geneid | 23176 |
---|---|
ensemblid | ENSG00000164402.14 |
hgncid | 16511 |
symbol | SEPTIN8 |
name | septin 8 |
refseq_nuc | NM_001098811.2 |
refseq_prot | NP_001092281.1 |
ensembl_nuc | ENST00000378719.7 |
ensembl_prot | ENSP00000367991.2 |
mane_status | MANE Select |
chr | chr5 |
start | 132750819 |
end | 132777239 |
strand | - |
ver | v1.2 |
region | chr5:132750819-132777239 |
region5000 | chr5:132745819-132782239 |
regionname0 | SEPTIN8_chr5_132750819_132777239 |
regionname5000 | SEPTIN8_chr5_132745819_132782239 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 483 | 318 | 89 | 53 | 144 | 4 | 26 | 108 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0002 | 0/0 | 483 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0003 | 0/0 | 483 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0004 | 0/0 | 483 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0005 | 0/0 | 483 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0006 | 0/0 | 483 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0007 | 0/0 | 483 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1452 | 214 | 79 | 22 | 106 | 0 | 7 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
c0002 | 1/1 | 1452 | 97 | 5 | 30 | 37 | 4 | 19 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
c0003 | 0/0 | 1452 | 5 | 4 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
c0004 | 0/0 | 1452 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
c0005 | 0/0 | 1452 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
c0006 | 0/0 | 1452 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
c0007 | 0/0 | 1452 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
c0008 | 0/0 | 1452 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
c0009 | 0/0 | 1452 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
c0010 | 0/0 | 1452 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
c0011 | 0/0 | 1452 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 1300 | 174 | 58 | 23 | 87 | 0 | 6 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
t0002 | 1/1 | 1300 | 110 | 10 | 29 | 46 | 4 | 19 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
t0003 | 0/0 | 1294 | 12 | 11 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
t0004 | 0/0 | 1300 | 11 | 10 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
t0005 | 0/0 | 1300 | 9 | 0 | 0 | 9 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
t0006 | 0/0 | 1300 | 6 | 0 | 0 | 5 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
t0007 | 0/0 | 1300 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
t0008 | 0/0 | 1300 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
t0009 | 0/0 | 1300 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0002 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0004 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0005 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0007 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0009 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0014 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0024 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0213 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0257 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1452 | 214 | 79 | 22 | 106 | 0 | 7 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0001c0002 | 1/1 | 1452 | 97 | 5 | 30 | 37 | 4 | 19 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0001c0003 | 0/0 | 1452 | 5 | 4 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0001c0007 | 0/0 | 1452 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0001c0010 | 0/0 | 1452 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0002c0005 | 0/0 | 1452 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0003c0004 | 0/0 | 1452 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0004c0006 | 0/0 | 1452 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0005c0008 | 0/0 | 1452 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0006c0009 | 0/0 | 1452 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0007c0011 | 0/0 | 1452 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2751 | 169 | 57 | 20 | 86 | 0 | 6 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0001c0001t0002 | 0/0 | 2751 | 12 | 5 | 1 | 6 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0001c0001t0003 | 0/0 | 2745 | 7 | 7 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0001c0001t0004 | 0/0 | 2751 | 10 | 9 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0001c0001t0005 | 0/0 | 2751 | 9 | 0 | 0 | 9 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0001c0001t0006 | 0/0 | 2751 | 6 | 0 | 0 | 5 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0001c0001t0008 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0001c0002t0002 | 1/1 | 2751 | 94 | 5 | 28 | 36 | 4 | 19 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0001c0002t0007 | 0/0 | 2751 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0001c0002t0009 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0001c0003t0003 | 0/0 | 2745 | 5 | 4 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0001c0007t0001 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0001c0010t0004 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0002c0005t0002 | 0/0 | 2751 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0003c0004t0001 | 0/0 | 2751 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0004c0006t0001 | 0/0 | 2751 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0005c0008t0001 | 0/0 | 2751 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0006c0009t0002 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
a0007c0011t0002 | 0/0 | 2751 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | copy fasta | chr5 | 132745819 | 132782239 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 1 | 3 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0005 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0009 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0013 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0024 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0004g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0005g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0005g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0006g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0006g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0006g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0006g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0006g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0006g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0001t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0007 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0014 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0213 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0257 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0007g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0002t0009g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0003t0003g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0003t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0007t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0001c0010t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0002c0005t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0002c0005t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0003c0004t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0004c0006t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0005c0008t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0006c0009t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
a0007c0011t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00408 | hp1 | a0001 | c0001 | t0005 | g0040 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00408 | hp2 | a0001 | c0001 | t0005 | g0038 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0244 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00609 | hp2 | a0001 | c0002 | t0002 | g0175 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00621 | hp1 | a0001 | c0002 | t0002 | g0232 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0178 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00642 | hp1 | a0001 | c0003 | t0003 | g0151 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00642 | hp2 | a0001 | c0002 | t0002 | g0218 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0014 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0210 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01069 | hp1 | a0001 | c0002 | t0002 | g0199 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01070 | hp1 | a0001 | c0002 | t0002 | g0255 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0028 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01071 | hp2 | a0001 | c0002 | t0002 | g0028 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01074 | hp2 | a0001 | c0002 | t0002 | g0184 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0181 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01099 | hp2 | a0001 | c0002 | t0002 | g0187 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01167 | hp2 | a0003 | c0004 | t0001 | g0021 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0182 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01168 | hp2 | a0001 | c0002 | t0007 | g0033 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01169 | hp1 | a0003 | c0004 | t0001 | g0021 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01169 | hp2 | a0001 | c0002 | t0007 | g0033 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0180 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0020 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01257 | hp1 | a0001 | c0002 | t0002 | g0195 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0214 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01346 | hp1 | a0005 | c0008 | t0001 | g0171 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0186 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01361 | hp1 | a0001 | c0002 | t0002 | g0170 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0258 | AMR | CLM | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01515 | hp1 | a0001 | c0002 | t0002 | g0189 | EUR | IBS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01515 | hp2 | a0001 | c0002 | t0002 | g0205 | EUR | IBS | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01891 | hp1 | a0001 | c0002 | t0002 | g0241 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01934 | hp1 | a0001 | c0002 | t0002 | g0029 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01943 | hp1 | a0001 | c0002 | t0002 | g0204 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0248 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG01981 | hp2 | a0001 | c0002 | t0002 | g0185 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02004 | hp1 | a0001 | c0002 | t0002 | g0235 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02015 | hp2 | a0001 | c0002 | t0002 | g0196 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0041 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02074 | hp2 | a0001 | c0002 | t0002 | g0226 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02080 | hp1 | a0001 | c0002 | t0002 | g0201 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02129 | hp1 | a0001 | c0002 | t0002 | g0183 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02129 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02145 | hp1 | a0001 | c0002 | t0002 | g0200 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02148 | hp1 | a0001 | c0002 | t0002 | g0014 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02155 | hp1 | a0001 | c0001 | t0006 | g0265 | EAS | CDX | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CDX | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02257 | hp1 | a0001 | c0002 | t0002 | g0242 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0076 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02273 | hp1 | a0001 | c0002 | t0002 | g0030 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0251 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02300 | hp2 | a0001 | c0002 | t0002 | g0249 | AMR | PEL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0149 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0146 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02717 | hp1 | a0001 | c0003 | t0003 | g0006 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02723 | hp1 | a0001 | c0010 | t0004 | g0144 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02735 | hp1 | a0001 | c0002 | t0002 | g0007 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0208 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0262 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02895 | hp1 | a0001 | c0003 | t0003 | g0006 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02897 | hp1 | a0001 | c0003 | t0003 | g0006 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03017 | hp1 | a0001 | c0001 | t0006 | g0269 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03195 | hp1 | a0001 | c0001 | t0008 | g0059 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03491 | hp1 | a0001 | c0002 | t0002 | g0256 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0032 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03492 | hp1 | a0001 | c0002 | t0002 | g0007 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03492 | hp2 | a0001 | c0002 | t0002 | g0032 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0155 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03540 | hp1 | a0001 | c0003 | t0003 | g0006 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0254 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03654 | hp2 | a0001 | c0002 | t0002 | g0253 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03704 | hp1 | a0001 | c0002 | t0002 | g0211 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0179 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0194 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03710 | hp2 | a0001 | c0002 | t0002 | g0212 | SAS | PJL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0229 | SAS | BEB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | BEB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | BEB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG04115 | hp2 | a0001 | c0002 | t0002 | g0014 | SAS | STU | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG04184 | hp2 | a0001 | c0002 | t0002 | g0207 | SAS | BEB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG04199 | hp1 | a0001 | c0002 | t0002 | g0252 | SAS | STU | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0209 | SAS | STU | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18612 | hp1 | a0001 | c0002 | t0002 | g0198 | EAS | CHB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18747 | hp2 | a0001 | c0007 | t0001 | g0105 | EAS | CHB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0055 | AFR | YRI | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18940 | hp2 | a0001 | c0002 | t0002 | g0177 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18941 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18942 | hp1 | a0001 | c0002 | t0002 | g0197 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18945 | hp1 | a0001 | c0002 | t0002 | g0227 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18947 | hp1 | a0001 | c0002 | t0009 | g0238 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18948 | hp1 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18951 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18951 | hp2 | a0001 | c0001 | t0006 | g0268 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18952 | hp2 | a0002 | c0005 | t0002 | g0239 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18957 | hp2 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18960 | hp2 | a0001 | c0001 | t0005 | g0035 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18961 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18963 | hp2 | a0001 | c0002 | t0002 | g0176 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18964 | hp2 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18968 | hp2 | a0007 | c0011 | t0002 | g0188 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18973 | hp2 | a0001 | c0002 | t0002 | g0192 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18978 | hp1 | a0001 | c0001 | t0006 | g0266 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18981 | hp1 | a0001 | c0002 | t0002 | g0259 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18984 | hp1 | a0001 | c0002 | t0002 | g0246 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18986 | hp2 | a0006 | c0009 | t0002 | g0219 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18989 | hp1 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18989 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18990 | hp1 | a0001 | c0002 | t0002 | g0231 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18991 | hp2 | a0001 | c0001 | t0006 | g0264 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0236 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18995 | hp2 | a0001 | c0002 | t0002 | g0225 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18999 | hp2 | a0001 | c0002 | t0002 | g0173 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0267 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0036 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19010 | hp2 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | LWK | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0222 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19063 | hp1 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19066 | hp1 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19066 | hp2 | a0001 | c0002 | t0002 | g0202 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19070 | hp1 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0250 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0203 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19088 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19091 | hp2 | a0001 | c0001 | t0005 | g0042 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | YRI | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA19240 | hp2 | a0004 | c0006 | t0001 | g0128 | AFR | YRI | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ASW | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ASW | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0007 | EUR | TSI | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA20752 | hp2 | a0001 | c0002 | t0002 | g0029 | EUR | TSI | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA20905 | hp1 | a0001 | c0002 | t0002 | g0233 | SAS | GIH | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA20905 | hp2 | a0001 | c0002 | t0002 | g0190 | SAS | GIH | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02486 | hp2 | a0001 | c0002 | t0002 | g0191 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0075 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG02559 | hp2 | a0001 | c0001 | t0003 | g0152 | AFR | ACB | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | USA | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0172 | AFR | USA | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18955 | hp1 | a0002 | c0005 | t0002 | g0230 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | USA | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | LWK | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0002 | g0213 | REF | REF | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0257 | REF | REF | SEPTIN8_chr5_132745819_132782239 | SEPTIN8 | chr5 | 132745819 | 132782239 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:132761584
|
A | G | 1 | a0006 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.836T>C | p.Met279Thr | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 7/10 | 938/2751 | 836/1452 | 279/483 | chr5 | 132761584 | ||
chr5:132761600
|
C | T | 1 | a0005 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.820G>A | p.Val274Met | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 7/10 | 922/2751 | 820/1452 | 274/483 | chr5 | 132761600 | ||
chr5:132763867
|
C | T | 1 | a0002 | 2 | NA18952.hp2 NA18955.hp1 |
missense_variant | MODERATE | c.373G>A | p.Asp125Asn | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/10 | 475/2751 | 373/1452 | 125/483 | chr5 | 132763867 | ||
chr5:132764270
|
T | C | 1 | a0007 | 1 | NA18968.hp2 | missense_variant | MODERATE | c.301A>G | p.Ile101Val | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 3/10 | 403/2751 | 301/1452 | 101/483 | chr5 | 132764270 | ||
chr5:132764278
|
T | A | 1 | a0003 | 2 | HG01167.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.293A>T | p.Lys98Met | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 3/10 | 395/2751 | 293/1452 | 98/483 | chr5 | 132764278 | ||
chr5:132764320
|
C | T | 1 | a0004 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.251G>A | p.Arg84Gln | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 3/10 | 353/2751 | 251/1452 | 84/483 | chr5 | 132764320 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:132752040
|
C | T | 1 | a0001c0003 | 5 | HG00642.hp1 HG02717.hp1 HG02895.hp1 others(2): Show |
synonymous_variant | LOW | c.1428G>A | p.Ala476Ala | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 10/10 | 1530/2751 | 1428/1452 | 476/483 | chr5 | 132752040 | ||
chr5:132760876
|
C | T | 1 | a0001c0010 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.1212G>A | p.Ala404Ala | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/10 | 1314/2751 | 1212/1452 | 404/483 | chr5 | 132760876 | ||
chr5:132763766
|
C | T | 1 | a0001c0007 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.474G>A | p.Thr158Thr | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/10 | 576/2751 | 474/1452 | 158/483 | chr5 | 132763766 | ||
chr5:132764307
|
A | G | 9 | a0001c0001a0001c0003a0001c0007others(6): Show | 227 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(224): Show |
synonymous_variant | LOW | c.264T>C | p.Tyr88Tyr | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 3/10 | 366/2751 | 264/1452 | 88/483 | chr5 | 132764307 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:132750906
|
C | T | 1 | a0001c0002t0009 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1110G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 10/10 | 1110 | chr5 | 132750906 | |||||
chr5:132751125
|
G | C | 12 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(9): Show | 213 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*891C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 10/10 | 891 | chr5 | 132751125 | |||||
chr5:132751440
|
GTTTGTA | G | 2 | a0001c0001t0003a0001c0003t0003 | 12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*570_*575delTACAAA | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 10/10 | 570 | chr5 | 132751440 | |||||
chr5:132751601
|
C | T | 1 | a0001c0001t0008 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*415G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 10/10 | 415 | chr5 | 132751601 | |||||
