geneid | 54517 |
---|---|
ensemblid | ENSG00000091127.14 |
hgncid | 26033 |
symbol | PUS7 |
name | pseudouridine synthase 7 |
refseq_nuc | NM_019042.5 |
refseq_prot | NP_061915.2 |
ensembl_nuc | ENST00000469408.6 |
ensembl_prot | ENSP00000417402.1 |
mane_status | MANE Select |
chr | chr7 |
start | 105456503 |
end | 105522271 |
strand | - |
ver | v1.2 |
region | chr7:105456503-105522271 |
region5000 | chr7:105451503-105527271 |
regionname0 | PUS7_chr7_105456503_105522271 |
regionname5000 | PUS7_chr7_105451503_105527271 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 661 | 348 | 92 | 62 | 136 | 14 | 42 | 97 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0002 | 0/0 | 661 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0003 | 0/0 | 661 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1986 | 332 | 83 | 62 | 130 | 13 | 42 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
c0002 | 0/0 | 1986 | 5 | 0 | 0 | 5 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
c0003 | 0/0 | 1986 | 4 | 3 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
c0004 | 0/0 | 1986 | 4 | 4 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
c0005 | 0/0 | 1986 | 2 | 2 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
c0006 | 0/0 | 1986 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
c0007 | 0/0 | 1986 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
c0008 | 0/0 | 1986 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
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 | 1/1 | 1540 | 264 | 60 | 48 | 121 | 7 | 26 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
t0002 | 0/0 | 1540 | 29 | 3 | 10 | 4 | 5 | 7 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
t0003 | 0/0 | 1540 | 19 | 15 | 2 | 0 | 2 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
t0004 | 0/0 | 1540 | 15 | 1 | 0 | 10 | 0 | 4 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
t0005 | 0/0 | 1540 | 4 | 4 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
t0006 | 0/0 | 1540 | 3 | 0 | 2 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
t0007 | 0/0 | 1540 | 2 | 2 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
t0008 | 0/0 | 1540 | 2 | 0 | 0 | 0 | 0 | 2 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
t0009 | 0/0 | 1540 | 2 | 2 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
t0010 | 0/0 | 1540 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
t0011 | 0/0 | 1540 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
t0012 | 0/0 | 1540 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
t0013 | 0/0 | 1540 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
t0014 | 0/0 | 1540 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
t0015 | 0/0 | 1540 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
t0016 | 0/0 | 1540 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
t0017 | 0/0 | 1540 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
t0018 | 0/0 | 1540 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
t0019 | 0/0 | 1540 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
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 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0002 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0014 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1986 | 332 | 83 | 62 | 130 | 13 | 42 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0002 | 0/0 | 1986 | 5 | 0 | 0 | 5 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0003 | 0/0 | 1986 | 4 | 3 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0004 | 0/0 | 1986 | 4 | 4 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0005 | 0/0 | 1986 | 2 | 2 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0007 | 0/0 | 1986 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0002c0008 | 0/0 | 1986 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0003c0006 | 0/0 | 1986 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3525 | 251 | 54 | 48 | 114 | 7 | 26 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0001t0002 | 0/0 | 3525 | 29 | 3 | 10 | 4 | 5 | 7 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0001t0003 | 0/0 | 3525 | 15 | 12 | 2 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0001t0004 | 0/0 | 3525 | 15 | 1 | 0 | 10 | 0 | 4 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0001t0005 | 0/0 | 3525 | 4 | 4 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0001t0006 | 0/0 | 3525 | 3 | 0 | 2 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0001t0007 | 0/0 | 3525 | 2 | 2 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0001t0008 | 0/0 | 3525 | 2 | 0 | 0 | 0 | 0 | 2 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0001t0009 | 0/0 | 3525 | 2 | 2 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0001t0010 | 0/0 | 3525 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0001t0011 | 0/0 | 3525 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0001t0012 | 0/0 | 3525 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0001t0014 | 0/0 | 3525 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0001t0015 | 0/0 | 3525 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0001t0016 | 0/0 | 3525 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0001t0017 | 0/0 | 3525 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0001t0018 | 0/0 | 3525 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0001t0019 | 0/0 | 3525 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0002t0001 | 0/0 | 3525 | 4 | 0 | 0 | 4 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0002t0013 | 0/0 | 3525 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0003t0003 | 0/0 | 3525 | 4 | 3 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0004t0001 | 0/0 | 3525 | 4 | 4 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0005t0001 | 0/0 | 3525 | 2 | 2 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0001c0007t0001 | 0/0 | 3525 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0002c0008t0001 | 0/0 | 3525 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
a0003c0006t0001 | 0/0 | 3525 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | copy fasta | chr7 | 105451503 | 105527271 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0002 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0014 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0003g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0004g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0004g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0004g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0004g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0004g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0004g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0004g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0004g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0004g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0004g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0004g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0006g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0006g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0006g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0007g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0007g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0008g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0008g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0009g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0009g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0010g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0011g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0012g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0014g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0015g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0016g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0017g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0018g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0001t0019g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0002t0013g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0003t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0003t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0003t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0003t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0004t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0004t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0004t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0004t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0005t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0005t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0001c0007t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0002c0008t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
a0003c0006t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | GBR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0319 | EUR | GBR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0182 | EUR | FIN | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00423 | hp1 | a0002 | c0008 | t0001 | g0135 | EAS | CHS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | CHS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00597 | hp2 | a0001 | c0001 | t0004 | g0339 | EAS | CHS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00609 | hp1 | a0001 | c0001 | t0004 | g0343 | EAS | CHS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0005 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0318 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01070 | hp2 | a0001 | c0001 | t0006 | g0346 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01071 | hp1 | a0001 | c0001 | t0006 | g0347 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0301 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0237 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0310 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | CLM | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0306 | AMR | CLM | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | CLM | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | CLM | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | IBS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0323 | EUR | IBS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | IBS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | IBS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0215 | EUR | IBS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0304 | EUR | IBS | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01884 | hp1 | a0001 | c0001 | t0005 | g0285 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01891 | hp2 | a0001 | c0003 | t0003 | g0268 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0326 | AMR | PEL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0327 | AMR | PEL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PEL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0322 | AMR | PEL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0320 | AMR | PEL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0341 | EAS | KHV | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | KHV | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02055 | hp1 | a0001 | c0005 | t0001 | g0040 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | KHV | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02074 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | KHV | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | KHV | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | KHV | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02135 | hp2 | a0001 | c0001 | t0004 | g0342 | EAS | KHV | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0308 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02145 | hp2 | a0001 | c0001 | t0018 | g0331 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CDX | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0340 | EAS | CDX | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CDX | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0066 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02280 | hp2 | a0001 | c0004 | t0001 | g0093 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0055 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02647 | hp1 | a0001 | c0003 | t0003 | g0221 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0315 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02717 | hp1 | a0001 | c0001 | t0014 | g0239 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02723 | hp2 | a0001 | c0001 | t0011 | g0063 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02735 | hp1 | a0001 | c0001 | t0004 | g0335 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0334 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02809 | hp2 | a0001 | c0003 | t0003 | g0219 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02895 | hp1 | a0001 | c0001 | t0009 | g0068 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0029 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02897 | hp2 | a0001 | c0001 | t0009 | g0069 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ESN | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02965 | hp2 | a0001 | c0005 | t0001 | g0041 | AFR | ESN | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0289 | AFR | ESN | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ESN | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0350 | AFR | MSL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | MSL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0269 | AFR | MSL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03225 | hp2 | a0001 | c0004 | t0001 | g0294 | AFR | MSL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | MSL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0052 | AFR | MSL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | MSL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0321 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | ESN | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0223 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | GWD | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | MSL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03654 | hp1 | a0001 | c0001 | t0008 | g0154 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0307 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | STU | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03831 | hp1 | a0001 | c0001 | t0017 | g0330 | SAS | BEB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03831 | hp2 | a0001 | c0001 | t0006 | g0344 | SAS | BEB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0303 | SAS | BEB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | BEB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | BEB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0325 | SAS | BEB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | STU | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG04115 | hp2 | a0001 | c0001 | t0016 | g0311 | SAS | STU | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG04184 | hp2 | a0001 | c0001 | t0004 | g0349 | SAS | BEB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG04199 | hp1 | a0001 | c0001 | t0008 | g0293 | SAS | STU | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | STU | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | STU | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0329 | SAS | STU | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG04228 | hp2 | a0001 | c0001 | t0004 | g0336 | SAS | STU | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18522 | hp1 | a0001 | c0004 | t0001 | g0081 | AFR | YRI | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0232 | AFR | YRI | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18906 | hp1 | a0001 | c0001 | t0007 | g0233 | AFR | YRI | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | YRI | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18946 | hp1 | a0001 | c0001 | t0004 | g0337 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18956 | hp1 | a0001 | c0001 | t0004 | g0345 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18963 | hp2 | a0001 | c0007 | t0001 | g0123 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18969 | hp1 | a0001 | c0002 | t0013 | g0140 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18977 | hp2 | a0003 | c0006 | t0001 | g0098 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18989 | hp2 | a0001 | c0001 | t0004 | g0338 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | LWK | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | LWK | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19062 | hp2 | a0001 | c0001 | t0004 | g0348 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0333 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19068 | hp2 | a0001 | c0001 | t0012 | g0126 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19075 | hp2 | a0001 | c0001 | t0015 | g0299 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | ASW | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ASW | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | TSI | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0317 | EUR | TSI | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA20805 | hp1 | a0001 | c0003 | t0003 | g0288 | EUR | TSI | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0312 | EUR | TSI | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0314 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | USA | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
HG06807 | hp2 | a0001 | c0001 | t0019 | g0332 | AFR | USA | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | USA | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | USA | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | LWK | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
NA21309 | hp2 | a0001 | c0004 | t0001 | g0082 | AFR | LWK | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0002 | REF | REF | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0014 | REF | REF | PUS7_chr7_105451503_105527271 | PUS7 | chr7 | 105451503 | 105527271 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:105506007
|
C | T | 1 | a0003 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.533G>A | p.Arg178Gln | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/16 | 785/3525 | 533/1986 | 178/661 | chr7 | 105506007 | ||
chr7:105508434
|
C | A | 1 | a0002 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.79G>T | p.Val27Phe | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/16 | 331/3525 | 79/1986 | 27/661 | chr7 | 105508434 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:105465350
|
G | A | 1 | a0001c0007 | 1 | NA18963.hp2 | synonymous_variant | LOW | c.1590C>T | p.Pro530Pro | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/16 | 1842/3525 | 1590/1986 | 530/661 | chr7 | 105465350 | ||
chr7:105470697
|
T | C | 1 | a0001c0003 | 4 | HG01891.hp2 HG02647.hp1 HG02809.hp2 others(1): Show |
synonymous_variant | LOW | c.1389A>G | p.Ala463Ala | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/16 | 1641/3525 | 1389/1986 | 463/661 | chr7 | 105470697 | ||
chr7:105470772
|
T | C | 2 | a0001c0004a0001c0005 | 6 | HG02055.hp1 HG02280.hp2 HG02965.hp2 others(3): Show |
synonymous_variant | LOW | c.1314A>G | p.Leu438Leu | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/16 | 1566/3525 | 1314/1986 | 438/661 | chr7 | 105470772 | ||
chr7:105495156
|
G | A | 1 | a0001c0002 | 5 | HG02074.hp1 NA18963.hp1 NA18969.hp1 others(2): Show |
synonymous_variant | LOW | c.828C>T | p.Leu276Leu | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/16 | 1080/3525 | 828/1986 | 276/661 | chr7 | 105495156 | ||
chr7:105495168
|
A | G | 1 | a0001c0005 | 2 | HG02055.hp1 HG02965.hp2 |
synonymous_variant | LOW | c.816T>C | p.Ala272Ala | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/16 | 1068/3525 | 816/1986 | 272/661 | chr7 | 105495168 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:105456828
|
C | G | 3 | a0001c0001t0003a0001c0001t0017a0001c0003t0003 | 20 | HG00280.hp1 HG00642.hp1 HG01106.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*962G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 16/16 | 962 | chr7 | 105456828 | |||||
chr7:105456898
|
G | A | 1 | a0001c0001t0011 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*892C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 16/16 | 892 | chr7 | 105456898 | |||||
chr7:105456911
|
C | T | 1 | a0001c0002t0013 | 1 | NA18969.hp1 | 3_prime_UTR_variant | MODIFIER | c.*879G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 16/16 | 879 | chr7 | 105456911 | |||||
chr7:105456991
|
C | T | 1 | a0001c0001t0012 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*799G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 16/16 | 799 | chr7 | 105456991 | |||||
chr7:105457003
|
C | T | 1 | a0001c0001t0016 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*787G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 16/16 | 787 | chr7 | 105457003 | |||||
chr7:105457036
|
T | C | 1 | a0001c0001t0009 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*754A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 16/16 | 754 | chr7 | 105457036 | |||||
chr7:105457077
|
A | C | 1 | a0001c0001t0005 | 4 | HG01884.hp1 HG02572.hp2 HG02622.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*713T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 16/16 | 713 | chr7 | 105457077 | |||||
