geneid | 642574 |
---|---|
ensemblid | ENSG00000203499.12 |
hgncid | 49576 |
symbol | IQANK1 |
name | IQ motif and ankyrin repeat containing 1 |
refseq_nuc | NM_001381874.1 |
refseq_prot | NP_001368803.1 |
ensembl_nuc | ENST00000527139.7 |
ensembl_prot | ENSP00000489685.1 |
mane_status | MANE Select |
chr | chr8 |
start | 143734139 |
end | 143790645 |
strand | + |
ver | v1.2 |
region | chr8:143734139-143790645 |
region5000 | chr8:143729139-143795645 |
regionname0 | IQANK1_chr8_143734139_143790645 |
regionname5000 | IQANK1_chr8_143729139_143795645 |
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 | 0/1 | 560 | 107 | 9 | 12 | 66 | 3 | 16 | 44 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0002 | 0/0 | 560 | 90 | 1 | 17 | 64 | 3 | 5 | 41 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0003 | 0/0 | 560 | 38 | 36 | 1 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0004 | 0/0 | 560 | 31 | 1 | 16 | 1 | 8 | 5 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0005 | 0/0 | 560 | 16 | 3 | 1 | 8 | 1 | 3 | 5 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0006 | 0/0 | 560 | 8 | 4 | 3 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0007 | 0/0 | 560 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0008 | 0/0 | 560 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0009 | 0/0 | 560 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0010 | 0/0 | 560 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0011 | 0/0 | 561 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0012 | 0/0 | 560 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0013 | 0/0 | 560 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0014 | 0/0 | 560 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0015 | 0/0 | 560 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0016 | 0/0 | 560 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0017 | 0/0 | 561 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0018 | 0/0 | 560 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0019 | 0/0 | 560 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0020 | 0/0 | 560 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0021 | 0/0 | 560 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0022 | 0/0 | 560 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0023 | 0/0 | 560 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0024 | 0/0 | 560 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0025 | 0/0 | 560 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0026 | 0/0 | 560 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0027 | 0/0 | 560 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0028 | 0/0 | 560 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0029 | 0/0 | 560 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0030 | 0/0 | 560 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0031 | 0/0 | 560 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0032 | 0/0 | 560 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1683 | 103 | 5 | 12 | 66 | 3 | 16 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0002 | 0/0 | 1683 | 89 | 1 | 17 | 63 | 3 | 5 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0003 | 0/0 | 1683 | 38 | 36 | 1 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0004 | 0/0 | 1683 | 31 | 1 | 16 | 1 | 8 | 5 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0005 | 0/0 | 1683 | 16 | 3 | 1 | 8 | 1 | 3 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0006 | 0/0 | 1683 | 8 | 4 | 3 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0007 | 0/0 | 1683 | 8 | 8 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0008 | 0/0 | 1683 | 7 | 7 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0009 | 0/0 | 1683 | 6 | 5 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0010 | 0/0 | 1683 | 4 | 4 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0011 | 0/0 | 1683 | 4 | 4 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0012 | 0/0 | 1686 | 3 | 2 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0013 | 0/0 | 1683 | 3 | 0 | 0 | 0 | 0 | 3 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0014 | 0/0 | 1683 | 2 | 0 | 0 | 0 | 0 | 2 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0015 | 0/0 | 1683 | 2 | 0 | 1 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0016 | 0/0 | 1686 | 2 | 1 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0017 | 0/0 | 1683 | 2 | 2 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0018 | 0/0 | 1683 | 2 | 0 | 2 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0019 | 0/0 | 1683 | 2 | 0 | 1 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0020 | 0/0 | 1683 | 2 | 0 | 0 | 0 | 0 | 2 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0021 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0022 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0023 | 0/0 | 1683 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0024 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0025 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0026 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0027 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0028 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0029 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0030 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0031 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0032 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0033 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0034 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
c0035 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
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 | 123 | 347 | 92 | 58 | 140 | 16 | 40 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
t0002 | 0/0 | 123 | 2 | 0 | 0 | 2 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1683 | 103 | 5 | 12 | 66 | 3 | 16 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0001c0010 | 0/0 | 1683 | 4 | 4 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0002c0002 | 0/0 | 1683 | 89 | 1 | 17 | 63 | 3 | 5 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0002c0035 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0003c0003 | 0/0 | 1683 | 38 | 36 | 1 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0004c0004 | 0/0 | 1683 | 31 | 1 | 16 | 1 | 8 | 5 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0005c0005 | 0/0 | 1683 | 16 | 3 | 1 | 8 | 1 | 3 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0006c0006 | 0/0 | 1683 | 8 | 4 | 3 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0007c0007 | 0/0 | 1683 | 8 | 8 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0008c0008 | 0/0 | 1683 | 7 | 7 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0009c0009 | 0/0 | 1683 | 6 | 5 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0010c0011 | 0/0 | 1683 | 4 | 4 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0011c0012 | 0/0 | 1686 | 3 | 2 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0012c0017 | 0/0 | 1683 | 2 | 2 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0012c0027 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0013c0013 | 0/0 | 1683 | 3 | 0 | 0 | 0 | 0 | 3 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0014c0019 | 0/0 | 1683 | 2 | 0 | 1 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0015c0015 | 0/0 | 1683 | 2 | 0 | 1 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0016c0014 | 0/0 | 1683 | 2 | 0 | 0 | 0 | 0 | 2 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0017c0016 | 0/0 | 1686 | 2 | 1 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0018c0018 | 0/0 | 1683 | 2 | 0 | 2 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0019c0020 | 0/0 | 1683 | 2 | 0 | 0 | 0 | 0 | 2 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0020c0023 | 0/0 | 1683 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0021c0024 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0022c0025 | 0/0 | 1683 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0023c0026 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0024c0022 | 0/0 | 1683 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0025c0030 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0026c0029 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0027c0028 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0028c0031 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0029c0032 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0030c0021 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0031c0033 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0032c0034 | 0/0 | 1683 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1805 | 101 | 5 | 12 | 64 | 3 | 16 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0001c0001t0002 | 0/0 | 1805 | 2 | 0 | 0 | 2 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0001c0010t0001 | 0/0 | 1805 | 4 | 4 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0002c0002t0001 | 0/0 | 1805 | 89 | 1 | 17 | 63 | 3 | 5 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0002c0035t0001 | 0/0 | 1805 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0003c0003t0001 | 0/0 | 1805 | 38 | 36 | 1 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0004c0004t0001 | 0/0 | 1805 | 31 | 1 | 16 | 1 | 8 | 5 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0005c0005t0001 | 0/0 | 1805 | 16 | 3 | 1 | 8 | 1 | 3 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0006c0006t0001 | 0/0 | 1805 | 8 | 4 | 3 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0007c0007t0001 | 0/0 | 1805 | 8 | 8 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0008c0008t0001 | 0/0 | 1805 | 7 | 7 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0009c0009t0001 | 0/0 | 1805 | 6 | 5 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0010c0011t0001 | 0/0 | 1805 | 4 | 4 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0011c0012t0001 | 0/0 | 1808 | 3 | 2 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0012c0017t0001 | 0/0 | 1805 | 2 | 2 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0012c0027t0001 | 0/0 | 1805 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0013c0013t0001 | 0/0 | 1805 | 3 | 0 | 0 | 0 | 0 | 3 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0014c0019t0001 | 0/0 | 1805 | 2 | 0 | 1 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0015c0015t0001 | 0/0 | 1805 | 2 | 0 | 1 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0016c0014t0001 | 0/0 | 1805 | 2 | 0 | 0 | 0 | 0 | 2 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0017c0016t0001 | 0/0 | 1808 | 2 | 1 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0018c0018t0001 | 0/0 | 1805 | 2 | 0 | 2 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0019c0020t0001 | 0/0 | 1805 | 2 | 0 | 0 | 0 | 0 | 2 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0020c0023t0001 | 0/0 | 1805 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0021c0024t0001 | 0/0 | 1805 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0022c0025t0001 | 0/0 | 1805 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0023c0026t0001 | 0/0 | 1805 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0024c0022t0001 | 0/0 | 1805 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0025c0030t0001 | 0/0 | 1805 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0026c0029t0001 | 0/0 | 1805 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0027c0028t0001 | 0/0 | 1805 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0028c0031t0001 | 0/0 | 1805 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0029c0032t0001 | 0/0 | 1805 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0030c0021t0001 | 0/0 | 1805 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0031c0033t0001 | 0/0 | 1805 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
a0032c0034t0001 | 0/0 | 1805 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | copy fasta | chr8 | 143729139 | 143795645 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0010t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0010t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0010t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0001c0010t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0002c0035t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0003c0003t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0004c0004t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0005c0005t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0005c0005t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0005c0005t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0005c0005t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0005c0005t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0005c0005t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0005c0005t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0005c0005t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0005c0005t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0005c0005t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0005c0005t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0005c0005t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0005c0005t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0005c0005t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0005c0005t0001g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0005c0005t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0006c0006t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0006c0006t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0006c0006t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0006c0006t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0006c0006t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0006c0006t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0006c0006t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0006c0006t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0007c0007t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0007c0007t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0007c0007t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0007c0007t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0007c0007t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0007c0007t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0007c0007t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0007c0007t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0008c0008t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0008c0008t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0008c0008t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0008c0008t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0008c0008t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0008c0008t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0008c0008t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0009c0009t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0009c0009t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0009c0009t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0009c0009t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0009c0009t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0009c0009t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0010c0011t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0010c0011t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0010c0011t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0010c0011t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0011c0012t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0011c0012t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0011c0012t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0012c0017t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0012c0017t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0012c0027t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0013c0013t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0013c0013t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0013c0013t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0014c0019t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0014c0019t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0015c0015t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0015c0015t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0016c0014t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0016c0014t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0017c0016t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0017c0016t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0018c0018t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0018c0018t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0019c0020t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0019c0020t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0020c0023t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0021c0024t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0022c0025t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0023c0026t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0024c0022t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0025c0030t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0026c0029t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0027c0028t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0028c0031t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0029c0032t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0030c0021t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0031c0033t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
a0032c0034t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0004 | c0004 | t0001 | g0169 | EUR | GBR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00099 | hp2 | a0004 | c0004 | t0001 | g0176 | EUR | GBR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | GBR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0316 | EUR | GBR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0290 | EUR | FIN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00280 | hp2 | a0005 | c0005 | t0001 | g0211 | EUR | FIN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0298 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0272 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0337 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0334 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00544 | hp1 | a0005 | c0005 | t0001 | g0206 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0286 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0297 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0271 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0324 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0304 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0336 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0257 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00642 | hp1 | a0006 | c0006 | t0001 | g0168 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0308 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | CHS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00733 | hp1 | a0004 | c0004 | t0001 | g0072 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00733 | hp2 | a0014 | c0019 | t0001 | g0021 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00735 | hp1 | a0005 | c0005 | t0001 | g0210 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00735 | hp2 | a0006 | c0006 | t0001 | g0184 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00738 | hp1 | a0004 | c0004 | t0001 | g0071 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG00738 | hp2 | a0004 | c0004 | t0001 | g0181 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01069 | hp1 | a0020 | c0023 | t0001 | g0052 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01071 | hp1 | a0004 | c0004 | t0001 | g0173 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01074 | hp1 | a0004 | c0004 | t0001 | g0050 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0260 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0331 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01081 | hp2 | a0004 | c0004 | t0001 | g0157 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01109 | hp1 | a0017 | c0016 | t0001 | g0348 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01109 | hp2 | a0004 | c0004 | t0001 | g0154 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01168 | hp1 | a0018 | c0018 | t0001 | g0179 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01175 | hp1 | a0011 | c0012 | t0001 | g0345 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01175 | hp2 | a0004 | c0004 | t0001 | g0183 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01192 | hp1 | a0004 | c0004 | t0001 | g0073 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01192 | hp2 | a0009 | c0009 | t0001 | g0007 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01243 | hp1 | a0004 | c0004 | t0001 | g0177 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0282 | AMR | PUR | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0261 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01261 | hp2 | a0004 | c0004 | t0001 | g0160 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0267 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0301 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01358 | hp1 | a0004 | c0004 | t0001 | g0162 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01361 | hp2 | a0006 | c0006 | t0001 | g0167 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01496 | hp1 | a0018 | c0018 | t0001 | g0180 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01496 | hp2 | a0004 | c0004 | t0001 | g0185 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01515 | hp1 | a0004 | c0004 | t0001 | g0074 | EUR | IBS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01515 | hp2 | a0015 | c0015 | t0001 | g0172 | EUR | IBS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01516 | hp1 | a0004 | c0004 | t0001 | g0170 | EUR | IBS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | IBS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | IBS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01517 | hp2 | a0004 | c0004 | t0001 | g0075 | EUR | IBS | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01884 | hp1 | a0031 | c0033 | t0001 | g0332 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01884 | hp2 | a0003 | c0003 | t0001 | g0028 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01891 | hp1 | a0008 | c0008 | t0001 | g0020 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0254 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0317 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0258 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01975 | hp2 | a0003 | c0003 | t0001 | g0241 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0268 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0326 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01981 | hp1 | a0004 | c0004 | t0001 | g0174 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02004 | hp1 | a0004 | c0004 | t0001 | g0155 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0309 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0305 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02015 | hp2 | a0004 | c0004 | t0001 | g0246 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02027 | hp1 | a0005 | c0005 | t0001 | g0208 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0312 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02055 | hp1 | a0005 | c0005 | t0001 | g0323 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02055 | hp2 | a0027 | c0028 | t0001 | g0150 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02056 | hp2 | a0002 | c0002 | t0001 | g0306 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0307 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0259 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02083 | hp1 | a0006 | c0006 | t0001 | g0056 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0278 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0280 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02145 | hp1 | a0007 | c0007 | t0001 | g0201 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02145 | hp2 | a0005 | c0005 | t0001 | g0288 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CDX | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CDX | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CDX | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0295 | EAS | CDX | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0213 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02257 | hp2 | a0006 | c0006 | t0001 | g0030 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02258 | hp1 | a0003 | c0003 | t0001 | g0229 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02258 | hp2 | a0007 | c0007 | t0001 | g0044 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02280 | hp1 | a0003 | c0003 | t0001 | g0033 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02280 | hp2 | a0003 | c0003 | t0001 | g0223 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02293 | hp1 | a0015 | c0015 | t0001 | g0156 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02293 | hp2 | a0002 | c0002 | t0001 | g0276 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0320 | EAS | KHV | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02572 | hp1 | a0008 | c0008 | t0001 | g0029 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02572 | hp2 | a0007 | c0007 | t0001 | g0015 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02602 | hp2 | a0024 | c0022 | t0001 | g0059 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02615 | hp1 | a0003 | c0003 | t0001 | g0010 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02615 | hp2 | a0007 | c0007 | t0001 | g0041 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02622 | hp1 | a0025 | c0030 | t0001 | g0346 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02622 | hp2 | a0003 | c0003 | t0001 | g0225 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02630 | hp1 | a0003 | c0003 | t0001 | g0069 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02630 | hp2 | a0003 | c0003 | t0001 | g0230 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02647 | hp1 | a0003 | c0003 | t0001 | g0063 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02647 | hp2 | a0008 | c0008 | t0001 | g0238 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02683 | hp1 | a0016 | c0014 | t0001 | g0058 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02683 | hp2 | a0004 | c0004 | t0001 | g0152 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02698 | hp2 | a0004 | c0004 | t0001 | g0165 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02717 | hp1 | a0003 | c0003 | t0001 | g0036 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02723 | hp1 | a0009 | c0009 | t0001 | g0012 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02723 | hp2 | a0003 | c0003 | t0001 | g0134 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02809 | hp1 | a0003 | c0003 | t0001 | g0034 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02809 | hp2 | a0026 | c0029 | t0001 | g0221 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02886 | hp1 | a0010 | c0011 | t0001 | g0232 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02886 | hp2 | a0008 | c0008 | t0001 | g0239 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02895 | hp1 | a0003 | c0003 | t0001 | g0226 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02895 | hp2 | a0003 | c0003 | t0001 | g0035 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02896 | hp1 | a0003 | c0003 | t0001 | g0228 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02896 | hp2 | a0003 | c0003 | t0001 | g0235 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02897 | hp1 | a0003 | c0003 | t0001 | g0227 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02897 | hp2 | a0003 | c0003 | t0001 | g0234 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02922 | hp1 | a0032 | c0034 | t0001 | g0212 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02922 | hp2 | a0003 | c0003 | t0001 | g0199 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02965 | hp1 | a0010 | c0011 | t0001 | g0220 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02965 | hp2 | a0003 | c0003 | t0001 | g0054 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02970 | hp1 | a0010 | c0011 | t0001 | g0231 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02970 | hp2 | a0001 | c0010 | t0001 | g0038 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02976 | hp1 | a0030 | c0021 | t0001 | g0338 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02976 | hp2 | a0029 | c0032 | t0001 | g0025 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03041 | hp1 | a0003 | c0003 | t0001 | g0016 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03041 | hp2 | a0003 | c0003 | t0001 | g0032 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03098 | hp1 | a0003 | c0003 | t0001 | g0045 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03098 | hp2 | a0010 | c0011 | t0001 | g0009 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03130 | hp1 | a0007 | c0007 | t0001 | g0042 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03130 | hp2 | a0009 | c0009 | t0001 | g0024 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03139 | hp1 | a0003 | c0003 | t0001 | g0133 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03195 | hp1 | a0001 | c0010 | t0001 | g0039 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03195 | hp2 | a0003 | c0003 | t0001 | g0194 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03209 | hp1 | a0012 | c0027 | t0001 | g0014 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03209 | hp2 | a0003 | c0003 | t0001 | g0233 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03225 | hp1 | a0003 | c0003 | t0001 | g0224 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03225 | hp2 | a0003 | c0003 | t0001 | g0196 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03239 | hp2 | a0004 | c0004 | t0001 | g0166 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03453 | hp1 | a0009 | c0009 | t0001 | g0027 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03453 | hp2 | a0008 | c0008 | t0001 | g0240 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03486 | hp1 | a0003 | c0003 | t0001 | g0198 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03486 | hp2 | a0011 | c0012 | t0001 | g0347 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03490 | hp1 | a0013 | c0013 | t0001 | g0017 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03490 | hp2 | a0019 | c0020 | t0001 | g0281 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03492 | hp1 | a0013 | c0013 | t0001 | g0018 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03516 | hp1 | a0008 | c0008 | t0001 | g0128 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03516 | hp2 | a0001 | c0010 | t0001 | g0037 | AFR | ESN | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03540 | hp1 | a0009 | c0009 | t0001 | g0022 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03540 | hp2 | a0003 | c0003 | t0001 | g0222 | AFR | GWD | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03579 | hp1 | a0009 | c0009 | t0001 | g0026 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03579 | hp2 | a0011 | c0012 | t0001 | g0342 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03654 | hp1 | a0003 | c0003 | t0001 | g0089 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03669 | hp1 | a0013 | c0013 | t0001 | g0008 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03669 | hp2 | a0016 | c0014 | t0001 | g0057 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03704 | hp1 | a0005 | c0005 | t0001 | g0328 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03710 | hp1 | a0023 | c0026 | t0001 | g0149 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0274 | SAS | PJL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03834 | hp2 | a0005 | c0005 | t0001 | g0329 | SAS | BEB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03927 | hp1 | a0004 | c0004 | t0001 | g0178 | SAS | BEB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03927 | hp2 | a0002 | c0002 | t0001 | g0321 | SAS | BEB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0269 | SAS | BEB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | STU | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | STU | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | BEB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG04199 | hp1 | a0004 | c0004 | t0001 | g0151 | SAS | STU | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG04199 | hp2 | a0014 | c0019 | t0001 | g0023 | SAS | STU | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG04204 | hp2 | a0005 | c0005 | t0001 | g0209 | SAS | STU | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG04228 | hp2 | a0019 | c0020 | t0001 | g0294 | SAS | STU | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18522 | hp1 | a0017 | c0016 | t0001 | g0237 | AFR | YRI | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18522 | hp2 | a0008 | c0008 | t0001 | g0019 | AFR | YRI | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18612 | hp1 | a0005 | c0005 | t0001 | g0216 | EAS | CHB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | CHB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18747 | hp2 | a0002 | c0002 | t0001 | g0313 | EAS | CHB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18906 | hp1 | a0001 | c0010 | t0001 | g0040 | AFR | YRI | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18906 | hp2 | a0012 | c0017 | t0001 | g0195 | AFR | YRI | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18939 | hp1 | a0005 | c0005 | t0001 | g0207 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0299 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18943 | hp2 | a0021 | c0024 | t0001 | g0193 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18947 | hp2 | a0005 | c0005 | t0001 | g0214 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0314 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18950 | hp1 | a0005 | c0005 | t0001 | g0215 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0263 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0335 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0248 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18968 | hp1 | a0022 | c0025 | t0001 | g0101 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18968 | hp2 | a0002 | c0002 | t0001 | g0330 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0266 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18974 | hp2 | a0002 | c0002 | t0001 | g0325 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18979 | hp2 | a0002 | c0002 | t0001 | g0322 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0318 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0284 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0311 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18995 | hp1 | a0005 | c0005 | t0001 | g0218 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0283 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0285 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0253 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19000 | hp2 | a0005 | c0005 | t0001 | g0217 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0279 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19030 | hp1 | a0003 | c0003 | t0001 | g0236 | AFR | LWK | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19030 | hp2 | a0006 | c0006 | t0001 | g0060 | AFR | LWK | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19043 | hp1 | a0028 | c0031 | t0001 | g0244 | AFR | LWK | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19043 | hp2 | a0003 | c0003 | t0001 | g0011 | AFR | LWK | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0251 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0287 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19065 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0340 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19067 | hp1 | a0002 | c0002 | t0001 | g0300 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19070 | hp1 | a0002 | c0002 | t0001 | g0255 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19070 | hp2 | a0002 | c0035 | t0001 | g0310 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0265 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19074 | hp2 | a0002 | c0002 | t0001 | g0275 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0273 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0327 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19082 | hp1 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0315 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA20129 | hp1 | a0003 | c0003 | t0001 | g0219 | AFR | ASW | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA20129 | hp2 | a0007 | c0007 | t0001 | g0043 | AFR | ASW | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA20752 | hp1 | a0004 | c0004 | t0001 | g0175 | EUR | TSI | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA20752 | hp2 | a0004 | c0004 | t0001 | g0171 | EUR | TSI | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA20805 | hp1 | a0004 | c0004 | t0001 | g0189 | EUR | TSI | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0289 | EUR | TSI | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | GIH | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | GIH | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01123 | hp1 | a0004 | c0004 | t0001 | g0163 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02486 | hp1 | a0003 | c0003 | t0001 | g0343 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02486 | hp2 | a0007 | c0007 | t0001 | g0013 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG02559 | hp2 | a0003 | c0003 | t0001 | g0135 | AFR | ACB | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03471 | hp1 | a0007 | c0007 | t0001 | g0200 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG03471 | hp2 | a0006 | c0006 | t0001 | g0031 | AFR | MSL | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG06807 | hp1 | a0005 | c0005 | t0001 | g0333 | AFR | USA | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
HG06807 | hp2 | a0006 | c0006 | t0001 | g0182 | AFR | USA | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0249 | EAS | JPT | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA20300 | hp1 | a0003 | c0003 | t0001 | g0197 | AFR | USA | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | USA | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA21309 | hp1 | a0012 | c0017 | t0001 | g0064 | AFR | LWK | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
NA21309 | hp2 | a0004 | c0004 | t0001 | g0339 | AFR | LWK | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0095 | REF | REF | IQANK1_chr8_143729139_143795645 | IQANK1 | chr8 | 143729139 | 143795645 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:143739867
|
G | T | 5 | a0002a0005a0019others(2): Show | 110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
missense_variant | MODERATE | c.94G>T | p.Gly32Trp | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/14 | 179/1805 | 94/1683 | 32/560 | chr8 | 143739867 | ||
chr8:143739894
|
G | A | 1 | a0030 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.121G>A | p.Ala41Thr | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/14 | 206/1805 | 121/1683 | 41/560 | chr8 | 143739894 | ||
chr8:143739895
|
C | T | 1 | a0030 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.122C>T | p.Ala41Val | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/14 | 207/1805 | 122/1683 | 41/560 | chr8 | 143739895 | ||
chr8:143739922
|
C | T | 1 | a0014 | 2 | HG00733.hp2 HG04199.hp2 |
missense_variant | MODERATE | c.149C>T | p.Ser50Leu | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/14 | 234/1805 | 149/1683 | 50/560 | chr8 | 143739922 | ||
chr8:143739940
|
C | A | 1 | a0030 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.167C>A | p.Ala56Asp | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/14 | 252/1805 | 167/1683 | 56/560 | chr8 | 143739940 | ||
chr8:143771521
|
A | G | 6 | a0008a0009a0013others(3): Show | 20 | HG00733.hp2 HG01192.hp2 HG01891.hp1 others(17): Show |
missense_variant | MODERATE | c.209A>G | p.Gln70Arg | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 4/14 | 294/1805 | 209/1683 | 70/560 | chr8 | 143771521 | ||
chr8:143771614
|
A | G | 18 | a0002a0003a0005others(15): Show | 181 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(178): Show |
missense_variant | MODERATE | c.302A>G | p.Lys101Arg | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 4/14 | 387/1805 | 302/1683 | 101/560 | chr8 | 143771614 | ||
chr8:143772134
|
C | T | 2 | a0007a0030 | 9 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(6): Show |
missense_variant | MODERATE | c.554C>T | p.Ala185Val | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 6/14 | 639/1805 | 554/1683 | 185/560 | chr8 | 143772134 | ||
chr8:143772161
|
C | T | 1 | a0025 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.581C>T | p.Thr194Met | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 6/14 | 666/1805 | 581/1683 | 194/560 | chr8 | 143772161 | ||
chr8:143772435
|
G | A | 5 | a0002a0016a0019others(2): Show | 96 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(93): Show |
missense_variant | MODERATE | c.742G>A | p.Gly248Arg | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/14 | 827/1805 | 742/1683 | 248/560 | chr8 | 143772435 | ||
chr8:143789022
|
G | C | 1 | a0020 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.897G>C | p.Glu299Asp | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 8/14 | 982/1805 | 897/1683 | 299/560 | chr8 | 143789022 | ||
chr8:143789463
|
C | T | 10 | a0004a0013a0015others(7): Show | 45 | HG00099.hp1 HG00099.hp2 HG00733.hp1 others(42): Show |
missense_variant | MODERATE | c.1021C>T | p.Arg341Trp | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 10/14 | 1106/1805 | 1021/1683 | 341/560 | chr8 | 143789463 | ||
chr8:143789976
|
G | C | 1 | a0032 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.1201G>C | p.Glu401Gln | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 12/14 | 1286/1805 | 1201/1683 | 401/560 | chr8 | 143789976 | ||
chr8:143790018
|
G | A | 1 | a0027 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.1243G>A | p.Asp415Asn | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 12/14 | 1328/1805 | 1243/1683 | 415/560 | chr8 | 143790018 | ||
chr8:143790142
|
C | A | 1 | a0021 | 1 | NA18943.hp2 | missense_variant | MODERATE | c.1295C>A | p.Pro432His | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 13/14 | 1380/1805 | 1295/1683 | 432/560 | chr8 | 143790142 | ||
chr8:143790241
|
C | G | 18 | a0001a0002a0003others(15): Show | 289 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(286): Show |
missense_variant | MODERATE | c.1394C>G | p.Thr465Arg | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 13/14 | 1479/1805 | 1394/1683 | 465/560 | chr8 | 143790241 | ||
chr8:143790253
|
C | T | 3 | a0008a0010a0028 | 12 | HG01891.hp1 HG02572.hp1 HG02647.hp2 others(9): Show |
missense_variant | MODERATE | c.1406C>T | p.Ala469Val | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 13/14 | 1491/1805 | 1406/1683 | 469/560 | chr8 | 143790253 | ||
chr8:143790372
|
G | C | 2 | a0011a0017 | 5 | HG01109.hp1 HG01175.hp1 HG03486.hp2 others(2): Show |
missense_variant | MODERATE | c.1447G>C | p.Asp483His | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 14/14 | 1532/1805 | 1447/1683 | 483/560 | chr8 | 143790372 | ||
chr8:143790408
|
C | T | 1 | a0022 | 1 | NA18968.hp1 | missense_variant | MODERATE | c.1483C>T | p.Arg495Trp | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 14/14 | 1568/1805 | 1483/1683 | 495/560 | chr8 | 143790408 | ||
chr8:143790424
|
T | TGCA | 2 | a0011a0017 | 5 | HG01109.hp1 HG01175.hp1 HG03486.hp2 others(2): Show |
conservative_inframe_insertion | MODERATE | c.1501_1503dupCAG | p.Gln501dup | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 14/14 | 1589/1805 | 1504/1683 | 502/560 | INFO_REALIGN_3_PRIME | chr8 | 143790424 | |
chr8:143790459
|
G | A | 1 | a0023 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.1534G>A | p.Asp512Asn | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 14/14 | 1619/1805 | 1534/1683 | 512/560 | chr8 | 143790459 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:143772183
|
A | G | 3 | a0001c0010a0007c0007a0030c0021 | 13 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(10): Show |
synonymous_variant | LOW | c.603A>G | p.Ala201Ala | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 6/14 | 688/1805 | 603/1683 | 201/560 | chr8 | 143772183 | ||
chr8:143789480
|
C | T | 2 | a0012c0017a0029c0032 | 3 | HG02976.hp2 NA18906.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.1038C>T | p.His346His | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 10/14 | 1123/1805 | 1038/1683 | 346/560 | chr8 | 143789480 | ||
chr8:143789999
|
C | T | 1 | a0002c0035 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.1224C>T | p.Cys408Cys | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 12/14 | 1309/1805 | 1224/1683 | 408/560 | chr8 | 143789999 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:143790641
|
C | T | 1 | a0001c0001t0002 | 2 | NA18957.hp2 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*33C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 14/14 | 33 | chr8 | 143790641 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:143734223
|
A | G | 8 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0343others(5): Show | 8 | HG01109.hp1 HG01175.hp1 HG02486.hp1 others(5): Show |
splice_region_variant&intron_variant | LOW | c.-5+4A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734223 | ||||||
chr8:143734255
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-5+36G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734255 | ||||||
chr8:143734330
|
C | T | 1 | a0002c0002t0001g0340 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-5+111C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734330 | ||||||
chr8:143734379
|
C | T | 1 | a0004c0004t0001g0339 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-5+160C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734379 | ||||||
chr8:143734418
|
C | T | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-5+199C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734418 | ||||||
chr8:143734459
|
G | C | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-5+240G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734459 | ||||||
chr8:143734489
|
T | C | 1 | a0002c0002t0001g0005 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-5+270T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734489 | ||||||
chr8:143734498
|
G | GGACCCCG others(7): Show |
1 | a0002c0002t0001g0006 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-5+280_-5+293dupGA others(12): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr8 | 143734498 | |||||
chr8:143734589
|
C | T | 96 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(93): Show | 97 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.-5+370C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734589 | ||||||
chr8:143734622
|
C | T | 1 | a0002c0002t0001g0337 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-5+403C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734622 | ||||||
chr8:143734623
|
G | A | 23 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(20): Show | 23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-5+404G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734623 | ||||||
chr8:143734725
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-5+506C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734725 | ||||||
chr8:143734867
|
C | G | 1 | a0004c0004t0001g0246 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-5+648C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143734867 | ||||||
chr8:143735164
|
G | T | 1 | a0001c0001t0001g0245 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-4-686G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735164 | ||||||
chr8:143735167
|
T | G | 1 | a0001c0001t0001g0245 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-4-683T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735167 | ||||||
chr8:143735168
|
G | T | 1 | a0001c0001t0001g0245 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-4-682G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735168 | ||||||
chr8:143735199
|
C | T | 23 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(20): Show | 23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.-4-651C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735199 | ||||||
chr8:143735316
|
G | A | 345 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(342): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.-4-534G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735316 | ||||||
chr8:143735351
|
C | G | 1 | a0002c0002t0001g0336 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-4-499C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735351 | ||||||
chr8:143735483
|
TGATTAC | T | 23 | a0003c0003t0001g0219a0003c0003t0001g0222a0003c0003t0001g0223others(20): Show | 23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.-4-365_-4-360delAT others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr8 | 143735483 | |||||
chr8:143735523
|
G | A | 2 | a0006c0006t0001g0030a0006c0006t0001g0031 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-4-327G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735523 | ||||||
chr8:143735540
|
G | A | 5 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(2): Show | 5 | HG02280.hp1 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-310G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735540 | ||||||
chr8:143735734
|
G | A | 8 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(5): Show | 8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-116G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735734 | ||||||
chr8:143735748
|
C | A | 1 | a0003c0003t0001g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-4-102C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735748 | ||||||
chr8:143735833
|
C | T | 1 | a0002c0002t0001g0335 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-4-17C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 1/13 | chr8 | 143735833 | ||||||
chr8:143736008
|
A | C | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.85+70A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736008 | ||||||
chr8:143736010
|
C | T | 1 | a0002c0002t0001g0337 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.85+72C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736010 | ||||||
chr8:143736140
|
T | A | 1 | a0003c0003t0001g0219 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.85+202T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736140 | ||||||
chr8:143736141
|
A | AT | 110 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(107): Show | 111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.85+220dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr8 | 143736141 | |||||
chr8:143736141
|
AT | A | 16 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(13): Show | 16 | HG00558.hp1 HG01069.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.85+220delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr8 | 143736141 | |||||
chr8:143736177
|
T | C | 23 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(20): Show | 23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.85+239T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736177 | ||||||
chr8:143736334
|
G | C | 1 | a0002c0002t0001g0252 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.85+396G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736334 | ||||||
chr8:143736370
|
CCTGACCT others(20): Show |
C | 1 | a0002c0002t0001g0251 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.85+433_85+459delCT others(25): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736370 | ||||||
chr8:143736481
|
C | G | 1 | a0002c0002t0001g0252 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.85+543C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736481 | ||||||
chr8:143736547
|
G | T | 1 | a0002c0002t0001g0252 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.85+609G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736547 | ||||||
chr8:143736639
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0202 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.85+701C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736639 | ||||||
chr8:143736657
|
C | A | 23 | a0003c0003t0001g0219a0003c0003t0001g0222a0003c0003t0001g0223others(20): Show | 23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.85+719C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736657 | ||||||
chr8:143736690
|
T | A | 1 | a0006c0006t0001g0056 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.85+752T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736690 | ||||||
chr8:143736782
|
C | T | 23 | a0003c0003t0001g0219a0003c0003t0001g0222a0003c0003t0001g0223others(20): Show | 23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.85+844C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736782 | ||||||
chr8:143736806
|
C | T | 1 | a0002c0002t0001g0334 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.85+868C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736806 | ||||||
chr8:143736897
|
C | T | 10 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(7): Show | 10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.85+959C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143736897 | ||||||
chr8:143737049
|
C | T | 8 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(5): Show | 8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.85+1111C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737049 | ||||||
chr8:143737059
|
C | T | 2 | a0001c0001t0001g0192a0021c0024t0001g0193 | 2 | NA18943.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.85+1121C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737059 | ||||||
chr8:143737144
|
G | A | 1 | a0003c0003t0001g0194 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.85+1206G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737144 | ||||||
chr8:143737175
|
C | G | 110 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(107): Show | 111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.85+1237C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737175 | ||||||
chr8:143737333
|
A | G | 5 | a0001c0001t0001g0191a0001c0001t0001g0192a0001c0001t0002g0053others(2): Show | 5 | HG02129.hp2 NA18943.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.85+1395A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737333 | ||||||
chr8:143737450
|
G | C | 23 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(20): Show | 23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.85+1512G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737450 | ||||||
chr8:143737520
|
G | C | 1 | a0026c0029t0001g0221 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.85+1582G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737520 | ||||||
chr8:143737608
|
C | T | 1 | a0025c0030t0001g0346 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.85+1670C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737608 | ||||||
chr8:143737621
|
C | T | 1 | a0004c0004t0001g0189 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.85+1683C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737621 | ||||||
chr8:143737625
|
C | T | 1 | a0003c0003t0001g0241 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.85+1687C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737625 | ||||||
chr8:143737704
|
G | A | 1 | a0002c0002t0001g0253 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.85+1766G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737704 | ||||||
chr8:143737734
|
G | A | 3 | a0016c0014t0001g0057a0016c0014t0001g0058a0024c0022t0001g0059 | 3 | HG02602.hp2 HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.85+1796G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737734 | ||||||
chr8:143737814
|
G | A | 1 | a0002c0002t0001g0254 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.85+1876G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737814 | ||||||
chr8:143737850
|
C | G | 10 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(7): Show | 10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.85+1912C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737850 | ||||||
chr8:143737927
|
G | A | 1 | a0006c0006t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.86-1932G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143737927 | ||||||
chr8:143738136
|
C | T | 1 | a0005c0005t0001g0333 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.86-1723C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738136 | ||||||
chr8:143738172
|
C | T | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.86-1687C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738172 | ||||||
chr8:143738324
|
C | T | 3 | a0016c0014t0001g0057a0016c0014t0001g0058a0024c0022t0001g0059 | 3 | HG02602.hp2 HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.86-1535C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738324 | ||||||
chr8:143738506
|
G | A | 3 | a0001c0001t0001g0203a0001c0010t0001g0037a0001c0010t0001g0038 | 3 | HG02970.hp2 HG03516.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.86-1353G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738506 | ||||||
chr8:143738519
|
G | A | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.86-1340G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738519 | ||||||
chr8:143738550
|
C | T | 1 | a0008c0008t0001g0029 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.86-1309C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738550 | ||||||
chr8:143738559
|
G | A | 1 | a0001c0001t0001g0061 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.86-1300G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738559 | ||||||
chr8:143738648
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.86-1211C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738648 | ||||||
chr8:143738738
|
C | A | 8 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(5): Show | 8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.86-1121C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738738 | ||||||
chr8:143738854
|
C | T | 6 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0343others(3): Show | 6 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-1005C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738854 | ||||||
chr8:143738911
|
C | T | 1 | a0003c0003t0001g0028 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.86-948C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738911 | ||||||
chr8:143738943
|
G | T | 1 | a0001c0001t0001g0188 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.86-916G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143738943 | ||||||
chr8:143739023
|
G | A | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.86-836G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739023 | ||||||
chr8:143739065
|
G | A | 1 | a0009c0009t0001g0007 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.86-794G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739065 | ||||||
chr8:143739112
|
C | T | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.86-747C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739112 | ||||||
chr8:143739148
|
C | G | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.86-711C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739148 | ||||||
chr8:143739175
|
A | G | 345 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(342): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.86-684A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739175 | ||||||
chr8:143739253
|
TG | T | 8 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(5): Show | 8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.86-604delG | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr8 | 143739253 | |||||
chr8:143739268
|
C | T | 193 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.86-591C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739268 | ||||||
chr8:143739325
|
G | A | 5 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | NA18942.hp2 NA18951.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.86-534G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739325 | ||||||
chr8:143739327
|
C | T | 2 | a0003c0003t0001g0063a0012c0017t0001g0064 | 2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.86-532C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739327 | ||||||
chr8:143739332
|
C | T | 1 | a0031c0033t0001g0332 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.86-527C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739332 | ||||||
chr8:143739626
|
G | C | 2 | a0002c0002t0001g0255a0002c0002t0001g0256 | 2 | HG02080.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.86-233G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739626 | ||||||
chr8:143739722
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.86-137C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739722 | ||||||
chr8:143739774
|
C | T | 1 | a0012c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.86-85C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739774 | ||||||
chr8:143739787
|
A | G | 2 | a0007c0007t0001g0200a0007c0007t0001g0201 | 2 | HG02145.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.86-72A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739787 | ||||||
chr8:143739807
|
A | G | 9 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0063others(6): Show | 9 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.86-52A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739807 | ||||||
chr8:143739830
|
C | G | 2 | a0003c0003t0001g0063a0012c0017t0001g0064 | 2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.86-29C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 2/13 | chr8 | 143739830 | ||||||
chr8:143740001
|
A | T | 1 | a0001c0001t0001g0187 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.175+53A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740001 | ||||||
chr8:143740004
|
G | A | 23 | a0003c0003t0001g0219a0003c0003t0001g0222a0003c0003t0001g0223others(20): Show | 23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+56G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740004 | ||||||
chr8:143740038
|
C | G | 1 | a0002c0002t0001g0251 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.175+90C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740038 | ||||||