chr5:132751623
|
G | A | 1 | a0001c0002t0007 | 2 | HG01168.hp2 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*393C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 10/10 | 393 | chr5 | 132751623 | |||||
chr5:132751902
|
T | C | 2 | a0001c0001t0004a0001c0010t0004 | 11 | HG01243.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*114A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 10/10 | 114 | chr5 | 132751902 | |||||
chr5:132777186
|
G | T | 1 | a0001c0001t0005 | 9 | HG00408.hp1 HG00408.hp2 HG02027.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-49C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/10 | 49 | chr5 | 132777186 | |||||
chr5:132777203
|
T | C | 1 | a0001c0001t0006 | 6 | HG02155.hp1 HG03017.hp1 NA18951.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-66A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/10 | 66 | chr5 | 132777203 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:132752256
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1287-75G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132752256 | ||||||
chr5:132752361
|
G | A | 12 | a0001c0001t0001g0009a0001c0001t0001g0072a0001c0001t0001g0073others(9): Show | 14 | HG01069.hp2 HG01071.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.1287-180C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132752361 | ||||||
chr5:132752821
|
T | C | 1 | a0001c0001t0001g0168 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1287-640A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132752821 | ||||||
chr5:132752885
|
G | T | 1 | a0001c0001t0004g0147 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1287-704C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132752885 | ||||||
chr5:132752989
|
G | A | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1287-808C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132752989 | ||||||
chr5:132753175
|
G | A | 7 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0043others(4): Show | 10 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.1287-994C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753175 | ||||||
chr5:132753263
|
G | T | 18 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0027others(15): Show | 24 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.1287-1082C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753263 | ||||||
chr5:132753287
|
G | C | 9 | a0001c0001t0003g0054a0001c0001t0003g0150a0001c0001t0003g0152others(6): Show | 12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1287-1106C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753287 | ||||||
chr5:132753508
|
C | T | 8 | a0001c0001t0001g0009a0001c0001t0001g0079a0001c0001t0001g0080others(5): Show | 10 | HG01069.hp2 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1287-1327G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753508 | ||||||
chr5:132753534
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1287-1353T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753534 | ||||||
chr5:132753584
|
A | C | 1 | a0001c0001t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1287-1403T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753584 | ||||||
chr5:132753785
|
G | A | 1 | a0001c0002t0002g0225 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1287-1604C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753785 | ||||||
chr5:132753795
|
C | T | 9 | a0001c0001t0003g0054a0001c0001t0003g0150a0001c0001t0003g0152others(6): Show | 12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1287-1614G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753795 | ||||||
chr5:132753877
|
G | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1287-1696C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753877 | ||||||
chr5:132753956
|
G | GT | 32 | a0001c0001t0001g0048a0001c0001t0001g0125a0001c0001t0002g0056others(29): Show | 36 | HG00639.hp2 HG00642.hp1 HG01074.hp2 others(33): Show |
intron_variant | MODIFIER | c.1287-1776dupA | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753956 | ||||||
chr5:132753956
|
G | GTT | 27 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0027others(24): Show | 34 | HG00621.hp1 HG00735.hp2 HG01069.hp2 others(31): Show |
intron_variant | MODIFIER | c.1287-1777_1287-177 others(6): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753956 | ||||||
chr5:132753956
|
G | GTTT | 17 | a0001c0001t0001g0015a0001c0001t0001g0045a0001c0001t0001g0046others(14): Show | 20 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.1287-1778_1287-177 others(7): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753956 | ||||||
chr5:132753956
|
G | GTTTT | 6 | a0001c0001t0001g0082a0001c0001t0004g0075a0001c0001t0004g0145others(3): Show | 6 | HG02145.hp2 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1287-1779_1287-177 others(8): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753956 | ||||||
chr5:132753956
|
GT | G | 19 | a0001c0001t0001g0011a0001c0001t0001g0061a0001c0001t0001g0071others(16): Show | 21 | HG00438.hp2 HG00597.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.1287-1776delA | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753956 | ||||||
chr5:132753956
|
GTT | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(92): Show | 126 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1287-1777_1287-177 others(6): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753956 | ||||||
chr5:132753956
|
GTTT | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0129others(1): Show | 6 | HG02451.hp2 HG02630.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1287-1778_1287-177 others(7): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132753956 | ||||||
chr5:132754149
|
A | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0079a0001c0001t0001g0080 | 5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287-1968T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132754149 | ||||||
chr5:132754428
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1287-2247G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132754428 | ||||||
chr5:132754602
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1287-2421A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132754602 | ||||||
chr5:132754615
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1287-2434A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132754615 | ||||||
chr5:132754690
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1287-2509G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132754690 | ||||||
chr5:132754764
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0008g0059 | 3 | HG02630.hp1 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1287-2583G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132754764 | ||||||
chr5:132754946
|
C | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1287-2765G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132754946 | ||||||
chr5:132755136
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 218 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1287-2955A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132755136 | ||||||
chr5:132755257
|
C | A | 1 | a0001c0001t0001g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1287-3076G>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132755257 | ||||||
chr5:132755959
|
C | CTT | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 218 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1287-3779_1287-377 others(6): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132755959 | ||||||
chr5:132756251
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0079a0001c0001t0001g0080 | 5 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1287-4070C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132756251 | ||||||
chr5:132756374
|
G | T | 32 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0057others(29): Show | 37 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.1287-4193C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132756374 | ||||||
chr5:132756386
|
A | G | 1 | a0001c0002t0002g0247 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1287-4205T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132756386 | ||||||
chr5:132756438
|
T | C | 1 | a0001c0002t0002g0194 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1287-4257A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132756438 | ||||||
chr5:132756716
|
G | A | 1 | a0001c0002t0009g0238 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1286+4086C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132756716 | ||||||
chr5:132756792
|
G | A | 9 | a0001c0001t0005g0034a0001c0001t0005g0035a0001c0001t0005g0036others(6): Show | 9 | HG00408.hp1 HG00408.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.1286+4010C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132756792 | ||||||
chr5:132757112
|
T | A | 1 | a0001c0001t0001g0129 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1286+3690A>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757112 | ||||||
chr5:132757121
|
G | T | 1 | a0001c0002t0002g0234 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1286+3681C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757121 | ||||||
chr5:132757345
|
G | A | 120 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(117): Show | 155 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(152): Show |
intron_variant | MODIFIER | c.1286+3457C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757345 | ||||||
chr5:132757357
|
C | T | 9 | a0001c0001t0003g0054a0001c0001t0003g0150a0001c0001t0003g0152others(6): Show | 12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1286+3445G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757357 | ||||||
chr5:132757568
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1286+3234C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757568 | ||||||
chr5:132757590
|
T | C | 8 | a0001c0001t0001g0009a0001c0001t0001g0079a0001c0001t0001g0080others(5): Show | 10 | HG01069.hp2 HG01071.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1286+3212A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757590 | ||||||
chr5:132757628
|
G | C | 1 | a0001c0001t0001g0100 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1286+3174C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757628 | ||||||
chr5:132757720
|
C | G | 1 | a0001c0001t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1286+3082G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757720 | ||||||
chr5:132757723
|
G | A | 1 | a0001c0002t0002g0205 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1286+3079C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757723 | ||||||
chr5:132757957
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 218 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1286+2845A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757957 | ||||||
chr5:132757967
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1286+2835A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132757967 | ||||||
chr5:132758043
|
A | C | 1 | a0004c0006t0001g0128 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1286+2759T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132758043 | ||||||
chr5:132758302
|
C | T | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(125): Show | 166 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.1286+2500G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132758302 | ||||||
chr5:132758313
|