chr7:105457088
|
T | C | 1 | a0001c0001t0008 | 2 | HG03654.hp1 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*702A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 16/16 | 702 | chr7 | 105457088 | |||||
chr7:105457336
|
G | A | 1 | a0001c0001t0009 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*454C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 16/16 | 454 | chr7 | 105457336 | |||||
chr7:105457356
|
C | T | 1 | a0001c0001t0007 | 2 | NA18522.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*434G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 16/16 | 434 | chr7 | 105457356 | |||||
chr7:105457427
|
A | G | 1 | a0001c0001t0011 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*363T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 16/16 | 363 | chr7 | 105457427 | |||||
chr7:105457471
|
T | C | 1 | a0001c0001t0006 | 3 | HG01070.hp2 HG01071.hp1 HG03831.hp2 |
3_prime_UTR_variant | MODIFIER | c.*319A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 16/16 | 319 | chr7 | 105457471 | |||||
chr7:105457595
|
T | G | 1 | a0001c0001t0014 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*195A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 16/16 | 195 | chr7 | 105457595 | |||||
chr7:105457785
|
A | G | 1 | a0001c0001t0010 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 16/16 | 5 | chr7 | 105457785 | |||||
chr7:105522066
|
C | T | 1 | a0001c0001t0019 | 1 | HG06807.hp2 | 5_prime_UTR_variant | MODIFIER | c.-47G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/16 | 13554 | chr7 | 105522066 | |||||
chr7:105522092
|
G | A | 1 | a0001c0001t0015 | 1 | NA19075.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-73C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/16 | chr7 | 105522092 | ||||||
chr7:105522115
|
G | C | 3 | a0001c0001t0002a0001c0001t0016a0001c0001t0017 | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-96C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/16 | 13603 | chr7 | 105522115 | |||||
chr7:105522182
|
T | G | 3 | a0001c0001t0002a0001c0001t0016a0001c0001t0017 | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-163A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/16 | 13670 | chr7 | 105522182 | |||||
chr7:105522191
|
G | C | 3 | a0001c0001t0002a0001c0001t0016a0001c0001t0017 | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
5_prime_UTR_variant | MODIFIER | c.-172C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/16 | 13679 | chr7 | 105522191 | |||||
chr7:105522222
|
G | C | 1 | a0001c0001t0018 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-203C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/16 | 13710 | chr7 | 105522222 | |||||
chr7:105522260
|
C | A | 3 | a0001c0001t0004a0001c0001t0006a0001c0001t0019 | 19 | HG00597.hp2 HG00609.hp1 HG01070.hp2 others(16): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-241G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/16 | chr7 | 105522260 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:105458030
|
C | T | 4 | a0001c0001t0005g0036a0001c0001t0005g0055a0001c0001t0005g0223others(1): Show | 4 | HG01884.hp1 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1850-104G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 15/15 | chr7 | 105458030 | ||||||
chr7:105458351
|
C | G | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG01074.hp2 HG01175.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1850-425G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 15/15 | chr7 | 105458351 | ||||||
chr7:105458404
|
G | A | 1 | a0001c0001t0004g0336 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1850-478C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 15/15 | chr7 | 105458404 | ||||||
chr7:105458419
|
C | A | 3 | a0001c0001t0001g0261a0001c0001t0001g0282a0001c0001t0004g0333 | 3 | NA18992.hp2 NA19064.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1850-493G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 15/15 | chr7 | 105458419 | ||||||
chr7:105458456
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1850-530C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 15/15 | chr7 | 105458456 | ||||||
chr7:105458518
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1850-592G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 15/15 | chr7 | 105458518 | ||||||
chr7:105458549
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1849+619C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 15/15 | chr7 | 105458549 | ||||||
chr7:105458571
|
A | AT | 8 | a0001c0001t0001g0065a0001c0001t0001g0218a0001c0001t0001g0241others(5): Show | 8 | HG02109.hp2 HG02132.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.1849+596dupA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 15/15 | chr7 | 105458571 | ||||||
chr7:105458650
|
A | G | 1 | a0001c0001t0001g0161 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1849+518T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 15/15 | chr7 | 105458650 | ||||||
chr7:105458718
|
A | C | 347 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(344): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1849+450T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 15/15 | chr7 | 105458718 | ||||||
chr7:105458735
|
G | A | 3 | a0001c0001t0001g0150a0001c0001t0001g0161a0001c0001t0004g0337 | 3 | HG02027.hp1 NA18946.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.1849+433C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 15/15 | chr7 | 105458735 | ||||||
chr7:105458804
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0002g0305 | 2 | HG02056.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1849+364C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 15/15 | chr7 | 105458804 | ||||||
chr7:105458807
|
C | T | 1 | a0001c0001t0003g0269 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1849+361G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 15/15 | chr7 | 105458807 | ||||||
chr7:105458858
|
C | G | 347 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(344): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1849+310G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 15/15 | chr7 | 105458858 | ||||||
chr7:105458908
|
G | C | 2 | a0001c0001t0009g0068a0001c0001t0009g0069 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1849+260C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 15/15 | chr7 | 105458908 | ||||||
chr7:105459281
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1758-22T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105459281 | ||||||
chr7:105459439
|
A | AT | 19 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0118others(16): Show | 19 | HG01934.hp1 HG02027.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.1758-181dupA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105459439 | ||||||
chr7:105459439
|
AT | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0062others(6): Show | 9 | HG01256.hp2 HG01496.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1758-181delA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105459439 | ||||||
chr7:105459498
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0054a0001c0001t0010g0289 | 3 | HG02055.hp2 HG02970.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1758-239A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105459498 | ||||||
chr7:105459506
|
T | C | 1 | a0001c0001t0002g0309 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1758-247A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105459506 | ||||||
chr7:105459689
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1758-430G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105459689 | ||||||
chr7:105459835
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0001g0270 | 2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1758-576C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105459835 | ||||||
chr7:105459992
|
G | A | 9 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0014g0239others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1758-733C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105459992 | ||||||
chr7:105460032
|
G | A | 1 | a0001c0001t0001g0144 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1758-773C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460032 | ||||||
chr7:105460064
|
G | A | 9 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0014g0239others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1758-805C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460064 | ||||||
chr7:105460097
|
C | T | 4 | a0001c0001t0001g0088a0001c0001t0001g0095a0001c0001t0001g0096others(1): Show | 4 | HG02074.hp2 HG02083.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.1758-838G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460097 | ||||||
chr7:105460132
|
G | A | 3 | a0001c0001t0001g0086a0001c0001t0001g0220a0001c0001t0004g0350 | 3 | HG00738.hp1 HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1758-873C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460132 | ||||||
chr7:105460170
|
G | C | 347 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(344): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1758-911C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460170 | ||||||
chr7:105460206
|
G | C | 4 | a0001c0001t0001g0086a0001c0001t0001g0155a0001c0001t0001g0220others(1): Show | 4 | HG00639.hp2 HG00738.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1758-947C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460206 | ||||||
chr7:105460307
|
C | T | 315 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(312): Show | 315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1758-1048G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460307 | ||||||
chr7:105460506
|
C | T | 12 | a0001c0001t0001g0120a0001c0001t0001g0141a0001c0001t0001g0142others(9): Show | 12 | HG01975.hp2 HG01978.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.1758-1247G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460506 | ||||||
chr7:105460552
|
A | C | 2 | a0001c0001t0001g0238a0001c0001t0001g0270 | 2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1758-1293T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460552 | ||||||
chr7:105460629
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1758-1370G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460629 | ||||||
chr7:105460630
|
G | A | 8 | a0001c0001t0001g0062a0001c0001t0001g0073a0001c0001t0001g0094others(5): Show | 8 | HG02976.hp2 HG04184.hp2 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.1758-1371C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460630 | ||||||
chr7:105460630
|
G | T | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(16): Show | 19 | HG01074.hp2 HG01175.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.1758-1371C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460630 | ||||||
chr7:105460689
|
C | A | 1 | a0001c0001t0001g0125 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1758-1430G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460689 | ||||||
chr7:105460723
|
G | A | 20 | a0001c0001t0001g0083a0001c0001t0001g0198a0001c0001t0001g0199others(17): Show | 20 | HG00642.hp1 HG01106.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1758-1464C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460723 | ||||||
chr7:105460770
|
C | T | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(7): Show | 10 | NA18944.hp1 NA18945.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.1758-1511G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460770 | ||||||
chr7:105460772
|
C | T | 338 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(335): Show | 338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.1758-1513G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460772 | ||||||
chr7:105460802
|
C | T | 2 | a0001c0001t0009g0068a0001c0001t0009g0069 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1758-1543G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460802 | ||||||
chr7:105460849
|
G | A | 18 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0150others(15): Show | 18 | HG01934.hp1 HG02027.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.1758-1590C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460849 | ||||||
chr7:105460853
|
C | CA | 22 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0035others(19): Show | 22 | HG01106.hp1 HG01255.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1758-1595dupT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460853 | ||||||
chr7:105460853
|
C | CAA | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1758-1596_1758-159 others(6): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460853 | ||||||
chr7:105460853
|
C | CAAA | 45 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0022others(42): Show | 45 | HG00438.hp1 HG00438.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.1758-1597_1758-159 others(7): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460853 | ||||||
chr7:105460853
|
CA | C | 20 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0065others(17): Show | 20 | HG01433.hp1 HG01934.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.1758-1595delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460853 | ||||||
chr7:105460889
|
A | T | 2 | a0001c0001t0001g0101a0001c0001t0001g0172 | 2 | HG01192.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1758-1630T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460889 | ||||||
chr7:105460899
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0001g0270 | 2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1758-1640C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460899 | ||||||
chr7:105460928
|
C | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0270 | 2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1758-1669G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460928 | ||||||
chr7:105460983
|
T | C | 9 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0047others(6): Show | 9 | HG02055.hp2 HG02451.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1757+1638A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105460983 | ||||||
chr7:105461064
|
G | C | 1 | a0001c0001t0001g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1757+1557C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105461064 | ||||||
chr7:105461130
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1757+1491T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105461130 | ||||||
chr7:105461421
|
A | C | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(321): Show | 324 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1757+1200T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105461421 | ||||||
chr7:105461468
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1757+1153C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105461468 | ||||||
chr7:105461489
|
G | A | 5 | a0001c0001t0001g0153a0001c0001t0002g0304a0001c0001t0002g0306others(2): Show | 5 | HG01256.hp1 HG01515.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1757+1132C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105461489 | ||||||
chr7:105461584
|
G | A | 347 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(344): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1757+1037C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105461584 | ||||||
chr7:105461586
|
A | G | 20 | a0001c0001t0001g0083a0001c0001t0001g0198a0001c0001t0001g0199others(17): Show | 20 | HG00642.hp1 HG01106.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1757+1035T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105461586 | ||||||
chr7:105461709
|
C | T | 5 | a0001c0001t0003g0005a0001c0003t0003g0219a0001c0003t0003g0221others(2): Show | 5 | HG00642.hp1 HG01891.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1757+912G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105461709 | ||||||
chr7:105461821
|
T | C | 2 | a0001c0001t0001g0278a0001c0001t0001g0283 | 2 | HG01168.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1757+800A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105461821 | ||||||
chr7:105461844
|
G | A | 9 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0014g0239others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1757+777C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105461844 | ||||||
chr7:105461882
|
A | T | 18 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0150others(15): Show | 18 | HG01934.hp1 HG02027.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.1757+739T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105461882 | ||||||
chr7:105461986
|
G | A | 294 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(291): Show | 294 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.1757+635C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105461986 | ||||||
chr7:105462057
|
GAAAAGAA others(8): Show |
G | 18 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0150others(15): Show | 18 | HG01934.hp1 HG02027.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.1757+549_1757+563d others(17): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105462057 | ||||||
chr7:105462103
|
GGAAAA | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1757+513_1757+517d others(7): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105462103 | ||||||
chr7:105462168
|
G | C | 9 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0014g0239others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1757+453C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105462168 | ||||||
chr7:105462171
|
C | T | 1 | a0001c0001t0003g0005 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1757+450G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105462171 | ||||||
chr7:105462184
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1757+437G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105462184 | ||||||
chr7:105462303
|
G | A | 3 | a0001c0001t0001g0241a0001c0001t0003g0053a0001c0001t0003g0240 | 3 | HG02109.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1757+318C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105462303 | ||||||
chr7:105462347
|
G | A | 9 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0014g0239others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1757+274C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105462347 | ||||||
chr7:105462350
|
T | C | 304 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(301): Show | 304 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.1757+271A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105462350 | ||||||
chr7:105462378
|
G | C | 3 | a0001c0001t0001g0261a0001c0001t0001g0282a0001c0001t0004g0333 | 3 | NA18992.hp2 NA19064.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1757+243C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105462378 | ||||||
chr7:105462426
|
G | A | 3 | a0001c0004t0001g0081a0001c0004t0001g0082a0001c0004t0001g0093 | 3 | HG02280.hp2 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1757+195C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105462426 | ||||||
chr7:105462430
|
CA | C | 9 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0014g0239others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1757+190delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105462430 | ||||||
chr7:105462441
|
C | CA | 26 | a0001c0001t0001g0043a0001c0001t0001g0054a0001c0001t0001g0083others(23): Show | 26 | HG00642.hp1 HG01106.hp2 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.1757+179dupT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105462441 | ||||||
chr7:105462441
|
C | CAA | 18 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0150others(15): Show | 18 | HG01934.hp1 HG02027.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.1757+178_1757+179d others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105462441 | ||||||
chr7:105462451
|
A | C | 1 | a0001c0001t0005g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1757+170T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105462451 | ||||||
chr7:105462551
|
T | C | 3 | a0001c0004t0001g0294a0001c0005t0001g0040a0001c0005t0001g0041 | 3 | HG02055.hp1 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1757+70A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105462551 | ||||||
chr7:105462577
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1757+44A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 14/15 | chr7 | 105462577 | ||||||
chr7:105462916
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1628-166T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105462916 | ||||||
chr7:105462925
|
C | G | 29 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(26): Show | 29 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1628-175G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105462925 | ||||||
chr7:105462958
|
G | C | 2 | a0001c0001t0001g0260a0001c0001t0004g0339 | 2 | HG00597.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1628-208C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105462958 | ||||||
chr7:105463082
|
A | G | 1 | a0001c0001t0001g0255 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1628-332T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105463082 | ||||||
chr7:105463211
|
T | G | 1 | a0001c0001t0004g0333 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1628-461A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105463211 | ||||||
