geneid | 89970 |
---|---|
ensemblid | ENSG00000159579.14 |
hgncid | 29420 |
symbol | RSPRY1 |
name | ring finger and SPRY domain containing 1 |
refseq_nuc | NM_133368.3 |
refseq_prot | NP_588609.1 |
ensembl_nuc | ENST00000394420.9 |
ensembl_prot | ENSP00000377942.4 |
mane_status | MANE Select |
chr | chr16 |
start | 57186329 |
end | 57240469 |
strand | + |
ver | v1.2 |
region | chr16:57186329-57240469 |
region5000 | chr16:57181329-57245469 |
regionname0 | RSPRY1_chr16_57186329_57240469 |
regionname5000 | RSPRY1_chr16_57181329_57245469 |
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 | 576 | 355 | 85 | 62 | 160 | 14 | 32 | 122 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0002 | 0/0 | 576 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
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 | 1731 | 352 | 82 | 62 | 160 | 14 | 32 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
c0002 | 0/0 | 1731 | 3 | 3 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
c0003 | 0/0 | 1731 | 2 | 2 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
c0004 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
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 | 1/0 | 1773 | 188 | 61 | 45 | 64 | 8 | 9 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0002 | 0/0 | 1771 | 74 | 0 | 10 | 47 | 4 | 13 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0003 | 0/0 | 1764 | 40 | 0 | 1 | 31 | 0 | 8 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0004 | 0/0 | 1765 | 9 | 5 | 0 | 4 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0005 | 0/0 | 1773 | 7 | 4 | 2 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0006 | 0/1 | 1775 | 6 | 1 | 1 | 0 | 2 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0007 | 0/0 | 1773 | 4 | 4 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0008 | 0/0 | 1775 | 4 | 1 | 1 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0009 | 0/0 | 1772 | 3 | 0 | 0 | 3 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0010 | 0/0 | 1772 | 3 | 2 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0011 | 0/0 | 1771 | 2 | 0 | 0 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0012 | 0/0 | 1774 | 2 | 2 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0013 | 0/0 | 1765 | 2 | 0 | 0 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0014 | 0/0 | 1772 | 2 | 0 | 0 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0015 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0016 | 0/0 | 1765 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0017 | 0/0 | 1775 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0018 | 0/0 | 1774 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0019 | 0/0 | 1773 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0020 | 0/0 | 1772 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0021 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0022 | 0/0 | 1773 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0023 | 0/0 | 1771 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0024 | 0/0 | 1772 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0025 | 0/0 | 1772 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
t0026 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
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 | 2 | 0 | 0 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0291 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
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 | 1731 | 352 | 82 | 62 | 160 | 14 | 32 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0003 | 0/0 | 1731 | 2 | 2 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0004 | 0/0 | 1731 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0002c0002 | 0/0 | 1731 | 3 | 3 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3503 | 186 | 59 | 45 | 64 | 8 | 9 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0002 | 0/0 | 3501 | 74 | 0 | 10 | 47 | 4 | 13 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0003 | 0/0 | 3494 | 40 | 0 | 1 | 31 | 0 | 8 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0004 | 0/0 | 3495 | 9 | 5 | 0 | 4 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0005 | 0/0 | 3503 | 7 | 4 | 2 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0006 | 0/1 | 3505 | 6 | 1 | 1 | 0 | 2 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0007 | 0/0 | 3503 | 3 | 3 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0008 | 0/0 | 3505 | 4 | 1 | 1 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0009 | 0/0 | 3502 | 3 | 0 | 0 | 3 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0010 | 0/0 | 3502 | 3 | 2 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0011 | 0/0 | 3501 | 2 | 0 | 0 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0013 | 0/0 | 3495 | 2 | 0 | 0 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0014 | 0/0 | 3502 | 2 | 0 | 0 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0015 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0016 | 0/0 | 3495 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0017 | 0/0 | 3505 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0019 | 0/0 | 3503 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0020 | 0/0 | 3502 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0021 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0022 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0023 | 0/0 | 3501 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0024 | 0/0 | 3502 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0025 | 0/0 | 3502 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0001t0026 | 0/0 | 3481 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0003t0001 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0003t0007 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0001c0004t0001 | 0/0 | 3503 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0002c0002t0012 | 0/0 | 3504 | 2 | 2 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
a0002c0002t0018 | 0/0 | 3504 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | copy fasta | chr16 | 57181329 | 57245469 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0291 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0004g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0004g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0004g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0005g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0005g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0006g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0006g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0006g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0006g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0007g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0007g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0008g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0008g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0008g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0009g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0009g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0009g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0010g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0010g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0010g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0011g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0011g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0013g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0013g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0014g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0014g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0015g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0016g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0017g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0019g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0020g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0021g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0022g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0023g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0024g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0025g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0001t0026g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0003t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0001c0004t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0002c0002t0012g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0002c0002t0012g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
a0002c0002t0018g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | GBR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0265 | EUR | GBR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0072 | EUR | GBR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0196 | EUR | GBR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00280 | hp1 | a0001 | c0001 | t0006 | g0129 | EUR | FIN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | FIN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0293 | EUR | FIN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0355 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00609 | hp2 | a0001 | c0001 | t0011 | g0278 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0331 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00735 | hp1 | a0001 | c0001 | t0019 | g0113 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01070 | hp2 | a0001 | c0001 | t0006 | g0143 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01109 | hp1 | a0001 | c0001 | t0008 | g0158 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0344 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0250 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01361 | hp2 | a0001 | c0001 | t0005 | g0263 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0273 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01515 | hp1 | a0001 | c0001 | t0006 | g0142 | EUR | IBS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01884 | hp2 | a0001 | c0001 | t0010 | g0165 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0084 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0271 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0351 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0132 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | CDX | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | CDX | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0323 | EAS | CDX | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | CDX | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0136 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0290 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02280 | hp2 | a0001 | c0001 | t0025 | g0164 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02523 | hp1 | a0001 | c0001 | t0011 | g0240 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0337 | EAS | KHV | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0130 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02647 | hp1 | a0001 | c0001 | t0021 | g0146 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0345 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0215 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0314 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0118 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0023 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0268 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02818 | hp1 | a0002 | c0002 | t0018 | g0287 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0147 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0316 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0218 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03041 | hp2 | a0001 | c0001 | t0016 | g0131 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03130 | hp1 | a0001 | c0001 | t0008 | g0157 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03139 | hp1 | a0001 | c0003 | t0007 | g0018 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0289 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03195 | hp1 | a0001 | c0001 | t0022 | g0279 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03195 | hp2 | a0001 | c0001 | t0026 | g0237 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0317 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03453 | hp1 | a0001 | c0001 | t0020 | g0162 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0329 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0144 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0280 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03704 | hp2 | a0001 | c0001 | t0006 | g0145 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0347 | SAS | BEB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | BEB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0246 | SAS | BEB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0328 | SAS | BEB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | BEB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0283 | SAS | STU | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0117 | AFR | YRI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18522 | hp2 | a0001 | c0004 | t0001 | g0040 | AFR | YRI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0334 | EAS | CHB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | CHB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | YRI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | YRI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0341 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18942 | hp1 | a0001 | c0001 | t0014 | g0326 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18950 | hp2 | a0001 | c0001 | t0009 | g0221 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18953 | hp1 | a0001 | c0001 | t0008 | g0012 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18961 | hp1 | a0001 | c0001 | t0017 | g0292 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0336 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18963 | hp1 | a0001 | c0001 | t0009 | g0195 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0335 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18964 | hp2 | a0001 | c0001 | t0024 | g0330 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0324 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0356 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0332 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18973 | hp2 | a0001 | c0001 | t0023 | g0310 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0348 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0339 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0349 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0321 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18991 | hp2 | a0001 | c0001 | t0013 | g0319 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0352 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0327 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0353 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0350 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19030 | hp1 | a0002 | c0002 | t0012 | g0288 | AFR | LWK | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | LWK | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19043 | hp1 | a0001 | c0001 | t0010 | g0166 | AFR | LWK | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0035 | AFR | LWK | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19067 | hp1 | a0001 | c0001 | t0009 | g0254 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0342 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19076 | hp1 | a0001 | c0001 | t0003 | g0343 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0357 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0354 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19083 | hp2 | a0001 | c0001 | t0014 | g0325 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19084 | hp1 | a0001 | c0001 | t0008 | g0065 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19085 | hp2 | a0001 | c0001 | t0013 | g0311 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | YRI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA19240 | hp2 | a0001 | c0001 | t0015 | g0177 | AFR | YRI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ASW | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ASW | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0266 | EUR | TSI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0243 | EUR | TSI | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0333 | SAS | GIH | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0239 | SAS | GIH | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01123 | hp1 | a0001 | c0001 | t0010 | g0163 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0135 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG06807 | hp1 | a0002 | c0002 | t0012 | g0286 | AFR | USA | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | USA | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0346 | EAS | JPT | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | USA | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | USA | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
NA21309 | hp2 | a0001 | c0001 | t0005 | g0128 | AFR | LWK | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0006 | g0133 | REF | REF | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0291 | REF | REF | RSPRY1_chr16_57181329_57245469 | RSPRY1 | chr16 | 57181329 | 57245469 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:57204505
|
A | G | 1 | a0001 | 1 | HG03195.hp1 | splice_region_variant | LOW | c.-154A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/15 | chr16 | 57204505 | ||||||
chr16:57227432
|
A | G | 1 | a0002 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
missense_variant | MODERATE | c.1252A>G | p.Ile418Val | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/15 | 1530/3503 | 1252/1731 | 418/576 | chr16 | 57227432 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:57204847
|
C | T | 1 | a0001c0004 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.189C>T | p.Ala63Ala | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/15 | 467/3503 | 189/1731 | 63/576 | chr16 | 57204847 | ||
chr16:57227371
|
C | T | 1 | a0002c0002 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.1191C>T | p.Tyr397Tyr | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/15 | 1469/3503 | 1191/1731 | 397/576 | chr16 | 57227371 | ||
chr16:57235142
|
G | C | 1 | a0001c0003 | 2 | HG03139.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.1548G>C | p.Leu516Leu | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/15 | 1826/3503 | 1548/1731 | 516/576 | chr16 | 57235142 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:57186386
|
C | T | 1 | a0001c0001t0025 | 1 | HG02280.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-221C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/15 | chr16 | 57186386 | ||||||
chr16:57186428
|
C | G | 5 | a0001c0001t0003a0001c0001t0013a0001c0001t0014others(2): Show | 46 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(43): Show |
5_prime_UTR_variant | MODIFIER | c.-179C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/15 | 18231 | chr16 | 57186428 | |||||
chr16:57204578
|
C | A | 1 | a0001c0001t0015 | 1 | NA19240.hp2 | 5_prime_UTR_variant | MODIFIER | c.-81C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/15 | 81 | chr16 | 57204578 | |||||
chr16:57239039
|
GA | G | 3 | a0001c0001t0003a0001c0001t0014a0001c0001t0024 | 43 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*74delA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 74 | INFO_REALIGN_3_PRIME | chr16 | 57239039 | ||||
chr16:57239049
|
ACT | A | 4 | a0001c0001t0002a0001c0001t0009a0001c0001t0011others(1): Show | 80 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*79_*80delCT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 79 | INFO_REALIGN_3_PRIME | chr16 | 57239049 | ||||
chr16:57239079
|
C | G | 1 | a0001c0001t0021 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*104C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 104 | chr16 | 57239079 | |||||
chr16:57239088
|
A | C | 1 | a0001c0001t0020 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*113A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 113 | chr16 | 57239088 | |||||
chr16:57239163
|
C | G | 1 | a0001c0001t0019 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*188C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 188 | chr16 | 57239163 | |||||
