(27): Show |
intron_variant | MODIFIER | c.215+2903G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717574 | ||||||
chr22:44717621
|
A | G | 1 | a0002c0003t0002g0384 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.215+2950A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717621 | ||||||
chr22:44717654
|
C | T | 4 | a0001c0001t0007g0036a0001c0002t0017g0037a0001c0002t0019g0208others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.215+2983C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717654 | ||||||
chr22:44717666
|
AG | A | 6 | a0001c0001t0007g0036a0001c0002t0001g0058a0001c0002t0005g0129others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+2996delG | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717666 | ||||||
chr22:44717687
|
G | A | 1 | a0001c0004t0004g0345 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.215+3016G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717687 | ||||||
chr22:44717697
|
G | A | 167 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(164): Show | 172 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.215+3026G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717697 | ||||||
chr22:44717700
|
T | C | 356 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(353): Show | 372 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(369): Show |
intron_variant | MODIFIER | c.215+3029T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717700 | ||||||
chr22:44717717
|
C | CT | 10 | a0001c0001t0001g0309a0001c0001t0001g0350a0001c0001t0001g0370others(7): Show | 10 | HG01109.hp1 HG01168.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.215+3062dupT | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44717717 | |||||
chr22:44717717
|
CT | C | 11 | a0001c0001t0001g0051a0001c0001t0001g0174a0001c0001t0003g0097others(8): Show | 11 | HG01099.hp2 HG02129.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.215+3062delT | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44717717 | |||||
chr22:44717773
|
A | G | 1 | a0001c0001t0001g0104 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.215+3102A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717773 | ||||||
chr22:44717799
|
C | T | 1 | a0001c0004t0004g0240 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.215+3128C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717799 | ||||||
chr22:44717851
|
G | A | 6 | a0001c0001t0001g0310a0001c0001t0001g0361a0001c0001t0001g0382others(3): Show | 6 | HG00621.hp2 HG02056.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+3180G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717851 | ||||||
chr22:44717874
|
A | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(162): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.215+3203A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717874 | ||||||
chr22:44717876
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(162): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.215+3205C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717876 | ||||||
chr22:44717888
|
T | G | 1 | a0001c0001t0027g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.215+3217T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717888 | ||||||
chr22:44717953
|
G | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(132): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.215+3282G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717953 | ||||||
chr22:44717964
|
C | T | 1 | a0001c0004t0004g0263 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.215+3293C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717964 | ||||||
chr22:44717995
|
G | A | 16 | a0001c0001t0001g0116a0001c0001t0003g0056a0001c0001t0006g0030others(13): Show | 16 | HG01106.hp2 HG01243.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.215+3324G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44717995 | ||||||
chr22:44718014
|
C | T | 1 | a0001c0001t0003g0378 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.215+3343C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718014 | ||||||
chr22:44718024
|
C | T | 1 | a0002c0003t0002g0332 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.215+3353C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718024 | ||||||
chr22:44718042
|
A | G | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(162): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.215+3371A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718042 | ||||||
chr22:44718052
|
A | G | 6 | a0001c0001t0007g0036a0001c0002t0001g0058a0001c0002t0005g0129others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+3381A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718052 | ||||||
chr22:44718161
|
A | G | 7 | a0001c0001t0001g0397a0001c0001t0001g0399a0001c0002t0001g0016others(4): Show | 8 | HG00738.hp1 HG01192.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.215+3490A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718161 | ||||||
chr22:44718192
|
C | CT | 128 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(125): Show | 132 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.215+3541dupT | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718192 | |||||
chr22:44718192
|
C | CTT | 59 | a0001c0001t0001g0007a0001c0001t0001g0073a0001c0001t0001g0081others(56): Show | 60 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.215+3540_215+3541d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718192 | |||||
chr22:44718192
|
C | CTTTT | 6 | a0001c0001t0001g0391a0001c0001t0012g0084a0001c0004t0004g0356others(3): Show | 6 | HG01256.hp2 HG01943.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+3538_215+3541d others(6): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718192 | |||||
chr22:44718192
|
C | CTTTTT | 54 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0066others(51): Show | 62 | HG00408.hp1 HG00597.hp2 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.215+3537_215+3541d others(7): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718192 | |||||
chr22:44718192
|
C | CTTTTTT | 66 | a0001c0001t0001g0011a0001c0001t0001g0060a0001c0001t0001g0113others(63): Show | 69 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.215+3536_215+3541d others(8): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718192 | |||||
chr22:44718192
|
C | CTTTTTTT | 12 | a0001c0001t0001g0050a0001c0001t0001g0065a0001c0001t0001g0104others(9): Show | 12 | HG02258.hp2 HG02818.hp1 HG03486.hp1 others(9): Show |
intron_variant | MODIFIER | c.215+3535_215+3541d others(9): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718192 | |||||
chr22:44718192
|
C | CTTTTTTT others(1): Show |
14 | a0001c0001t0001g0168a0001c0001t0001g0247a0001c0001t0001g0309others(11): Show | 14 | HG00735.hp2 HG01167.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.215+3534_215+3541d others(10): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718192 | |||||
chr22:44718192
|
C | CTTTTTTT others(2): Show |
10 | a0001c0001t0001g0370a0001c0001t0001g0404a0001c0001t0006g0034others(7): Show | 10 | HG02572.hp2 HG02886.hp1 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.215+3533_215+3541d others(11): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718192 | |||||
chr22:44718192
|
C | CTTTTTTT others(3): Show |
1 | a0001c0002t0010g0405 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.215+3532_215+3541d others(12): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718192 | |||||
chr22:44718297
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(162): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.215+3626C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718297 | ||||||
chr22:44718342
|
G | A | 1 | a0001c0006t0001g0274 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.215+3671G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718342 | ||||||
chr22:44718440
|
C | T | 1 | a0001c0001t0009g0412 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.215+3769C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718440 | ||||||
chr22:44718637
|
AG | A | 166 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(163): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.215+3968delG | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44718637 | |||||
chr22:44718749
|
G | A | 6 | a0001c0001t0007g0036a0001c0002t0001g0058a0001c0002t0005g0129others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+4078G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718749 | ||||||
chr22:44718962
|
C | T | 1 | a0001c0001t0006g0034 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.215+4291C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718962 | ||||||
chr22:44718968
|
C | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(162): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.215+4297C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44718968 | ||||||
chr22:44719089
|
C | CT | 167 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(164): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.215+4433dupT | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44719089 | |||||
chr22:44719089
|
C | CTTT | 6 | a0001c0001t0007g0036a0001c0002t0001g0058a0001c0002t0005g0129others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+4431_215+4433d others(5): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44719089 | |||||
chr22:44719120
|
G | A | 3 | a0001c0001t0001g0055a0001c0001t0001g0245a0001c0001t0001g0363 | 3 | HG01261.hp2 HG01515.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.215+4449G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719120 | ||||||
chr22:44719142
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(162): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.215+4471T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719142 | ||||||
chr22:44719145
|
A | G | 2 | a0001c0001t0001g0107a0001c0001t0001g0128 | 2 | HG03704.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.215+4474A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719145 | ||||||
chr22:44719153
|
C | G | 1 | a0001c0001t0001g0127 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.215+4482C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719153 | ||||||
chr22:44719160
|
G | A | 1 | a0001c0004t0004g0364 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.215+4489G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719160 | ||||||
chr22:44719167
|
C | A | 7 | a0001c0001t0001g0065a0001c0001t0006g0034a0001c0001t0014g0265others(4): Show | 7 | HG02258.hp2 HG02717.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.215+4496C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719167 | ||||||
chr22:44719240
|
T | C | 6 | a0001c0001t0007g0036a0001c0002t0001g0058a0001c0002t0005g0129others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+4569T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719240 | ||||||
chr22:44719246
|
AT | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(169): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.215+4585delT | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44719246 | |||||
chr22:44719248
|
T | A | 1 | a0001c0001t0014g0264 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.215+4577T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719248 | ||||||
chr22:44719499
|
T | C | 1 | a0001c0001t0014g0264 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.215+4828T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719499 | ||||||
chr22:44719519
|
A | G | 39 | a0001c0001t0001g0116a0001c0001t0001g0247a0001c0001t0001g0309others(36): Show | 39 | HG00735.hp2 HG01106.hp2 HG01243.hp2 others(36): Show |
intron_variant | MODIFIER | c.215+4848A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719519 | ||||||
chr22:44719534
|
G | A | 6 | a0001c0001t0007g0036a0001c0002t0001g0058a0001c0002t0005g0129others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+4863G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719534 | ||||||
chr22:44719538
|
G | A | 3 | a0001c0001t0001g0197a0001c0001t0001g0271a0001c0002t0001g0207 | 3 | HG00099.hp1 HG03239.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.215+4867G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719538 | ||||||
chr22:44719544
|
G | A | 6 | a0001c0001t0007g0036a0001c0002t0001g0058a0001c0002t0005g0129others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+4873G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719544 | ||||||
chr22:44719604
|
G | A | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(139): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.215+4933G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719604 | ||||||
