geneid | 9791 |
---|---|
ensemblid | ENSG00000156471.13 |
hgncid | 9587 |
symbol | PTDSS1 |
name | phosphatidylserine synthase 1 |
refseq_nuc | NM_014754.3 |
refseq_prot | NP_055569.1 |
ensembl_nuc | ENST00000517309.6 |
ensembl_prot | ENSP00000430548.1 |
mane_status | MANE Select |
chr | chr8 |
start | 96261902 |
end | 96336995 |
strand | + |
ver | v1.2 |
region | chr8:96261902-96336995 |
region5000 | chr8:96256902-96341995 |
regionname0 | PTDSS1_chr8_96261902_96336995 |
regionname5000 | PTDSS1_chr8_96256902_96341995 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 473 | 254 | 83 | 56 | 72 | 12 | 29 | 58 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0002 | 0/0 | 473 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0003 | 0/0 | 473 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1422 | 246 | 75 | 56 | 72 | 12 | 29 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
c0002 | 0/0 | 1422 | 7 | 7 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
c0003 | 0/0 | 1422 | 5 | 5 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
c0004 | 0/0 | 1422 | 2 | 2 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
c0005 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
c0006 | 0/0 | 1422 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3569 | 73 | 3 | 21 | 33 | 4 | 12 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0002 | 0/1 | 3569 | 47 | 23 | 14 | 0 | 2 | 7 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0003 | 1/0 | 3569 | 35 | 1 | 3 | 24 | 2 | 4 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0004 | 0/0 | 3569 | 15 | 14 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0005 | 0/0 | 3569 | 15 | 2 | 2 | 4 | 2 | 5 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0006 | 0/0 | 3569 | 9 | 2 | 1 | 5 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0007 | 0/0 | 3569 | 7 | 6 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0008 | 0/0 | 3569 | 7 | 7 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0009 | 0/0 | 3569 | 5 | 4 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0010 | 0/0 | 3569 | 4 | 3 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0011 | 0/0 | 3569 | 4 | 4 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0012 | 0/0 | 2592 | 4 | 3 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0013 | 0/0 | 3569 | 4 | 1 | 1 | 0 | 2 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0014 | 0/0 | 3569 | 4 | 1 | 1 | 2 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0015 | 0/0 | 3569 | 2 | 0 | 2 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0016 | 0/0 | 3569 | 2 | 2 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0017 | 0/0 | 3569 | 2 | 1 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0018 | 0/0 | 3569 | 2 | 2 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0019 | 0/0 | 3569 | 2 | 0 | 0 | 2 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0020 | 0/0 | 3569 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0021 | 0/0 | 3569 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0022 | 0/0 | 3569 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0023 | 0/0 | 3569 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0024 | 0/0 | 3569 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0025 | 0/0 | 3569 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0026 | 0/0 | 3569 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0027 | 0/0 | 3569 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0028 | 0/0 | 3569 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0029 | 0/0 | 3569 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0030 | 0/0 | 3569 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0031 | 0/0 | 3569 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0032 | 0/0 | 3569 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0033 | 0/0 | 3569 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0034 | 0/0 | 3569 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0035 | 0/0 | 3569 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0036 | 0/0 | 3569 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0037 | 0/0 | 3569 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
t0038 | 0/0 | 3569 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0179 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0213 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1422 | 246 | 75 | 56 | 72 | 12 | 29 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0003 | 0/0 | 1422 | 5 | 5 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0004 | 0/0 | 1422 | 2 | 2 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0005 | 0/0 | 1422 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0002c0002 | 0/0 | 1422 | 7 | 7 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0003c0006 | 0/0 | 1422 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4990 | 73 | 3 | 21 | 33 | 4 | 12 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0002 | 0/1 | 4990 | 43 | 19 | 14 | 0 | 2 | 7 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0003 | 1/0 | 4990 | 35 | 1 | 3 | 24 | 2 | 4 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0004 | 0/0 | 4990 | 12 | 11 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0005 | 0/0 | 4990 | 15 | 2 | 2 | 4 | 2 | 5 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0006 | 0/0 | 4990 | 9 | 2 | 1 | 5 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0007 | 0/0 | 4990 | 7 | 6 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0009 | 0/0 | 4990 | 5 | 4 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0010 | 0/0 | 4990 | 4 | 3 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0011 | 0/0 | 4990 | 4 | 4 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0012 | 0/0 | 4013 | 4 | 3 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0013 | 0/0 | 4990 | 4 | 1 | 1 | 0 | 2 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0014 | 0/0 | 4990 | 4 | 1 | 1 | 2 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0015 | 0/0 | 4990 | 2 | 0 | 2 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0016 | 0/0 | 4990 | 2 | 2 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0017 | 0/0 | 4990 | 2 | 1 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0018 | 0/0 | 4990 | 2 | 2 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0019 | 0/0 | 4990 | 2 | 0 | 0 | 2 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0020 | 0/0 | 4990 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0021 | 0/0 | 4990 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0023 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0024 | 0/0 | 4990 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0025 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0026 | 0/0 | 4990 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0027 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0028 | 0/0 | 4990 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0029 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0030 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0031 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0032 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0033 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0034 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0035 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0036 | 0/0 | 4990 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0001t0038 | 0/0 | 4990 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0003t0002 | 0/0 | 4990 | 3 | 3 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0003t0004 | 0/0 | 4990 | 2 | 2 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0004t0004 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0004t0022 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0001c0005t0002 | 0/0 | 4990 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0002c0002t0008 | 0/0 | 4990 | 7 | 7 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
a0003c0006t0037 | 0/0 | 4990 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | copy fasta | chr8 | 96256902 | 96341995 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0213 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0179 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0004g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0005g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0005g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0005g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0005g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0006g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0006g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0006g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0006g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0007g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0007g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0009g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0009g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0009g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0009g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0009g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0010g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0010g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0010g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0010g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0011g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0011g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0011g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0011g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0012g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0012g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0012g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0012g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0013g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0013g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0013g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0013g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0014g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0014g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0014g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0014g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0015g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0015g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0016g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0016g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0017g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0017g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0018g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0018g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0019g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0019g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0020g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0021g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0023g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0024g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0025g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0026g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0027g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0028g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0029g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0030g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0031g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0032g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0033g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0034g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0035g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0036g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0001t0038g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0003t0002g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0003t0004g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0004t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0004t0022g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0001c0005t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0002c0002t0008g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0002c0002t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0002c0002t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0002c0002t0008g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0002c0002t0008g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0002c0002t0008g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0002c0002t0008g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
a0003c0006t0037g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | GBR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0248 | EUR | GBR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG00280 | hp1 | a0001 | c0001 | t0013 | g0088 | EUR | FIN | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0196 | EUR | FIN | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | CHS | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | CHS | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG00609 | hp2 | a0001 | c0001 | t0006 | g0176 | EAS | CHS | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | CHS | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG00733 | hp1 | a0001 | c0001 | t0005 | g0107 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG00741 | hp2 | a0001 | c0001 | t0013 | g0251 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01069 | hp1 | a0001 | c0001 | t0028 | g0184 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01070 | hp1 | a0001 | c0001 | t0012 | g0063 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0246 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0250 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0238 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01081 | hp1 | a0001 | c0001 | t0010 | g0127 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01109 | hp1 | a0001 | c0001 | t0004 | g0144 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01167 | hp1 | a0001 | c0001 | t0024 | g0156 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0049 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01168 | hp1 | a0001 | c0001 | t0020 | g0203 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01168 | hp2 | a0001 | c0001 | t0015 | g0100 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0048 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01169 | hp2 | a0001 | c0001 | t0015 | g0070 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01243 | hp1 | a0001 | c0001 | t0017 | g0111 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01255 | hp2 | a0001 | c0001 | t0005 | g0222 | AMR | CLM | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01257 | hp2 | a0001 | c0001 | t0009 | g0091 | AMR | CLM | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01261 | hp1 | a0001 | c0001 | t0007 | g0007 | AMR | CLM | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | CLM | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | CLM | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0149 | AMR | CLM | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01516 | hp1 | a0001 | c0001 | t0013 | g0247 | EUR | IBS | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | IBS | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0050 | EUR | IBS | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | IBS | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01884 | hp1 | a0001 | c0001 | t0018 | g0112 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0121 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0015 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01928 | hp1 | a0001 | c0001 | t0026 | g0228 | AMR | PEL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01934 | hp2 | a0001 | c0001 | t0038 | g0165 | AMR | PEL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01975 | hp1 | a0001 | c0001 | t0014 | g0209 | AMR | PEL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0227 | AMR | PEL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02004 | hp1 | a0001 | c0001 | t0006 | g0054 | AMR | PEL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | KHV | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02055 | hp1 | a0001 | c0001 | t0030 | g0233 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | KHV | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02145 | hp2 | a0001 | c0001 | t0010 | g0036 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02155 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | CDX | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02155 | hp2 | a0001 | c0001 | t0014 | g0229 | EAS | CDX | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02257 | hp2 | a0001 | c0001 | t0011 | g0211 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02258 | hp2 | a0001 | c0001 | t0016 | g0013 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02280 | hp2 | a0001 | c0001 | t0011 | g0208 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02451 | hp2 | a0001 | c0001 | t0010 | g0059 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0119 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02572 | hp2 | a0001 | c0004 | t0004 | g0148 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0122 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02615 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02630 | hp1 | a0001 | c0001 | t0005 | g0101 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0158 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0207 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02698 | hp2 | a0001 | c0001 | t0006 | g0115 | SAS | PJL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02717 | hp1 | a0002 | c0002 | t0008 | g0052 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02717 | hp2 | a0001 | c0001 | t0011 | g0035 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02723 | hp1 | a0001 | c0001 | t0006 | g0133 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0139 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02809 | hp2 | a0001 | c0001 | t0027 | g0151 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02818 | hp1 | a0001 | c0001 | t0009 | g0120 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02818 | hp2 | a0002 | c0002 | t0008 | g0157 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02886 | hp1 | a0001 | c0001 | t0012 | g0146 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02886 | hp2 | a0001 | c0001 | t0011 | g0031 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02895 | hp1 | a0001 | c0003 | t0002 | g0001 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02895 | hp2 | a0002 | c0002 | t0008 | g0135 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02896 | hp1 | a0001 | c0001 | t0016 | g0012 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02896 | hp2 | a0002 | c0002 | t0008 | g0136 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02897 | hp1 | a0001 | c0003 | t0002 | g0001 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02897 | hp2 | a0002 | c0002 | t0008 | g0131 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02922 | hp1 | a0001 | c0003 | t0004 | g0002 | AFR | ESN | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | ESN | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0152 | AFR | ESN | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | ESN | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02970 | hp1 | a0001 | c0004 | t0022 | g0154 | AFR | ESN | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | ESN | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | ESN | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02976 | hp2 | a0001 | c0001 | t0025 | g0085 | AFR | ESN | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0132 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03041 | hp2 | a0002 | c0002 | t0008 | g0159 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0090 | AFR | ESN | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03130 | hp2 | a0001 | c0001 | t0012 | g0062 | AFR | ESN | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03139 | hp1 | a0001 | c0001 | t0012 | g0051 | AFR | ESN | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03139 | hp2 | a0001 | c0003 | t0004 | g0002 | AFR | ESN | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03195 | hp1 | a0001 | c0001 | t0032 | g0130 | AFR | ESN | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0014 | AFR | ESN | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03209 | hp1 | a0001 | c0001 | t0033 | g0147 | AFR | MSL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03209 | hp2 | a0001 | c0005 | t0002 | g0011 | AFR | MSL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | MSL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | MSL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03453 | hp1 | a0001 | c0001 | t0023 | g0150 | AFR | MSL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03453 | hp2 | a0001 | c0001 | t0010 | g0037 | AFR | MSL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0072 | SAS | PJL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03491 | hp2 | a0001 | c0001 | t0005 | g0039 | SAS | PJL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03540 | hp1 | a0001 | c0001 | t0034 | g0129 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03540 | hp2 | a0001 | c0001 | t0017 | g0145 | AFR | GWD | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03579 | hp1 | a0001 | c0001 | t0009 | g0123 | AFR | MSL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | MSL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0045 | SAS | PJL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0092 | SAS | STU | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0019 | SAS | STU | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03710 | hp2 | a0001 | c0001 | t0005 | g0106 | SAS | PJL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03831 | hp1 | a0003 | c0006 | t0037 | g0044 | SAS | BEB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0171 | SAS | BEB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03927 | hp1 | a0001 | c0001 | t0005 | g0109 | SAS | BEB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | BEB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | STU | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG04115 | hp2 | a0001 | c0001 | t0005 | g0040 | SAS | STU | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0230 | SAS | STU | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | STU | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18522 | hp1 | a0001 | c0001 | t0013 | g0142 | AFR | YRI | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18522 | hp2 | a0001 | c0003 | t0002 | g0001 | AFR | YRI | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | CHB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | CHB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | YRI | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18906 | hp2 | a0001 | c0001 | t0031 | g0128 | AFR | YRI | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18943 | hp1 | a0001 | c0001 | t0006 | g0117 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18949 | hp1 | a0001 | c0001 | t0019 | g0253 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18952 | hp2 | a0001 | c0001 | t0021 | g0201 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18960 | hp1 | a0001 | c0001 | t0005 | g0071 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18964 | hp1 | a0001 | c0001 | t0006 | g0243 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18966 | hp1 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18969 | hp1 | a0001 | c0001 | t0006 | g0167 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18971 | hp2 | a0001 | c0001 | t0019 | g0255 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18979 | hp1 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19005 | hp1 | a0001 | c0001 | t0036 | g0027 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | LWK | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19030 | hp2 | a0002 | c0002 | t0008 | g0241 | AFR | LWK | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19043 | hp1 | a0001 | c0001 | t0029 | g0016 | AFR | LWK | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19043 | hp2 | a0001 | c0001 | t0035 | g0041 | AFR | LWK | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19056 | hp1 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19056 | hp2 | a0001 | c0001 | t0014 | g0169 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | YRI | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0153 | AFR | YRI | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0202 | EUR | TSI | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA20752 | hp2 | a0001 | c0001 | t0005 | g0163 | EUR | TSI | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | TSI | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA20805 | hp2 | a0001 | c0001 | t0005 | g0116 | EUR | TSI | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02486 | hp1 | a0001 | c0001 | t0007 | g0033 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0258 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG02559 | hp2 | a0001 | c0001 | t0004 | g0140 | AFR | ACB | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | MSL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG06807 | hp1 | a0001 | c0001 | t0005 | g0244 | AFR | USA | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | USA | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18955 | hp1 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA20300 | hp1 | a0001 | c0001 | t0018 | g0024 | AFR | USA | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA20300 | hp2 | a0001 | c0001 | t0014 | g0166 | AFR | USA | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA21309 | hp1 | a0001 | c0001 | t0006 | g0032 | AFR | LWK | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | LWK | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0213 | REF | REF | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0179 | REF | REF | PTDSS1_chr8_96256902_96341995 | PTDSS1 | chr8 | 96256902 | 96341995 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:96331051