chr16:57239216
|
T | G | 1 | a0001c0001t0016 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*241T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 241 | chr16 | 57239216 | |||||
chr16:57239613
|
G | GT | 3 | a0001c0001t0009a0002c0002t0012a0002c0002t0018 | 6 | HG02818.hp1 HG06807.hp1 NA18950.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*650dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 651 | INFO_REALIGN_3_PRIME | chr16 | 57239613 | ||||
chr16:57239973
|
G | T | 1 | a0001c0001t0022 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*998G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 998 | chr16 | 57239973 | |||||
chr16:57240004
|
C | T | 1 | a0001c0001t0017 | 1 | NA18961.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1029C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 1029 | chr16 | 57240004 | |||||
chr16:57240307
|
AT | A | 3 | a0001c0001t0010a0001c0001t0020a0001c0001t0025 | 5 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1339delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 1339 | INFO_REALIGN_3_PRIME | chr16 | 57240307 | ||||
chr16:57240339
|
C | CCA | 2 | a0001c0001t0008a0001c0001t0017 | 5 | HG01109.hp1 HG03130.hp1 NA18953.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1383_*1384dupCA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 1385 | INFO_REALIGN_3_PRIME | chr16 | 57240339 | ||||
chr16:57240339
|
CCACACAC others(1): Show |
C | 4 | a0001c0001t0003a0001c0001t0004a0001c0001t0013others(1): Show | 52 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*1377_*1384delCACA others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 1377 | INFO_REALIGN_3_PRIME | chr16 | 57240339 | ||||
chr16:57240358
|
C | A | 6 | a0001c0001t0006a0001c0001t0007a0001c0001t0014others(3): Show | 14 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1383C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 1383 | chr16 | 57240358 | |||||
chr16:57240360
|
A | C | 3 | a0001c0001t0005a0001c0001t0011a0002c0002t0018 | 10 | HG00609.hp2 HG01361.hp2 HG01934.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1385A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 1385 | chr16 | 57240360 | |||||
chr16:57240363
|
A | AAT | 1 | a0001c0001t0006 | 6 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1402_*1403dupTA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 1404 | INFO_REALIGN_3_PRIME | chr16 | 57240363 | ||||
chr16:57240363
|
A | T | 1 | a0001c0001t0014 | 2 | NA18942.hp1 NA19083.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1388A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 15/15 | 1388 | chr16 | 57240363 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr16:57186463
|
A | C | 49 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(46): Show | 50 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.-156+12A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57186463 | ||||||
chr16:57186480
|
C | T | 1 | a0001c0001t0003g0357 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-156+29C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57186480 | ||||||
chr16:57186614
|
G | A | 1 | a0001c0001t0002g0002 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-156+163G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57186614 | ||||||
chr16:57186746
|
G | T | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG02155.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-156+295G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57186746 | ||||||
chr16:57186762
|
G | C | 42 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(39): Show | 42 | HG00621.hp1 HG01255.hp1 HG02165.hp1 others(39): Show |
intron_variant | MODIFIER | c.-156+311G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57186762 | ||||||
chr16:57186775
|
A | G | 7 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(4): Show | 7 | HG02071.hp1 HG02155.hp2 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.-156+324A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57186775 | ||||||
chr16:57186833
|
G | A | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-156+382G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57186833 | ||||||
chr16:57186977
|
G | A | 343 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.-156+526G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57186977 | ||||||
chr16:57187028
|
C | T | 4 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0126others(1): Show | 4 | HG00438.hp2 NA18991.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.-156+577C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57187028 | ||||||
chr16:57187081
|
G | A | 3 | a0001c0001t0004g0001a0001c0001t0004g0351a0001c0001t0004g0352 | 4 | HG02015.hp1 NA18992.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-156+630G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57187081 | ||||||
chr16:57187224
|
A | C | 3 | a0001c0001t0004g0001a0001c0001t0004g0351a0001c0001t0004g0352 | 4 | HG02015.hp1 NA18992.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-156+773A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57187224 | ||||||
chr16:57187520
|
ACCT | A | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+1073_-156+107 others(7): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57187520 | |||||
chr16:57187522
|
C | T | 3 | a0001c0001t0003g0348a0001c0001t0003g0349a0001c0001t0003g0350 | 3 | NA18977.hp1 NA18985.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-156+1071C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57187522 | ||||||
chr16:57187525
|
C | T | 48 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(45): Show | 49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.-156+1074C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57187525 | ||||||
chr16:57187649
|
C | T | 45 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(42): Show | 45 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.-156+1198C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57187649 | ||||||
chr16:57187953
|
G | T | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-156+1502G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57187953 | ||||||
chr16:57188219
|
G | A | 1 | a0001c0001t0005g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-156+1768G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57188219 | ||||||
chr16:57188303
|
A | G | 1 | a0001c0001t0003g0347 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-156+1852A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57188303 | ||||||
chr16:57188304
|
C | G | 1 | a0001c0001t0003g0347 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-156+1853C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57188304 | ||||||
chr16:57188317
|
G | T | 1 | a0001c0001t0003g0347 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-156+1866G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57188317 | ||||||
chr16:57188401
|
C | T | 48 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(45): Show | 49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.-156+1950C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57188401 | ||||||
chr16:57188515
|
T | TTTTG | 67 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(64): Show | 68 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.-156+2076_-156+207 others(8): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57188515 | |||||
chr16:57188527
|
G | GTTTGT | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+2079_-156+208 others(9): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57188527 | |||||
chr16:57188758
|
C | A | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+2307C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57188758 | ||||||
chr16:57188776
|
A | G | 1 | a0001c0001t0002g0285 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-156+2325A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57188776 | ||||||
chr16:57188990
|
C | CT | 56 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(53): Show | 57 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(54): Show |
intron_variant | MODIFIER | c.-156+2559dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57188990 | |||||
chr16:57188990
|
CT | C | 16 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(13): Show | 16 | HG00280.hp1 HG01169.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-156+2559delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57188990 | |||||
chr16:57189090
|
T | G | 3 | a0001c0001t0004g0130a0001c0001t0004g0132a0001c0001t0016g0131 | 3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-156+2639T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189090 | ||||||
chr16:57189137
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010 | 3 | HG01074.hp1 HG01261.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.-156+2686G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189137 | ||||||
chr16:57189155
|
T | C | 343 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.-156+2704T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189155 | ||||||
chr16:57189175
|
A | G | 1 | a0001c0003t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-156+2724A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189175 | ||||||
chr16:57189194
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-156+2743C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189194 | ||||||
chr16:57189200
|
G | A | 1 | a0001c0001t0006g0133 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-156+2749G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189200 | ||||||
chr16:57189509
|
A | G | 7 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0142others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.-156+3058A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189509 | ||||||
chr16:57189593
|
C | CT | 143 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(140): Show | 143 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.-156+3158dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57189593 | |||||
chr16:57189593
|
C | CTT | 53 | a0001c0001t0001g0116a0001c0001t0001g0304a0001c0001t0001g0305others(50): Show | 54 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(51): Show |
intron_variant | MODIFIER | c.-156+3157_-156+315 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57189593 | |||||
chr16:57189674
|
C | T | 1 | a0001c0001t0003g0345 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-156+3223C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189674 | ||||||
chr16:57189823
|
A | T | 5 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0002g0271others(2): Show | 5 | HG01433.hp2 HG01496.hp1 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156+3372A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189823 | ||||||
chr16:57189838
|
AC | A | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+3389delC | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57189838 | |||||
chr16:57189893
|
G | A | 2 | a0001c0001t0008g0157a0001c0001t0008g0158 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-156+3442G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57189893 | ||||||
chr16:57190161
|
A | AGAAC | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0015 | 3 | HG03453.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-156+3711_-156+371 others(8): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57190161 | |||||
chr16:57190230
|
G | A | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+3779G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57190230 | ||||||
chr16:57190357
|
C | T | 7 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0142others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.-156+3906C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57190357 | ||||||
chr16:57190361
|
T | C | 2 | a0001c0001t0002g0159a0001c0001t0002g0160 | 2 | NA18975.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-156+3910T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57190361 | ||||||
chr16:57190488
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-156+4037A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57190488 | ||||||
chr16:57190651
|
G | A | 1 | a0001c0001t0001g0016 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-156+4200G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57190651 | ||||||
chr16:57190853
|
T | C | 1 | a0001c0001t0007g0289 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-156+4402T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57190853 | ||||||
chr16:57190928
|
A | G | 1 | a0001c0001t0004g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-156+4477A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57190928 | ||||||
chr16:57191119
|
A | G | 5 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0002g0266others(2): Show | 5 | HG00099.hp2 HG02735.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156+4668A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57191119 | ||||||
chr16:57191193
|
G | A | 48 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(45): Show | 49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.-156+4742G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57191193 | ||||||
chr16:57191295
|
T | C | 1 | a0001c0001t0004g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-156+4844T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57191295 | ||||||
chr16:57191445
|
G | A | 7 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0002g0266others(4): Show | 7 | HG00099.hp2 HG01109.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.-156+4994G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57191445 | ||||||
chr16:57191538
|
G | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0119others(3): Show | 6 | HG02258.hp1 HG02717.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.-156+5087G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57191538 | ||||||
chr16:57191561
|
G | C | 1 | a0001c0001t0001g0019 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-156+5110G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57191561 | ||||||
chr16:57192292
|
T | A | 1 | a0001c0001t0001g0161 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-156+5841T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57192292 | ||||||
chr16:57192393
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-156+5942C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57192393 | ||||||
chr16:57192564
|
A | C | 343 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.-156+6113A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57192564 | ||||||
chr16:57192708
|
C | CT | 12 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0302others(9): Show | 12 | HG00735.hp1 HG01361.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.-156+6277dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57192708 | |||||
chr16:57192708
|
C | CTT | 41 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0320others(38): Show | 42 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(39): Show |
intron_variant | MODIFIER | c.-156+6276_-156+627 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57192708 | |||||
chr16:57192708
|
CT | C | 11 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(8): Show | 11 | HG01167.hp1 HG01993.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-156+6277delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57192708 | |||||
chr16:57192708
|
CTTTTTTT others(4): Show |
C | 5 | a0001c0001t0010g0163a0001c0001t0010g0165a0001c0001t0010g0166others(2): Show | 5 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156+6267_-156+627 others(15): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57192708 | |||||
chr16:57192712
|
T | TTC | 7 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0142others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.-156+6262_-156+626 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57192712 | |||||
chr16:57192718
|
T | C | 6 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0142others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.-156+6267T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57192718 | ||||||
chr16:57192769
|
G | A | 264 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-156+6318G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57192769 | ||||||
chr16:57192798
|
C | T | 1 | a0001c0001t0022g0279 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-156+6347C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57192798 | ||||||
chr16:57192990
|
A | G | 5 | a0001c0001t0010g0163a0001c0001t0010g0165a0001c0001t0010g0166others(2): Show | 5 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-156+6539A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57192990 | ||||||
chr16:57193044
|
C | T | 343 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.-156+6593C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193044 | ||||||
chr16:57193101
|
A | G | 1 | a0001c0001t0003g0344 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-156+6650A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193101 | ||||||
chr16:57193164
|
T | C | 1 | a0001c0001t0005g0023 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-156+6713T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193164 | ||||||
chr16:57193295
|
C | G | 1 | a0001c0001t0005g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-156+6844C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193295 | ||||||
chr16:57193446
|
A | G | 1 | a0001c0001t0021g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-156+6995A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193446 | ||||||
chr16:57193491
|
CT | C | 95 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0208others(92): Show | 96 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.-156+7054delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57193491 | |||||
chr16:57193491
|
CTT | C | 30 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(27): Show | 30 | HG00642.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-156+7053_-156+705 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57193491 | |||||
chr16:57193505
|
T | A | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+7054T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193505 | ||||||
chr16:57193506
|
C | A | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+7055C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193506 | ||||||
chr16:57193654
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-156+7203G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193654 | ||||||
chr16:57193708
|
T | G | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+7257T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193708 | ||||||
chr16:57193716
|
G | T | 1 | a0001c0001t0001g0111 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-156+7265G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193716 | ||||||
chr16:57193911
|
C | G | 1 | a0001c0001t0006g0145 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-156+7460C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57193911 | ||||||
chr16:57194096
|
A | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0107a0001c0001t0001g0108others(2): Show | 5 | HG01106.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.-156+7645A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57194096 | ||||||
chr16:57194105
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-156+7654C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57194105 | ||||||
chr16:57194188
|
A | G | 1 | a0001c0001t0002g0253 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-156+7737A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57194188 | ||||||
chr16:57194251
|
C | G | 1 | a0001c0001t0003g0343 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-156+7800C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57194251 | ||||||
chr16:57194530
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-156+8079C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57194530 | ||||||
chr16:57194554
|
G | T | 1 | a0001c0001t0003g0342 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-156+8103G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57194554 | ||||||
chr16:57194556
|
C | T | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+8105C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57194556 | ||||||
chr16:57195094
|
T | C | 1 | a0001c0001t0001g0025 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-156+8643T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195094 | ||||||