chr22:44719617
|
G | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(139): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.215+4946G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719617 | ||||||
chr22:44719652
|
T | C | 142 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(139): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.215+4981T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719652 | ||||||
chr22:44719671
|
T | C | 6 | a0001c0001t0007g0036a0001c0002t0001g0058a0001c0002t0005g0129others(3): Show | 6 | HG01109.hp1 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.215+5000T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719671 | ||||||
chr22:44719699
|
A | G | 357 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(354): Show | 373 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(370): Show |
intron_variant | MODIFIER | c.215+5028A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719699 | ||||||
chr22:44719871
|
GCAAACCC others(11): Show |
G | 1 | a0001c0002t0005g0285 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.215+5201_215+5218d others(20): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719871 | ||||||
chr22:44719877
|
C | T | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(178): Show | 192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.215+5206C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44719877 | ||||||
chr22:44720024
|
G | A | 175 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(172): Show | 180 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.216-5220G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720024 | ||||||
chr22:44720076
|
C | G | 1 | a0001c0002t0008g0086 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.216-5168C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720076 | ||||||
chr22:44720168
|
C | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(131): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.216-5076C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720168 | ||||||
chr22:44720247
|
G | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(131): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.216-4997G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720247 | ||||||
chr22:44720287
|
C | T | 3 | a0001c0001t0018g0132a0001c0002t0012g0133a0001c0002t0023g0134 | 3 | HG02647.hp2 HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.216-4957C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720287 | ||||||
chr22:44720290
|
G | A | 76 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0060others(73): Show | 79 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.216-4954G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720290 | ||||||
chr22:44720291
|
G | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(131): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.216-4953G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720291 | ||||||
chr22:44720311
|
C | T | 167 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(164): Show | 172 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.216-4933C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720311 | ||||||
chr22:44720323
|
A | G | 342 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(339): Show | 358 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.216-4921A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720323 | ||||||
chr22:44720364
|
C | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(131): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.216-4880C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720364 | ||||||
chr22:44720561
|
A | G | 169 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(166): Show | 174 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.216-4683A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720561 | ||||||
chr22:44720570
|
G | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(131): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.216-4674G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720570 | ||||||
chr22:44720608
|
C | T | 1 | a0001c0002t0033g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.216-4636C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720608 | ||||||
chr22:44720614
|
G | A | 356 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(353): Show | 372 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(369): Show |
intron_variant | MODIFIER | c.216-4630G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720614 | ||||||
chr22:44720727
|
T | C | 2 | a0001c0002t0001g0058a0001c0002t0005g0129 | 2 | HG01109.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.216-4517T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720727 | ||||||
chr22:44720727
|
T | G | 4 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0053others(1): Show | 4 | HG00323.hp2 HG01099.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-4517T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720727 | ||||||
chr22:44720784
|
T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(144): Show | 158 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.216-4460T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720784 | ||||||
chr22:44720814
|
C | T | 1 | a0001c0001t0003g0418 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.216-4430C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720814 | ||||||
chr22:44720920
|
A | G | 315 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(312): Show | 331 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(328): Show |
intron_variant | MODIFIER | c.216-4324A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720920 | ||||||
chr22:44720982
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.216-4262G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44720982 | ||||||
chr22:44721097
|
C | A | 55 | a0001c0001t0001g0007a0001c0001t0001g0073a0001c0001t0001g0118others(52): Show | 56 | HG00438.hp1 HG00609.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.216-4147C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721097 | ||||||
chr22:44721099
|
G | A | 3 | a0001c0002t0003g0253a0001c0002t0005g0251a0001c0002t0005g0252 | 3 | HG01884.hp1 HG01943.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.216-4145G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721099 | ||||||
chr22:44721099
|
G | T | 3 | a0001c0004t0004g0263a0001c0004t0004g0340a0001c0004t0004g0381 | 3 | HG02809.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.216-4145G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721099 | ||||||
chr22:44721248
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.216-3996G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721248 | ||||||
chr22:44721298
|
C | G | 140 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(137): Show | 151 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.216-3946C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721298 | ||||||
chr22:44721423
|
C | T | 4 | a0001c0001t0001g0241a0001c0001t0003g0242a0001c0001t0003g0243others(1): Show | 4 | NA18960.hp1 NA18979.hp1 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-3821C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721423 | ||||||
chr22:44721551
|
G | A | 1 | a0001c0009t0001g0111 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.216-3693G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721551 | ||||||
chr22:44721554
|
T | C | 282 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(279): Show | 295 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(292): Show |
intron_variant | MODIFIER | c.216-3690T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721554 | ||||||
chr22:44721676
|
C | A | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(107): Show | 113 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.216-3568C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721676 | ||||||
chr22:44721679
|
C | G | 4 | a0001c0001t0001g0310a0001c0001t0001g0382a0001c0002t0005g0231others(1): Show | 4 | NA18944.hp1 NA18973.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-3565C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721679 | ||||||
chr22:44721714
|
T | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(219): Show | 235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.216-3530T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721714 | ||||||
chr22:44721749
|
C | G | 94 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0009others(91): Show | 97 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.216-3495C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721749 | ||||||
chr22:44721750
|
G | A | 1 | a0007c0016t0001g0138 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.216-3494G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721750 | ||||||
chr22:44721760
|
C | A | 1 | a0001c0001t0001g0009 | 2 | NA19004.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.216-3484C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721760 | ||||||
chr22:44721917
|
G | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(283): Show | 301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.216-3327G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721917 | ||||||
chr22:44721993
|
T | A | 1 | a0001c0001t0001g0315 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.216-3251T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44721993 | ||||||
chr22:44722022
|
C | T | 1 | a0001c0001t0001g0099 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.216-3222C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722022 | ||||||
chr22:44722037
|
G | A | 1 | a0001c0001t0024g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.216-3207G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722037 | ||||||
chr22:44722073
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0315 | 2 | HG00099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.216-3171C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722073 | ||||||
chr22:44722086
|
G | A | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.216-3158G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722086 | ||||||
chr22:44722183
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.216-3061G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722183 | ||||||
chr22:44722239
|
T | C | 1 | a0002c0003t0002g0100 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.216-3005T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722239 | ||||||
chr22:44722401
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.216-2843C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722401 | ||||||
chr22:44722435
|
G | A | 1 | a0001c0002t0017g0037 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.216-2809G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722435 | ||||||
chr22:44722653
|
T | G | 107 | a0001c0001t0001g0009a0001c0001t0001g0078a0001c0001t0001g0079others(104): Show | 110 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.216-2591T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722653 | ||||||
chr22:44722670
|
T | A | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0007others(323): Show | 343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.216-2574T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722670 | ||||||
chr22:44722744
|
G | T | 105 | a0001c0001t0001g0009a0001c0001t0001g0078a0001c0001t0001g0079others(102): Show | 108 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.216-2500G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722744 | ||||||
chr22:44722767
|
T | C | 128 | a0001c0001t0001g0009a0001c0001t0001g0078a0001c0001t0001g0079others(125): Show | 132 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.216-2477T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722767 | ||||||
chr22:44722948
|
G | A | 1 | a0001c0001t0001g0200 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.216-2296G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722948 | ||||||
chr22:44722983
|
C | T | 1 | a0001c0002t0005g0085 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.216-2261C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44722983 | ||||||
chr22:44722988
|
CT | C | 76 | a0001c0001t0001g0007a0001c0001t0001g0075a0001c0001t0001g0079others(73): Show | 78 | HG00438.hp1 HG00438.hp2 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.216-2241delT | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44722988 | |||||
chr22:44722988
|