chr7:105463429
|
A | T | 1 | a0001c0001t0008g0154 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1628-679T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105463429 | ||||||
chr7:105463460
|
T | C | 3 | a0001c0001t0001g0241a0001c0001t0003g0053a0001c0001t0003g0240 | 3 | HG02109.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1628-710A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105463460 | ||||||
chr7:105463607
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1628-857C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105463607 | ||||||
chr7:105463633
|
C | G | 2 | a0001c0001t0001g0296a0001c0001t0002g0320 | 2 | HG01255.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1628-883G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105463633 | ||||||
chr7:105463645
|
CT | C | 334 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(331): Show | 334 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(331): Show |
intron_variant | MODIFIER | c.1628-896delA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105463645 | ||||||
chr7:105463645
|
CTT | C | 6 | a0001c0001t0001g0119a0001c0001t0004g0338a0001c0001t0014g0239others(3): Show | 6 | HG02055.hp1 HG02717.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1628-897_1628-896d others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105463645 | ||||||
chr7:105463647
|
T | C | 1 | a0001c0001t0001g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1628-897A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105463647 | ||||||
chr7:105463741
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1628-991A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105463741 | ||||||
chr7:105463832
|
C | T | 1 | a0001c0001t0001g0235 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1628-1082G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105463832 | ||||||
chr7:105463838
|
T | C | 1 | a0001c0001t0002g0313 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1628-1088A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105463838 | ||||||
chr7:105464033
|
T | C | 15 | a0001c0001t0001g0001a0001c0001t0001g0072a0001c0001t0001g0077others(12): Show | 15 | HG00735.hp2 HG00741.hp2 HG01192.hp2 others(12): Show |
intron_variant | MODIFIER | c.1627+1280A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105464033 | ||||||
chr7:105464223
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1627+1090A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105464223 | ||||||
chr7:105464241
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1627+1072A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105464241 | ||||||
chr7:105464245
|
CT | C | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1627+1067delA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105464245 | ||||||
chr7:105464328
|
A | C | 1 | a0001c0001t0001g0242 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1627+985T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105464328 | ||||||
chr7:105464361
|
G | C | 3 | a0001c0001t0001g0241a0001c0001t0003g0053a0001c0001t0003g0240 | 3 | HG02109.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1627+952C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105464361 | ||||||
chr7:105464526
|
C | T | 9 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0014g0239others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1627+787G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105464526 | ||||||
chr7:105464590
|
T | C | 1 | a0001c0001t0004g0336 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1627+723A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105464590 | ||||||
chr7:105464607
|
G | A | 1 | a0001c0001t0002g0318 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1627+706C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105464607 | ||||||
chr7:105464753
|
G | A | 2 | a0001c0001t0001g0238a0001c0001t0001g0270 | 2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1627+560C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105464753 | ||||||
chr7:105464813
|
C | CT | 37 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0150others(34): Show | 37 | HG00642.hp1 HG01106.hp2 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.1627+499dupA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105464813 | ||||||
chr7:105464813
|
CT | C | 6 | a0001c0001t0001g0169a0001c0001t0001g0185a0001c0001t0001g0241others(3): Show | 6 | HG02056.hp2 HG02109.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.1627+499delA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105464813 | ||||||
chr7:105464813
|
CTT | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(283): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.1627+498_1627+499d others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105464813 | ||||||
chr7:105464813
|
CTTT | C | 6 | a0001c0001t0001g0028a0001c0001t0001g0047a0001c0001t0001g0094others(3): Show | 6 | HG02451.hp1 HG02602.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1627+497_1627+499d others(5): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105464813 | ||||||
chr7:105464813
|
CTTTT | C | 9 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0014g0239others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1627+496_1627+499d others(6): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105464813 | ||||||
chr7:105464978
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1627+335G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105464978 | ||||||
chr7:105465038
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1627+275G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105465038 | ||||||
chr7:105465059
|
T | C | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG01074.hp2 HG01175.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.1627+254A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105465059 | ||||||
chr7:105465085
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1627+228A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105465085 | ||||||
chr7:105465099
|
A | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1627+214T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105465099 | ||||||
chr7:105465119
|
G | C | 3 | a0001c0001t0001g0241a0001c0001t0003g0053a0001c0001t0003g0240 | 3 | HG02109.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1627+194C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 13/15 | chr7 | 105465119 | ||||||
chr7:105465558
|
T | C | 347 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(344): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1526-144A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105465558 | ||||||
chr7:105465571
|
A | G | 347 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(344): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1526-157T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105465571 | ||||||
chr7:105465628
|
T | G | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1526-214A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105465628 | ||||||
chr7:105465748
|
G | A | 1 | a0001c0001t0001g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1526-334C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105465748 | ||||||
chr7:105465764
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1526-350G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105465764 | ||||||
chr7:105465773
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1526-359G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105465773 | ||||||
chr7:105465978
|
C | T | 5 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0153others(2): Show | 5 | NA18959.hp2 NA18965.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1526-564G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105465978 | ||||||
chr7:105466024
|
G | A | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(270): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1526-610C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105466024 | ||||||
chr7:105466110
|
A | C | 295 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(292): Show | 295 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.1526-696T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105466110 | ||||||
chr7:105466126
|
C | G | 22 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(19): Show | 22 | HG01074.hp2 HG01175.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.1526-712G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105466126 | ||||||
chr7:105466162
|
GA | G | 41 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0083others(38): Show | 41 | HG00642.hp1 HG01106.hp2 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.1526-749delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105466162 | ||||||
chr7:105466162
|
GAA | G | 305 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(302): Show | 305 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.1526-750_1526-749d others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105466162 | ||||||
chr7:105466249
|
G | T | 9 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0014g0239others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1526-835C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105466249 | ||||||
chr7:105466382
|
C | T | 18 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0150others(15): Show | 18 | HG01934.hp1 HG02027.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.1526-968G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105466382 | ||||||
chr7:105466414
|
C | T | 274 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(271): Show | 274 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.1526-1000G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105466414 | ||||||
chr7:105466489
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1526-1075C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105466489 | ||||||
chr7:105466539
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1526-1125A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105466539 | ||||||
chr7:105466705
|
C | G | 264 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(261): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1526-1291G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105466705 | ||||||
chr7:105466746
|
A | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0270 | 2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1526-1332T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105466746 | ||||||
chr7:105466758
|
G | A | 2 | a0001c0001t0001g0162a0001c0001t0001g0169 | 2 | HG02523.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1526-1344C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105466758 | ||||||
chr7:105466760
|
TA | T | 8 | a0001c0001t0001g0083a0001c0001t0001g0183a0001c0001t0001g0198others(5): Show | 8 | HG01515.hp1 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1526-1347delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105466760 | ||||||
chr7:105466802
|
C | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0270 | 2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1526-1388G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105466802 | ||||||
chr7:105466878
|
T | C | 9 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0014g0239others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1525+1459A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105466878 | ||||||
chr7:105467001
|
A | G | 1 | a0001c0001t0001g0255 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1525+1336T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467001 | ||||||
chr7:105467034
|
G | GT | 22 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0019others(19): Show | 22 | HG00280.hp1 HG00673.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.1525+1302dupA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467034 | ||||||
chr7:105467034
|
G | GTT | 29 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0020others(26): Show | 29 | HG00438.hp2 HG01175.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1525+1301_1525+130 others(6): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467034 | ||||||
chr7:105467034
|
G | GTTT | 17 | a0001c0001t0001g0026a0001c0001t0001g0046a0001c0001t0001g0084others(14): Show | 17 | HG01934.hp1 HG01978.hp1 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.1525+1300_1525+130 others(7): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467034 | ||||||
chr7:105467034
|
GT | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(148): Show |
intron_variant | MODIFIER | c.1525+1302delA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467034 | ||||||
chr7:105467034
|
GTT | G | 19 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0045others(16): Show | 19 | HG01175.hp1 HG01192.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.1525+1301_1525+130 others(6): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467034 | ||||||
chr7:105467034
|
GTTT | G | 15 | a0001c0001t0001g0083a0001c0001t0001g0198a0001c0001t0001g0199others(12): Show | 15 | HG00642.hp1 HG01106.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1525+1300_1525+130 others(7): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467034 | ||||||
chr7:105467034
|
GTTTTTTT others(2): Show |
G | 6 | a0001c0001t0001g0238a0001c0001t0001g0270a0001c0003t0003g0219others(3): Show | 6 | HG01433.hp1 HG01891.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1525+1294_1525+130 others(13): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467034 | ||||||
chr7:105467034
|
GTTTTTTT others(3): Show |
G | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1525+1293_1525+130 others(14): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467034 | ||||||
chr7:105467034
|
GTTTTTTT others(7): Show |
G | 4 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0115others(1): Show | 4 | HG01257.hp1 HG02602.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.1525+1289_1525+130 others(18): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467034 | ||||||
chr7:105467087
|
G | C | 1 | a0001c0001t0001g0207 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1525+1250C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467087 | ||||||
chr7:105467193
|
C | A | 9 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0270others(6): Show | 9 | HG01433.hp1 HG01891.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1525+1144G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467193 | ||||||
chr7:105467248
|
T | C | 347 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(344): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1525+1089A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467248 | ||||||
chr7:105467294
|
CT | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(288): Show | 291 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.1525+1042delA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467294 | ||||||
chr7:105467340
|
A | G | 2 | a0001c0001t0007g0232a0001c0001t0007g0233 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1525+997T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467340 | ||||||
chr7:105467341
|
A | G | 2 | a0001c0001t0007g0232a0001c0001t0007g0233 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1525+996T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467341 | ||||||
chr7:105467352
|
T | C | 2 | a0001c0001t0007g0232a0001c0001t0007g0233 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1525+985A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467352 | ||||||
chr7:105467359
|
G | A | 7 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 7 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1525+978C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467359 | ||||||
chr7:105467359
|
G | T | 2 | a0001c0001t0007g0232a0001c0001t0007g0233 | 2 | NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1525+978C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467359 | ||||||
chr7:105467368
|
C | A | 9 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0270others(6): Show | 9 | HG01433.hp1 HG01891.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1525+969G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467368 | ||||||
chr7:105467376
|
G | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0282 | 2 | NA18992.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1525+961C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467376 | ||||||
chr7:105467381
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1525+956G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467381 | ||||||
chr7:105467390
|
C | G | 16 | a0001c0001t0001g0083a0001c0001t0001g0198a0001c0001t0001g0199others(13): Show | 16 | HG00642.hp1 HG01106.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1525+947G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467390 | ||||||
chr7:105467438
|
T | C | 25 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0048others(22): Show | 25 | HG01074.hp2 HG01884.hp2 HG01934.hp1 others(22): Show |
intron_variant | MODIFIER | c.1525+899A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467438 | ||||||
chr7:105467479
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1525+858G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467479 | ||||||
chr7:105467482
|
C | G | 1 | a0001c0001t0001g0132 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1525+855G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467482 | ||||||
chr7:105467511
|
G | C | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 259 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1525+826C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467511 | ||||||
chr7:105467525
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0088 | 2 | HG01261.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.1525+812C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467525 | ||||||
chr7:105467531
|
T | C | 1 | a0001c0001t0002g0305 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1525+806A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467531 | ||||||
chr7:105467642
|
T | C | 8 | a0001c0001t0001g0044a0001c0001t0001g0241a0001c0001t0003g0053others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1525+695A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467642 | ||||||
chr7:105467674
|
A | C | 2 | a0001c0001t0001g0166a0001c0001t0001g0243 | 2 | HG02818.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1525+663T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467674 | ||||||
chr7:105467832
|
C | G | 1 | a0001c0001t0008g0154 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1525+505G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467832 | ||||||
chr7:105467939
|
CT | C | 7 | a0001c0001t0001g0043a0001c0001t0001g0054a0001c0001t0001g0222others(4): Show | 7 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1525+397delA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105467939 | ||||||
chr7:105468185
|
G | A | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 241 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1525+152C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105468185 | ||||||
chr7:105468292
|
C | T | 1 | a0001c0001t0004g0336 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1525+45G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 12/15 | chr7 | 105468292 | ||||||
chr7:105468563
|
G | A | 16 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0150others(13): Show | 16 | HG01934.hp1 HG02027.hp1 HG03491.hp2 others(13): Show |
intron_variant | MODIFIER | c.1399-100C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105468563 | ||||||
chr7:105468611
|
G | A | 17 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0150others(14): Show | 17 | HG01934.hp1 HG02027.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.1399-148C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105468611 | ||||||
chr7:105468680
|
T | TCTAATTT others(304): Show |
1 | a0001c0001t0001g0270 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1399-218_1399-217i others(313): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105468680 | ||||||
chr7:105468680
|
T | TCTAATTT others(317): Show |
1 | a0001c0001t0001g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1399-218_1399-217i others(326): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105468680 | ||||||
chr7:105469032
|
G | C | 3 | a0001c0004t0001g0081a0001c0004t0001g0082a0001c0004t0001g0093 | 3 | HG02280.hp2 NA18522.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1399-569C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105469032 | ||||||
chr7:105469091
|
G | A | 255 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(252): Show | 255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1399-628C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105469091 | ||||||
chr7:105469190
|
C | G | 1 | a0001c0001t0001g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1399-727G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105469190 | ||||||
chr7:105469234
|
C | T | 3 | a0001c0001t0001g0097a0001c0001t0001g0099a0003c0006t0001g0098 | 3 | NA18944.hp2 NA18977.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1399-771G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105469234 | ||||||
chr7:105469301
|
