geneid | 5635 |
---|---|
ensemblid | ENSG00000161542.17 |
hgncid | 9466 |
symbol | PRPSAP1 |
name | phosphoribosyl pyrophosphate synthetase associated protein 1 |
refseq_nuc | NM_002766.3 |
refseq_prot | NP_002757.2 |
ensembl_nuc | ENST00000446526.8 |
ensembl_prot | ENSP00000414624.2 |
mane_status | MANE Select |
chr | chr17 |
start | 76309478 |
end | 76353916 |
strand | - |
ver | v1.2 |
region | chr17:76309478-76353916 |
region5000 | chr17:76304478-76358916 |
regionname0 | PRPSAP1_chr17_76309478_76353916 |
regionname5000 | PRPSAP1_chr17_76304478_76358916 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 385 | 365 | 91 | 66 | 146 | 16 | 44 | 108 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0002 | 0/0 | 176 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1158 | 249 | 68 | 49 | 78 | 13 | 39 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
c0002 | 0/0 | 1158 | 116 | 23 | 17 | 68 | 3 | 5 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
c0003 | 0/0 | 1147 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2278 | 104 | 10 | 27 | 38 | 10 | 17 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0002 | 0/0 | 2278 | 70 | 4 | 12 | 46 | 3 | 5 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0003 | 0/0 | 2279 | 39 | 8 | 5 | 17 | 0 | 9 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0004 | 0/0 | 2279 | 34 | 2 | 9 | 11 | 3 | 9 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0005 | 0/0 | 2278 | 19 | 17 | 1 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0006 | 0/0 | 2107 | 16 | 5 | 1 | 10 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0007 | 0/0 | 2108 | 13 | 10 | 3 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0008 | 0/0 | 2277 | 6 | 1 | 0 | 4 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0009 | 0/0 | 2277 | 5 | 5 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0010 | 0/0 | 2278 | 5 | 5 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0011 | 0/0 | 2107 | 4 | 0 | 0 | 4 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0012 | 0/0 | 2277 | 4 | 4 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0013 | 0/0 | 2108 | 4 | 0 | 0 | 4 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0014 | 0/0 | 2278 | 3 | 2 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0015 | 0/0 | 2280 | 3 | 3 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0016 | 0/0 | 2277 | 3 | 3 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0017 | 0/0 | 2279 | 3 | 2 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0018 | 0/0 | 2277 | 3 | 0 | 0 | 3 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0019 | 0/0 | 2278 | 2 | 2 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0020 | 0/0 | 2280 | 2 | 0 | 0 | 1 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0021 | 0/0 | 2279 | 2 | 2 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0022 | 0/0 | 2277 | 2 | 1 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0023 | 0/0 | 2279 | 2 | 1 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0024 | 0/0 | 2278 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0025 | 0/0 | 2278 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0026 | 0/0 | 2277 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0027 | 0/0 | 2278 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0028 | 0/0 | 2279 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0029 | 0/0 | 2278 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0030 | 0/0 | 2279 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0031 | 0/0 | 2278 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0032 | 0/0 | 2277 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0033 | 0/0 | 2278 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0034 | 0/0 | 2278 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0035 | 0/0 | 2278 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0036 | 0/0 | 2278 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0037 | 0/0 | 2279 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0038 | 0/0 | 2278 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0039 | 0/0 | 2278 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0040 | 0/0 | 2277 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
t0041 | 0/0 | 2278 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1158 | 249 | 68 | 49 | 78 | 13 | 39 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0002 | 0/0 | 1158 | 116 | 23 | 17 | 68 | 3 | 5 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0002c0003 | 0/0 | 1147 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3435 | 103 | 10 | 27 | 38 | 10 | 16 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0002 | 0/0 | 3435 | 2 | 0 | 0 | 1 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0003 | 0/0 | 3436 | 37 | 7 | 4 | 17 | 0 | 9 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0004 | 0/0 | 3436 | 34 | 2 | 9 | 11 | 3 | 9 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0005 | 0/0 | 3435 | 19 | 17 | 1 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0008 | 0/0 | 3434 | 6 | 1 | 0 | 4 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0009 | 0/0 | 3434 | 5 | 5 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0010 | 0/0 | 3435 | 5 | 5 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0012 | 0/0 | 3434 | 4 | 4 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0014 | 0/0 | 3435 | 3 | 2 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0016 | 0/0 | 3434 | 3 | 3 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0017 | 0/0 | 3436 | 3 | 2 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0019 | 0/0 | 3435 | 2 | 2 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0020 | 0/0 | 3437 | 2 | 0 | 0 | 1 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0021 | 0/0 | 3436 | 2 | 2 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0022 | 0/0 | 3434 | 2 | 1 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0023 | 0/0 | 3436 | 2 | 1 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0024 | 0/0 | 3435 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0025 | 0/0 | 3435 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0027 | 0/0 | 3435 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0028 | 0/0 | 3436 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0029 | 0/0 | 3435 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0030 | 0/0 | 3436 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0031 | 0/0 | 3435 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0032 | 0/0 | 3434 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0033 | 0/0 | 3435 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0034 | 0/0 | 3435 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0035 | 0/0 | 3435 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0037 | 0/0 | 3436 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0038 | 0/0 | 3435 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0040 | 0/0 | 3434 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0001t0041 | 0/0 | 3435 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0002t0001 | 0/0 | 3435 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0002t0002 | 0/0 | 3435 | 68 | 4 | 12 | 45 | 3 | 4 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0002t0003 | 0/0 | 3436 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0002t0006 | 0/0 | 3264 | 16 | 5 | 1 | 10 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0002t0007 | 0/0 | 3265 | 13 | 10 | 3 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0002t0011 | 0/0 | 3264 | 4 | 0 | 0 | 4 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0002t0013 | 0/0 | 3265 | 4 | 0 | 0 | 4 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0002t0015 | 0/0 | 3437 | 3 | 3 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0002t0018 | 0/0 | 3434 | 3 | 0 | 0 | 3 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0002t0026 | 0/0 | 3434 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0002t0036 | 0/0 | 3435 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0001c0002t0039 | 0/0 | 3435 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
a0002c0003t0003 | 0/0 | 3425 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | copy fasta | chr17 | 76304478 | 76358916 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0138 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0004g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0005g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0008g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0008g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0008g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0008g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0008g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0008g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0009g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0009g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0009g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0009g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0009g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0010g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0010g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0010g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0010g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0010g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0012g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0012g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0012g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0012g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0014g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0014g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0014g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0016g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0016g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0016g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0017g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0017g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0017g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0019g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0019g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0020g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0020g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0021g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0021g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0022g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0022g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0023g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0023g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0024g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0025g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0027g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0028g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0029g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0030g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0031g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0032g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0033g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0034g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0035g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0037g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0038g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0040g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0001t0041g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0006g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0006g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0006g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0006g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0006g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0006g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0006g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0006g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0006g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0006g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0006g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0006g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0006g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0007g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0007g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0007g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0007g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0007g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0007g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0007g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0007g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0007g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0011g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0011g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0011g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0011g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0013g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0013g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0013g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0013g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0015g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0015g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0015g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0018g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0018g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0018g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0026g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0036g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0001c0002t0039g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
a0002c0003t0003g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0321 | EUR | GBR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | GBR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00140 | hp1 | a0001 | c0001 | t0004 | g0232 | EUR | GBR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0176 | EUR | GBR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0263 | EUR | FIN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | FIN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | FIN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0249 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0272 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00438 | hp1 | a0001 | c0001 | t0008 | g0278 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0269 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0239 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00597 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0148 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0102 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0288 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00639 | hp1 | a0001 | c0001 | t0005 | g0295 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0342 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00738 | hp2 | a0001 | c0002 | t0007 | g0333 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00741 | hp1 | a0001 | c0002 | t0002 | g0062 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG00741 | hp2 | a0001 | c0002 | t0002 | g0085 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01069 | hp1 | a0001 | c0002 | t0007 | g0325 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01069 | hp2 | a0001 | c0001 | t0022 | g0282 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0082 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01071 | hp1 | a0001 | c0002 | t0007 | g0326 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0083 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01074 | hp1 | a0001 | c0002 | t0002 | g0147 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0129 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01099 | hp1 | a0001 | c0002 | t0006 | g0054 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01106 | hp1 | a0001 | c0001 | t0014 | g0011 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0344 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0130 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01167 | hp1 | a0001 | c0001 | t0040 | g0357 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01167 | hp2 | a0001 | c0001 | t0034 | g0334 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01169 | hp2 | a0001 | c0001 | t0038 | g0356 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0345 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01243 | hp1 | a0001 | c0002 | t0002 | g0301 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01255 | hp2 | a0001 | c0002 | t0002 | g0180 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0079 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01261 | hp2 | a0001 | c0002 | t0002 | g0065 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01361 | hp2 | a0001 | c0001 | t0017 | g0318 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01433 | hp1 | a0001 | c0002 | t0002 | g0234 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0284 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | IBS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0184 | EUR | IBS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | IBS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0267 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0311 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01891 | hp2 | a0001 | c0001 | t0016 | g0052 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01928 | hp1 | a0001 | c0002 | t0003 | g0200 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0211 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01952 | hp2 | a0001 | c0001 | t0004 | g0126 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0196 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0084 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02004 | hp2 | a0001 | c0001 | t0004 | g0128 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02055 | hp1 | a0001 | c0001 | t0023 | g0361 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02055 | hp2 | a0001 | c0001 | t0009 | g0305 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02074 | hp2 | a0001 | c0002 | t0002 | g0168 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02080 | hp1 | a0001 | c0002 | t0013 | g0355 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02080 | hp2 | a0001 | c0002 | t0002 | g0248 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02129 | hp2 | a0001 | c0002 | t0006 | g0259 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0110 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02135 | hp2 | a0001 | c0001 | t0004 | g0343 | EAS | KHV | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02145 | hp2 | a0001 | c0001 | t0019 | g0007 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0221 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02148 | hp2 | a0001 | c0001 | t0030 | g0119 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CDX | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02165 | hp2 | a0001 | c0002 | t0018 | g0111 | EAS | CDX | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02257 | hp1 | a0001 | c0002 | t0006 | g0347 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02258 | hp1 | a0001 | c0002 | t0007 | g0003 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02258 | hp2 | a0001 | c0001 | t0005 | g0238 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02280 | hp1 | a0001 | c0001 | t0017 | g0323 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0233 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0058 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02300 | hp2 | a0001 | c0001 | t0029 | g0081 | AMR | PEL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02451 | hp2 | a0001 | c0001 | t0008 | g0309 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02572 | hp1 | a0001 | c0002 | t0007 | g0330 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02572 | hp2 | a0001 | c0002 | t0007 | g0324 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0162 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02615 | hp2 | a0001 | c0001 | t0010 | g0331 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02622 | hp1 | a0002 | c0003 | t0003 | g0307 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02622 | hp2 | a0001 | c0001 | t0025 | g0010 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02630 | hp1 | a0001 | c0002 | t0007 | g0327 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0328 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0231 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0198 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02809 | hp1 | a0001 | c0001 | t0012 | g0030 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02809 | hp2 | a0001 | c0001 | t0032 | g0057 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02818 | hp1 | a0001 | c0002 | t0006 | g0313 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0314 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02886 | hp2 | a0001 | c0001 | t0010 | g0038 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02895 | hp1 | a0001 | c0002 | t0026 | g0317 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0055 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0056 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02896 | hp2 | a0001 | c0001 | t0010 | g0037 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02922 | hp1 | a0001 | c0001 | t0016 | g0046 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02922 | hp2 | a0001 | c0001 | t0010 | g0041 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0245 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0236 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02970 | hp1 | a0001 | c0001 | t0017 | g0329 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02970 | hp2 | a0001 | c0001 | t0009 | g0304 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02976 | hp1 | a0001 | c0002 | t0007 | g0025 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0266 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03017 | hp1 | a0001 | c0001 | t0020 | g0132 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03041 | hp1 | a0001 | c0001 | t0035 | g0316 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0163 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03098 | hp2 | a0001 | c0002 | t0006 | g0310 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03130 | hp2 | a0001 | c0001 | t0016 | g0193 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03139 | hp1 | a0001 | c0002 | t0007 | g0308 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03139 | hp2 | a0001 | c0001 | t0005 | g0237 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03195 | hp1 | a0001 | c0002 | t0007 | g0291 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03195 | hp2 | a0001 | c0002 | t0002 | g0036 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03209 | hp1 | a0001 | c0001 | t0014 | g0008 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03209 | hp2 | a0001 | c0002 | t0015 | g0053 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03225 | hp1 | a0001 | c0002 | t0015 | g0027 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0244 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0223 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03453 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0243 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03486 | hp1 | a0001 | c0002 | t0006 | g0241 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03486 | hp2 | a0001 | c0001 | t0014 | g0009 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0067 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0209 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0265 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0210 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03516 | hp1 | a0001 | c0002 | t0002 | g0042 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0298 | AFR | ESN | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0283 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0050 | AFR | GWD | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0319 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03579 | hp2 | a0001 | c0001 | t0009 | g0303 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0144 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0080 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03669 | hp1 | a0001 | c0001 | t0004 | g0145 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03704 | hp1 | a0001 | c0001 | t0008 | g0187 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0299 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03710 | hp2 | a0001 | c0001 | t0004 | g0066 | SAS | PJL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03834 | hp1 | a0001 | c0001 | t0004 | g0177 | SAS | BEB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03927 | hp2 | a0001 | c0001 | t0005 | g0320 | SAS | BEB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0199 | SAS | BEB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03942 | hp2 | a0001 | c0001 | t0004 | g0294 | SAS | BEB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0290 | SAS | STU | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG04115 | hp2 | a0001 | c0002 | t0001 | g0068 | SAS | STU | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0293 | SAS | BEB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | STU | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0273 | SAS | STU | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG04204 | hp1 | a0001 | c0001 | t0004 | g0143 | SAS | STU | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0224 | SAS | STU | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0251 | SAS | STU | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0296 | SAS | STU | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18522 | hp1 | a0001 | c0001 | t0021 | g0039 | AFR | YRI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18522 | hp2 | a0001 | c0002 | t0007 | g0003 | AFR | YRI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0206 | EAS | CHB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0108 | EAS | CHB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0051 | AFR | YRI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0246 | AFR | YRI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18939 | hp2 | a0001 | c0002 | t0013 | g0352 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0013 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18941 | hp2 | a0001 | c0002 | t0011 | g0336 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18944 | hp1 | a0001 | c0002 | t0002 | g0020 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0142 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18945 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18946 | hp2 | a0001 | c0002 | t0006 | g0340 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18947 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18949 | hp2 | a0001 | c0001 | t0008 | g0114 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18950 | hp1 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18950 | hp2 | a0001 | c0002 | t0006 | g0335 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18953 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18954 | hp2 | a0001 | c0001 | t0008 | g0254 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18956 | hp1 | a0001 | c0001 | t0027 | g0146 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18956 | hp2 | a0001 | c0002 | t0002 | g0024 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18957 | hp1 | a0001 | c0002 | t0002 | g0017 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18960 | hp1 | a0001 | c0002 | t0006 | g0197 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18960 | hp2 | a0001 | c0002 | t0002 | g0018 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18962 | hp1 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18964 | hp2 | a0001 | c0002 | t0011 | g0338 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0302 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18965 | hp2 | a0001 | c0002 | t0002 | g0107 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18966 | hp1 | a0001 | c0001 | t0031 | g0276 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18966 | hp2 | a0001 | c0002 | t0002 | g0287 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18968 | hp1 | a0001 | c0002 | t0006 | g0350 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18968 | hp2 | a0001 | c0002 | t0002 | g0099 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0087 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18971 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18973 | hp1 | a0001 | c0001 | t0004 | g0097 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18975 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18977 | hp1 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18977 | hp2 | a0001 | c0001 | t0023 | g0360 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18979 | hp1 | a0001 | c0002 | t0002 | g0285 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18979 | hp2 | a0001 | c0001 | t0020 | g0212 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18980 | hp1 | a0001 | c0002 | t0006 | g0205 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18980 | hp2 | a0001 | c0002 | t0011 | g0346 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18981 | hp1 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18982 | hp2 | a0001 | c0002 | t0018 | g0092 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18984 | hp1 | a0001 | c0002 | t0036 | g0098 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18984 | hp2 | a0001 | c0002 | t0013 | g0353 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18985 | hp1 | a0001 | c0002 | t0002 | g0086 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18985 | hp2 | a0001 | c0001 | t0028 | g0179 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18986 | hp2 | a0001 | c0002 | t0006 | g0341 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0109 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18991 | hp1 | a0001 | c0002 | t0002 | g0091 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18992 | hp1 | a0001 | c0002 | t0011 | g0339 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18992 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18993 | hp1 | a0001 | c0002 | t0002 | g0100 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18993 | hp2 | a0001 | c0001 | t0004 | g0203 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18994 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18998 | hp2 | a0001 | c0002 | t0002 | g0167 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18999 | hp1 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19003 | hp1 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19003 | hp2 | a0001 | c0001 | t0037 | g0351 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19004 | hp1 | a0001 | c0002 | t0018 | g0101 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19004 | hp2 | a0001 | c0002 | t0006 | g0337 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19010 | hp1 | a0001 | c0001 | t0008 | g0297 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19043 | hp1 | a0001 | c0001 | t0009 | g0315 | AFR | LWK | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19043 | hp2 | a0001 | c0002 | t0015 | g0028 | AFR | LWK | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19054 | hp1 | a0001 | c0002 | t0013 | g0354 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19060 | hp1 | a0001 | c0002 | t0002 | g0208 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0166 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19064 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0292 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0104 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19072 | hp1 | a0001 | c0002 | t0006 | g0348 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0103 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19081 | hp1 | a0001 | c0002 | t0039 | g0358 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19086 | hp1 | a0001 | c0002 | t0002 | g0093 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19086 | hp2 | a0001 | c0001 | t0033 | g0201 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19087 | hp1 | a0001 | c0002 | t0002 | g0165 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19087 | hp2 | a0001 | c0002 | t0006 | g0349 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19240 | hp1 | a0001 | c0001 | t0021 | g0031 | AFR | YRI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA19240 | hp2 | a0001 | c0001 | t0022 | g0033 | AFR | YRI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ASW | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA20129 | hp2 | a0001 | c0002 | t0007 | g0332 | AFR | ASW | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0089 | EUR | TSI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA20805 | hp1 | a0001 | c0002 | t0002 | g0222 | EUR | TSI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA20805 | hp2 | a0001 | c0002 | t0002 | g0088 | EUR | TSI | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA20905 | hp1 | a0001 | c0001 | t0041 | g0359 | SAS | GIH | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0090 | SAS | GIH | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0281 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02109 | hp2 | a0001 | c0001 | t0019 | g0006 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02486 | hp2 | a0001 | c0001 | t0012 | g0235 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02559 | hp1 | a0001 | c0002 | t0007 | g0151 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | ACB | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03471 | hp1 | a0001 | c0001 | t0010 | g0040 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG03471 | hp2 | a0001 | c0001 | t0024 | g0012 | AFR | MSL | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG06807 | hp1 | a0001 | c0002 | t0006 | g0312 | AFR | USA | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | USA | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | USA | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | USA | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA21309 | hp1 | a0001 | c0001 | t0012 | g0029 | AFR | LWK | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
NA21309 | hp2 | a0001 | c0001 | t0012 | g0070 | AFR | LWK | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0138 | REF | REF | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0077 | REF | REF | PRPSAP1_chr17_76304478_76358916 | PRPSAP1 | chr17 | 76304478 | 76358916 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:76344683
|
TGTATAAT others(4): Show |
T | 1 | a0002 | 1 | HG02622.hp1 | frameshift_variant | HIGH | c.267_277delTTTCATTA others(3): Show |
p.Phe90fs | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/10 | 490/3435 | 267/1158 | 89/385 | chr17 | 76344683 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:76311656
|
T | C | 1 | a0001c0002 | 116 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(113): Show |
synonymous_variant | LOW | c.1044A>G | p.Gln348Gln | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1257/3435 | 1044/1158 | 348/385 | chr17 | 76311656 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:76309588
|
C | G | 1 | a0001c0002t0011 | 4 | NA18941.hp2 NA18964.hp2 NA18980.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1954G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1954 | chr17 | 76309588 | |||||
chr17:76309603
|
A | G | 1 | a0001c0001t0031 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1939T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1939 | chr17 | 76309603 | |||||
chr17:76309624
|
C | T | 1 | a0001c0001t0016 | 3 | HG01891.hp2 HG02922.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1918G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1918 | chr17 | 76309624 | |||||
chr17:76309666
|
T | C | 4 | a0001c0001t0010a0001c0001t0012a0001c0001t0016others(1): Show | 13 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1876A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1876 | chr17 | 76309666 | |||||
chr17:76309990
|
C | CT | 9 | a0001c0001t0003a0001c0001t0017a0001c0001t0020others(6): Show | 50 | HG00408.hp1 HG00408.hp2 HG01361.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1551dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1551 | chr17 | 76309990 | |||||
chr17:76309990
|
C | CTTT | 5 | a0001c0002t0006a0001c0002t0007a0001c0002t0011others(2): Show | 40 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1549_*1551dupAAA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1551 | chr17 | 76309990 | |||||
chr17:76310110
|
C | T | 1 | a0001c0001t0009 | 5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1432G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1432 | chr17 | 76310110 | |||||
chr17:76310157
|
CGGCTAAT others(166): Show |
C | 4 | a0001c0002t0006a0001c0002t0007a0001c0002t0011others(1): Show | 37 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1212_*1384del | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1212 | chr17 | 76310157 | |||||
chr17:76310422
|
G | A | 4 | a0001c0001t0010a0001c0001t0012a0001c0001t0016others(1): Show | 13 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1120C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1120 | chr17 | 76310422 | |||||
chr17:76310445
|
C | A | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0020others(8): Show | 119 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(116): Show |
3_prime_UTR_variant | MODIFIER | c.*1097G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1097 | chr17 | 76310445 | |||||
chr17:76310471
|
G | GT | 5 | a0001c0001t0004a0001c0001t0020a0001c0001t0030others(2): Show | 39 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1070dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1070 | chr17 | 76310471 | |||||
chr17:76310471
|
GT | G | 9 | a0001c0001t0009a0001c0001t0012a0001c0001t0016others(6): Show | 53 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*1070delA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1070 | chr17 | 76310471 | |||||
chr17:76310507
|
C | G | 1 | a0001c0001t0017 | 3 | HG01361.hp2 HG02280.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1035G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1035 | chr17 | 76310507 | |||||
chr17:76310540
|
A | T | 1 | a0001c0001t0029 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1002T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 1002 | chr17 | 76310540 | |||||
chr17:76310749
|
T | C | 21 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(18): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*793A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 793 | chr17 | 76310749 | |||||
chr17:76310769
|
C | CT | 3 | a0001c0001t0028a0001c0002t0007a0001c0002t0013 | 18 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*772dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 772 | chr17 | 76310769 | |||||
chr17:76310769
|
CT | C | 8 | a0001c0001t0008a0001c0001t0022a0001c0001t0033others(5): Show | 16 | HG00438.hp1 HG01069.hp2 HG01167.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*772delA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 772 | chr17 | 76310769 | |||||
chr17:76311021
|
G | A | 1 | a0001c0001t0009 | 5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*521C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 521 | chr17 | 76311021 | |||||
chr17:76311030
|
T | C | 1 | a0001c0002t0036 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*512A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 512 | chr17 | 76311030 | |||||
chr17:76311371
|
C | G | 1 | a0001c0001t0027 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*171G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 171 | chr17 | 76311371 | |||||
chr17:76311391
|
T | C | 4 | a0001c0001t0010a0001c0001t0012a0001c0001t0016others(1): Show | 13 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*151A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 151 | chr17 | 76311391 | |||||
chr17:76311425
|
A | G | 11 | a0001c0001t0009a0001c0001t0010a0001c0001t0012others(8): Show | 59 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*117T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 10/10 | 117 | chr17 | 76311425 | |||||
chr17:76353753
|
T | G | 5 | a0001c0001t0037a0001c0001t0038a0001c0001t0040others(2): Show | 8 | HG01167.hp1 HG01169.hp2 HG02080.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-50A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/10 | 50 | chr17 | 76353753 | |||||
chr17:76353784
|
G | A | 1 | a0001c0001t0041 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-81C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/10 | 81 | chr17 | 76353784 | |||||
chr17:76353829
|
G | T | 3 | a0001c0001t0014a0001c0001t0024a0001c0001t0025 | 5 | HG01106.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-126C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/10 | 126 | chr17 | 76353829 | |||||
chr17:76353837
|
T | A | 1 | a0001c0001t0023 | 2 | HG02055.hp1 NA18977.hp2 |
5_prime_UTR_variant | MODIFIER | c.-134A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/10 | 134 | chr17 | 76353837 | |||||
chr17:76353867
|
A | T | 1 | a0001c0001t0019 | 2 | HG02109.hp2 HG02145.hp2 |
5_prime_UTR_variant | MODIFIER | c.-164T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/10 | 164 | chr17 | 76353867 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:76311931
|
T | C | 58 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(55): Show | 59 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.1000-231A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76311931 | ||||||
chr17:76312044
|
G | A | 60 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0079others(57): Show | 60 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.1000-344C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312044 | ||||||
chr17:76312054
|
T | C | 3 | a0001c0001t0016g0046a0001c0001t0016g0052a0001c0001t0016g0193 | 3 | HG01891.hp2 HG02922.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1000-354A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312054 | ||||||
chr17:76312076
|
A | G | 1 | a0001c0001t0010g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1000-376T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312076 | ||||||
chr17:76312123
|
A | G | 3 | a0001c0001t0017g0318a0001c0001t0017g0323a0001c0001t0017g0329 | 3 | HG01361.hp2 HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1000-423T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312123 | ||||||
chr17:76312127
|
G | A | 39 | a0001c0002t0006g0054a0001c0002t0006g0197a0001c0002t0006g0205others(36): Show | 40 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.1000-427C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312127 | ||||||
chr17:76312195
|
C | A | 1 | a0001c0001t0001g0152 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1000-495G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312195 | ||||||
chr17:76312277
|
A | C | 244 | a0001c0001t0001g0306a0001c0001t0002g0213a0001c0001t0003g0004others(241): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1000-577T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312277 | ||||||
chr17:76312291
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.999+579T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312291 | ||||||
chr17:76312352
|
G | A | 118 | a0001c0001t0002g0213a0001c0001t0003g0004a0001c0001t0003g0105others(115): Show | 119 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.999+518C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312352 | ||||||
chr17:76312353
|
T | C | 57 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(54): Show | 58 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.999+517A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312353 | ||||||
chr17:76312431
|
C | G | 36 | a0001c0002t0006g0054a0001c0002t0006g0197a0001c0002t0006g0205others(33): Show | 37 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.999+439G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312431 | ||||||
chr17:76312437
|
CA | C | 190 | a0001c0001t0002g0213a0001c0001t0003g0004a0001c0001t0003g0105others(187): Show | 192 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(189): Show |
intron_variant | MODIFIER | c.999+432delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312437 | ||||||
chr17:76312473
|
C | G | 2 | a0001c0001t0001g0116a0001c0001t0001g0121 | 2 | HG01516.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.999+397G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312473 | ||||||
chr17:76312558
|
C | T | 3 | a0001c0001t0017g0318a0001c0001t0017g0323a0001c0001t0017g0329 | 3 | HG01361.hp2 HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.999+312G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312558 | ||||||
chr17:76312653
|
T | C | 42 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0079others(39): Show | 42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.999+217A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312653 | ||||||
chr17:76312810
|
T | G | 58 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(55): Show | 59 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.999+60A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 9/9 | chr17 | 76312810 | ||||||
chr17:76313183
|
A | C | 1 | a0001c0001t0003g0328 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.853-167T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 8/9 | chr17 | 76313183 | ||||||
chr17:76313203
|
T | A | 45 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(42): Show | 46 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(43): Show |
intron_variant | MODIFIER | c.853-187A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 8/9 | chr17 | 76313203 | ||||||
chr17:76313344
|
T | C | 245 | a0001c0001t0001g0306a0001c0001t0002g0213a0001c0001t0003g0004others(242): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.853-328A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 8/9 | chr17 | 76313344 | ||||||
chr17:76313393
|
A | G | 245 | a0001c0001t0001g0306a0001c0001t0002g0213a0001c0001t0003g0004others(242): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.853-377T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 8/9 | chr17 | 76313393 | ||||||
chr17:76313461
|
A | G | 1 | a0001c0001t0001g0019 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.852+360T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 8/9 | chr17 | 76313461 | ||||||
chr17:76313471
|
C | T | 5 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.852+350G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 8/9 | chr17 | 76313471 | ||||||
chr17:76313480
|
C | G | 58 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(55): Show | 59 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.852+341G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 8/9 | chr17 | 76313480 | ||||||
chr17:76313491
|
G | A | 4 | a0001c0002t0006g0310a0001c0002t0006g0312a0001c0002t0006g0313others(1): Show | 4 | HG02818.hp1 HG02895.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.852+330C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 8/9 | chr17 | 76313491 | ||||||
chr17:76313810
|
T | C | 5 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.852+11A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 8/9 | chr17 | 76313810 | ||||||
chr17:76314003
|
A | C | 53 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0040others(50): Show | 54 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.782-112T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314003 | ||||||
chr17:76314111
|
T | C | 1 | a0001c0002t0002g0147 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.782-220A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314111 | ||||||
chr17:76314201
|
A | AATGT | 7 | a0001c0001t0003g0223a0001c0001t0003g0314a0001c0001t0009g0303others(4): Show | 7 | HG01891.hp1 HG02055.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.782-314_782-311dup others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314201 | ||||||
chr17:76314201
|
A | AATGTATG others(5): Show |
1 | a0001c0002t0015g0053 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.782-322_782-311dup others(12): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314201 | ||||||
chr17:76314201
|
A | AATGTATG others(9): Show |
36 | a0001c0002t0006g0054a0001c0002t0006g0197a0001c0002t0006g0205others(33): Show | 37 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.782-326_782-311dup others(16): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314201 | ||||||
chr17:76314201
|
A | AATGTATG others(13): Show |
3 | a0001c0002t0006g0347a0001c0002t0015g0027a0001c0002t0015g0028 | 3 | HG02257.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.782-330_782-311dup others(20): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314201 | ||||||
chr17:76314211
|
T | C | 11 | a0001c0002t0002g0024a0001c0002t0002g0082a0001c0002t0002g0083others(8): Show | 11 | HG01070.hp1 HG01071.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.782-320A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314211 | ||||||
chr17:76314228
|
G | GTATGTAT others(10): Show |
10 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0040others(7): Show | 10 | HG01891.hp2 HG02615.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.782-338_782-337ins others(17): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314228 | ||||||
chr17:76314228
|
G | GTATGTAT others(14): Show |
2 | a0001c0001t0012g0029a0001c0001t0012g0070 | 2 | NA21309.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.782-338_782-337ins others(21): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314228 | ||||||
chr17:76314228
|
G | GTATGTAT others(18): Show |
1 | a0001c0001t0012g0235 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.782-338_782-337ins others(25): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314228 | ||||||
chr17:76314281
|
G | A | 35 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0079others(32): Show | 35 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(32): Show |
intron_variant | MODIFIER | c.782-390C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314281 | ||||||
chr17:76314341
|
C | T | 13 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0040others(10): Show | 13 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.782-450G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314341 | ||||||
chr17:76314399
|
T | C | 37 | a0001c0002t0006g0054a0001c0002t0006g0197a0001c0002t0006g0205others(34): Show | 38 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.782-508A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314399 | ||||||
chr17:76314480
|
G | A | 5 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-589C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314480 | ||||||
chr17:76314514
|
A | G | 126 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0079others(123): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.782-623T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314514 | ||||||
chr17:76314552
|
T | C | 1 | a0001c0001t0004g0296 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.782-661A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314552 | ||||||
chr17:76314577