chr16:57195113
|
T | A | 1 | a0001c0001t0001g0026 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-156+8662T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195113 | ||||||
chr16:57195217
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-156+8766G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195217 | ||||||
chr16:57195314
|
C | T | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-156+8863C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195314 | ||||||
chr16:57195374
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-156+8923T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195374 | ||||||
chr16:57195462
|
A | G | 1 | a0001c0001t0002g0268 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-156+9011A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195462 | ||||||
chr16:57195664
|
C | CT | 53 | a0001c0001t0002g0252a0001c0001t0003g0312a0001c0001t0003g0313others(50): Show | 54 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(51): Show |
intron_variant | MODIFIER | c.-155-8827dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57195664 | |||||
chr16:57195664
|
CT | C | 9 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(6): Show | 9 | HG01884.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-155-8827delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57195664 | |||||
chr16:57195793
|
T | C | 62 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(59): Show | 63 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.-155-8711T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195793 | ||||||
chr16:57195904
|
C | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0100a0001c0001t0001g0101others(5): Show | 8 | HG01243.hp1 HG01496.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.-155-8600C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195904 | ||||||
chr16:57195914
|
C | T | 3 | a0001c0001t0001g0141a0001c0001t0008g0157a0001c0001t0008g0158 | 3 | HG01109.hp1 HG02486.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-155-8590C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195914 | ||||||
chr16:57195953
|
T | C | 1 | a0001c0001t0021g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-155-8551T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57195953 | ||||||
chr16:57196020
|
C | CA | 56 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(53): Show | 57 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(54): Show |
intron_variant | MODIFIER | c.-155-8469dupA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57196020 | |||||
chr16:57196020
|
C | CAA | 8 | a0001c0001t0001g0003a0001c0001t0001g0029a0001c0001t0001g0030others(5): Show | 8 | HG00738.hp1 HG01106.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-155-8470_-155-846 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57196020 | |||||
chr16:57196030
|
A | AAT | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(14): Show | 17 | HG00642.hp2 HG01168.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.-155-8473_-155-847 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57196030 | |||||
chr16:57196032
|
A | AAT | 162 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0020others(159): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.-155-8471_-155-847 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57196032 | |||||
chr16:57196032
|
A | ATAT | 4 | a0001c0001t0001g0193a0001c0001t0001g0282a0001c0001t0002g0002others(1): Show | 4 | HG02055.hp1 HG02083.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-155-8472_-155-847 others(7): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196032 | ||||||
chr16:57196032
|
A | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(14): Show | 17 | HG00642.hp2 HG01168.hp2 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.-155-8472A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196032 | ||||||
chr16:57196034
|
A | AAAT | 9 | a0001c0001t0001g0011a0001c0001t0001g0032a0001c0001t0001g0033others(6): Show | 9 | HG00140.hp2 HG02056.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.-155-8469_-155-846 others(7): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57196034 | |||||
chr16:57196034
|
A | AAT | 54 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(51): Show | 54 | HG00280.hp2 HG01074.hp1 HG01099.hp1 others(51): Show |
intron_variant | MODIFIER | c.-155-8452_-155-845 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57196034 | |||||
chr16:57196034
|
A | ATAT | 3 | a0001c0001t0001g0026a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG01257.hp1 HG01258.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.-155-8470_-155-846 others(7): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196034 | ||||||
chr16:57196034
|
A | T | 195 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(192): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.-155-8470A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196034 | ||||||
chr16:57196036
|
T | A | 52 | a0001c0001t0001g0028a0001c0001t0001g0134a0001c0001t0001g0137others(49): Show | 52 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(49): Show |
intron_variant | MODIFIER | c.-155-8468T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196036 | ||||||
chr16:57196038
|
T | A | 7 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(4): Show | 7 | HG02258.hp2 HG02486.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-155-8466T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196038 | ||||||
chr16:57196040
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-155-8464T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196040 | ||||||
chr16:57196334
|
G | T | 1 | a0001c0001t0004g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-155-8170G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196334 | ||||||
chr16:57196340
|
T | A | 1 | a0001c0001t0004g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-155-8164T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196340 | ||||||
chr16:57196532
|
T | C | 1 | a0001c0001t0002g0151 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-155-7972T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196532 | ||||||
chr16:57196675
|
A | T | 343 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.-155-7829A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57196675 | ||||||
chr16:57197171
|
T | C | 2 | a0002c0002t0012g0286a0002c0002t0012g0288 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-7333T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57197171 | ||||||
chr16:57197185
|
C | T | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-7319C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57197185 | ||||||
chr16:57197317
|
T | A | 1 | a0001c0001t0003g0345 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-155-7187T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57197317 | ||||||
chr16:57197667
|
C | T | 1 | a0001c0001t0002g0247 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-155-6837C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57197667 | ||||||
chr16:57197709
|
TTTTTTG | T | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-6772_-155-676 others(10): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57197709 | |||||
chr16:57197836
|
A | C | 1 | a0001c0001t0004g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-155-6668A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57197836 | ||||||
chr16:57197863
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-155-6641A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57197863 | ||||||
chr16:57197894
|
C | T | 272 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(269): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.-155-6610C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57197894 | ||||||
chr16:57197923
|
GCTACATT others(37): Show |
G | 59 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(56): Show | 60 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.-155-6578_-155-653 others(48): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57197923 | |||||
chr16:57198046
|
T | A | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-6458T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198046 | ||||||
chr16:57198110
|
G | A | 9 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(6): Show | 9 | HG01884.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-155-6394G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198110 | ||||||
chr16:57198167
|
C | T | 1 | a0001c0001t0002g0246 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-155-6337C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198167 | ||||||
chr16:57198294
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-155-6210G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198294 | ||||||
chr16:57198316
|
G | A | 2 | a0001c0001t0001g0193a0001c0001t0001g0282 | 2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-155-6188G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198316 | ||||||
chr16:57198371
|
A | G | 48 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(45): Show | 49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.-155-6133A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198371 | ||||||
chr16:57198383
|
C | CA | 128 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(125): Show | 128 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-155-6109dupA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57198383 | |||||
chr16:57198474
|
A | T | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-6030A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198474 | ||||||
chr16:57198558
|
T | C | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-5946T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198558 | ||||||
chr16:57198615
|
T | C | 1 | a0001c0001t0002g0207 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-155-5889T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198615 | ||||||
chr16:57198840
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-155-5664C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57198840 | ||||||
chr16:57199049
|
A | G | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-155-5455A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199049 | ||||||
chr16:57199125
|
A | G | 132 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(129): Show | 132 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-155-5379A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199125 | ||||||
chr16:57199173
|
A | G | 62 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(59): Show | 63 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.-155-5331A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199173 | ||||||
chr16:57199179
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-155-5325A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199179 | ||||||
chr16:57199220
|
C | T | 1 | a0001c0001t0005g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-155-5284C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199220 | ||||||
chr16:57199225
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-155-5279C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199225 | ||||||
chr16:57199448
|
T | C | 71 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(68): Show | 72 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.-155-5056T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199448 | ||||||
chr16:57199533
|
T | C | 3 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037 | 3 | HG02622.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-155-4971T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199533 | ||||||
chr16:57199535
|
T | C | 7 | a0001c0001t0001g0155a0001c0001t0001g0171a0001c0001t0001g0255others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-155-4969T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199535 | ||||||
chr16:57199696
|
T | G | 1 | a0001c0001t0001g0105 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-155-4808T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199696 | ||||||
chr16:57199838
|
CT | C | 289 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(286): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.-155-4652delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57199838 | |||||
chr16:57199838
|
CTT | C | 53 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(50): Show | 54 | HG00280.hp1 HG00621.hp1 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.-155-4653_-155-465 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57199838 | |||||
chr16:57199895
|
GT | G | 263 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(260): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.-155-4598delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57199895 | |||||
chr16:57199896
|
T | C | 9 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(6): Show | 9 | HG01884.hp1 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-155-4608T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57199896 | ||||||
chr16:57199913
|
CT | C | 19 | a0001c0001t0001g0024a0001c0001t0001g0140a0001c0001t0001g0148others(16): Show | 19 | HG01169.hp2 HG01884.hp1 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.-155-4576delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57199913 | |||||
chr16:57200217
|
TG | T | 14 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0161others(11): Show | 14 | HG01099.hp2 HG01109.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.-155-4282delG | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200217 | |||||
chr16:57200314
|
C | A | 1 | a0001c0001t0001g0208 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-155-4190C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200314 | ||||||
chr16:57200360
|
C | A | 1 | a0001c0001t0004g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-155-4144C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200360 | ||||||
chr16:57200417
|
T | G | 1 | a0001c0001t0022g0279 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-155-4087T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200417 | ||||||
chr16:57200557
|
G | A | 7 | a0001c0001t0001g0155a0001c0001t0001g0171a0001c0001t0001g0255others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-155-3947G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200557 | ||||||
chr16:57200558
|
G | T | 2 | a0001c0001t0004g0130a0001c0001t0004g0132 | 2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-155-3946G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200558 | ||||||
chr16:57200560
|
TGGGGCGG others(120): Show |
T | 1 | a0001c0001t0003g0316 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-155-3866_-155-374 others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200560 | |||||
chr16:57200636
|
G | C | 3 | a0001c0001t0004g0001a0001c0001t0004g0351a0001c0001t0004g0352 | 4 | HG02015.hp1 NA18992.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-155-3868G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200636 | ||||||
chr16:57200638
|
C | T | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3866C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200638 | ||||||
chr16:57200651
|
C | T | 1 | a0001c0001t0006g0129 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-155-3853C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200651 | ||||||
chr16:57200652
|
G | GGGCTGGG others(41): Show |
1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3849_-155-384 others(52): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200652 | |||||
chr16:57200661
|
G | A | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3843G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200661 | ||||||
chr16:57200661
|
G | GCTGACCC others(42): Show |
2 | a0001c0001t0001g0101a0001c0001t0002g0252 | 2 | HG02056.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-155-3832_-155-383 others(53): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200661 | |||||
chr16:57200661
|
G | GCTGACCC others(41): Show |
336 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(333): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.-155-3833_-155-383 others(52): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200661 | |||||
chr16:57200661
|
G | GCTGACCC others(41): Show |
7 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0142others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.-155-3833_-155-383 others(52): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200661 | |||||
chr16:57200661
|
G | GGCTGACC others(42): Show |
1 | a0001c0001t0002g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-155-3843_-155-384 others(53): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200661 | ||||||
chr16:57200663
|
TGACCCCC others(121): Show |
T | 7 | a0001c0001t0001g0155a0001c0001t0001g0171a0001c0001t0001g0255others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-155-3839_-155-371 others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200663 | |||||
chr16:57200665
|
A | ACCCCCCG others(42): Show |
1 | a0001c0001t0004g0352 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-155-3833_-155-383 others(53): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200665 | |||||
chr16:57200684
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-155-3820G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200684 | ||||||
chr16:57200696
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T | G | 1 | a0001c0001t0002g0209 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-155-3808T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200696 | ||||||
chr16:57200792
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GC | G | 335 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(332): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.-155-3704delC | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200792 | |||||
chr16:57200793
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C | G | 7 | a0001c0001t0001g0155a0001c0001t0001g0171a0001c0001t0001g0255others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-155-3711C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200793 | ||||||
chr16:57200816
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G | T | 1 | a0001c0001t0001g0182 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-155-3688G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200816 | ||||||
chr16:57200829
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G | GGGCAGAG others(71): Show |
2 | a0001c0001t0002g0241a0001c0001t0002g0242 | 2 | NA18962.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-155-3651_-155-357 others(82): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200829 | |||||
chr16:57200842
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C | G | 31 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(28): Show | 31 | HG00642.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.-155-3662C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200842 | ||||||
chr16:57200850
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C | T | 48 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(45): Show | 49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.-155-3654C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200850 | ||||||
chr16:57200856
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C | T | 1 | a0001c0001t0002g0243 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-155-3648C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200856 | ||||||
chr16:57200886
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T | C | 71 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(68): Show | 72 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.-155-3618T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200886 | ||||||
chr16:57200934
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C | T | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-155-3570C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200934 | ||||||
chr16:57200947
|
C | CG | 36 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0034others(33): Show | 36 | HG00642.hp1 HG00735.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.-155-3543dupG | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200947 | |||||
chr16:57200947
|
C | CGG | 21 | a0001c0001t0001g0104a0001c0001t0001g0149a0001c0001t0001g0150others(18): Show | 21 | HG00642.hp2 HG01074.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.-155-3544_-155-354 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200947 | |||||
chr16:57200947
|