CTT | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(110): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.216-2242_216-2241d others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44722988 | |||||
chr22:44723048
|
C | T | 64 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0113others(61): Show | 66 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.216-2196C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723048 | ||||||
chr22:44723054
|
C | G | 127 | a0001c0001t0001g0009a0001c0001t0001g0078a0001c0001t0001g0079others(124): Show | 131 | HG00323.hp1 HG00408.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.216-2190C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723054 | ||||||
chr22:44723059
|
C | T | 1 | a0001c0002t0005g0369 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.216-2185C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723059 | ||||||
chr22:44723078
|
C | T | 1 | a0001c0001t0007g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.216-2166C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723078 | ||||||
chr22:44723143
|
G | A | 53 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0113others(50): Show | 55 | HG00438.hp1 HG00438.hp2 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.216-2101G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723143 | ||||||
chr22:44723164
|
TTAG | T | 4 | a0001c0001t0001g0146a0001c0001t0001g0164a0001c0001t0001g0177others(1): Show | 4 | HG00558.hp2 NA18959.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.216-2076_216-2074d others(5): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr22 | 44723164 | |||||
chr22:44723203
|
C | T | 1 | a0001c0001t0027g0275 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.216-2041C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723203 | ||||||
chr22:44723317
|
G | A | 3 | a0001c0002t0008g0086a0001c0002t0008g0090a0001c0002t0008g0091 | 3 | HG02280.hp1 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.216-1927G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723317 | ||||||
chr22:44723421
|
A | G | 1 | a0001c0001t0006g0414 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.216-1823A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723421 | ||||||
chr22:44723437
|
G | T | 1 | a0001c0002t0005g0285 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.216-1807G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723437 | ||||||
chr22:44723458
|
G | A | 5 | a0001c0001t0006g0035a0001c0001t0007g0024a0001c0001t0007g0033others(2): Show | 5 | HG01109.hp2 HG01433.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.216-1786G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723458 | ||||||
chr22:44723523
|
C | G | 1 | a0001c0002t0005g0185 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.216-1721C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723523 | ||||||
chr22:44723551
|
C | G | 15 | a0001c0001t0001g0404a0001c0001t0003g0077a0001c0001t0014g0264others(12): Show | 15 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.216-1693C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723551 | ||||||
chr22:44723592
|
C | T | 1 | a0001c0004t0016g0028 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.216-1652C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723592 | ||||||
chr22:44723593
|
G | T | 2 | a0001c0004t0004g0010a0001c0004t0004g0204 | 3 | HG00642.hp2 HG01175.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.216-1651G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723593 | ||||||
chr22:44723674
|
C | T | 11 | a0001c0001t0001g0195a0001c0001t0003g0182a0001c0001t0003g0194others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.216-1570C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723674 | ||||||
chr22:44723779
|
G | A | 114 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(111): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.216-1465G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723779 | ||||||
chr22:44723801
|
A | G | 2 | a0002c0003t0002g0064a0002c0003t0002g0256 | 2 | NA19003.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.216-1443A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44723801 | ||||||
chr22:44724019
|
T | C | 1 | a0001c0015t0031g0359 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.216-1225T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724019 | ||||||
chr22:44724048
|
G | A | 15 | a0001c0001t0001g0404a0001c0001t0003g0077a0001c0001t0014g0264others(12): Show | 15 | HG02257.hp1 HG02486.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.216-1196G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724048 | ||||||
chr22:44724080
|
T | G | 1 | a0001c0001t0001g0318 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.216-1164T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724080 | ||||||
chr22:44724102
|
C | T | 1 | a0001c0001t0006g0034 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.216-1142C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724102 | ||||||
chr22:44724320
|
C | T | 1 | a0001c0004t0004g0368 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.216-924C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724320 | ||||||
chr22:44724333
|
G | A | 1 | a0001c0002t0005g0403 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.216-911G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724333 | ||||||
chr22:44724424
|
A | C | 1 | a0002c0003t0002g0286 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.216-820A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724424 | ||||||
chr22:44724490
|
T | C | 1 | a0002c0003t0002g0286 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.216-754T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724490 | ||||||
chr22:44724491
|
C | T | 1 | a0002c0003t0002g0286 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.216-753C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724491 | ||||||
chr22:44724492
|
T | G | 1 | a0002c0003t0002g0286 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.216-752T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724492 | ||||||
chr22:44724543
|
G | A | 10 | a0001c0001t0001g0142a0001c0001t0001g0278a0001c0002t0001g0210others(7): Show | 10 | HG00609.hp1 HG00673.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.216-701G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724543 | ||||||
chr22:44724625
|
A | G | 1 | a0001c0002t0005g0285 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.216-619A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724625 | ||||||
chr22:44724719
|
T | C | 4 | a0001c0001t0003g0186a0001c0001t0014g0265a0001c0004t0004g0137others(1): Show | 4 | HG01168.hp1 HG02683.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.216-525T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724719 | ||||||
chr22:44724758
|
A | G | 2 | a0001c0001t0001g0088a0001c0002t0017g0037 | 2 | HG02886.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.216-486A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724758 | ||||||
chr22:44724769
|
T | A | 1 | a0001c0002t0005g0285 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.216-475T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44724769 | ||||||
chr22:44725058
|
C | G | 15 | a0001c0002t0001g0058a0001c0002t0005g0067a0001c0002t0005g0068others(12): Show | 15 | HG01109.hp1 HG01496.hp2 HG01934.hp1 others(12): Show |
intron_variant | MODIFIER | c.216-186C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44725058 | ||||||
chr22:44725070
|
G | C | 1 | a0001c0002t0005g0285 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.216-174G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 2/7 | chr22 | 44725070 | ||||||
chr22:44725548
|
G | A | 50 | a0001c0001t0001g0009a0001c0001t0001g0055a0001c0001t0001g0078others(47): Show | 51 | HG00408.hp2 HG00423.hp1 HG01255.hp2 others(48): Show |
intron_variant | MODIFIER | c.264+256G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44725548 | ||||||
chr22:44725627
|
C | T | 1 | a0001c0002t0001g0058 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.264+335C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44725627 | ||||||
chr22:44725659
|
T | TTTG | 88 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0001g0161others(85): Show | 92 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.264+389_264+391dup others(3): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr22 | 44725659 | |||||
chr22:44725659
|
TTTGTTG | T | 4 | a0001c0001t0015g0268a0001c0002t0003g0302a0001c0002t0007g0022others(1): Show | 4 | HG01891.hp1 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.264+386_264+391del others(6): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr22 | 44725659 | |||||
chr22:44725917
|
A | G | 328 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(325): Show | 346 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.264+625A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44725917 | ||||||
chr22:44725940
|
C | T | 3 | a0001c0002t0003g0258a0001c0002t0005g0252a0001c0002t0023g0134 | 3 | HG01943.hp1 HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.265-637C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44725940 | ||||||
chr22:44725945
|
G | A | 36 | a0001c0001t0001g0009a0001c0001t0001g0055a0001c0001t0001g0078others(33): Show | 37 | HG00408.hp2 HG00423.hp1 HG02015.hp2 others(34): Show |
intron_variant | MODIFIER | c.265-632G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44725945 | ||||||
chr22:44725957
|
G | A | 1 | a0001c0008t0001g0279 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.265-620G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44725957 | ||||||
chr22:44725961
|
G | A | 2 | a0001c0001t0001g0088a0001c0002t0005g0254 | 2 | HG02886.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.265-616G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44725961 | ||||||
chr22:44725984
|
T | C | 346 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(343): Show | 365 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(362): Show |
intron_variant | MODIFIER | c.265-593T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44725984 | ||||||
chr22:44725999
|
G | C | 1 | a0001c0002t0001g0080 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.265-578G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44725999 | ||||||
chr22:44726001
|
C | G | 342 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(339): Show | 360 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(357): Show |
intron_variant | MODIFIER | c.265-576C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44726001 | ||||||
chr22:44726034
|
A | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(174): Show | 189 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.265-543A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44726034 | ||||||
chr22:44726097
|
A | G | 14 | a0001c0001t0006g0027a0001c0001t0018g0057a0001c0002t0001g0058others(11): Show | 14 | HG01109.hp1 HG01934.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.265-480A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44726097 | ||||||
chr22:44726184
|
G | A | 1 | a0001c0001t0003g0077 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.265-393G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44726184 | ||||||
chr22:44726196
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.265-381T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44726196 | ||||||
chr22:44726379
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.265-198C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 3/7 | chr22 | 44726379 | ||||||
chr22:44726657
|
C | T | 1 | a0001c0002t0012g0269 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.322+23C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44726657 | ||||||
chr22:44726696
|
T | C | 5 | a0001c0001t0009g0412a0001c0001t0014g0266a0001c0002t0005g0185others(2): Show | 5 | HG02717.hp1 HG02895.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.322+62T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44726696 | ||||||
chr22:44726767
|
C | T | 1 | a0001c0001t0003g0077 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.322+133C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44726767 | ||||||
chr22:44726835
|
C | T | 1 | a0001c0002t0005g0261 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.322+201C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44726835 | ||||||
chr22:44726881
|
C | G | 1 | a0001c0001t0001g0181 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.322+247C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44726881 | ||||||