|
T | C | 40 | a0001c0002t0006g0054a0001c0002t0006g0197a0001c0002t0006g0205others(37): Show | 41 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.782-686A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314577 | ||||||
chr17:76314620
|
TCAGCCTC others(5): Show |
T | 1 | a0001c0002t0002g0264 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.782-741_782-730del others(12): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314620 | ||||||
chr17:76314673
|
C | T | 7 | a0001c0001t0005g0032a0001c0001t0005g0034a0001c0001t0005g0035others(4): Show | 7 | HG02818.hp2 HG02965.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.782-782G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314673 | ||||||
chr17:76314824
|
A | T | 1 | a0001c0001t0001g0185 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.782-933T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314824 | ||||||
chr17:76314826
|
A | G | 37 | a0001c0002t0006g0054a0001c0002t0006g0197a0001c0002t0006g0205others(34): Show | 38 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.782-935T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314826 | ||||||
chr17:76314838
|
C | T | 71 | a0001c0002t0001g0068a0001c0002t0002g0013a0001c0002t0002g0015others(68): Show | 71 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.782-947G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314838 | ||||||
chr17:76314892
|
T | C | 58 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(55): Show | 59 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.782-1001A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314892 | ||||||
chr17:76314895
|
C | A | 19 | a0001c0002t0006g0197a0001c0002t0006g0205a0001c0002t0006g0259others(16): Show | 19 | HG02080.hp1 HG02129.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.782-1004G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314895 | ||||||
chr17:76314903
|
T | C | 19 | a0001c0002t0006g0197a0001c0002t0006g0205a0001c0002t0006g0259others(16): Show | 19 | HG02080.hp1 HG02129.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.782-1012A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314903 | ||||||
chr17:76314922
|
T | C | 1 | a0001c0001t0003g0189 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.782-1031A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314922 | ||||||
chr17:76314998
|
T | C | 2 | a0001c0001t0001g0122a0001c0001t0001g0125 | 2 | HG01975.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.782-1107A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76314998 | ||||||
chr17:76315170
|
T | C | 53 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0040others(50): Show | 54 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.782-1279A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315170 | ||||||
chr17:76315262
|
C | T | 245 | a0001c0001t0001g0306a0001c0001t0002g0213a0001c0001t0003g0004others(242): Show | 247 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.782-1371G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315262 | ||||||
chr17:76315483
|
C | G | 57 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(54): Show | 58 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.782-1592G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315483 | ||||||
chr17:76315511
|
A | G | 15 | a0001c0001t0005g0032a0001c0001t0005g0034a0001c0001t0005g0035others(12): Show | 15 | HG01361.hp2 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.782-1620T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315511 | ||||||
chr17:76315580
|
C | T | 58 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(55): Show | 59 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.782-1689G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315580 | ||||||
chr17:76315700
|
C | CT | 17 | a0001c0001t0001g0048a0001c0001t0001g0069a0001c0001t0001g0071others(14): Show | 17 | HG00323.hp2 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.782-1810dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | ||||||
chr17:76315700
|
C | CTTT | 10 | a0001c0001t0005g0043a0001c0001t0005g0050a0001c0001t0005g0051others(7): Show | 10 | HG01106.hp1 HG02559.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.782-1812_782-1810d others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | ||||||
chr17:76315700
|
C | CTTTT | 16 | a0001c0001t0005g0163a0001c0002t0006g0054a0001c0002t0006g0205others(13): Show | 16 | HG01099.hp1 HG02080.hp1 HG02129.hp2 others(13): Show |
intron_variant | MODIFIER | c.782-1813_782-1810d others(6): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | ||||||
chr17:76315700
|
C | CTTTTT | 8 | a0001c0001t0005g0320a0001c0002t0006g0197a0001c0002t0006g0335others(5): Show | 9 | HG02258.hp1 HG02976.hp1 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.782-1814_782-1810d others(7): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | ||||||
chr17:76315700
|
C | CTTTTTTT others(4): Show |
1 | a0001c0002t0007g0308 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.782-1820_782-1810d others(13): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | ||||||
chr17:76315700
|
CT | C | 105 | a0001c0001t0001g0113a0001c0001t0001g0184a0001c0001t0001g0226others(102): Show | 106 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.782-1810delA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | ||||||
chr17:76315700
|
CTTTTTTT others(2): Show |
C | 41 | a0001c0001t0003g0299a0001c0001t0004g0066a0001c0001t0004g0067others(38): Show | 41 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(38): Show |
intron_variant | MODIFIER | c.782-1818_782-1810d others(11): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | ||||||
chr17:76315700
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0034g0334 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.782-1819_782-1810d others(12): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | ||||||
chr17:76315700
|
CTTTTTTT others(5): Show |
C | 5 | a0001c0002t0002g0016a0001c0002t0002g0017a0001c0002t0002g0018others(2): Show | 5 | NA18945.hp1 NA18947.hp2 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.782-1821_782-1810d others(14): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | ||||||
chr17:76315700
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0149 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.782-1822_782-1810d others(15): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315700 | ||||||
chr17:76315729
|
T | C | 12 | a0001c0001t0010g0037a0001c0001t0010g0040a0001c0001t0010g0041others(9): Show | 12 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.782-1838A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315729 | ||||||
chr17:76315841
|
A | T | 5 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-1950T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315841 | ||||||
chr17:76315861
|
C | T | 53 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0079others(50): Show | 53 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.782-1970G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315861 | ||||||
chr17:76315862
|
G | A | 5 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-1971C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315862 | ||||||
chr17:76315922
|
G | T | 1 | a0001c0002t0011g0336 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.782-2031C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315922 | ||||||
chr17:76315953
|
G | A | 7 | a0001c0001t0005g0032a0001c0001t0005g0034a0001c0001t0005g0035others(4): Show | 7 | HG02818.hp2 HG02965.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.782-2062C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76315953 | ||||||
chr17:76316021
|
T | C | 53 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0040others(50): Show | 54 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.782-2130A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316021 | ||||||
chr17:76316031
|
A | T | 53 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0040others(50): Show | 54 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.782-2140T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316031 | ||||||
chr17:76316174
|
T | TA | 6 | a0001c0001t0001g0135a0001c0001t0004g0293a0001c0001t0005g0050others(3): Show | 6 | HG02055.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.782-2284dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316174 | ||||||
chr17:76316174
|
TA | T | 7 | a0001c0001t0001g0113a0001c0001t0003g0189a0001c0001t0003g0299others(4): Show | 7 | HG02109.hp1 HG02895.hp1 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.782-2284delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316174 | ||||||
chr17:76316190
|
A | G | 1 | a0001c0001t0010g0037 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.782-2299T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316190 | ||||||
chr17:76316191
|
A | AAG | 32 | a0001c0002t0006g0054a0001c0002t0006g0205a0001c0002t0006g0241others(29): Show | 33 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.782-2301_782-2300i others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316191 | ||||||
chr17:76316191
|
A | G | 17 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(14): Show | 17 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.782-2300T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316191 | ||||||
chr17:76316192
|
G | A | 50 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(47): Show | 51 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.782-2301C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316192 | ||||||
chr17:76316192
|
G | GA | 9 | a0001c0001t0001g0123a0001c0001t0001g0218a0001c0001t0001g0306others(6): Show | 9 | HG01934.hp2 HG02145.hp1 HG03209.hp2 others(6): Show |
intron_variant | MODIFIER | c.782-2302dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316192 | ||||||
chr17:76316266
|
G | A | 4 | a0001c0001t0005g0032a0001c0001t0005g0034a0001c0001t0005g0035others(1): Show | 4 | HG02818.hp2 HG03453.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.782-2375C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316266 | ||||||
chr17:76316300
|
C | T | 15 | a0001c0001t0005g0032a0001c0001t0005g0034a0001c0001t0005g0035others(12): Show | 15 | HG01361.hp2 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.782-2409G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316300 | ||||||
chr17:76316524
|
C | A | 5 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-2633G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316524 | ||||||
chr17:76316673
|
C | T | 36 | a0001c0002t0006g0054a0001c0002t0006g0197a0001c0002t0006g0205others(33): Show | 37 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.782-2782G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316673 | ||||||
chr17:76316778
|
C | T | 57 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(54): Show | 58 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.782-2887G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316778 | ||||||
chr17:76316800
|
T | C | 2 | a0001c0001t0021g0031a0001c0001t0021g0039 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.782-2909A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316800 | ||||||
chr17:76316958
|
CTAAAG | C | 38 | a0001c0001t0002g0213a0001c0001t0003g0004a0001c0001t0003g0105others(35): Show | 39 | HG00408.hp1 HG00408.hp2 HG01952.hp1 others(36): Show |
intron_variant | MODIFIER | c.782-3072_782-3068d others(7): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76316958 | ||||||
chr17:76317005
|
C | T | 53 | a0001c0001t0004g0066a0001c0001t0004g0067a0001c0001t0004g0079others(50): Show | 53 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(50): Show |
intron_variant | MODIFIER | c.782-3114G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317005 | ||||||
chr17:76317022
|
A | G | 1 | a0001c0001t0001g0258 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.782-3131T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317022 | ||||||
chr17:76317166
|
AT | A | 52 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0040others(49): Show | 53 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.782-3276delA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317166 | ||||||
chr17:76317219
|
A | G | 57 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(54): Show | 58 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.782-3328T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317219 | ||||||
chr17:76317220
|
C | G | 13 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0040others(10): Show | 13 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.782-3329G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317220 | ||||||
chr17:76317233
|
T | C | 57 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(54): Show | 58 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.782-3342A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317233 | ||||||
chr17:76317267
|
T | G | 5 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-3376A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317267 | ||||||
chr17:76317285
|
G | C | 4 | a0001c0002t0002g0087a0001c0002t0002g0108a0001c0002t0002g0148others(1): Show | 4 | HG00609.hp1 HG00621.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.782-3394C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317285 | ||||||
chr17:76317316
|
C | T | 74 | a0001c0002t0002g0013a0001c0002t0002g0015a0001c0002t0002g0016others(71): Show | 74 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.782-3425G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317316 | ||||||
chr17:76317364
|
A | G | 8 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(5): Show | 8 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.782-3473T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317364 | ||||||
chr17:76317448
|
C | G | 3 | a0001c0002t0015g0027a0001c0002t0015g0028a0001c0002t0015g0053 | 3 | HG03209.hp2 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.782-3557G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317448 | ||||||
chr17:76317449
|
G | A | 12 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0040others(9): Show | 12 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.782-3558C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317449 | ||||||
chr17:76317461
|
A | C | 244 | a0001c0001t0001g0149a0001c0001t0001g0306a0001c0001t0002g0213others(241): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.782-3570T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317461 | ||||||
chr17:76317470
|
G | A | 12 | a0001c0001t0001g0048a0001c0001t0001g0069a0001c0001t0001g0133others(9): Show | 12 | HG00099.hp1 HG00323.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.782-3579C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317470 | ||||||
chr17:76317510
|
G | C | 52 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0040others(49): Show | 53 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.782-3619C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317510 | ||||||
chr17:76317620
|
A | C | 2 | a0001c0001t0019g0006a0001c0001t0019g0007 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.782-3729T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317620 | ||||||
chr17:76317663
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.782-3772A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317663 | ||||||
chr17:76317704
|
G | A | 3 | a0001c0001t0017g0318a0001c0001t0017g0323a0001c0001t0017g0329 | 3 | HG01361.hp2 HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.782-3813C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317704 | ||||||
chr17:76317728
|
C | T | 1 | a0001c0001t0008g0187 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.782-3837G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317728 | ||||||
chr17:76317729
|
G | A | 1 | a0001c0002t0006g0347 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.782-3838C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317729 | ||||||
chr17:76317816
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.782-3925G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317816 | ||||||
chr17:76317883
|
T | A | 1 | a0001c0001t0004g0271 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.782-3992A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317883 | ||||||
chr17:76317968
|
TA | T | 52 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0040others(49): Show | 53 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.782-4078delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76317968 | ||||||
chr17:76318014
|
G | A | 13 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0040others(10): Show | 13 | HG01891.hp2 HG02486.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.782-4123C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318014 | ||||||
chr17:76318099
|
A | G | 36 | a0001c0002t0006g0054a0001c0002t0006g0197a0001c0002t0006g0205others(33): Show | 37 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.782-4208T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318099 | ||||||
chr17:76318146
|
T | C | 5 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(2): Show | 5 | HG01891.hp1 HG02055.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-4255A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318146 | ||||||
chr17:76318220
|
T | C | 67 | a0001c0001t0001g0122a0001c0001t0001g0125a0001c0001t0003g0139others(64): Show | 68 | HG00408.hp2 HG00738.hp2 HG01069.hp1 others(65): Show |
intron_variant | MODIFIER | c.782-4329A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318220 | ||||||
chr17:76318397
|
C | T | 2 | a0001c0001t0003g0209a0001c0001t0003g0210 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.782-4506G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318397 | ||||||
chr17:76318431
|
C | T | 51 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0040others(48): Show | 52 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.782-4540G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318431 | ||||||
chr17:76318504
|
A | G | 2 | a0001c0002t0015g0027a0001c0002t0015g0028 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.782-4613T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318504 | ||||||
chr17:76318692
|
T | C | 56 | a0001c0001t0001g0268a0001c0001t0003g0265a0001c0001t0004g0066others(53): Show | 56 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(53): Show |
intron_variant | MODIFIER | c.782-4801A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318692 | ||||||
chr17:76318694
|
A | C | 1 | a0001c0001t0001g0268 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.782-4803T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318694 | ||||||
chr17:76318748
|
T | C | 65 | a0001c0001t0001g0152a0001c0001t0003g0139a0001c0001t0003g0188others(62): Show | 66 | HG00408.hp2 HG00738.hp2 HG01069.hp1 others(63): Show |
intron_variant | MODIFIER | c.782-4857A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318748 | ||||||
chr17:76318804
|
C | G | 1 | a0001c0002t0002g0264 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.782-4913G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318804 | ||||||
chr17:76318805
|
G | C | 1 | a0001c0002t0002g0264 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.782-4914C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76318805 | ||||||
chr17:76319001
|
G | A | 2 | a0001c0001t0004g0128a0001c0002t0002g0062 | 2 | HG00741.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.782-5110C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319001 | ||||||
chr17:76319038
|
C | T | 40 | a0001c0002t0006g0054a0001c0002t0006g0197a0001c0002t0006g0205others(37): Show | 41 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.782-5147G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319038 | ||||||
chr17:76319088
|
T | C | 2 | a0001c0002t0002g0141a0001c0002t0002g0142 | 2 | NA18944.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.782-5197A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319088 | ||||||
chr17:76319089
|
G | A | 1 | a0001c0001t0005g0320 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.782-5198C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319089 | ||||||
chr17:76319096
|
G | C | 128 | a0001c0001t0003g0298a0001c0001t0005g0320a0001c0001t0009g0303others(125): Show | 129 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(126): Show |
intron_variant | MODIFIER | c.782-5205C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319096 | ||||||
chr17:76319308
|
G | C | 1 | a0001c0001t0030g0119 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.782-5417C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319308 | ||||||
chr17:76319326
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.782-5435G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319326 | ||||||
chr17:76319333
|
T | C | 12 | a0001c0001t0005g0032a0001c0001t0005g0034a0001c0001t0005g0035others(9): Show | 12 | HG01243.hp1 HG01891.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.782-5442A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319333 | ||||||
chr17:76319476
|
A | AT | 11 | a0001c0001t0001g0174a0001c0001t0003g0298a0001c0001t0005g0049others(8): Show | 11 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.782-5586dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319476 | ||||||
chr17:76319491
|
C | T | 1 | a0001c0001t0005g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.782-5600G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319491 | ||||||
chr17:76319520
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.782-5629T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319520 | ||||||
chr17:76319542
|
C | T | 2 | a0001c0001t0001g0064a0001c0001t0001g0134 | 2 | HG03239.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.782-5651G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319542 | ||||||
chr17:76319555
|
G | A | 1 | a0001c0002t0002g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.782-5664C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319555 | ||||||
chr17:76319564
|
G | T | 1 | a0001c0002t0002g0264 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.782-5673C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319564 | ||||||
chr17:76319600
|
T | C | 56 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0075others(53): Show | 56 | HG00423.hp2 HG00597.hp2 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.782-5709A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319600 | ||||||
chr17:76319606
|
T | C | 19 | a0001c0001t0003g0298a0001c0001t0005g0049a0001c0001t0005g0236others(16): Show | 19 | HG01361.hp2 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.782-5715A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319606 | ||||||
chr17:76319617
|
C | G | 1 | a0001c0002t0002g0264 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.782-5726G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319617 | ||||||
chr17:76319617
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.782-5726G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319617 | ||||||
chr17:76319618
|
G | A | 36 | a0001c0001t0001g0060a0001c0001t0001g0063a0001c0001t0001g0120others(33): Show | 36 | HG00408.hp1 HG00423.hp2 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.782-5727C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319618 | ||||||
chr17:76319618
|
G | C | 1 | a0001c0002t0002g0264 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.782-5727C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319618 | ||||||
chr17:76319618
|
G | GCCACCAT others(522): Show |
1 | a0001c0002t0002g0023 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.782-5728_782-5727i others(531): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319618 | ||||||
chr17:76319625
|
T | C | 2 | a0001c0001t0004g0126a0001c0001t0005g0032 | 2 | HG01952.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.782-5734A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319625 | ||||||
chr17:76319628
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.782-5737A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319628 | ||||||
chr17:76319630
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.782-5739C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319630 | ||||||
chr17:76319657
|
C | T | 2 | a0001c0002t0002g0221a0001c0002t0002g0222 | 2 | HG02148.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.782-5766G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319657 | ||||||
chr17:76319668
|
C | T | 4 | a0001c0001t0001g0096a0001c0001t0001g0277a0001c0002t0002g0109others(1): Show | 4 | HG00597.hp1 HG02129.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.782-5777G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319668 | ||||||
chr17:76319669
|
G | A | 55 | a0001c0001t0001g0048a0001c0001t0001g0069a0001c0001t0001g0078others(52): Show | 56 | HG00323.hp2 HG00438.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.782-5778C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319669 | ||||||
chr17:76319669
|
GTGTTGGC others(959): Show |
G | 1 | a0001c0002t0011g0346 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.782-6744_782-5779d others(2): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319669 | ||||||
chr17:76319820
|
G | T | 4 | a0001c0001t0001g0306a0001c0001t0004g0145a0001c0001t0004g0232others(1): Show | 4 | HG00140.hp1 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.782-5929C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319820 | ||||||
chr17:76319848
|
A | G | 1 | a0001c0001t0033g0201 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.782-5957T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319848 | ||||||
chr17:76319952
|
C | G | 1 | a0001c0001t0004g0344 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.782-6061G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319952 | ||||||