CG | C | 73 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0013others(70): Show | 73 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.-155-3543delG | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200947 | |||||
chr16:57200947
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CGG | C | 75 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(72): Show | 75 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.-155-3544_-155-354 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200947 | |||||
chr16:57200947
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CGGGG | C | 56 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(53): Show | 57 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(54): Show |
intron_variant | MODIFIER | c.-155-3546_-155-354 others(8): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200947 | |||||
chr16:57200952
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G | T | 1 | a0001c0001t0001g0026 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-155-3552G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200952 | ||||||
chr16:57200953
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G | T | 1 | a0001c0001t0002g0267 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-155-3551G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200953 | ||||||
chr16:57200953
|
GGGGGGGG others(43): Show |
G | 1 | a0001c0001t0001g0075 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-155-3544_-155-349 others(54): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200953 | |||||
chr16:57200954
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G | T | 1 | a0001c0001t0005g0128 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-155-3550G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200954 | ||||||
chr16:57200954
|
GGGGGGGG others(42): Show |
G | 1 | a0001c0001t0002g0222 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-155-3543_-155-349 others(53): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200954 | |||||
chr16:57200955
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GGGGGGGC others(41): Show |
G | 3 | a0001c0001t0002g0234a0001c0001t0002g0252a0001c0001t0023g0310 | 3 | HG02056.hp1 NA18973.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.-155-3517_-155-347 others(52): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57200955 | |||||
chr16:57200958
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G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0256 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-155-3546G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200958 | ||||||
chr16:57200959
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G | T | 54 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(51): Show | 55 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.-155-3545G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200959 | ||||||
chr16:57200995
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T | G | 2 | a0001c0001t0001g0140a0001c0001t0001g0141 | 2 | HG01884.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-155-3509T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57200995 | ||||||
chr16:57201035
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T | C | 3 | a0001c0001t0001g0050a0001c0001t0001g0076a0002c0002t0018g0287 | 3 | HG02818.hp1 NA18974.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-155-3469T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201035 | ||||||
chr16:57201056
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G | C | 264 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-155-3448G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201056 | ||||||
chr16:57201066
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C | G | 1 | a0001c0001t0009g0221 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-155-3438C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201066 | ||||||
chr16:57201078
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A | G | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3426A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201078 | ||||||
chr16:57201080
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A | C | 2 | a0002c0002t0012g0286a0002c0002t0012g0288 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-3424A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201080 | ||||||
chr16:57201082
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G | T | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3422G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201082 | ||||||
chr16:57201086
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T | C | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3418T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201086 | ||||||
chr16:57201102
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A | G | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3402A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201102 | ||||||
chr16:57201103
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C | CGCTCCTC others(33): Show |
1 | a0001c0001t0001g0185 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-155-3388_-155-334 others(44): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57201103 | |||||
chr16:57201103
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C | G | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3401C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201103 | ||||||
chr16:57201109
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T | C | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3395T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201109 | ||||||
chr16:57201113
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T | C | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3391T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201113 | ||||||
chr16:57201117
|
CAGGCGGA others(29): Show |
C | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3386_-155-335 others(40): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201117 | ||||||
chr16:57201124
|
AGTGGCTG others(73): Show |
A | 2 | a0002c0002t0012g0286a0002c0002t0012g0288 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-3300_-155-322 others(84): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57201124 | |||||
chr16:57201137
|
C | CGGAGGGG others(33): Show |
59 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(56): Show | 60 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.-155-3330_-155-329 others(44): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57201137 | |||||
chr16:57201156
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T | C | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3348T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201156 | ||||||
chr16:57201160
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A | C | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3344A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201160 | ||||||
chr16:57201162
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G | A | 1 | a0001c0001t0002g0213 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-155-3342G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201162 | ||||||
chr16:57201164
|
T | G | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3340T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201164 | ||||||
chr16:57201174
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A | G | 2 | a0001c0001t0002g0273a0002c0002t0018g0287 | 2 | HG01496.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-155-3330A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201174 | ||||||
chr16:57201177
|
T | C | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3327T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201177 | ||||||
chr16:57201182
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G | A | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3322G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201182 | ||||||
chr16:57201183
|
G | C | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3321G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201183 | ||||||
chr16:57201196
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T | C | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3308T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201196 | ||||||
chr16:57201200
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A | G | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3304A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201200 | ||||||
chr16:57201204
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T | A | 1 | a0002c0002t0018g0287 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-155-3300T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201204 | ||||||
chr16:57201214
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G | A | 1 | a0001c0003t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-155-3290G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201214 | ||||||
chr16:57201217
|
C | T | 1 | a0001c0003t0001g0117 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-155-3287C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201217 | ||||||
chr16:57201281
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-155-3223C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201281 | ||||||
chr16:57201286
|
C | T | 1 | a0001c0001t0022g0279 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-155-3218C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201286 | ||||||
chr16:57201287
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-155-3217G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201287 | ||||||
chr16:57201304
|
TCTCCTCA others(30): Show |
T | 6 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-155-3191_-155-315 others(41): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57201304 | |||||
chr16:57201358
|
C | T | 59 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(56): Show | 60 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.-155-3146C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201358 | ||||||
chr16:57201407
|
TGGCAGAG others(33): Show |
T | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG01074.hp1 HG01175.hp1 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.-155-3076_-155-303 others(44): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57201407 | |||||
chr16:57201442
|
C | T | 1 | a0001c0001t0001g0074 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-155-3062C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201442 | ||||||
chr16:57201461
|
C | T | 3 | a0001c0001t0004g0001a0001c0001t0004g0351a0001c0001t0004g0352 | 4 | HG02015.hp1 NA18992.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-155-3043C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201461 | ||||||
chr16:57201550
|
C | CG | 8 | a0001c0001t0001g0051a0001c0001t0001g0115a0001c0001t0001g0174others(5): Show | 8 | HG01243.hp2 HG01496.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-155-2950dupG | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57201550 | |||||
chr16:57201551
|
G | C | 7 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0142others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.-155-2953G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201551 | ||||||
chr16:57201686
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-155-2818C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201686 | ||||||
chr16:57201690
|
A | C | 59 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(56): Show | 60 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.-155-2814A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201690 | ||||||
chr16:57201692
|
T | A | 1 | a0002c0002t0012g0286 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-155-2812T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201692 | ||||||
chr16:57201732
|
G | A | 135 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 135 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.-155-2772G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201732 | ||||||
chr16:57201778
|
G | A | 2 | a0001c0001t0008g0157a0001c0001t0008g0158 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-155-2726G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201778 | ||||||
chr16:57201794
|
C | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0122 | 2 | HG02074.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.-155-2710C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201794 | ||||||
chr16:57201799
|
A | G | 2 | a0001c0001t0004g0042a0001c0001t0004g0043 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-155-2705A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201799 | ||||||
chr16:57201824
|
C | T | 48 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(45): Show | 49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.-155-2680C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201824 | ||||||
chr16:57201851
|
C | A | 1 | a0001c0001t0001g0297 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-155-2653C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201851 | ||||||
chr16:57201864
|
C | T | 48 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(45): Show | 49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.-155-2640C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201864 | ||||||
chr16:57201958
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-155-2546A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57201958 | ||||||
chr16:57201960
|
AGAGGGAG others(8): Show |
A | 1 | a0001c0001t0001g0020 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-155-2525_-155-251 others(19): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57201960 | |||||
chr16:57202053
|
A | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0280 | 2 | HG00735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.-155-2451A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57202053 | ||||||
chr16:57202056
|
T | C | 3 | a0001c0001t0004g0130a0001c0001t0004g0132a0001c0001t0016g0131 | 3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.-155-2448T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57202056 | ||||||
chr16:57202293
|
G | C | 1 | a0001c0001t0001g0052 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-155-2211G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57202293 | ||||||
chr16:57202878
|
T | TTA | 13 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0161others(10): Show | 13 | HG00735.hp2 HG01099.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-155-1598_-155-159 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
T | TTATA | 6 | a0001c0001t0001g0284a0001c0001t0002g0196a0001c0001t0002g0218others(3): Show | 6 | HG00140.hp2 HG01071.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-155-1600_-155-159 others(8): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
T | TTATATA | 3 | a0001c0001t0002g0217a0001c0001t0002g0231a0001c0001t0002g0239 | 3 | HG03492.hp1 NA19002.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-155-1602_-155-159 others(10): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
T | TTATATAT others(1): Show |
19 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0169others(16): Show | 19 | HG00099.hp2 HG00408.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.-155-1604_-155-159 others(12): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
T | TTATATAT others(3): Show |
25 | a0001c0001t0001g0226a0001c0001t0002g0002a0001c0001t0002g0197others(22): Show | 26 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.-155-1606_-155-159 others(14): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
T | TTATATAT others(5): Show |
6 | a0001c0001t0001g0276a0001c0001t0002g0203a0001c0001t0002g0249others(3): Show | 6 | HG02559.hp1 HG02922.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.-155-1608_-155-159 others(16): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
T | TTATATAT others(7): Show |
13 | a0001c0001t0001g0236a0001c0001t0002g0202a0001c0001t0002g0214others(10): Show | 13 | HG00642.hp1 HG00738.hp1 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.-155-1610_-155-159 others(18): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
T | TTATATAT others(9): Show |
15 | a0001c0001t0002g0151a0001c0001t0002g0152a0001c0001t0002g0159others(12): Show | 15 | HG01257.hp2 HG02165.hp1 HG03239.hp1 others(12): Show |
intron_variant | MODIFIER | c.-155-1612_-155-159 others(20): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
T | TTATATAT others(11): Show |
11 | a0001c0001t0002g0209a0001c0001t0002g0246a0001c0001t0003g0320others(8): Show | 11 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.-155-1614_-155-159 others(22): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
T | TTATATAT others(13): Show |
7 | a0001c0001t0002g0156a0001c0001t0002g0224a0001c0001t0002g0266others(4): Show | 7 | HG02074.hp1 HG03017.hp1 NA18964.hp2 others(4): Show |
intron_variant | MODIFIER | c.-155-1616_-155-159 others(24): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
T | TTATATAT others(15): Show |
8 | a0001c0001t0002g0285a0001c0001t0003g0313a0001c0001t0003g0315others(5): Show | 8 | HG02145.hp2 HG02155.hp1 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.-155-1618_-155-159 others(26): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
T | TTATATAT others(17): Show |
6 | a0001c0001t0002g0154a0001c0001t0002g0170a0001c0001t0002g0245others(3): Show | 6 | HG02132.hp1 HG02523.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.-155-1620_-155-159 others(28): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
T | TTATATAT others(19): Show |
1 | a0001c0001t0003g0348 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-155-1622_-155-159 others(30): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
T | TTATATAT others(21): Show |
3 | a0001c0001t0003g0341a0001c0001t0003g0343a0001c0001t0014g0325 | 3 | NA18939.hp2 NA19076.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.-155-1624_-155-159 others(32): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
T | TTATATAT others(27): Show |
1 | a0001c0001t0013g0319 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-155-1597_-155-159 others(38): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
T | TTTTATAT others(11): Show |
1 | a0001c0001t0003g0346 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-155-1625_-155-162 others(22): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
T | TTTTATAT others(13): Show |
2 | a0001c0001t0003g0318a0001c0001t0003g0336 | 2 | NA18951.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.-155-1625_-155-162 others(24): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
T | TTTTATAT others(15): Show |
1 | a0001c0001t0003g0342 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-155-1625_-155-162 others(26): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
TTA | T | 17 | a0001c0001t0001g0155a0001c0001t0001g0171a0001c0001t0001g0193others(14): Show | 17 | HG01891.hp2 HG01934.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.-155-1598_-155-159 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
TTATA | T | 13 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(10): Show | 13 | HG00280.hp1 HG00609.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.-155-1600_-155-159 others(8): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
TTATATA | T | 51 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(48): Show | 51 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.-155-1602_-155-159 others(10): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
TTATATAT others(1): Show |
T | 86 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(83): Show | 86 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.-155-1604_-155-159 others(12): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202878
|
TTATATAT others(3): Show |
T | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-1606_-155-159 others(14): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202878 | |||||
chr16:57202888
|
A | ATATATAT others(3): Show |
5 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0223others(2): Show | 5 | NA18946.hp1 NA18959.hp1 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.-155-1607_-155-160 others(14): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57202888 | |||||
chr16:57202939
|
T | C | 1 | a0001c0001t0003g0316 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-155-1565T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57202939 | ||||||
chr16:57202959
|