chr22:44726904
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.322+270C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44726904 | ||||||
chr22:44726986
|
C | G | 327 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(324): Show | 346 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.322+352C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44726986 | ||||||
chr22:44727126
|
A | G | 1 | a0001c0012t0004g0372 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.322+492A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727126 | ||||||
chr22:44727140
|
G | A | 1 | a0001c0001t0001g0342 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.322+506G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727140 | ||||||
chr22:44727155
|
CA | C | 8 | a0001c0001t0006g0045a0001c0001t0006g0046a0001c0001t0006g0414others(5): Show | 8 | HG00280.hp2 HG00735.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.322+522delA | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727155 | ||||||
chr22:44727161
|
T | C | 1 | a0001c0002t0033g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.322+527T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727161 | ||||||
chr22:44727161
|
T | G | 7 | a0001c0001t0006g0045a0001c0001t0006g0046a0001c0001t0006g0414others(4): Show | 7 | HG00280.hp2 HG00735.hp2 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.322+527T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727161 | ||||||
chr22:44727204
|
A | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(132): Show | 147 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.322+570A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727204 | ||||||
chr22:44727210
|
T | C | 1 | a0001c0002t0008g0410 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.322+576T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727210 | ||||||
chr22:44727228
|
C | T | 1 | a0002c0003t0002g0248 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.322+594C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727228 | ||||||
chr22:44727238
|
C | T | 2 | a0001c0001t0003g0294a0001c0005t0001g0015 | 3 | HG02071.hp1 NA18984.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.322+604C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727238 | ||||||
chr22:44727304
|
G | A | 3 | a0001c0002t0005g0129a0001c0002t0005g0276a0001c0004t0004g0206 | 3 | HG02647.hp1 HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.322+670G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727304 | ||||||
chr22:44727335
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.322+701C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727335 | ||||||
chr22:44727339
|
G | A | 1 | a0001c0001t0001g0397 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.322+705G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727339 | ||||||
chr22:44727370
|
G | T | 1 | a0001c0001t0003g0170 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.322+736G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727370 | ||||||
chr22:44727480
|
G | T | 1 | a0001c0001t0001g0350 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.322+846G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727480 | ||||||
chr22:44727536
|
G | A | 6 | a0001c0002t0003g0193a0001c0002t0003g0253a0001c0002t0003g0302others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.322+902G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727536 | ||||||
chr22:44727601
|
C | T | 3 | a0001c0001t0006g0034a0001c0004t0004g0263a0001c0004t0016g0028 | 3 | HG02622.hp1 HG02809.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.322+967C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727601 | ||||||
chr22:44727623
|
G | C | 57 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(54): Show | 60 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.322+989G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727623 | ||||||
chr22:44727673
|
C | T | 10 | a0001c0002t0008g0086a0001c0002t0008g0087a0001c0002t0008g0090others(7): Show | 10 | HG01934.hp1 HG02109.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.322+1039C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727673 | ||||||
chr22:44727685
|
C | G | 1 | a0001c0001t0003g0294 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.322+1051C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727685 | ||||||
chr22:44727745
|
G | A | 45 | a0001c0001t0001g0241a0001c0001t0001g0260a0001c0001t0003g0013others(42): Show | 46 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.322+1111G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727745 | ||||||
chr22:44727800
|
C | A | 1 | a0001c0002t0026g0061 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.322+1166C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727800 | ||||||
chr22:44727812
|
A | G | 4 | a0001c0002t0001g0016a0001c0002t0001g0080a0001c0002t0001g0395others(1): Show | 5 | HG01257.hp2 HG01258.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.322+1178A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727812 | ||||||
chr22:44727866
|
C | G | 51 | a0001c0001t0001g0241a0001c0001t0001g0260a0001c0001t0003g0013others(48): Show | 52 | HG00558.hp1 HG00597.hp2 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.322+1232C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727866 | ||||||
chr22:44727874
|
C | T | 1 | a0001c0002t0001g0246 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.322+1240C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727874 | ||||||
chr22:44727926
|
C | T | 1 | a0001c0002t0005g0276 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.322+1292C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727926 | ||||||
chr22:44727961
|
C | G | 389 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(386): Show | 409 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(406): Show |
intron_variant | MODIFIER | c.322+1327C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727961 | ||||||
chr22:44727994
|
G | A | 4 | a0001c0002t0001g0016a0001c0002t0001g0080a0001c0002t0001g0395others(1): Show | 5 | HG01257.hp2 HG01258.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.322+1360G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44727994 | ||||||
chr22:44728093
|
G | A | 1 | a0001c0002t0005g0102 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.322+1459G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728093 | ||||||
chr22:44728097
|
G | C | 169 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(166): Show | 176 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.322+1463G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728097 | ||||||
chr22:44728099
|
C | T | 1 | a0002c0003t0002g0291 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.322+1465C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728099 | ||||||
chr22:44728156
|
A | G | 168 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(165): Show | 175 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.322+1522A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728156 | ||||||
chr22:44728283
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.322+1649G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728283 | ||||||
chr22:44728415
|
A | C | 155 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(152): Show | 162 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.322+1781A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728415 | ||||||
chr22:44728470
|
C | T | 91 | a0001c0001t0001g0348a0001c0001t0001g0361a0001c0001t0003g0109others(88): Show | 94 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.322+1836C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728470 | ||||||
chr22:44728471
|
G | A | 2 | a0001c0001t0014g0266a0001c0002t0026g0061 | 2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.322+1837G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728471 | ||||||
chr22:44728482
|
T | C | 3 | a0001c0002t0005g0213a0001c0009t0001g0111a0002c0003t0002g0255 | 3 | HG00673.hp1 NA18965.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.322+1848T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728482 | ||||||
chr22:44728497
|
G | A | 1 | a0001c0004t0004g0263 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.322+1863G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728497 | ||||||
chr22:44728540
|
C | T | 4 | a0001c0001t0001g0195a0001c0001t0009g0412a0001c0001t0014g0266others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.322+1906C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728540 | ||||||
chr22:44728560
|
T | G | 6 | a0001c0002t0003g0193a0001c0002t0003g0253a0001c0002t0003g0302others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.322+1926T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728560 | ||||||
chr22:44728634
|
C | T | 2 | a0001c0001t0001g0247a0002c0003t0002g0248 | 2 | HG02683.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.322+2000C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728634 | ||||||
chr22:44728661
|
C | T | 1 | a0001c0002t0008g0410 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.322+2027C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728661 | ||||||
chr22:44728665
|
T | C | 1 | a0002c0003t0002g0306 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.322+2031T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728665 | ||||||
chr22:44728715
|
T | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(63): Show | 75 | HG00280.hp1 HG00438.hp1 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.322+2081T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728715 | ||||||
chr22:44728729
|
G | A | 1 | a0002c0003t0002g0298 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.322+2095G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728729 | ||||||
chr22:44728730
|
A | G | 1 | a0002c0003t0002g0298 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.322+2096A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728730 | ||||||
chr22:44728731
|
G | C | 1 | a0002c0003t0002g0298 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.322+2097G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728731 | ||||||
chr22:44728773
|
G | A | 3 | a0001c0001t0001g0195a0001c0001t0014g0266a0001c0002t0026g0061 | 3 | HG01891.hp2 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.322+2139G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728773 | ||||||
chr22:44728782
|
A | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0082a0001c0001t0001g0142others(1): Show | 5 | NA18969.hp1 NA18999.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.322+2148A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728782 | ||||||
chr22:44728825
|
C | G | 12 | a0001c0001t0006g0027a0001c0001t0018g0057a0001c0002t0008g0086others(9): Show | 12 | HG01934.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.322+2191C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728825 | ||||||
chr22:44728883
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0082a0001c0001t0009g0412 | 4 | HG02922.hp1 NA18969.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.322+2249G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728883 | ||||||
chr22:44728962
|
G | A | 12 | a0001c0001t0006g0027a0001c0001t0018g0057a0001c0002t0008g0086others(9): Show | 12 | HG01934.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.322+2328G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728962 | ||||||
chr22:44728966
|
C | T | 59 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(56): Show | 63 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.322+2332C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728966 | ||||||
chr22:44728971
|
G | T | 1 | a0001c0004t0004g0236 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.322+2337G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44728971 | ||||||
chr22:44729015
|
A | G | 172 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 180 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.322+2381A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729015 | ||||||
chr22:44729025
|
A | G | 12 | a0001c0001t0006g0027a0001c0001t0018g0057a0001c0002t0008g0086others(9): Show | 12 | HG01934.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.322+2391A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729025 | ||||||
chr22:44729026
|
A | G | 12 | a0001c0001t0006g0027a0001c0001t0018g0057a0001c0002t0008g0086others(9): Show | 12 | HG01934.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.322+2392A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729026 | ||||||