A | C | 3 | a0001c0001t0001g0228a0001c0001t0001g0298a0001c0001t0004g0343 | 3 | HG00609.hp1 HG02896.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1399-838T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105469301 | ||||||
chr7:105469444
|
C | A | 4 | a0001c0001t0001g0086a0001c0001t0001g0155a0001c0001t0001g0220others(1): Show | 4 | HG00639.hp2 HG00738.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1399-981G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105469444 | ||||||
chr7:105469507
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1399-1044A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105469507 | ||||||
chr7:105469528
|
C | T | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1399-1065G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105469528 | ||||||
chr7:105469620
|
T | C | 4 | a0001c0001t0001g0047a0001c0001t0001g0062a0001c0001t0009g0068others(1): Show | 4 | HG02895.hp1 HG02897.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1398+1068A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105469620 | ||||||
chr7:105469753
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1398+935G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105469753 | ||||||
chr7:105469812
|
C | T | 1 | a0001c0001t0004g0348 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1398+876G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105469812 | ||||||
chr7:105469842
|
C | A | 1 | a0001c0001t0001g0102 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1398+846G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105469842 | ||||||
chr7:105470399
|
C | G | 2 | a0001c0001t0001g0238a0001c0001t0001g0270 | 2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1398+289G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105470399 | ||||||
chr7:105470399
|
C | T | 3 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0014g0239 | 3 | HG02717.hp1 NA18522.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1398+289G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105470399 | ||||||
chr7:105470501
|
C | T | 16 | a0001c0001t0001g0047a0001c0001t0001g0062a0001c0001t0001g0083others(13): Show | 16 | HG00642.hp1 HG01106.hp2 HG02818.hp2 others(13): Show |
intron_variant | MODIFIER | c.1398+187G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105470501 | ||||||
chr7:105470543
|
C | T | 94 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(91): Show | 94 | HG00642.hp1 HG00642.hp2 HG01074.hp2 others(91): Show |
intron_variant | MODIFIER | c.1398+145G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105470543 | ||||||
chr7:105470579
|
T | G | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1398+109A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 11/15 | chr7 | 105470579 | ||||||
chr7:105470862
|
A | C | 1 | a0001c0001t0001g0119 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1238-14T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 10/15 | chr7 | 105470862 | ||||||
chr7:105471013
|
A | G | 12 | a0001c0001t0001g0083a0001c0001t0001g0198a0001c0001t0001g0199others(9): Show | 12 | HG00642.hp1 HG01106.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.1238-165T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 10/15 | chr7 | 105471013 | ||||||
chr7:105471184
|
T | C | 1 | a0001c0001t0010g0289 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1238-336A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 10/15 | chr7 | 105471184 | ||||||
chr7:105471214
|
C | T | 94 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(91): Show | 94 | HG00642.hp1 HG00642.hp2 HG01074.hp2 others(91): Show |
intron_variant | MODIFIER | c.1238-366G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 10/15 | chr7 | 105471214 | ||||||
chr7:105471469
|
T | A | 1 | a0001c0001t0003g0029 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1238-621A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 10/15 | chr7 | 105471469 | ||||||
chr7:105471538
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0058 | 2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1237+594G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 10/15 | chr7 | 105471538 | ||||||
chr7:105471554
|
G | A | 7 | a0001c0001t0001g0083a0001c0001t0001g0198a0001c0001t0001g0199others(4): Show | 7 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.1237+578C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 10/15 | chr7 | 105471554 | ||||||
chr7:105471633
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1237+499G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 10/15 | chr7 | 105471633 | ||||||
chr7:105471638
|
C | T | 26 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0044others(23): Show | 26 | HG00642.hp2 HG01081.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1237+494G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 10/15 | chr7 | 105471638 | ||||||
chr7:105471776
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1237+356C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 10/15 | chr7 | 105471776 | ||||||
chr7:105471912
|
C | CA | 13 | a0001c0001t0001g0085a0001c0001t0001g0103a0001c0001t0001g0104others(10): Show | 13 | HG00099.hp2 HG01884.hp1 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1237+219dupT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 10/15 | chr7 | 105471912 | ||||||
chr7:105471912
|
CA | C | 78 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(75): Show | 78 | HG00642.hp1 HG00642.hp2 HG01074.hp2 others(75): Show |
intron_variant | MODIFIER | c.1237+219delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 10/15 | chr7 | 105471912 | ||||||
chr7:105471912
|
CAA | C | 17 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0150others(14): Show | 17 | HG01934.hp1 HG02027.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.1237+218_1237+219d others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 10/15 | chr7 | 105471912 | ||||||
chr7:105471940
|
ATATAAAT | A | 17 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0150others(14): Show | 17 | HG01934.hp1 HG02027.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.1237+185_1237+191d others(9): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 10/15 | chr7 | 105471940 | ||||||
chr7:105471941
|
T | C | 46 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(43): Show | 46 | HG00642.hp1 HG01074.hp2 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.1237+191A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 10/15 | chr7 | 105471941 | ||||||
chr7:105471948
|
T | C | 17 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0150others(14): Show | 17 | HG01934.hp1 HG02027.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.1237+184A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 10/15 | chr7 | 105471948 | ||||||
chr7:105471968
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1237+164T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 10/15 | chr7 | 105471968 | ||||||
chr7:105472042
|
C | A | 94 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(91): Show | 94 | HG00642.hp1 HG00642.hp2 HG01074.hp2 others(91): Show |
intron_variant | MODIFIER | c.1237+90G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 10/15 | chr7 | 105472042 | ||||||
chr7:105472293
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1176-100G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105472293 | ||||||
chr7:105472320
|
C | A | 5 | a0001c0001t0001g0044a0001c0003t0003g0219a0001c0003t0003g0221others(2): Show | 5 | HG01891.hp2 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1176-127G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105472320 | ||||||
chr7:105472584
|
C | T | 94 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(91): Show | 94 | HG00642.hp1 HG00642.hp2 HG01074.hp2 others(91): Show |
intron_variant | MODIFIER | c.1176-391G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105472584 | ||||||
chr7:105472663
|
C | T | 1 | a0001c0001t0003g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1176-470G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105472663 | ||||||
chr7:105472664
|
G | A | 1 | a0001c0001t0001g0012 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1176-471C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105472664 | ||||||
chr7:105472816
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1176-623G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105472816 | ||||||
chr7:105472904
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1176-711G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105472904 | ||||||
chr7:105472920
|
C | CT | 40 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0059others(37): Show | 40 | HG00597.hp1 HG01433.hp1 HG01891.hp1 others(37): Show |
intron_variant | MODIFIER | c.1176-728dupA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105472920 | ||||||
chr7:105472920
|
C | CTT | 46 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(43): Show | 46 | HG00642.hp2 HG01074.hp2 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.1176-729_1176-728d others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105472920 | ||||||
chr7:105472920
|
CT | C | 7 | a0001c0001t0001g0043a0001c0001t0001g0054a0001c0001t0001g0168others(4): Show | 7 | HG02055.hp2 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176-728delA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105472920 | ||||||
chr7:105472993
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1176-800G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105472993 | ||||||
chr7:105473039
|
G | C | 1 | a0001c0001t0003g0237 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1176-846C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473039 | ||||||
chr7:105473085
|
G | A | 3 | a0001c0004t0001g0294a0001c0005t0001g0040a0001c0005t0001g0041 | 3 | HG02055.hp1 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1176-892C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473085 | ||||||
chr7:105473100
|
C | T | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(44): Show | 47 | HG00642.hp2 HG01074.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.1176-907G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473100 | ||||||
chr7:105473101
|
G | A | 1 | a0001c0001t0003g0248 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1176-908C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473101 | ||||||
chr7:105473137
|
T | C | 7 | a0001c0001t0001g0043a0001c0001t0001g0054a0001c0001t0001g0222others(4): Show | 7 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176-944A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473137 | ||||||
chr7:105473138
|
C | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0270 | 2 | HG01433.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1176-945G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473138 | ||||||
chr7:105473187
|
CTT | C | 12 | a0001c0001t0001g0083a0001c0001t0001g0198a0001c0001t0001g0199others(9): Show | 12 | HG00642.hp1 HG01106.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.1176-996_1176-995d others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473187 | ||||||
chr7:105473251
|
T | A | 1 | a0001c0001t0001g0206 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1176-1058A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473251 | ||||||
chr7:105473266
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1176-1073A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473266 | ||||||
chr7:105473298
|
G | A | 1 | a0001c0007t0001g0123 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1176-1105C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473298 | ||||||
chr7:105473337
|
C | T | 9 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0014g0239others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1176-1144G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473337 | ||||||
chr7:105473339
|
T | G | 94 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(91): Show | 94 | HG00642.hp1 HG00642.hp2 HG01074.hp2 others(91): Show |
intron_variant | MODIFIER | c.1176-1146A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473339 | ||||||
chr7:105473415
|
A | AT | 87 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(84): Show | 87 | HG00642.hp1 HG00642.hp2 HG01081.hp1 others(84): Show |
intron_variant | MODIFIER | c.1176-1223dupA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473415 | ||||||
chr7:105473415
|
AT | A | 9 | a0001c0001t0001g0003a0001c0001t0001g0023a0001c0001t0001g0168others(6): Show | 9 | HG01069.hp2 HG01081.hp2 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1176-1223delA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473415 | ||||||
chr7:105473420
|
T | A | 1 | a0001c0001t0001g0006 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1176-1227A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473420 | ||||||
chr7:105473421
|
T | A | 1 | a0001c0001t0001g0003 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1176-1228A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473421 | ||||||
chr7:105473482
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1176-1289T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473482 | ||||||
chr7:105473511
|
C | G | 17 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0150others(14): Show | 17 | HG01934.hp1 HG02027.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.1176-1318G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473511 | ||||||
chr7:105473639
|
G | C | 1 | a0001c0001t0001g0220 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1176-1446C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473639 | ||||||
chr7:105473718
|
C | T | 9 | a0001c0001t0007g0232a0001c0001t0007g0233a0001c0001t0014g0239others(6): Show | 9 | HG02055.hp1 HG02280.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1176-1525G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473718 | ||||||
chr7:105473774
|
G | C | 9 | a0001c0001t0001g0032a0001c0001t0001g0046a0001c0001t0001g0057others(6): Show | 9 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1176-1581C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473774 | ||||||
chr7:105473986
|
T | C | 2 | a0001c0001t0009g0068a0001c0001t0009g0069 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1176-1793A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105473986 | ||||||
chr7:105474021
|
A | G | 7 | a0001c0001t0001g0043a0001c0001t0001g0054a0001c0001t0001g0222others(4): Show | 7 | HG02055.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176-1828T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105474021 | ||||||
chr7:105474192
|
G | A | 1 | a0001c0001t0003g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1176-1999C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105474192 | ||||||
chr7:105474491
|
G | A | 25 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0010others(22): Show | 25 | HG00280.hp2 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.1176-2298C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105474491 | ||||||
chr7:105474612
|
CA | C | 26 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0047others(23): Show | 26 | HG01433.hp1 HG01934.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.1176-2420delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105474612 | ||||||
chr7:105474612
|
CAA | C | 28 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0044others(25): Show | 28 | HG00642.hp2 HG01081.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1176-2421_1176-242 others(6): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105474612 | ||||||
chr7:105474612
|
CAAA | C | 21 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0045others(18): Show | 21 | HG01243.hp1 HG01433.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1176-2422_1176-242 others(7): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105474612 | ||||||
chr7:105474612
|
CAAAA | C | 225 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(222): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1176-2423_1176-242 others(8): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105474612 | ||||||
chr7:105474612
|
CAAAAA | C | 8 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0143others(5): Show | 8 | HG02717.hp1 HG02723.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.1176-2424_1176-242 others(9): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105474612 | ||||||
chr7:105474627
|
A | T | 13 | a0001c0001t0001g0047a0001c0001t0001g0083a0001c0001t0001g0198others(10): Show | 13 | HG00642.hp1 HG01106.hp2 HG02818.hp2 others(10): Show |
intron_variant | MODIFIER | c.1176-2434T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105474627 | ||||||
chr7:105474630
|
A | T | 31 | a0001c0001t0001g0043a0001c0001t0001g0054a0001c0001t0001g0083others(28): Show | 31 | HG00642.hp1 HG01106.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.1176-2437T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105474630 | ||||||
chr7:105474642
|
G | A | 63 | a0001c0001t0001g0004a0001c0001t0001g0015a0001c0001t0001g0042others(60): Show | 63 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.1176-2449C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105474642 | ||||||
chr7:105474707
|
G | C | 1 | a0001c0001t0014g0239 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1176-2514C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105474707 | ||||||
chr7:105474740
|
C | T | 27 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(24): Show | 27 | HG00438.hp2 HG00673.hp2 HG01975.hp2 others(24): Show |
intron_variant | MODIFIER | c.1176-2547G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105474740 | ||||||
chr7:105474823
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1176-2630G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105474823 | ||||||
chr7:105475193
|
C | CT | 30 | a0001c0001t0001g0039a0001c0001t0001g0044a0001c0001t0001g0048others(27): Show | 30 | HG00099.hp2 HG01074.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.1176-3001dupA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475193 | ||||||
chr7:105475219
|
T | C | 46 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0032others(43): Show | 46 | HG00280.hp1 HG01106.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.1176-3026A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475219 | ||||||
chr7:105475225
|
A | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(187): Show | 190 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.1176-3032T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475225 | ||||||
chr7:105475234
|
A | G | 191 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(188): Show | 191 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.1176-3041T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475234 | ||||||
chr7:105475266
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1176-3073T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475266 | ||||||
chr7:105475272
|
G | A | 103 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0026others(100): Show | 103 | HG00280.hp1 HG01106.hp1 HG01106.hp2 others(100): Show |
intron_variant | MODIFIER | c.1176-3079C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475272 | ||||||
chr7:105475284
|
C | T | 94 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0026others(91): Show | 94 | HG00280.hp1 HG01106.hp1 HG01106.hp2 others(91): Show |
intron_variant | MODIFIER | c.1176-3091G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475284 | ||||||
chr7:105475286
|
C | T | 95 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0026others(92): Show | 95 | HG00280.hp1 HG01106.hp1 HG01106.hp2 others(92): Show |
intron_variant | MODIFIER | c.1176-3093G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475286 | ||||||
chr7:105475295
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1176-3102A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475295 | ||||||
chr7:105475311
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0003g0182 | 2 | HG00280.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.1176-3118T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475311 | ||||||
chr7:105475333
|
G | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(110): Show | 113 | HG00423.hp2 HG00597.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.1176-3140C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475333 | ||||||
chr7:105475333
|
G | T | 1 | a0001c0001t0001g0027 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1176-3140C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475333 | ||||||
chr7:105475334
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1176-3141G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475334 | ||||||
chr7:105475346
|
T | C | 7 | a0001c0001t0001g0127a0001c0001t0001g0222a0001c0001t0001g0245others(4): Show | 7 | HG02257.hp1 HG02572.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176-3153A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475346 | ||||||
chr7:105475364
|
G | GTTAGTAG others(130): Show |
1 | a0001c0001t0001g0094 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1176-3172_1176-317 others(141): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475364 | ||||||
chr7:105475364
|
G | GTTAGTAG others(130): Show |
1 | a0001c0001t0001g0157 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1176-3172_1176-317 others(141): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475364 | ||||||
chr7:105475364
|
GTTAGTAG others(130): Show |
G | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1176-3308_1176-317 others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475364 | ||||||
chr7:105475375
|
T | C | 94 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0026others(91): Show | 94 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.1176-3182A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475375 | ||||||
chr7:105475395
|
C | T | 265 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(262): Show | 265 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(262): Show |
intron_variant | MODIFIER | c.1176-3202G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475395 | ||||||
chr7:105475395
|
CAGGATGG others(130): Show |
C | 1 | a0001c0001t0002g0313 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1176-3339_1176-320 others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475395 | ||||||
chr7:105475396
|
A | G | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 272 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(269): Show |
intron_variant | MODIFIER | c.1176-3203T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475396 | ||||||
chr7:105475397
|
G | A | 6 | a0001c0001t0001g0075a0001c0001t0001g0103a0001c0001t0001g0104others(3): Show | 6 | HG00099.hp2 HG01069.hp1 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1176-3204C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475397 | ||||||
chr7:105475403
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(209): Show | 212 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.1176-3210A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475403 | ||||||
chr7:105475406
|
C | T | 251 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(248): Show | 251 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1176-3213G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475406 | ||||||
chr7:105475407
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1176-3214C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475407 | ||||||
chr7:105475407
|
G | C | 3 | a0001c0001t0001g0241a0001c0001t0003g0053a0001c0001t0003g0240 | 3 | HG02109.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1176-3214C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475407 | ||||||
chr7:105475417
|
C | T | 7 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0155others(4): Show | 7 | HG00639.hp2 HG01975.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.1176-3224G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475417 | ||||||
chr7:105475420
|
T | C | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0192 | 3 | HG02074.hp2 HG02083.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1176-3227A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475420 | ||||||
chr7:105475460
|
C | T | 1 | a0001c0001t0001g0150 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1176-3267G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475460 | ||||||
chr7:105475467
|
C | G | 1 | a0001c0001t0001g0211 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1176-3274G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475467 | ||||||
chr7:105475476
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1176-3283A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475476 | ||||||
chr7:105475533
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1176-3340T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475533 | ||||||
chr7:105475537
|
T | C | 1 | a0001c0001t0001g0255 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1176-3344A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475537 | ||||||
chr7:105475543
|
C | G | 1 | a0001c0001t0001g0208 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1176-3350G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475543 | ||||||
chr7:105475600
|
G | C | 3 | a0001c0001t0001g0032a0001c0001t0001g0057a0001c0001t0001g0067 | 3 | HG01243.hp1 HG02717.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1176-3407C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475600 | ||||||
chr7:105475654
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1176-3461G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475654 | ||||||
chr7:105475693
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1176-3500A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475693 | ||||||
chr7:105475792
|
C | G | 118 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0030others(115): Show | 118 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.1176-3599G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475792 | ||||||
chr7:105475826
|
C | T | 28 | a0001c0001t0001g0039a0001c0001t0001g0044a0001c0001t0001g0045others(25): Show | 28 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.1176-3633G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475826 | ||||||
chr7:105475929
|
A | T | 1 | a0001c0001t0001g0163 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1176-3736T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475929 | ||||||
chr7:105475992
|
G | A | 1 | a0001c0001t0018g0331 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1176-3799C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105475992 | ||||||
chr7:105476001
|
C | T | 69 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(66): Show | 69 | HG00423.hp2 HG00735.hp2 HG01074.hp1 others(66): Show |
intron_variant | MODIFIER | c.1176-3808G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105476001 | ||||||
chr7:105476012
|
G | A | 33 | a0001c0001t0001g0021a0001c0001t0001g0089a0001c0001t0001g0100others(30): Show | 33 | HG00438.hp1 HG00544.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.1176-3819C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105476012 | ||||||
chr7:105476102
|
C | T | 14 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(11): Show | 14 | HG02155.hp2 HG02258.hp1 HG02976.hp1 others(11): Show |
intron_variant | MODIFIER | c.1176-3909G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105476102 | ||||||
chr7:105476123
|
C | CA | 47 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(44): Show | 47 | HG00438.hp1 HG00438.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1176-3931dupT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105476123 | ||||||
chr7:105476123
|
CA | C | 26 | a0001c0001t0001g0021a0001c0001t0001g0027a0001c0001t0001g0030others(23): Show | 26 | HG00558.hp2 HG01069.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1176-3931delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105476123 | ||||||
chr7:105476123
|
CAA | C | 16 | a0001c0001t0001g0039a0001c0001t0001g0044a0001c0001t0001g0054others(13): Show | 16 | HG02055.hp2 HG02056.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1176-3932_1176-393 others(6): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105476123 | ||||||
chr7:105476327
|
G | A | 1 | a0001c0001t0001g0235 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1176-4134C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105476327 | ||||||
chr7:105476345
|
T | C | 15 | a0001c0001t0001g0061a0001c0001t0001g0164a0001c0001t0001g0165others(12): Show | 15 | HG00423.hp2 HG01175.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1176-4152A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105476345 | ||||||
chr7:105476380
|
A | G | 13 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(10): Show | 13 | HG02155.hp2 NA18945.hp2 NA18946.hp1 others(10): Show |
intron_variant | MODIFIER | c.1176-4187T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105476380 | ||||||
chr7:105476451
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0130 | 2 | HG02602.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1176-4258C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105476451 | ||||||
chr7:105476514
|
C | T | 16 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0164others(13): Show | 16 | HG00423.hp2 HG01175.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.1176-4321G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105476514 | ||||||
chr7:105476519
|
G | A | 1 | a0001c0001t0001g0274 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1176-4326C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105476519 | ||||||
chr7:105476591
|
C | T | 16 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0164others(13): Show | 16 | HG00423.hp2 HG01175.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.1176-4398G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105476591 | ||||||
chr7:105476636
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1175+4416C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105476636 | ||||||
chr7:105476927
|
G | C | 15 | a0001c0001t0001g0061a0001c0001t0001g0164a0001c0001t0001g0165others(12): Show | 15 | HG00423.hp2 HG01175.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.1175+4125C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105476927 | ||||||
chr7:105477026
|
T | G | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1175+4026A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105477026 | ||||||
chr7:105477028
|
T | A | 15 | a0001c0001t0001g0030a0001c0001t0001g0043a0001c0001t0001g0047others(12): Show | 15 | HG01074.hp1 HG01081.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.1175+4024A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105477028 | ||||||
chr7:105477128
|
C | G | 28 | a0001c0001t0001g0031a0001c0001t0001g0045a0001c0001t0001g0054others(25): Show | 28 | HG00423.hp2 HG01175.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.1175+3924G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105477128 | ||||||
chr7:105477257
|
A | AT | 8 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0129others(5): Show | 8 | HG01934.hp1 HG02027.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1175+3794dupA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105477257 | ||||||
chr7:105477341
|
G | A | 7 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0295others(4): Show | 7 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175+3711C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105477341 | ||||||
chr7:105477393
|
G | C | 7 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0295others(4): Show | 7 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175+3659C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105477393 | ||||||
chr7:105477400
|
C | A | 1 | a0001c0001t0014g0239 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1175+3652G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105477400 | ||||||
chr7:105477518
|
G | C | 1 | a0001c0001t0001g0171 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1175+3534C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105477518 | ||||||
chr7:105477527
|
A | G | 7 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0295others(4): Show | 7 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175+3525T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105477527 | ||||||
chr7:105477571
|
G | A | 7 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0295others(4): Show | 7 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175+3481C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105477571 | ||||||
chr7:105477607
|
T | C | 7 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0295others(4): Show | 7 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175+3445A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105477607 | ||||||
chr7:105477619
|
G | A | 4 | a0001c0001t0001g0173a0001c0001t0001g0177a0001c0001t0001g0180others(1): Show | 4 | HG00558.hp1 NA18973.hp1 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.1175+3433C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105477619 | ||||||
chr7:105477808
|
C | G | 1 | a0001c0001t0001g0031 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1175+3244G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105477808 | ||||||
chr7:105477971
|
T | G | 1 | a0001c0001t0001g0054 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1175+3081A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105477971 | ||||||
chr7:105478392
|
G | C | 7 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0295others(4): Show | 7 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175+2660C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105478392 | ||||||
chr7:105478658
|
C | T | 1 | a0001c0001t0018g0331 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1175+2394G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105478658 | ||||||
chr7:105478713
|
C | T | 1 | a0001c0003t0003g0219 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1175+2339G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105478713 | ||||||
chr7:105478717
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1175+2335A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105478717 | ||||||
chr7:105478861
|
C | T | 60 | a0001c0001t0001g0021a0001c0001t0001g0032a0001c0001t0001g0048others(57): Show | 60 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1175+2191G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105478861 | ||||||
chr7:105478862
|
G | A | 10 | a0001c0001t0001g0030a0001c0001t0001g0198a0001c0001t0001g0199others(7): Show | 10 | HG01074.hp1 HG01081.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.1175+2190C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105478862 | ||||||
chr7:105478959
|
G | T | 6 | a0001c0001t0001g0222a0001c0001t0001g0228a0001c0001t0001g0229others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1175+2093C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105478959 | ||||||
chr7:105479195
|
G | A | 7 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0295others(4): Show | 7 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175+1857C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105479195 | ||||||
chr7:105479221
|
T | C | 1 | a0001c0001t0002g0325 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1175+1831A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105479221 | ||||||
chr7:105479355
|
C | T | 1 | a0001c0001t0001g0015 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1175+1697G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105479355 | ||||||
chr7:105479409
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1175+1643A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105479409 | ||||||
chr7:105479591
|
T | C | 18 | a0001c0001t0001g0017a0001c0001t0001g0026a0001c0001t0001g0088others(15): Show | 18 | HG01106.hp1 HG01255.hp2 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.1175+1461A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105479591 | ||||||
chr7:105479649
|
G | A | 14 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0174others(11): Show | 14 | HG00423.hp2 HG01175.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.1175+1403C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105479649 | ||||||
chr7:105479769
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0047a0001c0001t0001g0062 | 3 | HG02976.hp2 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1175+1283C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105479769 | ||||||
chr7:105479946
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1175+1106C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105479946 | ||||||
chr7:105479983
|
A | G | 140 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(137): Show | 140 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.1175+1069T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105479983 | ||||||
chr7:105480033
|
G | A | 16 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0174others(13): Show | 16 | HG00423.hp2 HG01175.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.1175+1019C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105480033 | ||||||
chr7:105480059
|
A | T | 7 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0295others(4): Show | 7 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175+993T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105480059 | ||||||
chr7:105480062
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1175+990G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105480062 | ||||||
chr7:105480136
|
T | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0238 | 2 | HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1175+916A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105480136 | ||||||
chr7:105480226
|
C | G | 2 | a0001c0001t0005g0285a0001c0004t0001g0294 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1175+826G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105480226 | ||||||
chr7:105480246
|
C | A | 1 | a0001c0001t0001g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1175+806G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105480246 | ||||||
chr7:105480292
|
TG | T | 7 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0295others(4): Show | 7 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1175+759delC | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105480292 | ||||||
chr7:105480558
|
C | T | 13 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(10): Show | 13 | HG02155.hp2 NA18945.hp2 NA18946.hp1 others(10): Show |
intron_variant | MODIFIER | c.1175+494G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105480558 | ||||||
chr7:105480701
|
G | A | 15 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(12): Show | 15 | HG02055.hp1 HG02155.hp2 HG02965.hp2 others(12): Show |
intron_variant | MODIFIER | c.1175+351C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105480701 | ||||||
chr7:105480839
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1175+213T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105480839 | ||||||
chr7:105480951
|
C | T | 6 | a0001c0001t0001g0031a0001c0001t0001g0054a0001c0001t0001g0295others(3): Show | 6 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1175+101G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 9/15 | chr7 | 105480951 | ||||||
chr7:105481184
|
G | C | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp1 | splice_region_variant&intron_variant | LOW | c.1050-7C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 8/15 | chr7 | 105481184 | ||||||
chr7:105481405
|
T | A | 1 | a0001c0001t0001g0284 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1050-228A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 8/15 | chr7 | 105481405 | ||||||
chr7:105481437
|
T | C | 1 | a0001c0001t0001g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1050-260A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 8/15 | chr7 | 105481437 | ||||||
chr7:105481453
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0160 | 2 | NA18992.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1050-276G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 8/15 | chr7 | 105481453 | ||||||
chr7:105481577
|
C | G | 1 | a0001c0001t0016g0311 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1050-400G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 8/15 | chr7 | 105481577 | ||||||
chr7:105481638
|
C | G | 2 | a0001c0005t0001g0040a0001c0005t0001g0041 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1050-461G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 8/15 | chr7 | 105481638 | ||||||
chr7:105481734
|
C | CT | 19 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0065others(16): Show | 19 | HG00423.hp2 HG01175.hp2 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.1050-558dupA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 8/15 | chr7 | 105481734 | ||||||
chr7:105481824
|
C | G | 16 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0065others(13): Show | 16 | HG00423.hp2 HG01175.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.1049+488G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 8/15 | chr7 | 105481824 | ||||||
chr7:105481825
|
G | A | 1 | a0001c0001t0003g0240 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1049+487C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 8/15 | chr7 | 105481825 | ||||||
chr7:105481856
|
G | C | 2 | a0001c0001t0005g0285a0001c0004t0001g0294 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1049+456C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 8/15 | chr7 | 105481856 | ||||||
chr7:105481891
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1049+421G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 8/15 | chr7 | 105481891 | ||||||
chr7:105481920
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1049+392G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 8/15 | chr7 | 105481920 | ||||||
chr7:105481921
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1049+391T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 8/15 | chr7 | 105481921 | ||||||
chr7:105481952
|
G | T | 1 | a0001c0001t0001g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1049+360C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 8/15 | chr7 | 105481952 | ||||||
chr7:105481973
|
A | G | 16 | a0001c0001t0001g0045a0001c0001t0001g0061a0001c0001t0001g0065others(13): Show | 16 | HG00423.hp2 HG01175.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.1049+339T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 8/15 | chr7 | 105481973 | ||||||
chr7:105482009
|
C | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0017g0330 | 3 | HG00738.hp2 HG03831.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1049+303G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 8/15 | chr7 | 105482009 | ||||||
chr7:105482081
|