A | G | 3 | a0001c0001t0004g0001a0001c0001t0004g0351a0001c0001t0004g0352 | 4 | HG02015.hp1 NA18992.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.-155-1545A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57202959 | ||||||
chr16:57203008
|
TAAA | T | 6 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0142others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.-155-1494_-155-149 others(7): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57203008 | |||||
chr16:57203113
|
A | G | 1 | a0001c0001t0021g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-155-1391A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57203113 | ||||||
chr16:57203125
|
C | T | 1 | a0001c0001t0016g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-155-1379C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57203125 | ||||||
chr16:57203349
|
T | A | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-1155T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57203349 | ||||||
chr16:57203460
|
A | G | 1 | a0001c0001t0022g0279 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-155-1044A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57203460 | ||||||
chr16:57203496
|
TTTTG | T | 3 | a0001c0001t0001g0072a0001c0001t0002g0200a0001c0001t0002g0203 | 3 | HG00140.hp1 NA19056.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.-155-992_-155-989d others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr16 | 57203496 | |||||
chr16:57203543
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-155-961A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57203543 | ||||||
chr16:57203746
|
C | G | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-155-758C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57203746 | ||||||
chr16:57203960
|
A | C | 1 | a0001c0001t0002g0167 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-155-544A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57203960 | ||||||
chr16:57204030
|
G | A | 2 | a0001c0001t0003g0314a0001c0003t0001g0117 | 2 | HG02698.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-155-474G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57204030 | ||||||
chr16:57204034
|
G | A | 2 | a0001c0001t0008g0157a0001c0001t0008g0158 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-155-470G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57204034 | ||||||
chr16:57204084
|
G | A | 8 | a0001c0001t0001g0027a0001c0001t0001g0100a0001c0001t0001g0101others(5): Show | 8 | HG01243.hp1 HG01496.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.-155-420G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57204084 | ||||||
chr16:57204190
|
C | T | 7 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0142others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.-155-314C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57204190 | ||||||
chr16:57204397
|
A | C | 1 | a0001c0001t0001g0083 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-155-107A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 1/14 | chr16 | 57204397 | ||||||
chr16:57205059
|
C | T | 2 | a0001c0001t0006g0133a0001c0001t0006g0143 | 2 | HG01070.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.350+51C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57205059 | ||||||
chr16:57205060
|
G | A | 2 | a0001c0001t0001g0137a0001c0001t0001g0139 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.350+52G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57205060 | ||||||
chr16:57205068
|
G | A | 7 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0142others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.350+60G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57205068 | ||||||
chr16:57205151
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037 | 3 | HG02622.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.350+143G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57205151 | ||||||
chr16:57205155
|
A | G | 6 | a0001c0001t0010g0163a0001c0001t0010g0165a0001c0001t0010g0166others(3): Show | 6 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.350+147A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57205155 | ||||||
chr16:57205384
|
A | G | 3 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0143 | 3 | HG00280.hp1 HG01070.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.350+376A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57205384 | ||||||
chr16:57205730
|
T | C | 1 | a0001c0001t0001g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.350+722T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57205730 | ||||||
chr16:57205804
|
T | C | 65 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(62): Show | 66 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.350+796T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57205804 | ||||||
chr16:57205924
|
G | T | 48 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(45): Show | 49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.350+916G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57205924 | ||||||
chr16:57206166
|
G | A | 1 | a0001c0001t0002g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.350+1158G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57206166 | ||||||
chr16:57206313
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.350+1305G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57206313 | ||||||
chr16:57206429
|
T | A | 3 | a0001c0001t0004g0130a0001c0001t0004g0132a0001c0001t0016g0131 | 3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.350+1421T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57206429 | ||||||
chr16:57206757
|
G | GTC | 3 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037 | 3 | HG02622.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.351-1299_351-1298d others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 57206757 | |||||
chr16:57206889
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.351-1169G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57206889 | ||||||
chr16:57207096
|
C | T | 1 | a0001c0001t0003g0332 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.351-962C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57207096 | ||||||
chr16:57207258
|
A | G | 125 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(122): Show | 125 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.351-800A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57207258 | ||||||
chr16:57207461
|
G | C | 2 | a0001c0001t0008g0157a0001c0001t0008g0158 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.351-597G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57207461 | ||||||
chr16:57207462
|
A | T | 2 | a0001c0001t0008g0157a0001c0001t0008g0158 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.351-596A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57207462 | ||||||
chr16:57207617
|
G | A | 3 | a0001c0001t0005g0128a0001c0001t0005g0135a0001c0001t0005g0136 | 3 | HG02258.hp2 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.351-441G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57207617 | ||||||
chr16:57207833
|
G | A | 48 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(45): Show | 49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.351-225G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57207833 | ||||||
chr16:57207862
|
A | G | 2 | a0001c0001t0003g0348a0001c0001t0003g0349 | 2 | NA18977.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.351-196A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57207862 | ||||||
chr16:57207890
|
A | AC | 6 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0142others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.351-167dupC | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr16 | 57207890 | |||||
chr16:57207893
|
T | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0091a0001c0001t0005g0084 | 3 | HG01934.hp1 HG02132.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.351-165T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 2/14 | chr16 | 57207893 | ||||||
chr16:57208174
|
CT | C | 3 | a0001c0001t0001g0274a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02559.hp1 HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.403+68delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 57208174 | |||||
chr16:57208181
|
TTTTTG | T | 3 | a0001c0001t0004g0130a0001c0001t0004g0132a0001c0001t0016g0131 | 3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.403+87_403+91delTT others(3): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 57208181 | |||||
chr16:57208228
|
T | G | 47 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0003g0312others(44): Show | 47 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.403+118T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208228 | ||||||
chr16:57208231
|
A | C | 1 | a0001c0001t0021g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.403+121A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208231 | ||||||
chr16:57208297
|
T | G | 1 | a0001c0001t0001g0025 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.403+187T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208297 | ||||||
chr16:57208302
|
C | CT | 60 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0017others(57): Show | 60 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.403+215dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 57208302 | |||||
chr16:57208302
|
CT | C | 6 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0030others(3): Show | 6 | HG02257.hp1 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.403+215delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 57208302 | |||||
chr16:57208376
|
TTA | T | 213 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(210): Show | 213 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.403+290_403+291del others(2): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 57208376 | |||||
chr16:57208376
|
TTATATA | T | 3 | a0001c0001t0005g0128a0001c0001t0005g0135a0001c0001t0005g0136 | 3 | HG02258.hp2 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.403+286_403+291del others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 57208376 | |||||
chr16:57208378
|
A | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0061a0001c0001t0001g0063others(1): Show | 4 | HG02886.hp1 HG03540.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+268A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208378 | ||||||
chr16:57208392
|
A | T | 1 | a0001c0001t0021g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.403+282A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208392 | ||||||
chr16:57208393
|
TA | T | 4 | a0001c0001t0006g0129a0001c0001t0006g0142a0001c0001t0006g0143others(1): Show | 4 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.403+284delA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208393 | ||||||
chr16:57208394
|
A | T | 1 | a0001c0001t0021g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.403+284A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208394 | ||||||
chr16:57208395
|
TA | T | 9 | a0001c0001t0001g0180a0001c0001t0001g0233a0001c0001t0001g0236others(6): Show | 10 | HG00642.hp1 HG02015.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.403+286delA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208395 | ||||||
chr16:57208395
|
TATA | T | 5 | a0001c0001t0001g0176a0001c0001t0001g0274a0001c0001t0002g0206others(2): Show | 5 | HG01167.hp2 HG01433.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.403+286_403+288del others(3): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208395 | ||||||
chr16:57208396
|
A | T | 15 | a0001c0001t0001g0148a0001c0001t0001g0181a0001c0001t0002g0214others(12): Show | 15 | HG00280.hp1 HG01070.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.403+286A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208396 | ||||||
chr16:57208397
|
TA | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0226a0001c0001t0002g0275 | 3 | HG00438.hp1 HG00738.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.403+288delA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208397 | ||||||
chr16:57208397
|
TATA | T | 15 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0064others(12): Show | 15 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.403+288_403+290del others(3): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208397 | ||||||
chr16:57208398
|
A | AT | 3 | a0001c0001t0001g0038a0001c0001t0001g0302a0001c0001t0003g0317 | 3 | HG03239.hp1 NA18997.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.403+289dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 57208398 | |||||
chr16:57208398
|
A | T | 134 | a0001c0001t0001g0031a0001c0001t0001g0062a0001c0001t0001g0070others(131): Show | 135 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.403+288A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208398 | ||||||
chr16:57208399
|
TA | T | 8 | a0001c0001t0001g0052a0001c0001t0001g0057a0001c0001t0001g0061others(5): Show | 8 | HG00738.hp2 HG02886.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.403+290delA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208399 | ||||||
chr16:57208400
|
A | AT | 39 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0100others(36): Show | 39 | HG00558.hp1 HG01255.hp1 HG02165.hp1 others(36): Show |
intron_variant | MODIFIER | c.403+305dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 57208400 | |||||
chr16:57208400
|
A | ATT | 12 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 12 | HG01496.hp2 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.403+304_403+305dup others(2): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr16 | 57208400 | |||||
chr16:57208400
|
A | T | 255 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(252): Show | 256 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.403+290A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208400 | ||||||
chr16:57208403
|
T | A | 1 | a0001c0001t0017g0292 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.403+293T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208403 | ||||||
chr16:57208438
|
C | T | 138 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(135): Show | 138 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.403+328C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208438 | ||||||
chr16:57208451
|
G | A | 268 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(265): Show | 268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.403+341G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208451 | ||||||
chr16:57208460
|
C | T | 125 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(122): Show | 125 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.403+350C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208460 | ||||||
chr16:57208864
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.404-211G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208864 | ||||||
chr16:57208920
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.404-155G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57208920 | ||||||
chr16:57209015
|
C | T | 1 | a0001c0001t0001g0149 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.404-60C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57209015 | ||||||
chr16:57209057
|
T | A | 2 | a0001c0001t0004g0042a0001c0001t0004g0043 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.404-18T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 3/14 | chr16 | 57209057 | ||||||
chr16:57209583
|
T | G | 3 | a0001c0001t0004g0130a0001c0001t0004g0132a0001c0001t0016g0131 | 3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.516+396T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209583 | ||||||
chr16:57209594
|
C | G | 48 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(45): Show | 49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.516+407C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209594 | ||||||
chr16:57209611
|
G | A | 1 | a0001c0001t0001g0294 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.516+424G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209611 | ||||||
chr16:57209713
|
A | C | 3 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0121 | 3 | HG01891.hp1 HG02055.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.516+526A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209713 | ||||||
chr16:57209764
|
C | T | 3 | a0001c0001t0001g0236a0001c0001t0002g0219a0001c0001t0002g0243 | 3 | HG00642.hp1 HG01071.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.516+577C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209764 | ||||||
chr16:57209847
|
T | G | 2 | a0001c0001t0008g0157a0001c0001t0008g0158 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.516+660T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209847 | ||||||
chr16:57209849
|
T | A | 1 | a0001c0001t0001g0150 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.516+662T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209849 | ||||||
chr16:57209880
|
G | A | 15 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028others(12): Show | 15 | HG01243.hp1 HG01496.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.516+693G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209880 | ||||||
chr16:57209935
|
C | T | 7 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0142others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.516+748C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209935 | ||||||
chr16:57209976
|
A | C | 1 | a0001c0001t0001g0025 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.516+789A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209976 | ||||||
chr16:57209988
|
A | G | 3 | a0001c0001t0004g0130a0001c0001t0004g0132a0001c0001t0016g0131 | 3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.516+801A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57209988 | ||||||
chr16:57210027
|
T | TTCCC | 267 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(264): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.516+858_516+861dup others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 57210027 | |||||
chr16:57210041
|
C | CCCTCCCT others(5): Show |
1 | a0001c0001t0001g0082 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.516+861_516+862ins others(12): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 57210041 | |||||
chr16:57210061
|
C | CCCTT | 50 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0003g0312others(47): Show | 51 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.516+884_516+887dup others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 57210061 | |||||
chr16:57210075
|
T | C | 343 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.516+888T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210075 | ||||||
chr16:57210089
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.516+902C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210089 | ||||||
chr16:57210120
|
C | T | 1 | a0001c0001t0002g0283 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.516+933C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210120 | ||||||
chr16:57210329
|
C | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0020 | 2 | HG02723.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.516+1142C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210329 | ||||||
chr16:57210357
|
C | T | 1 | a0001c0001t0002g0159 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.516+1170C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210357 | ||||||
chr16:57210358
|
G | A | 1 | a0001c0001t0001g0074 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.516+1171G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210358 | ||||||
chr16:57210434
|
G | A | 1 | a0001c0001t0017g0292 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.516+1247G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210434 | ||||||
chr16:57210532
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.516+1345G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210532 | ||||||
chr16:57210577
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0112 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.516+1390G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210577 | ||||||
chr16:57210664
|
G | T | 1 | a0001c0001t0003g0344 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.516+1477G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210664 | ||||||
chr16:57210667
|
T | C | 343 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.516+1480T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210667 | ||||||
chr16:57210675
|