|
C | A | 1 | a0002 | 7 | HG02717.hp1 HG02818.hp2 HG02895.hp2 others(4): Show |
missense_variant | MODERATE | c.1268C>A | p.Thr423Asn | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/13 | 1407/4990 | 1268/1422 | 423/473 | chr8 | 96331051 | ||
chr8:96333492
|
A | C | 1 | a0003 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.1348A>C | p.Asn450His | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 1487/4990 | 1348/1422 | 450/473 | chr8 | 96333492 | ||
chr8:96336018
|
TTTTCCCT others(3536): Show |
T | 1 | a0001 | 4 | HG01070.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
splice_region_variant | LOW | c.*2453_*5995del | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | chr8 | 96336018 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:96273389
|
T | C | 1 | a0001c0004 | 2 | HG02572.hp2 HG02970.hp1 |
splice_region_variant&synonymous_variant | LOW | c.270T>C | p.Asn90Asn | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/13 | 409/4990 | 270/1422 | 90/473 | chr8 | 96273389 | ||
chr8:96304113
|
C | A | 1 | a0001c0005 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.826C>A | p.Arg276Arg | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/13 | 965/4990 | 826/1422 | 276/473 | chr8 | 96304113 | ||
chr8:96320309
|
C | G | 1 | a0001c0003 | 5 | HG02895.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
synonymous_variant | LOW | c.1137C>G | p.Thr379Thr | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/13 | 1276/4990 | 1137/1422 | 379/473 | chr8 | 96320309 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:96333651
|
C | T | 2 | a0001c0001t0014a0001c0001t0038 | 5 | HG01934.hp2 HG01975.hp1 HG02155.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*85C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 85 | chr8 | 96333651 | |||||
chr8:96333691
|
G | A | 1 | a0001c0001t0020 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*125G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 125 | chr8 | 96333691 | |||||
chr8:96333733
|
T | C | 1 | a0001c0001t0015 | 2 | HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*167T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 167 | chr8 | 96333733 | |||||
chr8:96333770
|
G | C | 1 | a0001c0001t0021 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*204G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 204 | chr8 | 96333770 | |||||
chr8:96333863
|
A | G | 1 | a0003c0006t0037 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*297A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 297 | chr8 | 96333863 | |||||
chr8:96333869
|
C | G | 1 | a0001c0001t0036 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*303C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 303 | chr8 | 96333869 | |||||
chr8:96333915
|
C | T | 3 | a0001c0001t0034a0001c0001t0035a0002c0002t0008 | 9 | HG02717.hp1 HG02818.hp2 HG02895.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*349C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 349 | chr8 | 96333915 | |||||
chr8:96334117
|
G | T | 1 | a0001c0001t0033 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*551G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 551 | chr8 | 96334117 | |||||
chr8:96334156
|
G | A | 3 | a0001c0001t0010a0001c0001t0016a0001c0004t0022 | 7 | HG01081.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*590G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 590 | chr8 | 96334156 | |||||
chr8:96334212
|
C | T | 1 | a0001c0001t0032 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*646C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 646 | chr8 | 96334212 | |||||
chr8:96334363
|
A | T | 3 | a0001c0001t0010a0001c0001t0016a0001c0004t0022 | 7 | HG01081.hp1 HG02145.hp2 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*797A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 797 | chr8 | 96334363 | |||||
chr8:96334413
|
T | C | 1 | a0001c0001t0023 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*847T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 847 | chr8 | 96334413 | |||||
chr8:96334500
|
C | G | 2 | a0001c0001t0010a0001c0001t0016 | 6 | HG01081.hp1 HG02145.hp2 HG02258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*934C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 934 | chr8 | 96334500 | |||||
chr8:96334762
|
T | A | 5 | a0001c0001t0001a0001c0001t0011a0001c0001t0017others(2): Show | 81 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*1196T>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 1196 | chr8 | 96334762 | |||||
chr8:96334909
|
G | A | 1 | a0001c0001t0024 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1343G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 1343 | chr8 | 96334909 | |||||
chr8:96334913
|
T | C | 34 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(31): Show | 216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*1347T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 1347 | chr8 | 96334913 | |||||
chr8:96335090
|
C | T | 2 | a0001c0001t0005a0001c0001t0013 | 19 | HG00280.hp1 HG00733.hp1 HG00741.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1524C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 1524 | chr8 | 96335090 | |||||
chr8:96335288
|
G | T | 1 | a0001c0001t0031 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1722G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 1722 | chr8 | 96335288 | |||||
chr8:96335397
|
G | A | 7 | a0001c0001t0001a0001c0001t0019a0001c0001t0020others(4): Show | 80 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1831G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 1831 | chr8 | 96335397 | |||||
chr8:96335409
|
C | T | 7 | a0001c0001t0001a0001c0001t0009a0001c0001t0017others(4): Show | 84 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1843C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 1843 | chr8 | 96335409 | |||||
chr8:96335462
|
T | C | 1 | a0001c0001t0027 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1896T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 1896 | chr8 | 96335462 | |||||
chr8:96335490
|
A | T | 1 | a0001c0004t0022 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1924A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 1924 | chr8 | 96335490 | |||||
chr8:96335540
|
C | T | 1 | a0001c0001t0030 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1974C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 1974 | chr8 | 96335540 | |||||
chr8:96336330
|
G | A | 1 | a0001c0001t0027 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2764G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 2764 | chr8 | 96336330 | |||||
chr8:96336361
|
T | C | 8 | a0001c0001t0004a0001c0001t0016a0001c0001t0024others(5): Show | 21 | HG01109.hp1 HG01167.hp1 HG02258.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2795T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 2795 | chr8 | 96336361 | |||||
chr8:96336410
|
A | G | 1 | a0001c0001t0029 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2844A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 2844 | chr8 | 96336410 | |||||
chr8:96336683
|
T | C | 2 | a0001c0001t0028a0002c0002t0008 | 8 | HG01069.hp1 HG02717.hp1 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3117T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 3117 | chr8 | 96336683 | |||||
chr8:96336723
|
G | A | 3 | a0001c0001t0005a0001c0001t0006a0001c0001t0032 | 25 | HG00609.hp2 HG00733.hp1 HG01255.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3157G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 3157 | chr8 | 96336723 | |||||
chr8:96336734
|
G | A | 3 | a0001c0001t0027a0001c0001t0028a0002c0002t0008 | 9 | HG01069.hp1 HG02717.hp1 HG02809.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3168G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 3168 | chr8 | 96336734 | |||||
chr8:96336831
|
G | A | 2 | a0001c0001t0028a0002c0002t0008 | 8 | HG01069.hp1 HG02717.hp1 HG02818.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3265G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 3265 | chr8 | 96336831 | |||||
chr8:96336953
|
G | A | 1 | a0001c0001t0007 | 7 | HG01261.hp1 HG01891.hp2 HG02486.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3387G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 3387 | chr8 | 96336953 | |||||
chr8:96336967
|
T | C | 4 | a0001c0001t0018a0001c0001t0028a0001c0004t0022others(1): Show | 11 | HG01069.hp1 HG01884.hp1 HG02717.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3401T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 13/13 | 3401 | chr8 | 96336967 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:96262400
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.179+181C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96262400 | ||||||
chr8:96262428
|
C | T | 1 | a0001c0001t0002g0257 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.179+209C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96262428 | ||||||
chr8:96262459
|
G | C | 1 | a0001c0001t0002g0004 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.179+240G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96262459 | ||||||
chr8:96262502
|
A | T | 1 | a0001c0001t0001g0256 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.179+283A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96262502 | ||||||
chr8:96262716
|
GGT | G | 6 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0009others(3): Show | 6 | HG01261.hp1 HG02622.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.179+498_179+499del others(2): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96262716 | ||||||
chr8:96262762
|
G | A | 164 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0001g0046others(161): Show | 167 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.179+543G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96262762 | ||||||
chr8:96263295
|
A | G | 1 | a0001c0001t0019g0255 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.179+1076A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96263295 | ||||||
chr8:96263403
|
GC | G | 31 | a0001c0001t0001g0034a0001c0001t0002g0006a0001c0001t0002g0008others(28): Show | 31 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.179+1186delC | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 96263403 | |||||
chr8:96263759
|
C | T | 1 | a0001c0001t0005g0163 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.179+1540C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96263759 | ||||||
chr8:96264003
|
C | G | 1 | a0001c0001t0001g0162 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.179+1784C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96264003 | ||||||
chr8:96264197
|
G | A | 3 | a0001c0001t0010g0036a0001c0001t0010g0037a0001c0001t0011g0035 | 3 | HG02145.hp2 HG02717.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.179+1978G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96264197 | ||||||
chr8:96264528
|
T | C | 1 | a0001c0001t0004g0038 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.179+2309T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96264528 | ||||||
chr8:96264765
|
AATTGCAG others(3): Show |
A | 1 | a0001c0001t0001g0161 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.179+2547_179+2556d others(12): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96264765 | ||||||
chr8:96264797
|
C | T | 2 | a0001c0001t0001g0160a0002c0002t0008g0159 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.179+2578C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96264797 | ||||||
chr8:96264986
|
C | T | 9 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0004g0152others(6): Show | 9 | HG01167.hp1 HG02630.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.179+2767C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96264986 | ||||||
chr8:96265004
|
C | T | 2 | a0001c0001t0001g0160a0002c0002t0008g0159 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.179+2785C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96265004 | ||||||
chr8:96265485
|
C | A | 2 | a0001c0001t0005g0039a0001c0001t0005g0040 | 2 | HG03491.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.179+3266C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96265485 | ||||||
chr8:96265573
|
A | G | 1 | a0001c0001t0002g0149 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.179+3354A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96265573 | ||||||
chr8:96265584
|
C | CAAACAAA others(3): Show |
2 | a0001c0001t0010g0036a0001c0001t0010g0037 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.179+3394_179+3403d others(12): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 96265584 | |||||
chr8:96265584
|
CAAACAAA others(3): Show |
C | 5 | a0001c0001t0001g0043a0001c0001t0001g0164a0001c0001t0005g0042others(2): Show | 5 | HG01934.hp2 HG01975.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.179+3394_179+3403d others(12): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 96265584 | |||||
chr8:96265584
|
CAAACAAA others(8): Show |
C | 1 | a0001c0001t0035g0041 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.179+3389_179+3403d others(17): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 96265584 | |||||
chr8:96265667
|
G | A | 1 | a0001c0001t0023g0150 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.179+3448G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96265667 | ||||||
chr8:96265745
|
G | C | 5 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0256others(2): Show | 5 | HG03669.hp2 HG03831.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.179+3526G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96265745 | ||||||
chr8:96265746
|
A | G | 2 | a0001c0001t0033g0147a0001c0004t0004g0148 | 2 | HG02572.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.179+3527A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96265746 | ||||||
chr8:96265830
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.179+3611G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96265830 | ||||||
chr8:96265861
|
G | A | 1 | a0001c0005t0002g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.179+3642G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96265861 | ||||||
chr8:96266051
|
C | A | 1 | a0001c0001t0006g0167 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.179+3832C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96266051 | ||||||
chr8:96266077
|
G | GTTGGTAA others(11): Show |
1 | a0001c0001t0001g0254 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.179+3862_179+3879d others(20): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 96266077 | |||||
chr8:96266148
|
A | G | 5 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0023g0150others(2): Show | 5 | HG01167.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.179+3929A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96266148 | ||||||
chr8:96266182
|
C | G | 1 | a0001c0001t0012g0146 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.179+3963C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96266182 | ||||||
chr8:96266265
|
G | A | 31 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(28): Show | 31 | HG00642.hp1 HG01070.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.179+4046G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96266265 | ||||||
chr8:96266304
|
A | G | 1 | a0001c0001t0019g0253 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.179+4085A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96266304 | ||||||
chr8:96266450
|
C | T | 18 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(15): Show | 18 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.179+4231C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96266450 | ||||||
chr8:96266492
|
T | A | 2 | a0001c0001t0001g0160a0002c0002t0008g0159 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.179+4273T>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96266492 | ||||||
chr8:96266505
|
T | C | 2 | a0001c0001t0010g0036a0001c0001t0010g0037 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.179+4286T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96266505 | ||||||
chr8:96266513
|
A | C | 53 | a0001c0001t0001g0053a0001c0001t0001g0141a0001c0001t0001g0160others(50): Show | 53 | HG00642.hp1 HG01070.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.179+4294A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96266513 | ||||||
chr8:96266645
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.179+4426G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96266645 | ||||||
chr8:96266890
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0168 | 2 | NA19007.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.179+4671G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96266890 | ||||||
chr8:96266961
|
T | C | 5 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0023g0150others(2): Show | 5 | HG01167.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.179+4742T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96266961 | ||||||
chr8:96267062
|
A | G | 32 | a0001c0001t0001g0034a0001c0001t0002g0006a0001c0001t0002g0008others(29): Show | 32 | HG01081.hp1 HG01261.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.179+4843A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96267062 | ||||||
chr8:96267124
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.179+4905A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96267124 | ||||||
chr8:96267204
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.179+4985C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96267204 | ||||||
chr8:96267216
|
C | T | 16 | a0001c0001t0001g0141a0001c0001t0002g0143a0001c0001t0004g0132others(13): Show | 16 | HG01109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.179+4997C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96267216 | ||||||
chr8:96267534
|
C | T | 9 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0162others(6): Show | 9 | HG00140.hp2 HG00741.hp2 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.179+5315C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96267534 | ||||||
chr8:96267648
|
T | C | 4 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0024g0156others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.179+5429T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96267648 | ||||||
chr8:96267829
|
G | A | 1 | a0001c0001t0001g0067 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.180-5470G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96267829 | ||||||
chr8:96267840
|
C | G | 1 | a0001c0001t0002g0124 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.180-5459C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96267840 | ||||||
chr8:96268019
|
T | A | 2 | a0001c0001t0007g0014a0001c0001t0007g0015 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.180-5280T>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96268019 | ||||||
chr8:96268634
|
C | CT | 11 | a0001c0001t0003g0245a0001c0001t0010g0036a0001c0001t0010g0037others(8): Show | 11 | HG01070.hp1 HG02145.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.180-4646dupT | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 96268634 | |||||
chr8:96268634
|
CT | C | 13 | a0001c0001t0001g0003a0001c0001t0001g0068a0001c0001t0001g0069others(10): Show | 14 | HG01070.hp2 HG01169.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.180-4646delT | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 96268634 | |||||
chr8:96268974
|
G | T | 1 | a0001c0001t0007g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.180-4325G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96268974 | ||||||
chr8:96269245
|
G | T | 1 | a0001c0005t0002g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.180-4054G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96269245 | ||||||
chr8:96269330
|
A | G | 2 | a0001c0001t0010g0036a0001c0001t0010g0037 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.180-3969A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96269330 | ||||||
chr8:96269516
|
A | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0161 | 2 | NA19088.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.180-3783A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96269516 | ||||||
chr8:96269659
|
C | A | 1 | a0001c0001t0001g0254 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.180-3640C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96269659 | ||||||
chr8:96269910
|
G | A | 18 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(15): Show | 18 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.180-3389G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96269910 | ||||||
chr8:96269913
|
C | T | 1 | a0001c0001t0001g0254 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.180-3386C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96269913 | ||||||
chr8:96269914
|
T | C | 1 | a0001c0001t0001g0254 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.180-3385T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96269914 | ||||||
chr8:96270171
|
C | T | 5 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0016g0012others(2): Show | 5 | HG02258.hp2 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.180-3128C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96270171 | ||||||
chr8:96270332
|
A | G | 42 | a0001c0001t0001g0053a0001c0001t0001g0141a0001c0001t0001g0160others(39): Show | 42 | HG00642.hp1 HG01070.hp1 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.180-2967A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96270332 | ||||||
chr8:96270386
|
G | A | 1 | a0001c0001t0029g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.180-2913G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96270386 | ||||||
chr8:96270409
|
C | A | 5 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0016g0012others(2): Show | 5 | HG02258.hp2 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.180-2890C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96270409 | ||||||
chr8:96270749
|
CAAAT | C | 4 | a0001c0001t0032g0130a0001c0001t0033g0147a0001c0004t0004g0148others(1): Show | 4 | HG02572.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.180-2548_180-2545d others(6): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr8 | 96270749 | |||||
chr8:96271085
|
G | A | 18 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(15): Show | 18 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.180-2214G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96271085 | ||||||
chr8:96271479
|
T | A | 1 | a0001c0001t0001g0254 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.180-1820T>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96271479 | ||||||
chr8:96271562
|
C | A | 1 | a0001c0001t0001g0254 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.180-1737C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96271562 | ||||||
chr8:96271644
|
T | C | 4 | a0001c0001t0032g0130a0001c0001t0033g0147a0001c0004t0004g0148others(1): Show | 4 | HG02572.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.180-1655T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96271644 | ||||||
chr8:96272042
|
G | A | 1 | a0001c0001t0006g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.180-1257G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96272042 | ||||||
chr8:96272261
|
A | G | 2 | a0001c0001t0001g0160a0002c0002t0008g0159 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.180-1038A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96272261 | ||||||
chr8:96272274
|
A | G | 1 | a0001c0001t0002g0124 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.180-1025A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96272274 | ||||||
chr8:96272322
|
T | A | 18 | a0001c0001t0001g0141a0001c0001t0002g0143a0001c0001t0004g0132others(15): Show | 18 | HG01109.hp1 HG02145.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.180-977T>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96272322 | ||||||
chr8:96272394
|
G | A | 1 | a0001c0001t0034g0129 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.180-905G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96272394 | ||||||
chr8:96272539
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.180-760C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96272539 | ||||||
chr8:96272542
|
G | C | 4 | a0001c0001t0032g0130a0001c0001t0033g0147a0001c0004t0004g0148others(1): Show | 4 | HG02572.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.180-757G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96272542 | ||||||