chr17:76319978
|
A | C | 2 | a0001c0002t0002g0082a0001c0002t0002g0083 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.782-6087T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76319978 | ||||||
chr17:76320009
|
T | C | 1 | a0001c0001t0031g0276 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.782-6118A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320009 | ||||||
chr17:76320045
|
G | A | 1 | a0001c0002t0039g0358 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.782-6154C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320045 | ||||||
chr17:76320127
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.782-6236C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320127 | ||||||
chr17:76320132
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.782-6241A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320132 | ||||||
chr17:76320178
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.782-6287C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320178 | ||||||
chr17:76320256
|
GAAAGAAA others(2): Show |
G | 6 | a0001c0001t0003g0298a0001c0001t0010g0037a0001c0001t0010g0038others(3): Show | 6 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.782-6374_782-6366d others(11): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320256 | ||||||
chr17:76320264
|
G | A | 130 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(127): Show | 132 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.782-6373C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320264 | ||||||
chr17:76320265
|
A | G | 130 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(127): Show | 132 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.782-6374T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320265 | ||||||
chr17:76320277
|
G | GA | 130 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(127): Show | 132 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.782-6387dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320277 | ||||||
chr17:76320281
|
GA | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(94): Show | 100 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.782-6391delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320281 | ||||||
chr17:76320285
|
A | G | 130 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(127): Show | 132 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.782-6394T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320285 | ||||||
chr17:76320286
|
G | A | 131 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(128): Show | 133 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.782-6395C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320286 | ||||||
chr17:76320287
|
A | G | 1 | a0001c0002t0002g0264 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.782-6396T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320287 | ||||||
chr17:76320290
|
G | GA | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(141): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.782-6400dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320290 | ||||||
chr17:76320290
|
GAAAGAAA others(2): Show |
G | 7 | a0001c0001t0003g0298a0001c0001t0005g0320a0001c0001t0010g0037others(4): Show | 7 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.782-6408_782-6400d others(11): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320290 | ||||||
chr17:76320295
|
A | G | 130 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(127): Show | 132 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.782-6404T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320295 | ||||||
chr17:76320298
|
GA | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(141): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.782-6408delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320298 | ||||||
chr17:76320299
|
A | G | 130 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(127): Show | 132 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.782-6408T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320299 | ||||||
chr17:76320300
|
A | G | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(278): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.782-6409T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320300 | ||||||
chr17:76320302
|
A | G | 131 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(128): Show | 133 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.782-6411T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320302 | ||||||
chr17:76320304
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.782-6413T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320304 | ||||||
chr17:76320305
|
A | AGGG | 131 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(128): Show | 133 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.782-6415_782-6414i others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320305 | ||||||
chr17:76320305
|
A | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(148): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.782-6414T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320305 | ||||||
chr17:76320317
|
A | G | 131 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(128): Show | 133 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.782-6426T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320317 | ||||||
chr17:76320321
|
G | A | 4 | a0001c0001t0016g0046a0001c0001t0016g0052a0001c0001t0016g0193others(1): Show | 4 | HG01891.hp2 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.782-6430C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320321 | ||||||
chr17:76320341
|
G | GAGGAAGG others(1): Show |
7 | a0001c0001t0001g0306a0001c0001t0005g0032a0001c0001t0005g0034others(4): Show | 7 | HG02145.hp1 HG02818.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.782-6458_782-6451d others(10): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320341 | ||||||
chr17:76320345
|
A | G | 128 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(125): Show | 130 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.782-6454T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320345 | ||||||
chr17:76320349
|
A | G | 1 | a0001c0001t0001g0277 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.782-6458T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320349 | ||||||
chr17:76320352
|
G | GAAGA | 6 | a0001c0001t0004g0145a0001c0001t0004g0232a0001c0001t0004g0233others(3): Show | 6 | HG00140.hp1 HG01106.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.782-6465_782-6462d others(6): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320352 | ||||||
chr17:76320352
|
G | GAAGGAAG others(1): Show |
36 | a0001c0001t0003g0198a0001c0001t0004g0343a0001c0001t0005g0238others(33): Show | 36 | HG01361.hp2 HG01891.hp1 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.782-6462_782-6461i others(10): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320352 | ||||||
chr17:76320353
|
A | AAGGAAGG others(9): Show |
129 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(126): Show | 131 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.782-6463_782-6462i others(18): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320353 | ||||||
chr17:76320362
|
G | T | 5 | a0001c0001t0001g0117a0001c0001t0001g0169a0001c0001t0001g0181others(2): Show | 5 | HG01070.hp2 HG01074.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-6471C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320362 | ||||||
chr17:76320423
|
C | CT | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(95): Show | 101 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.782-6533dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320423 | ||||||
chr17:76320423
|
C | CTT | 13 | a0001c0001t0001g0071a0001c0001t0001g0094a0001c0001t0001g0137others(10): Show | 14 | HG00438.hp1 HG00558.hp1 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.782-6534_782-6533d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320423 | ||||||
chr17:76320423
|
C | CTTT | 84 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0152others(81): Show | 85 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(82): Show |
intron_variant | MODIFIER | c.782-6535_782-6533d others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320423 | ||||||
chr17:76320423
|
C | CTTTT | 39 | a0001c0001t0001g0127a0001c0001t0001g0171a0001c0001t0001g0268others(36): Show | 39 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.782-6536_782-6533d others(6): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320423 | ||||||
chr17:76320423
|
CT | C | 15 | a0001c0001t0005g0320a0001c0001t0014g0009a0001c0001t0014g0011others(12): Show | 15 | HG01106.hp1 HG03225.hp1 HG03471.hp2 others(12): Show |
intron_variant | MODIFIER | c.782-6533delA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320423 | ||||||
chr17:76320488
|
G | A | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.782-6597C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320488 | ||||||
chr17:76320539
|
C | G | 2 | a0001c0001t0010g0040a0001c0001t0010g0041 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.782-6648G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320539 | ||||||
chr17:76320546
|
T | A | 2 | a0001c0002t0002g0036a0001c0002t0002g0042 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.782-6655A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320546 | ||||||
chr17:76320591
|
A | AT | 6 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0063others(3): Show | 6 | HG00323.hp1 HG02145.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.782-6701dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320591 | ||||||
chr17:76320591
|
A | ATT | 125 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(122): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.782-6702_782-6701d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320591 | ||||||
chr17:76320591
|
A | ATTT | 9 | a0001c0001t0002g0213a0001c0001t0003g0252a0001c0001t0003g0299others(6): Show | 9 | HG00597.hp2 HG00639.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.782-6703_782-6701d others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320591 | ||||||
chr17:76320786
|
C | CT | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(92): Show | 98 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.782-6896dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320786 | ||||||
chr17:76320788
|
T | C | 2 | a0001c0001t0021g0031a0001c0001t0021g0039 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.782-6897A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320788 | ||||||
chr17:76320845
|
G | A | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(146): Show | 152 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.782-6954C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320845 | ||||||
chr17:76320972
|
A | G | 136 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(133): Show | 138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.782-7081T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76320972 | ||||||
chr17:76321010
|
T | C | 1 | a0001c0001t0028g0179 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.782-7119A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321010 | ||||||
chr17:76321011
|
G | T | 1 | a0001c0001t0028g0179 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.782-7120C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321011 | ||||||
chr17:76321178
|
C | G | 1 | a0001c0001t0010g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.782-7287G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321178 | ||||||
chr17:76321238
|
C | A | 2 | a0001c0001t0019g0006a0001c0001t0019g0007 | 2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.782-7347G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321238 | ||||||
chr17:76321322
|
C | T | 2 | a0001c0001t0001g0306a0001c0001t0005g0244 | 2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.781+7395G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321322 | ||||||
chr17:76321358
|
C | T | 1 | a0001c0001t0005g0320 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.781+7359G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321358 | ||||||
chr17:76321387
|
G | A | 2 | a0001c0001t0004g0067a0001c0002t0001g0068 | 2 | HG03490.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.781+7330C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321387 | ||||||
chr17:76321487
|
G | A | 2 | a0001c0001t0005g0236a0001c0001t0005g0237 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.781+7230C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321487 | ||||||
chr17:76321640
|
T | C | 3 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305 | 3 | HG02055.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.781+7077A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321640 | ||||||
chr17:76321884
|
TAC | T | 131 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(128): Show | 133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.781+6831_781+6832d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321884 | ||||||
chr17:76321922
|
A | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(280): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.781+6795T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76321922 | ||||||
chr17:76322042
|
T | C | 131 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(128): Show | 133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.781+6675A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322042 | ||||||
chr17:76322065
|
G | A | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+6652C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322065 | ||||||
chr17:76322075
|
C | G | 1 | a0001c0001t0001g0156 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.781+6642G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322075 | ||||||
chr17:76322118
|
C | T | 12 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305others(9): Show | 12 | HG02055.hp2 HG02970.hp2 HG03579.hp2 others(9): Show |
intron_variant | MODIFIER | c.781+6599G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322118 | ||||||
chr17:76322206
|
G | A | 131 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(128): Show | 133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.781+6511C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322206 | ||||||
chr17:76322345
|
G | A | 1 | a0001c0001t0031g0276 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.781+6372C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322345 | ||||||
chr17:76322428
|
G | A | 131 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(128): Show | 133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.781+6289C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322428 | ||||||
chr17:76322475
|
C | T | 1 | a0001c0001t0005g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.781+6242G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322475 | ||||||
chr17:76322551
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.781+6166T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322551 | ||||||
chr17:76322695
|
T | C | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+6022A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322695 | ||||||
chr17:76322743
|
C | T | 8 | a0001c0001t0003g0105a0001c0002t0002g0102a0001c0002t0002g0103others(5): Show | 8 | HG00408.hp1 HG00609.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.781+5974G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322743 | ||||||
chr17:76322744
|
G | A | 1 | a0001c0001t0005g0320 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.781+5973C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322744 | ||||||
chr17:76322911
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.781+5806G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322911 | ||||||
chr17:76322948
|
C | T | 1 | a0001c0002t0015g0053 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.781+5769G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322948 | ||||||
chr17:76322959
|
A | G | 131 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(128): Show | 133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.781+5758T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322959 | ||||||
chr17:76322976
|
G | C | 4 | a0001c0001t0001g0161a0001c0001t0008g0187a0001c0001t0008g0309others(1): Show | 4 | HG01433.hp1 HG02451.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+5741C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76322976 | ||||||
chr17:76323001
|
C | T | 1 | a0001c0001t0003g0188 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.781+5716G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323001 | ||||||
chr17:76323008
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.781+5709C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323008 | ||||||
chr17:76323025
|
C | A | 1 | a0001c0001t0033g0201 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.781+5692G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323025 | ||||||
chr17:76323027
|
C | G | 1 | a0001c0001t0001g0115 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.781+5690G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323027 | ||||||
chr17:76323154
|
C | T | 2 | a0001c0002t0002g0202a0001c0002t0002g0208 | 2 | NA18975.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.781+5563G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323154 | ||||||
chr17:76323171
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.781+5546C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323171 | ||||||
chr17:76323179
|
T | TAAAAATA others(3045): Show |
1 | a0001c0001t0004g0284 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3054): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3052): Show |
1 | a0001c0001t0003g0224 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3061): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3050): Show |
1 | a0001c0001t0001g0268 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3049): Show |
1 | a0001c0001t0004g0206 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3045): Show |
1 | a0001c0001t0003g0204 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3054): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3038): Show |
1 | a0001c0001t0004g0286 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3047): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3038): Show |
1 | a0001c0001t0004g0261 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3047): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3051): Show |
1 | a0001c0001t0033g0201 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3060): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(2698): Show |
1 | a0001c0001t0003g0215 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(2707): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3046): Show |
1 | a0001c0001t0004g0097 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3055): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3045): Show |
1 | a0001c0001t0004g0293 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3054): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3050): Show |
1 | a0001c0001t0012g0030 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3044): Show |
1 | a0001c0001t0004g0130 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3053): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3045): Show |
1 | a0001c0001t0001g0171 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3054): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3044): Show |
2 | a0001c0001t0003g0267a0001c0001t0004g0283 | 2 | HG01884.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3053): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3043): Show |
1 | a0001c0002t0006g0054 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3052): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3051): Show |
1 | a0001c0001t0016g0052 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3060): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3050): Show |
2 | a0001c0001t0016g0046a0001c0002t0007g0291 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3050): Show |
1 | a0001c0001t0016g0193 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3050): Show |
1 | a0001c0001t0003g0188 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3044): Show |
4 | a0001c0001t0005g0162a0001c0001t0005g0243a0001c0001t0005g0281others(1): Show | 4 | HG00639.hp1 HG02109.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3053): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3051): Show |
1 | a0001c0001t0001g0161 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3060): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3049): Show |
1 | a0001c0001t0012g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3049): Show |
1 | a0001c0001t0003g0246 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3042): Show |
1 | a0001c0002t0002g0285 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3051): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3043): Show |
11 | a0001c0001t0001g0127a0001c0001t0004g0079a0001c0001t0004g0126others(8): Show | 12 | HG00280.hp1 HG00423.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3052): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3044): Show |
1 | a0001c0001t0004g0271 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3053): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3048): Show |
1 | a0001c0001t0003g0328 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3057): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3049): Show |
3 | a0001c0001t0001g0156a0001c0001t0001g0158a0001c0001t0003g0314 | 3 | HG01515.hp1 HG01516.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3050): Show |
5 | a0001c0001t0001g0045a0001c0001t0001g0178a0001c0001t0008g0187others(2): Show | 5 | HG01169.hp1 HG02451.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3051): Show |
1 | a0001c0002t0002g0319 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3060): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3053): Show |
1 | a0001c0001t0003g0299 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3062): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3051): Show |
1 | a0001c0001t0001g0160 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3060): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3048): Show |
1 | a0001c0001t0003g0195 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3057): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3049): Show |
6 | a0001c0001t0003g0004a0001c0001t0003g0192a0001c0001t0003g0210others(3): Show | 7 | HG01993.hp1 HG02055.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3050): Show |
4 | a0001c0001t0001g0061a0001c0001t0003g0216a0001c0001t0003g0290others(1): Show | 4 | HG00408.hp2 HG00597.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3042): Show |
1 | a0001c0001t0005g0049 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3051): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3043): Show |
1 | a0001c0001t0004g0176 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3052): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3049): Show |
1 | a0001c0001t0019g0006 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3047): Show |
1 | a0001c0001t0003g0220 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3056): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3048): Show |
1 | a0001c0001t0003g0211 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3057): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3040): Show |
1 | a0001c0001t0005g0055 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3049): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3041): Show |
1 | a0001c0001t0034g0334 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3050): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3040): Show |
1 | a0001c0001t0004g0177 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3049): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3048): Show |
1 | a0001c0002t0006g0197 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3057): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3043): Show |
1 | a0001c0001t0022g0282 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3052): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3051): Show |
1 | a0001c0001t0020g0212 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3060): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3047): Show |
1 | a0002c0003t0003g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3056): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3048): Show |
1 | a0001c0001t0003g0245 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3057): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3049): Show |
1 | a0001c0001t0004g0203 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3042): Show |
4 | a0001c0001t0003g0266a0001c0001t0004g0292a0001c0001t0004g0342others(1): Show | 4 | HG00735.hp2 HG01071.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3051): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3044): Show |
1 | a0001c0002t0007g0308 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3053): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3049): Show |
1 | a0001c0002t0007g0333 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3050): Show |
1 | a0001c0002t0007g0330 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3042): Show |
1 | a0001c0001t0003g0252 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3051): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3047): Show |
1 | a0001c0001t0003g0300 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3056): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3048): Show |