chr22:44729101
|
C | T | 12 | a0001c0001t0006g0027a0001c0001t0018g0057a0001c0002t0008g0086others(9): Show | 12 | HG01934.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.322+2467C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729101 | ||||||
chr22:44729201
|
C | T | 4 | a0001c0002t0001g0016a0001c0002t0001g0080a0001c0002t0001g0395others(1): Show | 5 | HG01257.hp2 HG01258.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.323-2529C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729201 | ||||||
chr22:44729233
|
C | T | 12 | a0001c0001t0006g0027a0001c0001t0018g0057a0001c0002t0008g0086others(9): Show | 12 | HG01934.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.323-2497C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729233 | ||||||
chr22:44729363
|
C | G | 1 | a0001c0001t0001g0177 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.323-2367C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729363 | ||||||
chr22:44729430
|
G | A | 82 | a0001c0001t0001g0348a0001c0001t0001g0361a0001c0001t0003g0109others(79): Show | 85 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.323-2300G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729430 | ||||||
chr22:44729506
|
G | A | 3 | a0001c0001t0009g0412a0001c0001t0014g0266a0001c0002t0026g0061 | 3 | HG02451.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.323-2224G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729506 | ||||||
chr22:44729533
|
C | G | 1 | a0001c0002t0001g0229 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.323-2197C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729533 | ||||||
chr22:44729539
|
T | C | 1 | a0001c0001t0009g0412 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.323-2191T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729539 | ||||||
chr22:44729577
|
T | G | 12 | a0001c0001t0006g0027a0001c0001t0018g0057a0001c0002t0008g0086others(9): Show | 12 | HG01934.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.323-2153T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729577 | ||||||
chr22:44729672
|
C | CA | 6 | a0001c0001t0001g0088a0001c0001t0001g0404a0001c0001t0006g0035others(3): Show | 6 | HG01433.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.323-2057dupA | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr22 | 44729672 | |||||
chr22:44729731
|
C | T | 1 | a0002c0003t0002g0209 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.323-1999C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729731 | ||||||
chr22:44729740
|
G | A | 1 | a0002c0003t0002g0291 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.323-1990G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729740 | ||||||
chr22:44729766
|
G | A | 1 | a0001c0001t0009g0412 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.323-1964G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729766 | ||||||
chr22:44729800
|
C | T | 2 | a0001c0001t0001g0200a0001c0001t0001g0352 | 2 | HG02602.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.323-1930C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729800 | ||||||
chr22:44729877
|
G | A | 54 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(51): Show | 57 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.323-1853G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729877 | ||||||
chr22:44729920
|
G | T | 1 | a0001c0001t0001g0065 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.323-1810G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729920 | ||||||
chr22:44729952
|
G | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0055a0001c0001t0001g0317others(2): Show | 6 | HG00738.hp2 HG01934.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.323-1778G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729952 | ||||||
chr22:44729961
|
G | A | 2 | a0001c0001t0014g0266a0001c0002t0026g0061 | 2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.323-1769G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729961 | ||||||
chr22:44729971
|
G | A | 1 | a0001c0001t0009g0412 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.323-1759G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44729971 | ||||||
chr22:44730195
|
G | A | 1 | a0001c0001t0030g0112 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.323-1535G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730195 | ||||||
chr22:44730252
|
C | T | 5 | a0001c0002t0001g0016a0001c0002t0001g0080a0001c0002t0001g0395others(2): Show | 6 | HG01257.hp2 HG01258.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.323-1478C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730252 | ||||||
chr22:44730255
|
G | A | 1 | a0002c0003t0002g0256 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.323-1475G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730255 | ||||||
chr22:44730277
|
G | A | 1 | a0001c0002t0019g0208 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.323-1453G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730277 | ||||||
chr22:44730319
|
C | T | 1 | a0001c0001t0003g0077 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.323-1411C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730319 | ||||||
chr22:44730423
|
G | A | 1 | a0001c0002t0005g0331 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.323-1307G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730423 | ||||||
chr22:44730426
|
C | G | 1 | a0002c0003t0002g0311 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.323-1304C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730426 | ||||||
chr22:44730524
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.323-1206C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730524 | ||||||
chr22:44730547
|
T | C | 161 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(158): Show | 168 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.323-1183T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730547 | ||||||
chr22:44730580
|
C | T | 1 | a0001c0001t0009g0412 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.323-1150C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730580 | ||||||
chr22:44730671
|
C | T | 3 | a0001c0001t0015g0268a0001c0002t0003g0202a0001c0002t0012g0269 | 3 | HG02630.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.323-1059C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730671 | ||||||
chr22:44730725
|
C | T | 1 | a0001c0001t0009g0412 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.323-1005C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730725 | ||||||
chr22:44730735
|
C | T | 4 | a0001c0001t0001g0195a0001c0001t0009g0412a0001c0001t0014g0266others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.323-995C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730735 | ||||||
chr22:44730755
|
A | C | 6 | a0001c0002t0003g0193a0001c0002t0003g0253a0001c0002t0003g0302others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.323-975A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730755 | ||||||
chr22:44730758
|
G | T | 172 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 180 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.323-972G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730758 | ||||||
chr22:44730766
|
G | A | 1 | a0001c0002t0005g0021 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.323-964G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730766 | ||||||
chr22:44730772
|
C | T | 3 | a0001c0001t0007g0026a0001c0001t0007g0033a0001c0001t0009g0025 | 3 | HG03130.hp1 HG03225.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.323-958C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730772 | ||||||
chr22:44730815
|
T | A | 12 | a0001c0001t0006g0027a0001c0001t0018g0057a0001c0002t0008g0086others(9): Show | 12 | HG01934.hp1 HG02055.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.323-915T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730815 | ||||||
chr22:44730895
|
T | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(273): Show | 293 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.323-835T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730895 | ||||||
chr22:44730967
|
G | C | 1 | a0002c0003t0002g0311 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.323-763G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44730967 | ||||||
chr22:44731037
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.323-693A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731037 | ||||||
chr22:44731051
|
A | G | 1 | a0001c0002t0026g0061 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.323-679A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731051 | ||||||
chr22:44731054
|
G | A | 1 | a0001c0002t0026g0061 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.323-676G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731054 | ||||||
chr22:44731063
|
G | A | 1 | a0001c0001t0001g0293 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.323-667G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731063 | ||||||
chr22:44731170
|
G | A | 1 | a0001c0002t0001g0246 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.323-560G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731170 | ||||||
chr22:44731186
|
C | T | 1 | a0001c0001t0007g0033 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.323-544C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731186 | ||||||
chr22:44731276
|
G | A | 1 | a0001c0002t0006g0049 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.323-454G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731276 | ||||||
chr22:44731452
|
G | A | 6 | a0001c0002t0003g0193a0001c0002t0003g0253a0001c0002t0003g0302others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.323-278G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731452 | ||||||
chr22:44731555
|
G | T | 92 | a0001c0001t0001g0055a0001c0001t0001g0152a0001c0001t0001g0241others(89): Show | 95 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.323-175G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731555 | ||||||
chr22:44731600
|
T | C | 1 | a0001c0002t0005g0252 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.323-130T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731600 | ||||||
chr22:44731661
|
C | T | 1 | a0001c0001t0001g0314 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.323-69C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731661 | ||||||
chr22:44731688
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.323-42C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731688 | ||||||
chr22:44731692
|
C | T | 1 | a0001c0001t0001g0361 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.323-38C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731692 | ||||||
chr22:44731701
|
C | T | 2 | a0002c0003t0002g0148a0002c0003t0002g0150 | 2 | HG00408.hp2 HG00423.hp1 |
intron_variant | MODIFIER | c.323-29C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 4/7 | chr22 | 44731701 | ||||||
chr22:44731859
|
C | T | 43 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0018others(40): Show | 44 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.414+38C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44731859 | ||||||
chr22:44731882
|
A | G | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.414+61A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44731882 | ||||||
chr22:44731892
|
G | C | 8 | a0001c0001t0001g0124a0001c0001t0001g0142a0001c0002t0003g0337others(5): Show | 8 | NA18947.hp2 NA18961.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+71G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44731892 | ||||||
chr22:44731900
|
G | A | 1 | a0001c0004t0004g0135 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.414+79G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44731900 | ||||||
chr22:44731926
|
CTCTGCTC others(3): Show |
C | 47 | a0001c0002t0001g0016a0001c0002t0001g0080a0001c0002t0001g0190others(44): Show | 49 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.414+106_414+115del others(10): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44731926 | ||||||
chr22:44731927
|
T | G | 30 | a0001c0001t0001g0157a0001c0001t0003g0077a0001c0001t0007g0026others(27): Show | 31 | HG00609.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.414+106T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44731927 | ||||||
chr22:44731936
|
T | C | 19 | a0001c0001t0003g0077a0001c0001t0007g0026a0001c0001t0007g0033others(16): Show | 19 | HG00408.hp1 HG00673.hp1 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.414+115T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44731936 | ||||||