chr8:96272646
|
A | T | 1 | a0001c0001t0001g0254 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.180-653A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96272646 | ||||||
chr8:96272694
|
C | T | 162 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0001g0046others(159): Show | 165 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(162): Show |
intron_variant | MODIFIER | c.180-605C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96272694 | ||||||
chr8:96272765
|
A | T | 1 | a0001c0001t0001g0254 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.180-534A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96272765 | ||||||
chr8:96272848
|
A | C | 16 | a0001c0001t0001g0141a0001c0001t0002g0143a0001c0001t0004g0132others(13): Show | 16 | HG01109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.180-451A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96272848 | ||||||
chr8:96273061
|
G | C | 1 | a0001c0001t0002g0074 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.180-238G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96273061 | ||||||
chr8:96273201
|
G | A | 36 | a0001c0001t0001g0053a0001c0001t0001g0141a0001c0001t0002g0055others(33): Show | 36 | HG00642.hp1 HG01070.hp1 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.180-98G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96273201 | ||||||
chr8:96273225
|
T | C | 3 | a0001c0001t0003g0048a0001c0001t0003g0049a0001c0001t0003g0050 | 3 | HG01167.hp2 HG01169.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.180-74T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96273225 | ||||||
chr8:96273232
|
C | T | 1 | a0001c0001t0019g0253 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.180-67C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96273232 | ||||||
chr8:96273277
|
A | T | 1 | a0001c0001t0001g0254 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.180-22A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 1/12 | chr8 | 96273277 | ||||||
chr8:96273429
|
G | C | 1 | a0001c0001t0013g0247 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.271+39G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96273429 | ||||||
chr8:96273588
|
T | G | 4 | a0001c0001t0032g0130a0001c0001t0033g0147a0001c0004t0004g0148others(1): Show | 4 | HG02572.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+198T>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96273588 | ||||||
chr8:96273614
|
G | C | 53 | a0001c0001t0001g0053a0001c0001t0001g0141a0001c0001t0001g0160others(50): Show | 53 | HG00642.hp1 HG01070.hp1 HG01109.hp1 others(50): Show |
intron_variant | MODIFIER | c.271+224G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96273614 | ||||||
chr8:96273929
|
C | T | 4 | a0001c0001t0009g0120a0001c0001t0009g0121a0001c0001t0009g0122others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+539C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96273929 | ||||||
chr8:96274083
|
A | G | 4 | a0001c0001t0032g0130a0001c0001t0033g0147a0001c0004t0004g0148others(1): Show | 4 | HG02572.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+693A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96274083 | ||||||
chr8:96274209
|
A | G | 1 | a0001c0001t0004g0144 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.271+819A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96274209 | ||||||
chr8:96274290
|
A | G | 3 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0019g0255 | 3 | NA18951.hp1 NA18966.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.271+900A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96274290 | ||||||
chr8:96274456
|
C | T | 2 | a0001c0001t0001g0160a0002c0002t0008g0159 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.271+1066C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96274456 | ||||||
chr8:96274468
|
G | A | 3 | a0001c0001t0003g0171a0001c0001t0003g0172a0001c0001t0003g0173 | 3 | HG03834.hp2 NA18955.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.271+1078G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96274468 | ||||||
chr8:96274588
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.271+1198G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96274588 | ||||||
chr8:96274595
|
C | T | 1 | a0001c0001t0005g0042 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.271+1205C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96274595 | ||||||
chr8:96274620
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.271+1230G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96274620 | ||||||
chr8:96274741
|
T | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.271+1351T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96274741 | ||||||
chr8:96274774
|
G | A | 1 | a0001c0001t0034g0129 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.271+1384G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96274774 | ||||||
chr8:96274807
|
C | T | 1 | a0001c0001t0034g0129 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.271+1417C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96274807 | ||||||
chr8:96274820
|
G | C | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.271+1430G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96274820 | ||||||
chr8:96274970
|
G | T | 4 | a0001c0001t0009g0120a0001c0001t0009g0121a0001c0001t0009g0122others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+1580G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96274970 | ||||||
chr8:96275120
|
G | A | 4 | a0001c0001t0009g0120a0001c0001t0009g0121a0001c0001t0009g0122others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+1730G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96275120 | ||||||
chr8:96275175
|
T | G | 50 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(47): Show | 50 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(47): Show |
intron_variant | MODIFIER | c.271+1785T>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96275175 | ||||||
chr8:96275624
|
T | C | 18 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(15): Show | 18 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.271+2234T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96275624 | ||||||
chr8:96275685
|
C | G | 2 | a0001c0001t0001g0160a0002c0002t0008g0159 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.271+2295C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96275685 | ||||||
chr8:96275826
|
C | T | 1 | a0001c0001t0006g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.271+2436C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96275826 | ||||||
chr8:96276391
|
T | C | 1 | a0001c0001t0033g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.271+3001T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96276391 | ||||||
chr8:96276539
|
T | C | 1 | a0001c0001t0001g0175 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.271+3149T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96276539 | ||||||
chr8:96276598
|
C | G | 50 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(47): Show | 50 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(47): Show |
intron_variant | MODIFIER | c.271+3208C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96276598 | ||||||
chr8:96276611
|
C | T | 18 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(15): Show | 18 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.271+3221C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96276611 | ||||||
chr8:96276629
|
C | T | 4 | a0001c0001t0032g0130a0001c0001t0033g0147a0001c0004t0004g0148others(1): Show | 4 | HG02572.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+3239C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96276629 | ||||||
chr8:96276671
|
G | A | 1 | a0003c0006t0037g0044 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.271+3281G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96276671 | ||||||
chr8:96276718
|
G | T | 1 | a0001c0001t0034g0129 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.271+3328G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96276718 | ||||||
chr8:96276863
|
T | C | 18 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(15): Show | 18 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.271+3473T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96276863 | ||||||
chr8:96276884
|
T | C | 1 | a0001c0001t0004g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.271+3494T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96276884 | ||||||
chr8:96276961
|
T | TAC | 6 | a0001c0001t0002g0006a0001c0001t0002g0258a0001c0001t0007g0005others(3): Show | 6 | HG02486.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.271+3574_271+3575d others(4): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96276961 | |||||
chr8:96276965
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.271+3575C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96276965 | ||||||
chr8:96276966
|
G | A | 43 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0008others(40): Show | 43 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.271+3576G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96276966 | ||||||
chr8:96276968
|
G | A | 1 | a0001c0001t0007g0005 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.271+3578G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96276968 | ||||||
chr8:96276968
|
GCGCA | G | 7 | a0001c0001t0001g0034a0001c0001t0002g0029a0001c0001t0003g0028others(4): Show | 7 | HG01884.hp2 HG02155.hp1 NA18949.hp2 others(4): Show |
intron_variant | MODIFIER | c.271+3582_271+3585d others(6): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96276968 | |||||
chr8:96276970
|
G | A | 2 | a0001c0001t0006g0032a0001c0001t0013g0142 | 2 | NA18522.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.271+3580G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96276970 | ||||||
chr8:96276970
|
G | GCACA | 13 | a0001c0001t0001g0141a0001c0001t0004g0132a0001c0001t0004g0134others(10): Show | 13 | HG01109.hp1 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.271+3583_271+3584i others(6): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96276970 | |||||
chr8:96276970
|
G | GCGCACAC others(5): Show |
1 | a0001c0001t0031g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.271+3581_271+3582i others(14): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96276970 | |||||
chr8:96276970
|
GCA | G | 3 | a0001c0001t0002g0010a0001c0001t0010g0036a0001c0001t0010g0037 | 3 | HG02145.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.271+3582_271+3583d others(4): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96276970 | |||||
chr8:96276972
|
A | G | 17 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0018others(14): Show | 17 | HG01261.hp1 HG01891.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.271+3582A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96276972 | ||||||
chr8:96276972
|
ACG | A | 4 | a0001c0001t0003g0118a0001c0001t0005g0244a0001c0001t0032g0130others(1): Show | 4 | HG02056.hp1 HG03195.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+3590_271+3591d others(4): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96276972 | |||||
chr8:96276974
|
G | A | 40 | a0001c0001t0001g0141a0001c0001t0002g0006a0001c0001t0002g0008others(37): Show | 40 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.271+3584G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96276974 | ||||||
chr8:96276976
|
G | A | 43 | a0001c0001t0001g0141a0001c0001t0002g0006a0001c0001t0002g0008others(40): Show | 43 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.271+3586G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96276976 | ||||||
chr8:96276976
|
G | GCACACAC others(7): Show |
2 | a0001c0004t0004g0148a0001c0004t0022g0154 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.271+3587_271+3588i others(16): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96276976 | |||||
chr8:96276978
|
G | A | 60 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0001g0160others(57): Show | 60 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(57): Show |
intron_variant | MODIFIER | c.271+3588G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96276978 | ||||||
chr8:96276978
|
G | GCA | 19 | a0001c0001t0001g0068a0001c0001t0001g0086a0001c0001t0002g0060others(16): Show | 20 | HG00280.hp1 HG00642.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.271+3589_271+3590i others(4): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96276978 | |||||
chr8:96276978
|
G | GCACA | 17 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(14): Show | 17 | HG00438.hp2 HG00621.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.271+3589_271+3590i others(6): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96276978 | |||||
chr8:96276978
|
G | GCACACAC others(1): Show |
4 | a0001c0001t0004g0038a0001c0001t0012g0051a0001c0001t0012g0063others(1): Show | 4 | HG01070.hp1 HG02886.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+3589_271+3590i others(10): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96276978 | |||||
chr8:96276980
|
G | A | 150 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0001g0053others(147): Show | 153 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.271+3590G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96276980 | ||||||
chr8:96276980
|
GCA | G | 75 | a0001c0001t0001g0003a0001c0001t0001g0066a0001c0001t0001g0125others(72): Show | 76 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.271+3622_271+3623d others(4): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96276980 | |||||
chr8:96276980
|
GCACA | G | 4 | a0001c0001t0001g0235a0001c0001t0002g0234a0001c0001t0003g0173others(1): Show | 4 | NA18940.hp1 NA18979.hp2 NA19090.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+3620_271+3623d others(6): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96276980 | |||||
chr8:96276980
|
GCACACA | G | 4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0003g0238others(1): Show | 4 | HG01074.hp2 HG01516.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+3618_271+3623d others(8): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96276980 | |||||
chr8:96277113
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.271+3723G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96277113 | ||||||
chr8:96277119
|
G | A | 2 | a0001c0001t0005g0039a0001c0001t0005g0040 | 2 | HG03491.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.271+3729G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96277119 | ||||||
chr8:96277426
|
C | T | 1 | a0001c0001t0012g0051 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.271+4036C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96277426 | ||||||
chr8:96277626
|
C | T | 49 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(46): Show | 49 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(46): Show |
intron_variant | MODIFIER | c.271+4236C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96277626 | ||||||
chr8:96277845
|
G | T | 1 | a0001c0001t0030g0233 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.271+4455G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96277845 | ||||||
chr8:96277872
|
A | G | 84 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0141others(81): Show | 84 | HG00642.hp1 HG01070.hp1 HG01081.hp1 others(81): Show |
intron_variant | MODIFIER | c.271+4482A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96277872 | ||||||
chr8:96277926
|
T | C | 1 | a0001c0001t0009g0091 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.271+4536T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96277926 | ||||||
chr8:96277937
|
C | T | 1 | a0001c0001t0007g0025 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.271+4547C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96277937 | ||||||
chr8:96277986
|
C | T | 1 | a0001c0001t0004g0153 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.271+4596C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96277986 | ||||||
chr8:96278111
|
G | A | 4 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0024g0156others(1): Show | 4 | HG01167.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.271+4721G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96278111 | ||||||
chr8:96278121
|
T | C | 5 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0016g0012others(2): Show | 5 | HG02258.hp2 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.271+4731T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96278121 | ||||||
chr8:96278390
|
T | G | 2 | a0001c0004t0004g0148a0001c0004t0022g0154 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.271+5000T>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96278390 | ||||||
chr8:96278400
|
A | G | 5 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0023g0150others(2): Show | 5 | HG01167.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.271+5010A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96278400 | ||||||
chr8:96278482
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.271+5092G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96278482 | ||||||
chr8:96278691
|
A | G | 2 | a0001c0001t0005g0039a0001c0001t0005g0040 | 2 | HG03491.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.271+5301A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96278691 | ||||||
chr8:96278726
|
C | T | 1 | a0001c0001t0002g0061 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.271+5336C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96278726 | ||||||
chr8:96278727
|
G | A | 2 | a0001c0001t0001g0160a0002c0002t0008g0159 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.271+5337G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96278727 | ||||||
chr8:96278728
|
G | A | 4 | a0001c0001t0009g0120a0001c0001t0009g0121a0001c0001t0009g0122others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.271+5338G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96278728 | ||||||
chr8:96278810
|
A | C | 18 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(15): Show | 18 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.272-5299A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96278810 | ||||||
chr8:96278851
|
AT | A | 50 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(47): Show | 50 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(47): Show |
intron_variant | MODIFIER | c.272-5256delT | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96278851 | |||||
chr8:96278899
|
T | C | 1 | a0001c0001t0002g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.272-5210T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96278899 | ||||||
chr8:96278966
|
G | GCC | 16 | a0001c0001t0002g0143a0001c0001t0004g0132a0001c0001t0004g0134others(13): Show | 16 | HG01109.hp1 HG02145.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.272-5138_272-5137d others(4): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96278966 | |||||
chr8:96278972
|
C | CCCT | 23 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(20): Show | 23 | HG01081.hp1 HG01261.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.272-5137_272-5136i others(5): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96278972 | ||||||
chr8:96278972
|
C | CT | 77 | a0001c0001t0001g0043a0001c0001t0001g0064a0001c0001t0001g0065others(74): Show | 77 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.272-5118dupT | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96278972 | |||||
chr8:96278972
|
C | CTT | 7 | a0001c0001t0001g0161a0001c0001t0002g0182a0001c0001t0003g0082others(4): Show | 7 | HG00621.hp2 HG03453.hp1 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.272-5119_272-5118d others(4): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96278972 | |||||
chr8:96278972
|
C | T | 1 | a0001c0001t0018g0024 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.272-5137C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96278972 | ||||||
chr8:96278973
|
T | C | 22 | a0001c0001t0001g0053a0001c0001t0001g0239a0001c0001t0001g0240others(19): Show | 22 | HG00642.hp1 HG01069.hp1 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.272-5136T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96278973 | ||||||
chr8:96278994
|
G | A | 14 | a0001c0001t0001g0141a0001c0001t0002g0143a0001c0001t0004g0132others(11): Show | 14 | HG01109.hp1 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.272-5115G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96278994 | ||||||
chr8:96279112
|
A | G | 4 | a0001c0001t0012g0051a0001c0001t0012g0062a0001c0001t0012g0063others(1): Show | 4 | HG01070.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.272-4997A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96279112 | ||||||
chr8:96279137
|
A | AT | 7 | a0001c0001t0001g0181a0001c0001t0001g0240a0001c0001t0002g0058others(4): Show | 7 | HG01934.hp1 HG02615.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.272-4957dupT | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96279137 | |||||
chr8:96279220
|
A | G | 1 | a0001c0001t0003g0090 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.272-4889A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96279220 | ||||||
chr8:96279299
|
C | T | 4 | a0001c0001t0032g0130a0001c0001t0033g0147a0001c0004t0004g0148others(1): Show | 4 | HG02572.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.272-4810C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96279299 | ||||||
chr8:96279456
|
T | A | 1 | a0001c0001t0001g0185 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.272-4653T>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96279456 | ||||||
chr8:96279556
|
C | T | 1 | a0001c0001t0030g0233 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.272-4553C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96279556 | ||||||
chr8:96279589
|
T | C | 155 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0001g0053others(152): Show | 158 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(155): Show |
intron_variant | MODIFIER | c.272-4520T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96279589 | ||||||
chr8:96279693
|
C | T | 2 | a0001c0001t0001g0160a0002c0002t0008g0159 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.272-4416C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96279693 | ||||||
chr8:96279743
|
C | T | 2 | a0001c0001t0001g0047a0001c0001t0006g0115 | 2 | HG02698.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.272-4366C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96279743 | ||||||
chr8:96279818
|
C | CAAATAAA others(1): Show |
28 | a0001c0001t0001g0034a0001c0001t0002g0018a0001c0001t0002g0019others(25): Show | 28 | HG01081.hp1 HG01884.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.272-4262_272-4255d others(10): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96279818 | |||||
chr8:96279818
|
C | CAAATAAA others(5): Show |
11 | a0001c0001t0001g0141a0001c0001t0004g0134a0001c0001t0004g0137others(8): Show | 11 | HG01109.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.272-4266_272-4255d others(14): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96279818 | |||||
chr8:96279818
|
C | CAAATAAA others(9): Show |
1 | a0001c0001t0002g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.272-4270_272-4255d others(18): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96279818 | |||||
chr8:96279818
|
CAAAT | C | 115 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0047others(112): Show | 118 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.272-4258_272-4255d others(6): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96279818 | |||||
chr8:96279818
|
CAAATAAA others(5): Show |
C | 5 | a0001c0001t0001g0160a0001c0001t0002g0158a0001c0001t0024g0156others(2): Show | 5 | HG01167.hp1 HG02257.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.272-4266_272-4255d others(14): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96279818 | |||||
chr8:96279912
|
T | A | 1 | a0001c0001t0003g0076 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.272-4197T>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96279912 | ||||||
chr8:96280407
|
A | C | 1 | a0001c0001t0003g0076 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.272-3702A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96280407 | ||||||
chr8:96280408
|
G | A | 1 | a0001c0001t0003g0076 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.272-3701G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96280408 | ||||||
chr8:96280454
|
A | AAAGCCTG others(16): Show |
1 | a0001c0001t0014g0229 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.272-3610_272-3588d others(25): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96280454 | |||||
chr8:96280454
|
AAAGCCTG others(16): Show |
A | 1 | a0001c0001t0001g0186 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.272-3610_272-3588d others(25): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96280454 | |||||
chr8:96280617
|
G | A | 18 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(15): Show | 18 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.272-3492G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96280617 | ||||||
chr8:96280651
|
T | C | 2 | a0001c0001t0007g0014a0001c0001t0007g0015 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.272-3458T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96280651 | ||||||
chr8:96280675
|