4 | a0001c0001t0003g0196a0001c0001t0003g0209a0001c0001t0012g0029others(1): Show | 4 | HG01928.hp1 HG01975.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3057): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3049): Show |
1 | a0001c0001t0023g0360 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3041): Show |
3 | a0001c0001t0005g0043a0001c0001t0005g0050a0001c0001t0005g0051 | 3 | HG02559.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3050): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3047): Show |
1 | a0001c0001t0003g0194 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3056): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3063): Show |
1 | a0001c0001t0001g0175 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3072): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3043): Show |
1 | a0001c0002t0007g0332 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3052): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3047): Show |
1 | a0001c0001t0001g0152 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3056): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3049): Show |
2 | a0001c0002t0007g0025a0001c0002t0007g0151 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3042): Show |
1 | a0001c0001t0003g0265 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3051): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3049): Show |
1 | a0001c0001t0001g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3044): Show |
1 | a0001c0001t0004g0296 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3053): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3039): Show |
1 | a0001c0001t0004g0232 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3048): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3049): Show |
2 | a0001c0001t0004g0145a0001c0001t0004g0233 | 2 | HG02280.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3058): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3050): Show |
1 | a0001c0001t0003g0189 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3053): Show |
1 | a0001c0001t0019g0007 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3062): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3046): Show |
1 | a0001c0001t0004g0294 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3055): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3052): Show |
1 | a0001c0001t0001g0157 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3061): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(2698): Show |
1 | a0001c0001t0002g0213 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(2707): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3046): Show |
1 | a0001c0001t0003g0270 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3055): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3052): Show |
1 | a0001c0001t0020g0132 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3061): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3046): Show |
1 | a0001c0001t0004g0273 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3055): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3045): Show |
1 | a0001c0001t0004g0269 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3054): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3044): Show |
2 | a0001c0001t0004g0345a0001c0002t0007g0325 | 2 | HG01069.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3053): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3051): Show |
1 | a0001c0002t0002g0042 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3060): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3050): Show |
1 | a0001c0001t0003g0191 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3051): Show |
2 | a0001c0001t0003g0139a0001c0002t0006g0205 | 2 | NA18964.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.781+5537_781+5538i others(3060): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3043): Show |
1 | a0001c0001t0005g0163 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3052): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3044): Show |
1 | a0001c0001t0004g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3053): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3050): Show |
1 | a0001c0001t0003g0190 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3059): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3042): Show |
1 | a0001c0001t0005g0056 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3051): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3042): Show |
1 | a0001c0002t0002g0262 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3051): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3024): Show |
1 | a0001c0001t0032g0057 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3033): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(2776): Show |
1 | a0001c0002t0006g0241 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(2785): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323179
|
T | TAAAAATA others(3046): Show |
1 | a0001c0002t0002g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.781+5537_781+5538i others(3055): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323179 | ||||||
chr17:76323277
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.781+5440C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323277 | ||||||
chr17:76323296
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(280): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.781+5421A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323296 | ||||||
chr17:76323341
|
C | CA | 11 | a0001c0001t0003g0224a0001c0001t0003g0328a0001c0001t0004g0271others(8): Show | 11 | HG02280.hp1 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.781+5375dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323341 | ||||||
chr17:76323354
|
G | A | 129 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(126): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.781+5363C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323354 | ||||||
chr17:76323387
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.781+5330T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323387 | ||||||
chr17:76323466
|
C | T | 130 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(127): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.781+5251G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323466 | ||||||
chr17:76323529
|
T | C | 2 | a0001c0001t0021g0031a0001c0001t0021g0039 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.781+5188A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323529 | ||||||
chr17:76323549
|
G | A | 2 | a0001c0001t0001g0306a0001c0001t0005g0244 | 2 | HG02145.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.781+5168C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323549 | ||||||
chr17:76323716
|
G | GT | 22 | a0001c0001t0003g0198a0001c0001t0004g0343a0001c0001t0005g0238others(19): Show | 22 | HG02080.hp1 HG02129.hp2 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.781+5000dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323716 | ||||||
chr17:76323847
|
T | C | 2 | a0001c0001t0023g0360a0001c0001t0023g0361 | 2 | HG02055.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.781+4870A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323847 | ||||||
chr17:76323859
|
C | A | 1 | a0001c0001t0001g0321 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.781+4858G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323859 | ||||||
chr17:76323861
|
T | G | 1 | a0001c0001t0001g0306 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.781+4856A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323861 | ||||||
chr17:76323921
|
A | G | 135 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(132): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.781+4796T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76323921 | ||||||
chr17:76324051
|
C | CAGG | 360 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(357): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.781+4665_781+4666i others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324051 | ||||||
chr17:76324140
|
C | CA | 128 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0125others(125): Show | 130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.781+4576dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324140 | ||||||
chr17:76324140
|
C | CAA | 6 | a0001c0001t0003g0190a0001c0001t0004g0126a0001c0001t0004g0294others(3): Show | 6 | HG01952.hp2 HG02896.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.781+4575_781+4576d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324140 | ||||||
chr17:76324217
|
G | A | 1 | a0001c0001t0003g0314 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.781+4500C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324217 | ||||||
chr17:76324235
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.781+4482G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324235 | ||||||
chr17:76324236
|
G | A | 11 | a0001c0001t0001g0173a0001c0001t0001g0258a0001c0002t0002g0024others(8): Show | 11 | HG01070.hp1 HG01071.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.781+4481C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324236 | ||||||
chr17:76324286
|
T | C | 1 | a0001c0001t0003g0314 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.781+4431A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324286 | ||||||
chr17:76324325
|
G | A | 2 | a0001c0002t0002g0110a0001c0002t0018g0111 | 2 | HG02132.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.781+4392C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324325 | ||||||
chr17:76324520
|
A | G | 130 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(127): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.781+4197T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324520 | ||||||
chr17:76324527
|
G | A | 2 | a0001c0001t0005g0236a0001c0001t0005g0237 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.781+4190C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324527 | ||||||
chr17:76324571
|
A | G | 1 | a0001c0001t0031g0276 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.781+4146T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324571 | ||||||
chr17:76324602
|
CAA | C | 130 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(127): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.781+4113_781+4114d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324602 | ||||||
chr17:76324674
|
C | T | 5 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0011others(2): Show | 5 | HG01106.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.781+4043G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324674 | ||||||
chr17:76324741
|
G | A | 3 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305 | 3 | HG02055.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.781+3976C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324741 | ||||||
chr17:76324777
|
G | A | 9 | a0001c0002t0002g0062a0001c0002t0002g0065a0001c0002t0002g0080others(6): Show | 9 | HG00741.hp1 HG01261.hp2 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.781+3940C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324777 | ||||||
chr17:76324905
|
C | CA | 6 | a0001c0001t0001g0071a0001c0001t0001g0112a0001c0001t0001g0113others(3): Show | 6 | HG01928.hp2 HG02886.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.781+3811dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324905 | ||||||
chr17:76324954
|
G | A | 6 | a0001c0001t0001g0152a0001c0002t0007g0025a0001c0002t0007g0151others(3): Show | 6 | HG00738.hp2 HG02451.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.781+3763C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324954 | ||||||
chr17:76324992
|
T | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(283): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.781+3725A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324992 | ||||||
chr17:76324996
|
G | A | 130 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(127): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.781+3721C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76324996 | ||||||
chr17:76325025
|
C | A | 1 | a0001c0002t0002g0015 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.781+3692G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325025 | ||||||
chr17:76325045
|
G | A | 1 | a0001c0002t0015g0053 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.781+3672C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325045 | ||||||
chr17:76325069
|
CA | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(152): Show | 158 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.781+3647delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325069 | ||||||
chr17:76325136
|
A | G | 140 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(137): Show | 142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.781+3581T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325136 | ||||||
chr17:76325263
|
C | G | 360 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(357): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.781+3454G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325263 | ||||||
chr17:76325289
|
G | C | 1 | a0001c0001t0005g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.781+3428C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325289 | ||||||
chr17:76325334
|
G | A | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+3383C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325334 | ||||||
chr17:76325363
|
C | T | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+3354G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325363 | ||||||
chr17:76325392
|
G | A | 9 | a0001c0001t0005g0043a0001c0001t0005g0049a0001c0001t0005g0050others(6): Show | 9 | HG01099.hp1 HG02559.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.781+3325C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325392 | ||||||
chr17:76325411
|
C | CA | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(125): Show | 130 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.781+3305dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325411 | ||||||
chr17:76325411
|
C | CAA | 47 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0001g0064others(44): Show | 48 | HG00099.hp1 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.781+3304_781+3305d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325411 | ||||||
chr17:76325411
|
CA | C | 73 | a0001c0001t0001g0045a0001c0001t0001g0127a0001c0001t0001g0152others(70): Show | 74 | HG00140.hp1 HG00140.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.781+3305delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325411 | ||||||
chr17:76325411
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0047 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.781+3291_781+3305d others(17): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325411 | ||||||
chr17:76325535
|
C | T | 1 | a0001c0001t0005g0320 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.781+3182G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325535 | ||||||
chr17:76325598
|
A | AT | 137 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0064others(134): Show | 139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.781+3118dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325598 | ||||||
chr17:76325598
|
A | ATT | 13 | a0001c0001t0001g0061a0001c0001t0003g0188a0001c0001t0003g0191others(10): Show | 13 | HG00735.hp2 HG01106.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.781+3117_781+3118d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325598 | ||||||
chr17:76325598
|
AT | A | 34 | a0001c0001t0003g0198a0001c0001t0003g0298a0001c0001t0004g0343others(31): Show | 34 | HG01361.hp2 HG01891.hp1 HG02080.hp1 others(31): Show |
intron_variant | MODIFIER | c.781+3118delA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325598 | ||||||
chr17:76325643
|
G | A | 1 | a0001c0001t0003g0298 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.781+3074C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325643 | ||||||
chr17:76325733
|
T | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0164 | 2 | HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.781+2984A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325733 | ||||||
chr17:76325762
|
G | A | 1 | a0001c0002t0006g0241 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.781+2955C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325762 | ||||||
chr17:76325766
|
G | A | 1 | a0001c0001t0005g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.781+2951C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325766 | ||||||
chr17:76325860
|
C | G | 130 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(127): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.781+2857G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325860 | ||||||
chr17:76325914
|
G | C | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(96): Show | 102 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.781+2803C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325914 | ||||||
chr17:76325947
|
G | T | 130 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(127): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.781+2770C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325947 | ||||||
chr17:76325992
|
A | T | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+2725T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76325992 | ||||||
chr17:76326045
|
G | A | 130 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(127): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.781+2672C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326045 | ||||||
chr17:76326152
|
T | C | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+2565A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326152 | ||||||
chr17:76326201
|
A | G | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+2516T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326201 | ||||||
chr17:76326343
|
A | C | 1 | a0001c0001t0001g0258 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.781+2374T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326343 | ||||||
chr17:76326399
|
GA | G | 131 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(128): Show | 133 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.781+2317delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326399 | ||||||
chr17:76326640
|
G | A | 130 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(127): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.781+2077C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326640 | ||||||
chr17:76326644
|
C | T | 359 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(356): Show | 364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.781+2073G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326644 | ||||||
chr17:76326784
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.781+1933A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326784 | ||||||
chr17:76326930
|
G | GA | 9 | a0001c0001t0001g0124a0001c0001t0001g0173a0001c0001t0001g0242others(6): Show | 9 | HG01081.hp1 HG02056.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.781+1786dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326930 | ||||||
chr17:76326942
|
C | A | 17 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0059others(14): Show | 17 | HG00323.hp1 HG01346.hp1 HG02129.hp1 others(14): Show |
intron_variant | MODIFIER | c.781+1775G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76326942 | ||||||
chr17:76327063
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.781+1654A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327063 | ||||||
chr17:76327116
|
G | A | 130 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(127): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.781+1601C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327116 | ||||||
chr17:76327164
|
A | G | 7 | a0001c0001t0003g0298a0001c0001t0005g0032a0001c0001t0005g0034others(4): Show | 7 | HG02818.hp2 HG02965.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.781+1553T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327164 | ||||||
chr17:76327257
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.781+1460T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327257 | ||||||
chr17:76327430
|
G | A | 2 | a0001c0002t0015g0027a0001c0002t0015g0028 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.781+1287C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327430 | ||||||
chr17:76327449
|
T | C | 135 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(132): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.781+1268A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327449 | ||||||
chr17:76327522
|
G | A | 21 | a0001c0001t0003g0198a0001c0001t0004g0343a0001c0001t0005g0238others(18): Show | 21 | HG02080.hp1 HG02129.hp2 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.781+1195C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327522 | ||||||
chr17:76327592
|
G | A | 8 | a0001c0001t0009g0311a0001c0001t0009g0315a0001c0001t0017g0318others(5): Show | 8 | HG01361.hp2 HG01891.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.781+1125C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327592 | ||||||
chr17:76327642
|
A | T | 1 | a0001c0002t0006g0347 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.781+1075T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327642 | ||||||
chr17:76327652
|
AAAAT | A | 4 | a0001c0001t0001g0182a0001c0001t0001g0228a0001c0001t0001g0289others(1): Show | 4 | NA18969.hp1 NA18969.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.781+1061_781+1064d others(6): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327652 | ||||||
chr17:76327769
|
T | TA | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+947dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327769 | ||||||
chr17:76327806
|
G | A | 4 | a0001c0001t0003g0004a0001c0001t0003g0196a0001c0001t0003g0211others(1): Show | 5 | HG01928.hp1 HG01952.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+911C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327806 | ||||||
chr17:76327917
|
T | C | 3 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305 | 3 | HG02055.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.781+800A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76327917 | ||||||
chr17:76328009
|
C | G | 3 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305 | 3 | HG02055.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.781+708G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328009 | ||||||
chr17:76328186
|
C | CA | 12 | a0001c0001t0001g0182a0001c0001t0001g0253a0001c0001t0001g0279others(9): Show | 12 | HG00438.hp1 HG00597.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.781+530dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328186 | ||||||
chr17:76328186
|
CA | C | 112 | a0001c0001t0001g0061a0001c0001t0001g0127a0001c0001t0001g0152others(109): Show | 114 | HG00280.hp1 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.781+530delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328186 | ||||||
chr17:76328211
|
G | A | 1 | a0001c0001t0005g0320 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.781+506C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328211 | ||||||
chr17:76328246
|
A | C | 1 | a0001c0002t0013g0352 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.781+471T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328246 | ||||||
chr17:76328290
|
C | T | 1 | a0001c0001t0003g0188 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.781+427G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328290 | ||||||
chr17:76328295
|
T | C | 3 | a0001c0002t0002g0109a0001c0002t0002g0239a0001c0002t0002g0251 | 3 | HG00597.hp1 HG04228.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.781+422A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328295 | ||||||
chr17:76328635
|
A | C | 3 | a0001c0001t0001g0071a0001c0001t0001g0112a0001c0001t0001g0113 | 3 | HG01928.hp2 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.781+82T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328635 | ||||||
chr17:76328648
|
C | A | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(280): Show | 288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.781+69G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328648 | ||||||
chr17:76328661
|
C | CA | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+55dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328661 | ||||||
chr17:76328670
|
A | C | 5 | a0001c0001t0003g0314a0001c0001t0003g0328a0001c0002t0002g0036others(2): Show | 5 | HG02630.hp2 HG02886.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.781+47T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 7/9 | chr17 | 76328670 | ||||||
chr17:76329074
|
A | AT | 125 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(122): Show | 127 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.636-213dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329074 | ||||||
chr17:76329087
|
T | C | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.636-225A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329087 | ||||||
chr17:76329112
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.636-250G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329112 | ||||||
chr17:76329138
|
T | C | 1 | a0001c0001t0003g0298 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.636-276A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329138 | ||||||
chr17:76329195
|
C | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(140): Show | 146 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.636-333G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329195 | ||||||