chr8:143740132
|
A | G | 1 | a0006c0006t0001g0056 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.175+184A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740132 | ||||||
chr8:143740160
|
C | A | 6 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+212C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740160 | ||||||
chr8:143740197
|
G | T | 1 | a0001c0001t0001g0186 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.175+249G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740197 | ||||||
chr8:143740273
|
C | T | 3 | a0009c0009t0001g0007a0009c0009t0001g0026a0009c0009t0001g0027 | 3 | HG01192.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.175+325C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740273 | ||||||
chr8:143740313
|
C | T | 1 | a0029c0032t0001g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.175+365C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740313 | ||||||
chr8:143740340
|
G | C | 2 | a0003c0003t0001g0063a0012c0017t0001g0064 | 2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.175+392G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740340 | ||||||
chr8:143740421
|
C | T | 47 | a0001c0001t0001g0051a0001c0001t0001g0153a0001c0001t0001g0158others(44): Show | 47 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(44): Show |
intron_variant | MODIFIER | c.175+473C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740421 | ||||||
chr8:143740479
|
C | T | 7 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0343others(4): Show | 7 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+531C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740479 | ||||||
chr8:143740550
|
C | T | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+602C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740550 | ||||||
chr8:143740580
|
A | G | 1 | a0010c0011t0001g0220 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.175+632A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740580 | ||||||
chr8:143740614
|
GCGGAGCC others(3): Show |
G | 1 | a0001c0001t0001g0148 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.175+667_175+676del others(10): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740614 | ||||||
chr8:143740645
|
G | A | 1 | a0012c0017t0001g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.175+697G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740645 | ||||||
chr8:143740652
|
C | T | 3 | a0007c0007t0001g0042a0007c0007t0001g0043a0007c0007t0001g0044 | 3 | HG02258.hp2 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.175+704C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740652 | ||||||
chr8:143740732
|
T | C | 1 | a0005c0005t0001g0206 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.175+784T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740732 | ||||||
chr8:143740748
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.175+800G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740748 | ||||||
chr8:143740830
|
G | T | 110 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(107): Show | 111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.175+882G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740830 | ||||||
chr8:143740833
|
G | A | 121 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.175+885G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143740833 | ||||||
chr8:143741013
|
G | A | 1 | a0023c0026t0001g0149 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.175+1065G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741013 | ||||||
chr8:143741139
|
C | T | 23 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(20): Show | 23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+1191C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741139 | ||||||
chr8:143741228
|
C | T | 1 | a0006c0006t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+1280C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741228 | ||||||
chr8:143741245
|
G | A | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+1297G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741245 | ||||||
chr8:143741249
|
G | T | 345 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(342): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.175+1301G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741249 | ||||||
chr8:143741355
|
G | A | 10 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(7): Show | 10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+1407G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741355 | ||||||
chr8:143741566
|
C | T | 3 | a0016c0014t0001g0057a0016c0014t0001g0058a0024c0022t0001g0059 | 3 | HG02602.hp2 HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.175+1618C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741566 | ||||||
chr8:143741629
|
C | T | 1 | a0004c0004t0001g0185 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.175+1681C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741629 | ||||||
chr8:143741662
|
G | A | 1 | a0027c0028t0001g0150 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.175+1714G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741662 | ||||||
chr8:143741724
|
C | T | 2 | a0001c0001t0001g0146a0001c0001t0001g0147 | 2 | NA18986.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.175+1776C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741724 | ||||||
chr8:143741725
|
G | A | 10 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(7): Show | 10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+1777G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741725 | ||||||
chr8:143741741
|
C | T | 151 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(148): Show |
intron_variant | MODIFIER | c.175+1793C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741741 | ||||||
chr8:143741778
|
A | T | 111 | a0001c0001t0001g0062a0002c0002t0001g0001a0002c0002t0001g0003others(108): Show | 112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.175+1830A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741778 | ||||||
chr8:143741857
|
T | C | 1 | a0002c0002t0001g0257 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.175+1909T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741857 | ||||||
chr8:143741877
|
G | A | 12 | a0002c0002t0001g0258a0002c0002t0001g0259a0002c0002t0001g0260others(9): Show | 12 | HG00609.hp1 HG00639.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.175+1929G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741877 | ||||||
chr8:143741888
|
T | G | 1 | a0001c0001t0001g0341 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.175+1940T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741888 | ||||||
chr8:143741930
|
T | A | 1 | a0002c0002t0001g0269 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.175+1982T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143741930 | ||||||
chr8:143742037
|
C | T | 1 | a0002c0002t0001g0331 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.175+2089C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742037 | ||||||
chr8:143742040
|
C | G | 2 | a0006c0006t0001g0030a0006c0006t0001g0031 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.175+2092C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742040 | ||||||
chr8:143742063
|
C | T | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+2115C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742063 | ||||||
chr8:143742064
|
G | A | 1 | a0004c0004t0001g0151 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.175+2116G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742064 | ||||||
chr8:143742119
|
G | A | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+2171G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742119 | ||||||
chr8:143742229
|
GGTGTCCG others(3641): Show |
G | 1 | a0004c0004t0001g0246 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.175+2284_175+5931d others(2): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143742229 | |||||
chr8:143742304
|
C | T | 1 | a0003c0003t0001g0036 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.175+2356C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742304 | ||||||
chr8:143742309
|
G | C | 5 | a0004c0004t0001g0071a0004c0004t0001g0072a0004c0004t0001g0073others(2): Show | 5 | HG00733.hp1 HG00738.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.175+2361G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742309 | ||||||
chr8:143742470
|
C | T | 10 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(7): Show | 10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+2522C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742470 | ||||||
chr8:143742497
|
C | T | 1 | a0006c0006t0001g0184 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.175+2549C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742497 | ||||||
chr8:143742510
|
C | CCCCACAA others(3): Show |
1 | a0001c0001t0001g0148 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.175+2565_175+2574d others(12): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143742510 | |||||
chr8:143742571
|
G | A | 1 | a0012c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.175+2623G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742571 | ||||||
chr8:143742595
|
C | T | 1 | a0025c0030t0001g0346 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.175+2647C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742595 | ||||||
chr8:143742671
|
C | T | 1 | a0002c0002t0001g0268 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.175+2723C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742671 | ||||||
chr8:143742681
|
A | G | 1 | a0002c0002t0001g0330 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.175+2733A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742681 | ||||||
chr8:143742682
|
G | A | 1 | a0002c0002t0001g0330 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.175+2734G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742682 | ||||||
chr8:143742728
|
A | C | 344 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(341): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.175+2780A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742728 | ||||||
chr8:143742767
|
A | G | 1 | a0002c0002t0001g0254 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.175+2819A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742767 | ||||||
chr8:143742770
|
G | GTGGC | 23 | a0003c0003t0001g0219a0003c0003t0001g0222a0003c0003t0001g0223others(20): Show | 23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+2823_175+2826d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143742770 | |||||
chr8:143742865
|
T | C | 1 | a0002c0002t0001g0270 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.175+2917T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742865 | ||||||
chr8:143742865
|
T | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(147): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.175+2917T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742865 | ||||||
chr8:143742896
|
G | A | 1 | a0002c0002t0001g0271 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.175+2948G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742896 | ||||||
chr8:143742977
|
C | T | 1 | a0001c0001t0001g0145 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.175+3029C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143742977 | ||||||
chr8:143743102
|
A | G | 165 | a0001c0001t0001g0062a0001c0001t0001g0341a0001c0001t0001g0344others(162): Show | 166 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.175+3154A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143743102 | ||||||
chr8:143743115
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.175+3167G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143743115 | ||||||
chr8:143743120
|
T | C | 111 | a0001c0001t0001g0062a0002c0002t0001g0001a0002c0002t0001g0003others(108): Show | 112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.175+3172T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143743120 | ||||||
chr8:143743282
|
A | T | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0205 | 3 | NA18966.hp1 NA18998.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.175+3334A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143743282 | ||||||
chr8:143743497
|
C | T | 4 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG02040.hp2 HG02132.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+3549C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143743497 | ||||||
chr8:143743611
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.175+3663A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143743611 | ||||||
chr8:143743705
|
G | A | 1 | a0013c0013t0001g0008 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.175+3757G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143743705 | ||||||
chr8:143743846
|
C | G | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+3898C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143743846 | ||||||
chr8:143744053
|
C | T | 8 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(5): Show | 8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+4105C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744053 | ||||||
chr8:143744329
|
C | T | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+4381C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744329 | ||||||
chr8:143744330
|
A | G | 6 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+4382A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744330 | ||||||
chr8:143744352
|
A | G | 111 | a0001c0001t0001g0062a0002c0002t0001g0001a0002c0002t0001g0003others(108): Show | 112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.175+4404A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744352 | ||||||
chr8:143744411
|
T | G | 23 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(20): Show | 23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+4463T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744411 | ||||||
chr8:143744443
|
A | C | 6 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+4495A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744443 | ||||||
chr8:143744482
|
G | A | 1 | a0007c0007t0001g0041 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.175+4534G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744482 | ||||||
chr8:143744495
|
G | A | 2 | a0007c0007t0001g0042a0007c0007t0001g0043 | 2 | HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.175+4547G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744495 | ||||||
chr8:143744501
|
A | G | 222 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(219): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.175+4553A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744501 | ||||||
chr8:143744519
|
G | A | 1 | a0011c0012t0001g0342 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.175+4571G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744519 | ||||||
chr8:143744723
|
T | C | 23 | a0003c0003t0001g0219a0003c0003t0001g0222a0003c0003t0001g0223others(20): Show | 23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+4775T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744723 | ||||||
chr8:143744792
|
C | T | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+4844C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744792 | ||||||
chr8:143744932
|
G | T | 1 | a0006c0006t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+4984G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744932 | ||||||
chr8:143744976
|
G | A | 1 | a0003c0003t0001g0063 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.175+5028G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744976 | ||||||
chr8:143744993
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.175+5045C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143744993 | ||||||
chr8:143745035
|
C | CTT | 111 | a0001c0001t0001g0062a0002c0002t0001g0001a0002c0002t0001g0003others(108): Show | 112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.175+5087_175+5088i others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745035 | ||||||
chr8:143745107
|
C | T | 111 | a0001c0001t0001g0062a0002c0002t0001g0001a0002c0002t0001g0003others(108): Show | 112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.175+5159C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745107 | ||||||
chr8:143745151
|
C | T | 3 | a0009c0009t0001g0007a0009c0009t0001g0026a0009c0009t0001g0027 | 3 | HG01192.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.175+5203C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745151 | ||||||
chr8:143745259
|
C | T | 1 | a0004c0004t0001g0183 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.175+5311C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745259 | ||||||
chr8:143745309
|
A | G | 111 | a0001c0001t0001g0062a0002c0002t0001g0001a0002c0002t0001g0003others(108): Show | 112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.175+5361A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745309 | ||||||
chr8:143745316
|
A | G | 9 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(6): Show | 9 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.175+5368A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745316 | ||||||
chr8:143745321
|
G | A | 1 | a0002c0002t0001g0331 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.175+5373G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745321 | ||||||
chr8:143745411
|
C | T | 8 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(5): Show | 8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+5463C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745411 | ||||||
chr8:143745412
|
G | A | 1 | a0006c0006t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+5464G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745412 | ||||||
chr8:143745509
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.175+5561G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745509 | ||||||
chr8:143745512
|
T | G | 3 | a0016c0014t0001g0057a0016c0014t0001g0058a0024c0022t0001g0059 | 3 | HG02602.hp2 HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.175+5564T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745512 | ||||||
chr8:143745550
|
G | A | 1 | a0004c0004t0001g0152 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.175+5602G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745550 | ||||||
chr8:143745579
|
T | C | 345 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(342): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.175+5631T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745579 | ||||||
chr8:143745592
|
T | C | 1 | a0006c0006t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+5644T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745592 | ||||||
chr8:143745596
|
T | C | 2 | a0001c0001t0001g0242a0028c0031t0001g0244 | 2 | HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.175+5648T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745596 | ||||||
chr8:143745785
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.175+5837G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745785 | ||||||
chr8:143745813
|
C | T | 10 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(7): Show | 10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+5865C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745813 | ||||||
chr8:143745966
|
A | C | 345 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(342): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.175+6018A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143745966 | ||||||
chr8:143746000
|
C | T | 2 | a0009c0009t0001g0024a0011c0012t0001g0345 | 2 | HG01175.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.175+6052C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746000 | ||||||
chr8:143746026
|
G | A | 2 | a0006c0006t0001g0030a0006c0006t0001g0031 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.175+6078G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746026 | ||||||
chr8:143746045
|
T | G | 239 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.175+6097T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746045 | ||||||
chr8:143746074
|
A | G | 8 | a0003c0003t0001g0234a0003c0003t0001g0235a0003c0003t0001g0236others(5): Show | 8 | HG01975.hp2 HG02647.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+6126A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746074 | ||||||
chr8:143746342
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.175+6394G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746342 | ||||||
chr8:143746354
|
T | G | 2 | a0006c0006t0001g0030a0006c0006t0001g0031 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.175+6406T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746354 | ||||||
chr8:143746426
|
A | G | 23 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(20): Show | 23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+6478A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746426 | ||||||
chr8:143746513
|
G | C | 6 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0343others(3): Show | 6 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+6565G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746513 | ||||||
chr8:143746758
|
T | G | 5 | a0001c0001t0001g0061a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG01358.hp2 HG01981.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.175+6810T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746758 | ||||||
chr8:143746980
|
C | T | 19 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0045others(16): Show | 19 | HG01175.hp1 HG02145.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.175+7032C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143746980 | ||||||
chr8:143747023
|
G | A | 2 | a0003c0003t0001g0063a0012c0017t0001g0064 | 2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.175+7075G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747023 | ||||||
chr8:143747168
|
C | G | 2 | a0003c0003t0001g0063a0012c0017t0001g0064 | 2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.175+7220C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747168 | ||||||
chr8:143747230
|
G | A | 8 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(5): Show | 8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+7282G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747230 | ||||||
chr8:143747237
|
T | G | 83 | a0001c0001t0001g0341a0001c0001t0001g0344a0001c0010t0001g0037others(80): Show | 83 | HG00733.hp2 HG01175.hp1 HG01192.hp2 others(80): Show |
intron_variant | MODIFIER | c.175+7289T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747237 | ||||||
chr8:143747493
|
C | T | 1 | a0002c0002t0001g0250 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.175+7545C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747493 | ||||||
chr8:143747598
|
CT | C | 10 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(7): Show | 10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+7653delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747598 | |||||
chr8:143747601
|
T | G | 1 | a0007c0007t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.175+7653T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747601 | ||||||
chr8:143747638
|
G | GT | 169 | a0001c0001t0001g0062a0002c0002t0001g0001a0002c0002t0001g0003others(166): Show | 170 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.175+7699dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747638 | |||||
chr8:143747638
|
G | GTT | 13 | a0001c0001t0001g0341a0001c0010t0001g0037a0001c0010t0001g0038others(10): Show | 13 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+7698_175+7699d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747638 | |||||
chr8:143747647
|
T | A | 1 | a0001c0001t0001g0247 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.175+7699T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747647 | ||||||
chr8:143747647
|
T | TA | 6 | a0002c0002t0001g0258a0003c0003t0001g0234a0003c0003t0001g0235others(3): Show | 6 | HG01975.hp1 HG01975.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+7705dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747647 | |||||
chr8:143747648
|
A | T | 2 | a0001c0001t0001g0137a0006c0006t0001g0060 | 2 | HG02071.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.175+7700A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747648 | ||||||
chr8:143747753
|
G | A | 1 | a0002c0002t0001g0273 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.175+7805G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747753 | ||||||
chr8:143747802
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.175+7854A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747802 | ||||||
chr8:143747910
|
G | GTCCTT | 61 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0062others(58): Show | 61 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.175+8021_175+8025d others(7): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | |||||
chr8:143747910
|
G | GTCCTTTC others(3): Show |
39 | a0001c0001t0001g0002a0001c0001t0001g0049a0001c0001t0001g0051others(36): Show | 39 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.175+8016_175+8025d others(12): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | |||||
chr8:143747910
|
G | GTCCTTTC others(8): Show |
26 | a0001c0001t0001g0070a0001c0001t0001g0124a0001c0001t0001g0125others(23): Show | 26 | HG00099.hp2 HG00738.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.175+8011_175+8025d others(17): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | |||||
chr8:143747910
|
G | GTCCTTTC others(13): Show |
10 | a0001c0001t0001g0132a0003c0003t0001g0133a0004c0004t0001g0151others(7): Show | 10 | HG00733.hp2 HG01891.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+8006_175+8025d others(22): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | |||||
chr8:143747910
|
G | GTCCTTTC others(18): Show |
3 | a0003c0003t0001g0134a0014c0019t0001g0023a0029c0032t0001g0025 | 3 | HG02723.hp2 HG02976.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.175+8001_175+8025d others(27): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | |||||
chr8:143747910
|
G | GTCCTTTC others(23): Show |
1 | a0003c0003t0001g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.175+7996_175+8025d others(32): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | |||||
chr8:143747910
|
G | GTCCTTTC others(28): Show |
1 | a0013c0013t0001g0008 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.175+7991_175+8025d others(37): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | |||||
chr8:143747910
|
GTCCTT | G | 26 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(23): Show | 26 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.175+8021_175+8025d others(7): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | |||||
chr8:143747910
|
GTCCTTTC others(3): Show |
G | 34 | a0002c0002t0001g0258a0002c0002t0001g0273a0002c0002t0001g0324others(31): Show | 34 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.175+8016_175+8025d others(12): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | |||||
chr8:143747910
|
GTCCTTTC others(8): Show |
G | 82 | a0001c0001t0001g0242a0001c0001t0001g0243a0002c0002t0001g0001others(79): Show | 83 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.175+8011_175+8025d others(17): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | |||||
chr8:143747910
|
GTCCTTTC others(13): Show |
G | 13 | a0002c0002t0001g0006a0002c0002t0001g0269a0002c0002t0001g0274others(10): Show | 13 | HG01081.hp1 HG01243.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+8006_175+8025d others(22): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | |||||
chr8:143747910
|
GTCCTTTC others(18): Show |
G | 1 | a0003c0003t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.175+8001_175+8025d others(27): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747910 | |||||
chr8:143747961
|
T | TC | 4 | a0001c0010t0001g0039a0007c0007t0001g0042a0007c0007t0001g0043others(1): Show | 4 | HG02258.hp2 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+8015dupC | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747961 | |||||
chr8:143747966
|
T | TCCTTTCC others(22): Show |
2 | a0008c0008t0001g0029a0009c0009t0001g0027 | 2 | HG02572.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.175+8025_175+8026i others(31): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747966 | |||||
chr8:143747966
|
T | TCCTTTCC others(28): Show |
2 | a0003c0003t0001g0011a0003c0003t0001g0028 | 2 | HG01884.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.175+8025_175+8026i others(37): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747966 | |||||
chr8:143747966
|
T | TCCTTTCC others(21): Show |
1 | a0009c0009t0001g0007 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.175+8025_175+8026i others(30): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747966 | |||||
chr8:143747966
|
T | TCCTTTCC others(33): Show |
1 | a0012c0027t0001g0014 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.175+8025_175+8026i others(42): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747966 | |||||
chr8:143747966
|
T | TCCTTTCC others(38): Show |
1 | a0003c0003t0001g0016 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.175+8025_175+8026i others(47): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747966 | |||||
chr8:143747977
|
T | TC | 7 | a0003c0003t0001g0011a0003c0003t0001g0016a0003c0003t0001g0028others(4): Show | 7 | HG01192.hp2 HG01884.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+8031dupC | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747977 | |||||
chr8:143747977
|
T | TCCCTTTC others(18): Show |
1 | a0009c0009t0001g0026 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.175+8031_175+8032i others(27): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747977 | |||||
chr8:143747977
|
T | TCCCTTTC others(24): Show |
1 | a0003c0003t0001g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.175+8031_175+8032i others(33): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747977 | |||||
chr8:143747977
|
T | TCCCTTTC others(30): Show |
1 | a0010c0011t0001g0009 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.175+8031_175+8032i others(39): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747977 | |||||
chr8:143747985
|
CTTTCCTT others(3): Show |
C | 5 | a0001c0010t0001g0038a0001c0010t0001g0039a0007c0007t0001g0042others(2): Show | 5 | HG02258.hp2 HG02970.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.175+8052_175+8061d others(12): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747985 | |||||
chr8:143747993
|
T | TC | 5 | a0001c0010t0001g0037a0001c0010t0001g0040a0006c0006t0001g0060others(2): Show | 5 | HG02615.hp2 HG02976.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+8046dupC | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143747993 | |||||
chr8:143747995
|
T | C | 5 | a0001c0010t0001g0037a0001c0010t0001g0040a0006c0006t0001g0060others(2): Show | 5 | HG02615.hp2 HG02976.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+8047T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143747995 | ||||||
chr8:143748449
|
A | G | 1 | a0006c0006t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+8501A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748449 | ||||||
chr8:143748465
|
C | CATGATAT others(26): Show |