G | A | 8 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0006g0032others(5): Show | 8 | HG02258.hp2 HG02809.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.272-3434G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96280675 | ||||||
chr8:96280973
|
A | T | 2 | a0001c0001t0001g0160a0002c0002t0008g0159 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.272-3136A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96280973 | ||||||
chr8:96281035
|
C | A | 18 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(15): Show | 18 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.272-3074C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96281035 | ||||||
chr8:96281089
|
G | A | 1 | a0001c0001t0005g0163 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.272-3020G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96281089 | ||||||
chr8:96281186
|
T | A | 3 | a0001c0001t0011g0035a0001c0003t0002g0001a0001c0003t0004g0002 | 6 | HG02717.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.272-2923T>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96281186 | ||||||
chr8:96281561
|
A | G | 166 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0001g0046others(163): Show | 169 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(166): Show |
intron_variant | MODIFIER | c.272-2548A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96281561 | ||||||
chr8:96281593
|
G | A | 9 | a0001c0001t0001g0043a0001c0001t0001g0069a0001c0001t0001g0093others(6): Show | 9 | HG02148.hp1 HG02273.hp1 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.272-2516G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96281593 | ||||||
chr8:96281677
|
C | T | 46 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(43): Show | 46 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.272-2432C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96281677 | ||||||
chr8:96281680
|
G | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.272-2429G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96281680 | ||||||
chr8:96281725
|
T | C | 64 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0141others(61): Show | 64 | HG00642.hp1 HG01070.hp1 HG01081.hp1 others(61): Show |
intron_variant | MODIFIER | c.272-2384T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96281725 | ||||||
chr8:96281836
|
C | A | 2 | a0001c0001t0003g0076a0001c0001t0003g0078 | 2 | NA19066.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.272-2273C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96281836 | ||||||
chr8:96281922
|
G | A | 2 | a0001c0001t0032g0130a0001c0001t0033g0147 | 2 | HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.272-2187G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96281922 | ||||||
chr8:96282115
|
G | A | 1 | a0001c0001t0034g0129 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.272-1994G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96282115 | ||||||
chr8:96282237
|
A | G | 1 | a0001c0001t0006g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.272-1872A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96282237 | ||||||
chr8:96282341
|
G | A | 1 | a0001c0001t0010g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.272-1768G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96282341 | ||||||
chr8:96282419
|
C | T | 10 | a0001c0001t0001g0164a0001c0001t0001g0183a0001c0001t0001g0224others(7): Show | 10 | HG01358.hp1 HG01496.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.272-1690C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96282419 | ||||||
chr8:96282604
|
C | A | 84 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0141others(81): Show | 84 | HG00642.hp1 HG01070.hp1 HG01081.hp1 others(81): Show |
intron_variant | MODIFIER | c.272-1505C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96282604 | ||||||
chr8:96282648
|
A | C | 2 | a0001c0001t0001g0160a0002c0002t0008g0159 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.272-1461A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96282648 | ||||||
chr8:96282903
|
C | T | 16 | a0001c0001t0001g0068a0001c0001t0001g0114a0001c0001t0003g0076others(13): Show | 16 | HG00280.hp1 HG00438.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.272-1206C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96282903 | ||||||
chr8:96282985
|
A | G | 2 | a0001c0001t0001g0160a0002c0002t0008g0159 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.272-1124A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96282985 | ||||||
chr8:96283192
|
A | G | 46 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(43): Show | 46 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.272-917A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283192 | ||||||
chr8:96283435
|
G | A | 1 | a0001c0001t0034g0129 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.272-674G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283435 | ||||||
chr8:96283449
|
T | G | 84 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0141others(81): Show | 84 | HG00642.hp1 HG01070.hp1 HG01081.hp1 others(81): Show |
intron_variant | MODIFIER | c.272-660T>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283449 | ||||||
chr8:96283503
|
T | C | 2 | a0001c0001t0001g0160a0002c0002t0008g0159 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.272-606T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283503 | ||||||
chr8:96283598
|
GTC | G | 28 | a0001c0001t0001g0034a0001c0001t0002g0006a0001c0001t0002g0008others(25): Show | 28 | HG01081.hp1 HG01261.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.272-494_272-493del others(2): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96283598 | |||||
chr8:96283598
|
GTCTC | G | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0256others(6): Show | 9 | HG01891.hp1 HG02615.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.272-496_272-493del others(4): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96283598 | |||||
chr8:96283615
|
T | A | 46 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(43): Show | 46 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.272-494T>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283615 | ||||||
chr8:96283615
|
TCA | T | 54 | a0001c0001t0001g0043a0001c0001t0001g0064a0001c0001t0001g0065others(51): Show | 54 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.272-476_272-475del others(2): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96283615 | |||||
chr8:96283617
|
A | T | 4 | a0001c0001t0003g0076a0001c0001t0006g0032a0001c0001t0011g0031others(1): Show | 4 | HG02886.hp2 HG03209.hp2 NA19091.hp2 others(1): Show |
intron_variant | MODIFIER | c.272-492A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283617 | ||||||
chr8:96283619
|
A | T | 1 | a0001c0001t0006g0243 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.272-490A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283619 | ||||||
chr8:96283624
|
C | A | 1 | a0001c0001t0001g0189 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.272-485C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283624 | ||||||
chr8:96283631
|
A | C | 1 | a0001c0001t0029g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.272-478A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283631 | ||||||
chr8:96283633
|
A | C | 2 | a0001c0001t0007g0005a0001c0003t0004g0002 | 3 | HG02622.hp1 HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.272-476A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283633 | ||||||
chr8:96283642
|
T | C | 68 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0141others(65): Show | 68 | HG00642.hp1 HG01070.hp1 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.272-467T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283642 | ||||||
chr8:96283758
|
G | T | 19 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0009others(16): Show | 19 | HG01261.hp1 HG01891.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.272-351G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283758 | ||||||
chr8:96283791
|
C | T | 5 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0256others(2): Show | 5 | HG03669.hp2 HG03831.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.272-318C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283791 | ||||||
chr8:96283817
|
A | G | 46 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(43): Show | 46 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.272-292A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283817 | ||||||
chr8:96283863
|
A | C | 1 | a0001c0001t0004g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.272-246A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283863 | ||||||
chr8:96283922
|
G | T | 46 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(43): Show | 46 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.272-187G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283922 | ||||||
chr8:96283930
|
G | A | 1 | a0001c0001t0023g0150 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.272-179G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283930 | ||||||
chr8:96283966
|
G | T | 2 | a0001c0001t0010g0127a0001c0001t0031g0128 | 2 | HG01081.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.272-143G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283966 | ||||||
chr8:96283977
|
G | GA | 11 | a0001c0001t0001g0043a0001c0001t0001g0069a0001c0001t0001g0093others(8): Show | 11 | HG01069.hp1 HG02148.hp1 HG02273.hp1 others(8): Show |
intron_variant | MODIFIER | c.272-118dupA | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr8 | 96283977 | |||||
chr8:96283993
|
T | C | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.272-116T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 2/12 | chr8 | 96283993 | ||||||
chr8:96284203
|
T | C | 3 | a0001c0001t0002g0246a0001c0001t0002g0249a0001c0001t0002g0250 | 3 | HG01070.hp2 HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.316+50T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96284203 | ||||||
chr8:96284337
|
G | C | 1 | a0001c0001t0001g0068 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.316+184G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96284337 | ||||||
chr8:96284339
|
C | T | 44 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(41): Show | 44 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(41): Show |
intron_variant | MODIFIER | c.316+186C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96284339 | ||||||
chr8:96284403
|
T | C | 1 | a0001c0001t0032g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.316+250T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96284403 | ||||||
chr8:96284458
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.316+305T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96284458 | ||||||
chr8:96284556
|
A | G | 1 | a0001c0001t0003g0082 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.316+403A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96284556 | ||||||
chr8:96284557
|
G | T | 44 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(41): Show | 44 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(41): Show |
intron_variant | MODIFIER | c.316+404G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96284557 | ||||||
chr8:96284790
|
C | A | 1 | a0001c0001t0007g0017 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.316+637C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96284790 | ||||||
chr8:96284807
|
A | G | 1 | a0001c0001t0011g0031 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.316+654A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96284807 | ||||||
chr8:96284809
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.316+656G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96284809 | ||||||
chr8:96284843
|
C | T | 1 | a0001c0001t0002g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.316+690C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96284843 | ||||||
chr8:96285033
|
C | T | 1 | a0001c0001t0023g0150 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316+880C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96285033 | ||||||
chr8:96285034
|
A | G | 80 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0141others(77): Show | 80 | HG00642.hp1 HG01070.hp1 HG01081.hp1 others(77): Show |
intron_variant | MODIFIER | c.316+881A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96285034 | ||||||
chr8:96285035
|
A | G | 153 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0001g0053others(150): Show | 156 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(153): Show |
intron_variant | MODIFIER | c.316+882A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96285035 | ||||||
chr8:96285057
|
A | G | 1 | a0001c0001t0002g0191 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.316+904A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96285057 | ||||||
chr8:96285086
|
C | T | 1 | a0001c0001t0019g0253 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.316+933C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96285086 | ||||||
chr8:96285265
|
G | A | 1 | a0001c0001t0006g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.316+1112G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96285265 | ||||||
chr8:96285361
|
G | T | 1 | a0001c0001t0003g0072 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.316+1208G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96285361 | ||||||
chr8:96285422
|
G | GA | 46 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(43): Show | 46 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.316+1271dupA | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr8 | 96285422 | |||||
chr8:96285666
|
A | G | 18 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(15): Show | 18 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.317-1356A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96285666 | ||||||
chr8:96286099
|
C | T | 3 | a0001c0001t0001g0181a0001c0001t0001g0223a0001c0001t0005g0222 | 3 | HG01255.hp2 HG02738.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.317-923C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96286099 | ||||||
chr8:96286263
|
G | C | 1 | a0001c0005t0002g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.317-759G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96286263 | ||||||
chr8:96286303
|
G | A | 4 | a0001c0001t0032g0130a0001c0001t0033g0147a0001c0004t0004g0148others(1): Show | 4 | HG02572.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.317-719G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96286303 | ||||||
chr8:96286664
|
A | G | 43 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(40): Show | 43 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.317-358A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96286664 | ||||||
chr8:96286728
|
T | C | 18 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(15): Show | 18 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.317-294T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96286728 | ||||||
chr8:96286753
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0003g0193 | 2 | HG00609.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.317-269G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96286753 | ||||||
chr8:96286840
|
G | A | 45 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(42): Show | 45 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(42): Show |
intron_variant | MODIFIER | c.317-182G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96286840 | ||||||
chr8:96286918
|
A | G | 4 | a0001c0001t0001g0186a0001c0001t0001g0190a0001c0001t0001g0221others(1): Show | 4 | HG01074.hp2 HG01243.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-104A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96286918 | ||||||
chr8:96286991
|
C | A | 1 | a0001c0001t0002g0060 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.317-31C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 3/12 | chr8 | 96286991 | ||||||
chr8:96287345
|
C | T | 2 | a0001c0001t0010g0036a0001c0001t0010g0037 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.441+199C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96287345 | ||||||
chr8:96287369
|
T | G | 13 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0004g0152others(10): Show | 13 | HG01167.hp1 HG02258.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+223T>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96287369 | ||||||
chr8:96287541
|
C | T | 1 | a0001c0001t0032g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.441+395C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96287541 | ||||||
chr8:96287572
|
AC | A | 37 | a0001c0001t0001g0043a0001c0001t0001g0064a0001c0001t0001g0065others(34): Show | 37 | HG00609.hp2 HG00642.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.441+430delC | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 96287572 | |||||
chr8:96287706
|
C | A | 46 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(43): Show | 46 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.441+560C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96287706 | ||||||
chr8:96287734
|
A | G | 13 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0004g0152others(10): Show | 13 | HG01167.hp1 HG02258.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+588A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96287734 | ||||||
chr8:96287748
|
A | G | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.441+602A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96287748 | ||||||
chr8:96287748
|
A | T | 1 | a0001c0001t0002g0220 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.441+602A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96287748 | ||||||
chr8:96287776
|
A | G | 1 | a0001c0001t0005g0092 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.441+630A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96287776 | ||||||
chr8:96287805
|
G | A | 4 | a0001c0001t0032g0130a0001c0001t0033g0147a0001c0004t0004g0148others(1): Show | 4 | HG02572.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+659G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96287805 | ||||||
chr8:96288119
|
C | T | 46 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(43): Show | 46 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.441+973C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96288119 | ||||||
chr8:96288281
|
T | C | 5 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0016g0012others(2): Show | 5 | HG02258.hp2 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.441+1135T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96288281 | ||||||
chr8:96288319
|
C | T | 5 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0023g0150others(2): Show | 5 | HG01167.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.441+1173C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96288319 | ||||||
chr8:96288320
|
G | A | 1 | a0001c0001t0001g0194 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.441+1174G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96288320 | ||||||
chr8:96288366
|
C | T | 8 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0006g0032others(5): Show | 8 | HG02258.hp2 HG02809.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.441+1220C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96288366 | ||||||
chr8:96288380
|
A | C | 1 | a0001c0001t0003g0090 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.441+1234A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96288380 | ||||||
chr8:96288402
|
G | A | 46 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(43): Show | 46 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.441+1256G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96288402 | ||||||
chr8:96288414
|
T | A | 4 | a0001c0001t0009g0120a0001c0001t0009g0121a0001c0001t0009g0122others(1): Show | 4 | HG01891.hp1 HG02615.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.441+1268T>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96288414 | ||||||
chr8:96288514
|
G | A | 19 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0009others(16): Show | 19 | HG01261.hp1 HG01891.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.441+1368G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96288514 | ||||||
chr8:96288544
|
G | A | 1 | a0001c0001t0034g0129 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.441+1398G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96288544 | ||||||
chr8:96288575
|
T | C | 46 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(43): Show | 46 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.441+1429T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96288575 | ||||||
chr8:96288625
|
C | CT | 97 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0053others(94): Show | 100 | HG00280.hp1 HG00438.hp1 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.441+1501dupT | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 96288625 | |||||
chr8:96288625
|
C | CTT | 34 | a0001c0001t0001g0047a0001c0001t0001g0075a0001c0001t0001g0086others(31): Show | 34 | HG00438.hp2 HG00621.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.441+1500_441+1501d others(4): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 96288625 | |||||
chr8:96288625
|
C | CTTT | 17 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0004g0132others(14): Show | 17 | HG01081.hp1 HG02258.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.441+1499_441+1501d others(5): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 96288625 | |||||
chr8:96288625
|
C | CTTTT | 16 | a0001c0001t0001g0034a0001c0001t0002g0010a0001c0001t0002g0021others(13): Show | 16 | HG01109.hp1 HG02145.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.441+1498_441+1501d others(6): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 96288625 | |||||
chr8:96288625
|
C | CTTTTT | 20 | a0001c0001t0001g0141a0001c0001t0002g0006a0001c0001t0002g0008others(17): Show | 20 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.441+1497_441+1501d others(7): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 96288625 | |||||
chr8:96288829
|
G | C | 3 | a0001c0001t0003g0048a0001c0001t0003g0049a0001c0001t0003g0050 | 3 | HG01167.hp2 HG01169.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.441+1683G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96288829 | ||||||
chr8:96288969
|
C | T | 6 | a0001c0001t0001g0034a0001c0001t0002g0029a0001c0001t0003g0028others(3): Show | 6 | HG01884.hp2 NA18949.hp2 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.441+1823C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96288969 | ||||||
chr8:96289169
|
A | G | 1 | a0001c0001t0033g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.441+2023A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96289169 | ||||||
chr8:96289863
|
T | C | 68 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0141others(65): Show | 68 | HG00642.hp1 HG01070.hp1 HG01081.hp1 others(65): Show |
intron_variant | MODIFIER | c.441+2717T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96289863 | ||||||
chr8:96289888
|
T | G | 1 | a0001c0001t0002g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.441+2742T>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96289888 | ||||||
chr8:96289914
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.441+2768G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96289914 | ||||||
chr8:96290087
|
G | A | 6 | a0001c0001t0002g0246a0001c0001t0002g0249a0001c0001t0002g0250others(3): Show | 6 | HG00140.hp2 HG00741.hp2 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.441+2941G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96290087 | ||||||
chr8:96290256
|
C | T | 18 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(15): Show | 18 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.441+3110C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96290256 | ||||||
chr8:96290343
|
G | A | 1 | a0001c0001t0001g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.441+3197G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96290343 | ||||||
chr8:96290366
|
C | T | 1 | a0001c0001t0035g0041 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.441+3220C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96290366 | ||||||
chr8:96290481
|
TA | T | 18 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(15): Show | 18 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.441+3336delA | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96290481 | ||||||
chr8:96290549
|
C | T | 1 | a0001c0001t0001g0232 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.441+3403C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96290549 | ||||||
chr8:96290558
|
G | A | 2 | a0001c0001t0001g0242a0001c0001t0003g0104 | 2 | NA18948.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.441+3412G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96290558 | ||||||
chr8:96290861
|
A | G | 1 | a0001c0001t0023g0150 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.441+3715A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96290861 | ||||||
chr8:96290867
|
T | C | 13 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0004g0152others(10): Show | 13 | HG01167.hp1 HG02258.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+3721T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96290867 | ||||||
chr8:96291056
|