G | C | 16 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(13): Show | 16 | HG02155.hp2 HG02976.hp1 NA18945.hp2 others(13): Show |
intron_variant | MODIFIER | c.1049+231C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 8/15 | chr7 | 105482081 | ||||||
chr7:105482444
|
TA | T | 75 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(72): Show | 75 | HG00423.hp2 HG00735.hp2 HG01069.hp1 others(72): Show |
splice_region_variant&intron_variant | LOW | c.921-5delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105482444 | ||||||
chr7:105482513
|
T | C | 105 | a0001c0001t0001g0021a0001c0001t0001g0031a0001c0001t0001g0039others(102): Show | 105 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.921-73A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105482513 | ||||||
chr7:105482701
|
C | T | 96 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(93): Show | 96 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.921-261G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105482701 | ||||||
chr7:105482911
|
A | C | 1 | a0001c0001t0001g0031 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.921-471T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105482911 | ||||||
chr7:105483194
|
C | CAG | 333 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(330): Show | 333 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.921-756_921-755dup others(2): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105483194 | ||||||
chr7:105483221
|
G | C | 1 | a0001c0001t0001g0271 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.921-781C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105483221 | ||||||
chr7:105483324
|
G | A | 5 | a0001c0002t0001g0137a0001c0002t0001g0138a0001c0002t0001g0139others(2): Show | 5 | HG02074.hp1 NA18963.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.921-884C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105483324 | ||||||
chr7:105483359
|
T | A | 1 | a0001c0001t0008g0293 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.921-919A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105483359 | ||||||
chr7:105483388
|
C | G | 15 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(12): Show | 15 | NA18945.hp2 NA18950.hp1 NA18952.hp1 others(12): Show |
intron_variant | MODIFIER | c.921-948G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105483388 | ||||||
chr7:105483407
|
C | T | 3 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0260 | 3 | NA18944.hp1 NA18982.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.921-967G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105483407 | ||||||
chr7:105483618
|
G | A | 3 | a0001c0001t0006g0344a0001c0001t0006g0346a0001c0001t0006g0347 | 3 | HG01070.hp2 HG01071.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.921-1178C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105483618 | ||||||
chr7:105483625
|
T | C | 1 | a0001c0001t0001g0042 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.921-1185A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105483625 | ||||||
chr7:105484397
|
T | G | 1 | a0001c0001t0001g0132 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.921-1957A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105484397 | ||||||
chr7:105484398
|
T | G | 3 | a0001c0001t0002g0313a0001c0001t0002g0314a0001c0001t0002g0316 | 3 | HG01257.hp2 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.921-1958A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105484398 | ||||||
chr7:105484510
|
TA | T | 312 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(309): Show | 312 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.921-2071delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105484510 | ||||||
chr7:105484510
|
TAA | T | 16 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(13): Show | 16 | HG00544.hp2 HG01081.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.921-2072_921-2071d others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105484510 | ||||||
chr7:105484527
|
A | G | 1 | a0001c0001t0001g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.921-2087T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105484527 | ||||||
chr7:105484681
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.921-2241A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105484681 | ||||||
chr7:105484718
|
T | C | 1 | a0001c0001t0001g0292 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.921-2278A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105484718 | ||||||
chr7:105484757
|
G | A | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(48): Show | 51 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.921-2317C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105484757 | ||||||
chr7:105484759
|
A | G | 11 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(8): Show | 11 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.921-2319T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105484759 | ||||||
chr7:105484855
|
A | AT | 76 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0015others(73): Show | 76 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.921-2416dupA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105484855 | ||||||
chr7:105484855
|
A | ATT | 11 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0025others(8): Show | 11 | HG01978.hp1 HG02145.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.921-2417_921-2416d others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105484855 | ||||||
chr7:105484855
|
AT | A | 14 | a0001c0001t0001g0062a0001c0001t0001g0158a0001c0001t0001g0163others(11): Show | 14 | HG01168.hp1 HG01346.hp2 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.921-2416delA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105484855 | ||||||
chr7:105484855
|
ATT | A | 42 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(39): Show | 42 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.921-2417_921-2416d others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105484855 | ||||||
chr7:105485100
|
C | A | 2 | a0001c0001t0005g0285a0001c0004t0001g0294 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.921-2660G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105485100 | ||||||
chr7:105485146
|
C | T | 2 | a0001c0005t0001g0040a0001c0005t0001g0041 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.921-2706G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105485146 | ||||||
chr7:105485172
|
T | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0200a0001c0001t0001g0201 | 3 | HG01074.hp1 HG01081.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.921-2732A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105485172 | ||||||
chr7:105485240
|
T | A | 2 | a0001c0005t0001g0040a0001c0005t0001g0041 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.921-2800A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105485240 | ||||||
chr7:105485266
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.921-2826T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105485266 | ||||||
chr7:105485543
|
T | A | 1 | a0001c0001t0001g0211 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.921-3103A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105485543 | ||||||
chr7:105485557
|
C | A | 2 | a0001c0001t0005g0285a0001c0004t0001g0294 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.921-3117G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105485557 | ||||||
chr7:105485649
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.921-3209C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105485649 | ||||||
chr7:105485832
|
G | A | 3 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0156 | 3 | NA18942.hp2 NA18983.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.921-3392C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105485832 | ||||||
chr7:105485834
|
C | T | 1 | a0001c0001t0001g0056 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.921-3394G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105485834 | ||||||
chr7:105485835
|
G | A | 1 | a0001c0001t0001g0260 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.921-3395C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105485835 | ||||||
chr7:105485850
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.921-3410G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105485850 | ||||||
chr7:105485941
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.921-3501A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105485941 | ||||||
chr7:105486044
|
T | G | 1 | a0001c0001t0001g0043 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.921-3604A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105486044 | ||||||
chr7:105486096
|
G | C | 1 | a0001c0001t0001g0230 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.921-3656C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105486096 | ||||||
chr7:105486197
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.921-3757G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105486197 | ||||||
chr7:105486334
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.921-3894A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105486334 | ||||||
chr7:105486342
|
C | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0028 | 2 | NA19003.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.921-3902G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105486342 | ||||||
chr7:105486392
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.921-3952G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105486392 | ||||||
chr7:105486669
|
G | A | 1 | a0001c0001t0002g0325 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.921-4229C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105486669 | ||||||
chr7:105486680
|
C | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0003g0070 | 3 | HG02630.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.921-4240G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105486680 | ||||||
chr7:105486820
|
G | C | 5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.921-4380C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105486820 | ||||||
chr7:105486835
|
G | A | 1 | a0001c0001t0004g0335 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.921-4395C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105486835 | ||||||
chr7:105486931
|
A | T | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.921-4491T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105486931 | ||||||
chr7:105487008
|
C | T | 1 | a0001c0001t0001g0247 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.920+4532G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105487008 | ||||||
chr7:105487249
|
G | A | 61 | a0001c0001t0001g0030a0001c0001t0001g0057a0001c0001t0001g0058others(58): Show | 61 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.920+4291C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105487249 | ||||||
chr7:105487300
|
T | C | 1 | a0001c0004t0001g0093 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.920+4240A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105487300 | ||||||
chr7:105487311
|
A | G | 3 | a0001c0001t0001g0054a0001c0001t0003g0053a0001c0001t0011g0063 | 3 | HG02055.hp2 HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.920+4229T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105487311 | ||||||
chr7:105487344
|
A | G | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.920+4196T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105487344 | ||||||
chr7:105487474
|
T | C | 14 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | NA18945.hp2 NA18950.hp1 NA18955.hp1 others(11): Show |
intron_variant | MODIFIER | c.920+4066A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105487474 | ||||||
chr7:105487893
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.920+3647G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105487893 | ||||||
chr7:105487977
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.920+3563G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105487977 | ||||||
chr7:105488026
|
G | A | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | NA18612.hp2 NA18954.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.920+3514C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105488026 | ||||||
chr7:105488029
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.920+3511C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105488029 | ||||||
chr7:105488061
|
C | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013 | 3 | HG01175.hp1 HG01261.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.920+3479G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105488061 | ||||||
chr7:105488264
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG01993.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.920+3276T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105488264 | ||||||
chr7:105488287
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.920+3253A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105488287 | ||||||
chr7:105488335
|
C | T | 1 | a0001c0001t0001g0276 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.920+3205G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105488335 | ||||||
chr7:105488502
|
T | C | 104 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(101): Show | 104 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.920+3038A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105488502 | ||||||
chr7:105488770
|
T | C | 48 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(45): Show | 48 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.920+2770A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105488770 | ||||||
chr7:105488844
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.920+2696G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105488844 | ||||||
chr7:105488889
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.920+2651G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105488889 | ||||||
chr7:105488935
|
T | C | 6 | a0001c0001t0001g0222a0001c0001t0001g0241a0001c0001t0003g0240others(3): Show | 6 | HG02109.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.920+2605A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105488935 | ||||||
chr7:105489045
|
C | G | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.920+2495G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105489045 | ||||||
chr7:105489135
|
G | A | 72 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(69): Show | 72 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.920+2405C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105489135 | ||||||
chr7:105489147
|
C | CA | 19 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0049others(16): Show | 19 | HG00735.hp1 HG01074.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.920+2392dupT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105489147 | ||||||
chr7:105489147
|
C | CAA | 21 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(18): Show | 21 | HG01884.hp2 HG02145.hp2 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.920+2391_920+2392d others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105489147 | ||||||
chr7:105489147
|
C | CAAA | 13 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(10): Show | 13 | HG02976.hp2 NA18945.hp2 NA18955.hp1 others(10): Show |
intron_variant | MODIFIER | c.920+2390_920+2392d others(5): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105489147 | ||||||
chr7:105489147
|
C | CAAAAA | 16 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(13): Show | 16 | HG01069.hp1 HG01071.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.920+2388_920+2392d others(7): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105489147 | ||||||
chr7:105489147
|
CA | C | 20 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0074others(17): Show | 20 | HG00099.hp2 HG01074.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.920+2392delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105489147 | ||||||
chr7:105489165
|
A | G | 1 | a0001c0001t0001g0235 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.920+2375T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105489165 | ||||||
chr7:105489205
|
CT | C | 12 | a0001c0001t0001g0030a0001c0001t0001g0124a0001c0001t0001g0198others(9): Show | 12 | HG01074.hp1 HG01081.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.920+2334delA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105489205 | ||||||
chr7:105489323
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.920+2217C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105489323 | ||||||
chr7:105489359
|
C | T | 1 | a0001c0001t0001g0189 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.920+2181G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105489359 | ||||||
chr7:105489505
|
C | T | 16 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(13): Show | 16 | HG02976.hp2 NA18945.hp2 NA18950.hp1 others(13): Show |
intron_variant | MODIFIER | c.920+2035G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105489505 | ||||||
chr7:105489989
|
T | C | 331 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(328): Show | 331 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(328): Show |
intron_variant | MODIFIER | c.920+1551A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105489989 | ||||||
chr7:105490001
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.920+1539G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105490001 | ||||||
chr7:105490111
|
T | TA | 10 | a0001c0001t0001g0020a0001c0001t0001g0103a0001c0001t0001g0157others(7): Show | 10 | HG01255.hp1 HG01361.hp2 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.920+1428dupT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105490111 | ||||||
chr7:105490154
|
G | T | 1 | a0001c0001t0001g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.920+1386C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105490154 | ||||||
chr7:105490159
|
T | A | 1 | a0001c0001t0001g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.920+1381A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105490159 | ||||||
chr7:105490377
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.920+1163T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105490377 | ||||||
chr7:105490573
|
T | A | 5 | a0001c0001t0001g0222a0001c0001t0001g0241a0001c0001t0003g0240others(2): Show | 5 | HG02109.hp2 HG02257.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.920+967A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105490573 | ||||||
chr7:105490745
|
T | C | 92 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(89): Show | 92 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(89): Show |
intron_variant | MODIFIER | c.920+795A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105490745 | ||||||
chr7:105490928
|
C | T | 1 | a0001c0001t0001g0257 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.920+612G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105490928 | ||||||
chr7:105491266
|
G | T | 88 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(85): Show | 88 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.920+274C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105491266 | ||||||
chr7:105491364
|
A | G | 8 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0260others(5): Show | 8 | HG02074.hp1 NA18944.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.920+176T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105491364 | ||||||
chr7:105491402
|
C | G | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(48): Show | 51 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.920+138G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105491402 | ||||||
chr7:105491525
|
G | A | 2 | a0001c0003t0003g0219a0001c0003t0003g0221 | 2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.920+15C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 7/15 | chr7 | 105491525 | ||||||
chr7:105491789
|
G | A | 1 | a0001c0001t0001g0175 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.843-172C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105491789 | ||||||
chr7:105491913
|
T | G | 1 | a0001c0001t0001g0083 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.843-296A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105491913 | ||||||
chr7:105492006
|
G | A | 11 | a0001c0001t0001g0030a0001c0001t0001g0198a0001c0001t0001g0199others(8): Show | 11 | HG01074.hp1 HG01081.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.843-389C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492006 | ||||||
chr7:105492052
|
C | CA | 206 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(203): Show | 206 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.843-436dupT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492052 | ||||||
chr7:105492052
|
C | CAA | 48 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(45): Show | 48 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.843-437_843-436dup others(2): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492052 | ||||||
chr7:105492052
|
CAA | C | 49 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(46): Show | 49 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.843-437_843-436del others(2): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492052 | ||||||
chr7:105492112
|
T | A | 1 | a0001c0001t0001g0062 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.843-495A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492112 | ||||||