T | G | 53 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0003g0312others(50): Show | 54 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(51): Show |
intron_variant | MODIFIER | c.516+1488T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210675 | ||||||
chr16:57210699
|
C | T | 11 | a0001c0001t0002g0167a0001c0001t0002g0197a0001c0001t0002g0198others(8): Show | 11 | NA18953.hp2 NA18962.hp1 NA18963.hp1 others(8): Show |
intron_variant | MODIFIER | c.516+1512C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210699 | ||||||
chr16:57210788
|
C | T | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.516+1601C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57210788 | ||||||
chr16:57211007
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.516+1820G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211007 | ||||||
chr16:57211022
|
G | A | 48 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(45): Show | 49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.516+1835G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211022 | ||||||
chr16:57211026
|
C | T | 1 | a0001c0001t0002g0199 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.516+1839C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211026 | ||||||
chr16:57211067
|
C | T | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.516+1880C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211067 | ||||||
chr16:57211155
|
G | A | 1 | a0001c0001t0022g0279 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.517-1817G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211155 | ||||||
chr16:57211244
|
C | G | 1 | a0001c0001t0022g0279 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.517-1728C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211244 | ||||||
chr16:57211266
|
T | TA | 121 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0030others(118): Show | 121 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.517-1688dupA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr16 | 57211266 | |||||
chr16:57211281
|
A | G | 1 | a0001c0001t0001g0093 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.517-1691A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211281 | ||||||
chr16:57211431
|
C | T | 1 | a0001c0001t0003g0324 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.517-1541C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211431 | ||||||
chr16:57211580
|
C | A | 1 | a0001c0001t0002g0285 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.517-1392C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211580 | ||||||
chr16:57211583
|
A | C | 7 | a0001c0001t0001g0155a0001c0001t0001g0171a0001c0001t0001g0255others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-1389A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211583 | ||||||
chr16:57211720
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.517-1252T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211720 | ||||||
chr16:57211956
|
G | A | 1 | a0001c0001t0001g0303 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.517-1016G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57211956 | ||||||
chr16:57212054
|
A | G | 7 | a0001c0001t0001g0060a0001c0001t0001g0080a0001c0001t0001g0094others(4): Show | 7 | HG00438.hp2 HG00673.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.517-918A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212054 | ||||||
chr16:57212187
|
G | T | 62 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(59): Show | 63 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.517-785G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212187 | ||||||
chr16:57212426
|
A | C | 1 | a0001c0001t0002g0209 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.517-546A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212426 | ||||||
chr16:57212550
|
A | T | 52 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(49): Show | 53 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.517-422A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212550 | ||||||
chr16:57212637
|
C | T | 3 | a0001c0001t0004g0130a0001c0001t0004g0132a0001c0001t0016g0131 | 3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.517-335C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212637 | ||||||
chr16:57212684
|
G | T | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.517-288G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212684 | ||||||
chr16:57212745
|
G | A | 48 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(45): Show | 49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.517-227G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212745 | ||||||
chr16:57212799
|
G | C | 1 | a0001c0001t0002g0219 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.517-173G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212799 | ||||||
chr16:57212835
|
G | A | 4 | a0001c0001t0001g0033a0002c0002t0012g0286a0002c0002t0012g0288others(1): Show | 4 | HG02818.hp1 HG06807.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.517-137G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212835 | ||||||
chr16:57212860
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.517-112G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 4/14 | chr16 | 57212860 | ||||||
chr16:57213150
|
G | A | 3 | a0001c0001t0004g0001a0001c0001t0004g0351a0001c0001t0004g0352 | 4 | HG02015.hp1 NA18992.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.643+52G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 5/14 | chr16 | 57213150 | ||||||
chr16:57213196
|
G | T | 1 | a0001c0001t0001g0048 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.643+98G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 5/14 | chr16 | 57213196 | ||||||
chr16:57213347
|
G | A | 3 | a0001c0001t0004g0042a0001c0001t0004g0043a0001c0003t0001g0117 | 3 | HG02922.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.643+249G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 5/14 | chr16 | 57213347 | ||||||
chr16:57213458
|
G | A | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.643+360G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 5/14 | chr16 | 57213458 | ||||||
chr16:57213664
|
G | C | 125 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(122): Show | 125 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.644-224G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 5/14 | chr16 | 57213664 | ||||||
chr16:57213674
|
T | C | 1 | a0001c0001t0001g0186 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.644-214T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 5/14 | chr16 | 57213674 | ||||||
chr16:57213742
|
A | G | 71 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(68): Show | 72 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.644-146A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 5/14 | chr16 | 57213742 | ||||||
chr16:57213787
|
A | C | 1 | a0001c0001t0003g0322 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.644-101A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 5/14 | chr16 | 57213787 | ||||||
chr16:57213791
|
T | A | 2 | a0001c0001t0004g0042a0001c0001t0004g0043 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.644-97T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 5/14 | chr16 | 57213791 | ||||||
chr16:57213962
|
A | G | 1 | a0001c0001t0002g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.702+16A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57213962 | ||||||
chr16:57213965
|
CTATT | C | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.702+24_702+27delTA others(2): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 57213965 | |||||
chr16:57214069
|
T | G | 2 | a0002c0002t0012g0286a0002c0002t0012g0288 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.702+123T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214069 | ||||||
chr16:57214082
|
T | G | 5 | a0001c0001t0001g0011a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG03471.hp2 HG03486.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+136T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214082 | ||||||
chr16:57214218
|
G | A | 3 | a0001c0001t0004g0001a0001c0001t0004g0351a0001c0001t0004g0352 | 4 | HG02015.hp1 NA18992.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+272G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214218 | ||||||
chr16:57214465
|
A | G | 1 | a0001c0001t0003g0334 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.702+519A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214465 | ||||||
chr16:57214534
|
TG | T | 3 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037 | 3 | HG02622.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.702+589delG | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214534 | ||||||
chr16:57214567
|
G | T | 52 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(49): Show | 53 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(50): Show |
intron_variant | MODIFIER | c.702+621G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214567 | ||||||
chr16:57214722
|
A | C | 1 | a0001c0001t0001g0192 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.702+776A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214722 | ||||||
chr16:57214750
|
C | T | 3 | a0001c0001t0001g0174a0001c0001t0001g0179a0001c0001t0001g0251 | 3 | HG02015.hp2 NA18994.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.702+804C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214750 | ||||||
chr16:57214771
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.702+825A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214771 | ||||||
chr16:57214860
|
C | G | 1 | a0001c0001t0001g0174 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.702+914C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214860 | ||||||
chr16:57214906
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0036a0001c0001t0001g0037 | 3 | HG02622.hp1 HG03098.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.702+960G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214906 | ||||||
chr16:57214921
|
C | T | 3 | a0001c0001t0001g0274a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02559.hp1 HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.702+975C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57214921 | ||||||
chr16:57215055
|
G | A | 2 | a0002c0002t0012g0286a0002c0002t0012g0288 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.703-1052G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57215055 | ||||||
chr16:57215107
|
A | G | 1 | a0001c0001t0003g0321 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.703-1000A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57215107 | ||||||
chr16:57215196
|
A | C | 2 | a0001c0001t0001g0210a0001c0001t0001g0256 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.703-911A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57215196 | ||||||
chr16:57215355
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0074 | 2 | NA18964.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.703-752A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57215355 | ||||||
chr16:57215397
|
G | C | 1 | a0001c0001t0001g0305 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.703-710G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57215397 | ||||||
chr16:57215466
|
A | G | 3 | a0001c0001t0004g0001a0001c0001t0004g0351a0001c0001t0004g0352 | 4 | HG02015.hp1 NA18992.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.703-641A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57215466 | ||||||
chr16:57215917
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.703-190A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | chr16 | 57215917 | ||||||
chr16:57216069
|
A | AT | 314 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(311): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.703-20dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 57216069 | |||||
chr16:57216069
|
A | ATT | 7 | a0001c0001t0001g0007a0001c0001t0001g0069a0001c0001t0001g0079others(4): Show | 7 | HG01109.hp1 HG01943.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.703-21_703-20dupTT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr16 | 57216069 | |||||
chr16:57216475
|
T | G | 1 | a0001c0001t0002g0266 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.769+302T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 7/14 | chr16 | 57216475 | ||||||
chr16:57216489
|
C | T | 4 | a0001c0001t0001g0153a0001c0001t0001g0238a0001c0001t0001g0284others(1): Show | 4 | HG02257.hp2 HG02976.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+316C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 7/14 | chr16 | 57216489 | ||||||
chr16:57216683
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.770-221G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 7/14 | chr16 | 57216683 | ||||||
chr16:57216684
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.770-220C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 7/14 | chr16 | 57216684 | ||||||
chr16:57216728
|
A | C | 1 | a0001c0001t0001g0029 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.770-176A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 7/14 | chr16 | 57216728 | ||||||
chr16:57216735
|
C | G | 64 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0003g0312others(61): Show | 65 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.770-169C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 7/14 | chr16 | 57216735 | ||||||
chr16:57217591
|
A | G | 4 | a0001c0001t0003g0338a0001c0001t0003g0339a0001c0001t0003g0340others(1): Show | 4 | NA18939.hp2 NA18981.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.901+556A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57217591 | ||||||
chr16:57217659
|
C | A | 1 | a0001c0001t0002g0219 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.901+624C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57217659 | ||||||
chr16:57217707
|
A | G | 3 | a0001c0001t0004g0130a0001c0001t0004g0132a0001c0001t0016g0131 | 3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.901+672A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57217707 | ||||||
chr16:57217771
|
G | C | 1 | a0001c0001t0001g0161 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.901+736G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57217771 | ||||||
chr16:57217791
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.901+756A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57217791 | ||||||
chr16:57218008
|
T | C | 13 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(10): Show | 13 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.901+973T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218008 | ||||||
chr16:57218158
|
A | G | 3 | a0001c0001t0004g0130a0001c0001t0004g0132a0001c0001t0016g0131 | 3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.901+1123A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218158 | ||||||
chr16:57218352
|
A | G | 6 | a0001c0001t0002g0228a0001c0001t0002g0269a0001c0001t0002g0270others(3): Show | 6 | HG00621.hp2 HG01433.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.901+1317A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218352 | ||||||
chr16:57218581
|
C | A | 1 | a0001c0001t0001g0079 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.901+1546C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218581 | ||||||
chr16:57218590
|
T | G | 50 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0003g0312others(47): Show | 51 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.901+1555T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218590 | ||||||
chr16:57218621
|
C | T | 1 | a0001c0001t0006g0142 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.901+1586C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218621 | ||||||
chr16:57218669
|
A | G | 138 | a0001c0001t0001g0134a0001c0001t0001g0137a0001c0001t0001g0138others(135): Show | 138 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.901+1634A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218669 | ||||||
chr16:57218670
|
T | A | 1 | a0001c0001t0001g0079 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.901+1635T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218670 | ||||||
chr16:57218709
|
TGCCACAT others(316): Show |
T | 67 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0003g0312others(64): Show | 68 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.901+1689_902-1686d others(2): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 57218709 | |||||
chr16:57218720
|
CT | C | 14 | a0001c0001t0001g0050a0001c0001t0001g0066a0001c0001t0001g0067others(11): Show | 14 | HG00735.hp2 HG01361.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.901+1718delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 57218720 | |||||
chr16:57218720
|
CTT | C | 80 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(77): Show | 80 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.901+1717_901+1718d others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 57218720 | |||||
chr16:57218720
|
CTTT | C | 172 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0009others(169): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.901+1716_901+1718d others(5): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 57218720 | |||||
chr16:57218720
|
CTTTT | C | 6 | a0001c0001t0001g0005a0001c0001t0001g0020a0001c0001t0001g0109others(3): Show | 6 | HG01169.hp2 HG01257.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.901+1715_901+1718d others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr16 | 57218720 | |||||
chr16:57218721
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.901+1686T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218721 | ||||||
chr16:57218738
|
T | C | 8 | a0001c0001t0001g0025a0001c0001t0001g0053a0001c0001t0001g0054others(5): Show | 8 | HG00408.hp1 HG00609.hp1 HG02056.hp2 others(5): Show |
intron_variant | MODIFIER | c.901+1703T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218738 | ||||||
chr16:57218937
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.902-1795C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57218937 | ||||||
chr16:57219031
|
C | T | 1 | a0001c0001t0001g0303 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.902-1701C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57219031 | ||||||
chr16:57219190
|
C | T | 1 | a0001c0001t0003g0333 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.902-1542C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57219190 | ||||||
chr16:57219239
|
G | C | 3 | a0001c0001t0005g0128a0001c0001t0005g0135a0001c0001t0005g0136 | 3 | HG02258.hp2 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.902-1493G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57219239 | ||||||
chr16:57219361
|
G | A | 3 | a0001c0001t0004g0130a0001c0001t0004g0132a0001c0001t0016g0131 | 3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.902-1371G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57219361 | ||||||
chr16:57219411
|
A | G | 1 | a0001c0001t0005g0136 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.902-1321A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57219411 | ||||||
chr16:57219433
|
A | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(9): Show | 12 | HG00280.hp2 HG01074.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.902-1299A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57219433 | ||||||
chr16:57219702
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.902-1030G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57219702 | ||||||
chr16:57219835
|
G | A | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.902-897G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57219835 | ||||||
chr16:57220249
|
G | A | 1 | a0001c0001t0022g0279 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.902-483G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57220249 | ||||||
chr16:57220475
|
T | C | 47 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0003g0312others(44): Show | 47 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.902-257T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57220475 | ||||||
chr16:57220723
|
C | T | 1 | a0001c0001t0005g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.902-9C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 8/14 | chr16 | 57220723 | ||||||
chr16:57220866
|
G | A | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1017+19G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 9/14 | chr16 | 57220866 | ||||||
chr16:57221132
|