T | C | 13 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0004g0152others(10): Show | 13 | HG01167.hp1 HG02258.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.441+3910T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96291056 | ||||||
chr8:96291107
|
C | T | 2 | a0001c0001t0010g0036a0001c0001t0010g0037 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.441+3961C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96291107 | ||||||
chr8:96291171
|
G | A | 1 | a0001c0001t0004g0020 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.442-3927G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96291171 | ||||||
chr8:96291235
|
G | T | 2 | a0001c0001t0010g0036a0001c0001t0010g0037 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.442-3863G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96291235 | ||||||
chr8:96291271
|
G | C | 18 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(15): Show | 18 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-3827G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96291271 | ||||||
chr8:96291452
|
C | CT | 20 | a0001c0001t0001g0103a0001c0001t0001g0126a0001c0001t0001g0141others(17): Show | 20 | HG01109.hp1 HG01175.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.442-3629dupT | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 96291452 | |||||
chr8:96291508
|
T | C | 6 | a0001c0001t0001g0141a0001c0001t0002g0143a0001c0001t0006g0133others(3): Show | 6 | HG02145.hp1 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.442-3590T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96291508 | ||||||
chr8:96291776
|
C | G | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.442-3322C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96291776 | ||||||
chr8:96291780
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.442-3318G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96291780 | ||||||
chr8:96291853
|
G | A | 1 | a0001c0001t0003g0083 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.442-3245G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96291853 | ||||||
chr8:96291938
|
G | A | 46 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(43): Show | 46 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.442-3160G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96291938 | ||||||
chr8:96291985
|
A | G | 18 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(15): Show | 18 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-3113A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96291985 | ||||||
chr8:96292289
|
C | CA | 25 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0053others(22): Show | 25 | HG01175.hp2 HG01358.hp1 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.442-2788dupA | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 96292289 | |||||
chr8:96292289
|
C | CAA | 73 | a0001c0001t0001g0043a0001c0001t0001g0064a0001c0001t0001g0065others(70): Show | 76 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.442-2789_442-2788d others(4): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 96292289 | |||||
chr8:96292289
|
CA | C | 14 | a0001c0001t0001g0180a0001c0001t0002g0155a0001c0001t0002g0158others(11): Show | 14 | HG01167.hp1 HG02258.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.442-2788delA | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 96292289 | |||||
chr8:96292306
|
A | AG | 18 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0009others(15): Show | 18 | HG01261.hp1 HG01891.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.442-2792_442-2791i others(3): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96292306 | ||||||
chr8:96292306
|
A | G | 26 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0023others(23): Show | 26 | HG01081.hp1 HG01109.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.442-2792A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96292306 | ||||||
chr8:96292398
|
A | G | 64 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0141others(61): Show | 64 | HG00642.hp1 HG01070.hp1 HG01081.hp1 others(61): Show |
intron_variant | MODIFIER | c.442-2700A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96292398 | ||||||
chr8:96292520
|
C | A | 4 | a0001c0001t0032g0130a0001c0001t0033g0147a0001c0004t0004g0148others(1): Show | 4 | HG02572.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-2578C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96292520 | ||||||
chr8:96292524
|
C | T | 1 | a0001c0001t0004g0134 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.442-2574C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96292524 | ||||||
chr8:96292817
|
A | G | 4 | a0001c0001t0032g0130a0001c0001t0033g0147a0001c0004t0004g0148others(1): Show | 4 | HG02572.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.442-2281A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96292817 | ||||||
chr8:96293059
|
C | G | 1 | a0001c0001t0002g0102 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.442-2039C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96293059 | ||||||
chr8:96293087
|
C | G | 2 | a0001c0001t0001g0160a0002c0002t0008g0159 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.442-2011C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96293087 | ||||||
chr8:96293365
|
C | T | 1 | a0001c0001t0029g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.442-1733C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96293365 | ||||||
chr8:96293397
|
C | T | 1 | a0001c0001t0031g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.442-1701C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96293397 | ||||||
chr8:96293675
|
C | G | 1 | a0001c0001t0002g0102 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.442-1423C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96293675 | ||||||
chr8:96293679
|
T | C | 164 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0001g0046others(161): Show | 167 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(164): Show |
intron_variant | MODIFIER | c.442-1419T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96293679 | ||||||
chr8:96293716
|
A | G | 18 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(15): Show | 18 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.442-1382A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96293716 | ||||||
chr8:96293808
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.442-1290T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96293808 | ||||||
chr8:96293903
|
G | GC | 84 | a0001c0001t0001g0034a0001c0001t0001g0053a0001c0001t0001g0141others(81): Show | 84 | HG00642.hp1 HG01070.hp1 HG01081.hp1 others(81): Show |
intron_variant | MODIFIER | c.442-1194dupC | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr8 | 96293903 | |||||
chr8:96294059
|
A | G | 46 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(43): Show | 46 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.442-1039A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96294059 | ||||||
chr8:96294829
|
T | A | 1 | a0001c0001t0001g0053 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.442-269T>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96294829 | ||||||
chr8:96294864
|
T | G | 1 | a0001c0001t0002g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.442-234T>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 4/12 | chr8 | 96294864 | ||||||
chr8:96295379
|
T | C | 1 | a0001c0001t0010g0036 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.600+123T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96295379 | ||||||
chr8:96295949
|
A | G | 1 | a0001c0001t0002g0227 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.600+693A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96295949 | ||||||
chr8:96296057
|
C | T | 22 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(19): Show | 22 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.600+801C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96296057 | ||||||
chr8:96296068
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.600+812G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96296068 | ||||||
chr8:96296100
|
C | A | 22 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(19): Show | 22 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.600+844C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96296100 | ||||||
chr8:96296132
|
C | CT | 45 | a0001c0001t0001g0103a0001c0001t0001g0125a0001c0001t0001g0141others(42): Show | 45 | HG00609.hp1 HG00621.hp1 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.600+902dupT | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 96296132 | |||||
chr8:96296132
|
CT | C | 80 | a0001c0001t0001g0043a0001c0001t0001g0064a0001c0001t0001g0065others(77): Show | 83 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.600+902delT | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 96296132 | |||||
chr8:96296161
|
G | A | 44 | a0001c0001t0001g0034a0001c0001t0001g0141a0001c0001t0002g0006others(41): Show | 44 | HG01081.hp1 HG01109.hp1 HG01261.hp1 others(41): Show |
intron_variant | MODIFIER | c.600+905G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96296161 | ||||||
chr8:96296263
|
C | T | 28 | a0001c0001t0001g0034a0001c0001t0002g0006a0001c0001t0002g0008others(25): Show | 28 | HG01081.hp1 HG01261.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.600+1007C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96296263 | ||||||
chr8:96296264
|
G | A | 6 | a0001c0001t0001g0192a0001c0001t0003g0193a0001c0001t0009g0120others(3): Show | 6 | HG00609.hp1 HG01891.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.600+1008G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96296264 | ||||||
chr8:96296695
|
C | T | 4 | a0001c0001t0032g0130a0001c0001t0033g0147a0001c0004t0004g0148others(1): Show | 4 | HG02572.hp2 HG02970.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.600+1439C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96296695 | ||||||
chr8:96296751
|
A | C | 1 | a0001c0001t0002g0124 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.600+1495A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96296751 | ||||||
chr8:96297176
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.600+1920T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96297176 | ||||||
chr8:96297448
|
T | G | 167 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0001g0046others(164): Show | 170 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(167): Show |
intron_variant | MODIFIER | c.600+2192T>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96297448 | ||||||
chr8:96297788
|
G | A | 16 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0002g0009others(13): Show | 16 | HG01891.hp2 HG02280.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.601-1906G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96297788 | ||||||
chr8:96297984
|
C | T | 1 | a0001c0001t0006g0167 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.601-1710C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96297984 | ||||||
chr8:96298318
|
T | C | 2 | a0001c0001t0003g0087a0001c0001t0003g0089 | 2 | NA18951.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.601-1376T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96298318 | ||||||
chr8:96298425
|
T | C | 4 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0016g0012others(1): Show | 4 | HG02258.hp2 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.601-1269T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96298425 | ||||||
chr8:96298531
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.601-1163C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96298531 | ||||||
chr8:96298563
|
C | G | 1 | a0001c0001t0004g0038 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.601-1131C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96298563 | ||||||
chr8:96298572
|
C | T | 1 | a0001c0003t0004g0002 | 2 | HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.601-1122C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96298572 | ||||||
chr8:96298844
|
A | G | 7 | a0001c0001t0004g0132a0001c0001t0004g0134a0001c0001t0004g0137others(4): Show | 7 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.601-850A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96298844 | ||||||
chr8:96298894
|
G | A | 1 | a0001c0001t0032g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.601-800G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96298894 | ||||||
chr8:96298965
|
G | A | 3 | a0001c0001t0002g0158a0001c0001t0024g0156a0002c0002t0008g0157 | 3 | HG01167.hp1 HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.601-729G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96298965 | ||||||
chr8:96299041
|
G | GA | 11 | a0001c0001t0001g0066a0001c0001t0001g0168a0001c0001t0002g0155others(8): Show | 11 | HG01167.hp1 HG02630.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.601-637dupA | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr8 | 96299041 | |||||
chr8:96299136
|
T | G | 2 | a0001c0001t0007g0014a0001c0001t0007g0015 | 2 | HG01891.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.601-558T>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96299136 | ||||||
chr8:96299294
|
A | G | 1 | a0001c0005t0002g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.601-400A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96299294 | ||||||
chr8:96299597
|
C | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0195 | 2 | HG01109.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.601-97C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96299597 | ||||||
chr8:96299602
|
A | G | 41 | a0001c0001t0001g0141a0001c0001t0002g0006a0001c0001t0002g0008others(38): Show | 41 | HG01069.hp1 HG01081.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.601-92A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 5/12 | chr8 | 96299602 | ||||||
chr8:96300126
|
C | T | 1 | a0001c0001t0003g0079 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.752+281C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96300126 | ||||||
chr8:96300214
|
T | G | 22 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(19): Show | 22 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.752+369T>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96300214 | ||||||
chr8:96300258
|
G | C | 159 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0047others(156): Show | 162 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(159): Show |
intron_variant | MODIFIER | c.752+413G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96300258 | ||||||
chr8:96300369
|
C | T | 5 | a0001c0001t0001g0141a0001c0001t0002g0143a0002c0002t0008g0131others(2): Show | 5 | HG02145.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.752+524C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96300369 | ||||||
chr8:96300499
|
A | G | 2 | a0001c0001t0003g0083a0001c0001t0003g0118 | 2 | HG02015.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.752+654A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96300499 | ||||||
chr8:96300585
|
G | A | 16 | a0001c0001t0001g0141a0001c0001t0002g0143a0001c0001t0004g0132others(13): Show | 16 | HG01109.hp1 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.752+740G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96300585 | ||||||
chr8:96301077
|
A | C | 1 | a0001c0001t0006g0176 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.752+1232A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96301077 | ||||||
chr8:96301116
|
T | C | 4 | a0001c0001t0006g0032a0001c0001t0011g0031a0001c0001t0027g0151others(1): Show | 4 | HG02809.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.752+1271T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96301116 | ||||||
chr8:96301145
|
A | G | 1 | a0001c0001t0003g0087 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.752+1300A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96301145 | ||||||
chr8:96301375
|
G | A | 1 | a0001c0001t0002g0227 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.752+1530G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96301375 | ||||||
chr8:96301382
|
A | G | 1 | a0001c0001t0009g0091 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.752+1537A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96301382 | ||||||
chr8:96301414
|
A | G | 2 | a0001c0001t0010g0036a0001c0001t0010g0037 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.752+1569A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96301414 | ||||||
chr8:96301565
|
G | A | 5 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0256others(2): Show | 5 | HG03669.hp2 HG03831.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.752+1720G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96301565 | ||||||
chr8:96301576
|
A | G | 4 | a0001c0001t0001g0186a0001c0001t0001g0190a0001c0001t0001g0221others(1): Show | 4 | HG01074.hp2 HG01243.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.752+1731A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96301576 | ||||||
chr8:96301578
|
G | A | 10 | a0001c0001t0001g0183a0001c0001t0001g0224a0001c0001t0002g0225others(7): Show | 10 | HG01358.hp1 HG01496.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.752+1733G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96301578 | ||||||
chr8:96301613
|
A | T | 2 | a0001c0001t0002g0057a0001c0001t0002g0061 | 2 | HG02683.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.752+1768A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96301613 | ||||||
chr8:96301668
|
G | A | 2 | a0001c0001t0010g0036a0001c0001t0010g0037 | 2 | HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.752+1823G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96301668 | ||||||
chr8:96301790
|
A | G | 2 | a0001c0001t0001g0160a0002c0002t0008g0159 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.752+1945A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96301790 | ||||||
chr8:96302003
|
A | G | 2 | a0001c0004t0004g0148a0001c0004t0022g0154 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.753-2037A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96302003 | ||||||
chr8:96302161
|
A | C | 1 | a0001c0001t0001g0114 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.753-1879A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96302161 | ||||||
chr8:96302306
|
A | G | 1 | a0001c0001t0002g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.753-1734A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96302306 | ||||||
chr8:96302521
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.753-1519G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96302521 | ||||||
chr8:96302576
|
C | CTTG | 105 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0047others(102): Show | 108 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.753-1446_753-1444d others(5): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr8 | 96302576 | |||||
chr8:96302735
|
C | T | 1 | a0001c0001t0011g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.753-1305C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96302735 | ||||||
chr8:96302754
|
G | A | 2 | a0001c0001t0004g0152a0001c0001t0004g0153 | 2 | HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.753-1286G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96302754 | ||||||
chr8:96303037
|
A | G | 1 | a0001c0001t0007g0025 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.753-1003A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96303037 | ||||||
chr8:96303244
|
C | T | 22 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(19): Show | 22 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.753-796C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96303244 | ||||||
chr8:96303330
|
C | T | 4 | a0001c0001t0006g0032a0001c0001t0011g0031a0001c0001t0027g0151others(1): Show | 4 | HG02809.hp2 HG02886.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.753-710C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96303330 | ||||||
chr8:96303417
|
A | C | 22 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(19): Show | 22 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.753-623A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96303417 | ||||||
chr8:96303437
|
T | C | 2 | a0001c0001t0001g0160a0002c0002t0008g0159 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.753-603T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96303437 | ||||||
chr8:96303628
|
G | T | 1 | a0001c0001t0001g0114 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.753-412G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96303628 | ||||||
chr8:96303785
|
G | A | 256 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(253): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.753-255G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96303785 | ||||||
chr8:96303849
|
T | C | 5 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0023g0150others(2): Show | 5 | HG01167.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.753-191T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96303849 | ||||||
chr8:96303933
|
C | T | 3 | a0001c0001t0010g0036a0001c0001t0010g0037a0001c0001t0010g0127 | 3 | HG01081.hp1 HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.753-107C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96303933 | ||||||
chr8:96304004
|
C | A | 1 | a0001c0001t0035g0041 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.753-36C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 6/12 | chr8 | 96304004 | ||||||
chr8:96304593
|
T | G | 109 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0047others(106): Show | 112 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.894+412T>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96304593 | ||||||
chr8:96304598
|
C | A | 1 | a0002c0002t0008g0157 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.894+417C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96304598 | ||||||
chr8:96304666
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.894+485G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96304666 | ||||||
chr8:96304706
|
G | A | 22 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0009others(19): Show | 22 | HG01069.hp1 HG01261.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.894+525G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96304706 | ||||||
chr8:96304775
|
A | G | 2 | a0001c0001t0001g0160a0002c0002t0008g0159 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.894+594A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96304775 | ||||||
chr8:96304953
|
T | C | 26 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(23): Show | 26 | HG00642.hp1 HG01070.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.894+772T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96304953 | ||||||
chr8:96304978
|
A | G | 2 | a0001c0001t0017g0111a0001c0001t0018g0112 | 2 | HG01243.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.894+797A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96304978 | ||||||
chr8:96305022
|
G | A | 2 | a0001c0001t0032g0130a0001c0001t0033g0147 | 2 | HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.894+841G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96305022 | ||||||
chr8:96305044
|
A | T | 21 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(18): Show | 21 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.894+863A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96305044 | ||||||
chr8:96305081
|
A | G | 5 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0023g0150others(2): Show | 5 | HG01167.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.894+900A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96305081 | ||||||
chr8:96305181
|
G | A | 82 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0047others(79): Show | 85 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.894+1000G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96305181 | ||||||
chr8:96305214
|
C | T | 2 | a0001c0001t0004g0038a0001c0005t0002g0011 | 2 | HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.894+1033C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96305214 | ||||||
chr8:96305487
|
A | G | 1 | a0001c0001t0002g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.895-957A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96305487 | ||||||
chr8:96305591
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.895-853T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96305591 | ||||||
chr8:96305736
|
A | T | 5 | a0001c0001t0002g0155a0001c0001t0002g0158a0001c0001t0023g0150others(2): Show | 5 | HG01167.hp1 HG02630.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.895-708A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96305736 | ||||||
chr8:96305749
|
C | T | 2 | a0001c0001t0032g0130a0001c0001t0033g0147 | 2 | HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.895-695C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96305749 | ||||||
chr8:96305872
|
G | C | 1 | a0001c0003t0002g0001 | 3 | HG02895.hp1 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.895-572G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96305872 | ||||||
chr8:96306083
|
G | A | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0256others(6): Show | 9 | HG01891.hp1 HG02615.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.895-361G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96306083 | ||||||
chr8:96306275
|