3 | a0001c0001t0001g0113a0002c0002t0001g0249a0004c0004t0001g0173 | 3 | HG01071.hp1 NA18955.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.175+8577_175+8609d others(35): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748465 | |||||
chr8:143748555
|
GAT | G | 5 | a0001c0001t0001g0242a0006c0006t0001g0030a0006c0006t0001g0031others(2): Show | 5 | HG01884.hp1 HG02257.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+8616_175+8617d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748555 | |||||
chr8:143748564
|
A | G | 23 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(20): Show | 23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+8616A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748564 | ||||||
chr8:143748622
|
T | G | 1 | a0006c0006t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+8674T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748622 | ||||||
chr8:143748630
|
CATATATA others(1): Show |
C | 3 | a0008c0008t0001g0019a0008c0008t0001g0020a0009c0009t0001g0007 | 3 | HG01192.hp2 HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.175+8698_175+8705d others(10): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748630 | |||||
chr8:143748642
|
TATAAATA others(35): Show |
T | 20 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(17): Show | 20 | HG00733.hp2 HG01884.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.175+8698_175+8739d others(44): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748642 | |||||
chr8:143748655
|
C | A | 1 | a0006c0006t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+8707C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748655 | ||||||
chr8:143748656
|
A | AATCATAT others(27): Show |
3 | a0001c0001t0001g0112a0001c0001t0001g0123a0002c0002t0001g0282 | 3 | HG00544.hp2 HG01243.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.175+8776_175+8809d others(36): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748656 | |||||
chr8:143748656
|
A | T | 1 | a0006c0006t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+8708A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748656 | ||||||
chr8:143748656
|
AATCATAT others(27): Show |
A | 58 | a0001c0001t0001g0341a0001c0001t0001g0344a0001c0010t0001g0037others(55): Show | 58 | HG01175.hp1 HG01975.hp2 HG02145.hp1 others(55): Show |
intron_variant | MODIFIER | c.175+8776_175+8809d others(36): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748656 | |||||
chr8:143748675
|
AATATATA others(31): Show |
A | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+8732_175+8769d others(40): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748675 | |||||
chr8:143748689
|
A | C | 20 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(17): Show | 20 | HG00733.hp2 HG01884.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.175+8741A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748689 | ||||||
chr8:143748690
|
T | A | 20 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(17): Show | 20 | HG00733.hp2 HG01884.hp2 HG02486.hp2 others(17): Show |
intron_variant | MODIFIER | c.175+8742T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748690 | ||||||
chr8:143748693
|
CATATATA others(29): Show |
C | 2 | a0008c0008t0001g0019a0008c0008t0001g0020 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.175+8751_175+8786d others(38): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748693 | |||||
chr8:143748720
|
TATATATC others(31): Show |
T | 1 | a0009c0009t0001g0007 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.175+8779_175+8816d others(40): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748720 | |||||
chr8:143748724
|
T | A | 12 | a0002c0002t0001g0248a0002c0002t0001g0250a0002c0002t0001g0253others(9): Show | 12 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+8776T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748724 | ||||||
chr8:143748726
|
TC | T | 12 | a0002c0002t0001g0248a0002c0002t0001g0250a0002c0002t0001g0253others(9): Show | 12 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+8779delC | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748726 | ||||||
chr8:143748733
|
TA | T | 12 | a0002c0002t0001g0248a0002c0002t0001g0250a0002c0002t0001g0253others(9): Show | 12 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+8788delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748733 | |||||
chr8:143748749
|
TATCATAT others(1): Show |
T | 12 | a0002c0002t0001g0248a0002c0002t0001g0250a0002c0002t0001g0253others(9): Show | 12 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+8803_175+8810d others(10): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748749 | |||||
chr8:143748758
|
A | C | 12 | a0002c0002t0001g0248a0002c0002t0001g0250a0002c0002t0001g0253others(9): Show | 12 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+8810A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748758 | ||||||
chr8:143748758
|
A | T | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.175+8810A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748758 | ||||||
chr8:143748762
|
T | A | 1 | a0009c0009t0001g0007 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.175+8814T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748762 | ||||||
chr8:143748765
|
AT | A | 12 | a0002c0002t0001g0248a0002c0002t0001g0250a0002c0002t0001g0253others(9): Show | 12 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+8818delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748765 | ||||||
chr8:143748782
|
C | A | 12 | a0002c0002t0001g0248a0002c0002t0001g0250a0002c0002t0001g0253others(9): Show | 12 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+8834C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748782 | ||||||
chr8:143748783
|
A | T | 12 | a0002c0002t0001g0248a0002c0002t0001g0250a0002c0002t0001g0253others(9): Show | 12 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+8835A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748783 | ||||||
chr8:143748784
|
T | C | 12 | a0002c0002t0001g0248a0002c0002t0001g0250a0002c0002t0001g0253others(9): Show | 12 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.175+8836T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748784 | ||||||
chr8:143748788
|
T | A | 2 | a0002c0002t0001g0003a0002c0002t0001g0004 | 2 | HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.175+8840T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748788 | ||||||
chr8:143748803
|
A | T | 1 | a0001c0001t0001g0112 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.175+8855A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748803 | ||||||
chr8:143748805
|
A | C | 3 | a0001c0001t0001g0112a0002c0002t0001g0003a0002c0002t0001g0004 | 3 | HG02698.hp1 HG04115.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.175+8857A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748805 | ||||||
chr8:143748806
|
T | A | 3 | a0001c0001t0001g0112a0002c0002t0001g0003a0002c0002t0001g0004 | 3 | HG02698.hp1 HG04115.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.175+8858T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748806 | ||||||
chr8:143748806
|
T | TTTCA | 14 | a0002c0002t0001g0248a0002c0002t0001g0250a0002c0002t0001g0253others(11): Show | 14 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.175+8858_175+8859i others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748806 | ||||||
chr8:143748807
|
C | A | 1 | a0002c0002t0001g0270 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.175+8859C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748807 | ||||||
chr8:143748807
|
C | CATATAAA others(20): Show |
9 | a0001c0001t0001g0161a0001c0001t0001g0164a0004c0004t0001g0151others(6): Show | 9 | HG01123.hp1 HG01358.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.175+8881_175+8882i others(29): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748807 | |||||
chr8:143748807
|
C | CATATAAA others(20): Show |
2 | a0001c0001t0001g0092a0001c0001t0001g0111 | 2 | NA18951.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.175+8882_175+8908d others(29): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748807 | |||||
chr8:143748807
|
C | CATATAAA others(47): Show |
2 | a0002c0002t0001g0319a0002c0002t0001g0320 | 2 | HG02523.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.175+8908_175+8909i others(56): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748807 | |||||
chr8:143748807
|
C | T | 17 | a0001c0001t0001g0112a0002c0002t0001g0003a0002c0002t0001g0004others(14): Show | 17 | HG00558.hp2 HG00597.hp2 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.175+8859C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748807 | ||||||
chr8:143748813
|
A | T | 1 | a0002c0002t0001g0270 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.175+8865A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748813 | ||||||
chr8:143748815
|
T | A | 1 | a0002c0002t0001g0270 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.175+8867T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748815 | ||||||
chr8:143748821
|
A | C | 1 | a0002c0002t0001g0270 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.175+8873A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748821 | ||||||
chr8:143748828
|
ATT | A | 3 | a0007c0007t0001g0042a0007c0007t0001g0043a0007c0007t0001g0044 | 3 | HG02258.hp2 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.175+8882_175+8883d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748828 | |||||
chr8:143748830
|
T | A | 19 | a0001c0001t0001g0112a0001c0001t0001g0124a0001c0001t0001g0125others(16): Show | 19 | HG01123.hp1 HG01358.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.175+8882T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748830 | ||||||
chr8:143748830
|
T | TTCATATA others(20): Show |
133 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(130): Show |
intron_variant | MODIFIER | c.175+8915_175+8941d others(29): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748830 | |||||
chr8:143748830
|
T | TTCATATA others(47): Show |
1 | a0001c0001t0001g0122 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.175+8888_175+8941d others(56): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748830 | |||||
chr8:143748832
|
C | A | 1 | a0002c0002t0001g0270 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.175+8884C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748832 | ||||||
chr8:143748840
|
A | AATATATA others(16): Show |
1 | a0002c0002t0001g0322 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.175+8908_175+8909i others(25): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748840 | |||||
chr8:143748840
|
AATAT | A | 10 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(7): Show | 10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+8896_175+8899d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748840 | |||||
chr8:143748848
|
A | AATATATA others(22): Show |
3 | a0004c0004t0001g0173a0004c0004t0001g0175a0006c0006t0001g0182 | 3 | HG01071.hp1 HG06807.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.175+8909_175+8937d others(31): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748848 | |||||
chr8:143748848
|
AAT | A | 6 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+8909_175+8910d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748848 | |||||
chr8:143748850
|
T | TATATATA others(18): Show |
1 | a0006c0006t0001g0184 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.175+8911_175+8935d others(27): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748850 | |||||
chr8:143748857
|
A | T | 90 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(87): Show | 91 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.175+8909A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748857 | ||||||
chr8:143748884
|
A | T | 1 | a0002c0002t0001g0321 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.175+8936A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748884 | ||||||
chr8:143748886
|
C | CATAT | 99 | a0001c0001t0001g0341a0001c0001t0001g0344a0001c0010t0001g0037others(96): Show | 99 | HG00558.hp2 HG00597.hp2 HG00733.hp2 others(96): Show |
intron_variant | MODIFIER | c.175+8941_175+8942i others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748886 | |||||
chr8:143748886
|
C | CATATATA others(24): Show |
79 | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(76): Show | 80 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.175+8941_175+8942i others(33): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748886 | |||||
chr8:143748886
|
C | CATATATA others(51): Show |
1 | a0002c0002t0001g0321 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.175+8941_175+8942i others(60): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748886 | |||||
chr8:143748886
|
C | T | 2 | a0002c0002t0001g0250a0003c0003t0001g0069 | 2 | HG02630.hp1 NA18942.hp1 |
intron_variant | MODIFIER | c.175+8938C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748886 | ||||||
chr8:143748890
|
A | T | 11 | a0005c0005t0001g0206a0005c0005t0001g0207a0005c0005t0001g0208others(8): Show | 11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8942A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748890 | ||||||
chr8:143748891
|
ATACT | A | 11 | a0005c0005t0001g0206a0005c0005t0001g0207a0005c0005t0001g0208others(8): Show | 11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8946_175+8949d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748891 | |||||
chr8:143748900
|
A | T | 11 | a0005c0005t0001g0206a0005c0005t0001g0207a0005c0005t0001g0208others(8): Show | 11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8952A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748900 | ||||||
chr8:143748906
|
C | A | 11 | a0005c0005t0001g0206a0005c0005t0001g0207a0005c0005t0001g0208others(8): Show | 11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8958C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748906 | ||||||
chr8:143748912
|
T | C | 1 | a0028c0031t0001g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.175+8964T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748912 | ||||||
chr8:143748915
|
C | A | 11 | a0005c0005t0001g0206a0005c0005t0001g0207a0005c0005t0001g0208others(8): Show | 11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8967C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748915 | ||||||
chr8:143748916
|
T | TC | 11 | a0005c0005t0001g0206a0005c0005t0001g0207a0005c0005t0001g0208others(8): Show | 11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8968_175+8969i others(3): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748916 | ||||||
chr8:143748928
|
T | C | 11 | a0005c0005t0001g0206a0005c0005t0001g0207a0005c0005t0001g0208others(8): Show | 11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8980T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748928 | ||||||
chr8:143748929
|
A | T | 11 | a0005c0005t0001g0206a0005c0005t0001g0207a0005c0005t0001g0208others(8): Show | 11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8981A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748929 | ||||||
chr8:143748940
|
T | C | 11 | a0005c0005t0001g0206a0005c0005t0001g0207a0005c0005t0001g0208others(8): Show | 11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8992T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748940 | ||||||
chr8:143748942
|
C | T | 11 | a0005c0005t0001g0206a0005c0005t0001g0207a0005c0005t0001g0208others(8): Show | 11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+8994C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748942 | ||||||
chr8:143748960
|
TATATATC others(8): Show |
T | 1 | a0001c0001t0001g0083 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.175+9034_175+9048d others(17): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748960 | |||||
chr8:143748964
|
T | TA | 11 | a0005c0005t0001g0206a0005c0005t0001g0207a0005c0005t0001g0208others(8): Show | 11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+9017dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748964 | |||||
chr8:143748966
|
T | A | 11 | a0005c0005t0001g0206a0005c0005t0001g0207a0005c0005t0001g0208others(8): Show | 11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+9018T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748966 | ||||||
chr8:143748967
|
C | A | 11 | a0005c0005t0001g0206a0005c0005t0001g0207a0005c0005t0001g0208others(8): Show | 11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+9019C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748967 | ||||||
chr8:143748975
|
A | C | 11 | a0005c0005t0001g0206a0005c0005t0001g0207a0005c0005t0001g0208others(8): Show | 11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+9027A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748975 | ||||||
chr8:143748982
|
C | CT | 11 | a0005c0005t0001g0206a0005c0005t0001g0207a0005c0005t0001g0208others(8): Show | 11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+9034_175+9035i others(3): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143748982 | ||||||
chr8:143748986
|
TATAAATA others(6): Show |
T | 104 | a0001c0001t0001g0341a0001c0001t0001g0344a0002c0002t0001g0001others(101): Show | 105 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.175+9055_175+9067d others(15): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748986 | |||||
chr8:143748999
|
C | CATAT | 11 | a0005c0005t0001g0206a0005c0005t0001g0207a0005c0005t0001g0208others(8): Show | 11 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(8): Show |
intron_variant | MODIFIER | c.175+9054_175+9055i others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143748999 | |||||
chr8:143749115
|
C | T | 3 | a0002c0002t0001g0003a0002c0002t0001g0004a0006c0006t0001g0056 | 3 | HG02083.hp1 HG02698.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.175+9167C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749115 | ||||||
chr8:143749166
|
CAA | C | 44 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0045others(41): Show | 44 | HG01175.hp1 HG01975.hp2 HG02145.hp1 others(41): Show |
intron_variant | MODIFIER | c.175+9219_175+9220d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749166 | ||||||
chr8:143749172
|
A | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.175+9224A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749172 | ||||||
chr8:143749219
|
TATATAA | T | 23 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(20): Show | 23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+9277_175+9282d others(8): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749219 | |||||
chr8:143749249
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.175+9301G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749249 | ||||||
chr8:143749257
|
T | G | 10 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0077others(7): Show | 10 | HG00544.hp2 HG01358.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+9309T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749257 | ||||||
chr8:143749284
|
TA | T | 4 | a0001c0001t0001g0070a0001c0001t0001g0121a0001c0001t0001g0130others(1): Show | 4 | NA18948.hp1 NA18970.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+9341delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749284 | |||||
chr8:143749346
|
C | CAT | 339 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(336): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.175+9400_175+9401d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749346 | |||||
chr8:143749346
|
C | T | 1 | a0002c0002t0001g0318 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.175+9398C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749346 | ||||||
chr8:143749353
|
A | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.175+9405A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749353 | ||||||
chr8:143749365
|
A | G | 1 | a0002c0002t0001g0326 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.175+9417A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749365 | ||||||
chr8:143749428
|
ATC | A | 9 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0063others(6): Show | 9 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.175+9483_175+9484d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749428 | |||||
chr8:143749432
|
CAT | C | 23 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(20): Show | 23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+9490_175+9491d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749432 | |||||
chr8:143749441
|
T | G | 1 | a0001c0001t0001g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.175+9493T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749441 | ||||||
chr8:143749485
|
TATATAAA others(8): Show |
T | 1 | a0004c0004t0001g0165 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.175+9551_175+9565d others(17): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749485 | |||||
chr8:143749500
|
CAT | C | 33 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(30): Show | 33 | HG01975.hp2 HG02145.hp1 HG02258.hp1 others(30): Show |
intron_variant | MODIFIER | c.175+9556_175+9557d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749500 | |||||
chr8:143749510
|
TATAAAAA others(10): Show |
T | 3 | a0016c0014t0001g0057a0016c0014t0001g0058a0024c0022t0001g0059 | 3 | HG02602.hp2 HG02683.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.175+9575_175+9591d others(19): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749510 | |||||
chr8:143749527
|
CAT | C | 5 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(2): Show | 5 | HG02615.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.175+9581_175+9582d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749527 | |||||
chr8:143749538
|
A | G | 1 | a0001c0001t0001g0203 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.175+9590A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749538 | ||||||
chr8:143749548
|
TGATATAT others(4): Show |
T | 4 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(1): Show | 4 | HG02280.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+9601_175+9611d others(13): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749548 | ||||||
chr8:143749558
|
C | G | 1 | a0006c0006t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+9610C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749558 | ||||||
chr8:143749560
|
T | C | 4 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(1): Show | 4 | HG02280.hp1 HG02809.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+9612T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749560 | ||||||
chr8:143749571
|
C | CAT | 110 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(107): Show | 111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.175+9634_175+9635d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749571 | |||||
chr8:143749581
|
TA | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0115 | 3 | NA18947.hp1 NA18964.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.175+9634delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749581 | ||||||
chr8:143749582
|
A | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(106): Show | 109 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.175+9634A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749582 | ||||||
chr8:143749584
|
T | A | 178 | a0001c0001t0001g0111a0001c0001t0001g0341a0001c0001t0001g0344others(175): Show | 179 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(176): Show |
intron_variant | MODIFIER | c.175+9636T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749584 | ||||||
chr8:143749587
|
A | T | 338 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(335): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.175+9639A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749587 | ||||||
chr8:143749599
|
A | AT | 7 | a0004c0004t0001g0050a0004c0004t0001g0160a0004c0004t0001g0178others(4): Show | 7 | HG00642.hp1 HG00735.hp2 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+9665dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143749599 | |||||
chr8:143749602
|
T | TA | 6 | a0002c0002t0001g0252a0002c0002t0001g0313a0002c0002t0001g0314others(3): Show | 6 | HG00438.hp1 HG02976.hp1 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+9654_175+9655i others(3): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749602 | ||||||
chr8:143749603
|
T | A | 186 | a0001c0001t0001g0080a0001c0001t0001g0126a0001c0001t0001g0191others(183): Show | 187 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.175+9655T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749603 | ||||||
chr8:143749604
|
T | A | 1 | a0002c0002t0001g0254 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.175+9656T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749604 | ||||||
chr8:143749607
|
T | A | 9 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0343others(6): Show | 9 | HG01175.hp1 HG02257.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.175+9659T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143749607 | ||||||
chr8:143750067
|
C | T | 2 | a0006c0006t0001g0030a0006c0006t0001g0031 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.175+10119C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750067 | ||||||
chr8:143750130
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.175+10182C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750130 | ||||||
chr8:143750147
|
C | T | 1 | a0003c0003t0001g0343 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.175+10199C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750147 | ||||||
chr8:143750155
|
C | T | 8 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(5): Show | 8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+10207C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750155 | ||||||
chr8:143750199
|
T | A | 1 | a0001c0001t0001g0098 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.175+10251T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750199 | ||||||
chr8:143750218
|
G | A | 1 | a0017c0016t0001g0348 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.175+10270G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750218 | ||||||
chr8:143750245
|
G | A | 1 | a0025c0030t0001g0346 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.175+10297G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750245 | ||||||
chr8:143750522
|
A | G | 12 | a0007c0007t0001g0013a0007c0007t0001g0015a0008c0008t0001g0019others(9): Show | 12 | HG00733.hp2 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.175+10574A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750522 | ||||||
chr8:143750574
|
G | A | 23 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(20): Show | 23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+10626G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750574 | ||||||
chr8:143750610
|
A | G | 1 | a0021c0024t0001g0193 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.175+10662A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750610 | ||||||
chr8:143750717
|
G | A | 109 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(106): Show | 110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.175+10769G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750717 | ||||||
chr8:143750771
|
A | C | 23 | a0003c0003t0001g0219a0003c0003t0001g0222a0003c0003t0001g0223others(20): Show | 23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+10823A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750771 | ||||||
chr8:143750786
|
C | A | 1 | a0003c0003t0001g0222 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.175+10838C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750786 | ||||||
chr8:143750798
|
A | G | 1 | a0029c0032t0001g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.175+10850A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750798 | ||||||
chr8:143750944
|
T | TTG | 5 | a0001c0001t0001g0047a0001c0001t0001g0048a0003c0003t0001g0010others(2): Show | 5 | HG02145.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+11018_175+1101 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143750944 | |||||
chr8:143750944
|
T | TTGTG | 145 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0049others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.175+11016_175+1101 others(8): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143750944 | |||||
chr8:143750944
|
T | TTGTGTG | 4 | a0001c0001t0001g0187a0004c0004t0001g0151a0018c0018t0001g0179others(1): Show | 4 | HG00408.hp1 HG01168.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+11014_175+1101 others(10): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143750944 | |||||
chr8:143750944
|
T | TTGTGTGT others(3): Show |
1 | a0001c0001t0001g0085 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.175+11010_175+1101 others(14): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143750944 | |||||
chr8:143750961
|
T | TGG | 9 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0063others(6): Show | 9 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.175+11014_175+1101 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143750961 | |||||
chr8:143750968
|
T | G | 137 | a0001c0001t0001g0055a0001c0001t0001g0086a0001c0001t0001g0202others(134): Show | 138 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.175+11020T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143750968 | ||||||
chr8:143751064
|
C | T | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+11116C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751064 | ||||||
chr8:143751073
|
C | T | 1 | a0002c0002t0001g0287 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.175+11125C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751073 | ||||||
chr8:143751383
|
C | T | 10 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(7): Show | 10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+11435C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751383 | ||||||
chr8:143751568
|
T | C | 9 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0063others(6): Show | 9 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.175+11620T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751568 | ||||||
chr8:143751611
|
CA | C | 6 | a0001c0001t0001g0120a0001c0010t0001g0037a0001c0010t0001g0038others(3): Show | 6 | HG02970.hp2 HG03195.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+11677delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751611 | |||||
chr8:143751625
|
A | AT | 4 | a0001c0001t0001g0076a0002c0002t0001g0270a0003c0003t0001g0063others(1): Show | 4 | HG02056.hp1 HG02257.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+11677_175+1167 others(5): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751625 | ||||||
chr8:143751625
|
A | T | 2 | a0001c0001t0001g0119a0003c0003t0001g0036 | 2 | HG02717.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.175+11677A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751625 | ||||||
chr8:143751625
|
AGT | A | 4 | a0001c0001t0001g0243a0002c0002t0001g0249a0005c0005t0001g0210others(1): Show | 4 | HG00280.hp2 HG00735.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+11716_175+1171 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751625 | |||||
chr8:143751625
|
AGTGTGTG others(1): Show |
A | 6 | a0003c0003t0001g0230a0003c0003t0001g0236a0010c0011t0001g0220others(3): Show | 6 | HG02630.hp2 HG02809.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+11710_175+1171 others(12): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751625 | |||||
chr8:143751625
|
AGTGTGTG others(3): Show |