A | G | 3 | a0001c0001t0001g0013a0001c0001t0001g0134a0001c0001t0001g0141 | 5 | HG01243.hp2 HG02809.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1286+2489T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132758313 | ||||||
chr5:132758411
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1286+2391C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132758411 | ||||||
chr5:132758513
|
G | A | 18 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0074others(15): Show | 21 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.1286+2289C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132758513 | ||||||
chr5:132758634
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1286+2168C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132758634 | ||||||
chr5:132758664
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1286+2138G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132758664 | ||||||
chr5:132758665
|
G | A | 7 | a0001c0001t0001g0094a0001c0001t0004g0145a0001c0001t0004g0146others(4): Show | 7 | HG02145.hp2 HG02300.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1286+2137C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132758665 | ||||||
chr5:132758718
|
G | A | 2 | a0001c0002t0002g0179a0001c0002t0002g0180 | 2 | HG01175.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1286+2084C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132758718 | ||||||
chr5:132759036
|
T | G | 5 | a0001c0001t0001g0101a0001c0001t0001g0106a0001c0001t0001g0108others(2): Show | 5 | HG02040.hp1 HG02155.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286+1766A>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759036 | ||||||
chr5:132759060
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1286+1742G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759060 | ||||||
chr5:132759089
|
G | A | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1286+1713C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759089 | ||||||
chr5:132759200
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1286+1602G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759200 | ||||||
chr5:132759218
|
G | GTCATGGG others(10): Show |
1 | a0001c0001t0002g0174 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1286+1567_1286+158 others(21): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759218 | ||||||
chr5:132759225
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1286+1577C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759225 | ||||||
chr5:132759230
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0073 | 2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1286+1572C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759230 | ||||||
chr5:132759282
|
G | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(169): Show | 218 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.1286+1520C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759282 | ||||||
chr5:132759350
|
A | G | 1 | a0001c0002t0002g0247 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1286+1452T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759350 | ||||||
chr5:132759467
|
CCT | C | 9 | a0001c0001t0003g0054a0001c0001t0003g0150a0001c0001t0003g0152others(6): Show | 12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.1286+1333_1286+133 others(6): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759467 | ||||||
chr5:132759554
|
G | A | 1 | a0001c0002t0002g0253 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1286+1248C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759554 | ||||||
chr5:132759696
|
C | T | 1 | a0001c0002t0002g0213 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1286+1106G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759696 | ||||||
chr5:132759916
|
G | T | 1 | a0001c0002t0002g0232 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1286+886C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132759916 | ||||||
chr5:132760074
|
G | T | 1 | a0001c0002t0002g0222 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1286+728C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132760074 | ||||||
chr5:132760431
|
A | G | 37 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0015others(34): Show | 45 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.1286+371T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132760431 | ||||||
chr5:132760603
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1286+199C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132760603 | ||||||
chr5:132760631
|
A | AAAAG | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 216 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.1286+167_1286+170d others(6): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132760631 | ||||||
chr5:132760779
|
C | T | 6 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0136others(3): Show | 8 | HG02055.hp1 HG02155.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1286+23G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132760779 | ||||||
chr5:132760785
|
C | T | 10 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0086others(7): Show | 13 | HG00438.hp2 HG02015.hp1 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.1286+17G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132760785 | ||||||
chr5:132760786
|
G | A | 6 | a0001c0001t0004g0145a0001c0001t0004g0146a0001c0001t0004g0147others(3): Show | 6 | HG02145.hp2 HG02615.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1286+16C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 9/9 | chr5 | 132760786 | ||||||
chr5:132761010
|
G | A | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1096-18C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 8/9 | chr5 | 132761010 | ||||||
chr5:132761104
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1095+29G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 8/9 | chr5 | 132761104 | ||||||
chr5:132761110
|
C | G | 1 | a0001c0002t0002g0032 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1095+23G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 8/9 | chr5 | 132761110 | ||||||
chr5:132761359
|
G | T | 38 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0015others(35): Show | 46 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.963-94C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 7/9 | chr5 | 132761359 | ||||||
chr5:132761733
|
T | A | 5 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0165others(2): Show | 5 | HG00639.hp1 HG01358.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.793+67A>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 6/9 | chr5 | 132761733 | ||||||
chr5:132761902
|
A | G | 1 | a0001c0002t0002g0190 | 1 | NA20905.hp2 | splice_region_variant&intron_variant | LOW | c.697-6T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 5/9 | chr5 | 132761902 | ||||||
chr5:132762071
|
G | A | 1 | a0001c0002t0002g0195 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.697-175C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 5/9 | chr5 | 132762071 | ||||||
chr5:132762225
|
G | T | 1 | a0001c0001t0001g0138 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.696+259C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 5/9 | chr5 | 132762225 | ||||||
chr5:132762226
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.696+258G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 5/9 | chr5 | 132762226 | ||||||
chr5:132762728
|
A | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(161): Show | 210 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.535-83T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/9 | chr5 | 132762728 | ||||||
chr5:132762841
|
A | C | 4 | a0001c0001t0001g0016a0001c0001t0001g0019a0001c0001t0001g0068others(1): Show | 6 | NA18954.hp1 NA18991.hp1 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.535-196T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/9 | chr5 | 132762841 | ||||||
chr5:132762874
|
TC | T | 9 | a0001c0001t0003g0054a0001c0001t0003g0150a0001c0001t0003g0152others(6): Show | 12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.535-230delG | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/9 | chr5 | 132762874 | ||||||
chr5:132763074
|
C | T | 4 | a0001c0001t0001g0027a0001c0001t0001g0087a0001c0001t0008g0059others(1): Show | 6 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.535-429G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/9 | chr5 | 132763074 | ||||||
chr5:132763433
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0087a0001c0001t0008g0059others(1): Show | 6 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.534+273C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/9 | chr5 | 132763433 | ||||||
chr5:132763443
|
C | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.534+263G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/9 | chr5 | 132763443 | ||||||
chr5:132763546
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.534+160T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/9 | chr5 | 132763546 | ||||||
chr5:132763559
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.534+147G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/9 | chr5 | 132763559 | ||||||
chr5:132763687
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.534+19G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 4/9 | chr5 | 132763687 | ||||||
chr5:132764206
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.347+18C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 3/9 | chr5 | 132764206 | ||||||
chr5:132764448
|
G | A | 10 | a0001c0001t0001g0135a0001c0001t0001g0161a0001c0001t0001g0162others(7): Show | 10 | HG00639.hp1 HG01358.hp1 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.152-29C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 2/9 | chr5 | 132764448 | ||||||
chr5:132764668
|
T | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0087a0001c0001t0008g0059others(1): Show | 6 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.152-249A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 2/9 | chr5 | 132764668 | ||||||
chr5:132764780
|
T | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 216 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.152-361A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 2/9 | chr5 | 132764780 | ||||||
chr5:132764807
|
A | G | 1 | a0001c0001t0005g0038 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.152-388T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 2/9 | chr5 | 132764807 | ||||||
chr5:132764913
|
A | G | 50 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0015others(47): Show | 61 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.152-494T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 2/9 | chr5 | 132764913 | ||||||
chr5:132765036
|
A | G | 9 | a0001c0001t0003g0054a0001c0001t0003g0150a0001c0001t0003g0152others(6): Show | 12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.151+373T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 2/9 | chr5 | 132765036 | ||||||
chr5:132765561
|
C | T | 6 | a0001c0001t0004g0145a0001c0001t0004g0146a0001c0001t0004g0147others(3): Show | 6 | HG02145.hp2 HG02615.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-32G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132765561 | ||||||
chr5:132765649
|
A | C | 2 | a0001c0001t0001g0052a0001c0001t0001g0098 | 2 | HG03927.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.31-120T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132765649 | ||||||
chr5:132765754
|
G | A | 1 | a0001c0002t0002g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.31-225C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132765754 | ||||||
