geneid | 124976 |
---|---|
ensemblid | ENSG00000183018.9 |
hgncid | 26992 |
symbol | SPNS2 |
name | SPNS lysolipid transporter 2, sphingosine-1-phosphate |
refseq_nuc | NM_001124758.3 |
refseq_prot | NP_001118230.1 |
ensembl_nuc | ENST00000329078.8 |
ensembl_prot | ENSP00000333292.3 |
mane_status | MANE Select |
chr | chr17 |
start | 4498881 |
end | 4539035 |
strand | + |
ver | v1.2 |
region | chr17:4498881-4539035 |
region5000 | chr17:4493881-4544035 |
regionname0 | SPNS2_chr17_4498881_4539035 |
regionname5000 | SPNS2_chr17_4493881_4544035 |
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 | 549 | 403 | 95 | 88 | 158 | 14 | 46 | 118 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0002 | 0/0 | 549 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1650 | 361 | 71 | 87 | 142 | 13 | 46 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
c0002 | 0/0 | 1650 | 9 | 9 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
c0003 | 0/0 | 1650 | 8 | 8 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
c0004 | 0/0 | 1650 | 7 | 0 | 0 | 7 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
c0005 | 0/0 | 1650 | 5 | 0 | 0 | 5 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
c0006 | 0/0 | 1650 | 2 | 1 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
c0007 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
c0008 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
c0009 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
c0010 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
c0011 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
c0012 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
c0013 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
c0014 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
c0015 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
c0016 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
c0017 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
c0018 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
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 | 0/1 | 1751 | 136 | 10 | 38 | 68 | 5 | 14 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0002 | 0/0 | 1751 | 98 | 2 | 17 | 70 | 0 | 9 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0003 | 1/0 | 1755 | 40 | 6 | 19 | 1 | 5 | 8 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0004 | 0/0 | 1751 | 27 | 23 | 4 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0005 | 0/0 | 1751 | 10 | 2 | 2 | 1 | 0 | 5 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0006 | 0/0 | 1751 | 10 | 10 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0007 | 0/0 | 1751 | 6 | 5 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0008 | 0/0 | 1751 | 5 | 0 | 0 | 4 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0009 | 0/0 | 1755 | 5 | 4 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0010 | 0/0 | 1751 | 5 | 0 | 3 | 0 | 1 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0011 | 0/0 | 1751 | 4 | 4 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0012 | 0/0 | 1751 | 4 | 0 | 0 | 4 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0013 | 0/0 | 1751 | 4 | 0 | 2 | 0 | 2 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0014 | 0/0 | 1755 | 4 | 1 | 1 | 0 | 0 | 2 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0015 | 0/0 | 1751 | 3 | 3 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0016 | 0/0 | 1755 | 3 | 2 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0017 | 0/0 | 1755 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0018 | 0/0 | 1740 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0019 | 0/0 | 1751 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0020 | 0/0 | 1751 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0021 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0022 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0023 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0024 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0025 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0026 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0027 | 0/0 | 1751 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0028 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0029 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0030 | 0/0 | 1751 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0031 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0032 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0033 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0034 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0035 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0036 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0037 | 0/0 | 1751 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0038 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0039 | 0/0 | 1751 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0040 | 0/0 | 1751 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0041 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0042 | 0/0 | 1751 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0043 | 0/0 | 1751 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0044 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0045 | 0/0 | 1755 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0046 | 0/0 | 1751 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0047 | 0/0 | 1751 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0048 | 0/0 | 1751 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0049 | 0/0 | 1751 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0050 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0051 | 0/0 | 1751 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
t0052 | 0/0 | 1751 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
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 | 4 | 0 | 0 | 4 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0002 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0003 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0005 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0037 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
g0371 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1650 | 361 | 71 | 87 | 142 | 13 | 46 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0002 | 0/0 | 1650 | 9 | 9 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0003 | 0/0 | 1650 | 8 | 8 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0004 | 0/0 | 1650 | 7 | 0 | 0 | 7 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0005 | 0/0 | 1650 | 5 | 0 | 0 | 5 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0006 | 0/0 | 1650 | 2 | 1 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0007 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0008 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0009 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0010 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0012 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0013 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0014 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0015 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0016 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0017 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0018 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0002c0011 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3400 | 132 | 10 | 38 | 65 | 4 | 14 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0002 | 0/0 | 3400 | 83 | 0 | 17 | 57 | 0 | 9 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0003 | 1/0 | 3404 | 40 | 6 | 19 | 1 | 5 | 8 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0004 | 0/0 | 3400 | 16 | 12 | 4 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0005 | 0/0 | 3400 | 9 | 1 | 2 | 1 | 0 | 5 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0006 | 0/0 | 3400 | 8 | 8 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0007 | 0/0 | 3400 | 5 | 4 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0008 | 0/0 | 3400 | 5 | 0 | 0 | 4 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0009 | 0/0 | 3404 | 5 | 4 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0010 | 0/0 | 3400 | 5 | 0 | 3 | 0 | 1 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0011 | 0/0 | 3400 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0012 | 0/0 | 3400 | 4 | 0 | 0 | 4 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0013 | 0/0 | 3400 | 4 | 0 | 2 | 0 | 2 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0014 | 0/0 | 3404 | 4 | 1 | 1 | 0 | 0 | 2 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0015 | 0/0 | 3400 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0016 | 0/0 | 3404 | 3 | 2 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0017 | 0/0 | 3404 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0018 | 0/0 | 3389 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0019 | 0/0 | 3400 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0020 | 0/0 | 3400 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0021 | 0/0 | 3404 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0022 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0023 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0025 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0026 | 0/0 | 3404 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0028 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0029 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0030 | 0/0 | 3400 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0031 | 0/0 | 3404 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0033 | 0/0 | 3404 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0034 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0035 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0036 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0037 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0038 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0039 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0040 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0042 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0043 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0046 | 0/0 | 3400 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0047 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0048 | 0/0 | 3400 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0049 | 0/0 | 3400 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0050 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0051 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0001t0052 | 0/0 | 3400 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0002t0004 | 0/0 | 3400 | 5 | 5 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0002t0006 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0002t0011 | 0/0 | 3400 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0002t0044 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0003t0004 | 0/0 | 3400 | 3 | 3 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0003t0005 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0003t0006 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0003t0007 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0003t0024 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0003t0041 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0004t0001 | 0/0 | 3400 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0004t0002 | 0/0 | 3400 | 5 | 0 | 0 | 5 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0005t0002 | 0/0 | 3400 | 5 | 0 | 0 | 5 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0006t0002 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0006t0027 | 0/0 | 3400 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0007t0004 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0008t0004 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0009t0015 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0010t0001 | 0/0 | 3400 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0012t0002 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0013t0045 | 0/0 | 3404 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0014t0002 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0015t0002 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0016t0001 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0017t0002 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0001c0018t0004 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
a0002c0011t0032 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | copy fasta | chr17 | 4493881 | 4544035 |
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 | 3 | 0 | 0 | 3 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0005 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0037 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0003g0371 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0004g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0004g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0004g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0004g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0004g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0004g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0004g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0005g0003 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0005g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0005g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0006g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0006g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0006g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0007g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0007g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0007g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0007g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0007g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0008g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0008g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0008g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0009g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0009g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0009g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0009g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0009g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0010g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0010g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0010g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0010g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0010g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0011g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0011g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0012g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0012g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0012g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0012g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0013g0002 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0013g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0014g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0014g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0014g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0014g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0015g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0015g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0016g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0016g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0016g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0017g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0017g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0018g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0018g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0019g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0019g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0020g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0020g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0021g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0022g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0023g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0025g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0026g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0028g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0029g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0030g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0031g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0033g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0034g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0035g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0036g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0037g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0038g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0039g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0040g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0042g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0043g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0046g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0047g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0048g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0049g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0050g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0051g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0001t0052g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0002t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0002t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0002t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0002t0004g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0002t0004g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0002t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0002t0011g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0002t0011g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0002t0044g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0003t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0003t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0003t0004g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0003t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0003t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0003t0007g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0003t0024g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0003t0041g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0004t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0004t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0004t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0004t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0004t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0004t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0005t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0005t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0005t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0005t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0005t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0006t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0006t0027g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0007t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0008t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0009t0015g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0010t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0012t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0013t0045g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0014t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0015t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0016t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0017t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0001c0018t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