A | 10 | a0003c0003t0001g0219a0003c0003t0001g0222a0003c0003t0001g0225others(7): Show | 10 | HG01975.hp2 HG02622.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+11708_175+1171 others(14): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751625 | |||||
chr8:143751625
|
AGTGTGTG others(5): Show |
A | 7 | a0003c0003t0001g0223a0003c0003t0001g0224a0003c0003t0001g0226others(4): Show | 7 | HG02258.hp1 HG02280.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+11706_175+1171 others(16): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751625 | |||||
chr8:143751640
|
G | C | 1 | a0001c0001t0001g0051 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.175+11692G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751640 | ||||||
chr8:143751650
|
G | GTA | 8 | a0003c0003t0001g0010a0003c0003t0001g0011a0009c0009t0001g0007others(5): Show | 8 | HG01192.hp2 HG02615.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+11703_175+1170 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751650 | |||||
chr8:143751652
|
G | A | 18 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(15): Show | 18 | HG01192.hp2 HG01884.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.175+11704G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751652 | ||||||
chr8:143751652
|
G | GTA | 10 | a0007c0007t0001g0013a0007c0007t0001g0015a0008c0008t0001g0019others(7): Show | 10 | HG00733.hp2 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+11705_175+1170 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751652 | |||||
chr8:143751654
|
G | A | 36 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(33): Show | 36 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.175+11706G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751654 | ||||||
chr8:143751654
|
G | GTATATAT others(17): Show |
1 | a0001c0001t0001g0121 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.175+11707_175+1170 others(28): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751654 | |||||
chr8:143751656
|
G | A | 48 | a0001c0001t0001g0121a0003c0003t0001g0010a0003c0003t0001g0011others(45): Show | 48 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(45): Show |
intron_variant | MODIFIER | c.175+11708G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751656 | ||||||
chr8:143751658
|
G | A | 50 | a0001c0001t0001g0121a0003c0003t0001g0010a0003c0003t0001g0011others(47): Show | 50 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(47): Show |
intron_variant | MODIFIER | c.175+11710G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751658 | ||||||
chr8:143751658
|
G | GTATATAT others(7): Show |
2 | a0004c0004t0001g0185a0027c0028t0001g0150 | 2 | HG01496.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.175+11711_175+1171 others(18): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751658 | |||||
chr8:143751658
|
G | GTATATAT others(9): Show |
2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | NA19011.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.175+11711_175+1171 others(20): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751658 | |||||
chr8:143751658
|
G | GTATATAT others(13): Show |
2 | a0004c0004t0001g0183a0030c0021t0001g0338 | 2 | HG01175.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.175+11711_175+1171 others(24): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751658 | |||||
chr8:143751660
|
G | A | 62 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0121others(59): Show | 62 | HG00733.hp2 HG01175.hp2 HG01192.hp2 others(59): Show |
intron_variant | MODIFIER | c.175+11712G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751660 | ||||||
chr8:143751660
|
G | GTATATAT others(11): Show |
2 | a0001c0001t0001g0161a0004c0004t0001g0174 | 2 | HG01981.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.175+11713_175+1171 others(22): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751660 | |||||
chr8:143751660
|
G | GTATATAT others(17): Show |
1 | a0001c0010t0001g0040 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.175+11713_175+1171 others(28): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751660 | |||||
chr8:143751660
|
G | GTATATAT others(19): Show |
3 | a0004c0004t0001g0169a0004c0004t0001g0181a0008c0008t0001g0128 | 3 | HG00099.hp1 HG00738.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.175+11713_175+1171 others(30): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751660 | |||||
chr8:143751660
|
G | GTATATAT others(21): Show |
1 | a0001c0010t0001g0039 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.175+11713_175+1171 others(32): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751660 | |||||
chr8:143751660
|
G | GTATATAT others(23): Show |
1 | a0007c0007t0001g0044 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.175+11713_175+1171 others(34): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751660 | |||||
chr8:143751660
|
G | GTATATAT others(31): Show |
1 | a0007c0007t0001g0041 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.175+11713_175+1171 others(42): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751660 | |||||
chr8:143751662
|
G | A | 83 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0121others(80): Show | 83 | HG00099.hp1 HG00544.hp1 HG00733.hp2 others(80): Show |
intron_variant | MODIFIER | c.175+11714G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751662 | ||||||
chr8:143751662
|
G | GTA | 20 | a0002c0002t0001g0258a0002c0002t0001g0260a0002c0002t0001g0261others(17): Show | 20 | HG00609.hp1 HG00639.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.175+11715_175+1171 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | |||||
chr8:143751662
|
G | GTATATA | 4 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0196others(1): Show | 4 | HG02965.hp2 HG03098.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+11715_175+1171 others(10): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | |||||
chr8:143751662
|
G | GTATATAT others(11): Show |
7 | a0001c0001t0001g0136a0001c0001t0001g0247a0004c0004t0001g0154others(4): Show | 7 | HG01109.hp2 HG01123.hp1 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+11715_175+1171 others(22): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | |||||
chr8:143751662
|
G | GTATATAT others(13): Show |
13 | a0001c0001t0001g0095a0001c0001t0001g0126a0001c0001t0001g0132others(10): Show | 13 | HG00140.hp1 HG00735.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.175+11715_175+1171 others(24): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | |||||
chr8:143751662
|
G | GTATATAT others(15): Show |
9 | a0001c0001t0001g0065a0001c0001t0001g0070a0001c0001t0001g0139others(6): Show | 9 | HG01261.hp2 HG02004.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.175+11715_175+1171 others(26): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | |||||
chr8:143751662
|
G | GTATATAT others(17): Show |
8 | a0001c0001t0001g0066a0001c0001t0001g0102a0001c0001t0001g0153others(5): Show | 8 | HG01069.hp1 HG02148.hp2 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.175+11715_175+1171 others(28): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | |||||
chr8:143751662
|
G | GTATATAT others(19): Show |
3 | a0001c0001t0001g0067a0004c0004t0001g0152a0004c0004t0001g0171 | 3 | HG02683.hp2 NA18995.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.175+11715_175+1171 others(30): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | |||||
chr8:143751662
|
G | GTATATAT others(21): Show |
1 | a0001c0001t0001g0146 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.175+11715_175+1171 others(32): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | |||||
chr8:143751662
|
G | GTATATAT others(23): Show |
2 | a0001c0001t0001g0147a0001c0010t0001g0037 | 2 | HG03516.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.175+11715_175+1171 others(34): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | |||||
chr8:143751662
|
G | GTATATAT others(25): Show |
1 | a0001c0010t0001g0038 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.175+11715_175+1171 others(36): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751662 | |||||
chr8:143751664
|
G | A | 157 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(154): Show | 157 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.175+11716G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751664 | ||||||
chr8:143751664
|
G | GTA | 4 | a0002c0002t0001g0290a0002c0002t0001g0313a0002c0002t0001g0340others(1): Show | 4 | HG00280.hp1 HG02055.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+11729_175+1173 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTATA | 53 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0213others(50): Show | 54 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.175+11727_175+1173 others(8): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTATATAT others(1): Show |
4 | a0001c0001t0001g0341a0003c0003t0001g0198a0007c0007t0001g0200others(1): Show | 4 | HG01109.hp1 HG03139.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+11723_175+1173 others(12): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTATATAT others(11): Show |
3 | a0001c0001t0001g0081a0001c0001t0001g0096a0001c0001t0001g0119 | 3 | HG02602.hp1 NA18939.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.175+11730_175+1173 others(22): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTATATAT others(13): Show |
10 | a0001c0001t0001g0083a0001c0001t0001g0116a0001c0001t0001g0145others(7): Show | 10 | HG00099.hp2 HG00738.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.175+11730_175+1173 others(24): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTATATAT others(15): Show |
26 | a0001c0001t0001g0049a0001c0001t0001g0061a0001c0001t0001g0078others(23): Show | 26 | HG00544.hp2 HG00558.hp1 HG00642.hp1 others(23): Show |
intron_variant | MODIFIER | c.175+11730_175+1173 others(26): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTATATAT others(17): Show |
9 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0111others(6): Show | 9 | HG02132.hp1 HG03491.hp1 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.175+11730_175+1173 others(28): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTATATAT others(19): Show |
7 | a0001c0001t0001g0047a0001c0001t0001g0055a0001c0001t0001g0076others(4): Show | 7 | HG01516.hp2 HG01517.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.175+11730_175+1173 others(30): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTATATAT others(21): Show |
4 | a0001c0001t0001g0048a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG01361.hp1 NA18955.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+11730_175+1173 others(32): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTATATAT others(23): Show |
2 | a0001c0001t0001g0062a0001c0001t0001g0068 | 2 | HG03654.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.175+11730_175+1173 others(34): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTA | 4 | a0002c0002t0001g0004a0002c0002t0001g0282a0002c0002t0001g0308others(1): Show | 4 | HG00642.hp2 HG01243.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.175+11717_175+1171 others(8): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTATA | 12 | a0002c0002t0001g0006a0002c0002t0001g0255a0002c0002t0001g0256others(9): Show | 12 | HG00140.hp2 HG01928.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.175+11717_175+1171 others(10): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTATAT others(3): Show |
6 | a0001c0001t0001g0344a0003c0003t0001g0194a0003c0003t0001g0343others(3): Show | 6 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+11717_175+1171 others(14): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTATAT others(5): Show |
1 | a0011c0012t0001g0347 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.175+11717_175+1171 others(16): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTATAT others(11): Show |
3 | a0001c0001t0001g0107a0001c0001t0001g0122a0001c0001t0001g0187 | 3 | HG00408.hp1 HG00621.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.175+11717_175+1171 others(22): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTATAT others(13): Show |
4 | a0001c0001t0001g0051a0001c0001t0001g0108a0003c0003t0001g0089others(1): Show | 4 | HG03491.hp2 HG03654.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+11717_175+1171 others(24): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTATAT others(15): Show |
5 | a0001c0001t0001g0090a0001c0001t0001g0117a0001c0001t0001g0138others(2): Show | 5 | HG00438.hp2 HG01981.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.175+11717_175+1171 others(26): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTATAT others(17): Show |
7 | a0001c0001t0001g0046a0001c0001t0001g0082a0001c0001t0001g0120others(4): Show | 7 | HG01069.hp2 HG01071.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.175+11717_175+1171 others(28): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTATAT others(19): Show |
9 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0001g0094others(6): Show | 9 | HG00673.hp1 HG02027.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.175+11717_175+1171 others(30): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTATAT others(21): Show |
1 | a0001c0001t0001g0084 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.175+11717_175+1171 others(32): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTATAT others(23): Show |
1 | a0007c0007t0001g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.175+11717_175+1171 others(34): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTATAT others(25): Show |
1 | a0001c0001t0001g0131 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.175+11717_175+1171 others(36): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTATAT others(27): Show |
1 | a0006c0006t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+11717_175+1171 others(38): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTGTAT others(13): Show |
1 | a0004c0004t0001g0173 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.175+11717_175+1171 others(24): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTGTAT others(15): Show |
1 | a0001c0001t0001g0002 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.175+11717_175+1171 others(26): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTGTAT others(17): Show |
2 | a0001c0001t0001g0077a0001c0001t0001g0110 | 2 | HG02300.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.175+11717_175+1171 others(28): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTGTAT others(19): Show |
1 | a0006c0006t0001g0056 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.175+11717_175+1171 others(30): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTGTAT others(29): Show |
1 | a0003c0003t0001g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.175+11717_175+1171 others(40): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTGTAT others(37): Show |
1 | a0003c0003t0001g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.175+11717_175+1171 others(48): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTGTAT others(47): Show |
1 | a0003c0003t0001g0133 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.175+11717_175+1171 others(58): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751664
|
G | GTGTGTGT others(3): Show |
1 | a0002c0002t0001g0318 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.175+11717_175+1171 others(14): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751664 | |||||
chr8:143751666
|
A | G | 3 | a0001c0001t0001g0242a0028c0031t0001g0244a0031c0033t0001g0332 | 3 | HG01884.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.175+11718A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751666 | ||||||
chr8:143751668
|
A | G | 3 | a0001c0001t0001g0242a0028c0031t0001g0244a0031c0033t0001g0332 | 3 | HG01884.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.175+11720A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751668 | ||||||
chr8:143751670
|
A | G | 1 | a0028c0031t0001g0244 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.175+11722A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751670 | ||||||
chr8:143751679
|
A | T | 12 | a0002c0002t0001g0258a0002c0002t0001g0259a0002c0002t0001g0260others(9): Show | 12 | HG00609.hp1 HG00639.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.175+11731A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751679 | ||||||
chr8:143751683
|
C | T | 1 | a0001c0001t0001g0106 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.175+11735C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143751683 | ||||||
chr8:143751930
|
GT | G | 343 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(340): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.175+11992delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143751930 | |||||
chr8:143752005
|
G | T | 1 | a0001c0001t0001g0094 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.175+12057G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752005 | ||||||
chr8:143752043
|
G | A | 10 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+12095G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752043 | ||||||
chr8:143752090
|
C | T | 109 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(106): Show | 110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.175+12142C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752090 | ||||||
chr8:143752106
|
T | C | 2 | a0003c0003t0001g0011a0010c0011t0001g0009 | 2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.175+12158T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752106 | ||||||
chr8:143752111
|
G | A | 2 | a0003c0003t0001g0011a0010c0011t0001g0009 | 2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.175+12163G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752111 | ||||||
chr8:143752113
|
C | T | 2 | a0003c0003t0001g0011a0010c0011t0001g0009 | 2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.175+12165C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752113 | ||||||
chr8:143752114
|
T | C | 2 | a0003c0003t0001g0011a0010c0011t0001g0009 | 2 | HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.175+12166T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752114 | ||||||
chr8:143752215
|
C | G | 1 | a0007c0007t0001g0041 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.175+12267C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752215 | ||||||
chr8:143752245
|
C | T | 1 | a0017c0016t0001g0348 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.175+12297C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752245 | ||||||
chr8:143752246
|
G | A | 10 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(7): Show | 10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+12298G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752246 | ||||||
chr8:143752312
|
CAAGTTTC others(17): Show |
C | 1 | a0002c0002t0001g0249 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.175+12365_175+1238 others(28): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752312 | ||||||
chr8:143752510
|
A | G | 1 | a0006c0006t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+12562A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752510 | ||||||
chr8:143752744
|
G | A | 6 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+12796G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752744 | ||||||
chr8:143752810
|
A | G | 73 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0010others(70): Show | 73 | HG00733.hp2 HG01175.hp1 HG01192.hp2 others(70): Show |
intron_variant | MODIFIER | c.175+12862A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752810 | ||||||
chr8:143752852
|
G | A | 1 | a0002c0002t0001g0327 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.175+12904G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752852 | ||||||
chr8:143752995
|
CG | C | 4 | a0003c0003t0001g0194a0003c0003t0001g0199a0007c0007t0001g0200others(1): Show | 4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+13048delG | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752995 | ||||||
chr8:143752996
|
G | A | 5 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0196others(2): Show | 5 | HG02965.hp2 HG03098.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.175+13048G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752996 | ||||||
chr8:143752996
|
G | GGT | 3 | a0003c0003t0001g0343a0011c0012t0001g0342a0025c0030t0001g0346 | 3 | HG02486.hp1 HG02622.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.175+13048_175+1304 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752996 | ||||||
chr8:143752996
|
G | GT | 146 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.175+13073dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143752996 | |||||
chr8:143752996
|
G | GTT | 29 | a0001c0001t0001g0002a0001c0001t0001g0065a0001c0001t0001g0076others(26): Show | 29 | HG00642.hp1 HG00735.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.175+13072_175+1307 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143752996 | |||||
chr8:143752996
|
G | GTTTT | 6 | a0001c0001t0001g0122a0003c0003t0001g0226a0003c0003t0001g0236others(3): Show | 6 | HG01975.hp2 HG02071.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.175+13070_175+1307 others(8): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143752996 | |||||
chr8:143752996
|
G | GTTTTT | 14 | a0003c0003t0001g0219a0003c0003t0001g0222a0003c0003t0001g0223others(11): Show | 14 | HG02258.hp1 HG02280.hp2 HG02809.hp2 others(11): Show |
intron_variant | MODIFIER | c.175+13069_175+1307 others(9): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143752996 | |||||
chr8:143752996
|
G | T | 1 | a0003c0003t0001g0197 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.175+13048G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752996 | ||||||
chr8:143752996
|
GT | G | 75 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(72): Show | 76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.175+13073delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143752996 | |||||
chr8:143752996
|
GTT | G | 8 | a0002c0002t0001g0260a0002c0002t0001g0277a0002c0002t0001g0315others(5): Show | 8 | HG00544.hp1 HG01074.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.175+13072_175+1307 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143752996 | |||||
chr8:143752996
|
GTTTTTTT others(3): Show |
G | 1 | a0010c0011t0001g0009 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.175+13064_175+1307 others(14): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143752996 | |||||
chr8:143752997
|
T | A | 4 | a0003c0003t0001g0194a0003c0003t0001g0199a0007c0007t0001g0200others(1): Show | 4 | HG02145.hp1 HG02922.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.175+13049T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143752997 | ||||||
chr8:143753002
|
T | G | 1 | a0001c0001t0001g0344 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.175+13054T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753002 | ||||||
chr8:143753009
|
T | G | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+13061T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753009 | ||||||
chr8:143753110
|
C | T | 109 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(106): Show | 110 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.175+13162C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753110 | ||||||
chr8:143753124
|
C | T | 3 | a0001c0001t0001g0242a0028c0031t0001g0244a0031c0033t0001g0332 | 3 | HG01884.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.175+13176C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753124 | ||||||
chr8:143753177
|
T | C | 1 | a0002c0002t0001g0316 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.175+13229T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753177 | ||||||
chr8:143753267
|
G | T | 1 | a0002c0002t0001g0331 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.175+13319G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753267 | ||||||
chr8:143753303
|
C | T | 1 | a0006c0006t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.175+13355C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753303 | ||||||
chr8:143753304
|
G | A | 1 | a0005c0005t0001g0207 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.175+13356G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753304 | ||||||
chr8:143753458
|
C | CT | 26 | a0001c0001t0001g0144a0002c0002t0001g0303a0003c0003t0001g0219others(23): Show | 26 | HG01975.hp2 HG02055.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.175+13527dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143753458 | |||||
chr8:143753458
|
CT | C | 14 | a0001c0001t0001g0051a0001c0001t0001g0096a0001c0001t0001g0344others(11): Show | 14 | HG01175.hp1 HG01243.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.175+13527delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143753458 | |||||
chr8:143753489
|
G | A | 2 | a0003c0003t0001g0063a0012c0017t0001g0064 | 2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.175+13541G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753489 | ||||||
chr8:143753497
|
A | G | 2 | a0006c0006t0001g0030a0006c0006t0001g0031 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.175+13549A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753497 | ||||||
chr8:143753515
|
A | G | 1 | a0003c0003t0001g0028 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.175+13567A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753515 | ||||||
chr8:143753566
|
G | A | 23 | a0003c0003t0001g0219a0003c0003t0001g0222a0003c0003t0001g0223others(20): Show | 23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+13618G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753566 | ||||||
chr8:143753699
|
C | A | 1 | a0017c0016t0001g0237 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.175+13751C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753699 | ||||||
chr8:143753711
|
T | TCCTAAGC others(17): Show |
1 | a0002c0002t0001g0249 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.175+13765_175+1376 others(28): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143753711 | |||||
chr8:143753975
|
C | T | 1 | a0005c0005t0001g0215 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.175+14027C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143753975 | ||||||
chr8:143754006
|
G | T | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.175+14058G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754006 | ||||||
chr8:143754051
|
TCC | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.175+14106_175+1410 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143754051 | |||||
chr8:143754305
|
G | A | 10 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(7): Show | 10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.175+14357G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754305 | ||||||
chr8:143754309
|
G | A | 44 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0045others(41): Show | 44 | HG01175.hp1 HG01975.hp2 HG02145.hp1 others(41): Show |
intron_variant | MODIFIER | c.175+14361G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754309 | ||||||
chr8:143754379
|
C | T | 2 | a0003c0003t0001g0063a0012c0017t0001g0064 | 2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.175+14431C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754379 | ||||||
chr8:143754380
|
G | A | 1 | a0008c0008t0001g0029 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.175+14432G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754380 | ||||||
chr8:143754438
|
C | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.175+14490C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754438 | ||||||
chr8:143754526
|
A | G | 23 | a0003c0003t0001g0219a0003c0003t0001g0222a0003c0003t0001g0223others(20): Show | 23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.175+14578A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754526 | ||||||
chr8:143754636
|
T | A | 111 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(108): Show | 112 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.175+14688T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754636 | ||||||
chr8:143754837
|
A | G | 1 | a0003c0003t0001g0036 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.175+14889A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754837 | ||||||
chr8:143754868
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.175+14920C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754868 | ||||||
chr8:143754878
|
G | A | 1 | a0029c0032t0001g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.175+14930G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754878 | ||||||
chr8:143754916
|
G | A | 6 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+14968G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143754916 | ||||||
chr8:143755160
|
G | C | 47 | a0001c0001t0001g0051a0001c0001t0001g0153a0001c0001t0001g0158others(44): Show | 47 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(44): Show |
intron_variant | MODIFIER | c.175+15212G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143755160 | ||||||
chr8:143755578
|
G | C | 6 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.175+15630G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143755578 | ||||||
chr8:143755629
|
G | T | 1 | a0017c0016t0001g0348 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.175+15681G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143755629 | ||||||
chr8:143755759
|
G | A | 1 | a0002c0002t0001g0331 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.176-15729G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143755759 | ||||||
chr8:143755899
|
G | C | 6 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.176-15589G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143755899 | ||||||
chr8:143755984
|
C | T | 1 | a0003c0003t0001g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.176-15504C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143755984 | ||||||
chr8:143755987
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0085 | 2 | NA18612.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.176-15501G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143755987 | ||||||
chr8:143756009
|
G | C | 6 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.176-15479G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143756009 | ||||||
chr8:143756222
|
T | G | 1 | a0003c0003t0001g0197 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.176-15266T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143756222 | ||||||
chr8:143756332
|
C | T | 3 | a0002c0002t0001g0255a0002c0002t0001g0256a0002c0002t0001g0302 | 3 | HG02080.hp2 NA18944.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.176-15156C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143756332 | ||||||
chr8:143756382
|
C | T | 10 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(7): Show | 10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.176-15106C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143756382 | ||||||
chr8:143756420
|
T | G | 83 | a0001c0001t0001g0341a0001c0001t0001g0344a0001c0010t0001g0037others(80): Show | 83 | HG00733.hp2 HG01175.hp1 HG01192.hp2 others(80): Show |
intron_variant | MODIFIER | c.176-15068T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143756420 | ||||||
chr8:143756519
|
C | T | 5 | a0001c0001t0001g0344a0003c0003t0001g0343a0011c0012t0001g0342others(2): Show | 5 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.176-14969C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143756519 | ||||||