chr7:105492307
|
T | C | 1 | a0001c0001t0002g0315 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.843-690A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492307 | ||||||
chr7:105492332
|
C | CT | 20 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.843-716dupA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492332 | ||||||
chr7:105492371
|
C | G | 1 | a0001c0001t0001g0189 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.843-754G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492371 | ||||||
chr7:105492439
|
T | C | 336 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(333): Show | 336 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.843-822A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492439 | ||||||
chr7:105492500
|
A | AT | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 102 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.843-884dupA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492500 | ||||||
chr7:105492500
|
A | ATT | 8 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0022others(5): Show | 8 | HG01884.hp2 HG02896.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.843-885_843-884dup others(2): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492500 | ||||||
chr7:105492500
|
AT | A | 36 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0067others(33): Show | 36 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.843-884delA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492500 | ||||||
chr7:105492500
|
ATTTT | A | 16 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(13): Show | 16 | HG01069.hp1 HG01071.hp2 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.843-887_843-884del others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492500 | ||||||
chr7:105492507
|
T | A | 2 | a0001c0005t0001g0040a0001c0005t0001g0041 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.843-890A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492507 | ||||||
chr7:105492599
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.843-982C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492599 | ||||||
chr7:105492635
|
A | G | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.843-1018T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492635 | ||||||
chr7:105492666
|
C | A | 1 | a0001c0001t0001g0197 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.843-1049G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492666 | ||||||
chr7:105492717
|
C | T | 18 | a0001c0001t0001g0030a0001c0001t0001g0054a0001c0001t0001g0198others(15): Show | 18 | HG01074.hp1 HG01081.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.843-1100G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492717 | ||||||
chr7:105492729
|
G | A | 2 | a0001c0001t0001g0241a0001c0001t0003g0240 | 2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.843-1112C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492729 | ||||||
chr7:105492749
|
C | T | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.843-1132G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492749 | ||||||
chr7:105492802
|
C | T | 49 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(46): Show | 49 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.843-1185G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492802 | ||||||
chr7:105492840
|
G | C | 2 | a0001c0005t0001g0040a0001c0005t0001g0041 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.843-1223C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492840 | ||||||
chr7:105492871
|
G | C | 48 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(45): Show | 48 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.843-1254C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492871 | ||||||
chr7:105492934
|
C | T | 1 | a0001c0001t0002g0324 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.843-1317G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105492934 | ||||||
chr7:105493032
|
G | T | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.843-1415C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105493032 | ||||||
chr7:105493067
|
C | A | 14 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | NA18945.hp2 NA18950.hp1 NA18955.hp1 others(11): Show |
intron_variant | MODIFIER | c.843-1450G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105493067 | ||||||
chr7:105493316
|
G | A | 3 | a0001c0001t0001g0188a0001c0001t0001g0215a0001c0001t0001g0216 | 3 | HG00735.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.843-1699C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105493316 | ||||||
chr7:105493368
|
G | C | 1 | a0001c0001t0001g0133 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.843-1751C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105493368 | ||||||
chr7:105493368
|
G | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0012g0126 | 3 | NA18946.hp2 NA18950.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.843-1751C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105493368 | ||||||
chr7:105493377
|
G | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(1): Show | 4 | HG02630.hp2 HG03486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.843-1760C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105493377 | ||||||
chr7:105493506
|
G | C | 48 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(45): Show | 48 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.842+1636C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105493506 | ||||||
chr7:105493637
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18983.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.842+1505C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105493637 | ||||||
chr7:105493714
|
G | C | 48 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(45): Show | 48 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.842+1428C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105493714 | ||||||
chr7:105493732
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG01978.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.842+1410C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105493732 | ||||||
chr7:105493795
|
G | A | 1 | a0001c0001t0001g0013 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.842+1347C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105493795 | ||||||
chr7:105493828
|
T | C | 2 | a0001c0001t0001g0099a0003c0006t0001g0098 | 2 | NA18944.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.842+1314A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105493828 | ||||||
chr7:105493837
|
T | C | 2 | a0001c0001t0001g0072a0001c0001t0001g0212 | 2 | HG00099.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.842+1305A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105493837 | ||||||
chr7:105493868
|
T | C | 1 | a0001c0004t0001g0093 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.842+1274A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105493868 | ||||||
chr7:105493930
|
C | T | 1 | a0001c0001t0001g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.842+1212G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105493930 | ||||||
chr7:105494163
|
C | A | 1 | a0001c0003t0003g0288 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.842+979G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105494163 | ||||||
chr7:105494302
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.842+840T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105494302 | ||||||
chr7:105494362
|
C | T | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.842+780G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105494362 | ||||||
chr7:105494402
|
A | AT | 109 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(106): Show | 109 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.842+739dupA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105494402 | ||||||
chr7:105494402
|
A | ATT | 7 | a0001c0001t0001g0164a0001c0001t0001g0290a0001c0001t0001g0295others(4): Show | 7 | HG01255.hp1 HG01934.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.842+738_842+739dup others(2): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105494402 | ||||||
chr7:105494402
|
A | ATTT | 12 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(9): Show | 12 | HG01069.hp1 HG01071.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.842+737_842+739dup others(3): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105494402 | ||||||
chr7:105494402
|
AT | A | 11 | a0001c0001t0001g0038a0001c0001t0001g0048a0001c0001t0001g0056others(8): Show | 11 | HG00621.hp1 HG01074.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.842+739delA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105494402 | ||||||
chr7:105494487
|
G | A | 1 | a0001c0001t0019g0332 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.842+655C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105494487 | ||||||
chr7:105494565
|
A | G | 5 | a0001c0001t0001g0209a0001c0001t0001g0258a0001c0001t0001g0265others(2): Show | 5 | HG01433.hp2 HG01496.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.842+577T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105494565 | ||||||
chr7:105494813
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.842+329T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105494813 | ||||||
chr7:105494851
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.842+291G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105494851 | ||||||
chr7:105494894
|
T | G | 1 | a0001c0001t0001g0150 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.842+248A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105494894 | ||||||
chr7:105494903
|
G | T | 1 | a0001c0001t0001g0166 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.842+239C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105494903 | ||||||
chr7:105494973
|
T | TA | 11 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(8): Show | 11 | HG02004.hp2 HG02615.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.842+168dupT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105494973 | ||||||
chr7:105494973
|
TA | T | 9 | a0001c0001t0001g0003a0001c0001t0001g0190a0001c0001t0001g0201others(6): Show | 9 | HG01074.hp1 HG01256.hp2 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.842+168delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105494973 | ||||||
chr7:105494989
|
A | G | 4 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0062others(1): Show | 4 | HG00642.hp2 HG01081.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.842+153T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105494989 | ||||||
chr7:105495095
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.842+47G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105495095 | ||||||
chr7:105495098
|
T | C | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.842+44A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 6/15 | chr7 | 105495098 | ||||||
chr7:105495348
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.731-95T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105495348 | ||||||
chr7:105495528
|
CA | C | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.731-276delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105495528 | ||||||
chr7:105495599
|
G | T | 2 | a0001c0001t0005g0285a0001c0004t0001g0294 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.731-346C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105495599 | ||||||
chr7:105495613
|
T | G | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.731-360A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105495613 | ||||||
chr7:105495684
|
G | A | 4 | a0001c0001t0001g0062a0001c0001t0001g0295a0001c0001t0005g0285others(1): Show | 4 | HG01884.hp1 HG02976.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.731-431C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105495684 | ||||||
chr7:105495776
|
TA | T | 14 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | NA18945.hp2 NA18950.hp1 NA18955.hp1 others(11): Show |
intron_variant | MODIFIER | c.731-524delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105495776 | ||||||
chr7:105495854
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.731-601G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105495854 | ||||||
chr7:105496031
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.731-778C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496031 | ||||||
chr7:105496032
|
T | C | 1 | a0001c0001t0001g0030 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.731-779A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496032 | ||||||
chr7:105496082
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.731-829G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496082 | ||||||
chr7:105496139
|
C | T | 1 | a0001c0001t0002g0302 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.731-886G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496139 | ||||||
chr7:105496153
|
C | A | 50 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(47): Show | 50 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.731-900G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496153 | ||||||
chr7:105496184
|
T | TAC | 7 | a0001c0001t0002g0304a0001c0001t0002g0306a0001c0001t0002g0312others(4): Show | 7 | HG01256.hp1 HG01257.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.731-933_731-932dup others(2): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496184 | ||||||
chr7:105496184
|
TAC | T | 100 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(97): Show | 100 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.731-933_731-932del others(2): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496184 | ||||||
chr7:105496194
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.731-941G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496194 | ||||||
chr7:105496194
|
CACAT | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0009a0001c0001t0001g0016others(40): Show | 43 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.731-945_731-942del others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496194 | ||||||
chr7:105496194
|
CACATAT | C | 11 | a0001c0001t0001g0039a0001c0001t0001g0047a0001c0001t0001g0086others(8): Show | 11 | HG00642.hp1 HG02523.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.731-947_731-942del others(6): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496194 | ||||||
chr7:105496194
|
CACATATA others(1): Show |
C | 5 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0085others(2): Show | 5 | HG02280.hp2 HG02486.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.731-949_731-942del others(8): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496194 | ||||||
chr7:105496194
|
CACATATA others(3): Show |
C | 3 | a0001c0001t0001g0061a0001c0001t0001g0146a0001c0001t0001g0149 | 3 | HG03209.hp1 NA18964.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.731-951_731-942del others(10): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496194 | ||||||
chr7:105496196
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.731-943G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496196 | ||||||
chr7:105496196
|
CAT | C | 17 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0054others(14): Show | 17 | HG01069.hp1 HG01071.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.731-945_731-944del others(2): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496196 | ||||||
chr7:105496196
|
CATAT | C | 14 | a0001c0001t0001g0031a0001c0001t0001g0033a0001c0001t0001g0034others(11): Show | 14 | HG01070.hp2 HG01071.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.731-947_731-944del others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496196 | ||||||
chr7:105496196
|
CATATATA others(1): Show |
C | 11 | a0001c0001t0001g0030a0001c0001t0001g0198a0001c0001t0001g0199others(8): Show | 11 | HG01074.hp1 HG01081.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.731-951_731-944del others(8): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496196 | ||||||
chr7:105496196
|
CATATATA others(3): Show |
C | 1 | a0001c0001t0001g0043 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.731-953_731-944del others(10): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496196 | ||||||
chr7:105496196
|
CATATATA others(5): Show |
C | 2 | a0001c0001t0001g0046a0001c0001t0003g0070 | 2 | HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.731-955_731-944del others(12): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496196 | ||||||
chr7:105496198
|
T | C | 5 | a0001c0001t0001g0133a0001c0001t0002g0310a0001c0001t0002g0314others(2): Show | 5 | HG01175.hp2 HG02109.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.731-945A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496198 | ||||||
chr7:105496200
|
T | C | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-947A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496200 | ||||||
chr7:105496204
|
T | C | 2 | a0001c0001t0002g0309a0001c0001t0002g0328 | 2 | HG02040.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.731-951A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496204 | ||||||
chr7:105496214
|
T | G | 3 | a0001c0001t0001g0102a0001c0001t0001g0122a0001c0001t0001g0187 | 3 | NA18612.hp1 NA18965.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.731-961A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496214 | ||||||
chr7:105496216
|
T | G | 18 | a0001c0001t0001g0010a0001c0001t0001g0089a0001c0001t0001g0102others(15): Show | 18 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.731-963A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496216 | ||||||
chr7:105496216
|
T | TAG | 6 | a0001c0001t0001g0067a0001c0001t0001g0251a0001c0001t0001g0252others(3): Show | 6 | HG01243.hp1 HG02165.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.731-964_731-963ins others(2): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496216 | ||||||
chr7:105496216
|
T | TAGAGAGA others(3): Show |
1 | a0001c0001t0001g0062 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.731-964_731-963ins others(10): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496216 | ||||||
chr7:105496216
|
TATATATA others(11): Show |
T | 1 | a0001c0001t0001g0242 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.731-981_731-964del others(18): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496216 | ||||||
chr7:105496218
|
T | G | 81 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0009others(78): Show | 81 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.731-965A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496218 | ||||||
chr7:105496218
|
T | TAG | 7 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0259others(4): Show | 7 | HG02071.hp1 HG02083.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.731-966_731-965ins others(2): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496218 | ||||||
chr7:105496218
|
T | TAGAG | 4 | a0001c0001t0001g0275a0001c0001t0001g0290a0001c0001t0002g0319others(1): Show | 4 | HG00099.hp2 HG01993.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.731-966_731-965ins others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496218 | ||||||
chr7:105496218
|
T | TAGAGAGA others(7): Show |
1 | a0001c0001t0001g0119 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.731-966_731-965ins others(14): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496218 | ||||||
chr7:105496218
|
T | TAGAGAGA others(9): Show |
1 | a0001c0001t0001g0023 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.731-966_731-965ins others(16): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496218 | ||||||
chr7:105496218
|
T | TAGAGAGA others(11): Show |
2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | NA18945.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.731-966_731-965ins others(18): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496218 | ||||||
chr7:105496218
|
T | TAGAGAGA others(15): Show |
1 | a0001c0001t0001g0015 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.731-966_731-965ins others(22): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496218 | ||||||
chr7:105496218
|
TATATATA others(5): Show |
T | 1 | a0001c0001t0001g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.731-977_731-966del others(12): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496218 | ||||||
chr7:105496220
|
T | G | 175 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(172): Show | 175 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.731-967A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496220 | ||||||
chr7:105496220
|
T | TAG | 6 | a0001c0001t0001g0006a0001c0001t0001g0209a0001c0001t0001g0280others(3): Show | 6 | HG01496.hp1 HG02004.hp2 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.731-968_731-967ins others(2): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496220 | ||||||
chr7:105496220
|
T | TAGAG | 3 | a0001c0001t0002g0308a0001c0001t0002g0321a0001c0001t0002g0327 | 3 | HG01952.hp1 HG02145.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.731-968_731-967ins others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496220 | ||||||
chr7:105496220
|
T | TAGAGAGA others(5): Show |
1 | a0001c0001t0001g0024 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.731-968_731-967ins others(12): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496220 | ||||||
chr7:105496222