a0002c0011t0032g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0073 | EUR | GBR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00099 | hp2 | a0001 | c0010 | t0001 | g0149 | EUR | GBR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | FIN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0049 | EUR | FIN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00323 | hp1 | a0001 | c0001 | t0009 | g0185 | EUR | FIN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0152 | EUR | FIN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00423 | hp1 | a0001 | c0001 | t0043 | g0320 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00423 | hp2 | a0001 | c0004 | t0002 | g0267 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00438 | hp2 | a0001 | c0014 | t0002 | g0139 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00639 | hp1 | a0001 | c0001 | t0014 | g0078 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0101 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00673 | hp1 | a0001 | c0005 | t0002 | g0076 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00673 | hp2 | a0001 | c0015 | t0002 | g0064 | EAS | CHS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00735 | hp2 | a0001 | c0001 | t0010 | g0040 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00738 | hp1 | a0001 | c0001 | t0004 | g0150 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG00741 | hp2 | a0001 | c0001 | t0013 | g0002 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0355 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01081 | hp2 | a0001 | c0001 | t0010 | g0210 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0352 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0095 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01167 | hp1 | a0001 | c0006 | t0027 | g0191 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0055 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01192 | hp2 | a0001 | c0001 | t0003 | g0250 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01243 | hp2 | a0001 | c0001 | t0007 | g0186 | AMR | PUR | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01256 | hp1 | a0001 | c0001 | t0010 | g0215 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0184 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0017 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01346 | hp1 | a0001 | c0001 | t0005 | g0361 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0116 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0058 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01433 | hp2 | a0001 | c0001 | t0013 | g0002 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01515 | hp2 | a0001 | c0001 | t0013 | g0043 | EUR | IBS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01516 | hp1 | a0001 | c0001 | t0010 | g0199 | EUR | IBS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0008 | EUR | IBS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0008 | EUR | IBS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01517 | hp2 | a0001 | c0001 | t0013 | g0002 | EUR | IBS | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01884 | hp1 | a0001 | c0001 | t0007 | g0177 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01884 | hp2 | a0001 | c0001 | t0051 | g0192 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01891 | hp1 | a0001 | c0001 | t0022 | g0366 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0172 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0253 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0217 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0305 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0205 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0251 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02015 | hp1 | a0001 | c0001 | t0042 | g0154 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0322 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02055 | hp2 | a0001 | c0017 | t0002 | g0045 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0315 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02145 | hp1 | a0001 | c0009 | t0015 | g0164 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | CDX | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0342 | EAS | CDX | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02257 | hp1 | a0001 | c0001 | t0016 | g0261 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02257 | hp2 | a0001 | c0002 | t0004 | g0071 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02258 | hp1 | a0001 | c0003 | t0041 | g0067 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02258 | hp2 | a0001 | c0001 | t0009 | g0165 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0276 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0125 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0254 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0228 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02451 | hp2 | a0001 | c0006 | t0002 | g0194 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | KHV | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02572 | hp1 | a0001 | c0002 | t0011 | g0367 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02572 | hp2 | a0001 | c0001 | t0025 | g0173 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02622 | hp1 | a0002 | c0011 | t0032 | g0161 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02622 | hp2 | a0001 | c0001 | t0033 | g0028 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02630 | hp1 | a0001 | c0001 | t0021 | g0368 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02630 | hp2 | a0001 | c0003 | t0004 | g0068 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0231 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0236 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02698 | hp1 | a0001 | c0001 | t0049 | g0122 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0343 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0237 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0331 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02723 | hp1 | a0001 | c0002 | t0006 | g0158 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0003 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0097 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02738 | hp1 | a0001 | c0001 | t0010 | g0201 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02809 | hp1 | a0001 | c0001 | t0009 | g0166 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02809 | hp2 | a0001 | c0001 | t0016 | g0056 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02818 | hp2 | a0001 | c0007 | t0004 | g0193 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02886 | hp1 | a0001 | c0001 | t0034 | g0026 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02895 | hp1 | a0001 | c0002 | t0004 | g0349 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02896 | hp2 | a0001 | c0001 | t0038 | g0220 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02897 | hp2 | a0001 | c0002 | t0004 | g0350 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0233 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02922 | hp2 | a0001 | c0001 | t0019 | g0227 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02965 | hp1 | a0001 | c0001 | t0009 | g0168 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02970 | hp1 | a0001 | c0002 | t0004 | g0069 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02970 | hp2 | a0001 | c0001 | t0015 | g0175 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02976 | hp1 | a0001 | c0001 | t0014 | g0140 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0354 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0039 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0327 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03041 | hp1 | a0001 | c0001 | t0017 | g0369 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03041 | hp2 | a0001 | c0001 | t0035 | g0030 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03098 | hp1 | a0001 | c0001 | t0050 | g0130 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03098 | hp2 | a0001 | c0003 | t0004 | g0351 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03130 | hp1 | a0001 | c0003 | t0024 | g0170 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03130 | hp2 | a0001 | c0001 | t0017 | g0364 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03139 | hp1 | a0001 | c0003 | t0007 | g0167 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0162 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03195 | hp2 | a0001 | c0002 | t0011 | g0365 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0171 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03209 | hp2 | a0001 | c0001 | t0028 | g0178 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0032 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03225 | hp2 | a0001 | c0001 | t0031 | g0029 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03239 | hp1 | a0001 | c0001 | t0052 | g0180 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0003 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03453 | hp1 | a0001 | c0001 | t0026 | g0188 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03486 | hp2 | a0001 | c0001 | t0007 | g0163 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0196 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0337 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0356 | AFR | ESN | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0157 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03540 | hp2 | a0001 | c0013 | t0045 | g0222 | AFR | GWD | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03579 | hp1 | a0001 | c0001 | t0011 | g0362 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03579 | hp2 | a0001 | c0001 | t0019 | g0070 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03704 | hp2 | a0001 | c0001 | t0014 | g0339 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0207 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03831 | hp1 | a0001 | c0001 | t0046 | g0104 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03834 | hp1 | a0001 | c0001 | t0005 | g0179 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03834 | hp2 | a0001 | c0001 | t0008 | g0182 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03927 | hp1 | a0001 | c0001 | t0005 | g0003 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0360 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0323 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG04184 | hp2 | a0001 | c0001 | t0048 | g0136 | SAS | BEB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0077 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG04204 | hp1 | a0001 | c0001 | t0030 | g0183 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0216 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG04228 | hp2 | a0001 | c0001 | t0016 | g0317 | SAS | STU | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18522 | hp1 | a0001 | c0001 | t0011 | g0363 | AFR | YRI | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | YRI | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | CHB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18747 | hp2 | a0001 | c0016 | t0001 | g0334 | EAS | CHB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18906 | hp1 | a0001 | c0003 | t0004 | g0230 | AFR | YRI | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18906 | hp2 | a0001 | c0002 | t0004 | g0235 | AFR | YRI | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18945 | hp1 | a0001 | c0001 | t0040 | g0264 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18945 | hp2 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0348 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18957 | hp2 | a0001 | c0001 | t0012 | g0138 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18960 | hp2 | a0001 | c0001 | t0012 | g0325 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18963 | hp1 | a0001 | c0005 | t0002 | g0147 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18965 | hp1 | a0001 | c0005 | t0002 | g0047 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18970 | hp2 | a0001 | c0012 | t0002 | g0242 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18977 | hp1 | a0001 | c0001 | t0012 | g0118 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18980 | hp2 | a0001 | c0001 | t0005 | g0189 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18984 | hp1 | a0001 | c0001 | t0047 | g0345 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18986 | hp2 | a0001 | c0001 | t0039 | g0332 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18990 | hp1 | a0001 | c0001 | t0008 | g0181 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18991 | hp1 | a0001 | c0004 | t0001 | g0022 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18994 | hp1 | a0001 | c0001 | t0020 | g0263 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18994 | hp2 | a0001 | c0005 | t0002 | g0052 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18995 | hp2 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18997 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19003 | hp2 | a0001 | c0004 | t0002 | g0292 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19004 | hp2 | a0001 | c0004 | t0002 | g0123 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19005 | hp2 | a0001 | c0001 | t0018 | g0110 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19010 | hp1 | a0001 | c0004 | t0002 | g0294 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19012 | hp1 | a0001 | c0004 | t0002 | g0293 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19030 | hp1 | a0001 | c0008 | t0004 | g0072 | AFR | LWK | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19030 | hp2 | a0001 | c0018 | t0004 | g0044 | AFR | LWK | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19043 | hp1 | a0001 | c0001 | t0036 | g0224 | AFR | LWK | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0169 | AFR | LWK | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19057 | hp2 | a0001 | c0001 | t0018 | g0109 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19068 | hp2 | a0001 | c0004 | t0001 | g0022 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19074 | hp2 | a0001 | c0001 | t0020 | g0273 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19083 | hp2 | a0001 | c0005 | t0002 | g0119 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19085 | hp2 | a0001 | c0001 | t0037 | g0001 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19089 | hp2 | a0001 | c0001 | t0012 | g0085 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA19091 | hp2 | a0001 | c0001 | t0008 | g0004 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ASW | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA20129 | hp2 | a0001 | c0002 | t0044 | g0232 | AFR | ASW | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | TSI | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0009 | EUR | TSI | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0336 | SAS | GIH | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA20905 | hp2 | a0001 | c0001 | t0014 | g0335 | SAS | GIH | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02109 | hp2 | a0001 | c0001 | t0009 | g0190 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02486 | hp1 | a0001 | c0001 | t0006 | g0027 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02486 | hp2 | a0001 | c0001 | t0006 | g0160 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0223 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG02559 | hp2 | a0001 | c0001 | t0015 | g0187 | AFR | ACB | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03471 | hp1 | a0001 | c0001 | t0023 | g0370 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | MSL | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG06807 | hp1 | a0001 | c0001 | t0029 | g0174 | AFR | USA | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
HG06807 | hp2 | a0001 | c0003 | t0006 | g0159 | AFR | USA | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0031 | AFR | USA | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA21309 | hp1 | a0001 | c0003 | t0005 | g0176 | AFR | LWK | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | LWK | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0037 | REF | REF | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0371 | REF | REF | SPNS2_chr17_4493881_4544035 | SPNS2 | chr17 | 4493881 | 4544035 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:4536344
|
C | T | 1 | a0002 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.1525C>T | p.Pro509Ser | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/13 | 1692/3404 | 1525/1650 | 509/549 | chr17 | 4536344 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:4499263
|
C | T | 2 | a0001c0017a0001c0018 | 2 | HG02055.hp2 NA19030.hp2 |
synonymous_variant | LOW | c.216C>T | p.Pro72Pro | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/13 | 383/3404 | 216/1650 | 72/549 | chr17 | 4499263 | ||
chr17:4513248
|
C | T | 1 | a0001c0016 | 1 | NA18747.hp2 | splice_region_variant&synonymous_variant | LOW | c.372C>T | p.Gly124Gly | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/13 | 539/3404 | 372/1650 | 124/549 | chr17 | 4513248 | ||
chr17:4530634
|
C | T | 1 | a0001c0015 | 1 | HG00673.hp2 | splice_region_variant&synonymous_variant | LOW | c.576C>T | p.Tyr192Tyr | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/13 | 743/3404 | 576/1650 | 192/549 | chr17 | 4530634 | ||
chr17:4530667
|
G | A | 1 | a0001c0002 | 9 | HG02257.hp2 HG02572.hp1 HG02723.hp1 others(6): Show |
synonymous_variant | LOW | c.609G>A | p.Val203Val | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/13 | 776/3404 | 609/1650 | 203/549 | chr17 | 4530667 | ||
chr17:4530673
|
C | T | 1 | a0001c0014 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.615C>T | p.Ile205Ile | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/13 | 782/3404 | 615/1650 | 205/549 | chr17 | 4530673 | ||
chr17:4532550
|
T | G | 1 | a0001c0007 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.801T>G | p.Pro267Pro | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 6/13 | 968/3404 | 801/1650 | 267/549 | chr17 | 4532550 | ||
chr17:4533007
|
G | A | 2 | a0001c0006a0001c0017 | 3 | HG01167.hp1 HG02055.hp2 HG02451.hp2 |
synonymous_variant | LOW | c.966G>A | p.Thr322Thr | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 7/13 | 1133/3404 | 966/1650 | 322/549 | chr17 | 4533007 | ||
chr17:4533010
|
G | A | 1 | a0001c0008 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.969G>A | p.Ser323Ser | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 7/13 | 1136/3404 | 969/1650 | 323/549 | chr17 | 4533010 | ||
chr17:4533025
|
C | T | 1 | a0001c0013 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.984C>T | p.Ala328Ala | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 7/13 | 1151/3404 | 984/1650 | 328/549 | chr17 | 4533025 | ||
chr17:4533059
|
C | T | 1 | a0001c0003 | 8 | HG02258.hp1 HG02630.hp2 HG03098.hp2 others(5): Show |
synonymous_variant | LOW | c.1018C>T | p.Leu340Leu | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 7/13 | 1185/3404 | 1018/1650 | 340/549 | chr17 | 4533059 | ||
chr17:4533288
|
G | A | 1 | a0001c0009 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.1134G>A | p.Val378Val | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/13 | 1301/3404 | 1134/1650 | 378/549 | chr17 | 4533288 | ||
chr17:4536108
|
C | A | 1 | a0001c0005 | 5 | HG00673.hp1 NA18963.hp1 NA18965.hp1 others(2): Show |
synonymous_variant | LOW | c.1377C>A | p.Ala459Ala | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/13 | 1544/3404 | 1377/1650 | 459/549 | chr17 | 4536108 | ||
chr17:4536153
|
G | T | 1 | a0001c0012 | 1 | NA18970.hp2 | synonymous_variant | LOW | c.1422G>T | p.Gly474Gly | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/13 | 1589/3404 | 1422/1650 | 474/549 | chr17 | 4536153 | ||
chr17:4536328
|
C | T | 1 | a0001c0004 | 7 | HG00423.hp2 NA18991.hp1 NA19003.hp2 others(4): Show |
synonymous_variant | LOW | c.1509C>T | p.Tyr503Tyr | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/13 | 1676/3404 | 1509/1650 | 503/549 | chr17 | 4536328 | ||
chr17:4536388
|
G | C | 1 | a0001c0010 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.1569G>C | p.Ala523Ala | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/13 | 1736/3404 | 1569/1650 | 523/549 | chr17 | 4536388 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:4498886
|
G | T | 1 | a0001c0001t0052 | 1 | HG03239.hp1 | 5_prime_UTR_variant | MODIFIER | c.-162G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/13 | 162 | chr17 | 4498886 | |||||
chr17:4498895
|
G | C | 30 | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(27): Show | 61 | HG00323.hp1 HG01167.hp1 HG01243.hp2 others(58): Show |
5_prime_UTR_variant | MODIFIER | c.-153G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/13 | 153 | chr17 | 4498895 | |||||
chr17:4498919
|
G | C | 6 | a0001c0001t0011a0001c0001t0017a0001c0001t0021others(3): Show | 9 | HG01891.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-129G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/13 | 129 | chr17 | 4498919 | |||||
chr17:4499000
|
C | T | 8 | a0001c0001t0006a0001c0001t0031a0001c0001t0033others(5): Show | 15 | HG02486.hp1 HG02486.hp2 HG02622.hp1 others(12): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-48C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/13 | chr17 | 4499000 | ||||||
chr17:4499006
|
C | A | 1 | a0001c0001t0036 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-42C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/13 | 42 | chr17 | 4499006 | |||||
chr17:4499027
|
G | C | 1 | a0001c0001t0037 | 1 | NA19085.hp2 | 5_prime_UTR_variant | MODIFIER | c.-21G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/13 | 21 | chr17 | 4499027 | |||||
chr17:4537516
|
G | A | 1 | a0001c0001t0038 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*68G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 574 | chr17 | 4537516 | |||||
chr17:4537612
|
A | G | 21 | a0001c0001t0001a0001c0001t0005a0001c0001t0014others(18): Show | 165 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*164A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 670 | chr17 | 4537612 | |||||
chr17:4537663
|
G | A | 1 | a0001c0001t0039 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*215G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 721 | chr17 | 4537663 | |||||
chr17:4537696
|
G | A | 1 | a0001c0001t0040 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*248G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 754 | chr17 | 4537696 | |||||
chr17:4537706
|
T | C | 1 | a0001c0001t0020 | 2 | NA18994.hp1 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*258T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 764 | chr17 | 4537706 | |||||
chr17:4537742
|
C | T | 1 | a0001c0001t0030 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*294C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 800 | chr17 | 4537742 | |||||
chr17:4537743
|
G | A | 1 | a0001c0001t0046 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*295G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 801 | chr17 | 4537743 | |||||
chr17:4537835
|
C | A | 1 | a0001c0001t0047 | 1 | NA18984.hp1 | 3_prime_UTR_variant | MODIFIER | c.*387C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 893 | chr17 | 4537835 | |||||
chr17:4537855
|
G | A | 1 | a0001c0001t0048 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*407G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 913 | chr17 | 4537855 | |||||
chr17:4537895
|
G | A | 2 | a0001c0001t0021a0001c0001t0031 | 2 | HG02630.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*447G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 953 | chr17 | 4537895 | |||||
chr17:4537923
|
G | A | 2 | a0001c0003t0024a0001c0003t0041 | 2 | HG02258.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*475G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 981 | chr17 | 4537923 | |||||
chr17:4538000
|
A | C | 1 | a0001c0001t0035 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*552A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1058 | chr17 | 4538000 | |||||
chr17:4538014
|
C | A | 14 | a0001c0001t0002a0001c0001t0008a0001c0001t0018others(11): Show | 109 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*566C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1072 | chr17 | 4538014 | |||||
chr17:4538142
|
G | A | 4 | a0001c0001t0015a0001c0002t0044a0001c0009t0015others(1): Show | 5 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*694G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1200 | chr17 | 4538142 | |||||
chr17:4538224
|
A | C | 1 | a0001c0001t0034 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*776A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1282 | chr17 | 4538224 | |||||
chr17:4538241
|
C | T | 1 | a0001c0001t0013 | 4 | HG00741.hp2 HG01433.hp2 HG01515.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*793C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1299 | chr17 | 4538241 | |||||
chr17:4538246
|
C | T | 1 | a0001c0001t0029 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*798C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1304 | chr17 | 4538246 | |||||
chr17:4538380
|
A | C | 6 | a0001c0001t0012a0001c0001t0015a0001c0002t0044others(3): Show | 10 | HG02145.hp1 HG02559.hp2 HG02622.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*932A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1438 | chr17 | 4538380 | |||||
chr17:4538423
|
C | T | 3 | a0001c0001t0012a0001c0001t0015a0001c0009t0015 | 7 | HG02145.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*975C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1481 | chr17 | 4538423 | |||||
chr17:4538466
|