chr17:76329495
|
G | A | 1 | a0001c0002t0015g0053 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.635+548C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329495 | ||||||
chr17:76329735
|
C | CA | 13 | a0001c0001t0003g0298a0001c0001t0005g0032a0001c0001t0005g0034others(10): Show | 13 | HG02280.hp1 HG02615.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.635+307dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329735 | ||||||
chr17:76329746
|
C | A | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+297G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329746 | ||||||
chr17:76329787
|
T | C | 130 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(127): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.635+256A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329787 | ||||||
chr17:76329865
|
T | C | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+178A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329865 | ||||||
chr17:76329933
|
AG | A | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.635+109delC | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 6/9 | chr17 | 76329933 | ||||||
chr17:76330185
|
T | C | 4 | a0001c0001t0001g0161a0001c0001t0008g0187a0001c0001t0008g0309others(1): Show | 4 | HG01433.hp1 HG02451.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.580-87A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 5/9 | chr17 | 76330185 | ||||||
chr17:76330352
|
G | A | 1 | a0001c0001t0001g0322 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.579+199C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 5/9 | chr17 | 76330352 | ||||||
chr17:76330395
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.579+156C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 5/9 | chr17 | 76330395 | ||||||
chr17:76330472
|
G | A | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(283): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.579+79C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 5/9 | chr17 | 76330472 | ||||||
chr17:76330475
|
A | T | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(283): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.579+76T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 5/9 | chr17 | 76330475 | ||||||
chr17:76330706
|
C | T | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-40G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76330706 | ||||||
chr17:76330979
|
G | T | 1 | a0001c0001t0005g0320 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.464-313C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76330979 | ||||||
chr17:76330983
|
G | T | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-317C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76330983 | ||||||
chr17:76331040
|
C | T | 2 | a0001c0001t0003g0314a0001c0001t0003g0328 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.464-374G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76331040 | ||||||
chr17:76331197
|
T | C | 9 | a0001c0001t0005g0043a0001c0001t0005g0049a0001c0001t0005g0050others(6): Show | 9 | HG01099.hp1 HG02559.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.464-531A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76331197 | ||||||
chr17:76331241
|
C | T | 4 | a0001c0001t0001g0306a0001c0001t0009g0303a0001c0001t0009g0304others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.464-575G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76331241 | ||||||
chr17:76331361
|
C | T | 38 | a0001c0001t0003g0198a0001c0001t0003g0298a0001c0001t0004g0343others(35): Show | 38 | HG01361.hp2 HG01891.hp1 HG02080.hp1 others(35): Show |
intron_variant | MODIFIER | c.464-695G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76331361 | ||||||
chr17:76331371
|
G | C | 1 | a0001c0002t0026g0317 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.464-705C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76331371 | ||||||
chr17:76331381
|
T | C | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.464-715A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76331381 | ||||||
chr17:76331528
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0009g0303a0001c0001t0009g0304others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.463+735C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76331528 | ||||||
chr17:76331653
|
T | A | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+610A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76331653 | ||||||
chr17:76331854
|
G | A | 2 | a0001c0001t0004g0067a0001c0002t0001g0068 | 2 | HG03490.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.463+409C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76331854 | ||||||
chr17:76332088
|
C | A | 2 | a0001c0001t0021g0031a0001c0001t0021g0039 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.463+175G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76332088 | ||||||
chr17:76332102
|
A | T | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.463+161T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76332102 | ||||||
chr17:76332137
|
C | T | 3 | a0001c0001t0012g0029a0001c0001t0012g0030a0001c0001t0012g0235 | 3 | HG02486.hp2 HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.463+126G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76332137 | ||||||
chr17:76332251
|
G | A | 1 | a0001c0001t0003g0298 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.463+12C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 4/9 | chr17 | 76332251 | ||||||
chr17:76332495
|
C | G | 133 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(130): Show | 135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.291-60G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332495 | ||||||
chr17:76332550
|
C | G | 1 | a0001c0002t0006g0054 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.291-115G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332550 | ||||||
chr17:76332605
|
T | C | 135 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(132): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.291-170A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332605 | ||||||
chr17:76332606
|
T | G | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-171A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332606 | ||||||
chr17:76332623
|
T | C | 135 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(132): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.291-188A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332623 | ||||||
chr17:76332704
|
G | C | 1 | a0001c0001t0005g0320 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.291-269C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332704 | ||||||
chr17:76332892
|
A | AT | 8 | a0001c0001t0001g0026a0001c0001t0001g0071a0001c0001t0001g0112others(5): Show | 8 | HG01928.hp2 HG02145.hp2 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.291-458dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332892 | ||||||
chr17:76332892
|
AT | A | 6 | a0001c0001t0001g0125a0001c0001t0001g0306a0001c0001t0003g0298others(3): Show | 6 | HG01975.hp1 HG02145.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.291-458delA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332892 | ||||||
chr17:76332916
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0095 | 2 | NA18939.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.291-481C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332916 | ||||||
chr17:76332924
|
G | A | 38 | a0001c0001t0001g0061a0001c0001t0002g0213a0001c0001t0003g0004others(35): Show | 39 | HG00408.hp2 HG00597.hp2 HG01928.hp1 others(36): Show |
intron_variant | MODIFIER | c.291-489C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76332924 | ||||||
chr17:76333113
|
C | G | 135 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(132): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.291-678G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333113 | ||||||
chr17:76333265
|
C | T | 36 | a0001c0001t0003g0198a0001c0001t0003g0298a0001c0001t0004g0343others(33): Show | 36 | HG01361.hp2 HG01891.hp1 HG02080.hp1 others(33): Show |
intron_variant | MODIFIER | c.291-830G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333265 | ||||||
chr17:76333402
|
A | G | 135 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(132): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.291-967T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333402 | ||||||
chr17:76333581
|
G | A | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-1146C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333581 | ||||||
chr17:76333594
|
G | A | 1 | a0001c0001t0003g0190 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.291-1159C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333594 | ||||||
chr17:76333630
|
G | C | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-1195C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333630 | ||||||
chr17:76333670
|
C | CA | 130 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(127): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.291-1236dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333670 | ||||||
chr17:76333670
|
CA | C | 6 | a0001c0001t0005g0320a0001c0001t0014g0008a0001c0001t0014g0009others(3): Show | 6 | HG01106.hp1 HG02622.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.291-1236delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333670 | ||||||
chr17:76333850
|
G | GCATT | 105 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(102): Show | 108 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.291-1419_291-1416d others(6): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333850 | ||||||
chr17:76333876
|
T | A | 135 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(132): Show | 137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.291-1441A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333876 | ||||||
chr17:76333900
|
A | G | 1 | a0001c0002t0002g0287 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.291-1465T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333900 | ||||||
chr17:76333974
|
G | A | 134 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(131): Show | 136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.291-1539C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76333974 | ||||||
chr17:76334122
|
C | T | 1 | a0001c0001t0004g0302 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.291-1687G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334122 | ||||||
chr17:76334177
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.291-1742C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334177 | ||||||
chr17:76334368
|
T | C | 2 | a0001c0001t0017g0318a0001c0002t0006g0313 | 2 | HG01361.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.291-1933A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334368 | ||||||
chr17:76334431
|
G | A | 8 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0096others(5): Show | 8 | HG02129.hp1 HG02165.hp1 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.291-1996C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334431 | ||||||
chr17:76334533
|
A | G | 2 | a0001c0001t0021g0031a0001c0001t0021g0039 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.291-2098T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334533 | ||||||
chr17:76334542
|
C | T | 2 | a0001c0001t0003g0314a0001c0001t0003g0328 | 2 | HG02630.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.291-2107G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334542 | ||||||
chr17:76334557
|
T | C | 284 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(281): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.291-2122A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334557 | ||||||
chr17:76334582
|
T | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(285): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.291-2147A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334582 | ||||||
chr17:76334583
|
G | A | 127 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(124): Show | 129 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.291-2148C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334583 | ||||||
chr17:76334623
|
T | C | 12 | a0001c0001t0001g0173a0001c0001t0001g0258a0001c0002t0002g0024others(9): Show | 12 | HG01070.hp1 HG01071.hp2 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.291-2188A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334623 | ||||||
chr17:76334627
|
AAAAAAC | A | 130 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0127others(127): Show | 132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.291-2198_291-2193d others(8): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334627 | ||||||
chr17:76334641
|
A | G | 1 | a0001c0002t0002g0231 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.291-2206T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334641 | ||||||
chr17:76334649
|
A | T | 1 | a0001c0002t0015g0053 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.291-2214T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334649 | ||||||
chr17:76334761
|
C | A | 2 | a0001c0001t0003g0245a0001c0001t0003g0246 | 2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.291-2326G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334761 | ||||||
chr17:76334811
|
A | G | 1 | a0001c0001t0024g0012 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.291-2376T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76334811 | ||||||
chr17:76335147
|
C | T | 5 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0011others(2): Show | 5 | HG01106.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-2712G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335147 | ||||||
chr17:76335158
|
T | C | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-2723A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335158 | ||||||
chr17:76335167
|
T | C | 2 | a0001c0002t0015g0027a0001c0002t0015g0028 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.291-2732A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335167 | ||||||
chr17:76335212
|
G | C | 5 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0011others(2): Show | 5 | HG01106.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-2777C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335212 | ||||||
chr17:76335234
|
C | T | 8 | a0001c0001t0009g0311a0001c0001t0009g0315a0001c0001t0017g0318others(5): Show | 8 | HG01361.hp2 HG01891.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.291-2799G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335234 | ||||||
chr17:76335419
|
G | A | 1 | a0001c0001t0003g0298 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.291-2984C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335419 | ||||||
chr17:76335591
|
G | A | 1 | a0001c0001t0010g0038 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.291-3156C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335591 | ||||||
chr17:76335599
|
A | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(283): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.291-3164T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335599 | ||||||
chr17:76335720
|
T | C | 52 | a0001c0001t0001g0061a0001c0001t0002g0213a0001c0001t0003g0004others(49): Show | 53 | HG00408.hp2 HG00597.hp2 HG01891.hp2 others(50): Show |
intron_variant | MODIFIER | c.291-3285A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335720 | ||||||
chr17:76335887
|
G | C | 1 | a0001c0002t0006g0241 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.291-3452C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335887 | ||||||
chr17:76335897
|
G | A | 14 | a0001c0001t0001g0045a0001c0001t0001g0156a0001c0001t0001g0157others(11): Show | 14 | HG01169.hp1 HG01433.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.291-3462C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335897 | ||||||
chr17:76335967
|
G | T | 1 | a0001c0001t0004g0177 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.291-3532C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76335967 | ||||||
chr17:76336254
|
A | G | 1 | a0001c0001t0005g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.291-3819T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336254 | ||||||
chr17:76336255
|
T | C | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.291-3820A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336255 | ||||||
chr17:76336411
|
T | C | 360 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(357): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.291-3976A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336411 | ||||||
chr17:76336425
|
G | A | 1 | a0001c0001t0025g0010 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.291-3990C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336425 | ||||||
chr17:76336432
|
T | C | 360 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(357): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.291-3997A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336432 | ||||||
chr17:76336437
|
C | CA | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(185): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.291-4003dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336437 | ||||||
chr17:76336503
|
CA | C | 28 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0073others(25): Show | 30 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.291-4069delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336503 | ||||||
chr17:76336521
|
C | T | 1 | a0001c0002t0002g0015 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.291-4086G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336521 | ||||||
chr17:76336660
|
A | G | 1 | a0001c0001t0003g0298 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.291-4225T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336660 | ||||||
chr17:76336732
|
C | CA | 7 | a0001c0001t0010g0038a0001c0001t0010g0040a0001c0001t0010g0041others(4): Show | 7 | HG02615.hp2 HG02886.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-4298dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336732 | ||||||
chr17:76336732
|
CA | C | 24 | a0001c0001t0001g0242a0001c0001t0001g0274a0001c0001t0003g0199others(21): Show | 24 | HG00140.hp2 HG00735.hp2 HG01106.hp1 others(21): Show |
intron_variant | MODIFIER | c.291-4298delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336732 | ||||||
chr17:76336732
|
CAA | C | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(205): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.291-4299_291-4298d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336732 | ||||||
chr17:76336732
|
CAAA | C | 9 | a0001c0001t0001g0019a0001c0001t0001g0076a0001c0001t0001g0161others(6): Show | 9 | HG01169.hp2 HG02145.hp1 HG03834.hp2 others(6): Show |
intron_variant | MODIFIER | c.291-4300_291-4298d others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336732 | ||||||
chr17:76336732
|
CAAAAAAA | C | 40 | a0001c0001t0001g0061a0001c0001t0002g0213a0001c0001t0003g0004others(37): Show | 41 | HG00408.hp2 HG00597.hp2 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.291-4304_291-4298d others(9): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336732 | ||||||
chr17:76336732
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0002t0002g0147 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.291-4307_291-4298d others(12): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336732 | ||||||
chr17:76336772
|
G | A | 3 | a0001c0001t0021g0031a0001c0001t0021g0039a0001c0002t0015g0053 | 3 | HG03209.hp2 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.291-4337C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336772 | ||||||
chr17:76336822
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.291-4387G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336822 | ||||||
chr17:76336960
|
C | T | 5 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0011others(2): Show | 5 | HG01106.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.291-4525G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76336960 | ||||||
chr17:76337045
|
T | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(232): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.291-4610A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337045 | ||||||
chr17:76337054
|
A | T | 2 | a0001c0001t0003g0290a0001c0001t0003g0299 | 2 | HG03704.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.291-4619T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337054 | ||||||
chr17:76337080
|
T | C | 1 | a0001c0001t0003g0196 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.291-4645A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337080 | ||||||
chr17:76337216
|
A | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(283): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.291-4781T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337216 | ||||||
chr17:76337423
|
A | AAACAACA others(2): Show |
3 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331 | 3 | HG02615.hp2 HG02886.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.291-4997_291-4989d others(11): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337423 | ||||||
chr17:76337448
|
A | AAAC | 233 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(230): Show | 237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.291-5016_291-5014d others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337448 | ||||||
chr17:76337448
|
A | AACAAAC | 7 | a0001c0001t0003g0298a0001c0001t0005g0032a0001c0001t0005g0034others(4): Show | 7 | HG02818.hp2 HG02965.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.291-5014_291-5013i others(8): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337448 | ||||||
chr17:76337507
|
C | T | 1 | a0001c0001t0005g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.291-5072G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337507 | ||||||
chr17:76337652
|
C | T | 1 | a0001c0001t0004g0343 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.291-5217G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337652 | ||||||
chr17:76337653
|
G | A | 2 | a0001c0001t0004g0294a0001c0001t0005g0244 | 2 | HG03225.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.291-5218C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337653 | ||||||
chr17:76337658
|
T | C | 1 | a0001c0002t0002g0239 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.291-5223A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337658 | ||||||
chr17:76337749
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0009g0303a0001c0001t0009g0304others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-5314C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337749 | ||||||
chr17:76337809
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0009g0303a0001c0001t0009g0304others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.291-5374C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337809 | ||||||
chr17:76337853
|
C | A | 228 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(225): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.291-5418G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76337853 | ||||||
chr17:76338018
|
TC | T | 40 | a0001c0001t0003g0198a0001c0001t0003g0298a0001c0001t0004g0145others(37): Show | 40 | HG00140.hp1 HG01361.hp2 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.291-5584delG | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76338018 | ||||||
chr17:76338035
|
C | T | 2 | a0001c0002t0015g0027a0001c0002t0015g0028 | 2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.291-5600G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76338035 | ||||||
chr17:76338091
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.291-5656C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76338091 | ||||||
chr17:76338926
|
G | A | 1 | a0001c0001t0004g0343 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.290+5745C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76338926 | ||||||
chr17:76338947
|
C | T | 5 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0331others(2): Show | 5 | HG02280.hp1 HG02615.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.290+5724G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76338947 | ||||||
chr17:76338988
|
A | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(242): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.290+5683T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76338988 | ||||||
chr17:76339066
|
G | A | 1 | a0001c0001t0029g0081 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.290+5605C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76339066 | ||||||
chr17:76339153
|
TCAGCACT others(1479): Show |
T | 5 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0011others(2): Show | 5 | HG01106.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+4032_290+5517d others(2): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76339153 | ||||||
chr17:76339191
|
G | A | 4 | a0001c0001t0001g0306a0001c0001t0009g0303a0001c0001t0009g0304others(1): Show | 4 | HG02055.hp2 HG02145.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+5480C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76339191 | ||||||
chr17:76339353
|
C | T | 1 | a0001c0001t0010g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.290+5318G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76339353 | ||||||
chr17:76339606
|
G | A | 1 | a0001c0001t0022g0282 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.290+5065C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76339606 | ||||||
chr17:76339907
|
A | G | 1 | a0001c0001t0017g0323 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.290+4764T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76339907 | ||||||
chr17:76339948
|