chr8:143756638
|
A | G | 2 | a0001c0001t0001g0055a0001c0001t0001g0202 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.176-14850A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143756638 | ||||||
chr8:143756812
|
T | TA | 84 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(81): Show | 84 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.176-14660dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143756812 | |||||
chr8:143756812
|
TA | T | 10 | a0001c0001t0001g0139a0002c0002t0001g0006a0002c0002t0001g0313others(7): Show | 10 | HG01069.hp1 HG01516.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.176-14660delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143756812 | |||||
chr8:143756976
|
T | TA | 122 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(119): Show | 123 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.176-14500dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143756976 | |||||
chr8:143756977
|
A | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.176-14511A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143756977 | ||||||
chr8:143757002
|
A | G | 5 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(2): Show | 5 | HG02615.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.176-14486A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757002 | ||||||
chr8:143757040
|
C | G | 2 | a0016c0014t0001g0058a0024c0022t0001g0059 | 2 | HG02602.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.176-14448C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757040 | ||||||
chr8:143757044
|
G | A | 1 | a0017c0016t0001g0237 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.176-14444G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757044 | ||||||
chr8:143757127
|
A | T | 73 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0010others(70): Show | 73 | HG00733.hp2 HG01175.hp1 HG01192.hp2 others(70): Show |
intron_variant | MODIFIER | c.176-14361A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757127 | ||||||
chr8:143757205
|
C | T | 1 | a0002c0002t0001g0282 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.176-14283C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757205 | ||||||
chr8:143757221
|
C | T | 5 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(2): Show | 5 | HG02615.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.176-14267C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757221 | ||||||
chr8:143757238
|
A | G | 23 | a0003c0003t0001g0219a0003c0003t0001g0222a0003c0003t0001g0223others(20): Show | 23 | HG01975.hp2 HG02258.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.176-14250A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757238 | ||||||
chr8:143757337
|
T | G | 2 | a0002c0002t0001g0292a0002c0002t0001g0304 | 2 | HG00621.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.176-14151T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757337 | ||||||
chr8:143757338
|
T | C | 1 | a0001c0001t0001g0242 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.176-14150T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757338 | ||||||
chr8:143757339
|
CTTTT | C | 12 | a0007c0007t0001g0013a0007c0007t0001g0015a0008c0008t0001g0019others(9): Show | 12 | HG00733.hp2 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.176-14137_176-1413 others(8): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143757339 | |||||
chr8:143757422
|
C | T | 1 | a0005c0005t0001g0211 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.176-14066C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757422 | ||||||
chr8:143757647
|
T | C | 2 | a0006c0006t0001g0030a0006c0006t0001g0031 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.176-13841T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757647 | ||||||
chr8:143757952
|
TG | T | 6 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.176-13535delG | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143757952 | ||||||
chr8:143758061
|
T | C | 1 | a0002c0002t0001g0293 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.176-13427T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758061 | ||||||
chr8:143758176
|
C | G | 1 | a0002c0002t0001g0324 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.176-13312C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758176 | ||||||
chr8:143758356
|
C | T | 1 | a0001c0001t0001g0095 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.176-13132C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758356 | ||||||
chr8:143758414
|
G | T | 8 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(5): Show | 8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-13074G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758414 | ||||||
chr8:143758469
|
G | A | 1 | a0002c0002t0001g0277 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.176-13019G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758469 | ||||||
chr8:143758519
|
C | T | 2 | a0003c0003t0001g0224a0003c0003t0001g0229 | 2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.176-12969C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758519 | ||||||
chr8:143758697
|
T | C | 83 | a0001c0001t0001g0341a0001c0001t0001g0344a0001c0010t0001g0037others(80): Show | 83 | HG00733.hp2 HG01175.hp1 HG01192.hp2 others(80): Show |
intron_variant | MODIFIER | c.176-12791T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758697 | ||||||
chr8:143758725
|
C | T | 1 | a0023c0026t0001g0149 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.176-12763C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758725 | ||||||
chr8:143758735
|
C | T | 3 | a0002c0002t0001g0264a0002c0002t0001g0265a0002c0002t0001g0266 | 3 | HG00609.hp1 NA18971.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.176-12753C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758735 | ||||||
chr8:143758752
|
A | T | 6 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0104others(3): Show | 6 | HG02071.hp2 NA18747.hp1 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.176-12736A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758752 | ||||||
chr8:143758883
|
C | T | 1 | a0002c0002t0001g0318 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.176-12605C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758883 | ||||||
chr8:143758966
|
G | A | 3 | a0007c0007t0001g0042a0007c0007t0001g0043a0007c0007t0001g0044 | 3 | HG02258.hp2 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.176-12522G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758966 | ||||||
chr8:143758975
|
G | A | 2 | a0002c0002t0001g0311a0002c0035t0001g0310 | 2 | NA18989.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.176-12513G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143758975 | ||||||
chr8:143759040
|
G | A | 1 | a0004c0004t0001g0072 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.176-12448G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759040 | ||||||
chr8:143759104
|
C | T | 3 | a0002c0002t0001g0255a0002c0002t0001g0256a0002c0002t0001g0302 | 3 | HG02080.hp2 NA18944.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.176-12384C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759104 | ||||||
chr8:143759227
|
G | A | 1 | a0001c0001t0001g0095 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.176-12261G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759227 | ||||||
chr8:143759238
|
G | C | 4 | a0004c0004t0001g0154a0004c0004t0001g0171a0004c0004t0001g0185others(1): Show | 4 | HG01109.hp2 HG01496.hp2 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.176-12250G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759238 | ||||||
chr8:143759269
|
G | T | 23 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(20): Show | 23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.176-12219G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759269 | ||||||
chr8:143759270
|
C | T | 23 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(20): Show | 23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.176-12218C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759270 | ||||||
chr8:143759281
|
C | T | 23 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(20): Show | 23 | HG00733.hp2 HG01192.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.176-12207C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759281 | ||||||
chr8:143759380
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.176-12108G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759380 | ||||||
chr8:143759552
|
A | G | 1 | a0007c0007t0001g0042 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.176-11936A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759552 | ||||||
chr8:143759572
|
A | G | 11 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(8): Show | 11 | HG01192.hp2 HG01884.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.176-11916A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759572 | ||||||
chr8:143759576
|
G | T | 4 | a0002c0002t0001g0252a0002c0002t0001g0314a0002c0002t0001g0315others(1): Show | 4 | HG00438.hp1 NA18948.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.176-11912G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759576 | ||||||
chr8:143759648
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.176-11840C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759648 | ||||||
chr8:143759660
|
TCCAAGGA others(3): Show |
T | 1 | a0005c0005t0001g0207 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.176-11825_176-1181 others(14): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143759660 | |||||
chr8:143759793
|
T | C | 39 | a0001c0010t0001g0038a0003c0003t0001g0032a0003c0003t0001g0033others(36): Show | 39 | HG01975.hp2 HG02055.hp1 HG02145.hp1 others(36): Show |
intron_variant | MODIFIER | c.176-11695T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143759793 | ||||||
chr8:143760120
|
G | A | 2 | a0002c0002t0001g0006a0002c0002t0001g0278 | 2 | HG02083.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.176-11368G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143760120 | ||||||
chr8:143760134
|
T | C | 5 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | NA18942.hp2 NA18951.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.176-11354T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143760134 | ||||||
chr8:143760512
|
C | CA | 231 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(228): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.176-10959dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143760512 | |||||
chr8:143760512
|
C | CAA | 25 | a0001c0001t0001g0081a0001c0001t0001g0086a0001c0001t0001g0088others(22): Show | 25 | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.176-10960_176-1095 others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143760512 | |||||
chr8:143760512
|
CA | C | 40 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0032others(37): Show | 40 | HG01175.hp1 HG01975.hp2 HG02145.hp1 others(37): Show |
intron_variant | MODIFIER | c.176-10959delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143760512 | |||||
chr8:143760637
|
G | A | 71 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0010others(68): Show | 71 | HG00733.hp2 HG01175.hp1 HG01192.hp2 others(68): Show |
intron_variant | MODIFIER | c.176-10851G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143760637 | ||||||
chr8:143760663
|
C | G | 1 | a0002c0002t0001g0278 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.176-10825C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143760663 | ||||||
chr8:143760728
|
A | C | 1 | a0002c0002t0001g0335 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.176-10760A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143760728 | ||||||
chr8:143760770
|
C | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0132 | 2 | HG01123.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.176-10718C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143760770 | ||||||
chr8:143760904
|
C | A | 11 | a0003c0003t0001g0010a0003c0003t0001g0011a0003c0003t0001g0016others(8): Show | 11 | HG01192.hp2 HG01884.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.176-10584C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143760904 | ||||||
chr8:143760932
|
G | A | 1 | a0031c0033t0001g0332 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.176-10556G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143760932 | ||||||
chr8:143760965
|
C | G | 1 | a0005c0005t0001g0207 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.176-10523C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143760965 | ||||||
chr8:143761034
|
C | A | 274 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(271): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.176-10454C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143761034 | ||||||
chr8:143761053
|
T | G | 344 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(341): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.176-10435T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143761053 | ||||||
chr8:143761085
|
G | A | 83 | a0001c0001t0001g0341a0001c0001t0001g0344a0001c0010t0001g0037others(80): Show | 83 | HG00733.hp2 HG01175.hp1 HG01192.hp2 others(80): Show |
intron_variant | MODIFIER | c.176-10403G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143761085 | ||||||
chr8:143761278
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.176-10210G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143761278 | ||||||
chr8:143761808
|
G | GT | 156 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(153): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.176-9668dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143761808 | |||||
chr8:143761808
|
G | GTT | 19 | a0001c0001t0001g0080a0001c0001t0001g0098a0001c0001t0001g0113others(16): Show | 19 | HG00408.hp1 HG00733.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.176-9669_176-9668d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143761808 | |||||
chr8:143761886
|
CAT | C | 152 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.176-9597_176-9596d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143761886 | |||||
chr8:143761939
|
A | C | 1 | a0002c0002t0001g0274 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.176-9549A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143761939 | ||||||
chr8:143762060
|
G | A | 2 | a0006c0006t0001g0030a0006c0006t0001g0031 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.176-9428G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762060 | ||||||
chr8:143762172
|
G | A | 3 | a0006c0006t0001g0167a0006c0006t0001g0168a0006c0006t0001g0184 | 3 | HG00642.hp1 HG00735.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.176-9316G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762172 | ||||||
chr8:143762224
|
G | A | 8 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(5): Show | 8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-9264G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762224 | ||||||
chr8:143762263
|
C | T | 1 | a0004c0004t0001g0166 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.176-9225C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762263 | ||||||
chr8:143762326
|
A | AAGGG | 16 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(13): Show | 16 | HG01123.hp2 HG01361.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.176-9148_176-9145d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143762326 | |||||
chr8:143762326
|
A | G | 1 | a0005c0005t0001g0329 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.176-9162A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762326 | ||||||
chr8:143762341
|
G | GGAAAA | 29 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(26): Show | 29 | HG01975.hp2 HG02258.hp1 HG02280.hp1 others(26): Show |
intron_variant | MODIFIER | c.176-9132_176-9128d others(7): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143762341 | |||||
chr8:143762361
|
G | C | 1 | a0001c0001t0001g0103 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.176-9127G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762361 | ||||||
chr8:143762364
|
T | C | 5 | a0013c0013t0001g0008a0013c0013t0001g0017a0013c0013t0001g0018others(2): Show | 5 | HG00733.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.176-9124T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762364 | ||||||
chr8:143762394
|
C | A | 3 | a0013c0013t0001g0008a0013c0013t0001g0017a0013c0013t0001g0018 | 3 | HG03490.hp1 HG03492.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.176-9094C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762394 | ||||||
chr8:143762522
|
A | G | 1 | a0017c0016t0001g0348 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.176-8966A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762522 | ||||||
chr8:143762785
|
A | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.176-8703A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762785 | ||||||
chr8:143762868
|
G | T | 2 | a0003c0003t0001g0063a0012c0017t0001g0064 | 2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.176-8620G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762868 | ||||||
chr8:143762940
|
C | CT | 10 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(7): Show | 10 | HG02145.hp1 HG02922.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.176-8539dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143762940 | |||||
chr8:143762955
|
CTCTTT | C | 8 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(5): Show | 8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-8522_176-8518d others(7): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143762955 | |||||
chr8:143762970
|
T | G | 1 | a0002c0002t0001g0279 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.176-8518T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143762970 | ||||||
chr8:143763024
|
TTTC | T | 9 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0063others(6): Show | 9 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.176-8461_176-8459d others(5): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143763024 | |||||
chr8:143763051
|
C | G | 1 | a0001c0001t0001g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.176-8437C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143763051 | ||||||
chr8:143763145
|
A | G | 1 | a0002c0002t0001g0291 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.176-8343A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143763145 | ||||||
chr8:143763245
|
A | C | 31 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(28): Show | 31 | HG01975.hp2 HG02258.hp1 HG02280.hp1 others(28): Show |
intron_variant | MODIFIER | c.176-8243A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143763245 | ||||||
chr8:143763466
|
A | G | 1 | a0006c0006t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.176-8022A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143763466 | ||||||
chr8:143763778
|
C | G | 110 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(107): Show | 111 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.176-7710C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143763778 | ||||||
chr8:143763892
|
C | T | 2 | a0002c0002t0001g0292a0002c0002t0001g0304 | 2 | HG00621.hp1 HG00673.hp2 |
intron_variant | MODIFIER | c.176-7596C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143763892 | ||||||
chr8:143763899
|
A | G | 6 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(3): Show | 6 | HG02280.hp1 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.176-7589A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143763899 | ||||||
chr8:143763943
|
T | C | 1 | a0029c0032t0001g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.176-7545T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143763943 | ||||||
chr8:143764095
|
CT | C | 8 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(5): Show | 8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-7392delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143764095 | ||||||
chr8:143764175
|
C | A | 8 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(5): Show | 8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-7313C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143764175 | ||||||
chr8:143764360
|
A | G | 29 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(26): Show | 29 | HG01975.hp2 HG02258.hp1 HG02280.hp1 others(26): Show |
intron_variant | MODIFIER | c.176-7128A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143764360 | ||||||
chr8:143764431
|
A | G | 3 | a0007c0007t0001g0042a0007c0007t0001g0043a0007c0007t0001g0044 | 3 | HG02258.hp2 HG03130.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.176-7057A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143764431 | ||||||
chr8:143764451
|
C | CA | 191 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(188): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.176-7020dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143764451 | |||||
chr8:143764451
|
C | CAA | 21 | a0001c0001t0001g0081a0001c0001t0001g0090a0001c0001t0001g0096others(18): Show | 21 | HG00438.hp2 HG00642.hp1 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.176-7021_176-7020d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143764451 | |||||
chr8:143764551
|
G | A | 6 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0343others(3): Show | 6 | HG01175.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.176-6937G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143764551 | ||||||
chr8:143764661
|
A | G | 190 | a0001c0001t0001g0341a0001c0001t0001g0344a0001c0010t0001g0037others(187): Show | 191 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.176-6827A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143764661 | ||||||
chr8:143764769
|
A | G | 8 | a0001c0001t0001g0158a0004c0004t0001g0166a0004c0004t0001g0173others(5): Show | 8 | HG00099.hp2 HG01071.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.176-6719A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143764769 | ||||||
chr8:143764959
|
T | C | 3 | a0006c0006t0001g0030a0006c0006t0001g0031a0030c0021t0001g0338 | 3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-6529T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143764959 | ||||||
chr8:143764974
|
A | G | 1 | a0003c0003t0001g0219 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.176-6514A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143764974 | ||||||
chr8:143765075
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.176-6413G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143765075 | ||||||
chr8:143765226
|
G | A | 2 | a0001c0001t0001g0119a0001c0001t0001g0186 | 2 | NA18939.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.176-6262G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143765226 | ||||||
chr8:143765242
|
C | T | 1 | a0004c0004t0001g0163 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.176-6246C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143765242 | ||||||
chr8:143765315
|
C | G | 8 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(5): Show | 8 | HG02258.hp2 HG02615.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-6173C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143765315 | ||||||
chr8:143765356
|
C | CA | 11 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(8): Show | 11 | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.176-6120dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143765356 | |||||
chr8:143766448
|
A | G | 1 | a0004c0004t0001g0174 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.176-5040A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766448 | ||||||
chr8:143766457
|
G | A | 1 | a0002c0002t0001g0271 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.176-5031G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766457 | ||||||
chr8:143766477
|
C | T | 149 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.176-5011C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766477 | ||||||
chr8:143766516
|
C | CA | 3 | a0003c0003t0001g0063a0012c0017t0001g0064a0025c0030t0001g0346 | 3 | HG02622.hp1 HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.176-4967dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143766516 | |||||
chr8:143766562
|
C | T | 196 | a0001c0001t0001g0341a0001c0001t0001g0344a0001c0010t0001g0037others(193): Show | 197 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.176-4926C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766562 | ||||||
chr8:143766586
|
G | A | 48 | a0001c0001t0001g0051a0001c0001t0001g0153a0001c0001t0001g0158others(45): Show | 48 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(45): Show |
intron_variant | MODIFIER | c.176-4902G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766586 | ||||||
chr8:143766643
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.176-4845C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766643 | ||||||
chr8:143766657
|
C | T | 112 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(109): Show | 113 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.176-4831C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766657 | ||||||
chr8:143766769
|
T | C | 3 | a0006c0006t0001g0030a0006c0006t0001g0031a0030c0021t0001g0338 | 3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-4719T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766769 | ||||||
chr8:143766953
|
C | T | 1 | a0004c0004t0001g0157 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.176-4535C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766953 | ||||||
chr8:143766993
|
C | T | 29 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(26): Show | 29 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(26): Show |
intron_variant | MODIFIER | c.176-4495C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143766993 | ||||||
chr8:143767292
|
A | G | 13 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0063others(10): Show | 13 | HG02145.hp1 HG02622.hp1 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.176-4196A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143767292 | ||||||
chr8:143767345
|
A | AGTGT | 3 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0090 | 3 | HG00438.hp2 NA18955.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.176-4130_176-4127d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143767345 | |||||
chr8:143767379
|
G | A | 15 | a0001c0001t0001g0344a0001c0010t0001g0037a0001c0010t0001g0038others(12): Show | 15 | HG01175.hp1 HG02258.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.176-4109G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143767379 | ||||||
chr8:143767432
|
T | C | 345 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(342): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.176-4056T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143767432 | ||||||
chr8:143767477
|
T | A | 2 | a0001c0001t0001g0242a0031c0033t0001g0332 | 2 | HG01884.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.176-4011T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143767477 | ||||||
chr8:143767515
|
G | A | 1 | a0002c0002t0001g0006 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.176-3973G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143767515 | ||||||
chr8:143767742
|
G | T | 1 | a0029c0032t0001g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.176-3746G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143767742 | ||||||
chr8:143767877
|
C | CT | 72 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0061others(69): Show | 72 | HG00544.hp2 HG00642.hp1 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.176-3589dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143767877 | |||||
chr8:143767877
|
C | CTT | 11 | a0003c0003t0001g0034a0003c0003t0001g0035a0003c0003t0001g0036others(8): Show | 11 | HG02258.hp1 HG02622.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.176-3590_176-3589d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143767877 | |||||
chr8:143767877
|
CT | C | 91 | a0001c0001t0001g0245a0002c0002t0001g0001a0002c0002t0001g0004others(88): Show | 92 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.176-3589delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143767877 | |||||
chr8:143767970
|
T | A | 345 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(342): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.176-3518T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143767970 | ||||||
chr8:143768032
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.176-3456G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768032 | ||||||
chr8:143768088
|
G | A | 3 | a0003c0003t0001g0063a0012c0017t0001g0064a0025c0030t0001g0346 | 3 | HG02622.hp1 HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.176-3400G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768088 | ||||||
chr8:143768134
|
C | T | 3 | a0006c0006t0001g0030a0006c0006t0001g0031a0030c0021t0001g0338 | 3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-3354C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768134 | ||||||
chr8:143768238
|
T | C | 1 | a0002c0002t0001g0282 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.176-3250T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768238 | ||||||
chr8:143768380
|
C | A | 1 | a0002c0002t0001g0320 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.176-3108C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768380 | ||||||
chr8:143768381
|
G | A | 12 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(9): Show | 12 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.176-3107G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768381 | ||||||
chr8:143768505
|
C | T | 3 | a0006c0006t0001g0030a0006c0006t0001g0031a0030c0021t0001g0338 | 3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-2983C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768505 | ||||||
chr8:143768517
|
C | T | 1 | a0025c0030t0001g0346 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.176-2971C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768517 | ||||||
chr8:143768540
|
C | T | 1 | a0017c0016t0001g0348 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.176-2948C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768540 | ||||||
chr8:143768595
|
A | G | 3 | a0006c0006t0001g0030a0006c0006t0001g0031a0030c0021t0001g0338 | 3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-2893A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768595 | ||||||
chr8:143768664
|
G | A | 345 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(342): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.176-2824G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768664 | ||||||
chr8:143768711
|
A | C | 3 | a0006c0006t0001g0030a0006c0006t0001g0031a0030c0021t0001g0338 | 3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-2777A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768711 | ||||||
chr8:143768740
|
TTC | T | 3 | a0006c0006t0001g0030a0006c0006t0001g0031a0030c0021t0001g0338 | 3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-2746_176-2745d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr8 | 143768740 | |||||
chr8:143768744
|
G | T | 3 | a0006c0006t0001g0030a0006c0006t0001g0031a0030c0021t0001g0338 | 3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-2744G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768744 | ||||||