C | A | 1 | a0001c0001t0035 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1018C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1524 | chr17 | 4538466 | |||||
chr17:4538470
|
AGGGG | A | 63 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(60): Show | 345 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(342): Show |
3_prime_UTR_variant | MODIFIER | c.*1027_*1030delGGGG | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1533 | INFO_REALIGN_3_PRIME | chr17 | 4538470 | ||||
chr17:4538590
|
C | G | 24 | a0001c0001t0001a0001c0001t0005a0001c0001t0012others(21): Show | 171 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*1142C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1648 | chr17 | 4538590 | |||||
chr17:4538591
|
CCTGCACT others(4): Show |
C | 1 | a0001c0001t0018 | 2 | NA19005.hp2 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1149_*1159delCTTC others(7): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1655 | INFO_REALIGN_3_PRIME | chr17 | 4538591 | ||||
chr17:4538626
|
C | T | 2 | a0001c0001t0019a0001c0001t0022 | 3 | HG01891.hp1 HG02922.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1178C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1684 | chr17 | 4538626 | |||||
chr17:4538638
|
G | A | 1 | a0001c0001t0042 | 1 | HG02015.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1190G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1696 | chr17 | 4538638 | |||||
chr17:4538748
|
G | A | 1 | a0001c0001t0043 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1300G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1806 | chr17 | 4538748 | |||||
chr17:4538783
|
G | A | 2 | a0001c0001t0049a0001c0006t0027 | 2 | HG01167.hp1 HG02698.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1335G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1841 | chr17 | 4538783 | |||||
chr17:4538793
|
C | A | 3 | a0001c0001t0010a0001c0001t0036a0001c0001t0052 | 7 | HG00735.hp2 HG01081.hp2 HG01256.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1345C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1851 | chr17 | 4538793 | |||||
chr17:4538840
|
C | T | 1 | a0001c0001t0051 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1392C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1898 | chr17 | 4538840 | |||||
chr17:4538899
|
G | C | 1 | a0001c0001t0025 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1451G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 13/13 | 1957 | chr17 | 4538899 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:4499508
|
T | C | 371 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(368): Show | 403 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.370+91T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4499508 | ||||||
chr17:4499701
|
C | T | 9 | a0001c0001t0011g0362a0001c0001t0011g0363a0001c0001t0017g0364others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.370+284C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4499701 | ||||||
chr17:4499725
|
CCTCTGCG others(1): Show |
C | 7 | a0001c0001t0006g0027a0001c0001t0006g0031a0001c0001t0006g0032others(4): Show | 7 | HG02486.hp1 HG02622.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.370+313_370+320del others(8): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4499725 | |||||
chr17:4499757
|
C | A | 1 | a0001c0001t0003g0033 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.370+340C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4499757 | ||||||
chr17:4499839
|
G | A | 1 | a0001c0001t0003g0033 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.370+422G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4499839 | ||||||
chr17:4499873
|
C | G | 2 | a0001c0001t0005g0360a0001c0001t0005g0361 | 2 | HG01346.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.370+456C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4499873 | ||||||
chr17:4500104
|
T | C | 131 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(128): Show | 140 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.370+687T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4500104 | ||||||
chr17:4500576
|
A | G | 1 | a0001c0001t0006g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.370+1159A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4500576 | ||||||
chr17:4500580
|
AACAC | A | 21 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(18): Show | 24 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.370+1171_370+1174d others(6): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4500580 | |||||
chr17:4500707
|
T | C | 8 | a0001c0001t0003g0033a0001c0001t0006g0015a0001c0001t0006g0157others(5): Show | 9 | HG02486.hp2 HG02622.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.370+1290T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4500707 | ||||||
chr17:4500708
|
G | GC | 69 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(66): Show | 76 | HG00323.hp1 HG00735.hp2 HG00741.hp2 others(73): Show |
intron_variant | MODIFIER | c.370+1293dupC | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4500708 | |||||
chr17:4500770
|
G | T | 1 | a0001c0001t0003g0033 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.370+1353G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4500770 | ||||||
chr17:4500775
|
C | T | 42 | a0001c0001t0005g0003a0001c0001t0005g0169a0001c0001t0005g0179others(39): Show | 46 | HG00323.hp1 HG01167.hp1 HG01243.hp2 others(43): Show |
intron_variant | MODIFIER | c.370+1358C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4500775 | ||||||
chr17:4500824
|
C | T | 6 | a0001c0001t0006g0027a0001c0001t0006g0032a0001c0001t0031g0029others(3): Show | 6 | HG02486.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.370+1407C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4500824 | ||||||
chr17:4500838
|
G | T | 1 | a0001c0001t0001g0359 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.370+1421G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4500838 | ||||||
chr17:4500846
|
G | A | 237 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(234): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(252): Show |
intron_variant | MODIFIER | c.370+1429G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4500846 | ||||||
chr17:4500964
|
C | T | 27 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(24): Show | 30 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(27): Show |
intron_variant | MODIFIER | c.370+1547C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4500964 | ||||||
chr17:4501039
|
A | G | 2 | a0001c0017t0002g0045a0001c0018t0004g0044 | 2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.370+1622A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501039 | ||||||
chr17:4501087
|
G | A | 9 | a0001c0001t0011g0362a0001c0001t0011g0363a0001c0001t0017g0364others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.370+1670G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501087 | ||||||
chr17:4501113
|
G | A | 2 | a0001c0001t0007g0163a0001c0009t0015g0164 | 2 | HG02145.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.370+1696G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501113 | ||||||
chr17:4501129
|
A | G | 2 | a0001c0001t0001g0357a0001c0001t0002g0358 | 2 | NA18969.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.370+1712A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501129 | ||||||
chr17:4501263
|
T | C | 21 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(18): Show | 24 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.370+1846T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501263 | ||||||
chr17:4501279
|
C | G | 21 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(18): Show | 24 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.370+1862C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501279 | ||||||
chr17:4501280
|
C | T | 2 | a0001c0001t0003g0238a0001c0001t0003g0239 | 2 | HG01433.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.370+1863C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501280 | ||||||
chr17:4501322
|
CAG | C | 7 | a0001c0001t0001g0014a0001c0001t0003g0148a0001c0001t0003g0151others(4): Show | 8 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(5): Show |
intron_variant | MODIFIER | c.370+1910_370+1911d others(4): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4501322 | |||||
chr17:4501527
|
G | A | 9 | a0001c0001t0011g0362a0001c0001t0011g0363a0001c0001t0017g0364others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.370+2110G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501527 | ||||||
chr17:4501528
|
C | T | 9 | a0001c0001t0011g0362a0001c0001t0011g0363a0001c0001t0017g0364others(6): Show | 9 | HG01891.hp1 HG02572.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.370+2111C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501528 | ||||||
chr17:4501636
|
T | C | 2 | a0001c0001t0001g0241a0001c0001t0002g0240 | 2 | NA18948.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.370+2219T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501636 | ||||||
chr17:4501919
|
A | G | 6 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(3): Show | 6 | HG02083.hp1 HG02523.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.370+2502A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4501919 | ||||||
chr17:4502097
|
T | C | 361 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(358): Show | 393 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.370+2680T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502097 | ||||||
chr17:4502200
|
A | AC | 139 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0023others(136): Show | 153 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.370+2789dupC | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4502200 | |||||
chr17:4502324
|
G | C | 140 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0023others(137): Show | 154 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.370+2907G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502324 | ||||||
chr17:4502366
|
T | G | 1 | a0001c0001t0002g0046 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.370+2949T>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502366 | ||||||
chr17:4502379
|
CA | C | 144 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(141): Show | 154 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.370+2978delA | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4502379 | |||||
chr17:4502379
|
CAA | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0023others(150): Show | 168 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.370+2977_370+2978d others(4): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4502379 | |||||
chr17:4502418
|
ATGT | A | 3 | a0001c0001t0051g0192a0001c0006t0002g0194a0001c0007t0004g0193 | 3 | HG01884.hp2 HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.370+3006_370+3008d others(5): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4502418 | |||||
chr17:4502428
|
T | C | 30 | a0001c0001t0001g0001a0001c0001t0001g0241a0001c0001t0001g0243others(27): Show | 34 | HG00423.hp2 HG02004.hp2 HG02071.hp2 others(31): Show |
intron_variant | MODIFIER | c.370+3011T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502428 | ||||||
chr17:4502510
|
C | T | 1 | a0001c0001t0048g0136 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.370+3093C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502510 | ||||||
chr17:4502569
|
C | G | 5 | a0001c0001t0001g0234a0001c0001t0003g0236a0001c0001t0004g0233others(2): Show | 5 | HG02145.hp2 HG02683.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.370+3152C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502569 | ||||||
chr17:4502775
|
C | G | 1 | a0001c0001t0003g0153 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.370+3358C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502775 | ||||||
chr17:4502775
|
C | T | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | NA18983.hp2 NA19063.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.370+3358C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502775 | ||||||
chr17:4502854
|
A | G | 353 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(350): Show | 383 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.370+3437A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502854 | ||||||
chr17:4502910
|
G | A | 10 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(7): Show | 12 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.370+3493G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502910 | ||||||
chr17:4502950
|
C | T | 1 | a0001c0001t0010g0040 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.370+3533C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502950 | ||||||
chr17:4502954
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.370+3537C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4502954 | ||||||
chr17:4503161
|
G | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 179 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.370+3744G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4503161 | ||||||
chr17:4503166
|
C | T | 3 | a0001c0001t0051g0192a0001c0006t0002g0194a0001c0007t0004g0193 | 3 | HG01884.hp2 HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.370+3749C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4503166 | ||||||
chr17:4503175
|
G | C | 162 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(159): Show | 179 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.370+3758G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4503175 | ||||||
chr17:4503212
|
G | A | 1 | a0001c0001t0016g0056 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.370+3795G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4503212 | ||||||
chr17:4503678
|
G | A | 27 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0065others(24): Show | 31 | HG00099.hp2 HG00621.hp1 HG00639.hp2 others(28): Show |
intron_variant | MODIFIER | c.370+4261G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4503678 | ||||||
chr17:4503795
|
C | T | 2 | a0001c0001t0009g0190a0001c0006t0027g0191 | 2 | HG01167.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.370+4378C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4503795 | ||||||
chr17:4503924
|
G | A | 6 | a0001c0001t0006g0027a0001c0001t0006g0032a0001c0001t0031g0029others(3): Show | 6 | HG02486.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.370+4507G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4503924 | ||||||
chr17:4503982
|
C | CT | 86 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0025others(83): Show | 92 | HG00280.hp2 HG00558.hp2 HG00642.hp1 others(89): Show |
intron_variant | MODIFIER | c.370+4580dupT | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4503982 | |||||
chr17:4503982
|
C | CTT | 119 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(116): Show | 128 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.370+4579_370+4580d others(4): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4503982 | |||||
chr17:4503982
|
C | CTTT | 54 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(51): Show | 62 | HG00323.hp1 HG00735.hp2 HG00741.hp2 others(59): Show |
intron_variant | MODIFIER | c.370+4578_370+4580d others(5): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4503982 | |||||
chr17:4504080
|
G | C | 1 | a0001c0001t0001g0265 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.370+4663G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4504080 | ||||||
chr17:4504210
|
C | T | 1 | a0001c0001t0040g0264 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.370+4793C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4504210 | ||||||
chr17:4504299
|
T | C | 363 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(360): Show | 395 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(392): Show |
intron_variant | MODIFIER | c.370+4882T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4504299 | ||||||
chr17:4504379
|
C | A | 1 | a0001c0001t0003g0196 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.370+4962C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4504379 | ||||||
chr17:4504417
|
A | G | 150 | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0023others(147): Show | 163 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(160): Show |
intron_variant | MODIFIER | c.370+5000A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4504417 | ||||||
chr17:4504435
|
CAT | C | 2 | a0001c0001t0003g0008a0001c0001t0003g0058 | 3 | HG01361.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.370+5020_370+5021d others(4): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4504435 | |||||
chr17:4504464
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.370+5047G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4504464 | ||||||
chr17:4504709
|
C | T | 1 | a0001c0001t0004g0223 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.370+5292C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4504709 | ||||||
chr17:4504711
|
C | T | 140 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(137): Show | 150 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.370+5294C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4504711 | ||||||
chr17:4505046
|
C | T | 2 | a0001c0001t0006g0031a0001c0001t0036g0224 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.370+5629C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505046 | ||||||
chr17:4505146
|
C | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0247a0001c0001t0001g0255others(10): Show | 15 | HG00558.hp2 HG00642.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.370+5729C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505146 | ||||||
chr17:4505201
|
C | A | 2 | a0001c0001t0009g0165a0001c0001t0009g0166 | 2 | HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.370+5784C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505201 | ||||||
chr17:4505404
|
G | A | 1 | a0001c0008t0004g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.370+5987G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505404 | ||||||
chr17:4505415
|
C | G | 4 | a0001c0001t0001g0229a0001c0001t0003g0231a0001c0002t0044g0232others(1): Show | 4 | HG01243.hp1 HG02647.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.370+5998C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505415 | ||||||
chr17:4505431
|
A | G | 2 | a0001c0001t0005g0189a0001c0001t0008g0004 | 4 | NA18945.hp2 NA18980.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.370+6014A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505431 | ||||||
chr17:4505482
|
G | A | 1 | a0001c0001t0029g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.370+6065G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505482 | ||||||
chr17:4505516
|
A | G | 1 | a0001c0001t0004g0223 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.370+6099A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505516 | ||||||
chr17:4505526
|
G | C | 35 | a0001c0001t0001g0034a0001c0001t0001g0041a0001c0001t0001g0195others(32): Show | 37 | HG00099.hp1 HG00280.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.370+6109G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505526 | ||||||
chr17:4505549
|
G | A | 4 | a0001c0001t0007g0177a0001c0001t0015g0175a0001c0001t0028g0178others(1): Show | 4 | HG01884.hp1 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.370+6132G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505549 | ||||||
chr17:4505736
|
G | T | 160 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(157): Show | 174 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.370+6319G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505736 | ||||||
chr17:4505793
|
G | A | 4 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0290others(1): Show | 4 | NA18946.hp2 NA18948.hp1 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.370+6376G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505793 | ||||||
chr17:4505918
|
G | A | 1 | a0001c0001t0040g0264 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.370+6501G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4505918 | ||||||
chr17:4506078
|
C | A | 1 | a0001c0001t0002g0197 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.370+6661C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506078 | ||||||
chr17:4506158
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0066 | 2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.370+6741C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506158 | ||||||
chr17:4506171
|
T | C | 2 | a0001c0001t0003g0050a0001c0001t0003g0051 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.370+6754T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506171 | ||||||
chr17:4506236
|
G | A | 2 | a0001c0001t0006g0031a0001c0001t0036g0224 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.370+6819G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506236 | ||||||
chr17:4506251
|
C | T | 3 | a0001c0001t0001g0221a0001c0001t0004g0223a0001c0013t0045g0222 | 3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.370+6834C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506251 | ||||||
chr17:4506362
|
T | C | 1 | a0001c0001t0001g0285 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.371-6885T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506362 | ||||||
chr17:4506442
|
G | C | 2 | a0001c0001t0011g0363a0001c0001t0017g0364 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.371-6805G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506442 | ||||||
chr17:4506471
|
G | T | 1 | a0001c0001t0001g0346 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.371-6776G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506471 | ||||||
chr17:4506581
|
C | T | 1 | a0001c0002t0004g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.371-6666C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506581 | ||||||
chr17:4506774
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.371-6473T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506774 | ||||||
chr17:4506961
|
G | A | 3 | a0001c0001t0003g0207a0001c0001t0009g0190a0001c0006t0027g0191 | 3 | HG01167.hp1 HG02109.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.371-6286G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4506961 | ||||||
chr17:4507187
|
C | T | 95 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0053others(92): Show | 101 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.371-6060C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507187 | ||||||
chr17:4507188
|
G | A | 17 | a0001c0001t0003g0033a0001c0001t0005g0169a0001c0001t0007g0171others(14): Show | 17 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.371-6059G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507188 | ||||||
chr17:4507212
|
G | A | 3 | a0001c0004t0002g0292a0001c0004t0002g0293a0001c0004t0002g0294 | 3 | NA19003.hp2 NA19010.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.371-6035G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507212 | ||||||
chr17:4507331
|