chr5:132765937
|
T | C | 4 | a0001c0001t0001g0053a0001c0001t0001g0072a0001c0001t0001g0073others(1): Show | 4 | HG01884.hp1 HG01891.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-408A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132765937 | ||||||
chr5:132765977
|
C | G | 9 | a0001c0001t0003g0054a0001c0001t0003g0150a0001c0001t0003g0152others(6): Show | 12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.31-448G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132765977 | ||||||
chr5:132766077
|
C | T | 1 | a0001c0002t0002g0208 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.31-548G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132766077 | ||||||
chr5:132766184
|
G | C | 9 | a0001c0001t0003g0054a0001c0001t0003g0150a0001c0001t0003g0152others(6): Show | 12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.31-655C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132766184 | ||||||
chr5:132766211
|
G | A | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(150): Show | 195 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(192): Show |
intron_variant | MODIFIER | c.31-682C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132766211 | ||||||
chr5:132766368
|
G | A | 1 | a0001c0001t0003g0154 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.31-839C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132766368 | ||||||
chr5:132766400
|
G | C | 51 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0015others(48): Show | 62 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.31-871C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132766400 | ||||||
chr5:132766432
|
G | A | 8 | a0001c0002t0002g0031a0001c0002t0002g0203a0001c0002t0002g0222others(5): Show | 9 | NA18941.hp1 NA18945.hp1 NA18947.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-903C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132766432 | ||||||
chr5:132766976
|
A | C | 1 | a0001c0001t0001g0110 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.31-1447T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132766976 | ||||||
chr5:132767095
|
C | G | 4 | a0001c0001t0001g0027a0001c0001t0001g0087a0001c0001t0008g0059others(1): Show | 6 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-1566G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767095 | ||||||
chr5:132767549
|
C | T | 33 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0015others(30): Show | 41 | HG01069.hp2 HG01071.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.31-2020G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767549 | ||||||
chr5:132767579
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.31-2050C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767579 | ||||||
chr5:132767586
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0008g0059a0003c0004t0001g0021 | 4 | HG01167.hp2 HG01169.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.31-2057G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767586 | ||||||
chr5:132767664
|
C | T | 2 | a0001c0001t0002g0055a0001c0001t0002g0056 | 2 | HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.31-2135G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767664 | ||||||
chr5:132767676
|
A | G | 1 | a0001c0001t0001g0081 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.31-2147T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767676 | ||||||
chr5:132767885
|
G | A | 1 | a0001c0001t0001g0164 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.31-2356C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767885 | ||||||
chr5:132767916
|
C | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0109 | 2 | NA18943.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.31-2387G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767916 | ||||||
chr5:132767941
|
A | C | 1 | a0001c0002t0002g0212 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.31-2412T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767941 | ||||||
chr5:132767942
|
A | C | 2 | a0001c0001t0001g0064a0001c0001t0001g0095 | 2 | NA18982.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.31-2413T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767942 | ||||||
chr5:132767943
|
C | CACACACA others(6): Show |
1 | a0001c0001t0001g0119 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.31-2415_31-2414ins others(13): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132767943
|
C | CACACACA others(8): Show |
1 | a0001c0001t0001g0118 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.31-2415_31-2414ins others(15): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132767943
|
C | CACACACA others(10): Show |
3 | a0001c0001t0001g0062a0001c0001t0001g0064a0001c0001t0001g0095 | 3 | NA18968.hp1 NA18982.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.31-2415_31-2414ins others(17): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132767943
|
C | CCA | 17 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0015others(14): Show | 23 | HG01069.hp1 HG01243.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.31-2416_31-2415dup others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132767943
|
C | CCACA | 59 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0050others(56): Show | 66 | HG00639.hp1 HG00639.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.31-2418_31-2415dup others(4): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132767943
|
C | CCACACA | 35 | a0001c0001t0001g0052a0001c0001t0001g0073a0001c0001t0001g0090others(32): Show | 39 | HG00735.hp2 HG01257.hp1 HG01346.hp2 others(36): Show |
intron_variant | MODIFIER | c.31-2420_31-2415dup others(6): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132767943
|
C | CCACACAC others(1): Show |
30 | a0001c0001t0001g0002a0001c0001t0001g0057a0001c0001t0001g0094others(27): Show | 34 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.31-2422_31-2415dup others(8): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132767943
|
C | CCACACAC others(3): Show |
29 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0065others(26): Show | 34 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.31-2424_31-2415dup others(10): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132767943
|
C | CCACACAC others(5): Show |
18 | a0001c0001t0001g0004a0001c0001t0001g0019a0001c0001t0001g0023others(15): Show | 24 | HG00408.hp1 HG00438.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.31-2426_31-2415dup others(12): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132767943
|
C | CCACACAC others(7): Show |
10 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0016others(7): Show | 18 | HG00544.hp2 HG00597.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.31-2428_31-2415dup others(14): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132767943
|
C | CCACACAC others(9): Show |
10 | a0001c0001t0001g0001a0001c0001t0001g0060a0001c0001t0001g0063others(7): Show | 14 | HG00438.hp2 HG01975.hp1 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.31-2430_31-2415dup others(16): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132767943
|
C | CCACACAC others(11): Show |
6 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0061others(3): Show | 9 | HG02015.hp1 NA18612.hp2 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.31-2432_31-2415dup others(18): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132767943
|
C | CCACACAC others(13): Show |
4 | a0001c0001t0001g0018a0001c0001t0001g0092a0001c0001t0001g0117others(1): Show | 5 | HG02027.hp2 HG04115.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-2434_31-2415dup others(20): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132767943
|
C | CCACACAC others(17): Show |
1 | a0001c0001t0001g0069 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.31-2438_31-2415dup others(24): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132767943
|
CCA | C | 2 | a0001c0001t0001g0026a0004c0006t0001g0128 | 3 | HG02965.hp2 HG03540.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.31-2416_31-2415del others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132767943
|
CCACA | C | 4 | a0001c0001t0001g0025a0001c0001t0001g0136a0001c0001t0001g0159others(1): Show | 5 | HG02055.hp1 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-2418_31-2415del others(4): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132767943
|
CCACACA | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0079a0001c0001t0001g0080others(1): Show | 6 | HG01069.hp2 HG01071.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-2420_31-2415del others(6): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132767943
|
CCACACAC others(1): Show |
C | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0084others(1): Show | 4 | HG02451.hp1 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-2422_31-2415del others(8): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132767943
|
CCACACAC others(5): Show |
C | 4 | a0001c0001t0001g0072a0001c0001t0004g0020a0001c0001t0004g0075others(1): Show | 5 | HG01243.hp1 HG02258.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.31-2426_31-2415del others(12): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132767943 | ||||||
chr5:132768045
|
T | G | 1 | a0001c0001t0001g0072 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.31-2516A>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132768045 | ||||||
chr5:132768181
|
G | C | 1 | a0001c0001t0001g0158 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.31-2652C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132768181 | ||||||
chr5:132768299
|
G | C | 1 | a0001c0001t0001g0169 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.31-2770C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132768299 | ||||||
chr5:132768410
|
T | C | 1 | a0001c0003t0003g0151 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.31-2881A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132768410 | ||||||
chr5:132768464
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(114): Show | 152 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.31-2935G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132768464 | ||||||
chr5:132768690
|
C | T | 1 | a0001c0002t0002g0233 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.31-3161G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132768690 | ||||||
chr5:132768983
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.31-3454C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132768983 | ||||||
chr5:132769176
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.31-3647T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769176 | ||||||
chr5:132769405
|
T | C | 2 | a0001c0001t0004g0146a0001c0001t0004g0148 | 2 | HG02615.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.31-3876A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769405 | ||||||
chr5:132769592
|
A | T | 13 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0043others(10): Show | 16 | HG01167.hp1 HG02258.hp2 HG02622.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-4063T>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769592 | ||||||
chr5:132769683
|
C | G | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(115): Show | 153 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(150): Show |
intron_variant | MODIFIER | c.31-4154G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769683 | ||||||
chr5:132769704
|
G | C | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4175C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769704 | ||||||