G | A | 1 | a0001c0001t0033g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.895-169G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96306275 | ||||||
chr8:96306304
|
A | G | 3 | a0001c0001t0010g0036a0001c0001t0010g0037a0001c0001t0010g0127 | 3 | HG01081.hp1 HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.895-140A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96306304 | ||||||
chr8:96306362
|
A | G | 9 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0256others(6): Show | 9 | HG01891.hp1 HG02615.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.895-82A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96306362 | ||||||
chr8:96306432
|
C | T | 21 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(18): Show | 21 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.895-12C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 7/12 | chr8 | 96306432 | ||||||
chr8:96306607
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1007+51A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96306607 | ||||||
chr8:96306657
|
G | A | 1 | a0001c0001t0002g0009 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1007+101G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96306657 | ||||||
chr8:96306669
|
G | A | 1 | a0001c0001t0033g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1007+113G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96306669 | ||||||
chr8:96307051
|
G | C | 1 | a0001c0001t0001g0214 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1007+495G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96307051 | ||||||
chr8:96307449
|
C | CA | 23 | a0001c0001t0001g0126a0001c0001t0001g0168a0001c0001t0001g0183others(20): Show | 23 | HG00280.hp2 HG00621.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1007+923dupA | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 96307449 | |||||
chr8:96307449
|
CA | C | 11 | a0001c0001t0001g0206a0001c0001t0002g0158a0001c0001t0002g0234others(8): Show | 11 | HG00733.hp2 HG01167.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1007+923delA | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 96307449 | |||||
chr8:96307449
|
CAA | C | 6 | a0001c0001t0001g0141a0001c0001t0002g0143a0001c0001t0003g0028others(3): Show | 6 | HG02145.hp1 HG02698.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007+922_1007+923d others(4): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 96307449 | |||||
chr8:96307449
|
CAAA | C | 24 | a0001c0001t0001g0053a0001c0001t0001g0086a0001c0001t0001g0093others(21): Show | 24 | HG00438.hp2 HG00621.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.1007+921_1007+923d others(5): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 96307449 | |||||
chr8:96307449
|
CAAAA | C | 116 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0047others(113): Show | 119 | HG00609.hp2 HG00733.hp1 HG00741.hp1 others(116): Show |
intron_variant | MODIFIER | c.1007+920_1007+923d others(6): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 96307449 | |||||
chr8:96307449
|
CAAAAA | C | 5 | a0001c0001t0001g0065a0001c0001t0001g0160a0001c0001t0002g0023others(2): Show | 5 | HG01071.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1007+919_1007+923d others(7): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 96307449 | |||||
chr8:96307449
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0003g0072a0001c0001t0013g0088 | 2 | HG00280.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.1007+913_1007+923d others(13): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 96307449 | |||||
chr8:96307473
|
A | G | 1 | a0003c0006t0037g0044 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1007+917A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96307473 | ||||||
chr8:96307876
|
A | G | 22 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0009others(19): Show | 22 | HG01069.hp1 HG01261.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1007+1320A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96307876 | ||||||
chr8:96307889
|
C | T | 5 | a0001c0001t0001g0141a0001c0001t0002g0143a0002c0002t0008g0131others(2): Show | 5 | HG02145.hp1 HG02895.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1007+1333C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96307889 | ||||||
chr8:96307913
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1007+1357C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96307913 | ||||||
chr8:96308009
|
T | C | 1 | a0001c0001t0006g0032 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1007+1453T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96308009 | ||||||
chr8:96308037
|
G | A | 1 | a0001c0001t0001g0114 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1007+1481G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96308037 | ||||||
chr8:96308251
|
T | C | 1 | a0001c0001t0023g0150 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1008-1306T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96308251 | ||||||
chr8:96308339
|
A | G | 3 | a0001c0001t0010g0036a0001c0001t0010g0037a0001c0001t0010g0127 | 3 | HG01081.hp1 HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1008-1218A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96308339 | ||||||
chr8:96308377
|
G | A | 17 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(14): Show | 17 | HG00642.hp1 HG01070.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1008-1180G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96308377 | ||||||
chr8:96308628
|
A | G | 1 | a0001c0001t0035g0041 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1008-929A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96308628 | ||||||
chr8:96308799
|
C | T | 2 | a0001c0001t0002g0119a0001c0001t0025g0085 | 2 | HG02572.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1008-758C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96308799 | ||||||
chr8:96308804
|
GAATTTAA | G | 2 | a0001c0004t0004g0148a0001c0004t0022g0154 | 2 | HG02572.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1008-748_1008-742d others(9): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 96308804 | |||||
chr8:96308844
|
C | T | 1 | a0001c0001t0029g0016 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1008-713C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96308844 | ||||||
chr8:96309193
|
GT | G | 70 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0066others(67): Show | 71 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.1008-334delT | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 96309193 | |||||
chr8:96309193
|
GTT | G | 21 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0108others(18): Show | 21 | HG00642.hp1 HG00733.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1008-335_1008-334d others(4): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 96309193 | |||||
chr8:96309193
|
GTTT | G | 46 | a0001c0001t0001g0053a0001c0001t0001g0098a0001c0001t0001g0141others(43): Show | 46 | HG00438.hp2 HG01070.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.1008-336_1008-334d others(5): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 96309193 | |||||
chr8:96309193
|
GTTTT | G | 94 | a0001c0001t0001g0043a0001c0001t0001g0064a0001c0001t0001g0065others(91): Show | 97 | HG00280.hp1 HG00609.hp2 HG00621.hp2 others(94): Show |
intron_variant | MODIFIER | c.1008-337_1008-334d others(6): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr8 | 96309193 | |||||
chr8:96309196
|
T | G | 1 | a0001c0001t0002g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1008-361T>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96309196 | ||||||
chr8:96309204
|
T | G | 1 | a0001c0001t0003g0090 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1008-353T>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96309204 | ||||||
chr8:96309331
|
G | A | 1 | a0001c0001t0031g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1008-226G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 8/12 | chr8 | 96309331 | ||||||
chr8:96309670
|
T | A | 125 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0001g0046others(122): Show | 128 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(125): Show |
intron_variant | MODIFIER | c.1073+48T>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96309670 | ||||||
chr8:96309731
|
A | G | 23 | a0001c0001t0001g0053a0001c0001t0002g0055a0001c0001t0002g0056others(20): Show | 23 | HG00642.hp1 HG01070.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1073+109A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96309731 | ||||||
chr8:96309749
|
A | ATATATC | 36 | a0001c0001t0001g0053a0001c0001t0001g0141a0001c0001t0002g0055others(33): Show | 36 | HG00642.hp1 HG01070.hp1 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1073+145_1073+150d others(8): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96309749 | |||||
chr8:96309749
|
A | ATATATCT others(5): Show |
1 | a0001c0001t0034g0129 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1073+139_1073+150d others(14): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96309749 | |||||
chr8:96310012
|
AATTAGCT others(249): Show |
A | 1 | a0001c0001t0001g0125 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1073+394_1073+649d others(2): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96310012 | |||||
chr8:96310053
|
C | T | 1 | a0001c0001t0003g0072 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1073+431C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310053 | ||||||
chr8:96310129
|
A | T | 1 | a0001c0001t0001g0034 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1073+507A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310129 | ||||||
chr8:96310169
|
C | CT | 84 | a0001c0001t0001g0034a0001c0001t0001g0047a0001c0001t0001g0067others(81): Show | 84 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.1073+562dupT | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96310169 | |||||
chr8:96310169
|
C | CTT | 22 | a0001c0001t0002g0006a0001c0001t0002g0009a0001c0001t0002g0018others(19): Show | 22 | HG01069.hp1 HG01261.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1073+561_1073+562d others(4): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96310169 | |||||
chr8:96310169
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1073+547C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310169 | ||||||
chr8:96310282
|
AGCCTCCC others(125): Show |
A | 1 | a0001c0001t0001g0125 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1073+670_1073+801d others(2): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96310282 | |||||
chr8:96310289
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0221 | 2 | HG00140.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1073+667C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310289 | ||||||
chr8:96310312
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1073+690G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310312 | ||||||
chr8:96310332
|
G | T | 4 | a0001c0001t0001g0068a0001c0001t0002g0055a0001c0001t0002g0155others(1): Show | 4 | HG01517.hp1 HG02735.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073+710G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310332 | ||||||
chr8:96310365
|
G | A | 19 | a0001c0001t0001g0206a0001c0001t0002g0119a0001c0001t0002g0196others(16): Show | 22 | HG00280.hp2 HG00733.hp2 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.1073+743G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310365 | ||||||
chr8:96310411
|
C | G | 1 | a0001c0004t0022g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1073+789C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310411 | ||||||
chr8:96310411
|
C | T | 3 | a0001c0001t0011g0035a0001c0003t0002g0001a0001c0003t0004g0002 | 6 | HG02717.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1073+789C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310411 | ||||||
chr8:96310442
|
A | G | 5 | a0001c0001t0002g0008a0001c0001t0002g0084a0001c0001t0007g0005others(2): Show | 5 | HG02622.hp1 HG02965.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073+820A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310442 | ||||||
chr8:96310451
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1073+829C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310451 | ||||||
chr8:96310452
|
G | A | 2 | a0001c0001t0001g0174a0001c0001t0001g0195 | 2 | HG01109.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1073+830G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310452 | ||||||
chr8:96310470
|
CT | C | 7 | a0001c0001t0001g0053a0001c0001t0002g0056a0001c0001t0002g0058others(4): Show | 7 | HG00642.hp1 HG01168.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1073+861delT | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96310470 | |||||
chr8:96310484
|
A | T | 1 | a0001c0001t0028g0184 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1073+862A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310484 | ||||||
chr8:96310630
|
A | T | 5 | a0001c0001t0002g0008a0001c0001t0002g0084a0001c0001t0013g0142others(2): Show | 5 | HG02965.hp2 HG03540.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073+1008A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310630 | ||||||
chr8:96310636
|
T | C | 50 | a0001c0001t0001g0206a0001c0001t0001g0236a0001c0001t0002g0004others(47): Show | 50 | HG00140.hp2 HG00280.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1073+1014T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310636 | ||||||
chr8:96310709
|
A | G | 2 | a0001c0001t0001g0160a0002c0002t0008g0159 | 2 | HG02257.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1073+1087A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310709 | ||||||
chr8:96310753
|
G | A | 1 | a0001c0001t0006g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1073+1131G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310753 | ||||||
chr8:96310834
|
C | T | 1 | a0001c0001t0002g0202 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1073+1212C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310834 | ||||||
chr8:96310909
|
G | A | 5 | a0001c0001t0006g0026a0001c0001t0006g0117a0001c0001t0006g0167others(2): Show | 5 | HG00609.hp2 NA18943.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073+1287G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96310909 | ||||||
chr8:96311001
|
G | A | 8 | a0001c0001t0001g0141a0002c0002t0008g0052a0002c0002t0008g0131others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1073+1379G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96311001 | ||||||
chr8:96311061
|
C | T | 3 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0018g0112 | 3 | HG01884.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1073+1439C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96311061 | ||||||
chr8:96311253
|
G | A | 215 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(212): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1073+1631G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96311253 | ||||||
chr8:96311256
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1073+1634C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96311256 | ||||||
chr8:96311257
|
A | G | 81 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(78): Show | 82 | HG00438.hp1 HG00621.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1073+1635A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96311257 | ||||||
chr8:96311519
|
C | G | 1 | a0001c0004t0022g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1073+1897C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96311519 | ||||||
chr8:96311615
|
A | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(78): Show | 82 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.1073+1993A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96311615 | ||||||
chr8:96311680
|
T | A | 214 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(211): Show | 218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1073+2058T>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96311680 | ||||||
chr8:96311790
|
A | T | 1 | a0001c0001t0027g0151 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1073+2168A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96311790 | ||||||
chr8:96311854
|
A | C | 1 | a0001c0004t0022g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1073+2232A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96311854 | ||||||
chr8:96311888
|
G | A | 85 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(82): Show | 86 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.1073+2266G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96311888 | ||||||
chr8:96311940
|
G | C | 214 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(211): Show | 218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1073+2318G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96311940 | ||||||
chr8:96312054
|
T | C | 90 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(87): Show | 91 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.1073+2432T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96312054 | ||||||
chr8:96312277
|
G | A | 3 | a0001c0001t0010g0036a0001c0001t0010g0037a0001c0001t0010g0127 | 3 | HG01081.hp1 HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1073+2655G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96312277 | ||||||
chr8:96312287
|
C | T | 1 | a0001c0001t0033g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1073+2665C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96312287 | ||||||
chr8:96312462
|
C | CT | 15 | a0001c0001t0006g0133a0001c0001t0009g0091a0001c0001t0009g0120others(12): Show | 18 | HG01257.hp2 HG01891.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1073+2855dupT | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96312462 | |||||
chr8:96312462
|
CT | C | 34 | a0001c0001t0001g0094a0001c0001t0001g0164a0001c0001t0002g0004others(31): Show | 34 | HG00280.hp2 HG01069.hp1 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.1073+2855delT | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96312462 | |||||
chr8:96312478
|
A | T | 9 | a0001c0001t0001g0047a0001c0001t0009g0091a0001c0001t0009g0120others(6): Show | 9 | HG01257.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073+2856A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96312478 | ||||||
chr8:96312529
|
C | G | 1 | a0001c0001t0001g0189 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1073+2907C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96312529 | ||||||
chr8:96312745
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1073+3123G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96312745 | ||||||
chr8:96312794
|
A | G | 4 | a0001c0001t0010g0059a0001c0001t0016g0012a0001c0001t0016g0013others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1073+3172A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96312794 | ||||||
chr8:96312825
|
G | A | 1 | a0001c0001t0005g0163 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1073+3203G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96312825 | ||||||
chr8:96312958
|
C | A | 1 | a0001c0001t0002g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1073+3336C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96312958 | ||||||
chr8:96313095
|
C | T | 3 | a0001c0001t0003g0083a0001c0001t0034g0129a0001c0001t0035g0041 | 3 | HG02015.hp2 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1073+3473C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96313095 | ||||||
chr8:96313124
|
C | A | 1 | a0001c0001t0017g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1073+3502C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96313124 | ||||||
chr8:96313145
|
C | T | 2 | a0001c0001t0024g0156a0001c0004t0022g0154 | 2 | HG01167.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1073+3523C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96313145 | ||||||
chr8:96313293
|
C | T | 3 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0018g0112 | 3 | HG01884.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1073+3671C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96313293 | ||||||
chr8:96313294
|
G | A | 8 | a0001c0001t0001g0141a0002c0002t0008g0052a0002c0002t0008g0131others(5): Show | 8 | HG02145.hp1 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1073+3672G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96313294 | ||||||
chr8:96313394
|
C | T | 98 | a0001c0001t0001g0053a0001c0001t0002g0004a0001c0001t0002g0006others(95): Show | 98 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(95): Show |
intron_variant | MODIFIER | c.1073+3772C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96313394 | ||||||
chr8:96313543
|
G | A | 4 | a0001c0001t0010g0059a0001c0001t0016g0012a0001c0001t0016g0013others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1073+3921G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96313543 | ||||||
chr8:96313732
|
C | T | 1 | a0001c0001t0003g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1073+4110C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96313732 | ||||||
chr8:96313734
|
T | C | 1 | a0001c0001t0003g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1073+4112T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96313734 | ||||||
chr8:96313859
|
T | G | 114 | a0001c0001t0001g0053a0001c0001t0001g0141a0001c0001t0002g0004others(111): Show | 114 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.1073+4237T>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96313859 | ||||||
chr8:96314238
|
G | T | 100 | a0001c0001t0001g0053a0001c0001t0002g0004a0001c0001t0002g0006others(97): Show | 100 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.1073+4616G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96314238 | ||||||
chr8:96314340
|
C | T | 3 | a0001c0001t0010g0036a0001c0001t0010g0037a0001c0001t0010g0127 | 3 | HG01081.hp1 HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1073+4718C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96314340 | ||||||
chr8:96314341
|
G | A | 1 | a0001c0001t0013g0142 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1073+4719G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96314341 | ||||||
chr8:96314354
|
T | C | 1 | a0001c0001t0034g0129 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1073+4732T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96314354 | ||||||
chr8:96314421
|
G | A | 1 | a0001c0001t0013g0247 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1073+4799G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96314421 | ||||||
chr8:96314435
|
A | AG | 215 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(212): Show | 219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1073+4819dupG | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96314435 | |||||
chr8:96314443
|
C | A | 100 | a0001c0001t0001g0053a0001c0001t0002g0004a0001c0001t0002g0006others(97): Show | 100 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.1073+4821C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96314443 | ||||||
chr8:96314468
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1073+4846G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96314468 | ||||||
chr8:96314478
|
T | C | 1 | a0001c0001t0003g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1073+4856T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96314478 | ||||||
chr8:96314479
|
G | T | 1 | a0001c0001t0003g0172 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1073+4857G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96314479 | ||||||
chr8:96314553
|
C | G | 1 | a0001c0001t0024g0156 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1073+4931C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96314553 | ||||||
chr8:96314555
|
C | G | 6 | a0001c0001t0002g0009a0001c0001t0002g0021a0001c0001t0002g0022others(3): Show | 6 | HG02280.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1073+4933C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96314555 | ||||||
chr8:96314584
|
C | A | 1 | a0001c0001t0031g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1073+4962C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96314584 | ||||||
chr8:96314690
|
G | T | 28 | a0001c0001t0001g0053a0001c0001t0002g0006a0001c0001t0002g0008others(25): Show | 28 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1073+5068G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96314690 | ||||||
chr8:96314717
|
G | A | 1 | a0001c0001t0033g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1073+5095G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96314717 | ||||||
chr8:96314888
|
G | A | 100 | a0001c0001t0001g0053a0001c0001t0002g0004a0001c0001t0002g0006others(97): Show | 100 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.1073+5266G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96314888 | ||||||
chr8:96314978
|
G | C | 1 | a0001c0001t0002g0029 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1074-5268G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96314978 | ||||||
chr8:96315001
|
T | C | 112 | a0001c0001t0001g0053a0001c0001t0001g0141a0001c0001t0002g0004others(109): Show | 112 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.1074-5245T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96315001 | ||||||
chr8:96315066
|
G | T | 100 | a0001c0001t0001g0053a0001c0001t0002g0004a0001c0001t0002g0006others(97): Show | 100 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.1074-5180G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96315066 | ||||||