chr22:44731937
|
G | A | 1 | a0002c0003t0002g0123 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.414+116G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44731937 | ||||||
chr22:44731953
|
T | C | 2 | a0001c0001t0015g0268a0001c0002t0003g0202 | 2 | HG02630.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.414+132T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44731953 | ||||||
chr22:44732011
|
C | A | 5 | a0001c0002t0005g0129a0001c0002t0005g0184a0001c0002t0005g0261others(2): Show | 5 | HG02818.hp2 HG03041.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+190C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44732011 | ||||||
chr22:44732031
|
A | G | 26 | a0001c0001t0001g0181a0001c0001t0003g0077a0001c0001t0027g0275others(23): Show | 26 | HG00140.hp1 HG01243.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.414+210A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44732031 | ||||||
chr22:44732043
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.415-208C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44732043 | ||||||
chr22:44732166
|
C | G | 1 | a0001c0001t0001g0297 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.415-85C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44732166 | ||||||
chr22:44732234
|
G | A | 1 | a0001c0002t0012g0269 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.415-17G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 5/7 | chr22 | 44732234 | ||||||
chr22:44732408
|
G | C | 328 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(325): Show | 346 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(343): Show |
intron_variant | MODIFIER | c.555+17G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732408 | ||||||
chr22:44732494
|
C | G | 1 | a0001c0001t0001g0159 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.555+103C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732494 | ||||||
chr22:44732569
|
G | T | 241 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0052others(238): Show | 249 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.555+178G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732569 | ||||||
chr22:44732625
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.555+234A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732625 | ||||||
chr22:44732667
|
G | A | 1 | a0001c0004t0004g0322 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.555+276G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732667 | ||||||
chr22:44732673
|
G | A | 2 | a0001c0002t0003g0409a0001c0002t0012g0133 | 2 | HG01243.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.555+282G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732673 | ||||||
chr22:44732696
|
T | C | 47 | a0001c0002t0003g0070a0001c0002t0003g0071a0001c0002t0003g0202others(44): Show | 51 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.555+305T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732696 | ||||||
chr22:44732716
|
T | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(321): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.555+325T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732716 | ||||||
chr22:44732721
|
G | A | 40 | a0001c0002t0003g0202a0001c0002t0003g0337a0001c0004t0004g0010others(37): Show | 43 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.555+330G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732721 | ||||||
chr22:44732728
|
T | C | 47 | a0001c0002t0003g0070a0001c0002t0003g0071a0001c0002t0003g0202others(44): Show | 51 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.555+337T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732728 | ||||||
chr22:44732736
|
CACCA | C | 9 | a0001c0002t0003g0202a0001c0004t0004g0110a0001c0004t0004g0137others(6): Show | 9 | HG00140.hp1 HG01255.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.555+346_555+349del others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732736 | ||||||
chr22:44732738
|
CCA | C | 38 | a0001c0001t0001g0195a0001c0001t0003g0243a0001c0002t0001g0016others(35): Show | 42 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.555+353_555+354del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732738 | |||||
chr22:44732739
|
C | T | 1 | a0001c0002t0012g0269 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.555+348C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732739 | ||||||
chr22:44732744
|
A | G | 1 | a0001c0002t0005g0252 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.555+353A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732744 | ||||||
chr22:44732752
|
ACG | A | 15 | a0001c0001t0009g0025a0001c0001t0009g0412a0001c0002t0008g0086others(12): Show | 15 | HG01934.hp1 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.555+363_555+364del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732752 | |||||
chr22:44732754
|
G | A | 50 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0018others(47): Show | 51 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.555+363G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732754 | ||||||
chr22:44732760
|
G | A | 3 | a0001c0001t0015g0268a0001c0002t0001g0058a0001c0002t0012g0269 | 3 | HG01109.hp1 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.555+369G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732760 | ||||||
chr22:44732762
|
TAC | T | 6 | a0001c0002t0003g0193a0001c0002t0003g0253a0001c0002t0003g0302others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+377_555+378del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732762 | |||||
chr22:44732773
|
CTGTGTGC others(14): Show |
C | 98 | a0001c0002t0005g0021a0001c0002t0005g0067a0001c0002t0005g0068others(95): Show | 99 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.555+387_555+407del others(21): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732773 | |||||
chr22:44732778
|
T | C | 273 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(270): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.555+387T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732778 | ||||||
chr22:44732782
|
C | T | 2 | a0001c0004t0004g0206a0001c0004t0004g0277 | 2 | HG02055.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.555+391C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732782 | ||||||
chr22:44732787
|
ATAC | A | 67 | a0001c0001t0001g0392a0001c0001t0003g0013a0001c0001t0003g0014others(64): Show | 68 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.555+400_555+402del others(3): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732787 | |||||
chr22:44732800
|
A | G | 98 | a0001c0002t0005g0021a0001c0002t0005g0067a0001c0002t0005g0068others(95): Show | 99 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.555+409A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732800 | ||||||
chr22:44732803
|
C | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(160): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.555+412C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732803 | ||||||
chr22:44732804
|
G | A | 1 | a0001c0001t0007g0029 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.555+413G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732804 | ||||||
chr22:44732807
|
TAC | T | 44 | a0001c0002t0001g0058a0001c0002t0003g0202a0001c0002t0003g0337others(41): Show | 48 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.555+421_555+422del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732807 | |||||
chr22:44732813
|
CTA | C | 6 | a0001c0002t0003g0193a0001c0002t0003g0253a0001c0002t0003g0302others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+423_555+424del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732813 | ||||||
chr22:44732819
|
G | A | 2 | a0001c0001t0015g0268a0001c0002t0012g0269 | 2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.555+428G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732819 | ||||||
chr22:44732822
|
T | C | 43 | a0001c0002t0003g0202a0001c0002t0003g0337a0001c0002t0013g0008others(40): Show | 47 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.555+431T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732822 | ||||||
chr22:44732826
|
C | T | 2 | a0001c0001t0015g0267a0001c0002t0033g0059 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.555+435C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732826 | ||||||
chr22:44732827
|
G | A | 9 | a0001c0002t0003g0202a0001c0004t0004g0110a0001c0004t0004g0137others(6): Show | 9 | HG00140.hp1 HG01255.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.555+436G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732827 | ||||||
chr22:44732831
|
ATAC | A | 154 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(151): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.555+444_555+446del others(3): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732831 | |||||
chr22:44732831
|
ATACTACA others(29): Show |
A | 43 | a0001c0002t0003g0202a0001c0002t0003g0337a0001c0002t0013g0008others(40): Show | 47 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.555+444_555+479del others(36): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732831 | |||||
chr22:44732832
|
TACTACAC others(6): Show |
T | 5 | a0001c0001t0014g0266a0001c0002t0001g0016a0001c0002t0001g0229others(2): Show | 6 | HG01257.hp2 HG01258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+444_555+456del others(13): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732832 | |||||
chr22:44732835
|
TAC | T | 7 | a0001c0002t0003g0193a0001c0002t0003g0253a0001c0002t0003g0302others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.555+449_555+450del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732835 | |||||
chr22:44732835
|
TACACACG others(3): Show |
T | 98 | a0001c0002t0005g0021a0001c0002t0005g0067a0001c0002t0005g0068others(95): Show | 99 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.555+459_555+468del others(10): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732835 | |||||
chr22:44732836
|
A | G | 4 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0081others(1): Show | 4 | NA18612.hp1 NA19001.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.555+445A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732836 | ||||||
chr22:44732844
|
GCA | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(150): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.555+459_555+460del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732844 | |||||
chr22:44732860
|
G | A | 1 | a0001c0001t0009g0412 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.555+469G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732860 | ||||||
chr22:44732868
|
TAC | T | 15 | a0001c0001t0009g0025a0001c0001t0009g0412a0001c0002t0008g0086others(12): Show | 15 | HG01934.hp1 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.555+482_555+483del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732868 | |||||
chr22:44732883
|
C | T | 419 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(416): Show | 439 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(436): Show |
intron_variant | MODIFIER | c.555+492C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732883 | ||||||
chr22:44732887
|
CCA | C | 11 | a0001c0001t0003g0056a0001c0001t0003g0182a0001c0001t0003g0194others(8): Show | 11 | HG01109.hp2 HG02055.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.555+502_555+503del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732887 | |||||
chr22:44732892
|
C | T | 1 | a0001c0001t0006g0034 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.555+501C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732892 | ||||||
chr22:44732898
|
C | T | 43 | a0001c0002t0003g0202a0001c0002t0003g0337a0001c0002t0013g0008others(40): Show | 47 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.555+507C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732898 | ||||||
chr22:44732899
|
A | G | 43 | a0001c0002t0003g0202a0001c0002t0003g0337a0001c0002t0013g0008others(40): Show | 47 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.555+508A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732899 | ||||||
chr22:44732912
|
C | T | 1 | a0001c0004t0004g0010 | 2 | HG00642.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.555+521C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732912 | ||||||
chr22:44732913
|
TAC | T | 99 | a0001c0001t0003g0203a0001c0002t0005g0021a0001c0002t0005g0067others(96): Show | 100 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.555+527_555+528del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732913 | |||||
chr22:44732923
|