chr5:132769708
|
A | C | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4179T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769708 | ||||||
chr5:132769798
|
A | T | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4269T>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769798 | ||||||
chr5:132769815
|
G | T | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4286C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769815 | ||||||
chr5:132769825
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4296C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769825 | ||||||
chr5:132769829
|
A | T | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4300T>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769829 | ||||||
chr5:132769831
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4302C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769831 | ||||||
chr5:132769833
|
GGGAATGG others(18): Show |
G | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4329_31-4305del others(25): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769833 | ||||||
chr5:132769867
|
G | T | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4338C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769867 | ||||||
chr5:132769877
|
T | G | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4348A>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769877 | ||||||
chr5:132769878
|
G | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0074others(15): Show | 21 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.31-4349C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769878 | ||||||
chr5:132769879
|
G | T | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4350C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769879 | ||||||
chr5:132769913
|
G | A | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4384C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769913 | ||||||
chr5:132769915
|
A | G | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4386T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769915 | ||||||
chr5:132769924
|
T | TATGTGCC others(41): Show |
1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4396_31-4395ins others(48): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769924 | ||||||
chr5:132769926
|
G | C | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4397C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769926 | ||||||
chr5:132769937
|
T | A | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4408A>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769937 | ||||||
chr5:132769939
|
T | A | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4410A>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769939 | ||||||
chr5:132769940
|
T | C | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4411A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769940 | ||||||
chr5:132769941
|
C | A | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4412G>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769941 | ||||||
chr5:132769944
|
G | C | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4415C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769944 | ||||||
chr5:132769945
|
T | A | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4416A>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769945 | ||||||
chr5:132769946
|
T | C | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4417A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769946 | ||||||
chr5:132769973
|
C | A | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4444G>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769973 | ||||||
chr5:132769982
|
C | CAT | 4 | a0001c0001t0001g0143a0001c0001t0002g0174a0001c0002t0002g0177others(1): Show | 4 | HG03130.hp1 NA18940.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-4455_31-4454dup others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769982 | ||||||
chr5:132769982
|
C | CATAT | 8 | a0001c0001t0002g0055a0001c0001t0002g0056a0001c0002t0002g0173others(5): Show | 8 | HG01496.hp2 HG02080.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.31-4457_31-4454dup others(4): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769982 | ||||||
chr5:132769982
|
C | CATATATA others(3): Show |
1 | a0001c0002t0002g0222 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.31-4463_31-4454dup others(10): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769982 | ||||||
chr5:132769982
|
CAT | C | 12 | a0001c0001t0001g0072a0001c0001t0001g0078a0001c0001t0003g0150others(9): Show | 16 | HG00642.hp1 HG01168.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-4455_31-4454del others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769982 | ||||||
chr5:132769982
|
CATATAT | C | 9 | a0001c0001t0001g0009a0001c0001t0001g0053a0001c0001t0003g0152others(6): Show | 12 | HG01069.hp2 HG01071.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.31-4459_31-4454del others(6): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769982 | ||||||
chr5:132769982
|
CATATATA others(1): Show |
C | 7 | a0001c0001t0001g0073a0001c0001t0001g0079a0001c0001t0001g0080others(4): Show | 7 | HG01891.hp2 HG02970.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-4461_31-4454del others(8): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769982 | ||||||
chr5:132769982
|
CATATATA others(3): Show |
C | 2 | a0001c0001t0001g0081a0001c0001t0002g0261 | 2 | HG01884.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.31-4463_31-4454del others(10): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769982 | ||||||
chr5:132769982
|
CATATATA others(5): Show |
C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.31-4465_31-4454del others(12): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769982 | ||||||
chr5:132769982
|
CATATATA others(9): Show |
C | 3 | a0001c0001t0005g0034a0001c0001t0005g0041a0001c0001t0005g0042 | 3 | HG02027.hp1 NA18964.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.31-4469_31-4454del others(16): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769982 | ||||||
chr5:132769984
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.31-4455A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769984 | ||||||
chr5:132769998
|
TATATATA others(19): Show |
T | 2 | a0001c0001t0001g0022a0001c0001t0001g0093 | 3 | HG02257.hp2 HG02895.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.31-4495_31-4470del others(26): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132769998 | ||||||
chr5:132770002
|
TATATATA others(15): Show |
T | 1 | a0001c0001t0002g0221 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.31-4495_31-4474del others(22): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770002 | ||||||
chr5:132770004
|
T | C | 5 | a0001c0001t0001g0090a0001c0001t0001g0121a0001c0001t0001g0122others(2): Show | 5 | HG01496.hp1 HG02280.hp1 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-4475A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770004 | ||||||
chr5:132770006
|
T | C | 68 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(65): Show | 91 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.31-4477A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770006 | ||||||
chr5:132770006
|
TATATATA others(11): Show |
T | 2 | a0001c0001t0004g0145a0001c0002t0002g0256 | 2 | HG02145.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.31-4495_31-4478del others(18): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770006 | ||||||
chr5:132770008
|
T | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(32): Show | 45 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.31-4479A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770008 | ||||||
chr5:132770008
|
T | TAC | 5 | a0001c0001t0001g0018a0001c0001t0001g0064a0001c0001t0001g0094others(2): Show | 6 | HG02300.hp1 HG03017.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.31-4480_31-4479ins others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770008 | ||||||
chr5:132770008
|
TATATATA others(9): Show |
T | 2 | a0001c0001t0001g0051a0001c0001t0005g0036 | 2 | HG03195.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.31-4495_31-4480del others(16): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770008 | ||||||
chr5:132770010
|
TATATATA others(7): Show |
T | 7 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0043others(4): Show | 10 | HG02622.hp2 HG02896.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.31-4495_31-4482del others(14): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770010 | ||||||
chr5:132770011
|
A | C | 1 | a0001c0001t0001g0062 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.31-4482T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770011 | ||||||
chr5:132770012
|
TATATATA others(5): Show |
T | 2 | a0001c0001t0001g0044a0001c0001t0004g0149 | 2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.31-4495_31-4484del others(12): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770012 | ||||||
chr5:132770014
|
TATATATA others(3): Show |
T | 2 | a0001c0001t0001g0027a0001c0001t0008g0059 | 3 | HG02630.hp1 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.31-4495_31-4486del others(10): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770014 | ||||||
chr5:132770016
|
TATATATA others(1): Show |
T | 15 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0087others(12): Show | 16 | HG01070.hp1 HG01099.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.31-4495_31-4488del others(8): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770016 | ||||||
chr5:132770018
|
TATATAC | T | 23 | a0001c0001t0002g0220a0001c0002t0002g0007a0001c0002t0002g0028others(20): Show | 27 | HG00544.hp1 HG00558.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.31-4495_31-4490del others(6): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770018 | ||||||
chr5:132770020
|
TATAC | T | 22 | a0001c0001t0001g0090a0001c0001t0001g0123a0001c0001t0001g0132others(19): Show | 24 | HG00735.hp2 HG00738.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.31-4495_31-4492del others(4): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770020 | ||||||
chr5:132770022
|
TAC | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(62): Show | 87 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.31-4495_31-4494del others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770022 | ||||||
chr5:132770023
|
ACACACAC others(51): Show |
A | 1 | a0001c0001t0001g0070 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.31-4552_31-4495del others(58): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770023 | ||||||
chr5:132770024
|
C | T | 68 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(65): Show | 81 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.31-4495G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770024 | ||||||
chr5:132770026
|
C | T | 5 | a0001c0001t0001g0125a0001c0001t0001g0137a0001c0001t0001g0142others(2): Show | 6 | HG00558.hp1 HG03471.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-4497G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770026 | ||||||
chr5:132770028
|
CACAT | C | 14 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(11): Show | 17 | HG00621.hp2 HG02055.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.31-4503_31-4500del others(4): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770028 | ||||||
chr5:132770030
|
C | T | 3 | a0001c0002t0002g0173a0001c0002t0002g0248a0001c0002t0002g0249 | 3 | HG01975.hp2 HG02300.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.31-4501G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770030 | ||||||