C | G | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1018-140C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 9/14 | chr16 | 57221132 | ||||||
chr16:57221451
|
T | C | 343 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1161+36T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57221451 | ||||||
chr16:57221523
|
T | A | 3 | a0001c0001t0001g0274a0001c0001t0001g0276a0001c0001t0001g0277 | 3 | HG02559.hp1 HG02818.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1161+108T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57221523 | ||||||
chr16:57221542
|
A | T | 1 | a0001c0001t0001g0302 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1161+127A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57221542 | ||||||
chr16:57221621
|
C | T | 1 | a0001c0001t0002g0209 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1161+206C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57221621 | ||||||
chr16:57221622
|
T | C | 1 | a0001c0001t0002g0209 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1161+207T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57221622 | ||||||
chr16:57221755
|
C | A | 1 | a0001c0001t0001g0302 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1161+340C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57221755 | ||||||
chr16:57221761
|
A | G | 343 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1161+346A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57221761 | ||||||
chr16:57221892
|
T | C | 50 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0003g0312others(47): Show | 51 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.1161+477T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57221892 | ||||||
chr16:57222095
|
T | G | 3 | a0001c0001t0004g0130a0001c0001t0004g0132a0001c0001t0016g0131 | 3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1161+680T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222095 | ||||||
chr16:57222129
|
C | A | 1 | a0001c0001t0001g0302 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1161+714C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222129 | ||||||
chr16:57222130
|
C | G | 1 | a0001c0001t0001g0302 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1161+715C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222130 | ||||||
chr16:57222134
|
T | G | 1 | a0001c0001t0002g0197 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1161+719T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222134 | ||||||
chr16:57222137
|
A | AT | 50 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0003g0312others(47): Show | 51 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.1161+724dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 57222137 | |||||
chr16:57222194
|
G | A | 1 | a0001c0001t0004g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1161+779G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222194 | ||||||
chr16:57222212
|
A | G | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1161+797A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222212 | ||||||
chr16:57222217
|
A | AT | 4 | a0001c0001t0001g0148a0001c0001t0001g0181a0001c0001t0002g0246others(1): Show | 4 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1161+803dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 57222217 | |||||
chr16:57222343
|
C | G | 3 | a0001c0001t0004g0130a0001c0001t0004g0132a0001c0001t0016g0131 | 3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1161+928C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222343 | ||||||
chr16:57222372
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1161+957G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222372 | ||||||
chr16:57222526
|
C | T | 1 | a0001c0001t0001g0186 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1161+1111C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222526 | ||||||
chr16:57222924
|
C | G | 7 | a0001c0001t0001g0155a0001c0001t0001g0171a0001c0001t0001g0255others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1161+1509C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222924 | ||||||
chr16:57222940
|
C | T | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1161+1525C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222940 | ||||||
chr16:57222994
|
G | GT | 50 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0003g0312others(47): Show | 51 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.1161+1586dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 57222994 | |||||
chr16:57222996
|
T | A | 1 | a0001c0001t0002g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1161+1581T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57222996 | ||||||
chr16:57223001
|
T | TA | 3 | a0001c0001t0004g0130a0001c0001t0004g0132a0001c0001t0016g0131 | 3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1161+1587dupA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 57223001 | |||||
chr16:57223003
|
T | A | 1 | a0001c0001t0002g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1161+1588T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57223003 | ||||||
chr16:57223037
|
T | C | 130 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(127): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.1161+1622T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57223037 | ||||||
chr16:57223049
|
C | T | 343 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(340): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1161+1634C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57223049 | ||||||
chr16:57223275
|
T | C | 1 | a0001c0001t0004g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1161+1860T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57223275 | ||||||
chr16:57223589
|
A | G | 3 | a0001c0001t0001g0100a0001c0001t0001g0105a0001c0001t0005g0023 | 3 | HG02735.hp1 NA18945.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1161+2174A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57223589 | ||||||
chr16:57223796
|
C | A | 45 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(42): Show | 45 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.1161+2381C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57223796 | ||||||
chr16:57224025
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1161+2610G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224025 | ||||||
chr16:57224036
|
T | C | 2 | a0001c0001t0001g0235a0001c0001t0001g0280 | 2 | HG00735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1161+2621T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224036 | ||||||
chr16:57224070
|
A | C | 6 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0142others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161+2655A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224070 | ||||||
chr16:57224079
|
C | T | 1 | a0001c0001t0003g0324 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1161+2664C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224079 | ||||||
chr16:57224161
|
C | T | 6 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0142others(3): Show | 6 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.1161+2746C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224161 | ||||||
chr16:57224174
|
A | G | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1161+2759A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224174 | ||||||
chr16:57224196
|
C | T | 7 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0142others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161+2781C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224196 | ||||||
chr16:57224512
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1162-2830A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224512 | ||||||
chr16:57224630
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1162-2712G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224630 | ||||||
chr16:57224720
|
G | A | 1 | a0001c0001t0002g0216 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1162-2622G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224720 | ||||||
chr16:57224920
|
G | A | 3 | a0001c0001t0001g0051a0001c0001t0001g0059a0001c0001t0019g0113 | 3 | HG00735.hp1 HG01243.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1162-2422G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224920 | ||||||
chr16:57224925
|
G | A | 1 | a0001c0001t0001g0021 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1162-2417G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224925 | ||||||
chr16:57224960
|
C | T | 1 | a0001c0003t0007g0018 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1162-2382C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57224960 | ||||||
chr16:57225023
|
T | G | 64 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0003g0312others(61): Show | 65 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1162-2319T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225023 | ||||||
chr16:57225083
|
C | CAG | 64 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0003g0312others(61): Show | 65 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1162-2258_1162-225 others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 57225083 | |||||
chr16:57225151
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1162-2191C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225151 | ||||||
chr16:57225257
|
C | T | 64 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0003g0312others(61): Show | 65 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1162-2085C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225257 | ||||||
chr16:57225341
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1162-2001G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225341 | ||||||
chr16:57225562
|
C | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0115 | 3 | HG01261.hp1 HG01952.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1162-1780C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225562 | ||||||
chr16:57225571
|
A | AAGTGAGG others(23): Show |
1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1771_1162-177 others(34): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225571 | ||||||
chr16:57225574
|
A | T | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1768A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225574 | ||||||
chr16:57225576
|
C | A | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1766C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225576 | ||||||
chr16:57225578
|
G | T | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1764G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225578 | ||||||
chr16:57225583
|
T | A | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1759T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225583 | ||||||
chr16:57225620
|
T | A | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1722T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225620 | ||||||
chr16:57225625
|
T | G | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1717T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225625 | ||||||
chr16:57225633
|
T | G | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1709T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225633 | ||||||
chr16:57225636
|
A | G | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1706A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225636 | ||||||
chr16:57225638
|
C | A | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1704C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225638 | ||||||
chr16:57225639
|
T | C | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1703T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225639 | ||||||
chr16:57225640
|
T | G | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1702T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225640 | ||||||
chr16:57225644
|
A | T | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1698A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225644 | ||||||
chr16:57225648
|
T | G | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1694T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225648 | ||||||
chr16:57225651
|
T | A | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1691T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225651 | ||||||
chr16:57225654
|
C | T | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1688C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225654 | ||||||
chr16:57225657
|
A | G | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1685A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225657 | ||||||
chr16:57225660
|
G | A | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1682G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225660 | ||||||
chr16:57225670
|
G | A | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1672G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225670 | ||||||
chr16:57225688
|
T | C | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1654T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225688 | ||||||
chr16:57225692
|
A | C | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1650A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225692 | ||||||
chr16:57225694
|
T | A | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1648T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225694 | ||||||
chr16:57225701
|
A | G | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1641A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225701 | ||||||
chr16:57225703
|
G | C | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1639G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225703 | ||||||
chr16:57225704
|
C | T | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1638C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225704 | ||||||
chr16:57225713
|
T | G | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1629T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225713 | ||||||
chr16:57225716
|
T | G | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1626T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225716 | ||||||
chr16:57225721
|
T | A | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1621T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225721 | ||||||
chr16:57225723
|
A | T | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1619A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225723 | ||||||
chr16:57225726
|
T | G | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1616T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225726 | ||||||
chr16:57225730
|
A | T | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1612A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225730 | ||||||
chr16:57225751
|
G | T | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1591G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225751 | ||||||
chr16:57225753
|
T | G | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1589T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225753 | ||||||
chr16:57225755
|
T | C | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1587T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225755 | ||||||
chr16:57225756
|
G | T | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1586G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225756 | ||||||
chr16:57225758
|
G | A | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1584G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225758 | ||||||
chr16:57225759
|
A | G | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1583A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225759 | ||||||
chr16:57225766
|
TGAAAGGC others(9): Show |
T | 1 | a0001c0001t0003g0312 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1162-1575_1162-156 others(20): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225766 | ||||||
chr16:57225885
|
C | G | 2 | a0001c0001t0005g0135a0001c0001t0005g0136 | 2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1162-1457C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57225885 | ||||||
chr16:57226082
|
G | GA | 18 | a0001c0001t0001g0005a0001c0001t0001g0024a0001c0001t0001g0060others(15): Show | 18 | HG00438.hp2 HG00544.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.1162-1251dupA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr16 | 57226082 | |||||
chr16:57226314
|
C | T | 4 | a0001c0001t0002g0268a0002c0002t0012g0286a0002c0002t0012g0288others(1): Show | 4 | HG02738.hp2 HG02818.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162-1028C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57226314 | ||||||
chr16:57226375
|
A | G | 3 | a0001c0001t0005g0128a0001c0001t0005g0135a0001c0001t0005g0136 | 3 | HG02258.hp2 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1162-967A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57226375 | ||||||
chr16:57226410
|
C | T | 1 | a0001c0001t0004g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1162-932C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57226410 | ||||||
chr16:57226686
|
G | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(2): Show | 5 | HG01074.hp1 HG01168.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.1162-656G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57226686 | ||||||
chr16:57226739
|
C | T | 1 | a0001c0001t0004g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1162-603C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57226739 | ||||||
chr16:57226806
|
T | G | 1 | a0001c0001t0017g0292 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1162-536T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57226806 | ||||||
chr16:57226879
|
C | T | 6 | a0001c0001t0001g0172a0001c0001t0001g0175a0001c0001t0001g0178others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-463C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57226879 | ||||||
chr16:57227124
|
G | A | 1 | a0001c0001t0022g0279 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1162-218G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57227124 | ||||||
chr16:57227146
|
G | T | 1 | a0001c0001t0001g0026 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1162-196G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57227146 | ||||||
chr16:57227210
|
A | C | 6 | a0001c0001t0001g0172a0001c0001t0001g0175a0001c0001t0001g0178others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1162-132A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57227210 | ||||||
chr16:57227234
|
A | C | 270 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(267): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.1162-108A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57227234 | ||||||
chr16:57227267
|
C | T | 5 | a0001c0001t0010g0163a0001c0001t0010g0165a0001c0001t0010g0166others(2): Show | 5 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1162-75C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 10/14 | chr16 | 57227267 | ||||||
chr16:57227559
|
G | A | 1 | a0001c0001t0003g0345 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1273+106G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57227559 | ||||||
chr16:57227765
|
C | T | 3 | a0001c0001t0005g0128a0001c0001t0005g0135a0001c0001t0005g0136 | 3 | HG02258.hp2 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1273+312C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57227765 | ||||||
chr16:57227887
|
C | A | 3 | a0001c0001t0005g0128a0001c0001t0005g0135a0001c0001t0005g0136 | 3 | HG02258.hp2 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1273+434C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57227887 | ||||||
chr16:57227940
|
A | G | 3 | a0001c0001t0005g0128a0001c0001t0005g0135a0001c0001t0005g0136 | 3 | HG02258.hp2 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1273+487A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57227940 | ||||||
chr16:57228147
|
C | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0049a0001c0001t0001g0089others(2): Show | 5 | HG01261.hp1 HG01433.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1273+694C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57228147 | ||||||
chr16:57228168
|
G | T | 3 | a0001c0001t0004g0130a0001c0001t0004g0132a0001c0001t0016g0131 | 3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1273+715G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57228168 | ||||||
chr16:57228272
|
C | CA | 9 | a0001c0001t0001g0302a0001c0001t0006g0129a0001c0001t0006g0133others(6): Show | 9 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.1273+840dupA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57228272 | |||||
chr16:57228272
|