A | C | 2 | a0001c0001t0001g0291a0001c0001t0002g0343 | 2 | HG02602.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.371-5916A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507331 | ||||||
chr17:4507364
|
C | T | 6 | a0001c0001t0005g0169a0001c0001t0007g0171a0001c0001t0007g0172others(3): Show | 6 | HG01891.hp2 HG02145.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.371-5883C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507364 | ||||||
chr17:4507398
|
C | A | 5 | a0001c0001t0001g0198a0001c0001t0001g0209a0001c0001t0002g0074others(2): Show | 5 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.371-5849C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507398 | ||||||
chr17:4507418
|
A | C | 3 | a0001c0001t0001g0221a0001c0001t0004g0223a0001c0013t0045g0222 | 3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.371-5829A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507418 | ||||||
chr17:4507420
|
A | G | 3 | a0001c0001t0001g0221a0001c0001t0004g0223a0001c0013t0045g0222 | 3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.371-5827A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507420 | ||||||
chr17:4507461
|
C | T | 12 | a0001c0001t0003g0236a0001c0001t0004g0237a0001c0001t0006g0015others(9): Show | 13 | HG02055.hp2 HG02486.hp2 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.371-5786C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507461 | ||||||
chr17:4507552
|
T | G | 1 | a0001c0001t0002g0295 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.371-5695T>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507552 | ||||||
chr17:4507561
|
A | C | 15 | a0001c0001t0001g0262a0001c0001t0003g0236a0001c0001t0004g0237others(12): Show | 16 | HG01109.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.371-5686A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507561 | ||||||
chr17:4507628
|
G | A | 2 | a0001c0001t0006g0031a0001c0001t0036g0224 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.371-5619G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507628 | ||||||
chr17:4507670
|
G | A | 2 | a0001c0001t0006g0031a0001c0001t0036g0224 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.371-5577G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507670 | ||||||
chr17:4507766
|
G | A | 1 | a0001c0001t0001g0296 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.371-5481G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507766 | ||||||
chr17:4507831
|
C | T | 6 | a0001c0001t0006g0027a0001c0001t0006g0032a0001c0001t0031g0029others(3): Show | 6 | HG02486.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.371-5416C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4507831 | ||||||
chr17:4508022
|
C | T | 3 | a0001c0001t0001g0221a0001c0001t0004g0223a0001c0013t0045g0222 | 3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.371-5225C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508022 | ||||||
chr17:4508118
|
C | T | 3 | a0001c0001t0001g0221a0001c0001t0004g0223a0001c0013t0045g0222 | 3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.371-5129C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508118 | ||||||
chr17:4508139
|
A | G | 3 | a0001c0001t0001g0221a0001c0001t0004g0223a0001c0013t0045g0222 | 3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.371-5108A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508139 | ||||||
chr17:4508210
|
A | T | 95 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0053others(92): Show | 101 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.371-5037A>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508210 | ||||||
chr17:4508211
|
T | C | 3 | a0001c0001t0001g0221a0001c0001t0004g0223a0001c0013t0045g0222 | 3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.371-5036T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508211 | ||||||
chr17:4508230
|
T | C | 3 | a0001c0001t0001g0221a0001c0001t0004g0223a0001c0013t0045g0222 | 3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.371-5017T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508230 | ||||||
chr17:4508534
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(272): Show | 301 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.371-4713A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508534 | ||||||
chr17:4508561
|
G | T | 1 | a0001c0008t0004g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.371-4686G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508561 | ||||||
chr17:4508575
|
C | T | 1 | a0001c0001t0003g0017 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.371-4672C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508575 | ||||||
chr17:4508586
|
G | C | 22 | a0001c0001t0001g0141a0001c0001t0001g0225a0001c0001t0001g0229others(19): Show | 23 | HG00558.hp1 HG01243.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.371-4661G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508586 | ||||||
chr17:4508649
|
C | T | 1 | a0001c0001t0001g0284 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.371-4598C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508649 | ||||||
chr17:4508683
|
G | A | 4 | a0001c0001t0009g0165a0001c0001t0009g0166a0001c0001t0009g0168others(1): Show | 4 | HG02258.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.371-4564G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508683 | ||||||
chr17:4508760
|
C | T | 1 | a0001c0005t0002g0076 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.371-4487C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508760 | ||||||
chr17:4508984
|
C | T | 3 | a0001c0001t0001g0124a0001c0001t0002g0342a0001c0004t0002g0123 | 3 | HG02165.hp2 NA19004.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.371-4263C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508984 | ||||||
chr17:4508996
|
G | A | 1 | a0001c0001t0002g0057 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.371-4251G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508996 | ||||||
chr17:4508997
|
A | G | 1 | a0001c0001t0002g0057 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.371-4250A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508997 | ||||||
chr17:4508998
|
G | A | 1 | a0001c0001t0002g0057 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.371-4249G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4508998 | ||||||
chr17:4509038
|
G | A | 1 | a0001c0001t0001g0081 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.371-4209G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4509038 | ||||||
chr17:4509425
|
G | A | 12 | a0001c0001t0005g0003a0001c0001t0005g0179a0001c0001t0005g0184others(9): Show | 16 | HG00323.hp1 HG01257.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.371-3822G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4509425 | ||||||
chr17:4509575
|
G | A | 1 | a0001c0001t0009g0166 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.371-3672G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4509575 | ||||||
chr17:4509602
|
GGCCCAA | G | 8 | a0001c0001t0007g0177a0001c0001t0009g0165a0001c0001t0009g0166others(5): Show | 8 | HG01884.hp1 HG02258.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.371-3641_371-3636d others(8): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4509602 | |||||
chr17:4509720
|
C | T | 3 | a0001c0001t0007g0177a0001c0001t0028g0178a0001c0003t0005g0176 | 3 | HG01884.hp1 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.371-3527C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4509720 | ||||||
chr17:4509729
|
T | C | 4 | a0001c0001t0009g0165a0001c0001t0009g0166a0001c0001t0009g0168others(1): Show | 4 | HG02258.hp2 HG02809.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.371-3518T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4509729 | ||||||
chr17:4510037
|
G | A | 2 | a0001c0001t0003g0050a0001c0001t0003g0051 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.371-3210G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510037 | ||||||
chr17:4510093
|
G | A | 1 | a0001c0001t0002g0266 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.371-3154G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510093 | ||||||
chr17:4510096
|
C | T | 1 | a0001c0001t0004g0055 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.371-3151C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510096 | ||||||
chr17:4510135
|
C | A | 2 | a0001c0001t0006g0157a0001c0002t0011g0365 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.371-3112C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510135 | ||||||
chr17:4510147
|
C | T | 2 | a0001c0001t0005g0184a0001c0001t0009g0185 | 2 | HG00323.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.371-3100C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510147 | ||||||
chr17:4510187
|
C | T | 17 | a0001c0001t0003g0033a0001c0001t0005g0169a0001c0001t0007g0171others(14): Show | 17 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.371-3060C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510187 | ||||||
chr17:4510248
|
C | A | 9 | a0001c0001t0001g0225a0001c0001t0001g0229a0001c0001t0003g0231others(6): Show | 10 | HG01243.hp1 HG02451.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.371-2999C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510248 | ||||||
chr17:4510581
|
T | C | 2 | a0001c0001t0002g0082a0001c0014t0002g0139 | 2 | HG00438.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.371-2666T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510581 | ||||||
chr17:4510594
|
C | T | 2 | a0001c0001t0006g0031a0001c0001t0036g0224 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.371-2653C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510594 | ||||||
chr17:4510732
|
A | G | 222 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(219): Show | 240 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(237): Show |
intron_variant | MODIFIER | c.371-2515A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510732 | ||||||
chr17:4510840
|
C | T | 21 | a0001c0001t0001g0006a0001c0001t0001g0065a0001c0001t0001g0066others(18): Show | 23 | HG00099.hp1 HG00673.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.371-2407C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510840 | ||||||
chr17:4510874
|
C | T | 6 | a0001c0001t0001g0282a0001c0001t0001g0341a0001c0001t0002g0021others(3): Show | 7 | HG00597.hp1 NA18941.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.371-2373C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510874 | ||||||
chr17:4510944
|
T | C | 1 | a0001c0001t0002g0297 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.371-2303T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4510944 | ||||||
chr17:4511047
|
T | C | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0004t0002g0267 | 3 | HG00423.hp2 HG02071.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.371-2200T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511047 | ||||||
chr17:4511154
|
A | G | 1 | a0001c0001t0004g0228 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.371-2093A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511154 | ||||||
chr17:4511293
|
C | T | 2 | a0001c0001t0003g0050a0001c0001t0003g0051 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.371-1954C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511293 | ||||||
chr17:4511395
|
G | A | 16 | a0001c0001t0003g0033a0001c0001t0005g0169a0001c0001t0007g0171others(13): Show | 16 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.371-1852G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511395 | ||||||
chr17:4511499
|
A | C | 1 | a0001c0001t0009g0165 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.371-1748A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511499 | ||||||
chr17:4511753
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.371-1494G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511753 | ||||||
chr17:4511793
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.371-1454G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511793 | ||||||
chr17:4511796
|
C | T | 1 | a0001c0001t0001g0143 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.371-1451C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511796 | ||||||
chr17:4511808
|
A | G | 2 | a0001c0001t0001g0195a0001c0001t0003g0207 | 2 | HG03710.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.371-1439A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511808 | ||||||
chr17:4511812
|
C | T | 1 | a0001c0001t0047g0345 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.371-1435C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511812 | ||||||
chr17:4511883
|
A | AACACCCT others(3): Show |
1 | a0001c0001t0020g0263 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.371-1364_371-1363i others(12): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511883 | ||||||
chr17:4511885
|
A | C | 1 | a0001c0001t0020g0263 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.371-1362A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511885 | ||||||
chr17:4511893
|
T | C | 1 | a0001c0001t0020g0263 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.371-1354T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511893 | ||||||
chr17:4511922
|
C | T | 1 | a0001c0001t0002g0281 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.371-1325C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511922 | ||||||
chr17:4511976
|
G | A | 2 | a0001c0001t0001g0268a0001c0004t0002g0267 | 2 | HG00423.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.371-1271G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4511976 | ||||||
chr17:4512020
|
C | T | 3 | a0001c0001t0001g0221a0001c0001t0004g0223a0001c0013t0045g0222 | 3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.371-1227C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512020 | ||||||
chr17:4512041
|
C | T | 1 | a0001c0001t0020g0263 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.371-1206C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512041 | ||||||
chr17:4512064
|
T | C | 1 | a0001c0014t0002g0139 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.371-1183T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512064 | ||||||
chr17:4512099
|
T | A | 2 | a0001c0002t0004g0349a0001c0002t0004g0350 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.371-1148T>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512099 | ||||||
chr17:4512176
|
A | G | 1 | a0001c0001t0020g0263 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.371-1071A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512176 | ||||||
chr17:4512177
|
G | A | 1 | a0001c0001t0020g0263 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.371-1070G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512177 | ||||||
chr17:4512422
|
G | A | 19 | a0001c0001t0001g0013a0001c0001t0001g0075a0001c0001t0001g0128others(16): Show | 22 | HG01109.hp1 HG01123.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.371-825G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512422 | ||||||
chr17:4512462
|
G | A | 2 | a0001c0001t0003g0050a0001c0001t0003g0051 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.371-785G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512462 | ||||||
chr17:4512531
|
A | C | 98 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(95): Show | 106 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.371-716A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512531 | ||||||
chr17:4512636
|
G | GTGTGTGT others(19): Show |
2 | a0001c0001t0007g0177a0001c0001t0028g0178 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.371-600_371-575dup others(26): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4512636 | |||||
chr17:4512640
|
GTGTGCGT others(15): Show |
G | 1 | a0001c0001t0014g0339 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.371-602_371-581del others(22): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4512640 | |||||
chr17:4512647
|
T | C | 19 | a0001c0001t0001g0234a0001c0001t0004g0233a0001c0001t0005g0003others(16): Show | 23 | HG00323.hp1 HG01167.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.371-600T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512647 | ||||||
chr17:4512649
|
C | T | 1 | a0001c0017t0002g0045 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.371-598C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512649 | ||||||
chr17:4512673
|
C | CGAGCGGG others(13): Show |
3 | a0001c0001t0001g0221a0001c0001t0004g0223a0001c0013t0045g0222 | 3 | HG02559.hp1 HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.371-573_371-572ins others(20): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4512673 | |||||
chr17:4512675
|
C | CGCGGGTG others(13): Show |
2 | a0001c0001t0006g0031a0001c0001t0036g0224 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.371-571_371-570ins others(20): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4512675 | |||||
chr17:4512675
|
C | T | 4 | a0001c0001t0001g0221a0001c0001t0003g0051a0001c0001t0004g0223others(1): Show | 4 | HG02559.hp1 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.371-572C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512675 | ||||||
chr17:4512677
|
T | C | 143 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(140): Show | 152 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.371-570T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512677 | ||||||
chr17:4512708
|
A | G | 1 | a0001c0001t0049g0122 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.371-539A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512708 | ||||||
chr17:4512742
|
A | G | 23 | a0001c0001t0001g0013a0001c0001t0001g0075a0001c0001t0001g0128others(20): Show | 25 | HG01081.hp2 HG01123.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.371-505A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512742 | ||||||
chr17:4512758
|
G | A | 1 | a0001c0001t0012g0085 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.371-489G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512758 | ||||||
chr17:4512808
|
G | A | 9 | a0001c0001t0001g0225a0001c0001t0001g0229a0001c0001t0003g0231others(6): Show | 10 | HG01243.hp1 HG02451.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.371-439G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512808 | ||||||
chr17:4512825
|
C | G | 11 | a0001c0001t0001g0117a0001c0001t0001g0120a0001c0001t0002g0012others(8): Show | 12 | HG01257.hp1 HG01258.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.371-422C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512825 | ||||||
chr17:4512833
|
TC | T | 24 | a0001c0001t0001g0014a0001c0001t0001g0195a0001c0001t0001g0213others(21): Show | 27 | HG00099.hp2 HG00280.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.371-410delC | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 4512833 | |||||
chr17:4512862
|
C | T | 7 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(4): Show | 7 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.371-385C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512862 | ||||||
chr17:4512925
|
G | A | 1 | a0001c0001t0003g0086 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.371-322G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512925 | ||||||
chr17:4512929
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 152 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.371-318T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512929 | ||||||
chr17:4512961
|
C | G | 1 | a0001c0006t0002g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.371-286C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512961 | ||||||
chr17:4512968
|
G | A | 2 | a0001c0001t0005g0179a0001c0001t0052g0180 | 2 | HG03239.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.371-279G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512968 | ||||||
chr17:4512999
|
G | A | 141 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(138): Show | 150 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.371-248G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4512999 | ||||||
chr17:4513121
|
C | A | 3 | a0001c0001t0001g0262a0001c0001t0004g0260a0001c0001t0016g0261 | 3 | HG01109.hp2 HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.371-126C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 1/12 | chr17 | 4513121 | ||||||
chr17:4513340
|
C | A | 1 | a0001c0001t0001g0075 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.436+28C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513340 | ||||||
chr17:4513343
|
G | A | 120 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0016others(117): Show | 127 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.436+31G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513343 | ||||||
chr17:4513357
|
G | A | 1 | a0001c0001t0003g0212 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.436+45G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513357 | ||||||
chr17:4513379
|
T | C | 142 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(139): Show | 151 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(148): Show |
intron_variant | MODIFIER | c.436+67T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513379 | ||||||
chr17:4513574
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.436+262G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513574 | ||||||
chr17:4513685
|
G | A | 141 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(138): Show | 150 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(147): Show |
intron_variant | MODIFIER | c.436+373G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513685 | ||||||
chr17:4513766
|
T | G | 1 | a0001c0001t0020g0263 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.436+454T>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513766 | ||||||
chr17:4513800
|
C | T | 1 | a0001c0001t0040g0264 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.436+488C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513800 | ||||||
chr17:4513821
|
G | A | 27 | a0001c0001t0001g0141a0001c0001t0001g0225a0001c0001t0001g0229others(24): Show | 28 | HG01243.hp1 HG02074.hp2 HG02165.hp2 others(25): Show |
intron_variant | MODIFIER | c.436+509G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513821 | ||||||
chr17:4513956
|
C | T | 78 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0053others(75): Show | 84 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.436+644C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513956 | ||||||
chr17:4513963
|
G | C | 86 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(83): Show | 94 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.436+651G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513963 | ||||||
chr17:4513997
|
C | G | 10 | a0001c0001t0003g0033a0001c0001t0011g0362a0001c0001t0011g0363others(7): Show | 10 | HG01884.hp2 HG01891.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+685C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4513997 | ||||||
chr17:4514186
|
A | C | 10 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(7): Show | 10 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+874A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4514186 | ||||||