chr5:132770032
|
T | C | 8 | a0001c0001t0001g0077a0001c0001t0001g0125a0001c0001t0001g0137others(5): Show | 10 | HG00558.hp1 HG01243.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.31-4503A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770032 | ||||||
chr5:132770034
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.31-4505A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770034 | ||||||
chr5:132770039
|
A | G | 5 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0090others(2): Show | 5 | HG02280.hp1 HG02630.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-4510T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770039 | ||||||
chr5:132770041
|
A | G | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(142): Show | 189 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(186): Show |
intron_variant | MODIFIER | c.31-4512T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770041 | ||||||
chr5:132770043
|
G | A | 2 | a0001c0001t0002g0215a0001c0002t0002g0032 | 3 | HG03491.hp2 HG03492.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.31-4514C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770043 | ||||||
chr5:132770055
|
GTGTGTGT others(75): Show |
G | 1 | a0001c0001t0001g0079 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.31-4608_31-4527del others(82): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770055 | ||||||
chr5:132770059
|
GTGTGTAT others(83): Show |
G | 3 | a0001c0001t0001g0084a0001c0001t0001g0127a0001c0001t0002g0126 | 3 | HG01361.hp2 HG02027.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.31-4620_31-4531del others(90): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770059 | ||||||
chr5:132770061
|
GTGTA | G | 7 | a0001c0001t0002g0216a0001c0001t0002g0217a0001c0001t0002g0220others(4): Show | 7 | HG00642.hp2 NA18944.hp2 NA18954.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-4536_31-4533del others(4): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770061 | ||||||
chr5:132770061
|
GTGTATAT others(81): Show |
G | 19 | a0001c0001t0001g0024a0001c0001t0001g0085a0001c0001t0001g0124others(16): Show | 20 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.31-4620_31-4533del others(88): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770061 | ||||||
chr5:132770061
|
GTGTATAT others(83): Show |
G | 1 | a0001c0001t0001g0088 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.31-4622_31-4533del others(90): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770061 | ||||||
chr5:132770063
|
G | A | 2 | a0001c0002t0002g0248a0001c0002t0002g0249 | 2 | HG01975.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.31-4534C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770063 | ||||||
chr5:132770063
|
GTA | G | 42 | a0001c0001t0002g0193a0001c0001t0002g0215a0001c0001t0002g0260others(39): Show | 46 | HG00609.hp2 HG00639.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.31-4536_31-4535del others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770063 | ||||||
chr5:132770063
|
GTATATAT others(67): Show |
G | 1 | a0001c0001t0001g0131 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.31-4608_31-4535del others(74): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770063 | ||||||
chr5:132770063
|
GTATATAT others(77): Show |
G | 21 | a0001c0001t0001g0009a0001c0001t0001g0072a0001c0001t0001g0080others(18): Show | 27 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.31-4618_31-4535del others(84): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770063 | ||||||
chr5:132770063
|
GTATATAT others(79): Show |
G | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(104): Show | 142 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(139): Show |
intron_variant | MODIFIER | c.31-4620_31-4535del others(86): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770063 | ||||||
chr5:132770063
|
GTATATAT others(81): Show |
G | 14 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0043others(11): Show | 17 | HG02258.hp2 HG02622.hp2 HG02896.hp2 others(14): Show |
intron_variant | MODIFIER | c.31-4622_31-4535del others(88): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770063 | ||||||
chr5:132770063
|
GTATATAT others(83): Show |
G | 2 | a0001c0001t0001g0087a0003c0004t0001g0021 | 3 | HG01167.hp2 HG01169.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.31-4624_31-4535del others(90): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770063 | ||||||
chr5:132770065
|
A | G | 4 | a0001c0002t0002g0173a0001c0002t0002g0201a0001c0002t0002g0202others(1): Show | 4 | HG02080.hp1 NA18999.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-4536T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770065 | ||||||
chr5:132770067
|
A | G | 5 | a0001c0001t0002g0260a0001c0001t0002g0261a0001c0002t0002g0189others(2): Show | 5 | HG01069.hp1 HG01515.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.31-4538T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770067 | ||||||
chr5:132770089
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.31-4560C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770089 | ||||||
chr5:132770091
|
ATATATAT others(11): Show |
A | 1 | a0001c0002t0002g0250 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.31-4580_31-4563del others(18): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770091 | ||||||
chr5:132770092
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.31-4563A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770092 | ||||||
chr5:132770093
|
A | G | 1 | a0007c0011t0002g0188 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.31-4564T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770093 | ||||||
chr5:132770101
|
G | A | 3 | a0001c0001t0001g0070a0001c0001t0002g0260a0001c0001t0002g0261 | 3 | HG01884.hp2 HG02148.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.31-4572C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770101 | ||||||
chr5:132770103
|
A | G | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.31-4574T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770103 | ||||||
chr5:132770107
|
ATG | A | 3 | a0001c0002t0002g0187a0001c0002t0002g0251a0001c0002t0002g0252 | 3 | HG01099.hp2 HG02273.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.31-4580_31-4579del others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770107 | ||||||
chr5:132770109
|
G | A | 3 | a0001c0001t0001g0070a0001c0001t0002g0260a0001c0001t0002g0261 | 3 | HG01884.hp2 HG02148.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.31-4580C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770109 | ||||||
chr5:132770109
|
G | GTA | 77 | a0001c0001t0002g0174a0001c0001t0002g0215a0001c0001t0002g0216others(74): Show | 87 | HG00544.hp1 HG00558.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.31-4582_31-4581dup others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770109 | ||||||
chr5:132770109
|
G | GTATATAT others(41): Show |
1 | a0001c0002t0002g0256 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.31-4581_31-4580ins others(48): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770109 | ||||||
chr5:132770110
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.31-4581A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770110 | ||||||
chr5:132770111
|
A | G | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.31-4582T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770111 | ||||||
chr5:132770112
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.31-4583A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770112 | ||||||
chr5:132770114
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.31-4585A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770114 | ||||||
chr5:132770129
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.31-4600T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770129 | ||||||
chr5:132770131
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.31-4602T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770131 | ||||||
chr5:132770137
|
A | G | 1 | a0001c0001t0001g0070 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.31-4608T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770137 | ||||||
chr5:132770143
|
G | A | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.31-4614C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770143 | ||||||
chr5:132770145
|
G | A | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.31-4616C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770145 | ||||||
chr5:132770145
|
G | GTA | 5 | a0001c0002t0002g0032a0001c0002t0002g0253a0001c0002t0002g0254others(2): Show | 6 | HG01070.hp1 HG03491.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.31-4618_31-4617dup others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770145 | ||||||
chr5:132770147
|
A | G | 8 | a0001c0001t0001g0070a0001c0001t0001g0079a0001c0002t0002g0028others(5): Show | 9 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.31-4618T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770147 | ||||||
chr5:132770149
|
A | G | 16 | a0001c0001t0001g0009a0001c0001t0001g0070a0001c0001t0001g0072others(13): Show | 22 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.31-4620T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770149 | ||||||
chr5:132770151
|
A | G | 17 | a0001c0001t0001g0027a0001c0001t0001g0077a0001c0001t0001g0142others(14): Show | 21 | HG00642.hp1 HG02258.hp1 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.31-4622T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770151 | ||||||
chr5:132770153
|
A | G | 2 | a0001c0001t0001g0044a0001c0001t0001g0045 | 2 | HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.31-4624T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770153 | ||||||
chr5:132770163
|
A | G | 4 | a0001c0002t0002g0179a0001c0002t0002g0180a0001c0002t0002g0181others(1): Show | 4 | HG01099.hp1 HG01168.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.31-4634T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770163 | ||||||
chr5:132770333
|
C | T | 1 | a0001c0002t0002g0178 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.31-4804G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770333 | ||||||
chr5:132770552
|
T | C | 7 | a0001c0001t0004g0145a0001c0001t0004g0146a0001c0001t0004g0147others(4): Show | 7 | HG02145.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.31-5023A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770552 | ||||||
chr5:132770640
|
C | T | 3 | a0001c0002t0002g0175a0001c0002t0002g0176a0001c0002t0002g0177 | 3 | HG00609.hp2 NA18940.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.31-5111G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770640 | ||||||
chr5:132770789
|
T | C | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.31-5260A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770789 | ||||||
chr5:132770856
|
C | T | 1 | a0001c0001t0004g0262 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.31-5327G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770856 | ||||||
chr5:132770869
|
A | T | 81 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(78): Show | 109 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.31-5340T>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132770869 | ||||||
chr5:132771093
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.31-5564G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132771093 | ||||||
chr5:132771333
|