CA | C | 319 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(316): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.1273+840delA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57228272 | |||||
chr16:57228272
|
CAA | C | 6 | a0001c0001t0001g0282a0001c0001t0004g0147a0001c0001t0005g0128others(3): Show | 6 | HG02055.hp1 HG02258.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1273+839_1273+840d others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57228272 | |||||
chr16:57228358
|
G | GA | 64 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0003g0312others(61): Show | 65 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.1273+912dupA | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57228358 | |||||
chr16:57228421
|
A | T | 1 | a0001c0001t0001g0025 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1273+968A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57228421 | ||||||
chr16:57228659
|
A | G | 1 | a0001c0001t0003g0328 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1273+1206A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57228659 | ||||||
chr16:57229281
|
A | G | 1 | a0001c0001t0006g0133 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1274-1430A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57229281 | ||||||
chr16:57229327
|
C | T | 1 | a0001c0001t0001g0277 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1274-1384C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57229327 | ||||||
chr16:57229434
|
A | T | 1 | a0001c0001t0004g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1274-1277A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57229434 | ||||||
chr16:57229652
|
C | CTTAGAGT others(1): Show |
3 | a0001c0001t0004g0130a0001c0001t0004g0132a0001c0001t0016g0131 | 3 | HG02145.hp2 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1274-1055_1274-104 others(12): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229652 | |||||
chr16:57229690
|
C | CT | 23 | a0001c0001t0001g0034a0001c0001t0001g0299a0001c0001t0001g0302others(20): Show | 23 | HG00621.hp1 HG02165.hp1 HG02523.hp2 others(20): Show |
intron_variant | MODIFIER | c.1274-988dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | |||||
chr16:57229690
|
C | CTT | 12 | a0001c0001t0001g0074a0001c0001t0003g0314a0001c0001t0003g0329others(9): Show | 12 | HG02698.hp1 HG03492.hp2 HG03831.hp1 others(9): Show |
intron_variant | MODIFIER | c.1274-989_1274-988d others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | |||||
chr16:57229690
|
C | CTTT | 15 | a0001c0001t0003g0317a0001c0001t0003g0324a0001c0001t0003g0328others(12): Show | 15 | HG00558.hp1 HG01255.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.1274-990_1274-988d others(5): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | |||||
chr16:57229690
|
C | CTTTT | 5 | a0001c0001t0001g0055a0001c0001t0003g0315a0001c0001t0003g0321others(2): Show | 6 | HG02280.hp1 NA18989.hp1 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.1274-991_1274-988d others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | |||||
chr16:57229690
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0004g0130 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1274-997_1274-988d others(12): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | |||||
chr16:57229690
|
CT | C | 43 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0011others(40): Show | 43 | HG00140.hp1 HG00438.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.1274-988delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | |||||
chr16:57229690
|
CTT | C | 76 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 76 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1274-989_1274-988d others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | |||||
chr16:57229690
|
CTTT | C | 91 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0022others(88): Show | 91 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1274-990_1274-988d others(5): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | |||||
chr16:57229690
|
CTTTT | C | 69 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0036others(66): Show | 69 | HG00099.hp2 HG00609.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.1274-991_1274-988d others(6): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | |||||
chr16:57229690
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0004g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1274-1001_1274-988 others(17): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57229690 | |||||
chr16:57229768
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0076 | 2 | NA18974.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1274-943C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57229768 | ||||||
chr16:57229892
|
A | G | 1 | a0001c0001t0003g0345 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1274-819A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57229892 | ||||||
chr16:57229908
|
T | A | 1 | a0001c0001t0002g0152 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1274-803T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57229908 | ||||||
chr16:57229917
|
T | G | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1274-794T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57229917 | ||||||
chr16:57229963
|
C | T | 7 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0142others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1274-748C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57229963 | ||||||
chr16:57230005
|
C | CT | 197 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(194): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.1274-683dupT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57230005 | |||||
chr16:57230005
|
C | CTT | 24 | a0001c0001t0001g0101a0001c0001t0001g0137a0001c0001t0001g0155others(21): Show | 24 | HG01074.hp2 HG01981.hp1 HG01981.hp2 others(21): Show |
intron_variant | MODIFIER | c.1274-684_1274-683d others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr16 | 57230005 | |||||
chr16:57230555
|
G | T | 1 | a0001c0001t0003g0331 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1274-156G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57230555 | ||||||
chr16:57230668
|
A | G | 1 | a0001c0001t0002g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1274-43A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 11/14 | chr16 | 57230668 | ||||||
chr16:57230904
|
C | T | 2 | a0002c0002t0012g0286a0002c0002t0012g0288 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1376+91C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 12/14 | chr16 | 57230904 | ||||||
chr16:57230907
|
T | C | 1 | a0001c0001t0004g0147 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1376+94T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 12/14 | chr16 | 57230907 | ||||||
chr16:57230957
|
G | T | 2 | a0001c0001t0003g0322a0001c0001t0003g0343 | 2 | NA18959.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.1376+144G>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 12/14 | chr16 | 57230957 | ||||||
chr16:57231370
|
A | G | 3 | a0001c0001t0005g0128a0001c0001t0005g0135a0001c0001t0005g0136 | 3 | HG02258.hp2 HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1529+51A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57231370 | ||||||
chr16:57231428
|
G | A | 2 | a0001c0001t0008g0157a0001c0001t0008g0158 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1529+109G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57231428 | ||||||
chr16:57231632
|
A | T | 1 | a0001c0001t0022g0279 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1529+313A>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57231632 | ||||||
chr16:57231769
|
ACT | A | 135 | a0001c0001t0001g0069a0001c0001t0001g0134a0001c0001t0001g0137others(132): Show | 135 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.1529+452_1529+453d others(4): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr16 | 57231769 | |||||
chr16:57231806
|
A | G | 7 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0142others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1529+487A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57231806 | ||||||
chr16:57231830
|
C | G | 2 | a0001c0001t0011g0240a0001c0001t0011g0278 | 2 | HG00609.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1529+511C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57231830 | ||||||
chr16:57232052
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1529+733A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57232052 | ||||||
chr16:57232063
|
T | G | 1 | a0001c0001t0009g0254 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1529+744T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57232063 | ||||||
chr16:57232168
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1529+849G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57232168 | ||||||
chr16:57232294
|
A | G | 2 | a0002c0002t0012g0286a0002c0002t0012g0288 | 2 | HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1529+975A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57232294 | ||||||
chr16:57232493
|
C | T | 1 | a0001c0001t0006g0133 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1529+1174C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57232493 | ||||||
chr16:57232542
|
G | A | 55 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(52): Show | 56 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(53): Show |
intron_variant | MODIFIER | c.1529+1223G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57232542 | ||||||
chr16:57232723
|
T | C | 1 | a0001c0001t0002g0249 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1529+1404T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57232723 | ||||||
chr16:57233002
|
G | A | 1 | a0001c0001t0002g0230 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1529+1683G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57233002 | ||||||
chr16:57233152
|
T | C | 7 | a0001c0001t0006g0129a0001c0001t0006g0133a0001c0001t0006g0142others(4): Show | 7 | HG00280.hp1 HG01070.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.1529+1833T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57233152 | ||||||
chr16:57233379
|
T | A | 1 | a0001c0001t0016g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1530-1745T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57233379 | ||||||
chr16:57233510
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1530-1614T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57233510 | ||||||
chr16:57233720
|
G | A | 5 | a0001c0001t0010g0163a0001c0001t0010g0165a0001c0001t0010g0166others(2): Show | 5 | HG01123.hp1 HG01884.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.1530-1404G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57233720 | ||||||
chr16:57233751
|
A | G | 3 | a0002c0002t0012g0286a0002c0002t0012g0288a0002c0002t0018g0287 | 3 | HG02818.hp1 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1530-1373A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57233751 | ||||||
chr16:57233791
|
C | G | 1 | a0001c0001t0002g0002 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1530-1333C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57233791 | ||||||
chr16:57234014
|
T | C | 3 | a0001c0001t0010g0163a0001c0001t0010g0166a0001c0001t0020g0162 | 3 | HG01123.hp1 HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1530-1110T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57234014 | ||||||
chr16:57234115
|
C | G | 18 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(15): Show | 18 | HG00280.hp2 HG01074.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1530-1009C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57234115 | ||||||
chr16:57234198
|
C | T | 1 | a0001c0001t0002g0169 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1530-926C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57234198 | ||||||
chr16:57234218
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0045 | 2 | HG01123.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1530-906C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57234218 | ||||||
chr16:57234496
|
C | T | 5 | a0001c0001t0001g0011a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 5 | HG03471.hp2 HG03486.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1530-628C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57234496 | ||||||
chr16:57234533
|
G | A | 3 | a0001c0001t0004g0001a0001c0001t0004g0351a0001c0001t0004g0352 | 4 | HG02015.hp1 NA18992.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.1530-591G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57234533 | ||||||
chr16:57234625
|
T | A | 1 | a0001c0001t0005g0263 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1530-499T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57234625 | ||||||
chr16:57234785
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1530-339T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57234785 | ||||||
chr16:57235019
|
G | A | 1 | a0001c0001t0005g0263 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1530-105G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57235019 | ||||||
chr16:57235041
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1530-83G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 13/14 | chr16 | 57235041 | ||||||
chr16:57235419
|
A | C | 1 | a0001c0001t0022g0279 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1634+191A>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57235419 | ||||||
chr16:57236077
|
C | A | 48 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(45): Show | 49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.1634+849C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236077 | ||||||
chr16:57236270
|
C | G | 1 | a0001c0003t0007g0018 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1634+1042C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236270 | ||||||
chr16:57236304
|
A | G | 1 | a0001c0001t0010g0163 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1634+1076A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236304 | ||||||
chr16:57236382
|
A | G | 1 | a0001c0001t0001g0026 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1634+1154A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236382 | ||||||
chr16:57236517
|
GAGGA | G | 5 | a0001c0001t0001g0017a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 5 | HG02258.hp1 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1634+1290_1634+129 others(8): Show |
RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236517 | ||||||
chr16:57236522
|
G | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 5 | HG02258.hp1 HG02717.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1634+1294G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236522 | ||||||
chr16:57236633
|
T | G | 4 | a0001c0001t0003g0353a0001c0001t0003g0354a0001c0001t0003g0355others(1): Show | 4 | HG00558.hp1 NA18969.hp1 NA19003.hp2 others(1): Show |
intron_variant | MODIFIER | c.1634+1405T>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236633 | ||||||
chr16:57236793
|
C | T | 1 | a0001c0001t0002g0229 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1634+1565C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236793 | ||||||
chr16:57236830
|
C | G | 1 | a0001c0001t0016g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1634+1602C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236830 | ||||||
chr16:57236842
|
G | C | 1 | a0001c0001t0002g0218 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1634+1614G>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236842 | ||||||
chr16:57236854
|
A | G | 1 | a0001c0001t0002g0247 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1634+1626A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236854 | ||||||
chr16:57236870
|
AT | A | 62 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(59): Show | 63 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1634+1644delT | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr16 | 57236870 | |||||
chr16:57236895
|
G | A | 62 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(59): Show | 63 | HG00280.hp1 HG00558.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.1634+1667G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236895 | ||||||
chr16:57236900
|
C | T | 1 | a0001c0001t0006g0145 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1634+1672C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236900 | ||||||
chr16:57236938
|
G | A | 2 | a0001c0001t0002g0223a0001c0001t0002g0232 | 2 | NA18959.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1634+1710G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236938 | ||||||
chr16:57236994
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1634+1766G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57236994 | ||||||
chr16:57237040
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1634+1812C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237040 | ||||||
chr16:57237060
|
C | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0100a0001c0001t0001g0101others(5): Show | 8 | HG01243.hp1 HG01496.hp2 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.1635-1819C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237060 | ||||||
chr16:57237099
|
G | A | 1 | a0001c0001t0003g0328 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1635-1780G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237099 | ||||||
chr16:57237155
|
T | A | 1 | a0001c0001t0001g0302 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1635-1724T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237155 | ||||||
chr16:57237234
|
C | T | 1 | a0001c0001t0009g0221 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1635-1645C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237234 | ||||||
chr16:57237332
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031 | 3 | HG02257.hp1 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1635-1547C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237332 | ||||||
chr16:57237333
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1635-1546G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237333 | ||||||
chr16:57237387
|
C | G | 1 | a0001c0001t0002g0194 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1635-1492C>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237387 | ||||||
chr16:57237585
|
G | A | 1 | a0001c0001t0002g0218 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1635-1294G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237585 | ||||||
chr16:57237735
|
G | A | 14 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0161others(11): Show | 14 | HG01099.hp2 HG01109.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1635-1144G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237735 | ||||||
chr16:57237938
|
C | T | 48 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(45): Show | 49 | HG00558.hp1 HG00621.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.1635-941C>T | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57237938 | ||||||
chr16:57238138
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1635-741G>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57238138 | ||||||
chr16:57238249
|
T | A | 7 | a0001c0001t0001g0155a0001c0001t0001g0171a0001c0001t0001g0255others(4): Show | 7 | HG02145.hp1 HG02451.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1635-630T>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57238249 | ||||||
chr16:57238262
|
A | G | 125 | a0001c0001t0001g0024a0001c0001t0001g0148a0001c0001t0001g0149others(122): Show | 125 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.1635-617A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57238262 | ||||||
chr16:57238644
|
T | C | 2 | a0001c0001t0008g0157a0001c0001t0008g0158 | 2 | HG01109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1635-235T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57238644 | ||||||
chr16:57238699
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1635-180A>G | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57238699 | ||||||
chr16:57238756
|
C | A | 8 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0220others(5): Show | 8 | HG00544.hp1 NA18946.hp1 NA18959.hp1 others(5): Show |
intron_variant | MODIFIER | c.1635-123C>A | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57238756 | ||||||
chr16:57238760
|
T | C | 1 | a0001c0001t0001g0261 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1635-119T>C | RSPRY1 | ENSG00000159579.14 | transcript | ENST00000394420.9 | protein_coding | 14/14 | chr16 | 57238760 |