chr17:4514238
|
C | G | 5 | a0001c0001t0001g0221a0001c0001t0004g0223a0001c0001t0006g0031others(2): Show | 5 | HG02559.hp1 HG02818.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+926C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4514238 | ||||||
chr17:4514274
|
G | T | 2 | a0001c0001t0007g0177a0001c0001t0028g0178 | 2 | HG01884.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.436+962G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4514274 | ||||||
chr17:4514283
|
C | T | 1 | a0001c0008t0004g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.436+971C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4514283 | ||||||
chr17:4514414
|
C | A | 1 | a0001c0001t0003g0039 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.436+1102C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4514414 | ||||||
chr17:4514601
|
C | T | 1 | a0001c0008t0004g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.436+1289C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4514601 | ||||||
chr17:4514892
|
C | T | 20 | a0001c0001t0001g0141a0001c0001t0001g0225a0001c0001t0001g0229others(17): Show | 21 | HG01243.hp1 HG02257.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.436+1580C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4514892 | ||||||
chr17:4515044
|
G | T | 76 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0016others(73): Show | 82 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.436+1732G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515044 | ||||||
chr17:4515051
|
C | T | 2 | a0001c0001t0003g0152a0001c0001t0025g0173 | 2 | HG00323.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.436+1739C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515051 | ||||||
chr17:4515104
|
G | A | 1 | a0001c0001t0002g0340 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.436+1792G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515104 | ||||||
chr17:4515189
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.436+1877T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515189 | ||||||
chr17:4515256
|
G | A | 251 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(248): Show | 272 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.436+1944G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515256 | ||||||
chr17:4515328
|
A | T | 1 | a0001c0001t0001g0290 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.436+2016A>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515328 | ||||||
chr17:4515410
|
C | T | 1 | a0001c0001t0009g0185 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.436+2098C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515410 | ||||||
chr17:4515630
|
T | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(245): Show | 269 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.436+2318T>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515630 | ||||||
chr17:4515726
|
G | A | 10 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(7): Show | 10 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+2414G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515726 | ||||||
chr17:4515729
|
A | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(245): Show | 269 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.436+2417A>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515729 | ||||||
chr17:4515795
|
T | TG | 248 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(245): Show | 269 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.436+2485dupG | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4515795 | |||||
chr17:4515834
|
G | A | 5 | a0001c0001t0005g0169a0001c0001t0007g0171a0001c0001t0007g0172others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+2522G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515834 | ||||||
chr17:4515834
|
G | T | 1 | a0001c0001t0029g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.436+2522G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515834 | ||||||
chr17:4515986
|
A | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(245): Show | 269 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.436+2674A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515986 | ||||||
chr17:4515995
|
G | C | 248 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(245): Show | 269 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.436+2683G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4515995 | ||||||
chr17:4516018
|
A | C | 1 | a0001c0001t0002g0084 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.436+2706A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516018 | ||||||
chr17:4516022
|
C | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(245): Show | 269 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.436+2710C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516022 | ||||||
chr17:4516051
|
C | T | 240 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(237): Show | 259 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.436+2739C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516051 | ||||||
chr17:4516058
|
A | G | 248 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(245): Show | 269 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(266): Show |
intron_variant | MODIFIER | c.436+2746A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516058 | ||||||
chr17:4516229
|
G | A | 2 | a0001c0001t0006g0031a0001c0001t0036g0224 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.436+2917G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516229 | ||||||
chr17:4516288
|
TG | T | 10 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(7): Show | 10 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+2979delG | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4516288 | |||||
chr17:4516305
|
C | G | 10 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(7): Show | 10 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+2993C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516305 | ||||||
chr17:4516313
|
C | CA | 5 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0010g0040others(2): Show | 7 | HG00735.hp2 HG00741.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.436+3001_436+3002i others(3): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516313 | ||||||
chr17:4516314
|
C | A | 366 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(363): Show | 396 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(393): Show |
intron_variant | MODIFIER | c.436+3002C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516314 | ||||||
chr17:4516316
|
C | A | 5 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0010g0040others(2): Show | 7 | HG00735.hp2 HG00741.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.436+3004C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516316 | ||||||
chr17:4516316
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0004g0223 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.436+3014_436+3031d others(20): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4516316 | |||||
chr17:4516316
|
C | CAAAAAAA others(13): Show |
1 | a0001c0001t0001g0221 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.436+3012_436+3031d others(22): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4516316 | |||||
chr17:4516316
|
CA | C | 75 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0065others(72): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.436+3031delA | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4516316 | |||||
chr17:4516316
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0052g0180 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.436+3018_436+3031d others(16): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4516316 | |||||
chr17:4516326
|
A | C | 5 | a0001c0001t0005g0169a0001c0001t0007g0171a0001c0001t0007g0172others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+3014A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516326 | ||||||
chr17:4516328
|
A | C | 1 | a0001c0001t0003g0035 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.436+3016A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516328 | ||||||
chr17:4516330
|
A | C | 21 | a0001c0001t0001g0234a0001c0001t0001g0259a0001c0001t0002g0113others(18): Show | 21 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.436+3018A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516330 | ||||||
chr17:4516331
|
A | C | 65 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0065others(62): Show | 74 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.436+3019A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516331 | ||||||
chr17:4516332
|
A | C | 21 | a0001c0001t0001g0141a0001c0001t0001g0225a0001c0001t0001g0229others(18): Show | 22 | HG00558.hp1 HG00597.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.436+3020A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516332 | ||||||
chr17:4516333
|
A | C | 14 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0206others(11): Show | 14 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.436+3021A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516333 | ||||||
chr17:4516334
|
A | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(209): Show | 232 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.436+3022A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516334 | ||||||
chr17:4516335
|
A | C | 11 | a0001c0001t0001g0128a0001c0001t0001g0247a0001c0001t0002g0046others(8): Show | 11 | HG00544.hp1 HG01978.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.436+3023A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516335 | ||||||
chr17:4516336
|
A | C | 21 | a0001c0001t0001g0141a0001c0001t0001g0225a0001c0001t0001g0229others(18): Show | 22 | HG00558.hp1 HG00597.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.436+3024A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516336 | ||||||
chr17:4516337
|
A | C | 5 | a0001c0001t0001g0206a0001c0001t0004g0125a0001c0002t0004g0069others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+3025A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516337 | ||||||
chr17:4516338
|
A | C | 211 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(208): Show | 231 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.436+3026A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516338 | ||||||
chr17:4516339
|
A | C | 11 | a0001c0001t0001g0128a0001c0001t0001g0247a0001c0001t0002g0046others(8): Show | 11 | HG00544.hp1 HG01978.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.436+3027A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516339 | ||||||
chr17:4516340
|
A | C | 21 | a0001c0001t0001g0141a0001c0001t0001g0225a0001c0001t0001g0229others(18): Show | 22 | HG00558.hp1 HG00597.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.436+3028A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516340 | ||||||
chr17:4516340
|
AAAAC | A | 210 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(207): Show | 230 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.436+3032_436+3035d others(6): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4516340 | |||||
chr17:4516341
|
A | C | 13 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(10): Show | 13 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.436+3029A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516341 | ||||||
chr17:4516341
|
AAAC | A | 12 | a0001c0001t0001g0053a0001c0001t0001g0128a0001c0001t0001g0247others(9): Show | 12 | HG00544.hp1 HG01978.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.436+3032_436+3034d others(5): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4516341 | |||||
chr17:4516342
|
A | C | 1 | a0001c0001t0003g0051 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.436+3030A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516342 | ||||||
chr17:4516342
|
AAC | A | 21 | a0001c0001t0001g0141a0001c0001t0001g0225a0001c0001t0001g0229others(18): Show | 22 | HG00558.hp1 HG00597.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.436+3032_436+3033d others(4): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4516342 | |||||
chr17:4516343
|
A | C | 1 | a0001c0001t0001g0259 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.436+3031A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516343 | ||||||
chr17:4516343
|
AC | A | 16 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(13): Show | 16 | HG01081.hp2 HG01099.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.436+3032delC | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516343 | ||||||
chr17:4516344
|
C | A | 9 | a0001c0001t0001g0221a0001c0001t0001g0259a0001c0001t0003g0051others(6): Show | 9 | HG02559.hp1 HG02818.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.436+3032C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516344 | ||||||
chr17:4516352
|
C | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(255): Show | 279 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.436+3040C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516352 | ||||||
chr17:4516367
|
G | T | 1 | a0001c0001t0010g0199 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.436+3055G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516367 | ||||||
chr17:4516394
|
T | A | 10 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(7): Show | 10 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+3082T>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516394 | ||||||
chr17:4516447
|
G | A | 1 | a0001c0001t0005g0361 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.436+3135G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516447 | ||||||
chr17:4516489
|
T | C | 1 | a0001c0001t0025g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.436+3177T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516489 | ||||||
chr17:4516556
|
G | A | 5 | a0001c0001t0005g0169a0001c0001t0007g0171a0001c0001t0007g0172others(2): Show | 5 | HG01891.hp2 HG02145.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+3244G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516556 | ||||||
chr17:4516581
|
C | T | 15 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(12): Show | 15 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.436+3269C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516581 | ||||||
chr17:4516602
|
C | CG | 255 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(252): Show | 276 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(273): Show |
intron_variant | MODIFIER | c.436+3291dupG | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4516602 | |||||
chr17:4516646
|
T | C | 10 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(7): Show | 10 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.436+3334T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516646 | ||||||
chr17:4516653
|
T | G | 1 | a0001c0001t0001g0229 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.436+3341T>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516653 | ||||||
chr17:4516691
|
A | G | 1 | a0001c0001t0010g0040 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.436+3379A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516691 | ||||||
chr17:4516702
|
C | T | 1 | a0001c0002t0044g0232 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.436+3390C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516702 | ||||||
chr17:4516757
|
A | G | 304 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(301): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.436+3445A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516757 | ||||||
chr17:4516885
|
A | G | 1 | a0001c0001t0001g0337 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.436+3573A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516885 | ||||||
chr17:4516887
|
C | T | 9 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(6): Show | 9 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.436+3575C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516887 | ||||||
chr17:4516905
|
C | T | 1 | a0001c0001t0030g0183 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.436+3593C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516905 | ||||||
chr17:4516963
|
G | A | 1 | a0001c0001t0001g0270 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.436+3651G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4516963 | ||||||
chr17:4517023
|
C | T | 1 | a0001c0001t0009g0166 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.436+3711C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517023 | ||||||
chr17:4517262
|
T | C | 25 | a0001c0001t0001g0141a0001c0001t0001g0225a0001c0001t0001g0229others(22): Show | 26 | HG00558.hp1 HG00597.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.436+3950T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517262 | ||||||
chr17:4517308
|
C | CT | 9 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(6): Show | 9 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.436+3996_436+3997i others(3): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517308 | ||||||
chr17:4517383
|
C | T | 1 | a0001c0001t0007g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.436+4071C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517383 | ||||||
chr17:4517386
|
G | A | 9 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(6): Show | 9 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.436+4074G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517386 | ||||||
chr17:4517411
|
A | C | 3 | a0001c0001t0001g0262a0001c0001t0004g0260a0001c0001t0016g0261 | 3 | HG01109.hp2 HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.436+4099A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517411 | ||||||
chr17:4517415
|
T | C | 1 | a0001c0008t0004g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.436+4103T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517415 | ||||||
chr17:4517428
|
C | T | 2 | a0001c0001t0006g0031a0001c0001t0036g0224 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.436+4116C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517428 | ||||||
chr17:4517469
|
A | G | 2 | a0001c0001t0006g0031a0001c0001t0036g0224 | 2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.436+4157A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517469 | ||||||
chr17:4517478
|
G | T | 13 | a0001c0001t0003g0033a0001c0001t0007g0171a0001c0001t0007g0172others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.436+4166G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517478 | ||||||
chr17:4517528
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.436+4216C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517528 | ||||||
chr17:4517672
|
T | C | 5 | a0001c0001t0001g0338a0001c0001t0002g0089a0001c0001t0002g0126others(2): Show | 5 | HG00558.hp1 HG00597.hp2 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.436+4360T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517672 | ||||||
chr17:4517999
|
C | A | 4 | a0001c0001t0001g0079a0001c0001t0001g0087a0001c0001t0001g0088others(1): Show | 4 | HG00733.hp2 HG01074.hp2 HG01255.hp1 others(1): Show |
intron_variant | MODIFIER | c.436+4687C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4517999 | ||||||
chr17:4518262
|
C | T | 66 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0053others(63): Show | 71 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.436+4950C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518262 | ||||||
chr17:4518290
|
T | C | 359 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(356): Show | 391 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(388): Show |
intron_variant | MODIFIER | c.436+4978T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518290 | ||||||
chr17:4518340
|
T | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(150): Show | 166 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.436+5028T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518340 | ||||||
chr17:4518396
|
T | C | 5 | a0001c0001t0001g0221a0001c0001t0004g0223a0001c0001t0006g0031others(2): Show | 5 | HG02559.hp1 HG02818.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.436+5084T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518396 | ||||||
chr17:4518501
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.436+5189C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518501 | ||||||
chr17:4518509
|
C | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(140): Show | 156 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.436+5197C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518509 | ||||||
chr17:4518535
|
A | AAAAC | 20 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(17): Show | 20 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.436+5235_436+5238d others(6): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4518535 | |||||
chr17:4518637
|
T | C | 5 | a0001c0001t0001g0225a0001c0001t0004g0019a0001c0001t0004g0226others(2): Show | 6 | HG02451.hp1 HG02922.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.436+5325T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518637 | ||||||
chr17:4518642
|
G | T | 7 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(4): Show | 7 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.436+5330G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518642 | ||||||
chr17:4518658
|
C | T | 1 | a0001c0009t0015g0164 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.436+5346C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518658 | ||||||
chr17:4518669
|
A | T | 1 | a0001c0001t0002g0280 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.436+5357A>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518669 | ||||||
chr17:4518795
|
G | A | 91 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0053others(88): Show | 96 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.436+5483G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518795 | ||||||
chr17:4518834
|
C | T | 80 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0053others(77): Show | 86 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.436+5522C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518834 | ||||||
chr17:4518967
|
G | A | 1 | a0001c0001t0038g0220 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.436+5655G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4518967 | ||||||
chr17:4519062
|
G | A | 1 | a0001c0001t0004g0237 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.436+5750G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519062 | ||||||
chr17:4519065
|
C | T | 2 | a0001c0001t0001g0336a0001c0001t0014g0335 | 2 | NA20905.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.436+5753C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519065 | ||||||
chr17:4519222
|
G | A | 3 | a0001c0001t0007g0171a0001c0001t0007g0172a0001c0009t0015g0164 | 3 | HG01891.hp2 HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.437-5835G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519222 | ||||||