A | G | 5 | a0001c0001t0001g0306a0001c0001t0009g0303a0001c0001t0009g0304others(2): Show | 5 | HG02055.hp2 HG02145.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.290+4723T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76339948 | ||||||
chr17:76340051
|
C | T | 1 | a0001c0002t0002g0319 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.290+4620G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340051 | ||||||
chr17:76340094
|
C | T | 3 | a0001c0001t0001g0306a0001c0002t0006g0241a0001c0002t0015g0053 | 3 | HG02145.hp1 HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.290+4577G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340094 | ||||||
chr17:76340142
|
T | C | 2 | a0001c0001t0001g0044a0001c0001t0001g0137 | 2 | HG00639.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.290+4529A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340142 | ||||||
chr17:76340145
|
C | CA | 119 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0064others(116): Show | 120 | HG00140.hp1 HG00408.hp2 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.290+4525dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340145 | ||||||
chr17:76340312
|
T | C | 1 | a0001c0001t0001g0173 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.290+4359A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340312 | ||||||
chr17:76340333
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.290+4338C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340333 | ||||||
chr17:76340371
|
T | C | 1 | a0001c0001t0001g0064 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.290+4300A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340371 | ||||||
chr17:76340391
|
T | A | 45 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0131others(42): Show | 46 | HG00673.hp2 HG00738.hp2 HG01109.hp1 others(43): Show |
intron_variant | MODIFIER | c.290+4280A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340391 | ||||||
chr17:76340400
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0005g0032 | 2 | HG01884.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.290+4271G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340400 | ||||||
chr17:76340419
|
T | C | 11 | a0001c0001t0003g0314a0001c0001t0005g0034a0001c0001t0005g0056others(8): Show | 11 | HG00738.hp2 HG01069.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.290+4252A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340419 | ||||||
chr17:76340464
|
T | C | 107 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0014others(104): Show | 109 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.290+4207A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340464 | ||||||
chr17:76340470
|
G | C | 2 | a0001c0001t0005g0035a0001c0001t0012g0030 | 2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.290+4201C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340470 | ||||||
chr17:76340499
|
GT | G | 54 | a0001c0001t0001g0074a0001c0001t0001g0112a0001c0001t0001g0113others(51): Show | 55 | HG00140.hp2 HG00639.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.290+4171delA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340499 | ||||||
chr17:76340576
|
T | G | 1 | a0001c0001t0004g0143 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.290+4095A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340576 | ||||||
chr17:76340585
|
G | A | 1 | a0001c0001t0003g0267 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.290+4086C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340585 | ||||||
chr17:76340627
|
G | A | 2 | a0001c0001t0021g0031a0001c0001t0021g0039 | 2 | NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.290+4044C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340627 | ||||||
chr17:76340651
|
G | A | 6 | a0001c0001t0001g0306a0001c0001t0014g0008a0001c0001t0014g0009others(3): Show | 6 | HG01106.hp1 HG02145.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.290+4020C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340651 | ||||||
chr17:76340720
|
G | A | 2 | a0001c0001t0004g0283a0001c0001t0004g0284 | 2 | HG01433.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.290+3951C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340720 | ||||||
chr17:76340746
|
C | T | 1 | a0001c0001t0005g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.290+3925G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340746 | ||||||
chr17:76340747
|
G | A | 2 | a0001c0001t0010g0040a0001c0001t0010g0041 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.290+3924C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340747 | ||||||
chr17:76340749
|
G | C | 2 | a0001c0001t0010g0040a0001c0001t0010g0041 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.290+3922C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340749 | ||||||
chr17:76340804
|
T | C | 105 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0075others(102): Show | 106 | HG00408.hp2 HG00597.hp2 HG00639.hp1 others(103): Show |
intron_variant | MODIFIER | c.290+3867A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340804 | ||||||
chr17:76340838
|
T | G | 1 | a0001c0001t0003g0188 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.290+3833A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340838 | ||||||
chr17:76340842
|
C | G | 47 | a0001c0001t0003g0314a0001c0001t0003g0328a0001c0001t0004g0343others(44): Show | 47 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.290+3829G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340842 | ||||||
chr17:76340896
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.290+3775G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340896 | ||||||
chr17:76340919
|
G | A | 1 | a0001c0002t0007g0291 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.290+3752C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340919 | ||||||
chr17:76340928
|
G | C | 4 | a0001c0001t0001g0048a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 4 | HG00323.hp2 HG03710.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+3743C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340928 | ||||||
chr17:76340972
|
T | C | 5 | a0001c0001t0005g0032a0001c0001t0005g0034a0001c0001t0005g0035others(2): Show | 5 | HG02818.hp2 HG03453.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+3699A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340972 | ||||||
chr17:76340991
|
C | CT | 39 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0003g0328others(36): Show | 39 | HG00099.hp1 HG00738.hp2 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.290+3679dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76340991 | ||||||
chr17:76341203
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.290+3468G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341203 | ||||||
chr17:76341234
|
G | GT | 8 | a0001c0001t0001g0173a0001c0001t0003g0189a0001c0001t0003g0190others(5): Show | 8 | HG02055.hp1 HG02056.hp2 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.290+3436dupA | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341234 | ||||||
chr17:76341234
|
GTT | G | 14 | a0001c0001t0001g0306a0001c0001t0005g0320a0001c0001t0009g0303others(11): Show | 14 | HG01106.hp1 HG01361.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.290+3435_290+3436d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341234 | ||||||
chr17:76341234
|
GTTT | G | 77 | a0001c0001t0001g0001a0001c0001t0001g0154a0001c0001t0001g0181others(74): Show | 78 | HG00099.hp1 HG00280.hp2 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.290+3434_290+3436d others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341234 | ||||||
chr17:76341234
|
GTTTT | G | 144 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0026others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.290+3433_290+3436d others(6): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341234 | ||||||
chr17:76341237
|
T | G | 6 | a0001c0001t0005g0320a0001c0001t0017g0318a0001c0001t0019g0007others(3): Show | 6 | HG01361.hp2 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.290+3434A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341237 | ||||||
chr17:76341238
|
T | G | 51 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0003g0314others(48): Show | 51 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.290+3433A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341238 | ||||||
chr17:76341240
|
T | G | 1 | a0001c0002t0006g0197 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.290+3431A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341240 | ||||||
chr17:76341241
|
T | G | 1 | a0001c0002t0006g0241 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.290+3430A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341241 | ||||||
chr17:76341244
|
T | G | 3 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0021g0039 | 3 | HG02886.hp2 HG02896.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.290+3427A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341244 | ||||||
chr17:76341245
|
T | G | 2 | a0001c0002t0002g0141a0001c0002t0002g0142 | 2 | NA18944.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.290+3426A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341245 | ||||||
chr17:76341246
|
T | G | 4 | a0001c0001t0004g0342a0001c0001t0004g0344a0001c0001t0004g0345others(1): Show | 4 | HG00735.hp2 HG01106.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+3425A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341246 | ||||||
chr17:76341247
|
T | G | 1 | a0001c0001t0004g0143 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.290+3424A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341247 | ||||||
chr17:76341281
|
A | C | 2 | a0001c0001t0004g0203a0001c0002t0002g0207 | 2 | HG00597.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.290+3390T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341281 | ||||||
chr17:76341313
|
C | G | 1 | a0001c0001t0001g0153 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.290+3358G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341313 | ||||||
chr17:76341323
|
G | A | 1 | a0001c0002t0002g0144 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.290+3348C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341323 | ||||||
chr17:76341394
|
C | T | 1 | a0001c0002t0002g0247 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.290+3277G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341394 | ||||||
chr17:76341535
|
C | T | 10 | a0001c0001t0005g0043a0001c0001t0005g0049a0001c0001t0005g0050others(7): Show | 10 | HG01099.hp1 HG01891.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.290+3136G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341535 | ||||||
chr17:76341553
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.290+3118A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341553 | ||||||
chr17:76341668
|
C | T | 10 | a0001c0001t0005g0043a0001c0001t0005g0049a0001c0001t0005g0050others(7): Show | 10 | HG01099.hp1 HG01891.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.290+3003G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341668 | ||||||
chr17:76341669
|
G | A | 4 | a0001c0001t0012g0029a0001c0001t0012g0030a0001c0002t0015g0027others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+3002C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341669 | ||||||
chr17:76341706
|
G | A | 10 | a0001c0001t0005g0043a0001c0001t0005g0049a0001c0001t0005g0050others(7): Show | 10 | HG01099.hp1 HG01891.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.290+2965C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341706 | ||||||
chr17:76341711
|
A | G | 9 | a0001c0001t0001g0306a0001c0001t0009g0303a0001c0001t0009g0304others(6): Show | 9 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.290+2960T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341711 | ||||||
chr17:76341722
|
G | A | 5 | a0001c0001t0005g0032a0001c0001t0005g0034a0001c0001t0005g0035others(2): Show | 5 | HG02818.hp2 HG03453.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+2949C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341722 | ||||||
chr17:76341796
|
G | A | 3 | a0001c0001t0004g0067a0001c0001t0004g0145a0001c0002t0001g0068 | 3 | HG03490.hp2 HG03669.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.290+2875C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341796 | ||||||
chr17:76341892
|
T | C | 2 | a0001c0001t0004g0232a0001c0001t0004g0233 | 2 | HG00140.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.290+2779A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341892 | ||||||
chr17:76341896
|
G | A | 2 | a0001c0001t0004g0203a0001c0002t0002g0207 | 2 | HG00597.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.290+2775C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341896 | ||||||
chr17:76341896
|
G | C | 2 | a0001c0001t0005g0236a0001c0001t0005g0237 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.290+2775C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76341896 | ||||||
chr17:76342024
|
T | C | 141 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0306others(138): Show | 142 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.290+2647A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76342024 | ||||||
chr17:76342148
|
A | C | 4 | a0001c0001t0012g0029a0001c0001t0012g0030a0001c0002t0015g0027others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+2523T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76342148 | ||||||
chr17:76342169
|
C | T | 2 | a0001c0002t0002g0221a0001c0002t0002g0222 | 2 | HG02148.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.290+2502G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76342169 | ||||||
chr17:76342314
|
G | A | 1 | a0001c0001t0003g0198 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.290+2357C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76342314 | ||||||
chr17:76342390
|
C | T | 141 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0306others(138): Show | 142 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.290+2281G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76342390 | ||||||
chr17:76342795
|
C | T | 49 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0002g0213others(46): Show | 50 | HG00408.hp2 HG00597.hp2 HG01433.hp1 others(47): Show |
intron_variant | MODIFIER | c.290+1876G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76342795 | ||||||
chr17:76342927
|
A | G | 38 | a0001c0001t0003g0328a0001c0001t0004g0342a0001c0001t0004g0343others(35): Show | 38 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.290+1744T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76342927 | ||||||
chr17:76343100
|
G | A | 49 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0002g0213others(46): Show | 50 | HG00408.hp2 HG00597.hp2 HG01433.hp1 others(47): Show |
intron_variant | MODIFIER | c.290+1571C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76343100 | ||||||
chr17:76343244
|
C | T | 3 | a0001c0001t0016g0046a0001c0001t0016g0193a0001c0002t0007g0025 | 3 | HG02922.hp1 HG02976.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.290+1427G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76343244 | ||||||
chr17:76343343
|
C | G | 1 | a0001c0001t0012g0235 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.290+1328G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76343343 | ||||||
chr17:76343645
|
G | C | 5 | a0001c0001t0001g0026a0001c0001t0001g0172a0001c0001t0001g0240others(2): Show | 5 | HG02129.hp2 HG02165.hp1 NA18956.hp1 others(2): Show |
intron_variant | MODIFIER | c.290+1026C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76343645 | ||||||
chr17:76343663
|
T | C | 4 | a0001c0001t0012g0029a0001c0001t0012g0030a0001c0002t0015g0027others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+1008A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76343663 | ||||||
chr17:76344219
|
C | T | 3 | a0001c0001t0003g0266a0001c0001t0003g0267a0001c0002t0007g0291 | 3 | HG01884.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.290+452G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76344219 | ||||||
chr17:76344230
|
C | T | 2 | a0001c0001t0004g0342a0001c0001t0034g0334 | 2 | HG00735.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.290+441G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76344230 | ||||||
chr17:76344507
|
C | T | 2 | a0001c0002t0002g0036a0001c0002t0002g0042 | 2 | HG03195.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.290+164G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76344507 | ||||||
chr17:76344517
|
G | A | 1 | a0001c0001t0025g0010 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.290+154C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76344517 | ||||||
chr17:76344537
|
T | C | 1 | a0001c0001t0024g0012 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.290+134A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76344537 | ||||||
chr17:76344649
|
ATAAAG | A | 4 | a0001c0001t0012g0029a0001c0001t0012g0030a0001c0002t0015g0027others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.290+17_290+21delCT others(3): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 3/9 | chr17 | 76344649 | ||||||
chr17:76344863
|
G | A | 1 | a0001c0002t0013g0355 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.224-126C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76344863 | ||||||
chr17:76344973
|
C | T | 1 | a0001c0002t0002g0080 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.224-236G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76344973 | ||||||
chr17:76345025
|
G | C | 3 | a0001c0001t0035g0316a0001c0002t0007g0308a0001c0002t0026g0317 | 3 | HG02895.hp1 HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.224-288C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345025 | ||||||
chr17:76345033
|
A | T | 1 | a0001c0001t0004g0079 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.224-296T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345033 | ||||||
chr17:76345095
|
C | T | 7 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0040others(4): Show | 7 | HG02886.hp2 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.224-358G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345095 | ||||||
chr17:76345107
|
T | C | 141 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0306others(138): Show | 142 | HG00099.hp1 HG00408.hp2 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.224-370A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345107 | ||||||
chr17:76345127
|
C | T | 8 | a0001c0001t0003g0265a0001c0001t0003g0290a0001c0001t0004g0261others(5): Show | 8 | HG00280.hp1 HG03491.hp2 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.224-390G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345127 | ||||||
chr17:76345130
|
G | A | 1 | a0001c0001t0005g0162 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.224-393C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345130 | ||||||
chr17:76345151
|
C | T | 5 | a0001c0001t0005g0032a0001c0001t0005g0034a0001c0001t0005g0035others(2): Show | 5 | HG02818.hp2 HG03453.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-414G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345151 | ||||||
chr17:76345237
|
T | TAA | 14 | a0001c0001t0001g0306a0001c0001t0009g0303a0001c0001t0009g0304others(11): Show | 14 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.224-502_224-501dup others(2): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345237 | ||||||
chr17:76345237
|
T | TAAAAA | 11 | a0001c0001t0001g0059a0001c0001t0001g0072a0001c0001t0001g0075others(8): Show | 11 | HG00099.hp2 HG00323.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.224-505_224-501dup others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345237 | ||||||
chr17:76345237
|
T | TAAAAAA | 197 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(194): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.224-506_224-501dup others(6): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345237 | ||||||
chr17:76345237
|
T | TAAAAAAA | 11 | a0001c0001t0001g0060a0001c0001t0001g0064a0001c0001t0001g0178others(8): Show | 11 | HG00609.hp1 HG01074.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.224-507_224-501dup others(7): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345237 | ||||||
chr17:76345237
|
T | TAAAAAAA others(13): Show |
3 | a0001c0001t0010g0040a0001c0002t0002g0036a0001c0002t0002g0042 | 3 | HG03195.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.224-501_224-500ins others(20): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345237 | ||||||
chr17:76345237
|
T | TAAAAAAA others(14): Show |
1 | a0001c0001t0010g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.224-501_224-500ins others(21): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345237 | ||||||
chr17:76345237
|
TA | T | 58 | a0001c0001t0003g0314a0001c0001t0003g0328a0001c0001t0004g0342others(55): Show | 58 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(55): Show |
intron_variant | MODIFIER | c.224-501delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345237 | ||||||
chr17:76345237
|
TAA | T | 55 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0002g0213others(52): Show | 56 | HG00408.hp2 HG00597.hp2 HG01433.hp1 others(53): Show |
intron_variant | MODIFIER | c.224-502_224-501del others(2): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345237 | ||||||
chr17:76345336
|
G | A | 3 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305 | 3 | HG02055.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.224-599C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345336 | ||||||
chr17:76345544
|
G | A | 5 | a0001c0001t0005g0032a0001c0001t0005g0034a0001c0001t0005g0035others(2): Show | 5 | HG02818.hp2 HG03453.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-807C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345544 | ||||||
chr17:76345555
|
G | T | 5 | a0001c0001t0005g0032a0001c0001t0005g0034a0001c0001t0005g0035others(2): Show | 5 | HG02818.hp2 HG03453.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-818C>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345555 | ||||||
chr17:76345607
|
G | C | 2 | a0001c0002t0002g0231a0001c0002t0002g0301 | 2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.224-870C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345607 | ||||||
chr17:76345609
|
G | GA | 77 | a0001c0001t0001g0075a0001c0001t0001g0149a0001c0001t0001g0150others(74): Show | 77 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.224-873dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345609 | ||||||
chr17:76345609
|
GA | G | 56 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0002g0213others(53): Show | 57 | HG00408.hp2 HG00597.hp2 HG01433.hp1 others(54): Show |
intron_variant | MODIFIER | c.224-873delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345609 | ||||||
chr17:76345789
|
C | CA | 4 | a0001c0001t0012g0029a0001c0001t0012g0030a0001c0002t0015g0027others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.224-1053dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345789 | ||||||
chr17:76345818
|
C | T | 8 | a0001c0001t0005g0043a0001c0001t0005g0049a0001c0001t0005g0050others(5): Show | 8 | HG01891.hp2 HG02559.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.224-1081G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345818 | ||||||
chr17:76345910
|
T | C | 1 | a0001c0002t0011g0346 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.224-1173A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345910 | ||||||
chr17:76345930
|
A | C | 1 | a0001c0001t0001g0076 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.224-1193T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345930 | ||||||
chr17:76345932
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.224-1195G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345932 | ||||||
chr17:76345981
|
AG | A | 5 | a0001c0001t0005g0032a0001c0001t0005g0034a0001c0001t0005g0035others(2): Show | 5 | HG02818.hp2 HG03453.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.224-1245delC | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345981 | ||||||
chr17:76345985
|
G | C | 6 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0011others(3): Show | 6 | HG01106.hp1 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.224-1248C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76345985 | ||||||
chr17:76346019
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.224-1282G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346019 | ||||||
chr17:76346104
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.224-1367G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346104 | ||||||
chr17:76346238
|
T | A | 1 | a0002c0003t0003g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.224-1501A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346238 | ||||||
chr17:76346271
|
T | C | 9 | a0001c0001t0001g0306a0001c0001t0009g0303a0001c0001t0009g0304others(6): Show | 9 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.224-1534A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346271 | ||||||
chr17:76346295
|
G | A | 2 | a0001c0001t0005g0055a0001c0001t0005g0056 | 2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.224-1558C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346295 | ||||||
chr17:76346336
|
C | T | 2 | a0001c0002t0002g0231a0001c0002t0002g0301 | 2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.224-1599G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346336 | ||||||
chr17:76346445
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.224-1708A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346445 | ||||||
chr17:76346558
|
T | C | 1 | a0001c0001t0003g0298 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.224-1821A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346558 | ||||||
chr17:76346640
|
T | G | 1 | a0001c0001t0004g0286 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.223+1889A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346640 | ||||||