chr8:96315067
|
G | T | 100 | a0001c0001t0001g0053a0001c0001t0002g0004a0001c0001t0002g0006others(97): Show | 100 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(97): Show |
intron_variant | MODIFIER | c.1074-5179G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96315067 | ||||||
chr8:96315235
|
A | T | 3 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0018g0112 | 3 | HG01884.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1074-5011A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96315235 | ||||||
chr8:96315256
|
G | A | 2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1074-4990G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96315256 | ||||||
chr8:96315306
|
A | G | 5 | a0001c0001t0001g0141a0002c0002t0008g0131a0002c0002t0008g0136others(2): Show | 5 | HG02145.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1074-4940A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96315306 | ||||||
chr8:96315451
|
A | T | 37 | a0001c0001t0004g0020a0001c0001t0004g0038a0001c0001t0004g0132others(34): Show | 37 | HG00280.hp1 HG00609.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.1074-4795A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96315451 | ||||||
chr8:96315600
|
C | G | 2 | a0001c0001t0001g0053a0001c0001t0002g0056 | 2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1074-4646C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96315600 | ||||||
chr8:96315647
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1074-4599C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96315647 | ||||||
chr8:96315696
|
A | G | 3 | a0001c0001t0010g0059a0001c0001t0016g0012a0001c0001t0016g0013 | 3 | HG02258.hp2 HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1074-4550A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96315696 | ||||||
chr8:96315861
|
C | A | 4 | a0001c0001t0032g0130a0001c0001t0034g0129a0001c0001t0035g0041others(1): Show | 4 | HG03195.hp1 HG03209.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074-4385C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96315861 | ||||||
chr8:96315891
|
C | T | 1 | a0001c0001t0019g0255 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1074-4355C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96315891 | ||||||
chr8:96315898
|
A | C | 1 | a0001c0001t0002g0061 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1074-4348A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96315898 | ||||||
chr8:96316045
|
C | A | 2 | a0001c0003t0002g0001a0001c0003t0004g0002 | 5 | HG02895.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-4201C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96316045 | ||||||
chr8:96316076
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1074-4170C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96316076 | ||||||
chr8:96316080
|
C | T | 212 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(209): Show | 216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1074-4166C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96316080 | ||||||
chr8:96316139
|
G | C | 1 | a0001c0001t0023g0150 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1074-4107G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96316139 | ||||||
chr8:96316141
|
T | A | 1 | a0001c0001t0031g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1074-4105T>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96316141 | ||||||
chr8:96316270
|
G | A | 3 | a0001c0001t0010g0036a0001c0001t0010g0037a0001c0001t0010g0127 | 3 | HG01081.hp1 HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1074-3976G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96316270 | ||||||
chr8:96316294
|
C | T | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1074-3952C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96316294 | ||||||
chr8:96316306
|
C | A | 11 | a0001c0001t0010g0036a0001c0001t0010g0037a0001c0001t0010g0127others(8): Show | 11 | HG01081.hp1 HG02145.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.1074-3940C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96316306 | ||||||
chr8:96316318
|
C | T | 3 | a0001c0001t0010g0036a0001c0001t0010g0037a0001c0001t0010g0127 | 3 | HG01081.hp1 HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1074-3928C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96316318 | ||||||
chr8:96316407
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1074-3839T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96316407 | ||||||
chr8:96316430
|
C | G | 1 | a0001c0001t0001g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1074-3816C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96316430 | ||||||
chr8:96316687
|
A | T | 1 | a0001c0001t0001g0086 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1074-3559A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96316687 | ||||||
chr8:96316720
|
G | A | 14 | a0001c0001t0010g0036a0001c0001t0010g0037a0001c0001t0010g0059others(11): Show | 14 | HG01081.hp1 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1074-3526G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96316720 | ||||||
chr8:96316733
|
C | G | 3 | a0001c0001t0003g0104a0001c0001t0003g0200a0001c0001t0021g0201 | 3 | NA18952.hp2 NA18971.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1074-3513C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96316733 | ||||||
chr8:96317033
|
C | CTA | 210 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(207): Show | 211 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.1074-3205_1074-320 others(6): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317033 | |||||
chr8:96317057
|
A | ATGTGTGT others(3): Show |
4 | a0001c0001t0010g0036a0001c0001t0010g0037a0001c0001t0010g0059others(1): Show | 4 | HG01081.hp1 HG02145.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1074-3183_1074-317 others(14): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317057 | |||||
chr8:96317071
|
G | A | 2 | a0001c0003t0002g0001a0001c0003t0004g0002 | 5 | HG02895.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-3175G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317071 | ||||||
chr8:96317071
|
G | GTGTGTAT others(1): Show |
26 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0042others(23): Show | 26 | HG00280.hp1 HG00609.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.1074-3174_1074-317 others(12): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317071 | |||||
chr8:96317071
|
G | GTGTGTGT others(1): Show |
69 | a0001c0001t0001g0053a0001c0001t0002g0004a0001c0001t0002g0009others(66): Show | 69 | HG00280.hp2 HG00642.hp1 HG01069.hp1 others(66): Show |
intron_variant | MODIFIER | c.1074-3174_1074-317 others(12): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317071 | |||||
chr8:96317071
|
G | GTGTGTGT others(3): Show |
2 | a0001c0001t0016g0012a0001c0001t0016g0013 | 2 | HG02258.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1074-3174_1074-317 others(14): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317071 | |||||
chr8:96317071
|
G | GTGTGTGT others(3): Show |
14 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0010others(11): Show | 14 | HG02647.hp2 HG02717.hp1 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.1074-3174_1074-317 others(14): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317071 | |||||
chr8:96317071
|
G | GTGTGTGT others(7): Show |
1 | a0001c0001t0002g0124 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1074-3174_1074-317 others(18): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317071 | |||||
chr8:96317073
|
A | G | 2 | a0001c0001t0034g0129a0001c0001t0035g0041 | 2 | HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1074-3173A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317073 | ||||||
chr8:96317075
|
A | G | 2 | a0001c0001t0034g0129a0001c0001t0035g0041 | 2 | HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1074-3171A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317075 | ||||||
chr8:96317077
|
A | G | 2 | a0001c0001t0034g0129a0001c0001t0035g0041 | 2 | HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1074-3169A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317077 | ||||||
chr8:96317079
|
A | G | 2 | a0001c0001t0034g0129a0001c0001t0035g0041 | 2 | HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1074-3167A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317079 | ||||||
chr8:96317090
|
G | T | 2 | a0001c0001t0034g0129a0001c0001t0035g0041 | 2 | HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1074-3156G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317090 | ||||||
chr8:96317092
|
G | T | 2 | a0001c0001t0034g0129a0001c0001t0035g0041 | 2 | HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1074-3154G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317092 | ||||||
chr8:96317094
|
G | T | 2 | a0001c0001t0034g0129a0001c0001t0035g0041 | 2 | HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1074-3152G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317094 | ||||||
chr8:96317096
|
G | T | 2 | a0001c0001t0034g0129a0001c0001t0035g0041 | 2 | HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1074-3150G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317096 | ||||||
chr8:96317098
|
C | T | 2 | a0001c0001t0034g0129a0001c0001t0035g0041 | 2 | HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1074-3148C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317098 | ||||||
chr8:96317099
|
A | G | 2 | a0001c0001t0034g0129a0001c0001t0035g0041 | 2 | HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1074-3147A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317099 | ||||||
chr8:96317138
|
C | A | 103 | a0001c0001t0001g0053a0001c0001t0002g0004a0001c0001t0002g0006others(100): Show | 103 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.1074-3108C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317138 | ||||||
chr8:96317288
|
T | C | 1 | a0001c0005t0002g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1074-2958T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317288 | ||||||
chr8:96317345
|
G | A | 1 | a0001c0001t0024g0156 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1074-2901G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317345 | ||||||
chr8:96317429
|
C | CT | 210 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(207): Show | 211 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.1074-2817_1074-281 others(5): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317429 | ||||||
chr8:96317533
|
G | A | 1 | a0001c0001t0003g0245 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1074-2713G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317533 | ||||||
chr8:96317715
|
A | G | 63 | a0001c0001t0001g0053a0001c0001t0002g0006a0001c0001t0002g0008others(60): Show | 63 | HG00280.hp1 HG00609.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1074-2531A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317715 | ||||||
chr8:96317729
|
G | A | 2 | a0001c0001t0034g0129a0001c0001t0035g0041 | 2 | HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1074-2517G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317729 | ||||||
chr8:96317753
|
A | C | 1 | a0001c0001t0001g0043 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1074-2493A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317753 | ||||||
chr8:96317757
|
G | GA | 80 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(77): Show | 81 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1074-2483dupA | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317757 | |||||
chr8:96317790
|
T | C | 3 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0018g0112 | 3 | HG01884.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1074-2456T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317790 | ||||||
chr8:96317838
|
C | G | 8 | a0001c0001t0033g0147a0002c0002t0008g0052a0002c0002t0008g0131others(5): Show | 8 | HG02717.hp1 HG02818.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1074-2408C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317838 | ||||||
chr8:96317878
|
A | AGT | 7 | a0001c0001t0003g0083a0001c0001t0003g0252a0001c0001t0014g0166others(4): Show | 9 | HG01934.hp2 HG02015.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.1074-2327_1074-232 others(6): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317878 | |||||
chr8:96317878
|
A | AGTGT | 3 | a0001c0001t0001g0231a0001c0001t0003g0081a0001c0001t0014g0209 | 3 | HG00438.hp2 HG01975.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1074-2329_1074-232 others(8): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317878 | |||||
chr8:96317878
|
A | AGTGTGT | 3 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0018g0112 | 3 | HG01884.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1074-2331_1074-232 others(10): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317878 | |||||
chr8:96317878
|
AGT | A | 9 | a0001c0001t0001g0086a0001c0001t0003g0045a0001c0001t0003g0082others(6): Show | 10 | HG00621.hp2 HG00642.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1074-2327_1074-232 others(6): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317878 | |||||
chr8:96317878
|
AGTGT | A | 10 | a0001c0001t0001g0180a0001c0001t0003g0096a0001c0001t0003g0099others(7): Show | 10 | HG00609.hp1 HG02056.hp1 HG03209.hp1 others(7): Show |
intron_variant | MODIFIER | c.1074-2329_1074-232 others(8): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317878 | |||||
chr8:96317878
|
AGTGTGT | A | 3 | a0001c0001t0034g0129a0001c0001t0035g0041a0001c0004t0022g0154 | 3 | HG02970.hp1 HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1074-2331_1074-232 others(10): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317878 | |||||
chr8:96317878
|
AGTGTGTG others(1): Show |
A | 8 | a0001c0001t0030g0233a0002c0002t0008g0052a0002c0002t0008g0131others(5): Show | 8 | HG02055.hp1 HG02717.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1074-2333_1074-232 others(12): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317878 | |||||
chr8:96317878
|
AGTGTGTG others(5): Show |
A | 3 | a0001c0001t0010g0036a0001c0001t0010g0037a0001c0001t0010g0127 | 3 | HG01081.hp1 HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1074-2337_1074-232 others(16): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317878 | |||||
chr8:96317878
|
AGTGTGTG others(17): Show |
A | 10 | a0001c0001t0001g0053a0001c0001t0002g0056a0001c0001t0002g0226others(7): Show | 10 | HG00642.hp1 HG01109.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1074-2349_1074-232 others(28): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317878 | |||||
chr8:96317878
|
AGTGTGTG others(19): Show |
A | 95 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0008others(92): Show | 95 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.1074-2351_1074-232 others(30): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317878 | |||||
chr8:96317897
|
G | A | 3 | a0001c0001t0010g0059a0001c0001t0016g0012a0001c0001t0016g0013 | 3 | HG02258.hp2 HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1074-2349G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317897 | ||||||
chr8:96317909
|
G | A | 3 | a0001c0001t0001g0086a0001c0001t0001g0160a0001c0001t0001g0186 | 3 | HG00642.hp2 HG02257.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1074-2337G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317909 | ||||||
chr8:96317909
|
G | GTGTA | 67 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(64): Show | 68 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.1074-2334_1074-233 others(8): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317909 | |||||
chr8:96317909
|
G | GTGTATA | 3 | a0001c0001t0009g0091a0001c0001t0009g0120a0001c0001t0009g0121 | 3 | HG01257.hp2 HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1074-2334_1074-233 others(10): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317909 | |||||
chr8:96317909
|
G | GTGTGTA | 8 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0103others(5): Show | 8 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1074-2332_1074-233 others(10): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96317909 | |||||
chr8:96317943
|
A | G | 1 | a0001c0001t0009g0091 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1074-2303A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317943 | ||||||
chr8:96317960
|
TC | T | 2 | a0001c0003t0002g0001a0001c0003t0004g0002 | 5 | HG02895.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-2285delC | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317960 | ||||||
chr8:96317967
|
A | G | 1 | a0001c0001t0013g0247 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1074-2279A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96317967 | ||||||
chr8:96318063
|
G | A | 2 | a0001c0001t0007g0025a0001c0001t0007g0033 | 2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1074-2183G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96318063 | ||||||
chr8:96318218
|
G | A | 1 | a0001c0001t0002g0258 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1074-2028G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96318218 | ||||||
chr8:96318227
|
A | T | 8 | a0001c0001t0033g0147a0002c0002t0008g0052a0002c0002t0008g0131others(5): Show | 8 | HG02717.hp1 HG02818.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1074-2019A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96318227 | ||||||
chr8:96318273
|
G | A | 1 | a0001c0001t0003g0028 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1074-1973G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96318273 | ||||||
chr8:96318296
|
C | T | 105 | a0001c0001t0001g0053a0001c0001t0002g0004a0001c0001t0002g0006others(102): Show | 105 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.1074-1950C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96318296 | ||||||
chr8:96318322
|
T | TA | 75 | a0001c0001t0001g0053a0001c0001t0002g0006a0001c0001t0002g0008others(72): Show | 75 | HG00280.hp1 HG00609.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1074-1913dupA | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96318322 | |||||
chr8:96318322
|
T | TAA | 30 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0018others(27): Show | 30 | HG00280.hp2 HG01069.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.1074-1914_1074-191 others(6): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96318322 | |||||
chr8:96318382
|
A | G | 2 | a0001c0001t0016g0012a0001c0001t0016g0013 | 2 | HG02258.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1074-1864A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96318382 | ||||||
chr8:96318407
|
T | C | 1 | a0001c0004t0022g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1074-1839T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96318407 | ||||||
chr8:96318421
|
C | T | 7 | a0001c0001t0001g0180a0001c0001t0003g0096a0001c0001t0003g0099others(4): Show | 7 | HG00609.hp1 NA18952.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.1074-1825C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96318421 | ||||||
chr8:96318422
|
A | G | 1 | a0001c0001t0011g0031 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1074-1824A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96318422 | ||||||
chr8:96318438
|
C | T | 3 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0018g0112 | 3 | HG01884.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1074-1808C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96318438 | ||||||
chr8:96318463
|
C | A | 103 | a0001c0001t0001g0053a0001c0001t0002g0004a0001c0001t0002g0006others(100): Show | 103 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.1074-1783C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96318463 | ||||||
chr8:96318523
|
A | C | 114 | a0001c0001t0001g0053a0001c0001t0002g0004a0001c0001t0002g0006others(111): Show | 114 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(111): Show |
intron_variant | MODIFIER | c.1074-1723A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96318523 | ||||||
chr8:96318775
|
A | G | 3 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0018g0112 | 3 | HG01884.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1074-1471A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96318775 | ||||||
chr8:96318798
|
T | C | 220 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(217): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1074-1448T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96318798 | ||||||
chr8:96318902
|
C | CT | 21 | a0001c0001t0001g0180a0001c0001t0003g0079a0001c0001t0003g0082others(18): Show | 24 | HG00621.hp2 HG01257.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1074-1318dupT | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96318902 | |||||
chr8:96318902
|
C | CTT | 6 | a0001c0001t0001g0162a0001c0001t0003g0076a0001c0001t0004g0153others(3): Show | 6 | HG01496.hp2 HG02615.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1074-1319_1074-131 others(6): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96318902 | |||||
chr8:96318902
|
C | CTTT | 45 | a0001c0001t0001g0003a0001c0001t0001g0046a0001c0001t0001g0047others(42): Show | 46 | HG01168.hp1 HG01243.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.1074-1320_1074-131 others(7): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96318902 | |||||
chr8:96318902
|
C | CTTTT | 35 | a0001c0001t0001g0034a0001c0001t0001g0043a0001c0001t0001g0064others(32): Show | 35 | HG00140.hp1 HG00438.hp1 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.1074-1321_1074-131 others(8): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96318902 | |||||
chr8:96318902
|
CT | C | 77 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0010others(74): Show | 77 | HG00280.hp1 HG00280.hp2 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.1074-1318delT | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96318902 | |||||
chr8:96318902
|
CTTTTT | C | 6 | a0001c0001t0010g0059a0001c0001t0010g0127a0001c0001t0016g0012others(3): Show | 6 | HG01081.hp1 HG02258.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1074-1322_1074-131 others(9): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96318902 | |||||
chr8:96318904
|
T | C | 1 | a0001c0001t0002g0019 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1074-1342T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96318904 | ||||||
chr8:96319137
|
C | A | 2 | a0001c0003t0002g0001a0001c0003t0004g0002 | 5 | HG02895.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-1109C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96319137 | ||||||
chr8:96319156
|
C | T | 1 | a0001c0001t0023g0150 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1074-1090C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96319156 | ||||||
chr8:96319157
|
G | A | 3 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0018g0112 | 3 | HG01884.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1074-1089G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96319157 | ||||||
chr8:96319248
|
A | C | 1 | a0001c0001t0017g0111 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1074-998A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96319248 | ||||||
chr8:96319488
|
C | T | 2 | a0001c0003t0002g0001a0001c0003t0004g0002 | 5 | HG02895.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1074-758C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96319488 | ||||||
chr8:96319495
|
T | TAA | 87 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(84): Show | 88 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(85): Show |
intron_variant | MODIFIER | c.1074-743_1074-742d others(4): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96319495 | |||||
chr8:96319495
|
T | TAAA | 10 | a0001c0001t0009g0123a0001c0001t0033g0147a0001c0004t0022g0154others(7): Show | 10 | HG02717.hp1 HG02818.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1074-744_1074-742d others(5): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr8 | 96319495 | |||||
chr8:96319584
|
A | G | 1 | a0001c0001t0031g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1074-662A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96319584 | ||||||
chr8:96319676
|
T | C | 1 | a0001c0001t0003g0090 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1074-570T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96319676 | ||||||
chr8:96319692
|
A | G | 1 | a0001c0001t0019g0253 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1074-554A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96319692 | ||||||
chr8:96319736
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1074-510C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96319736 | ||||||
chr8:96319938
|
G | A | 1 | a0001c0001t0006g0176 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1074-308G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96319938 | ||||||
chr8:96319940
|
G | A | 88 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(85): Show | 89 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.1074-306G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96319940 | ||||||
chr8:96319942
|
C | T | 1 | a0001c0001t0010g0059 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1074-304C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96319942 | ||||||
chr8:96320023
|