chr8:143768748
|
C | T | 3 | a0006c0006t0001g0030a0006c0006t0001g0031a0030c0021t0001g0338 | 3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-2740C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768748 | ||||||
chr8:143768944
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.176-2544C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143768944 | ||||||
chr8:143769095
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.176-2393C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769095 | ||||||
chr8:143769150
|
C | G | 2 | a0006c0006t0001g0030a0006c0006t0001g0031 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.176-2338C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769150 | ||||||
chr8:143769209
|
G | A | 3 | a0009c0009t0001g0007a0009c0009t0001g0026a0009c0009t0001g0027 | 3 | HG01192.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.176-2279G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769209 | ||||||
chr8:143769262
|
G | A | 1 | a0012c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.176-2226G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769262 | ||||||
chr8:143769370
|
T | A | 124 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(121): Show | 125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.176-2118T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769370 | ||||||
chr8:143769445
|
T | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(83): Show | 86 | HG00408.hp1 HG00438.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.176-2043T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769445 | ||||||
chr8:143769481
|
T | C | 197 | a0001c0001t0001g0341a0001c0001t0001g0344a0001c0010t0001g0037others(194): Show | 198 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.176-2007T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769481 | ||||||
chr8:143769482
|
G | A | 2 | a0005c0005t0001g0210a0005c0005t0001g0211 | 2 | HG00280.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.176-2006G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769482 | ||||||
chr8:143769500
|
A | T | 1 | a0002c0002t0001g0306 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.176-1988A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769500 | ||||||
chr8:143769536
|
G | A | 1 | a0007c0007t0001g0041 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.176-1952G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769536 | ||||||
chr8:143769652
|
C | T | 3 | a0006c0006t0001g0030a0006c0006t0001g0031a0030c0021t0001g0338 | 3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-1836C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769652 | ||||||
chr8:143769754
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.176-1734C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769754 | ||||||
chr8:143769784
|
T | C | 1 | a0006c0006t0001g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.176-1704T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769784 | ||||||
chr8:143769857
|
A | C | 1 | a0002c0002t0001g0278 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.176-1631A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143769857 | ||||||
chr8:143770320
|
C | T | 3 | a0006c0006t0001g0030a0006c0006t0001g0031a0030c0021t0001g0338 | 3 | HG02257.hp2 HG02976.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.176-1168C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770320 | ||||||
chr8:143770395
|
G | T | 176 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(173): Show | 177 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.176-1093G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770395 | ||||||
chr8:143770516
|
T | C | 345 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(342): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.176-972T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770516 | ||||||
chr8:143770564
|
C | T | 2 | a0003c0003t0001g0045a0003c0003t0001g0199 | 2 | HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.176-924C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770564 | ||||||
chr8:143770624
|
G | A | 1 | a0002c0002t0001g0268 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.176-864G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770624 | ||||||
chr8:143770638
|
G | A | 123 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(120): Show | 124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.176-850G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770638 | ||||||
chr8:143770709
|
G | A | 46 | a0001c0001t0001g0051a0001c0001t0001g0153a0001c0001t0001g0158others(43): Show | 46 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(43): Show |
intron_variant | MODIFIER | c.176-779G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770709 | ||||||
chr8:143770721
|
C | G | 1 | a0001c0001t0001g0153 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.176-767C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770721 | ||||||
chr8:143770746
|
G | T | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.176-742G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770746 | ||||||
chr8:143770848
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.176-640C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143770848 | ||||||
chr8:143771090
|
G | C | 2 | a0006c0006t0001g0030a0006c0006t0001g0031 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.176-398G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143771090 | ||||||
chr8:143771166
|
C | A | 1 | a0002c0002t0001g0305 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.176-322C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143771166 | ||||||
chr8:143771175
|
G | A | 7 | a0001c0001t0001g0088a0001c0001t0001g0091a0001c0001t0001g0102others(4): Show | 7 | HG02080.hp1 HG02129.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.176-313G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143771175 | ||||||
chr8:143771311
|
C | G | 1 | a0025c0030t0001g0346 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.176-177C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143771311 | ||||||
chr8:143771360
|
G | A | 1 | a0001c0001t0001g0116 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.176-128G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143771360 | ||||||
chr8:143771390
|
C | G | 172 | a0001c0001t0001g0082a0001c0001t0001g0084a0001c0001t0001g0086others(169): Show | 173 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.176-98C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 3/13 | chr8 | 143771390 | ||||||
chr8:143771644
|
G | T | 123 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(120): Show | 124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.306+26G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 4/13 | chr8 | 143771644 | ||||||
chr8:143771645
|
G | A | 1 | a0002c0002t0001g0295 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.306+27G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 4/13 | chr8 | 143771645 | ||||||
chr8:143771709
|
G | A | 8 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(5): Show | 8 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.306+91G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 4/13 | chr8 | 143771709 | ||||||
chr8:143771710
|
A | G | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.307-91A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 4/13 | chr8 | 143771710 | ||||||
chr8:143771743
|
C | CCTCGGGG | 3 | a0006c0006t0001g0030a0006c0006t0001g0031a0006c0006t0001g0060 | 3 | HG02257.hp2 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.307-49_307-43dupTC others(5): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr8 | 143771743 | |||||
chr8:143771983
|
G | A | 2 | a0006c0006t0001g0030a0006c0006t0001g0031 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.471+18G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 5/13 | chr8 | 143771983 | ||||||
chr8:143772315
|
A | G | 1 | a0003c0003t0001g0197 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.664-42A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 6/13 | chr8 | 143772315 | ||||||
chr8:143772494
|
AGAGGTGT others(25): Show |
A | 1 | a0012c0017t0001g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.789+25_789+56delCC others(30): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143772494 | |||||
chr8:143772507
|
CCGGGAGG others(25): Show |
C | 2 | a0001c0001t0001g0002a0001c0001t0001g0137 | 2 | HG02071.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.789+55_789+86delCC others(30): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143772507 | |||||
chr8:143772508
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.789+26C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143772508 | ||||||
chr8:143772539
|
T | C | 161 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(158): Show | 161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.789+57T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143772539 | ||||||
chr8:143772628
|
C | CTG | 15 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(12): Show | 15 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.789+148_789+149dup others(2): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143772628 | |||||
chr8:143772646
|
A | G | 24 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(21): Show | 24 | HG02258.hp1 HG02280.hp1 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.789+164A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143772646 | ||||||
chr8:143772875
|
T | C | 15 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(12): Show | 15 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.789+393T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143772875 | ||||||
chr8:143772884
|
T | C | 1 | a0031c0033t0001g0332 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.789+402T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143772884 | ||||||
chr8:143772904
|
C | T | 14 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(11): Show | 14 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.789+422C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143772904 | ||||||
chr8:143772909
|
C | T | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0205 | 3 | NA18966.hp1 NA18998.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.789+427C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143772909 | ||||||
chr8:143772936
|
T | G | 15 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(12): Show | 15 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.789+454T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143772936 | ||||||
chr8:143772956
|
C | T | 15 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(12): Show | 15 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.789+474C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143772956 | ||||||
chr8:143773015
|
T | C | 15 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(12): Show | 15 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.789+533T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773015 | ||||||
chr8:143773044
|
A | G | 15 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(12): Show | 15 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.789+562A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773044 | ||||||
chr8:143773175
|
C | T | 1 | a0003c0003t0001g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.789+693C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773175 | ||||||
chr8:143773251
|
G | A | 2 | a0006c0006t0001g0030a0006c0006t0001g0031 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.789+769G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773251 | ||||||
chr8:143773261
|
G | T | 15 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(12): Show | 15 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.789+779G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773261 | ||||||
chr8:143773300
|
C | CA | 8 | a0001c0001t0001g0048a0001c0001t0001g0084a0001c0001t0001g0088others(5): Show | 8 | HG00735.hp2 HG01168.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.789+834dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143773300 | |||||
chr8:143773307
|
A | AAACAAAA others(5): Show |
11 | a0001c0010t0001g0040a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+827_789+828ins others(12): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143773307 | |||||
chr8:143773308
|
A | AC | 8 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(5): Show | 8 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.789+826_789+827ins others(1): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773308 | ||||||
chr8:143773310
|
A | C | 10 | a0002c0002t0001g0254a0002c0002t0001g0276a0002c0002t0001g0280others(7): Show | 10 | HG00280.hp1 HG00639.hp1 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+828A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773310 | ||||||
chr8:143773314
|
A | AC | 10 | a0002c0002t0001g0248a0002c0002t0001g0250a0002c0002t0001g0253others(7): Show | 10 | HG00558.hp2 HG02622.hp1 NA18942.hp1 others(7): Show |
intron_variant | MODIFIER | c.789+832_789+833ins others(1): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773314 | ||||||
chr8:143773314
|
A | C | 114 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(111): Show | 115 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.789+832A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773314 | ||||||
chr8:143773316
|
ACAAAAAA others(3): Show |
A | 22 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(19): Show | 22 | HG02258.hp1 HG02280.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.789+835_789+844del others(10): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773316 | ||||||
chr8:143773317
|
C | A | 143 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(140): Show | 144 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.789+835C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773317 | ||||||
chr8:143773318
|
A | C | 144 | a0001c0010t0001g0040a0002c0002t0001g0001a0002c0002t0001g0003others(141): Show | 145 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.789+836A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773318 | ||||||
chr8:143773320
|
A | C | 1 | a0025c0030t0001g0346 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.789+838A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773320 | ||||||
chr8:143773322
|
A | C | 124 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(121): Show | 125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.789+840A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773322 | ||||||
chr8:143773325
|
AC | A | 17 | a0001c0001t0001g0341a0001c0001t0001g0344a0003c0003t0001g0045others(14): Show | 17 | HG01175.hp1 HG02559.hp1 HG02622.hp1 others(14): Show |
intron_variant | MODIFIER | c.789+844delC | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773325 | ||||||
chr8:143773326
|
C | A | 22 | a0001c0010t0001g0040a0008c0008t0001g0019a0008c0008t0001g0020others(19): Show | 22 | HG00733.hp2 HG01192.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.789+844C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773326 | ||||||
chr8:143773326
|
C | CCAAAAAA others(2): Show |
4 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(1): Show | 4 | HG02615.hp2 HG02970.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.789+844_789+845ins others(9): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773326 | ||||||
chr8:143773326
|
CA | C | 10 | a0006c0006t0001g0030a0006c0006t0001g0031a0007c0007t0001g0013others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+845delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773326 | ||||||
chr8:143773327
|
A | C | 1 | a0007c0007t0001g0041 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.789+845A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773327 | ||||||
chr8:143773328
|
C | A | 125 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(122): Show | 126 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.789+846C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773328 | ||||||
chr8:143773330
|
A | C | 2 | a0001c0001t0001g0109a0002c0002t0001g0254 | 2 | HG01928.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.789+848A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773330 | ||||||
chr8:143773454
|
G | T | 8 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(5): Show | 8 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.789+972G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773454 | ||||||
chr8:143773470
|
A | G | 5 | a0001c0001t0001g0341a0001c0001t0001g0344a0011c0012t0001g0342others(2): Show | 5 | HG01175.hp1 HG02559.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+988A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773470 | ||||||
chr8:143773797
|
G | C | 1 | a0001c0001t0002g0053 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.789+1315G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773797 | ||||||
chr8:143773867
|
G | T | 126 | a0001c0001t0001g0153a0002c0002t0001g0001a0002c0002t0001g0003others(123): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.789+1385G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143773867 | ||||||
chr8:143774164
|
A | G | 14 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(11): Show | 14 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.789+1682A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774164 | ||||||
chr8:143774177
|
CA | C | 283 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0049others(280): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.789+1710delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143774177 | |||||
chr8:143774189
|
A | C | 124 | a0001c0001t0001g0153a0002c0002t0001g0001a0002c0002t0001g0003others(121): Show | 125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.789+1707A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774189 | ||||||
chr8:143774232
|
T | C | 8 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(5): Show | 8 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.789+1750T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774232 | ||||||
chr8:143774273
|
G | T | 35 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(32): Show | 35 | HG02258.hp1 HG02280.hp1 HG02280.hp2 others(32): Show |
intron_variant | MODIFIER | c.789+1791G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774273 | ||||||
chr8:143774345
|
G | A | 2 | a0004c0004t0001g0074a0004c0004t0001g0075 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.789+1863G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774345 | ||||||
chr8:143774611
|
T | C | 15 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(12): Show | 15 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.789+2129T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774611 | ||||||
chr8:143774739
|
G | C | 1 | a0014c0019t0001g0023 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.789+2257G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774739 | ||||||
chr8:143774744
|
C | T | 3 | a0003c0003t0001g0063a0012c0017t0001g0064a0025c0030t0001g0346 | 3 | HG02622.hp1 HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.789+2262C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774744 | ||||||
chr8:143774821
|
A | C | 2 | a0004c0004t0001g0169a0004c0004t0001g0181 | 2 | HG00099.hp1 HG00738.hp2 |
intron_variant | MODIFIER | c.789+2339A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774821 | ||||||
chr8:143774890
|
G | T | 16 | a0001c0001t0001g0344a0001c0010t0001g0037a0001c0010t0001g0038others(13): Show | 16 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.789+2408G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774890 | ||||||
chr8:143774965
|
G | A | 2 | a0006c0006t0001g0030a0006c0006t0001g0031 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.789+2483G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774965 | ||||||
chr8:143774975
|
G | GGGGGCAG others(17): Show |
2 | a0005c0005t0001g0288a0005c0005t0001g0333 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.789+2499_789+2522d others(26): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143774975 | |||||
chr8:143774989
|
C | T | 17 | a0003c0003t0001g0219a0003c0003t0001g0222a0003c0003t0001g0223others(14): Show | 17 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.789+2507C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774989 | ||||||
chr8:143774993
|
G | C | 8 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(5): Show | 8 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.789+2511G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143774993 | ||||||
chr8:143775184
|
T | G | 1 | a0002c0002t0001g0267 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.789+2702T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775184 | ||||||
chr8:143775324
|
G | A | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+2842G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775324 | ||||||
chr8:143775335
|
T | TAC | 45 | a0001c0001t0001g0051a0001c0001t0001g0158a0001c0001t0001g0159others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.789+2871_789+2872d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775335 | |||||
chr8:143775335
|
T | TACAC | 5 | a0001c0001t0001g0341a0006c0006t0001g0182a0011c0012t0001g0342others(2): Show | 5 | HG01175.hp1 HG03139.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+2869_789+2872d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775335 | |||||
chr8:143775335
|
TAC | T | 4 | a0002c0002t0001g0001a0002c0002t0001g0251a0002c0002t0001g0293others(1): Show | 5 | NA18964.hp2 NA18970.hp1 NA19055.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+2871_789+2872d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775335 | |||||
chr8:143775353
|
C | CACAG | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+2872_789+2873i others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775353 | |||||
chr8:143775355
|
G | C | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+2873G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775355 | ||||||
chr8:143775526
|
C | T | 8 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(5): Show | 8 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.789+3044C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775526 | ||||||
chr8:143775622
|
C | T | 1 | a0025c0030t0001g0346 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.789+3140C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775622 | ||||||
chr8:143775673
|
A | G | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3191A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775673 | ||||||
chr8:143775747
|
G | A | 1 | a0002c0002t0001g0287 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.789+3265G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775747 | ||||||
chr8:143775787
|
T | TAC | 36 | a0001c0001t0001g0047a0001c0001t0001g0049a0001c0001t0001g0051others(33): Show | 36 | HG00558.hp1 HG00673.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.789+3340_789+3341d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | |||||
chr8:143775787
|
T | TACAC | 10 | a0001c0001t0001g0108a0001c0001t0001g0136a0001c0001t0001g0144others(7): Show | 10 | HG02165.hp1 HG02647.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+3338_789+3341d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | |||||
chr8:143775787
|
T | TACACAC | 19 | a0001c0001t0001g0110a0001c0001t0001g0242a0002c0002t0001g0257others(16): Show | 19 | HG00621.hp1 HG00639.hp2 HG00673.hp2 others(16): Show |
intron_variant | MODIFIER | c.789+3336_789+3341d others(8): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | |||||
chr8:143775787
|
T | TACACACA others(1): Show |
34 | a0001c0001t0001g0161a0002c0002t0001g0003a0002c0002t0001g0004others(31): Show | 34 | HG00609.hp1 HG01123.hp1 HG01192.hp2 others(31): Show |
intron_variant | MODIFIER | c.789+3334_789+3341d others(10): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | |||||
chr8:143775787
|
T | TACACACA others(3): Show |
72 | a0001c0001t0001g0127a0001c0001t0001g0153a0002c0002t0001g0213others(69): Show | 72 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.789+3332_789+3341d others(12): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | |||||
chr8:143775787
|
T | TACACACA others(5): Show |
41 | a0001c0010t0001g0037a0002c0002t0001g0001a0002c0002t0001g0005others(38): Show | 42 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.789+3330_789+3341d others(14): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | |||||
chr8:143775787
|
T | TACACACA others(7): Show |
6 | a0001c0010t0001g0038a0001c0010t0001g0039a0002c0002t0001g0320others(3): Show | 6 | HG00423.hp2 HG02523.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.789+3328_789+3341d others(16): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | |||||
chr8:143775787
|
T | TACACACA others(9): Show |
4 | a0002c0002t0001g0296a0002c0002t0001g0307a0002c0002t0001g0309others(1): Show | 4 | HG02004.hp2 HG02074.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.789+3326_789+3341d others(18): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | |||||
chr8:143775787
|
T | TACACACA others(13): Show |
1 | a0001c0010t0001g0040 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.789+3322_789+3341d others(22): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | |||||
chr8:143775787
|
T | TACACACA others(17): Show |
1 | a0002c0002t0001g0272 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.789+3318_789+3341d others(26): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | |||||
chr8:143775787
|
T | TACACGCA others(11): Show |
3 | a0003c0003t0001g0226a0003c0003t0001g0227a0003c0003t0001g0228 | 3 | HG02895.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.789+3309_789+3310i others(20): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | |||||
chr8:143775787
|
TAC | T | 6 | a0001c0001t0001g0097a0001c0001t0001g0112a0001c0001t0001g0115others(3): Show | 6 | HG01081.hp2 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.789+3340_789+3341d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775787 | |||||
chr8:143775816
|
ACACACAC | A | 3 | a0001c0001t0001g0344a0007c0007t0001g0044a0030c0021t0001g0338 | 3 | HG02258.hp2 HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.789+3337_789+3343d others(9): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775816 | |||||
chr8:143775818
|
ACACAC | A | 4 | a0007c0007t0001g0042a0007c0007t0001g0043a0007c0007t0001g0200others(1): Show | 4 | HG02145.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.789+3339_789+3343d others(7): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143775818 | |||||
chr8:143775869
|
T | C | 3 | a0003c0003t0001g0063a0012c0017t0001g0064a0025c0030t0001g0346 | 3 | HG02622.hp1 HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.789+3387T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775869 | ||||||
chr8:143775877
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.789+3395T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775877 | ||||||
chr8:143775887
|
G | A | 1 | a0005c0005t0001g0207 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.789+3405G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775887 | ||||||
chr8:143775919
|
A | G | 4 | a0001c0001t0001g0341a0011c0012t0001g0342a0011c0012t0001g0345others(1): Show | 4 | HG01175.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.789+3437A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775919 | ||||||
chr8:143775961
|
A | C | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3479A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775961 | ||||||
chr8:143775980
|
G | A | 198 | a0001c0001t0001g0153a0001c0001t0001g0341a0001c0001t0001g0344others(195): Show | 199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.789+3498G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143775980 | ||||||
chr8:143776004
|
GGGCCGGG others(28): Show |
G | 5 | a0001c0001t0001g0341a0007c0007t0001g0013a0011c0012t0001g0342others(2): Show | 5 | HG01175.hp1 HG02486.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+3535_789+3569d others(37): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143776004 | |||||
chr8:143776009
|
G | T | 10 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+3527G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776009 | ||||||
chr8:143776017
|
T | C | 10 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+3535T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776017 | ||||||
chr8:143776044
|
G | T | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3562G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776044 | ||||||
chr8:143776052
|
C | T | 10 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+3570C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776052 | ||||||
chr8:143776088
|
G | A | 5 | a0013c0013t0001g0008a0013c0013t0001g0017a0013c0013t0001g0018others(2): Show | 5 | HG00733.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.789+3606G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776088 | ||||||
chr8:143776096
|
C | G | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3614C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776096 | ||||||
chr8:143776097
|
A | G | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3615A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776097 | ||||||
chr8:143776101
|
T | C | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3619T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776101 | ||||||
chr8:143776105
|
G | A | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3623G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776105 | ||||||
chr8:143776118
|
A | G | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3636A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776118 | ||||||
chr8:143776121
|
C | A | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3639C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776121 | ||||||
chr8:143776137
|
C | A | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3655C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776137 | ||||||
chr8:143776149
|
G | T | 2 | a0003c0003t0001g0063a0012c0017t0001g0064 | 2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.789+3667G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776149 | ||||||
chr8:143776177
|
C | T | 4 | a0001c0001t0001g0341a0011c0012t0001g0342a0011c0012t0001g0345others(1): Show | 4 | HG01175.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.789+3695C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776177 | ||||||
chr8:143776182
|
G | A | 1 | a0003c0003t0001g0219 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.789+3700G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776182 | ||||||
chr8:143776213
|
C | T | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3731C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776213 | ||||||
chr8:143776259
|
T | C | 8 | a0001c0001t0001g0344a0007c0007t0001g0013a0007c0007t0001g0015others(5): Show | 8 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.789+3777T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776259 | ||||||
chr8:143776283
|
TGCAGTCC | T | 12 | a0001c0001t0001g0344a0002c0002t0001g0283a0006c0006t0001g0030others(9): Show | 12 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.789+3810_789+3816d others(9): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143776283 | |||||