chr17:4519248
|
C | T | 20 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(17): Show | 20 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.437-5809C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519248 | ||||||
chr17:4519338
|
G | A | 5 | a0001c0001t0001g0117a0001c0001t0002g0012a0001c0001t0002g0114others(2): Show | 6 | HG01257.hp1 HG01258.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-5719G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519338 | ||||||
chr17:4519357
|
C | T | 1 | a0001c0004t0002g0294 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.437-5700C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519357 | ||||||
chr17:4519605
|
G | GCACACGT others(20): Show |
371 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(368): Show | 403 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(400): Show |
intron_variant | MODIFIER | c.437-5447_437-5446i others(29): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4519605 | |||||
chr17:4519701
|
TCAAA | T | 3 | a0001c0001t0001g0229a0001c0001t0003g0231a0001c0003t0004g0230 | 3 | HG01243.hp1 HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.437-5347_437-5344d others(6): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 4519701 | |||||
chr17:4519722
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.437-5335G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519722 | ||||||
chr17:4519727
|
C | T | 1 | a0001c0001t0009g0166 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.437-5330C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519727 | ||||||
chr17:4519924
|
C | T | 72 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0053others(69): Show | 77 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.437-5133C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519924 | ||||||
chr17:4519972
|
T | C | 7 | a0001c0001t0003g0033a0001c0001t0011g0363a0001c0001t0017g0364others(4): Show | 7 | HG01884.hp2 HG01891.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.437-5085T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4519972 | ||||||
chr17:4520020
|
C | T | 2 | a0001c0001t0005g0003a0001c0001t0008g0182 | 4 | HG02735.hp1 HG03239.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.437-5037C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520020 | ||||||
chr17:4520093
|
G | T | 2 | a0001c0001t0003g0050a0001c0001t0003g0051 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.437-4964G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520093 | ||||||
chr17:4520115
|
C | T | 1 | a0001c0001t0003g0196 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.437-4942C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520115 | ||||||
chr17:4520194
|
G | A | 1 | a0001c0001t0002g0306 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.437-4863G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520194 | ||||||
chr17:4520246
|
G | T | 79 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0014others(76): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.437-4811G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520246 | ||||||
chr17:4520269
|
A | T | 16 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(13): Show | 16 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.437-4788A>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520269 | ||||||
chr17:4520379
|
G | A | 1 | a0001c0001t0006g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.437-4678G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520379 | ||||||
chr17:4520509
|
C | T | 1 | a0002c0011t0032g0161 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.437-4548C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520509 | ||||||
chr17:4520541
|
A | G | 1 | a0001c0001t0001g0333 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.437-4516A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520541 | ||||||
chr17:4520545
|
C | G | 3 | a0001c0001t0007g0177a0001c0001t0028g0178a0001c0003t0005g0176 | 3 | HG01884.hp1 HG03209.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.437-4512C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520545 | ||||||
chr17:4520864
|
A | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(119): Show | 134 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.437-4193A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520864 | ||||||
chr17:4520901
|
C | G | 7 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(4): Show | 7 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.437-4156C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520901 | ||||||
chr17:4520955
|
C | T | 10 | a0001c0001t0001g0141a0001c0001t0011g0362a0001c0001t0014g0140others(7): Show | 10 | HG02257.hp2 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.437-4102C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520955 | ||||||
chr17:4520956
|
G | A | 1 | a0001c0001t0030g0183 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.437-4101G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520956 | ||||||
chr17:4520967
|
T | C | 1 | a0001c0012t0002g0242 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.437-4090T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4520967 | ||||||
chr17:4521387
|
A | T | 71 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0053others(68): Show | 76 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.437-3670A>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521387 | ||||||
chr17:4521489
|
G | A | 1 | a0001c0001t0014g0335 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.437-3568G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521489 | ||||||
chr17:4521557
|
C | T | 248 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(245): Show | 266 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(263): Show |
intron_variant | MODIFIER | c.437-3500C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521557 | ||||||
chr17:4521570
|
G | A | 2 | a0001c0001t0021g0368a0001c0002t0011g0367 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.437-3487G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521570 | ||||||
chr17:4521670
|
G | A | 231 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(228): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.437-3387G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521670 | ||||||
chr17:4521772
|
G | C | 1 | a0001c0001t0002g0248 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.437-3285G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521772 | ||||||
chr17:4521820
|
C | T | 2 | a0001c0001t0036g0224a0001c0018t0004g0044 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.437-3237C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521820 | ||||||
chr17:4521856
|
G | A | 9 | a0001c0001t0006g0015a0001c0001t0006g0157a0001c0001t0006g0160others(6): Show | 10 | HG02486.hp2 HG02723.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.437-3201G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521856 | ||||||
chr17:4521885
|
G | A | 2 | a0001c0001t0021g0368a0001c0002t0011g0367 | 2 | HG02572.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.437-3172G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521885 | ||||||
chr17:4521921
|
G | A | 7 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(4): Show | 7 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.437-3136G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4521921 | ||||||
chr17:4522035
|
C | T | 3 | a0001c0001t0002g0093a0001c0001t0018g0109a0001c0001t0018g0110 | 3 | HG00544.hp1 NA19005.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.437-3022C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522035 | ||||||
chr17:4522038
|
A | C | 6 | a0001c0001t0001g0234a0001c0001t0006g0031a0001c0001t0009g0190others(3): Show | 6 | HG01167.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-3019A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522038 | ||||||
chr17:4522056
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.437-3001G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522056 | ||||||
chr17:4522099
|
C | T | 1 | a0001c0001t0003g0216 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.437-2958C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522099 | ||||||
chr17:4522123
|
C | T | 31 | a0001c0001t0001g0141a0001c0001t0003g0033a0001c0001t0004g0125others(28): Show | 32 | HG01884.hp2 HG01891.hp1 HG02257.hp2 others(29): Show |
intron_variant | MODIFIER | c.437-2934C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522123 | ||||||
chr17:4522131
|
A | G | 8 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(5): Show | 8 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-2926A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522131 | ||||||
chr17:4522135
|
A | G | 8 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(5): Show | 8 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.437-2922A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522135 | ||||||
chr17:4522138
|
G | T | 7 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(4): Show | 7 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.437-2919G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522138 | ||||||
chr17:4522167
|
C | G | 1 | a0001c0007t0004g0193 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.437-2890C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522167 | ||||||
chr17:4522178
|
G | A | 110 | a0001c0001t0001g0006a0001c0001t0001g0014a0001c0001t0001g0034others(107): Show | 122 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.437-2879G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522178 | ||||||
chr17:4522220
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.437-2837A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522220 | ||||||
chr17:4522315
|
G | A | 2 | a0001c0001t0003g0050a0001c0001t0003g0051 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.437-2742G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522315 | ||||||
chr17:4522370
|
C | T | 7 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(4): Show | 7 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.437-2687C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522370 | ||||||
chr17:4522389
|
C | T | 1 | a0001c0009t0015g0164 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.437-2668C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522389 | ||||||
chr17:4522455
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.437-2602C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522455 | ||||||
chr17:4522525
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.437-2532G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522525 | ||||||
chr17:4522543
|
G | A | 44 | a0001c0001t0001g0006a0001c0001t0001g0065a0001c0001t0001g0066others(41): Show | 50 | HG00099.hp1 HG00323.hp1 HG00621.hp2 others(47): Show |
intron_variant | MODIFIER | c.437-2514G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522543 | ||||||
chr17:4522573
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.437-2484T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522573 | ||||||
chr17:4522641
|
C | T | 1 | a0001c0001t0036g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.437-2416C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522641 | ||||||
chr17:4522703
|
C | T | 3 | a0001c0001t0002g0093a0001c0001t0018g0109a0001c0001t0018g0110 | 3 | HG00544.hp1 NA19005.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.437-2354C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522703 | ||||||
chr17:4522727
|
C | T | 2 | a0001c0001t0002g0077a0001c0001t0002g0283 | 2 | HG04199.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.437-2330C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522727 | ||||||
chr17:4522741
|
C | A | 1 | a0001c0005t0002g0052 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.437-2316C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522741 | ||||||
chr17:4522757
|
G | A | 2 | a0001c0001t0009g0168a0001c0003t0007g0167 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.437-2300G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522757 | ||||||
chr17:4522830
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0010g0201 | 2 | HG02738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.437-2227G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522830 | ||||||
chr17:4522946
|
C | T | 1 | a0001c0001t0010g0210 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.437-2111C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4522946 | ||||||
chr17:4523084
|
G | A | 210 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0011others(207): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.437-1973G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523084 | ||||||
chr17:4523192
|
C | A | 2 | a0001c0001t0036g0224a0001c0018t0004g0044 | 2 | NA19030.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.437-1865C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523192 | ||||||
chr17:4523204
|
G | A | 6 | a0001c0001t0001g0234a0001c0001t0006g0031a0001c0001t0009g0190others(3): Show | 6 | HG01167.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-1853G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523204 | ||||||
chr17:4523282
|
A | G | 6 | a0001c0001t0001g0234a0001c0001t0006g0031a0001c0001t0009g0190others(3): Show | 6 | HG01167.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-1775A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523282 | ||||||
chr17:4523311
|
G | A | 1 | a0001c0001t0003g0207 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.437-1746G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523311 | ||||||
chr17:4523366
|
A | G | 15 | a0001c0001t0001g0234a0001c0001t0006g0015a0001c0001t0006g0031others(12): Show | 16 | HG01167.hp1 HG02109.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.437-1691A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523366 | ||||||
chr17:4523370
|
G | A | 7 | a0001c0001t0001g0198a0001c0001t0001g0200a0001c0001t0001g0209others(4): Show | 7 | HG01081.hp2 HG01175.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.437-1687G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523370 | ||||||
chr17:4523551
|
T | C | 1 | a0001c0001t0003g0095 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.437-1506T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523551 | ||||||
chr17:4523585
|
C | T | 1 | a0001c0005t0002g0047 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.437-1472C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523585 | ||||||
chr17:4523650
|
G | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(165): Show | 183 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.437-1407G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523650 | ||||||
chr17:4523660
|
C | T | 1 | a0001c0015t0002g0064 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.437-1397C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523660 | ||||||
chr17:4523716
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.437-1341T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523716 | ||||||
chr17:4523880
|
A | G | 6 | a0001c0001t0001g0234a0001c0001t0006g0031a0001c0001t0009g0190others(3): Show | 6 | HG01167.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-1177A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523880 | ||||||
chr17:4523938
|
T | C | 6 | a0001c0001t0001g0234a0001c0001t0006g0031a0001c0001t0009g0190others(3): Show | 6 | HG01167.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.437-1119T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523938 | ||||||
chr17:4523963
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.437-1094G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4523963 | ||||||
chr17:4524069
|
G | A | 235 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(232): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.437-988G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4524069 | ||||||
chr17:4524515
|
T | C | 1 | a0001c0001t0029g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.437-542T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4524515 | ||||||
chr17:4524556
|
T | C | 3 | a0001c0001t0003g0231a0001c0001t0014g0140a0001c0001t0016g0056 | 3 | HG02647.hp1 HG02809.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.437-501T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4524556 | ||||||
chr17:4525009
|
C | T | 1 | a0002c0011t0032g0161 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.437-48C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4525009 | ||||||
chr17:4525034
|
C | G | 1 | a0001c0001t0014g0339 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.437-23C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4525034 | ||||||
chr17:4525034
|
C | T | 1 | a0001c0001t0036g0224 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.437-23C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 2/12 | chr17 | 4525034 | ||||||
chr17:4525245
|
G | T | 9 | a0001c0001t0003g0033a0001c0001t0004g0352a0001c0001t0004g0356others(6): Show | 9 | HG01099.hp2 HG01243.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.573+52G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525245 | ||||||
chr17:4525469
|
C | G | 6 | a0001c0001t0001g0234a0001c0001t0006g0031a0001c0001t0026g0188others(3): Show | 6 | HG01167.hp1 HG02145.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.573+276C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525469 | ||||||
chr17:4525469
|
C | T | 1 | a0001c0001t0025g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.573+276C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525469 | ||||||
chr17:4525628
|
G | A | 1 | a0001c0001t0029g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.573+435G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525628 | ||||||
chr17:4525747
|
C | A | 28 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(25): Show | 31 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.573+554C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525747 | ||||||
chr17:4525798
|
C | T | 2 | a0001c0001t0009g0168a0001c0003t0007g0167 | 2 | HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.573+605C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525798 | ||||||
chr17:4525851
|
C | T | 5 | a0001c0001t0003g0050a0001c0001t0003g0051a0001c0001t0009g0168others(2): Show | 5 | HG02886.hp2 HG02895.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+658C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525851 | ||||||
chr17:4525852
|
G | A | 39 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(36): Show | 42 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.573+659G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525852 | ||||||
chr17:4525970
|
C | G | 50 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(47): Show | 53 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.573+777C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525970 | ||||||
chr17:4525976
|
G | C | 5 | a0001c0001t0004g0125a0001c0001t0028g0178a0001c0003t0004g0068others(2): Show | 5 | HG02258.hp1 HG02280.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.573+783G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4525976 | ||||||
chr17:4526204
|
C | T | 1 | a0001c0001t0004g0237 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.573+1011C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4526204 | ||||||
chr17:4526295
|
G | A | 44 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(41): Show | 47 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.573+1102G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4526295 | ||||||
chr17:4526529
|
G | A | 2 | a0001c0001t0003g0050a0001c0001t0003g0051 | 2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.573+1336G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4526529 | ||||||
chr17:4526558
|
G | A | 44 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(41): Show | 47 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.573+1365G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4526558 | ||||||
chr17:4526603
|
CAA | C | 44 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0001g0037others(41): Show | 47 | HG00735.hp2 HG00741.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.573+1422_573+1423d others(4): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 4526603 | |||||
chr17:4526617
|
G | A | 1 | a0001c0004t0002g0292 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.573+1424G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4526617 | ||||||
chr17:4526618
|
A | G | 1 | a0001c0004t0002g0292 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.573+1425A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4526618 | ||||||
chr17:4526726
|
A | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(220): Show | 245 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.573+1533A>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4526726 | ||||||
chr17:4526761
|
C | T | 1 | a0001c0006t0027g0191 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.573+1568C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4526761 | ||||||
chr17:4526914
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(120): Show | 134 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.573+1721T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4526914 | ||||||
chr17:4527112
|
AGAAACAG others(12): Show |
A | 3 | a0001c0001t0001g0353a0001c0001t0004g0233a0001c0001t0004g0354 | 3 | HG02280.hp2 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.573+1923_573+1941d others(21): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 4527112 | |||||
chr17:4527156
|
C | G | 2 | a0001c0001t0001g0146a0001c0005t0002g0147 | 2 | NA18960.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.573+1963C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527156 | ||||||
chr17:4527470
|
T | C | 1 | a0001c0001t0002g0315 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.573+2277T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527470 | ||||||
chr17:4527486
|
C | T | 1 | a0001c0004t0002g0123 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.573+2293C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527486 | ||||||
chr17:4527533
|
A | G | 5 | a0001c0001t0004g0125a0001c0001t0009g0190a0001c0001t0022g0366others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.573+2340A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527533 | ||||||
chr17:4527579
|
C | T | 1 | a0001c0001t0028g0178 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.573+2386C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527579 | ||||||
chr17:4527663
|
C | T | 120 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0065others(117): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.573+2470C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527663 | ||||||
chr17:4527690
|