C | T | 9 | a0001c0001t0003g0054a0001c0001t0003g0150a0001c0001t0003g0152others(6): Show | 12 | HG00642.hp1 HG02559.hp2 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.30+5775G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132771333 | ||||||
chr5:132771359
|
G | T | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.30+5749C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132771359 | ||||||
chr5:132771548
|
G | A | 1 | a0001c0001t0001g0027 | 2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.30+5560C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132771548 | ||||||
chr5:132771654
|
T | C | 1 | a0001c0001t0001g0018 | 2 | NA18961.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.30+5454A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132771654 | ||||||
chr5:132771703
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.30+5405T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132771703 | ||||||
chr5:132771737
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0141 | 4 | HG01243.hp2 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+5371C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132771737 | ||||||
chr5:132771876
|
C | T | 1 | a0001c0001t0002g0174 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.30+5232G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132771876 | ||||||
chr5:132772008
|
T | C | 52 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0015others(49): Show | 63 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(60): Show |
intron_variant | MODIFIER | c.30+5100A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772008 | ||||||
chr5:132772015
|
A | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | NA18979.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.30+5093T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772015 | ||||||
chr5:132772086
|
TCA | T | 3 | a0001c0001t0001g0087a0001c0001t0008g0059a0003c0004t0001g0021 | 4 | HG01167.hp2 HG01169.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.30+5020_30+5021del others(2): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772086 | ||||||
chr5:132772302
|
G | C | 1 | a0001c0001t0006g0269 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.30+4806C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772302 | ||||||
chr5:132772315
|
G | C | 1 | a0001c0001t0001g0085 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.30+4793C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772315 | ||||||
chr5:132772334
|
G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(164): Show | 213 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(210): Show |
intron_variant | MODIFIER | c.30+4774C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772334 | ||||||
chr5:132772537
|
C | A | 1 | a0001c0002t0002g0256 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.30+4571G>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772537 | ||||||
chr5:132772626
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0071 | 3 | NA18954.hp1 NA18991.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.30+4482C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772626 | ||||||
chr5:132772649
|
C | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 216 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.30+4459G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772649 | ||||||
chr5:132772705
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.30+4403C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772705 | ||||||
chr5:132772993
|
G | A | 25 | a0001c0001t0001g0009a0001c0001t0001g0053a0001c0001t0001g0072others(22): Show | 31 | HG00642.hp1 HG01069.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.30+4115C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132772993 | ||||||
chr5:132773109
|
C | A | 1 | a0001c0001t0001g0169 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.30+3999G>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132773109 | ||||||
chr5:132773160
|
A | G | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.30+3948T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132773160 | ||||||
chr5:132773431
|
C | T | 16 | a0001c0001t0001g0009a0001c0001t0001g0053a0001c0001t0001g0072others(13): Show | 19 | HG01069.hp2 HG01071.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.30+3677G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132773431 | ||||||
chr5:132773593
|
A | G | 1 | a0001c0001t0001g0074 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.30+3515T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132773593 | ||||||
chr5:132773761
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.30+3347A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132773761 | ||||||
chr5:132773793
|
A | G | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.30+3315T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132773793 | ||||||
chr5:132773882
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.30+3226A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132773882 | ||||||
chr5:132773927
|
T | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.30+3181A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132773927 | ||||||
chr5:132774050
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.30+3058C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132774050 | ||||||
chr5:132774274
|
T | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.30+2834A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132774274 | ||||||
chr5:132774495
|
C | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0072a0001c0001t0001g0073 | 3 | HG01884.hp1 HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.30+2613G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132774495 | ||||||
chr5:132774780
|
C | T | 1 | a0001c0002t0002g0173 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.30+2328G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132774780 | ||||||
chr5:132774937
|
G | T | 1 | a0001c0001t0001g0043 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.30+2171C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132774937 | ||||||
chr5:132775046
|
G | T | 18 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(15): Show | 26 | HG00738.hp2 HG01975.hp1 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.30+2062C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132775046 | ||||||
chr5:132775238
|
A | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 216 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.30+1870T>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132775238 | ||||||
chr5:132775351
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 216 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.30+1757C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132775351 | ||||||
chr5:132775596
|
G | T | 1 | a0001c0001t0008g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.30+1512C>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132775596 | ||||||
chr5:132775626
|
C | G | 266 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(263): Show | 322 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(319): Show |
intron_variant | MODIFIER | c.30+1482G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132775626 | ||||||
chr5:132775651
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.30+1457T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132775651 | ||||||
chr5:132775889
|
T | C | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.30+1219A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132775889 | ||||||
chr5:132775898
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 216 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.30+1210T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132775898 | ||||||
chr5:132775931
|
C | G | 1 | a0001c0001t0001g0057 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.30+1177G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132775931 | ||||||
chr5:132776043
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 214 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.30+1065C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776043 | ||||||
chr5:132776297
|
T | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 216 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.30+811A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776297 | ||||||
chr5:132776313
|
C | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.30+795G>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776313 | ||||||
chr5:132776348
|
G | A | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 216 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.30+760C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776348 | ||||||
chr5:132776477
|
C | G | 1 | a0001c0001t0003g0054 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.30+631G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776477 | ||||||
chr5:132776558
|
TGGGGAGC others(8): Show |
T | 1 | a0001c0002t0002g0172 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.30+535_30+549delTC others(13): Show |
SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776558 | ||||||
chr5:132776699
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.30+409G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776699 | ||||||
chr5:132776741
|
A | G | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(167): Show | 216 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.30+367T>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776741 | ||||||
chr5:132776773
|
G | C | 9 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(6): Show | 9 | HG00639.hp1 HG01358.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.30+335C>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776773 | ||||||
chr5:132776778
|
G | A | 1 | a0001c0002t0002g0259 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.30+330C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776778 | ||||||
chr5:132776783
|
C | T | 1 | a0001c0002t0002g0170 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.30+325G>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776783 | ||||||
chr5:132776868
|
A | T | 169 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(166): Show | 215 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(212): Show |
intron_variant | MODIFIER | c.30+240T>A | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776868 | ||||||
chr5:132776922
|
C | G | 1 | a0001c0001t0001g0052 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.30+186G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776922 | ||||||
chr5:132776950
|
C | G | 1 | a0001c0001t0001g0263 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.30+158G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776950 | ||||||
chr5:132776977
|
T | C | 2 | a0001c0001t0002g0260a0001c0001t0002g0261 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.30+131A>G | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776977 | ||||||
chr5:132776994
|
C | G | 12 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0043others(9): Show | 15 | HG01167.hp1 HG02258.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.30+114G>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132776994 | ||||||
chr5:132777015
|
T | G | 1 | a0001c0001t0004g0262 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.30+93A>C | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132777015 | ||||||
chr5:132777080
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.30+28C>T | SEPTIN8 | ENSG00000164402.14 | transcript | ENST00000378719.7 | protein_coding | 1/9 | chr5 | 132777080 |