chr17:76346645
|
A | G | 4 | a0001c0002t0007g0324a0001c0002t0007g0325a0001c0002t0007g0326others(1): Show | 4 | HG01069.hp1 HG01071.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+1884T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346645 | ||||||
chr17:76346757
|
C | T | 4 | a0001c0001t0012g0029a0001c0001t0012g0030a0001c0002t0015g0027others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+1772G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346757 | ||||||
chr17:76346807
|
A | G | 1 | a0001c0001t0003g0204 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.223+1722T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346807 | ||||||
chr17:76346850
|
T | C | 217 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0045others(214): Show | 221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.223+1679A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346850 | ||||||
chr17:76346871
|
G | A | 5 | a0001c0001t0005g0032a0001c0001t0005g0034a0001c0001t0005g0035others(2): Show | 5 | HG02818.hp2 HG03453.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.223+1658C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346871 | ||||||
chr17:76346874
|
C | T | 7 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0040others(4): Show | 7 | HG02886.hp2 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.223+1655G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76346874 | ||||||
chr17:76347017
|
C | A | 4 | a0001c0001t0012g0029a0001c0001t0012g0030a0001c0002t0015g0027others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+1512G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347017 | ||||||
chr17:76347064
|
C | A | 2 | a0001c0001t0003g0220a0001c0001t0003g0300 | 2 | NA18959.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.223+1465G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347064 | ||||||
chr17:76347109
|
G | A | 1 | a0001c0002t0006g0348 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.223+1420C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347109 | ||||||
chr17:76347317
|
G | A | 1 | a0001c0001t0003g0299 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.223+1212C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347317 | ||||||
chr17:76347428
|
A | G | 2 | a0001c0001t0005g0236a0001c0001t0005g0237 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.223+1101T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347428 | ||||||
chr17:76347484
|
C | CA | 56 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0060others(53): Show | 56 | HG00140.hp1 HG00140.hp2 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.223+1044dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | ||||||
chr17:76347484
|
C | CAA | 19 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0229others(16): Show | 19 | HG00735.hp2 HG01106.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.223+1043_223+1044d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | ||||||
chr17:76347484
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0003g0189 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.223+1035_223+1044d others(12): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | ||||||
chr17:76347484
|
C | CAAAAAAA others(4): Show |
7 | a0001c0001t0003g0190a0001c0001t0003g0191a0001c0001t0003g0192others(4): Show | 7 | HG02132.hp2 HG02922.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.223+1034_223+1044d others(13): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | ||||||
chr17:76347484
|
C | CAAAAAAA others(5): Show |
12 | a0001c0001t0001g0061a0001c0001t0003g0004a0001c0001t0003g0194others(9): Show | 13 | HG01975.hp2 HG01993.hp1 HG02273.hp2 others(10): Show |
intron_variant | MODIFIER | c.223+1033_223+1044d others(14): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | ||||||
chr17:76347484
|
C | CAAAAAAA others(6): Show |
7 | a0001c0001t0001g0047a0001c0001t0003g0199a0001c0001t0003g0220others(4): Show | 7 | HG01928.hp1 HG02135.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.223+1032_223+1044d others(15): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | ||||||
chr17:76347484
|
C | CAAAAAAA others(7): Show |
6 | a0001c0001t0003g0204a0001c0001t0004g0206a0001c0001t0023g0361others(3): Show | 6 | HG00597.hp2 HG02055.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.223+1031_223+1044d others(16): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | ||||||
chr17:76347484
|
C | CAAAAAAA others(8): Show |
1 | a0001c0002t0002g0208 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.223+1030_223+1044d others(17): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | ||||||
chr17:76347484
|
C | CAAAAAAA others(9): Show |
1 | a0001c0001t0003g0223 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.223+1029_223+1044d others(18): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | ||||||
chr17:76347484
|
C | CAAAAAAA others(10): Show |
4 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0211others(1): Show | 4 | HG01952.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.223+1028_223+1044d others(19): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | ||||||
chr17:76347484
|
C | CAAAAAAA others(11): Show |
3 | a0001c0001t0002g0213a0001c0001t0003g0214a0001c0001t0020g0212 | 3 | NA18957.hp2 NA18979.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.223+1027_223+1044d others(20): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | ||||||
chr17:76347484
|
C | CAAAAAAA others(12): Show |
2 | a0001c0001t0003g0215a0001c0001t0003g0216 | 2 | HG00408.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.223+1026_223+1044d others(21): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | ||||||
chr17:76347484
|
CA | C | 16 | a0001c0001t0001g0059a0001c0001t0001g0072a0001c0001t0001g0073others(13): Show | 16 | HG00099.hp2 HG00323.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.223+1044delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | ||||||
chr17:76347484
|
CAA | C | 32 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0003g0314others(29): Show | 32 | HG00099.hp1 HG01069.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.223+1043_223+1044d others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347484 | ||||||
chr17:76347529
|
A | T | 1 | a0001c0001t0017g0323 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.223+1000T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347529 | ||||||
chr17:76347532
|
G | C | 5 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0005g0320others(2): Show | 5 | HG00099.hp1 HG01074.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.223+997C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347532 | ||||||
chr17:76347606
|
C | T | 3 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305 | 3 | HG02055.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.223+923G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347606 | ||||||
chr17:76347660
|
A | C | 1 | a0001c0002t0006g0241 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.223+869T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347660 | ||||||
chr17:76347668
|
A | G | 1 | a0002c0003t0003g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.223+861T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347668 | ||||||
chr17:76347670
|
G | A | 1 | a0002c0003t0003g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.223+859C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347670 | ||||||
chr17:76347759
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.223+770C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347759 | ||||||
chr17:76347872
|
C | T | 4 | a0001c0001t0012g0029a0001c0001t0012g0030a0001c0002t0015g0027others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.223+657G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76347872 | ||||||
chr17:76348043
|
C | T | 62 | a0001c0001t0001g0306a0001c0001t0001g0321a0001c0001t0001g0322others(59): Show | 62 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.223+486G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348043 | ||||||
chr17:76348160
|
A | AAAAT | 40 | a0001c0001t0001g0071a0001c0001t0003g0328a0001c0001t0004g0342others(37): Show | 40 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.223+365_223+368dup others(4): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348160 | ||||||
chr17:76348160
|
A | AAAATAAA others(1): Show |
21 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0003g0314others(18): Show | 21 | HG00099.hp1 HG01074.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.223+361_223+368dup others(8): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348160 | ||||||
chr17:76348160
|
A | AAAATAAA others(5): Show |
8 | a0001c0001t0001g0306a0001c0001t0008g0309a0001c0001t0009g0303others(5): Show | 8 | HG02055.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.223+357_223+368dup others(12): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348160 | ||||||
chr17:76348160
|
A | AAAATAAA others(9): Show |
2 | a0001c0001t0024g0012a0001c0002t0002g0319 | 2 | HG03471.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.223+353_223+368dup others(16): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348160 | ||||||
chr17:76348160
|
A | AAAATAAA others(13): Show |
2 | a0001c0001t0014g0008a0001c0001t0014g0009 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.223+349_223+368dup others(20): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348160 | ||||||
chr17:76348160
|
AAAATAAA others(5): Show |
A | 2 | a0001c0001t0003g0245a0001c0001t0003g0246 | 2 | HG02965.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.223+357_223+368del others(12): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348160 | ||||||
chr17:76348172
|
T | A | 1 | a0002c0003t0003g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.223+357A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348172 | ||||||
chr17:76348203
|
G | C | 6 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0183others(3): Show | 6 | HG00323.hp1 HG01346.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+326C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348203 | ||||||
chr17:76348310
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.223+219A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348310 | ||||||
chr17:76348310
|
TAAAAATA others(98): Show |
T | 1 | a0001c0001t0001g0044 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.223+114_223+218del | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348310 | ||||||
chr17:76348316
|
T | C | 38 | a0001c0001t0003g0328a0001c0001t0004g0342a0001c0001t0004g0343others(35): Show | 38 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.223+213A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348316 | ||||||
chr17:76348330
|
G | A | 1 | a0001c0001t0024g0012 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.223+199C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348330 | ||||||
chr17:76348346
|
G | A | 53 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0002g0213others(50): Show | 54 | HG00408.hp2 HG00597.hp2 HG01433.hp1 others(51): Show |
intron_variant | MODIFIER | c.223+183C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348346 | ||||||
chr17:76348497
|
A | C | 6 | a0001c0001t0037g0351a0001c0002t0013g0352a0001c0002t0013g0353others(3): Show | 6 | HG02080.hp1 NA18939.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.223+32T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348497 | ||||||
chr17:76348502
|
T | A | 1 | a0001c0001t0001g0217 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.223+27A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 2/9 | chr17 | 76348502 | ||||||
chr17:76348587
|
G | A | 2 | a0001c0001t0001g0218a0001c0001t0001g0219 | 2 | HG01109.hp1 HG01934.hp2 |
splice_region_variant&intron_variant | LOW | c.171-6C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76348587 | ||||||
chr17:76348686
|
C | T | 7 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0040others(4): Show | 7 | HG02886.hp2 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.171-105G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76348686 | ||||||
chr17:76348689
|
T | A | 1 | a0002c0003t0003g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.171-108A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76348689 | ||||||
chr17:76348878
|
C | T | 4 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0005g0243others(1): Show | 4 | HG02965.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.171-297G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76348878 | ||||||
chr17:76348910
|
T | A | 1 | a0002c0003t0003g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.171-329A>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76348910 | ||||||
chr17:76348936
|
G | A | 1 | a0001c0002t0002g0024 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.171-355C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76348936 | ||||||
chr17:76349061
|
A | G | 1 | a0001c0001t0012g0070 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.171-480T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349061 | ||||||
chr17:76349100
|
C | G | 1 | a0001c0001t0005g0320 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.171-519G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349100 | ||||||
chr17:76349178
|
C | A | 1 | a0001c0002t0006g0347 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.171-597G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349178 | ||||||
chr17:76349274
|
C | T | 1 | a0001c0002t0002g0301 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.171-693G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349274 | ||||||
chr17:76349406
|
C | T | 1 | a0001c0002t0002g0319 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.171-825G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349406 | ||||||
chr17:76349536
|
G | A | 3 | a0001c0001t0009g0303a0001c0001t0009g0304a0001c0001t0009g0305 | 3 | HG02055.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.171-955C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349536 | ||||||
chr17:76349558
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.171-977G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349558 | ||||||
chr17:76349561
|
G | C | 2 | a0001c0001t0003g0220a0001c0001t0003g0300 | 2 | NA18959.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.171-980C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349561 | ||||||
chr17:76349629
|
C | T | 10 | a0001c0001t0005g0043a0001c0001t0005g0049a0001c0001t0005g0050others(7): Show | 10 | HG01099.hp1 HG01891.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.171-1048G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349629 | ||||||
chr17:76349633
|
C | T | 1 | a0001c0001t0024g0012 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.171-1052G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349633 | ||||||
chr17:76349702
|
C | T | 2 | a0001c0001t0004g0067a0001c0002t0001g0068 | 2 | HG03490.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.171-1121G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349702 | ||||||
chr17:76349703
|
G | A | 4 | a0001c0001t0003g0223a0001c0001t0003g0224a0001c0002t0002g0221others(1): Show | 4 | HG02148.hp1 HG03239.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.171-1122C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349703 | ||||||
chr17:76349992
|
C | A | 9 | a0001c0001t0001g0306a0001c0001t0009g0303a0001c0001t0009g0304others(6): Show | 9 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.171-1411G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76349992 | ||||||
chr17:76350074
|
C | CA | 6 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228others(3): Show | 6 | HG02027.hp2 HG02145.hp1 NA18946.hp1 others(3): Show |
intron_variant | MODIFIER | c.171-1494dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350074 | ||||||
chr17:76350165
|
C | T | 1 | a0001c0001t0004g0066 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.171-1584G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350165 | ||||||
chr17:76350194
|
C | T | 2 | a0001c0002t0002g0062a0001c0002t0002g0065 | 2 | HG00741.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.171-1613G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350194 | ||||||
chr17:76350205
|
C | T | 1 | a0001c0001t0021g0031 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.171-1624G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350205 | ||||||
chr17:76350210
|
CG | C | 53 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0003g0314others(50): Show | 53 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.171-1630delC | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350210 | ||||||
chr17:76350232
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0230 | 2 | HG00323.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.171-1651C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350232 | ||||||
chr17:76350332
|
G | A | 4 | a0001c0001t0012g0029a0001c0001t0012g0030a0001c0002t0015g0027others(1): Show | 4 | HG02809.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.171-1751C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350332 | ||||||
chr17:76350355
|
C | T | 5 | a0001c0001t0005g0032a0001c0001t0005g0034a0001c0001t0005g0035others(2): Show | 5 | HG02818.hp2 HG03453.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.171-1774G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350355 | ||||||
chr17:76350356
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.171-1775C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350356 | ||||||
chr17:76350396
|
G | A | 1 | a0001c0002t0002g0301 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.171-1815C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350396 | ||||||
chr17:76350438
|
C | CA | 7 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0004g0232others(4): Show | 7 | HG00140.hp1 HG01243.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.171-1858dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350438 | ||||||
chr17:76350501
|
T | G | 1 | a0001c0001t0004g0302 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.171-1920A>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350501 | ||||||
chr17:76350656
|
A | G | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG03710.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.171-2075T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350656 | ||||||
chr17:76350846
|
A | C | 1 | a0001c0002t0002g0062 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.171-2265T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76350846 | ||||||
chr17:76351027
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.171-2446G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76351027 | ||||||
chr17:76351386
|
G | A | 1 | a0001c0002t0002g0234 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.170+2148C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76351386 | ||||||
chr17:76351494
|
G | A | 1 | a0001c0001t0012g0235 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.170+2040C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76351494 | ||||||
chr17:76351507
|
C | T | 3 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0242 | 3 | HG00323.hp1 HG02486.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.170+2027G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76351507 | ||||||
chr17:76351822
|
C | T | 1 | a0001c0002t0006g0241 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.170+1712G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76351822 | ||||||
chr17:76352046
|
C | A | 9 | a0001c0001t0001g0306a0001c0001t0009g0303a0001c0001t0009g0304others(6): Show | 9 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.170+1488G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352046 | ||||||
chr17:76352217
|
GAAAATGG others(12): Show |
G | 9 | a0001c0001t0001g0306a0001c0001t0009g0303a0001c0001t0009g0304others(6): Show | 9 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.170+1298_170+1316d others(21): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352217 | ||||||
chr17:76352367
|
C | G | 1 | a0001c0002t0002g0058 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.170+1167G>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352367 | ||||||
chr17:76352374
|
G | C | 1 | a0001c0002t0002g0021 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.170+1160C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352374 | ||||||
chr17:76352391
|
A | G | 10 | a0001c0001t0005g0043a0001c0001t0005g0049a0001c0001t0005g0050others(7): Show | 10 | HG01099.hp1 HG01891.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.170+1143T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352391 | ||||||
chr17:76352495
|
A | T | 1 | a0001c0001t0001g0240 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.170+1039T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352495 | ||||||
chr17:76352505
|
T | C | 2 | a0001c0001t0005g0236a0001c0001t0005g0237 | 2 | HG02965.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.170+1029A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352505 | ||||||
chr17:76352509
|
G | C | 1 | a0001c0001t0005g0238 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.170+1025C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352509 | ||||||
chr17:76352577
|
G | A | 1 | a0001c0002t0002g0239 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.170+957C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352577 | ||||||
chr17:76352644
|
C | CA | 71 | a0001c0001t0001g0005a0001c0001t0001g0240a0001c0001t0001g0242others(68): Show | 72 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.170+889dupT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352644 | ||||||
chr17:76352644
|
C | CG | 6 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0040others(3): Show | 6 | HG02886.hp2 HG02896.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.170+889_170+890ins others(1): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352644 | ||||||
chr17:76352644
|
CA | C | 11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0047others(8): Show | 11 | HG00323.hp2 HG00639.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.170+889delT | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352644 | ||||||
chr17:76352644
|
CAAA | C | 9 | a0001c0001t0001g0306a0001c0001t0009g0303a0001c0001t0009g0304others(6): Show | 9 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.170+887_170+889del others(3): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352644 | ||||||
chr17:76352644
|
CAAAAA | C | 34 | a0001c0001t0003g0328a0001c0001t0004g0342a0001c0001t0004g0343others(31): Show | 34 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.170+885_170+889del others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352644 | ||||||
chr17:76352663
|
A | G | 7 | a0001c0001t0010g0037a0001c0001t0010g0038a0001c0001t0010g0040others(4): Show | 7 | HG02886.hp2 HG02896.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.170+871T>C | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352663 | ||||||
chr17:76352680
|
AAAAAG | A | 5 | a0001c0001t0005g0032a0001c0001t0005g0034a0001c0001t0005g0035others(2): Show | 5 | HG02818.hp2 HG03453.hp1 NA19240.hp1 others(2): Show |
intron_variant | MODIFIER | c.170+849_170+853del others(5): Show |
PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352680 | ||||||
chr17:76352735
|
T | C | 5 | a0001c0001t0014g0008a0001c0001t0014g0009a0001c0001t0014g0011others(2): Show | 5 | HG01106.hp1 HG02622.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.170+799A>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352735 | ||||||
chr17:76352886
|
G | A | 9 | a0001c0001t0001g0306a0001c0001t0009g0303a0001c0001t0009g0304others(6): Show | 9 | HG01106.hp1 HG02055.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.170+648C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76352886 | ||||||
chr17:76353085
|
G | C | 1 | a0002c0003t0003g0307 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.170+449C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76353085 | ||||||
chr17:76353089
|
C | T | 9 | a0001c0001t0005g0032a0001c0001t0005g0034a0001c0001t0005g0035others(6): Show | 9 | HG02809.hp1 HG02818.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.170+445G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76353089 | ||||||
chr17:76353116
|
G | C | 1 | a0001c0001t0024g0012 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.170+418C>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76353116 | ||||||
chr17:76353301
|
A | C | 1 | a0001c0001t0001g0026 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.170+233T>G | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76353301 | ||||||
chr17:76353434
|
G | A | 53 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0003g0314others(50): Show | 53 | HG00099.hp1 HG00735.hp2 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.170+100C>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76353434 | ||||||
chr17:76353438
|
A | T | 1 | a0001c0002t0007g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.170+96T>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76353438 | ||||||
chr17:76353505
|
C | A | 36 | a0001c0001t0003g0328a0001c0001t0004g0342a0001c0001t0004g0343others(33): Show | 36 | HG00735.hp2 HG00738.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.170+29G>T | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76353505 | ||||||
chr17:76353526
|
C | T | 12 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0002t0002g0013others(9): Show | 12 | NA18941.hp1 NA18944.hp1 NA18945.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.170+8G>A | PRPSAP1 | ENSG00000161542.17 | transcript | ENST00000446526.8 | protein_coding | 1/9 | chr17 | 76353526 |