T | C | 16 | a0001c0001t0004g0125a0001c0001t0004g0226a0001c0001t0019g0227others(13): Show | 16 | HG01167.hp1 HG01891.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.573+2497T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527690 | ||||||
chr17:4527813
|
G | C | 114 | a0001c0001t0001g0016a0001c0001t0001g0025a0001c0001t0001g0034others(111): Show | 123 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(120): Show |
intron_variant | MODIFIER | c.573+2620G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527813 | ||||||
chr17:4527832
|
G | A | 1 | a0001c0001t0009g0185 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.573+2639G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527832 | ||||||
chr17:4527842
|
T | C | 1 | a0001c0001t0038g0220 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.573+2649T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527842 | ||||||
chr17:4527864
|
G | A | 4 | a0001c0001t0001g0079a0001c0001t0002g0042a0001c0001t0002g0090others(1): Show | 4 | HG01255.hp1 HG02683.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+2671G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527864 | ||||||
chr17:4527886
|
G | T | 2 | a0001c0001t0002g0107a0001c0012t0002g0242 | 2 | NA18970.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.573+2693G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527886 | ||||||
chr17:4527949
|
CA | C | 256 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(253): Show | 284 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.574-2668delA | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 4527949 | |||||
chr17:4527963
|
A | AC | 6 | a0001c0001t0001g0271a0001c0001t0002g0252a0001c0001t0003g0018others(3): Show | 7 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.574-2669_574-2668i others(3): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527963 | ||||||
chr17:4527963
|
A | C | 83 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0009others(80): Show | 91 | HG00323.hp1 HG00438.hp2 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.574-2669A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4527963 | ||||||
chr17:4528094
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0007others(132): Show | 149 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.574-2538T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528094 | ||||||
chr17:4528108
|
C | T | 2 | a0001c0001t0004g0228a0001c0001t0004g0331 | 2 | HG02451.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.574-2524C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528108 | ||||||
chr17:4528115
|
C | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0128a0001c0001t0001g0286others(1): Show | 5 | HG03490.hp1 HG03491.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.574-2517C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528115 | ||||||
chr17:4528171
|
C | T | 1 | a0001c0018t0004g0044 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574-2461C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528171 | ||||||
chr17:4528318
|
G | A | 1 | a0001c0001t0048g0136 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.574-2314G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528318 | ||||||
chr17:4528459
|
A | G | 12 | a0001c0001t0001g0065a0001c0001t0001g0141a0001c0001t0001g0229others(9): Show | 12 | HG01099.hp2 HG01109.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.574-2173A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528459 | ||||||
chr17:4528503
|
C | T | 11 | a0001c0001t0004g0019a0001c0001t0004g0223a0001c0001t0004g0226others(8): Show | 12 | HG01243.hp2 HG01891.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.574-2129C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528503 | ||||||
chr17:4528531
|
C | T | 2 | a0001c0001t0002g0093a0001c0001t0002g0315 | 2 | HG00544.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.574-2101C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528531 | ||||||
chr17:4528627
|
C | T | 2 | a0001c0001t0004g0237a0001c0018t0004g0044 | 2 | HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.574-2005C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528627 | ||||||
chr17:4528645
|
T | G | 122 | a0001c0001t0001g0016a0001c0001t0001g0272a0001c0001t0001g0309others(119): Show | 132 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.574-1987T>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528645 | ||||||
chr17:4528805
|
G | A | 1 | a0001c0008t0004g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.574-1827G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4528805 | ||||||
chr17:4528942
|
C | CT | 89 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(86): Show | 97 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.574-1678dupT | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 4528942 | |||||
chr17:4529067
|
C | A | 1 | a0001c0005t0002g0147 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.574-1565C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4529067 | ||||||
chr17:4529085
|
G | A | 1 | a0001c0001t0034g0026 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.574-1547G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4529085 | ||||||
chr17:4529093
|
A | G | 15 | a0001c0001t0001g0065a0001c0001t0001g0141a0001c0001t0001g0229others(12): Show | 15 | HG01109.hp2 HG01243.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.574-1539A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4529093 | ||||||
chr17:4529411
|
C | A | 1 | a0001c0001t0003g0048 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.574-1221C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4529411 | ||||||
chr17:4529587
|
G | A | 7 | a0001c0001t0003g0035a0001c0001t0003g0236a0001c0001t0004g0356others(4): Show | 8 | HG01192.hp1 HG02486.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.574-1045G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4529587 | ||||||
chr17:4529593
|
A | G | 32 | a0001c0001t0002g0077a0001c0001t0003g0008a0001c0001t0003g0017others(29): Show | 35 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.574-1039A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4529593 | ||||||
chr17:4529680
|
G | GA | 43 | a0001c0001t0001g0269a0001c0001t0002g0077a0001c0001t0003g0008others(40): Show | 47 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.574-943dupA | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 4529680 | |||||
chr17:4529979
|
A | G | 4 | a0001c0001t0001g0066a0001c0001t0001g0324a0001c0001t0001g0353others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-653A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4529979 | ||||||
chr17:4530004
|
G | A | 1 | a0001c0001t0009g0168 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.574-628G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530004 | ||||||
chr17:4530017
|
G | A | 4 | a0001c0001t0001g0102a0001c0001t0001g0144a0001c0001t0001g0244others(1): Show | 4 | HG02056.hp2 HG02083.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-615G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530017 | ||||||
chr17:4530081
|
C | T | 2 | a0001c0001t0005g0003a0001c0001t0030g0183 | 4 | HG02735.hp1 HG03239.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-551C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530081 | ||||||
chr17:4530123
|
G | T | 1 | a0001c0001t0003g0253 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.574-509G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530123 | ||||||
chr17:4530152
|
C | T | 1 | a0001c0001t0003g0008 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.574-480C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530152 | ||||||
chr17:4530305
|
G | T | 114 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 131 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.574-327G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530305 | ||||||
chr17:4530330
|
C | T | 3 | a0001c0001t0001g0146a0001c0001t0001g0195a0001c0001t0001g0277 | 3 | NA18960.hp1 NA18990.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.574-302C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530330 | ||||||
chr17:4530450
|
G | A | 1 | a0001c0001t0007g0163 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.574-182G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530450 | ||||||
chr17:4530463
|
C | T | 9 | a0001c0001t0004g0019a0001c0001t0004g0223a0001c0001t0004g0226others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.574-169C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530463 | ||||||
chr17:4530522
|
C | T | 1 | a0001c0001t0003g0207 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.574-110C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530522 | ||||||
chr17:4530528
|
C | G | 18 | a0001c0001t0001g0271a0001c0001t0002g0084a0001c0001t0002g0090others(15): Show | 18 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.574-104C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 3/12 | chr17 | 4530528 | ||||||
chr17:4530819
|
C | G | 1 | a0001c0001t0006g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.725+36C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/12 | chr17 | 4530819 | ||||||
chr17:4530882
|
G | A | 4 | a0001c0001t0006g0015a0001c0001t0006g0160a0001c0001t0025g0173others(1): Show | 5 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.725+99G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/12 | chr17 | 4530882 | ||||||
chr17:4530908
|
G | C | 4 | a0001c0004t0001g0022a0001c0004t0002g0292a0001c0004t0002g0293others(1): Show | 5 | NA18991.hp1 NA19003.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.725+125G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/12 | chr17 | 4530908 | ||||||
chr17:4530974
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.726-79C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/12 | chr17 | 4530974 | ||||||
chr17:4530979
|
C | T | 3 | a0001c0005t0002g0047a0001c0005t0002g0052a0001c0005t0002g0076 | 3 | HG00673.hp1 NA18965.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.726-74C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/12 | chr17 | 4530979 | ||||||
chr17:4531002
|
T | G | 1 | a0001c0001t0006g0160 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.726-51T>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/12 | chr17 | 4531002 | ||||||
chr17:4531050
|
C | T | 1 | a0001c0001t0001g0009 | 2 | HG01175.hp2 NA20805.hp2 |
splice_region_variant&intron_variant | LOW | c.726-3C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 4/12 | chr17 | 4531050 | ||||||
chr17:4531155
|
C | T | 11 | a0001c0001t0003g0073a0001c0003t0004g0068a0001c0003t0004g0230others(8): Show | 11 | HG00099.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.792+36C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531155 | ||||||
chr17:4531176
|
G | C | 38 | a0001c0001t0001g0065a0001c0001t0001g0079a0001c0001t0001g0141others(35): Show | 38 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.792+57G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531176 | ||||||
chr17:4531194
|
C | T | 6 | a0001c0001t0010g0199a0001c0001t0010g0201a0001c0001t0010g0210others(3): Show | 6 | HG01081.hp2 HG01256.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+75C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531194 | ||||||
chr17:4531289
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.792+170C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531289 | ||||||
chr17:4531310
|
G | C | 1 | a0001c0001t0029g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.792+191G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531310 | ||||||
chr17:4531322
|
G | A | 6 | a0001c0001t0010g0199a0001c0001t0010g0201a0001c0001t0010g0210others(3): Show | 6 | HG01081.hp2 HG01256.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+203G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531322 | ||||||
chr17:4531341
|
C | CG | 9 | a0001c0002t0004g0069a0001c0002t0004g0071a0001c0002t0004g0235others(6): Show | 9 | HG02257.hp2 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.792+226dupG | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr17 | 4531341 | |||||
chr17:4531342
|
G | A | 9 | a0001c0001t0004g0019a0001c0001t0004g0223a0001c0001t0004g0226others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.792+223G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531342 | ||||||
chr17:4531485
|
G | A | 1 | a0001c0001t0001g0316 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.792+366G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531485 | ||||||
chr17:4531507
|
G | A | 4 | a0001c0004t0001g0022a0001c0004t0002g0292a0001c0004t0002g0293others(1): Show | 5 | NA18991.hp1 NA19003.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.792+388G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531507 | ||||||
chr17:4531599
|
T | C | 368 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(365): Show | 400 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(397): Show |
intron_variant | MODIFIER | c.792+480T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531599 | ||||||
chr17:4531703
|
C | T | 1 | a0001c0001t0002g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.792+584C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531703 | ||||||
chr17:4531704
|
G | A | 11 | a0001c0002t0004g0069a0001c0002t0004g0071a0001c0002t0004g0235others(8): Show | 11 | HG02055.hp2 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.792+585G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531704 | ||||||
chr17:4531744
|
G | A | 1 | a0001c0001t0002g0060 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.792+625G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531744 | ||||||
chr17:4531750
|
A | C | 14 | a0001c0001t0001g0079a0001c0001t0004g0233a0001c0001t0004g0354others(11): Show | 14 | HG01255.hp1 HG01257.hp2 HG02698.hp1 others(11): Show |
intron_variant | MODIFIER | c.792+631A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531750 | ||||||
chr17:4531763
|
T | TGGGGGAG others(15): Show |
1 | a0001c0001t0001g0255 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.792+645_792+666dup others(22): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr17 | 4531763 | |||||
chr17:4531768
|
G | GA | 6 | a0001c0001t0002g0114a0001c0001t0002g0129a0001c0001t0002g0248others(3): Show | 6 | HG01975.hp2 HG01993.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.792+650dupA | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr17 | 4531768 | |||||
chr17:4531780
|
C | T | 2 | a0001c0001t0003g0151a0001c0006t0027g0191 | 2 | HG00639.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.792+661C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531780 | ||||||
chr17:4531781
|
G | C | 1 | a0001c0001t0003g0207 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.792+662G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531781 | ||||||
chr17:4531826
|
A | C | 1 | a0001c0001t0001g0310 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.792+707A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531826 | ||||||
chr17:4531828
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.792+709C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531828 | ||||||
chr17:4531881
|
C | T | 1 | a0001c0005t0002g0147 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.793-661C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531881 | ||||||
chr17:4531940
|
A | G | 25 | a0001c0001t0001g0065a0001c0001t0001g0141a0001c0001t0001g0229others(22): Show | 25 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.793-602A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531940 | ||||||
chr17:4531970
|
G | A | 1 | a0001c0001t0009g0166 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.793-572G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531970 | ||||||
chr17:4531980
|
C | T | 5 | a0001c0001t0004g0260a0001c0001t0004g0352a0001c0001t0019g0070others(2): Show | 5 | HG01099.hp2 HG01891.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.793-562C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4531980 | ||||||
chr17:4532016
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.793-526C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532016 | ||||||
chr17:4532051
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.793-491C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532051 | ||||||
chr17:4532068
|
C | T | 4 | a0001c0001t0001g0066a0001c0001t0001g0324a0001c0001t0001g0353others(1): Show | 4 | HG01884.hp2 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.793-474C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532068 | ||||||
chr17:4532120
|
G | T | 2 | a0001c0006t0002g0194a0001c0017t0002g0045 | 2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.793-422G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532120 | ||||||
chr17:4532135
|
C | G | 2 | a0001c0006t0002g0194a0001c0017t0002g0045 | 2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.793-407C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532135 | ||||||
chr17:4532135
|
C | T | 1 | a0001c0001t0001g0307 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.793-407C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532135 | ||||||
chr17:4532140
|
ATCCATCT others(13): Show |
A | 2 | a0001c0001t0003g0058a0001c0001t0006g0031 | 2 | HG01361.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.793-387_793-368del others(20): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr17 | 4532140 | |||||
chr17:4532156
|
GTCTGTCC others(1): Show |
G | 152 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(149): Show | 169 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.793-374_793-367del others(8): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr17 | 4532156 | |||||
chr17:4532260
|
C | T | 2 | a0001c0001t0001g0198a0001c0001t0001g0213 | 2 | HG01175.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.793-282C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532260 | ||||||
chr17:4532319
|
C | T | 1 | a0001c0001t0002g0314 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.793-223C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532319 | ||||||
chr17:4532358
|
C | T | 2 | a0001c0001t0001g0198a0001c0001t0001g0213 | 2 | HG01175.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.793-184C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532358 | ||||||
chr17:4532372
|
G | A | 23 | a0001c0001t0010g0199a0001c0001t0010g0201a0001c0001t0010g0210others(20): Show | 23 | HG01081.hp2 HG01256.hp1 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.793-170G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 5/12 | chr17 | 4532372 | ||||||
chr17:4532710
|
T | C | 368 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(365): Show | 400 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(397): Show |
intron_variant | MODIFIER | c.935+26T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 6/12 | chr17 | 4532710 | ||||||
chr17:4532719
|
A | G | 9 | a0001c0001t0004g0019a0001c0001t0004g0223a0001c0001t0004g0226others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.935+35A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 6/12 | chr17 | 4532719 | ||||||
chr17:4532924
|
AG | A | 9 | a0001c0002t0004g0069a0001c0002t0004g0071a0001c0002t0004g0235others(6): Show | 9 | HG02257.hp2 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.936-47delG | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr17 | 4532924 | |||||
chr17:4532926
|
G | A | 5 | a0001c0001t0004g0125a0001c0001t0004g0228a0001c0001t0034g0026others(2): Show | 5 | HG02280.hp1 HG02451.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.936-51G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 6/12 | chr17 | 4532926 | ||||||
chr17:4533134
|
G | A | 1 | a0001c0001t0001g0198 | 1 | HG01175.hp1 | splice_region_variant&intron_variant | LOW | c.1088+5G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 7/12 | chr17 | 4533134 | ||||||
chr17:4533475
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1278+43G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533475 | ||||||
chr17:4533479
|
C | T | 5 | a0001c0003t0004g0351a0001c0003t0006g0159a0001c0003t0007g0167others(2): Show | 5 | HG02258.hp1 HG03098.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278+47C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533479 | ||||||
chr17:4533480
|
G | T | 1 | a0001c0001t0006g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1278+48G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533480 | ||||||
chr17:4533528
|
C | T | 2 | a0001c0003t0004g0230a0001c0003t0005g0176 | 2 | NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1278+96C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533528 | ||||||
chr17:4533568
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1278+136C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533568 | ||||||
chr17:4533574
|
C | T | 111 | a0001c0001t0001g0016a0001c0001t0001g0087a0001c0001t0001g0088others(108): Show | 120 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1278+142C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533574 | ||||||
chr17:4533602
|
G | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(144): Show | 167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.1278+170G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533602 | ||||||
chr17:4533628
|
C | T | 1 | a0001c0001t0043g0320 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1279-160C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533628 | ||||||
chr17:4533636
|
G | A | 9 | a0001c0001t0001g0079a0001c0001t0004g0233a0001c0001t0004g0354others(6): Show | 9 | HG01255.hp1 HG01257.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1279-152G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533636 | ||||||
chr17:4533666
|
G | A | 9 | a0001c0001t0004g0019a0001c0001t0004g0223a0001c0001t0004g0226others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1279-122G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533666 | ||||||
chr17:4533757
|
G | A | 3 | a0001c0001t0012g0085a0001c0001t0012g0118a0001c0001t0012g0138 | 3 | NA18957.hp2 NA18977.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.1279-31G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 8/12 | chr17 | 4533757 | ||||||
chr17:4533870
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0329 | 2 | NA18977.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1344+17G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4533870 | ||||||
chr17:4533871
|
A | C | 1 | a0001c0001t0004g0233 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1344+18A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4533871 | ||||||
chr17:4533871
|
A | G | 1 | a0001c0005t0002g0119 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1344+18A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4533871 | ||||||
chr17:4533905
|
C | A | 5 | a0001c0001t0004g0125a0001c0001t0004g0228a0001c0001t0034g0026others(2): Show | 5 | HG02280.hp1 HG02451.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344+52C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4533905 | ||||||
chr17:4533919
|
C | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(146): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.1344+66C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4533919 | ||||||
chr17:4533944
|
G | T | 2 | a0001c0006t0002g0194a0001c0017t0002g0045 | 2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1344+91G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4533944 | ||||||
chr17:4534177
|
C | T | 2 | a0001c0001t0001g0333a0001c0001t0002g0303 | 2 | HG03927.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1344+324C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534177 | ||||||
chr17:4534182
|
G | C | 17 | a0001c0001t0001g0271a0001c0001t0002g0084a0001c0001t0002g0090others(14): Show | 17 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(14): Show |
intron_variant | MODIFIER | c.1344+329G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534182 | ||||||
chr17:4534240
|
C | CGGCTGG | 4 | a0001c0001t0004g0352a0001c0001t0019g0227a0001c0001t0022g0366others(1): Show | 4 | HG01099.hp2 HG01891.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+395_1344+400d others(8): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 4534240 | |||||
chr17:4534272
|
A | T | 10 | a0001c0001t0003g0035a0001c0001t0003g0236a0001c0001t0004g0356others(7): Show | 11 | HG01192.hp1 HG02486.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1344+419A>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534272 | ||||||
chr17:4534294
|
G | C | 1 | a0001c0001t0029g0174 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1344+441G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534294 | ||||||
chr17:4534297
|
C | T | 5 | a0001c0001t0001g0096a0001c0001t0001g0143a0001c0001t0001g0270others(2): Show | 5 | NA18941.hp1 NA18980.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344+444C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534297 | ||||||
chr17:4534334
|
G | A | 4 | a0001c0001t0004g0125a0001c0001t0004g0228a0001c0008t0004g0072others(1): Show | 4 | HG02280.hp1 HG02451.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344+481G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534334 | ||||||
chr17:4534416
|
C | T | 4 | a0001c0001t0004g0125a0001c0001t0004g0228a0001c0008t0004g0072others(1): Show | 4 | HG02280.hp1 HG02451.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344+563C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534416 | ||||||
chr17:4534417
|
G | A | 2 | a0001c0001t0006g0032a0001c0001t0007g0177 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1344+564G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534417 | ||||||
chr17:4534479
|
G | C | 1 | a0001c0009t0015g0164 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1344+626G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534479 | ||||||
chr17:4534496
|
T | A | 26 | a0001c0001t0001g0271a0001c0001t0002g0084a0001c0001t0002g0090others(23): Show | 26 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1344+643T>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534496 | ||||||
chr17:4534562
|
G | A | 1 | a0001c0001t0002g0280 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1344+709G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534562 | ||||||
chr17:4534605
|
G | GCCAGGC | 5 | a0001c0001t0004g0352a0001c0001t0019g0070a0001c0001t0019g0227others(2): Show | 5 | HG01099.hp2 HG01891.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1344+753_1344+758d others(8): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 4534605 | |||||
chr17:4534617
|
G | A | 1 | a0001c0003t0005g0176 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1344+764G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534617 | ||||||
chr17:4534630
|
C | T | 120 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(117): Show | 137 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1344+777C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534630 | ||||||
chr17:4534631
|
G | A | 21 | a0001c0001t0001g0065a0001c0001t0001g0141a0001c0001t0001g0229others(18): Show | 21 | HG01109.hp2 HG01243.hp1 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1344+778G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534631 | ||||||
chr17:4534642
|
C | G | 20 | a0001c0001t0004g0019a0001c0001t0004g0223a0001c0001t0004g0226others(17): Show | 21 | HG01081.hp2 HG01243.hp2 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.1344+789C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534642 | ||||||
chr17:4534658
|
C | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(267): Show | 300 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1344+805C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534658 | ||||||
chr17:4534665
|
G | A | 1 | a0001c0001t0002g0322 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1344+812G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534665 | ||||||
chr17:4534718
|
C | T | 1 | a0001c0001t0004g0233 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1344+865C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534718 | ||||||
chr17:4534719
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1344+866G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534719 | ||||||
chr17:4534767
|
A | G | 22 | a0001c0001t0001g0141a0001c0001t0002g0197a0001c0001t0002g0302others(19): Show | 23 | HG01099.hp1 HG01167.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.1344+914A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534767 | ||||||
chr17:4534771
|
G | A | 5 | a0001c0001t0002g0020a0001c0001t0002g0240a0001c0001t0002g0274others(2): Show | 6 | NA18948.hp1 NA18956.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.1344+918G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534771 | ||||||
chr17:4534771
|
G | C | 6 | a0001c0001t0003g0033a0001c0001t0003g0231a0001c0001t0009g0190others(3): Show | 6 | HG02109.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1344+918G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534771 | ||||||
chr17:4534800
|
C | T | 9 | a0001c0001t0004g0019a0001c0001t0004g0223a0001c0001t0004g0226others(6): Show | 10 | HG01243.hp2 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1344+947C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534800 | ||||||
chr17:4534805
|
CCA | C | 51 | a0001c0001t0004g0019a0001c0001t0004g0223a0001c0001t0004g0226others(48): Show | 52 | HG01081.hp2 HG01099.hp2 HG01167.hp1 others(49): Show |
intron_variant | MODIFIER | c.1344+953_1344+954d others(4): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534805 | ||||||
chr17:4534889
|
G | C | 358 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(355): Show | 389 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.1344+1036G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534889 | ||||||
chr17:4534920
|
G | A | 1 | a0001c0001t0002g0042 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1344+1067G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534920 | ||||||
chr17:4534928
|
C | T | 1 | a0001c0013t0045g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1344+1075C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534928 | ||||||
chr17:4534992
|
G | C | 16 | a0001c0001t0002g0084a0001c0001t0002g0090a0001c0001t0003g0048others(13): Show | 16 | HG00280.hp2 HG00639.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.1345-1084G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4534992 | ||||||
chr17:4535034
|
G | A | 1 | a0001c0001t0042g0154 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1345-1042G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535034 | ||||||
chr17:4535076
|
TAAGGCTG others(8): Show |
T | 120 | a0001c0001t0001g0016a0001c0001t0001g0037a0001c0001t0001g0041others(117): Show | 130 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.1345-996_1345-982d others(17): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 4535076 | |||||
chr17:4535114
|
C | T | 6 | a0001c0001t0001g0255a0001c0001t0004g0352a0001c0001t0019g0070others(3): Show | 6 | HG01099.hp2 HG01891.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-962C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535114 | ||||||
chr17:4535194
|
T | TGGCCTGC others(72): Show |
1 | a0001c0001t0003g0097 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1345-878_1345-800d others(81): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 4535194 | |||||
chr17:4535195
|
GGCCTGCC others(313): Show |
G | 1 | a0001c0001t0040g0264 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1345-877_1345-558d others(2): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 4535195 | |||||
chr17:4535261
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1345-815G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535261 | ||||||
chr17:4535296
|
C | G | 1 | a0001c0001t0001g0258 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1345-780C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535296 | ||||||
chr17:4535308
|
C | T | 1 | a0001c0001t0009g0165 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1345-768C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535308 | ||||||
chr17:4535309
|
G | A | 1 | a0001c0001t0017g0369 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1345-767G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535309 | ||||||
chr17:4535310
|
G | C | 128 | a0001c0001t0001g0016a0001c0001t0001g0036a0001c0001t0001g0037others(125): Show | 137 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.1345-766G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535310 | ||||||
chr17:4535319
|
G | C | 4 | a0001c0001t0004g0352a0001c0001t0019g0070a0001c0001t0019g0227others(1): Show | 4 | HG01099.hp2 HG01891.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-757G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535319 | ||||||
chr17:4535362
|
G | T | 7 | a0001c0001t0002g0297a0001c0001t0002g0314a0001c0004t0002g0123others(4): Show | 7 | HG00423.hp2 NA18951.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.1345-714G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535362 | ||||||
chr17:4535440
|
C | T | 2 | a0001c0001t0004g0125a0001c0001t0004g0228 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1345-636C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535440 | ||||||
chr17:4535459
|
G | A | 2 | a0001c0001t0004g0125a0001c0001t0004g0228 | 2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1345-617G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535459 | ||||||
chr17:4535492
|
C | T | 1 | a0001c0001t0001g0311 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1345-584C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535492 | ||||||
chr17:4535586
|
TGGCTCGG others(9): Show |
T | 1 | a0001c0001t0004g0260 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1345-482_1345-467d others(18): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 4535586 | |||||
chr17:4535732
|
A | C | 1 | a0001c0001t0002g0280 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1345-344A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535732 | ||||||
chr17:4535762
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1345-314G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535762 | ||||||
chr17:4535852
|
GGGA | G | 9 | a0001c0001t0004g0233a0001c0001t0004g0354a0001c0001t0005g0169others(6): Show | 9 | HG02922.hp1 HG02976.hp2 HG03540.hp1 others(6): Show |
intron_variant | MODIFIER | c.1345-219_1345-217d others(5): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 4535852 | |||||
chr17:4535857
|
G | A | 356 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(353): Show | 388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.1345-219G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535857 | ||||||
chr17:4535909
|
G | C | 1 | a0001c0001t0002g0254 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1345-167G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535909 | ||||||
chr17:4535952
|
G | A | 1 | a0001c0001t0046g0104 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1345-124G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535952 | ||||||
chr17:4535972
|
T | C | 1 | a0001c0008t0004g0072 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1345-104T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535972 | ||||||
chr17:4535987
|
G | A | 113 | a0001c0001t0001g0016a0001c0001t0001g0087a0001c0001t0001g0088others(110): Show | 123 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.1345-89G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4535987 | ||||||
chr17:4536006
|
C | T | 5 | a0001c0003t0004g0351a0001c0003t0006g0159a0001c0003t0007g0167others(2): Show | 5 | HG02258.hp1 HG03098.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1345-70C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4536006 | ||||||
chr17:4536018
|
A | G | 364 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(361): Show | 396 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(393): Show |
intron_variant | MODIFIER | c.1345-58A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4536018 | ||||||
chr17:4536029
|
C | T | 1 | a0001c0001t0001g0006 | 3 | NA18953.hp2 NA19060.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1345-47C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4536029 | ||||||
chr17:4536036
|
C | G | 1 | a0001c0001t0001g0206 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1345-40C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4536036 | ||||||
chr17:4536051
|
G | A | 2 | a0001c0001t0001g0206a0001c0001t0004g0125 | 2 | HG02280.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1345-25G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4536051 | ||||||
chr17:4536061
|
C | T | 6 | a0001c0001t0010g0040a0001c0001t0010g0199a0001c0001t0010g0201others(3): Show | 6 | HG00735.hp2 HG01081.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1345-15C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4536061 | ||||||
chr17:4536065
|
C | T | 2 | a0001c0001t0004g0354a0001c0001t0006g0157 | 2 | HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1345-11C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4536065 | ||||||
chr17:4536071
|
C | T | 9 | a0001c0001t0003g0095a0001c0001t0010g0040a0001c0001t0010g0199others(6): Show | 9 | HG00735.hp2 HG01081.hp2 HG01106.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.1345-5C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 9/12 | chr17 | 4536071 | ||||||
chr17:4536190
|
G | T | 1 | a0001c0001t0049g0122 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1443+16G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/12 | chr17 | 4536190 | ||||||
chr17:4536201
|
C | A | 102 | a0001c0001t0001g0016a0001c0001t0001g0087a0001c0001t0001g0088others(99): Show | 112 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1443+27C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/12 | chr17 | 4536201 | ||||||
chr17:4536202
|
A | G | 145 | a0001c0001t0001g0016a0001c0001t0001g0087a0001c0001t0001g0088others(142): Show | 158 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.1443+28A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/12 | chr17 | 4536202 | ||||||
chr17:4536206
|
C | G | 364 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(361): Show | 396 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(393): Show |
intron_variant | MODIFIER | c.1443+32C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/12 | chr17 | 4536206 | ||||||
chr17:4536217
|
A | C | 3 | a0001c0001t0019g0070a0001c0001t0019g0227a0001c0001t0022g0366 | 3 | HG01891.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1443+43A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/12 | chr17 | 4536217 | ||||||
chr17:4536217
|
A | G | 138 | a0001c0001t0001g0016a0001c0001t0001g0036a0001c0001t0001g0037others(135): Show | 149 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.1443+43A>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/12 | chr17 | 4536217 | ||||||
chr17:4536220
|
G | T | 137 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0087others(134): Show | 148 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.1444-43G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/12 | chr17 | 4536220 | ||||||
chr17:4536237
|
T | C | 311 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(308): Show | 340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.1444-26T>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/12 | chr17 | 4536237 | ||||||
chr17:4536238
|
G | A | 1 | a0001c0001t0002g0314 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1444-25G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 10/12 | chr17 | 4536238 | ||||||
chr17:4536431
|
G | GT | 12 | a0001c0001t0004g0331a0001c0001t0015g0187a0001c0002t0044g0232others(9): Show | 12 | HG02145.hp1 HG02258.hp1 HG02559.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.1607+6dupT | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 4536431 | |||||
chr17:4536432
|
T | TG | 44 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0013others(41): Show | 48 | HG00438.hp1 HG01069.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.1607+13dupG | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 4536432 | |||||
chr17:4536432
|
T | TGG | 27 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0002g0054others(24): Show | 29 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.1607+12_1607+13dup others(2): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr17 | 4536432 | |||||
chr17:4536433
|
G | T | 10 | a0001c0001t0004g0354a0001c0001t0006g0157a0001c0002t0004g0069others(7): Show | 10 | HG02257.hp2 HG02572.hp1 HG02723.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.1607+7G>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536433 | ||||||
chr17:4536436
|
G | GA | 73 | a0001c0001t0001g0016a0001c0001t0001g0041a0001c0001t0001g0087others(70): Show | 81 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1607+10_1607+11ins others(1): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536436 | ||||||
chr17:4536438
|
G | C | 2 | a0001c0004t0002g0292a0001c0004t0002g0293 | 2 | NA19003.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1607+12G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536438 | ||||||
chr17:4536439
|
G | GGA | 16 | a0001c0001t0002g0084a0001c0001t0002g0090a0001c0001t0003g0035others(13): Show | 16 | HG00738.hp1 HG01192.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.1607+13_1607+14ins others(2): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536439 | ||||||
chr17:4536459
|
C | T | 1 | a0001c0005t0002g0119 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1607+33C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536459 | ||||||
chr17:4536463
|
G | A | 2 | a0001c0001t0002g0306a0001c0001t0004g0354 | 2 | HG02976.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1607+37G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536463 | ||||||
chr17:4536500
|
C | G | 14 | a0001c0001t0003g0008a0001c0001t0003g0017a0001c0001t0003g0058others(11): Show | 18 | HG00323.hp1 HG00639.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1607+74C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536500 | ||||||
chr17:4536514
|
G | C | 9 | a0001c0001t0003g0033a0001c0001t0003g0231a0001c0001t0009g0190others(6): Show | 9 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1607+88G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536514 | ||||||
chr17:4536533
|
A | C | 98 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(95): Show | 112 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.1607+107A>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536533 | ||||||
chr17:4536686
|
C | A | 1 | a0001c0001t0002g0063 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1608-214C>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536686 | ||||||
chr17:4536689
|
C | T | 4 | a0001c0001t0015g0175a0001c0001t0015g0187a0001c0001t0021g0368others(1): Show | 4 | HG02559.hp2 HG02630.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1608-211C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536689 | ||||||
chr17:4536782
|
C | G | 1 | a0001c0001t0002g0089 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1608-118C>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536782 | ||||||
chr17:4536847
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1608-53G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536847 | ||||||
chr17:4536886
|
C | T | 6 | a0001c0001t0003g0033a0001c0001t0003g0231a0001c0001t0009g0190others(3): Show | 6 | HG02109.hp2 HG02622.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1608-14C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 11/12 | chr17 | 4536886 | ||||||
chr17:4537163
|
C | T | 1 | a0001c0001t0005g0184 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.*4+217C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | chr17 | 4537163 | ||||||
chr17:4537187
|
G | A | 1 | a0001c0001t0006g0031 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.*4+241G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | chr17 | 4537187 | ||||||
chr17:4537197
|
G | GGGCCAGG others(3): Show |
3 | a0001c0001t0016g0056a0001c0001t0016g0261a0001c0001t0026g0188 | 3 | HG02257.hp1 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.*5-247_*5-238dupCT others(8): Show |
SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 4537197 | |||||
chr17:4537207
|
T | A | 2 | a0001c0001t0002g0082a0001c0014t0002g0139 | 2 | HG00438.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.*5-246T>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | chr17 | 4537207 | ||||||
chr17:4537211
|
C | T | 103 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0020others(100): Show | 111 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.*5-242C>T | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | chr17 | 4537211 | ||||||
chr17:4537213
|
G | C | 1 | a0001c0001t0001g0337 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.*5-240G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | chr17 | 4537213 | ||||||
chr17:4537232
|
G | A | 4 | a0001c0001t0004g0125a0001c0001t0004g0228a0001c0008t0004g0072others(1): Show | 4 | HG02280.hp1 HG02451.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.*5-221G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | chr17 | 4537232 | ||||||
chr17:4537236
|
T | G | 27 | a0001c0001t0001g0079a0001c0001t0003g0033a0001c0001t0003g0231others(24): Show | 27 | HG01099.hp2 HG01255.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.*5-217T>G | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | chr17 | 4537236 | ||||||
chr17:4537259
|
G | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 176 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.*5-194G>C | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | chr17 | 4537259 | ||||||
chr17:4537342
|
G | A | 7 | a0001c0001t0003g0033a0001c0001t0003g0231a0001c0001t0009g0190others(4): Show | 7 | HG02109.hp2 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.*5-111G>A | SPNS2 | ENSG00000183018.9 | transcript | ENST00000329078.8 | protein_coding | 12/12 | chr17 | 4537342 |