C | T | 56 | a0001c0002t0003g0193a0001c0002t0003g0253a0001c0002t0003g0302others(53): Show | 57 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.555+532C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732923 | ||||||
chr22:44732924
|
G | A | 2 | a0001c0004t0004g0340a0001c0004t0004g0381 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.555+533G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732924 | ||||||
chr22:44732927
|
C | A | 2 | a0001c0001t0015g0268a0001c0002t0012g0269 | 2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.555+536C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732927 | ||||||
chr22:44732928
|
G | A | 1 | a0001c0001t0001g0009 | 2 | NA19004.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.555+537G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732928 | ||||||
chr22:44732936
|
TAC | T | 43 | a0001c0002t0003g0202a0001c0002t0003g0337a0001c0002t0013g0008others(40): Show | 47 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.555+550_555+551del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732936 | |||||
chr22:44732943
|
G | C | 1 | a0001c0001t0024g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.555+552G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732943 | ||||||
chr22:44732946
|
T | C | 65 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0018others(62): Show | 66 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.555+555T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732946 | ||||||
chr22:44732946
|
TGCACACA others(5): Show |
T | 1 | a0001c0001t0015g0267 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.555+557_555+568del others(12): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732946 | |||||
chr22:44732947
|
GCA | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(150): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.555+561_555+562del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732947 | |||||
chr22:44732954
|
TACGCGTG others(3): Show |
T | 1 | a0001c0002t0033g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.555+568_555+577del others(10): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732954 | |||||
chr22:44732977
|
TAC | T | 4 | a0001c0002t0001g0016a0001c0002t0001g0080a0001c0002t0001g0395others(1): Show | 5 | HG01257.hp2 HG01258.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.555+592_555+593del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732977 | |||||
chr22:44732981
|
CACAT | C | 17 | a0001c0001t0009g0025a0001c0001t0009g0412a0001c0002t0008g0086others(14): Show | 17 | HG01934.hp1 HG02109.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.555+595_555+598del others(4): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732981 | |||||
chr22:44732983
|
CAT | C | 6 | a0001c0002t0003g0193a0001c0002t0003g0253a0001c0002t0003g0302others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+594_555+595del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44732983 | |||||
chr22:44732990
|
G | T | 40 | a0001c0002t0003g0202a0001c0002t0003g0337a0001c0004t0004g0010others(37): Show | 43 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.555+599G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732990 | ||||||
chr22:44732998
|
A | G | 273 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(270): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(281): Show |
intron_variant | MODIFIER | c.555+607A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44732998 | ||||||
chr22:44733013
|
GTGCACA | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(156): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.555+630_555+635del others(6): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr22 | 44733013 | |||||
chr22:44733083
|
T | C | 2 | a0001c0001t0015g0268a0001c0002t0012g0269 | 2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.555+692T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733083 | ||||||
chr22:44733109
|
G | A | 3 | a0001c0002t0001g0016a0001c0002t0001g0395a0001c0002t0001g0396 | 4 | HG01257.hp2 HG01258.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.555+718G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733109 | ||||||
chr22:44733126
|
C | G | 1 | a0001c0004t0004g0220 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.555+735C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733126 | ||||||
chr22:44733196
|
C | T | 65 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0018others(62): Show | 66 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.555+805C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733196 | ||||||
chr22:44733219
|
A | G | 373 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(370): Show | 390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.555+828A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733219 | ||||||
chr22:44733228
|
T | C | 43 | a0001c0002t0003g0202a0001c0002t0003g0337a0001c0002t0013g0008others(40): Show | 47 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.555+837T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733228 | ||||||
chr22:44733276
|
C | G | 1 | a0001c0001t0001g0271 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.555+885C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733276 | ||||||
chr22:44733277
|
A | G | 43 | a0001c0002t0003g0202a0001c0002t0003g0337a0001c0002t0013g0008others(40): Show | 47 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.555+886A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733277 | ||||||
chr22:44733280
|
C | T | 1 | a0001c0002t0011g0044 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.555+889C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733280 | ||||||
chr22:44733359
|
T | C | 42 | a0001c0002t0003g0202a0001c0002t0013g0008a0001c0002t0013g0169others(39): Show | 46 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.555+968T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733359 | ||||||
chr22:44733365
|
C | T | 42 | a0001c0002t0003g0202a0001c0002t0013g0008a0001c0002t0013g0169others(39): Show | 46 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.555+974C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733365 | ||||||
chr22:44733377
|
T | C | 1 | a0001c0001t0014g0266 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.555+986T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733377 | ||||||
chr22:44733382
|
C | T | 69 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0011others(66): Show | 78 | HG00280.hp1 HG00438.hp1 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.555+991C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733382 | ||||||
chr22:44733386
|
G | C | 42 | a0001c0002t0003g0202a0001c0002t0013g0008a0001c0002t0013g0169others(39): Show | 46 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.555+995G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733386 | ||||||
chr22:44733391
|
C | T | 2 | a0003c0007t0004g0069a0003c0007t0025g0063 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.555+1000C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733391 | ||||||
chr22:44733434
|
C | G | 1 | a0001c0001t0001g0228 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.555+1043C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733434 | ||||||
chr22:44733479
|
G | C | 6 | a0001c0002t0003g0193a0001c0002t0003g0253a0001c0002t0003g0302others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+1088G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733479 | ||||||
chr22:44733594
|
G | C | 6 | a0001c0002t0003g0193a0001c0002t0003g0253a0001c0002t0003g0302others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.555+1203G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733594 | ||||||
chr22:44733625
|
C | T | 51 | a0002c0003t0002g0002a0002c0003t0002g0064a0002c0003t0002g0093others(48): Show | 52 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.555+1234C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733625 | ||||||
chr22:44733651
|
C | T | 33 | a0001c0002t0013g0008a0001c0002t0013g0169a0001c0004t0004g0010others(30): Show | 37 | HG00423.hp2 HG00609.hp1 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.555+1260C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733651 | ||||||
chr22:44733727
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.556-1300G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733727 | ||||||
chr22:44733810
|
A | G | 2 | a0001c0001t0015g0268a0001c0002t0012g0269 | 2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.556-1217A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733810 | ||||||
chr22:44733823
|
C | G | 3 | a0001c0002t0001g0080a0001c0002t0001g0395a0001c0002t0001g0396 | 3 | HG02738.hp2 HG03927.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.556-1204C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733823 | ||||||
chr22:44733929
|
G | A | 1 | a0001c0001t0001g0387 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.556-1098G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733929 | ||||||
chr22:44733940
|
T | G | 1 | a0001c0004t0004g0393 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.556-1087T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44733940 | ||||||
chr22:44734052
|
T | A | 2 | a0001c0001t0015g0268a0001c0002t0012g0269 | 2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.556-975T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734052 | ||||||
chr22:44734103
|
C | G | 1 | a0001c0002t0012g0269 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.556-924C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734103 | ||||||
chr22:44734131
|
G | A | 6 | a0001c0004t0004g0110a0001c0004t0004g0137a0001c0004t0004g0305others(3): Show | 6 | HG00140.hp1 HG01255.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.556-896G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734131 | ||||||
chr22:44734156
|
C | T | 49 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0018others(46): Show | 50 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.556-871C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734156 | ||||||
chr22:44734182
|
G | A | 91 | a0001c0002t0005g0021a0001c0002t0005g0067a0001c0002t0005g0068others(88): Show | 92 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.556-845G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734182 | ||||||
chr22:44734296
|
A | G | 7 | a0001c0002t0003g0193a0001c0002t0003g0253a0001c0002t0003g0302others(4): Show | 7 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.556-731A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734296 | ||||||
chr22:44734411
|
G | C | 1 | a0001c0002t0015g0270 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.556-616G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734411 | ||||||
chr22:44734428
|
A | C | 3 | a0001c0002t0001g0080a0001c0002t0001g0395a0001c0002t0001g0396 | 3 | HG02738.hp2 HG03927.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.556-599A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734428 | ||||||
chr22:44734493
|
A | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(154): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.556-534A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734493 | ||||||
chr22:44734535
|
G | A | 1 | a0001c0002t0033g0059 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.556-492G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734535 | ||||||
chr22:44734548
|
G | T | 153 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(150): Show | 164 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.556-479G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734548 | ||||||
chr22:44734582
|
G | T | 1 | a0001c0002t0005g0261 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.556-445G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734582 | ||||||
chr22:44734586
|
G | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(149): Show | 163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.556-441G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734586 | ||||||
chr22:44734613
|
C | T | 1 | a0001c0001t0003g0182 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.556-414C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734613 | ||||||
chr22:44734632
|
G | A | 5 | a0001c0001t0001g0088a0001c0001t0001g0260a0001c0001t0006g0030others(2): Show | 5 | HG02615.hp1 HG02886.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.556-395G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734632 | ||||||
chr22:44734684
|