A | G | 214 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(211): Show | 218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.1074-223A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96320023 | ||||||
chr8:96320030
|
G | A | 1 | a0001c0001t0005g0163 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1074-216G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96320030 | ||||||
chr8:96320053
|
A | C | 1 | a0001c0001t0002g0029 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1074-193A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 9/12 | chr8 | 96320053 | ||||||
chr8:96320418
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1173+73G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96320418 | ||||||
chr8:96320433
|
A | G | 105 | a0001c0001t0001g0053a0001c0001t0002g0004a0001c0001t0002g0006others(102): Show | 105 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.1173+88A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96320433 | ||||||
chr8:96320442
|
C | T | 1 | a0001c0004t0022g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1173+97C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96320442 | ||||||
chr8:96320582
|
C | T | 1 | a0001c0001t0007g0025 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1173+237C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96320582 | ||||||
chr8:96320624
|
T | C | 202 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(199): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1173+279T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96320624 | ||||||
chr8:96320758
|
C | T | 8 | a0001c0001t0033g0147a0002c0002t0008g0052a0002c0002t0008g0131others(5): Show | 8 | HG02717.hp1 HG02818.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1173+413C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96320758 | ||||||
chr8:96320969
|
A | G | 210 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(207): Show | 211 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.1173+624A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96320969 | ||||||
chr8:96321009
|
G | A | 1 | a0001c0004t0022g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1173+664G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96321009 | ||||||
chr8:96321038
|
T | C | 1 | a0001c0001t0005g0042 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1173+693T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96321038 | ||||||
chr8:96321148
|
C | T | 6 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0094others(3): Show | 6 | NA18948.hp1 NA18954.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1173+803C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96321148 | ||||||
chr8:96321597
|
A | G | 105 | a0001c0001t0001g0053a0001c0001t0002g0004a0001c0001t0002g0006others(102): Show | 105 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.1173+1252A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96321597 | ||||||
chr8:96321613
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1173+1268T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96321613 | ||||||
chr8:96321733
|
C | T | 1 | a0001c0001t0023g0150 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1173+1388C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96321733 | ||||||
chr8:96321787
|
A | G | 3 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0018g0112 | 3 | HG01884.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1173+1442A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96321787 | ||||||
chr8:96321891
|
T | C | 215 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(212): Show | 219 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.1173+1546T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96321891 | ||||||
chr8:96322133
|
C | T | 2 | a0001c0003t0002g0001a0001c0003t0004g0002 | 5 | HG02895.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+1788C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96322133 | ||||||
chr8:96322158
|
C | T | 5 | a0001c0001t0012g0051a0001c0001t0012g0062a0001c0001t0012g0063others(2): Show | 5 | HG01070.hp1 HG02809.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1173+1813C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96322158 | ||||||
chr8:96322240
|
C | T | 1 | a0001c0001t0026g0228 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1173+1895C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96322240 | ||||||
chr8:96322360
|
G | A | 3 | a0001c0001t0010g0036a0001c0001t0010g0037a0001c0001t0010g0127 | 3 | HG01081.hp1 HG02145.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1173+2015G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96322360 | ||||||
chr8:96322557
|
C | G | 1 | a0001c0004t0022g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1173+2212C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96322557 | ||||||
chr8:96322622
|
A | T | 113 | a0001c0001t0001g0053a0001c0001t0002g0004a0001c0001t0002g0006others(110): Show | 113 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(110): Show |
intron_variant | MODIFIER | c.1173+2277A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96322622 | ||||||
chr8:96322805
|
G | A | 8 | a0001c0001t0033g0147a0002c0002t0008g0052a0002c0002t0008g0131others(5): Show | 8 | HG02717.hp1 HG02818.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1173+2460G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96322805 | ||||||
chr8:96322839
|
C | T | 30 | a0001c0001t0001g0053a0001c0001t0002g0006a0001c0001t0002g0008others(27): Show | 30 | HG00642.hp1 HG01070.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.1173+2494C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96322839 | ||||||
chr8:96323180
|
G | A | 1 | a0001c0001t0012g0062 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1173+2835G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96323180 | ||||||
chr8:96323215
|
C | T | 2 | a0001c0001t0002g0257a0001c0001t0028g0184 | 2 | HG01069.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1173+2870C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96323215 | ||||||
chr8:96323260
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1173+2915T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96323260 | ||||||
chr8:96323389
|
G | A | 8 | a0001c0001t0033g0147a0002c0002t0008g0052a0002c0002t0008g0131others(5): Show | 8 | HG02717.hp1 HG02818.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1173+3044G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96323389 | ||||||
chr8:96323391
|
C | T | 1 | a0001c0001t0017g0111 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1173+3046C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96323391 | ||||||
chr8:96324269
|
G | T | 213 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(210): Show | 217 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1173+3924G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96324269 | ||||||
chr8:96324285
|
A | G | 3 | a0001c0001t0010g0059a0001c0001t0016g0012a0001c0001t0016g0013 | 3 | HG02258.hp2 HG02451.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.1173+3940A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96324285 | ||||||
chr8:96324553
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1173+4208C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96324553 | ||||||
chr8:96324972
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1173+4627C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96324972 | ||||||
chr8:96324975
|
G | A | 1 | a0001c0001t0006g0133 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1173+4630G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96324975 | ||||||
chr8:96325150
|
T | C | 2 | a0001c0001t0032g0130a0001c0005t0002g0011 | 2 | HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1173+4805T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96325150 | ||||||
chr8:96325285
|
C | T | 79 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(76): Show | 80 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.1174-4928C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96325285 | ||||||
chr8:96325428
|
A | G | 107 | a0001c0001t0001g0053a0001c0001t0002g0004a0001c0001t0002g0006others(104): Show | 107 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.1174-4785A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96325428 | ||||||
chr8:96325618
|
G | A | 1 | a0001c0001t0002g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1174-4595G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96325618 | ||||||
chr8:96326041
|
T | C | 212 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(209): Show | 216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1174-4172T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96326041 | ||||||
chr8:96326042
|
G | T | 73 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(70): Show | 74 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1174-4171G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96326042 | ||||||
chr8:96326068
|
G | C | 90 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(87): Show | 91 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.1174-4145G>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96326068 | ||||||
chr8:96326172
|
C | T | 6 | a0001c0001t0009g0091a0001c0001t0009g0120a0001c0001t0009g0121others(3): Show | 6 | HG01257.hp2 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174-4041C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96326172 | ||||||
chr8:96326234
|
C | T | 1 | a0001c0001t0018g0112 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1174-3979C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96326234 | ||||||
chr8:96326367
|
G | GT | 42 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0018others(39): Show | 42 | HG00280.hp2 HG01069.hp1 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.1174-3838dupT | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 96326367 | |||||
chr8:96326378
|
A | C | 1 | a0001c0001t0004g0038 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1174-3835A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96326378 | ||||||
chr8:96326607
|
C | T | 89 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(86): Show | 90 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.1174-3606C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96326607 | ||||||
chr8:96326703
|
A | G | 107 | a0001c0001t0001g0053a0001c0001t0002g0004a0001c0001t0002g0006others(104): Show | 107 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.1174-3510A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96326703 | ||||||
chr8:96326857
|
G | A | 2 | a0001c0003t0002g0001a0001c0003t0004g0002 | 5 | HG02895.hp1 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1174-3356G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96326857 | ||||||
chr8:96326863
|
G | T | 6 | a0001c0001t0009g0091a0001c0001t0009g0120a0001c0001t0009g0121others(3): Show | 6 | HG01257.hp2 HG01891.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1174-3350G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96326863 | ||||||
chr8:96327023
|
A | G | 213 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(210): Show | 217 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.1174-3190A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96327023 | ||||||
chr8:96327025
|
G | T | 26 | a0001c0001t0005g0039a0001c0001t0005g0040a0001c0001t0005g0042others(23): Show | 26 | HG00280.hp1 HG00609.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.1174-3188G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96327025 | ||||||
chr8:96327284
|
A | G | 2 | a0001c0001t0005g0039a0001c0001t0005g0040 | 2 | HG03491.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1174-2929A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96327284 | ||||||
chr8:96327284
|
A | T | 210 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(207): Show | 214 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1174-2929A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96327284 | ||||||
chr8:96327368
|
T | C | 6 | a0001c0001t0001g0069a0001c0001t0001g0093a0001c0001t0001g0094others(3): Show | 6 | NA18948.hp1 NA18954.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1174-2845T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96327368 | ||||||
chr8:96327485
|
C | T | 1 | a0001c0004t0022g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1174-2728C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96327485 | ||||||
chr8:96327555
|
C | T | 1 | a0001c0001t0011g0031 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1174-2658C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96327555 | ||||||
chr8:96327776
|
C | G | 105 | a0001c0001t0001g0053a0001c0001t0002g0004a0001c0001t0002g0006others(102): Show | 105 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.1174-2437C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96327776 | ||||||
chr8:96327863
|
G | A | 1 | a0001c0001t0033g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1174-2350G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96327863 | ||||||
chr8:96327888
|
C | G | 85 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(82): Show | 86 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.1174-2325C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96327888 | ||||||
chr8:96327999
|
C | T | 2 | a0001c0001t0004g0152a0001c0001t0004g0153 | 2 | HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1174-2214C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96327999 | ||||||
chr8:96328017
|
C | T | 1 | a0001c0004t0022g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1174-2196C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96328017 | ||||||
chr8:96328333
|
T | A | 39 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0018others(36): Show | 39 | HG00280.hp2 HG01069.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1174-1880T>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96328333 | ||||||
chr8:96328592
|
T | G | 2 | a0001c0001t0009g0120a0001c0001t0009g0121 | 2 | HG01891.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1174-1621T>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96328592 | ||||||
chr8:96328612
|
T | C | 1 | a0001c0001t0031g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1174-1601T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96328612 | ||||||
chr8:96328697
|
A | T | 106 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0008others(103): Show | 109 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(106): Show |
intron_variant | MODIFIER | c.1174-1516A>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96328697 | ||||||
chr8:96328731
|
C | T | 1 | a0001c0001t0003g0238 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1174-1482C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96328731 | ||||||
chr8:96328948
|
C | G | 1 | a0001c0001t0031g0128 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1174-1265C>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96328948 | ||||||
chr8:96329018
|
A | G | 3 | a0001c0001t0027g0151a0001c0001t0032g0130a0001c0005t0002g0011 | 3 | HG02809.hp2 HG03195.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1174-1195A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96329018 | ||||||
chr8:96329162
|
A | C | 88 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(85): Show | 89 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.1174-1051A>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96329162 | ||||||
chr8:96329178
|
G | A | 91 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(88): Show | 92 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.1174-1035G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96329178 | ||||||
chr8:96329347
|
CG | C | 88 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(85): Show | 89 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.1174-862delG | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr8 | 96329347 | |||||
chr8:96329454
|
T | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0065 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1174-759T>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96329454 | ||||||
chr8:96329673
|
A | G | 1 | a0001c0001t0011g0211 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1174-540A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96329673 | ||||||
chr8:96329827
|
C | A | 1 | a0001c0001t0005g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1174-386C>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96329827 | ||||||
chr8:96329828
|
G | T | 1 | a0001c0001t0033g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1174-385G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96329828 | ||||||
chr8:96329862
|
A | G | 91 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(88): Show | 92 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.1174-351A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96329862 | ||||||
chr8:96329891
|
T | A | 1 | a0001c0005t0002g0011 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1174-322T>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96329891 | ||||||
chr8:96330129
|
G | A | 1 | a0001c0001t0002g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1174-84G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96330129 | ||||||
chr8:96330205
|
T | C | 1 | a0001c0001t0003g0172 | 1 | NA18955.hp2 | splice_region_variant&intron_variant | LOW | c.1174-8T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 10/12 | chr8 | 96330205 | ||||||
chr8:96330308
|
A | G | 92 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(89): Show | 93 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.1242+27A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 11/12 | chr8 | 96330308 | ||||||
chr8:96330334
|
C | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0231a0001c0001t0001g0232 | 3 | HG01975.hp2 HG02148.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1242+53C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 11/12 | chr8 | 96330334 | ||||||
chr8:96330354
|
C | T | 105 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0008others(102): Show | 108 | HG00280.hp1 HG00280.hp2 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.1242+73C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 11/12 | chr8 | 96330354 | ||||||
chr8:96330469
|
G | GCT | 28 | a0001c0001t0002g0004a0001c0001t0002g0009a0001c0001t0002g0018others(25): Show | 28 | HG00280.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.1242+191_1242+192d others(4): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr8 | 96330469 | |||||
chr8:96330728
|
G | A | 1 | a0001c0004t0022g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1243-298G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 11/12 | chr8 | 96330728 | ||||||
chr8:96330948
|
G | T | 88 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(85): Show | 89 | HG00140.hp1 HG00438.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.1243-78G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 11/12 | chr8 | 96330948 | ||||||
chr8:96331098
|
ATCTTGT | A | 64 | a0001c0001t0002g0006a0001c0001t0002g0008a0001c0001t0002g0010others(61): Show | 64 | HG00140.hp2 HG00280.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1312+12_1312+17del others(6): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 96331098 | |||||
chr8:96331215
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1312+120G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96331215 | ||||||
chr8:96331255
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0004g0139 | 2 | HG02809.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.1312+160C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96331255 | ||||||
chr8:96331297
|
G | A | 1 | a0001c0004t0022g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1312+202G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96331297 | ||||||
chr8:96331426
|
C | T | 1 | a0001c0001t0033g0147 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1312+331C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96331426 | ||||||
chr8:96331436
|
G | A | 5 | a0001c0001t0006g0032a0001c0001t0012g0051a0001c0001t0012g0062others(2): Show | 5 | HG01070.hp1 HG02886.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1312+341G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96331436 | ||||||
chr8:96331443
|
C | T | 1 | a0001c0001t0002g0074 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1312+348C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96331443 | ||||||
chr8:96331546
|
G | T | 1 | a0001c0001t0002g0029 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1312+451G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96331546 | ||||||
chr8:96331574
|
CA | C | 8 | a0001c0001t0001g0069a0001c0001t0010g0036a0001c0001t0010g0037others(5): Show | 8 | HG01081.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1312+492delA | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 96331574 | |||||
chr8:96331583
|
A | G | 1 | a0001c0004t0022g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1312+488A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96331583 | ||||||
chr8:96331805
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1312+710G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96331805 | ||||||
chr8:96332010
|
T | C | 15 | a0001c0001t0010g0036a0001c0001t0010g0037a0001c0001t0010g0059others(12): Show | 15 | HG01081.hp1 HG02145.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1312+915T>C | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96332010 | ||||||
chr8:96332017
|
TA | T | 19 | a0001c0001t0003g0045a0001c0001t0003g0048a0001c0001t0003g0049others(16): Show | 19 | HG00438.hp2 HG00609.hp1 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.1312+952delA | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 96332017 | |||||
chr8:96332017
|
TAA | T | 22 | a0001c0001t0001g0053a0001c0001t0003g0030a0001c0001t0003g0083others(19): Show | 22 | HG00140.hp2 HG01175.hp2 HG01934.hp2 others(19): Show |
intron_variant | MODIFIER | c.1312+951_1312+952d others(4): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 96332017 | |||||
chr8:96332017
|
TAAA | T | 36 | a0001c0001t0001g0103a0001c0001t0001g0126a0001c0001t0001g0162others(33): Show | 36 | HG00280.hp1 HG00438.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.1312+950_1312+952d others(5): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 96332017 | |||||
chr8:96332017
|
TAAAA | T | 122 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(119): Show | 126 | HG00140.hp1 HG00621.hp1 HG00642.hp1 others(123): Show |
intron_variant | MODIFIER | c.1312+949_1312+952d others(6): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 96332017 | |||||
chr8:96332017
|
TAAAAA | T | 50 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0094others(47): Show | 50 | HG00280.hp2 HG01167.hp1 HG01168.hp2 others(47): Show |
intron_variant | MODIFIER | c.1312+948_1312+952d others(7): Show |
PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr8 | 96332017 | |||||
chr8:96332129
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1312+1034A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96332129 | ||||||
chr8:96332142
|
G | A | 1 | a0001c0001t0003g0171 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1312+1047G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96332142 | ||||||
chr8:96332160
|
C | T | 1 | a0001c0001t0024g0156 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1312+1065C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96332160 | ||||||
chr8:96332201
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1312+1106C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96332201 | ||||||
chr8:96332259
|
C | T | 1 | a0001c0001t0003g0199 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1312+1164C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96332259 | ||||||
chr8:96332726
|
G | T | 1 | a0001c0001t0001g0034 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1313-731G>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96332726 | ||||||
chr8:96332752
|
T | G | 1 | a0001c0001t0002g0010 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1313-705T>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96332752 | ||||||
chr8:96333099
|
G | A | 1 | a0001c0001t0028g0184 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1313-358G>A | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96333099 | ||||||
chr8:96333105
|
C | T | 3 | a0001c0001t0004g0152a0001c0001t0004g0153a0001c0001t0018g0112 | 3 | HG01884.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1313-352C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96333105 | ||||||
chr8:96333132
|
T | G | 13 | a0001c0001t0010g0036a0001c0001t0010g0037a0001c0001t0010g0059others(10): Show | 13 | HG01081.hp1 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1313-325T>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96333132 | ||||||
chr8:96333246
|
C | T | 1 | a0001c0004t0022g0154 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1313-211C>T | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96333246 | ||||||
chr8:96333362
|
A | G | 175 | a0001c0001t0001g0003a0001c0001t0001g0034a0001c0001t0001g0043others(172): Show | 179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.1313-95A>G | PTDSS1 | ENSG00000156471.13 | transcript | ENST00000517309.6 | protein_coding | 12/12 | chr8 | 96333362 |