chr8:143776294
|
G | C | 12 | a0001c0001t0001g0344a0002c0002t0001g0283a0006c0006t0001g0030others(9): Show | 12 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.789+3812G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776294 | ||||||
chr8:143776298
|
G | A | 35 | a0001c0001t0001g0344a0002c0002t0001g0283a0003c0003t0001g0032others(32): Show | 35 | HG02145.hp1 HG02257.hp2 HG02258.hp1 others(32): Show |
intron_variant | MODIFIER | c.789+3816G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776298 | ||||||
chr8:143776327
|
C | CA | 266 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(263): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.789+3863dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143776327 | |||||
chr8:143776327
|
C | CAA | 32 | a0001c0001t0001g0002a0001c0001t0001g0049a0001c0001t0001g0062others(29): Show | 32 | HG00438.hp2 HG00558.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.789+3862_789+3863d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143776327 | |||||
chr8:143776381
|
C | G | 2 | a0005c0005t0001g0210a0005c0005t0001g0211 | 2 | HG00280.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.789+3899C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776381 | ||||||
chr8:143776425
|
A | G | 124 | a0001c0001t0001g0153a0002c0002t0001g0001a0002c0002t0001g0003others(121): Show | 125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.789+3943A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776425 | ||||||
chr8:143776578
|
G | A | 1 | a0002c0002t0001g0259 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.789+4096G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776578 | ||||||
chr8:143776578
|
G | C | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+4096G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143776578 | ||||||
chr8:143777143
|
T | C | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+4661T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777143 | ||||||
chr8:143777164
|
G | A | 1 | a0005c0005t0001g0329 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.789+4682G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777164 | ||||||
chr8:143777261
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.789+4779A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777261 | ||||||
chr8:143777288
|
C | G | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+4806C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777288 | ||||||
chr8:143777388
|
C | T | 5 | a0001c0001t0001g0062a0001c0001t0001g0087a0002c0002t0001g0269others(2): Show | 5 | HG03490.hp2 HG03654.hp1 HG03654.hp2 others(2): Show |
intron_variant | MODIFIER | c.789+4906C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777388 | ||||||
chr8:143777520
|
T | TA | 38 | a0001c0001t0001g0046a0001c0001t0001g0049a0001c0001t0001g0061others(35): Show | 38 | HG00558.hp1 HG00642.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.789+5057dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143777520 | |||||
chr8:143777520
|
TA | T | 116 | a0001c0001t0001g0153a0002c0002t0001g0001a0002c0002t0001g0003others(113): Show | 117 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.789+5057delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143777520 | |||||
chr8:143777537
|
A | C | 9 | a0001c0001t0001g0344a0007c0007t0001g0013a0007c0007t0001g0015others(6): Show | 9 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.789+5055A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777537 | ||||||
chr8:143777539
|
AC | A | 8 | a0001c0001t0001g0082a0001c0001t0001g0148a0001c0001t0001g0205others(5): Show | 8 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.789+5058delC | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777539 | ||||||
chr8:143777540
|
C | A | 149 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(146): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.789+5058C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777540 | ||||||
chr8:143777544
|
C | A | 1 | a0024c0022t0001g0059 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.789+5062C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777544 | ||||||
chr8:143777548
|
T | TA | 12 | a0001c0001t0002g0190a0006c0006t0001g0030a0008c0008t0001g0029others(9): Show | 12 | HG01192.hp2 HG02257.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.789+5075dupA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143777548 | |||||
chr8:143777718
|
G | T | 123 | a0001c0001t0001g0153a0002c0002t0001g0001a0002c0002t0001g0003others(120): Show | 124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.789+5236G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777718 | ||||||
chr8:143777870
|
T | C | 2 | a0006c0006t0001g0030a0006c0006t0001g0031 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.789+5388T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143777870 | ||||||
chr8:143778197
|
AAC | A | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+5717_789+5718d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143778197 | |||||
chr8:143778199
|
CA | C | 333 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(330): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.789+5729delA | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143778199 | |||||
chr8:143778349
|
G | A | 7 | a0007c0007t0001g0013a0007c0007t0001g0015a0007c0007t0001g0042others(4): Show | 7 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.789+5867G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143778349 | ||||||
chr8:143778582
|
C | T | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+6100C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143778582 | ||||||
chr8:143778627
|
G | A | 50 | a0001c0001t0001g0051a0001c0001t0001g0158a0001c0001t0001g0159others(47): Show | 50 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(47): Show |
intron_variant | MODIFIER | c.789+6145G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143778627 | ||||||
chr8:143778707
|
A | G | 147 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.789+6225A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143778707 | ||||||
chr8:143778747
|
ATTATC | A | 8 | a0005c0005t0001g0206a0005c0005t0001g0207a0005c0005t0001g0208others(5): Show | 8 | HG00544.hp1 HG02027.hp1 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.789+6270_789+6274d others(7): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143778747 | |||||
chr8:143778827
|
C | T | 25 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(22): Show | 25 | HG00733.hp2 HG01192.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.789+6345C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143778827 | ||||||
chr8:143778843
|
C | A | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+6361C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143778843 | ||||||
chr8:143778871
|
C | A | 26 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(23): Show | 26 | HG00733.hp2 HG01192.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.789+6389C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143778871 | ||||||
chr8:143778918
|
C | T | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+6436C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143778918 | ||||||
chr8:143779114
|
A | G | 1 | a0002c0002t0001g0005 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.789+6632A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143779114 | ||||||
chr8:143779453
|
C | T | 1 | a0001c0001t0001g0095 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.789+6971C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143779453 | ||||||
chr8:143779569
|
CTCAT | C | 45 | a0001c0001t0001g0051a0001c0001t0001g0158a0001c0001t0001g0159others(42): Show | 45 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(42): Show |
intron_variant | MODIFIER | c.789+7096_789+7099d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143779569 | |||||
chr8:143779815
|
A | G | 348 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.789+7333A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143779815 | ||||||
chr8:143779862
|
C | T | 8 | a0001c0001t0001g0344a0007c0007t0001g0013a0007c0007t0001g0015others(5): Show | 8 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.789+7380C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143779862 | ||||||
chr8:143780023
|
A | G | 1 | a0001c0001t0002g0053 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.789+7541A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780023 | ||||||
chr8:143780076
|
A | G | 4 | a0001c0001t0001g0341a0011c0012t0001g0342a0011c0012t0001g0345others(1): Show | 4 | HG01175.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.789+7594A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780076 | ||||||
chr8:143780217
|
C | T | 1 | a0002c0002t0001g0263 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.789+7735C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780217 | ||||||
chr8:143780357
|
G | A | 1 | a0025c0030t0001g0346 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.789+7875G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780357 | ||||||
chr8:143780395
|
T | C | 25 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(22): Show | 25 | HG00733.hp2 HG01192.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.789+7913T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780395 | ||||||
chr8:143780426
|
C | G | 3 | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0205 | 3 | NA18966.hp1 NA18998.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.789+7944C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780426 | ||||||
chr8:143780505
|
C | G | 3 | a0003c0003t0001g0226a0003c0003t0001g0227a0003c0003t0001g0228 | 3 | HG02895.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.789+8023C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780505 | ||||||
chr8:143780787
|
A | G | 1 | a0003c0003t0001g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.790-8128A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780787 | ||||||
chr8:143780790
|
C | G | 147 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.790-8125C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780790 | ||||||
chr8:143780946
|
G | A | 1 | a0012c0017t0001g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.790-7969G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143780946 | ||||||
chr8:143781063
|
A | G | 4 | a0001c0001t0001g0341a0011c0012t0001g0342a0011c0012t0001g0345others(1): Show | 4 | HG01175.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-7852A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781063 | ||||||
chr8:143781171
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.790-7744G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781171 | ||||||
chr8:143781173
|
G | A | 4 | a0001c0001t0001g0341a0011c0012t0001g0342a0011c0012t0001g0345others(1): Show | 4 | HG01175.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-7742G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781173 | ||||||
chr8:143781193
|
A | G | 23 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(20): Show | 23 | HG02258.hp1 HG02280.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.790-7722A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781193 | ||||||
chr8:143781280
|
A | G | 4 | a0002c0002t0001g0252a0002c0002t0001g0314a0002c0002t0001g0315others(1): Show | 4 | HG00438.hp1 NA18948.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.790-7635A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781280 | ||||||
chr8:143781358
|
T | G | 345 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(342): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.790-7557T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781358 | ||||||
chr8:143781561
|
C | A | 1 | a0002c0002t0001g0309 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.790-7354C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781561 | ||||||
chr8:143781697
|
A | G | 1 | a0003c0003t0001g0036 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.790-7218A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781697 | ||||||
chr8:143781842
|
T | A | 1 | a0002c0002t0001g0005 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.790-7073T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781842 | ||||||
chr8:143781873
|
T | C | 4 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(1): Show | 4 | HG02970.hp2 HG03195.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-7042T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781873 | ||||||
chr8:143781945
|
G | A | 345 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(342): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.790-6970G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143781945 | ||||||
chr8:143782061
|
T | C | 23 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(20): Show | 23 | HG02258.hp1 HG02280.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.790-6854T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143782061 | ||||||
chr8:143782167
|
T | A | 1 | a0001c0001t0001g0242 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.790-6748T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143782167 | ||||||
chr8:143782316
|
G | A | 1 | a0003c0003t0001g0036 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.790-6599G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143782316 | ||||||
chr8:143782380
|
C | T | 2 | a0003c0003t0001g0063a0012c0017t0001g0064 | 2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.790-6535C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143782380 | ||||||
chr8:143782454
|
GCTTA | G | 146 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.790-6457_790-6454d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143782454 | |||||
chr8:143782665
|
C | T | 1 | a0005c0005t0001g0328 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.790-6250C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143782665 | ||||||
chr8:143782766
|
G | A | 1 | a0002c0002t0001g0261 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.790-6149G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143782766 | ||||||
chr8:143782971
|
T | A | 11 | a0001c0001t0001g0344a0006c0006t0001g0030a0006c0006t0001g0031others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.790-5944T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143782971 | ||||||
chr8:143782972
|
A | G | 5 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0067others(2): Show | 5 | NA18942.hp2 NA18951.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.790-5943A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143782972 | ||||||
chr8:143783134
|
A | G | 8 | a0003c0003t0001g0045a0003c0003t0001g0054a0003c0003t0001g0194others(5): Show | 8 | HG02922.hp2 HG02965.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.790-5781A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783134 | ||||||
chr8:143783161
|
T | C | 2 | a0006c0006t0001g0030a0006c0006t0001g0031 | 2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.790-5754T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783161 | ||||||
chr8:143783171
|
T | C | 1 | a0003c0003t0001g0063 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.790-5744T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783171 | ||||||
chr8:143783304
|
T | G | 4 | a0001c0001t0001g0341a0011c0012t0001g0342a0011c0012t0001g0345others(1): Show | 4 | HG01175.hp1 HG03139.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-5611T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783304 | ||||||
chr8:143783433
|
CTGATT | C | 6 | a0007c0007t0001g0013a0007c0007t0001g0015a0007c0007t0001g0042others(3): Show | 6 | HG02145.hp1 HG02486.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.790-5480_790-5476d others(7): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143783433 | |||||
chr8:143783472
|
A | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0132 | 2 | HG01123.hp2 HG01891.hp2 |
intron_variant | MODIFIER | c.790-5443A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783472 | ||||||
chr8:143783479
|
A | G | 1 | a0007c0007t0001g0015 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.790-5436A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783479 | ||||||
chr8:143783524
|
C | G | 3 | a0009c0009t0001g0007a0009c0009t0001g0026a0009c0009t0001g0027 | 3 | HG01192.hp2 HG03453.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.790-5391C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783524 | ||||||
chr8:143783656
|
A | G | 3 | a0008c0008t0001g0238a0008c0008t0001g0239a0008c0008t0001g0240 | 3 | HG02647.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.790-5259A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783656 | ||||||
chr8:143783802
|
T | C | 1 | a0009c0009t0001g0027 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.790-5113T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783802 | ||||||
chr8:143783839
|
C | T | 1 | a0017c0016t0001g0237 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.790-5076C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783839 | ||||||
chr8:143783925
|
T | A | 124 | a0001c0001t0001g0136a0001c0001t0001g0153a0002c0002t0001g0001others(121): Show | 125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.790-4990T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143783925 | ||||||
chr8:143784005
|
C | T | 26 | a0001c0010t0001g0037a0001c0010t0001g0038a0001c0010t0001g0039others(23): Show | 26 | HG00733.hp2 HG01192.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.790-4910C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143784005 | ||||||
chr8:143784202
|
A | T | 2 | a0005c0005t0001g0328a0005c0005t0001g0329 | 2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.790-4713A>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143784202 | ||||||
chr8:143784295
|
T | A | 17 | a0003c0003t0001g0219a0003c0003t0001g0222a0003c0003t0001g0223others(14): Show | 17 | HG02258.hp1 HG02280.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.790-4620T>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143784295 | ||||||
chr8:143784613
|
A | G | 8 | a0001c0001t0001g0344a0007c0007t0001g0013a0007c0007t0001g0015others(5): Show | 8 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.790-4302A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143784613 | ||||||
chr8:143784709
|
A | C | 1 | a0012c0017t0001g0195 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.790-4206A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143784709 | ||||||
chr8:143784748
|
AACACTTC others(1): Show |
A | 124 | a0001c0001t0001g0136a0001c0001t0001g0153a0002c0002t0001g0001others(121): Show | 125 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(122): Show |
intron_variant | MODIFIER | c.790-4164_790-4157d others(10): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143784748 | |||||
chr8:143784948
|
A | G | 3 | a0003c0003t0001g0234a0003c0003t0001g0235a0003c0003t0001g0241 | 3 | HG01975.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.790-3967A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143784948 | ||||||
chr8:143785107
|
CTCTT | C | 23 | a0003c0003t0001g0032a0003c0003t0001g0033a0003c0003t0001g0034others(20): Show | 23 | HG02258.hp1 HG02280.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.790-3806_790-3803d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143785107 | |||||
chr8:143785118
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.790-3797C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143785118 | ||||||
chr8:143785253
|
C | CT | 7 | a0003c0003t0001g0069a0003c0003t0001g0236a0006c0006t0001g0030others(4): Show | 7 | HG01175.hp1 HG02257.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.790-3641dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143785253 | |||||
chr8:143785253
|
CT | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.790-3641delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143785253 | |||||
chr8:143785253
|
CTT | C | 126 | a0001c0001t0001g0119a0001c0001t0001g0146a0001c0001t0001g0153others(123): Show | 127 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.790-3642_790-3641d others(4): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143785253 | |||||
chr8:143785253
|
CTTT | C | 7 | a0001c0001t0001g0096a0002c0002t0001g0249a0002c0002t0001g0277others(4): Show | 7 | HG02040.hp1 NA18948.hp2 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.790-3643_790-3641d others(5): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143785253 | |||||
chr8:143785466
|
G | C | 8 | a0001c0001t0001g0344a0007c0007t0001g0013a0007c0007t0001g0015others(5): Show | 8 | HG02145.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.790-3449G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143785466 | ||||||
chr8:143785513
|
C | T | 1 | a0003c0003t0001g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.790-3402C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143785513 | ||||||
chr8:143785725
|
A | AT | 153 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(150): Show | 153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.790-3175dupT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143785725 | |||||
chr8:143785725
|
AT | A | 38 | a0002c0002t0001g0251a0002c0002t0001g0252a0002c0002t0001g0253others(35): Show | 38 | HG02258.hp1 HG02280.hp1 HG02280.hp2 others(35): Show |
intron_variant | MODIFIER | c.790-3175delT | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143785725 | |||||
chr8:143785874
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.790-3041G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143785874 | ||||||
chr8:143785985
|
A | G | 4 | a0001c0001t0001g0139a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG02040.hp2 HG02132.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-2930A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143785985 | ||||||
chr8:143786115
|
A | G | 346 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(343): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.790-2800A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786115 | ||||||
chr8:143786196
|
A | G | 31 | a0001c0001t0001g0242a0001c0010t0001g0037a0001c0010t0001g0038others(28): Show | 31 | HG00099.hp1 HG00733.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.790-2719A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786196 | ||||||
chr8:143786266
|
C | T | 2 | a0004c0004t0001g0050a0004c0004t0001g0160 | 2 | HG01074.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.790-2649C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786266 | ||||||
chr8:143786411
|
C | T | 2 | a0003c0003t0001g0063a0012c0017t0001g0064 | 2 | HG02647.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.790-2504C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786411 | ||||||
chr8:143786451
|
A | C | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.790-2464A>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786451 | ||||||
chr8:143786456
|
T | G | 1 | a0029c0032t0001g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.790-2459T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786456 | ||||||
chr8:143786577
|
G | A | 2 | a0002c0002t0001g0267a0002c0002t0001g0295 | 2 | HG01346.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.790-2338G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786577 | ||||||
chr8:143786594
|
C | A | 2 | a0009c0009t0001g0012a0009c0009t0001g0024 | 2 | HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.790-2321C>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786594 | ||||||
chr8:143786798
|
T | G | 1 | a0002c0002t0001g0249 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.790-2117T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786798 | ||||||
chr8:143786812
|
T | G | 32 | a0001c0001t0001g0243a0003c0003t0001g0010a0003c0003t0001g0016others(29): Show | 32 | HG02055.hp1 HG02280.hp2 HG02300.hp2 others(29): Show |
intron_variant | MODIFIER | c.790-2103T>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786812 | ||||||
chr8:143786816
|
G | A | 1 | a0030c0021t0001g0338 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.790-2099G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786816 | ||||||
chr8:143786827
|
C | T | 79 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0070others(76): Show | 79 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.790-2088C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786827 | ||||||
chr8:143786838
|
T | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0051others(203): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.790-2077T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786838 | ||||||
chr8:143786970
|
G | A | 15 | a0001c0001t0001g0243a0003c0003t0001g0069a0005c0005t0001g0288others(12): Show | 15 | HG01109.hp1 HG01175.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.790-1945G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143786970 | ||||||
chr8:143787114
|
G | GGGTTTGT others(6): Show |
1 | a0002c0002t0001g0287 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.790-1800_790-1788d others(15): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143787114 | |||||
chr8:143787141
|
C | T | 26 | a0001c0001t0001g0242a0003c0003t0001g0032a0003c0003t0001g0033others(23): Show | 26 | HG01192.hp2 HG01884.hp1 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.790-1774C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787141 | ||||||
chr8:143787177
|
GGGTC | G | 203 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049others(200): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.790-1733_790-1730d others(6): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr8 | 143787177 | |||||
chr8:143787372
|
G | A | 5 | a0007c0007t0001g0042a0007c0007t0001g0043a0007c0007t0001g0044others(2): Show | 5 | HG02145.hp1 HG02258.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.790-1543G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787372 | ||||||
chr8:143787381
|
T | C | 3 | a0001c0001t0001g0145a0002c0002t0001g0264a0002c0002t0001g0275 | 3 | HG00609.hp1 NA18952.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.790-1534T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787381 | ||||||
chr8:143787416
|
C | T | 348 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0047others(345): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.790-1499C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787416 | ||||||
chr8:143787488
|
G | T | 1 | a0002c0002t0001g0249 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.790-1427G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787488 | ||||||
chr8:143787627
|
G | C | 5 | a0011c0012t0001g0342a0011c0012t0001g0345a0011c0012t0001g0347others(2): Show | 5 | HG01109.hp1 HG01175.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.790-1288G>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787627 | ||||||
chr8:143787665
|
G | A | 2 | a0003c0003t0001g0010a0003c0003t0001g0011 | 2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.790-1250G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787665 | ||||||
chr8:143787692
|
C | G | 1 | a0001c0001t0001g0145 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.790-1223C>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787692 | ||||||
chr8:143787827
|
C | T | 1 | a0011c0012t0001g0342 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.790-1088C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787827 | ||||||
chr8:143787846
|
G | A | 2 | a0012c0017t0001g0064a0012c0017t0001g0195 | 2 | NA18906.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.790-1069G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787846 | ||||||
chr8:143787872
|
C | T | 334 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(331): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.790-1043C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787872 | ||||||
chr8:143787940
|
A | G | 332 | a0001c0001t0001g0002a0001c0001t0001g0047a0001c0001t0001g0048others(329): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.790-975A>G | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143787940 | ||||||
chr8:143788008
|
C | T | 1 | a0004c0004t0001g0173 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.790-907C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143788008 | ||||||
chr8:143788365
|
C | T | 172 | a0001c0001t0001g0055a0001c0001t0001g0061a0001c0001t0001g0066others(169): Show | 173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.790-550C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143788365 | ||||||
chr8:143788374
|
T | C | 3 | a0006c0006t0001g0030a0006c0006t0001g0031a0012c0017t0001g0064 | 3 | HG02257.hp2 HG03471.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.790-541T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143788374 | ||||||
chr8:143788483
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.790-432T>C | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143788483 | ||||||
chr8:143788516
|
G | A | 1 | a0003c0003t0001g0028 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.790-399G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143788516 | ||||||
chr8:143788531
|
G | A | 48 | a0004c0004t0001g0050a0004c0004t0001g0071a0004c0004t0001g0072others(45): Show | 48 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.790-384G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143788531 | ||||||
chr8:143788577
|
C | T | 1 | a0001c0001t0001g0344 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.790-338C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143788577 | ||||||
chr8:143788636
|
G | T | 1 | a0001c0001t0001g0344 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.790-279G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 7/13 | chr8 | 143788636 | ||||||
chr8:143789080
|
A | AGGTGCTG others(6): Show |
1 | a0002c0002t0001g0272 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.938+27_938+39dupGA others(11): Show |
IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr8 | 143789080 | |||||
chr8:143789134
|
G | T | 1 | a0012c0017t0001g0064 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.939-55G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 8/13 | chr8 | 143789134 | ||||||
chr8:143789147
|
C | T | 1 | a0003c0003t0001g0035 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.939-42C>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 8/13 | chr8 | 143789147 | ||||||
chr8:143789148
|
G | A | 11 | a0001c0001t0001g0046a0001c0001t0001g0065a0001c0001t0001g0095others(8): Show | 11 | HG00733.hp2 HG01884.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.939-41G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 8/13 | chr8 | 143789148 | ||||||
chr8:143789891
|
G | A | 1 | a0003c0003t0001g0034 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1195+22G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 11/13 | chr8 | 143789891 | ||||||
chr8:143789924
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1196-47G>A | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 11/13 | chr8 | 143789924 | ||||||
chr8:143789936
|
G | T | 1 | a0001c0001t0001g0090 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1196-35G>T | IQANK1 | ENSG00000203499.12 | transcript | ENST00000527139.7 | protein_coding | 11/13 | chr8 | 143789936 |