T | G | 40 | a0001c0001t0006g0034a0001c0002t0005g0021a0001c0002t0005g0067others(37): Show | 40 | HG00323.hp1 HG00609.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.556-343T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734684 | ||||||
chr22:44734778
|
C | G | 1 | a0001c0001t0001g0195 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.556-249C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734778 | ||||||
chr22:44734811
|
C | A | 39 | a0001c0002t0003g0202a0001c0004t0004g0010a0001c0004t0004g0012others(36): Show | 42 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.556-216C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734811 | ||||||
chr22:44734815
|
C | T | 40 | a0001c0001t0014g0264a0001c0002t0003g0202a0001c0004t0004g0010others(37): Show | 43 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.556-212C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734815 | ||||||
chr22:44734968
|
G | T | 2 | a0001c0001t0015g0267a0001c0002t0033g0059 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.556-59G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44734968 | ||||||
chr22:44735014
|
C | A | 10 | a0001c0001t0001g0146a0001c0001t0001g0164a0001c0001t0001g0177others(7): Show | 10 | HG00544.hp2 HG00558.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.556-13C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44735014 | ||||||
chr22:44735020
|
C | A | 2 | a0001c0002t0005g0339a0001c0002t0005g0380 | 2 | HG01070.hp2 HG01071.hp2 |
splice_region_variant&intron_variant | LOW | c.556-7C>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 6/7 | chr22 | 44735020 | ||||||
chr22:44735173
|
G | A | 51 | a0002c0003t0002g0002a0002c0003t0002g0064a0002c0003t0002g0093others(48): Show | 52 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.691+11G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735173 | ||||||
chr22:44735206
|
G | T | 1 | a0001c0002t0006g0049 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.691+44G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735206 | ||||||
chr22:44735207
|
G | T | 1 | a0001c0002t0006g0049 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.691+45G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735207 | ||||||
chr22:44735212
|
C | T | 9 | a0001c0002t0003g0202a0001c0004t0004g0110a0001c0004t0004g0137others(6): Show | 9 | HG00140.hp1 HG01255.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.691+50C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735212 | ||||||
chr22:44735238
|
C | T | 4 | a0002c0003t0002g0117a0002c0003t0002g0149a0002c0003t0002g0256others(1): Show | 4 | NA18943.hp2 NA18960.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.691+76C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735238 | ||||||
chr22:44735249
|
G | A | 8 | a0001c0001t0003g0013a0001c0001t0003g0018a0001c0001t0003g0324others(5): Show | 8 | HG01975.hp2 NA18945.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.691+87G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735249 | ||||||
chr22:44735286
|
C | T | 39 | a0001c0002t0003g0202a0001c0004t0004g0010a0001c0004t0004g0012others(36): Show | 42 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.691+124C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735286 | ||||||
chr22:44735310
|
T | G | 1 | a0001c0004t0004g0206 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.691+148T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735310 | ||||||
chr22:44735311
|
A | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0316 | 2 | HG02129.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.691+149A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735311 | ||||||
chr22:44735359
|
C | G | 1 | a0001c0001t0001g0370 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.691+197C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735359 | ||||||
chr22:44735359
|
C | T | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(148): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.691+197C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735359 | ||||||
chr22:44735426
|
T | G | 4 | a0001c0001t0001g0078a0001c0001t0001g0079a0001c0001t0001g0081others(1): Show | 4 | NA18612.hp1 NA19001.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.691+264T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735426 | ||||||
chr22:44735474
|
C | G | 3 | a0001c0002t0001g0224a0001c0002t0001g0281a0001c0011t0001g0282 | 3 | HG00609.hp1 NA18990.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.691+312C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735474 | ||||||
chr22:44735480
|
C | T | 39 | a0001c0002t0003g0202a0001c0004t0004g0010a0001c0004t0004g0012others(36): Show | 42 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.691+318C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735480 | ||||||
chr22:44735533
|
G | A | 51 | a0002c0003t0002g0002a0002c0003t0002g0064a0002c0003t0002g0093others(48): Show | 52 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.691+371G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735533 | ||||||
chr22:44735539
|
G | T | 2 | a0001c0001t0015g0267a0001c0002t0033g0059 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.691+377G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735539 | ||||||
chr22:44735543
|
T | C | 2 | a0001c0001t0015g0267a0001c0002t0033g0059 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.691+381T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735543 | ||||||
chr22:44735548
|
A | T | 2 | a0001c0001t0015g0267a0001c0002t0033g0059 | 2 | HG02258.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.691+386A>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735548 | ||||||
chr22:44735582
|
T | A | 367 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(364): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.691+420T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735582 | ||||||
chr22:44735637
|
T | A | 39 | a0001c0002t0003g0202a0001c0004t0004g0010a0001c0004t0004g0012others(36): Show | 42 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.691+475T>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735637 | ||||||
chr22:44735646
|
A | G | 40 | a0001c0002t0003g0202a0001c0004t0004g0010a0001c0004t0004g0012others(37): Show | 43 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.691+484A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735646 | ||||||
chr22:44735653
|
C | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(153): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.691+491C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735653 | ||||||
chr22:44735675
|
T | G | 367 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(364): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.691+513T>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735675 | ||||||
chr22:44735718
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.691+556G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735718 | ||||||
chr22:44735732
|
C | T | 41 | a0001c0002t0003g0202a0001c0004t0004g0010a0001c0004t0004g0012others(38): Show | 44 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.691+570C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735732 | ||||||
chr22:44735786
|
G | T | 1 | a0001c0002t0005g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.691+624G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735786 | ||||||
chr22:44735814
|
C | T | 1 | a0002c0003t0002g0148 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.691+652C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735814 | ||||||
chr22:44735963
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.691+801G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735963 | ||||||
chr22:44735984
|
T | C | 1 | a0002c0003t0002g0209 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.692-788T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735984 | ||||||
chr22:44735986
|
T | C | 41 | a0001c0002t0003g0202a0001c0004t0004g0010a0001c0004t0004g0012others(38): Show | 44 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.692-786T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44735986 | ||||||
chr22:44736021
|
C | T | 2 | a0001c0004t0004g0263a0001c0004t0016g0028 | 2 | HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.692-751C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736021 | ||||||
chr22:44736046
|
T | C | 41 | a0001c0002t0003g0202a0001c0004t0004g0010a0001c0004t0004g0012others(38): Show | 44 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.692-726T>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736046 | ||||||
chr22:44736116
|
C | T | 6 | a0002c0003t0002g0100a0002c0003t0002g0148a0002c0003t0002g0150others(3): Show | 6 | HG00408.hp2 HG00423.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.692-656C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736116 | ||||||
chr22:44736239
|
C | G | 1 | a0001c0001t0001g0385 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.692-533C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736239 | ||||||
chr22:44736259
|
C | G | 3 | a0001c0002t0001g0080a0001c0002t0001g0395a0001c0002t0001g0396 | 3 | HG02738.hp2 HG03927.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.692-513C>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736259 | ||||||
chr22:44736333
|
G | A | 1 | a0001c0002t0012g0269 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.692-439G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736333 | ||||||
chr22:44736443
|
A | G | 138 | a0001c0002t0003g0202a0001c0002t0003g0258a0001c0002t0005g0021others(135): Show | 142 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.692-329A>G | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736443 | ||||||
chr22:44736474
|
CG | C | 41 | a0001c0002t0003g0202a0001c0004t0004g0010a0001c0004t0004g0012others(38): Show | 44 | HG00140.hp1 HG00423.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.692-293delG | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr22 | 44736474 | |||||
chr22:44736475
|
G | A | 6 | a0001c0002t0003g0193a0001c0002t0003g0253a0001c0002t0003g0302others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.692-297G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736475 | ||||||
chr22:44736479
|
G | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(153): Show | 167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.692-293G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736479 | ||||||
chr22:44736482
|
A | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0397a0001c0001t0001g0401others(2): Show | 7 | NA18948.hp2 NA18952.hp1 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.692-290A>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736482 | ||||||
chr22:44736568
|
G | T | 30 | a0001c0004t0004g0010a0001c0004t0004g0012a0001c0004t0004g0017others(27): Show | 33 | HG00423.hp2 HG00639.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.692-204G>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736568 | ||||||
chr22:44736611
|
G | A | 27 | a0001c0001t0001g0054a0001c0001t0001g0066a0001c0001t0001g0072others(24): Show | 28 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.692-161G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736611 | ||||||
chr22:44736613
|
CAG | C | 95 | a0001c0002t0005g0021a0001c0002t0005g0067a0001c0002t0005g0068others(92): Show | 96 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.692-158_692-157del others(2): Show |
PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736613 | ||||||
chr22:44736626
|
G | A | 97 | a0001c0002t0005g0021a0001c0002t0005g0067a0001c0002t0005g0068others(94): Show | 98 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.692-146G>A | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736626 | ||||||
chr22:44736651
|
G | C | 1 | a0001c0001t0001g0317 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.692-121G>C | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736651 | ||||||
chr22:44736655
|
C | T | 95 | a0001c0002t0005g0021a0001c0002t0005g0067a0001c0002t0005g0068others(92): Show | 96 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.692-117C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736655 | ||||||
chr22:44736660
|
C | T | 51 | a0002c0003t0002g0002a0002c0003t0002g0064a0002c0003t0002g0093others(48): Show | 52 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.692-112C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736660 | ||||||
chr22:44736757
|
C | T | 1 | a0001c0001t0006g0040 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.692-15C>T | PRR5 | ENSG00000186654.21 | transcript | ENST00000336985.11 | protein_coding | 7/7 | chr22 | 44736757 |