|
T | G | 231 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(228): Show | 231 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.731-969A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496222 | ||||||
chr7:105496222
|
T | TAG | 7 | a0001c0001t0001g0163a0001c0001t0001g0261a0001c0001t0001g0283others(4): Show | 7 | HG01346.hp2 HG01361.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.731-970_731-969ins others(2): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496222 | ||||||
chr7:105496222
|
T | TAGAG | 4 | a0001c0001t0002g0329a0001c0001t0010g0289a0001c0003t0003g0268others(1): Show | 4 | HG01891.hp2 HG02970.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.731-970_731-969ins others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496222 | ||||||
chr7:105496222
|
T | TAGAGAGA others(9): Show |
1 | a0001c0001t0001g0019 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.731-970_731-969ins others(16): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496222 | ||||||
chr7:105496224
|
T | G | 281 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(278): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.731-971A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496224 | ||||||
chr7:105496224
|
T | TAGAGAGA others(7): Show |
1 | a0001c0001t0001g0022 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.731-972_731-971ins others(14): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496224 | ||||||
chr7:105496224
|
T | TAGAGAGA others(11): Show |
1 | a0001c0001t0001g0028 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.731-972_731-971ins others(18): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496224 | ||||||
chr7:105496224
|
T | TAGAGAGA others(13): Show |
1 | a0001c0001t0001g0143 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.731-972_731-971ins others(20): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496224 | ||||||
chr7:105496226
|
T | G | 306 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(303): Show | 306 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.731-973A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496226 | ||||||
chr7:105496226
|
T | TAGAGAGA others(3): Show |
1 | a0001c0005t0001g0040 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.731-983_731-974dup others(10): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496226 | ||||||
chr7:105496226
|
T | TAGAGAGA others(5): Show |
1 | a0001c0005t0001g0041 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.731-985_731-974dup others(12): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496226 | ||||||
chr7:105496226
|
T | TAGAGAGA others(11): Show |
1 | a0001c0001t0001g0027 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.731-991_731-974dup others(18): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496226 | ||||||
chr7:105496226
|
T | TATAGAGA others(13): Show |
1 | a0001c0001t0001g0025 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.731-974_731-973ins others(20): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496226 | ||||||
chr7:105496226
|
TAG | T | 3 | a0001c0001t0004g0334a0001c0001t0004g0337a0001c0001t0004g0348 | 3 | HG02738.hp1 NA18946.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.731-975_731-974del others(2): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496226 | ||||||
chr7:105496228
|
G | T | 3 | a0001c0001t0001g0166a0001c0001t0004g0336a0001c0001t0004g0338 | 3 | HG02818.hp1 HG04228.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.731-975C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496228 | ||||||
chr7:105496230
|
G | T | 2 | a0001c0001t0004g0336a0001c0001t0004g0337 | 2 | HG04228.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.731-977C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496230 | ||||||
chr7:105496232
|
G | T | 2 | a0001c0001t0004g0337a0001c0001t0004g0349 | 2 | HG04184.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.731-979C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496232 | ||||||
chr7:105496251
|
A | G | 1 | a0001c0001t0005g0285 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.731-998T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496251 | ||||||
chr7:105496255
|
G | A | 9 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0112others(6): Show | 9 | HG01168.hp1 HG01192.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.731-1002C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496255 | ||||||
chr7:105496256
|
GA | G | 3 | a0001c0001t0001g0152a0001c0001t0001g0247a0001c0004t0001g0093 | 3 | HG01192.hp1 HG02280.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.731-1004delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496256 | ||||||
chr7:105496257
|
A | AGAGAGAG others(8): Show |
2 | a0001c0001t0001g0020a0001c0001t0001g0026 | 2 | NA18955.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.731-1005_731-1004i others(17): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496257 | ||||||
chr7:105496257
|
A | G | 1 | a0001c0001t0005g0285 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.731-1004T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496257 | ||||||
chr7:105496260
|
GAC | G | 339 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(336): Show | 339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.731-1009_731-1008d others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496260 | ||||||
chr7:105496262
|
C | G | 10 | a0001c0001t0001g0020a0001c0001t0001g0026a0001c0001t0001g0112others(7): Show | 10 | HG01168.hp1 HG01192.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.731-1009G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496262 | ||||||
chr7:105496324
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.731-1071T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496324 | ||||||
chr7:105496616
|
G | A | 2 | a0001c0001t0005g0285a0001c0004t0001g0294 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.731-1363C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496616 | ||||||
chr7:105496761
|
AAAGTATT others(2): Show |
A | 161 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(158): Show | 161 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.731-1517_731-1509d others(11): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496761 | ||||||
chr7:105496770
|
C | G | 1 | a0001c0001t0003g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.731-1517G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496770 | ||||||
chr7:105496786
|
C | A | 1 | a0001c0001t0001g0119 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.731-1533G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496786 | ||||||
chr7:105496894
|
C | G | 2 | a0001c0001t0002g0307a0001c0001t0002g0319 | 2 | HG00099.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.731-1641G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496894 | ||||||
chr7:105496959
|
G | A | 1 | a0001c0001t0002g0320 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.731-1706C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105496959 | ||||||
chr7:105497128
|
A | G | 4 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(1): Show | 4 | HG02630.hp2 HG03486.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.731-1875T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105497128 | ||||||
chr7:105497237
|
G | A | 5 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(2): Show | 5 | HG02559.hp2 HG02809.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-1984C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105497237 | ||||||
chr7:105497257
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.731-2004A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105497257 | ||||||
chr7:105497463
|
G | A | 1 | a0001c0001t0002g0317 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.731-2210C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105497463 | ||||||
chr7:105497631
|
T | G | 1 | a0001c0001t0001g0218 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.731-2378A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105497631 | ||||||
chr7:105497856
|
T | C | 2 | a0001c0001t0001g0259a0001c0001t0001g0279 | 2 | HG02071.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.731-2603A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105497856 | ||||||
chr7:105497929
|
T | C | 1 | a0001c0001t0014g0239 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.731-2676A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105497929 | ||||||
chr7:105498187
|
C | T | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.731-2934G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105498187 | ||||||
chr7:105498500
|
C | T | 87 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(84): Show | 87 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.731-3247G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105498500 | ||||||
chr7:105498813
|
G | A | 1 | a0001c0001t0001g0119 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.731-3560C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105498813 | ||||||
chr7:105498999
|
C | G | 2 | a0001c0005t0001g0040a0001c0005t0001g0041 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.730+3421G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105498999 | ||||||
chr7:105499127
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.730+3293C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105499127 | ||||||
chr7:105499292
|
A | G | 5 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+3128T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105499292 | ||||||
chr7:105499430
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.730+2990C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105499430 | ||||||
chr7:105499555
|
A | T | 155 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(152): Show | 155 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.730+2865T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105499555 | ||||||
chr7:105499556
|
A | T | 1 | a0001c0001t0001g0117 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.730+2864T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105499556 | ||||||
chr7:105499566
|
A | G | 3 | a0001c0001t0002g0303a0001c0001t0002g0309a0001c0001t0002g0328 | 3 | HG02040.hp1 HG02135.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.730+2854T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105499566 | ||||||
chr7:105499620
|
T | C | 1 | a0001c0001t0001g0160 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.730+2800A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105499620 | ||||||
chr7:105499804
|
TA | T | 5 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0010g0289others(2): Show | 5 | HG01891.hp2 HG02886.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+2615delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105499804 | ||||||
chr7:105500047
|
G | T | 1 | a0001c0001t0001g0263 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.730+2373C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105500047 | ||||||
chr7:105500110
|
C | T | 18 | a0001c0001t0001g0030a0001c0001t0001g0054a0001c0001t0001g0198others(15): Show | 18 | HG01074.hp1 HG01081.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.730+2310G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105500110 | ||||||
chr7:105500171
|
T | C | 7 | a0001c0001t0001g0054a0001c0001t0003g0053a0001c0001t0003g0237others(4): Show | 7 | HG01106.hp2 HG02055.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.730+2249A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105500171 | ||||||
chr7:105500327
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.730+2093G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105500327 | ||||||
chr7:105500375
|
C | T | 1 | a0001c0001t0001g0017 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.730+2045G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105500375 | ||||||
chr7:105500376
|
G | A | 3 | a0001c0001t0001g0222a0001c0003t0003g0219a0001c0003t0003g0221 | 3 | HG02257.hp1 HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.730+2044C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105500376 | ||||||
chr7:105500507
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.730+1913T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105500507 | ||||||
chr7:105500561
|
G | A | 47 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(44): Show | 47 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.730+1859C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105500561 | ||||||
chr7:105500690
|
C | T | 1 | a0001c0001t0014g0239 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.730+1730G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105500690 | ||||||
chr7:105500705
|
T | C | 91 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(88): Show | 91 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.730+1715A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105500705 | ||||||
chr7:105500743
|
C | T | 1 | a0001c0001t0003g0248 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.730+1677G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105500743 | ||||||
chr7:105500769
|
C | G | 1 | a0001c0001t0001g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.730+1651G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105500769 | ||||||
chr7:105500819
|
A | G | 1 | a0001c0001t0001g0230 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.730+1601T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105500819 | ||||||
chr7:105500912
|
G | T | 1 | a0001c0001t0001g0257 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.730+1508C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105500912 | ||||||
chr7:105501048
|
A | C | 2 | a0001c0001t0009g0068a0001c0001t0009g0069 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.730+1372T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501048 | ||||||
chr7:105501099
|
C | T | 2 | a0001c0005t0001g0040a0001c0005t0001g0041 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.730+1321G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501099 | ||||||
chr7:105501480
|
T | C | 1 | a0001c0001t0001g0255 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.730+940A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501480 | ||||||
chr7:105501722
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0022 | 2 | NA18955.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.730+698C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501722 | ||||||
chr7:105501726
|
C | T | 1 | a0001c0001t0005g0285 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.730+694G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501726 | ||||||
chr7:105501904
|
G | A | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.730+516C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501904 | ||||||
chr7:105501936
|
C | A | 11 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(8): Show | 11 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.730+484G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501936 | ||||||
chr7:105501940
|
G | T | 1 | a0001c0001t0001g0083 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.730+480C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501940 | ||||||
chr7:105501946
|
C | T | 1 | a0001c0001t0002g0326 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.730+474G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501946 | ||||||
chr7:105501954
|
CA | C | 8 | a0001c0001t0001g0031a0001c0001t0001g0067a0001c0001t0001g0102others(5): Show | 8 | HG01070.hp2 HG01243.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.730+465delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501954 | ||||||
chr7:105501954
|
CAAA | C | 21 | a0001c0001t0001g0071a0001c0001t0001g0092a0001c0001t0001g0120others(18): Show | 21 | HG00099.hp2 HG00609.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.730+463_730+465del others(3): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501954 | ||||||
chr7:105501966
|
AAAAATAT | A | 20 | a0001c0001t0001g0017a0001c0001t0001g0133a0001c0001t0002g0300others(17): Show | 20 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(17): Show |
intron_variant | MODIFIER | c.730+447_730+453del others(7): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501966 | ||||||
chr7:105501968
|
AAAT | A | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(193): Show | 196 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(193): Show |
intron_variant | MODIFIER | c.730+449_730+451del others(3): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501968 | ||||||
chr7:105501968
|
AAATATAT | A | 13 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0019others(10): Show | 13 | NA18945.hp2 NA18950.hp1 NA18955.hp1 others(10): Show |
intron_variant | MODIFIER | c.730+445_730+451del others(7): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501968 | ||||||
chr7:105501969
|
AAT | A | 8 | a0001c0001t0001g0089a0001c0001t0001g0158a0001c0001t0001g0161others(5): Show | 8 | HG00423.hp2 HG02027.hp1 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.730+449_730+450del others(2): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501969 | ||||||
chr7:105501969
|
AATAT | A | 6 | a0001c0001t0001g0048a0001c0001t0001g0083a0001c0001t0001g0200others(3): Show | 6 | HG01074.hp2 HG01081.hp2 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.730+447_730+450del others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501969 | ||||||
chr7:105501970
|
AT | A | 14 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(11): Show | 14 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.730+449delA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501970 | ||||||
chr7:105501970
|
ATAT | A | 38 | a0001c0001t0001g0010a0001c0001t0001g0030a0001c0001t0001g0039others(35): Show | 38 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.730+447_730+449del others(3): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501970 | ||||||
chr7:105501971
|
T | A | 3 | a0001c0001t0001g0047a0001c0001t0003g0037a0001c0001t0004g0333 | 3 | HG03516.hp1 NA19030.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.730+449A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501971 | ||||||
chr7:105501973
|
T | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0290a0001c0001t0002g0324 | 3 | HG00423.hp2 HG03486.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.730+447A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501973 | ||||||
chr7:105501975
|
T | A | 11 | a0001c0001t0001g0083a0001c0001t0001g0086a0001c0001t0001g0212others(8): Show | 11 | HG00099.hp1 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.730+445A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501975 | ||||||
chr7:105501977
|
T | A | 3 | a0001c0001t0001g0295a0001c0001t0005g0285a0001c0004t0001g0294 | 3 | HG01884.hp1 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.730+443A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105501977 | ||||||
chr7:105502058
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.730+362G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105502058 | ||||||
chr7:105502217
|
T | G | 1 | a0001c0001t0001g0260 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.730+203A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105502217 | ||||||
chr7:105502359
|
G | A | 1 | a0001c0001t0001g0254 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.730+61C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105502359 | ||||||
chr7:105502362
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0003g0070 | 3 | HG02630.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.730+58C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 5/15 | chr7 | 105502362 | ||||||
chr7:105502572
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG02818.hp1 | splice_region_variant&intron_variant | LOW | c.586-8T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105502572 | ||||||
chr7:105502577
|
A | C | 1 | a0001c0001t0001g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.586-13T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105502577 | ||||||
chr7:105502757
|
T | A | 5 | a0001c0001t0002g0304a0001c0001t0002g0306a0001c0001t0002g0310others(2): Show | 5 | HG01175.hp2 HG01256.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.586-193A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105502757 | ||||||
chr7:105502991
|
T | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18983.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.586-427A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105502991 | ||||||
chr7:105503063
|
A | G | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.586-499T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105503063 | ||||||
chr7:105503283
|
G | A | 33 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(30): Show | 33 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.586-719C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105503283 | ||||||
chr7:105503453
|
C | T | 47 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(44): Show | 47 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.586-889G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105503453 | ||||||
chr7:105503477
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.586-913C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105503477 | ||||||
chr7:105503612
|
G | A | 91 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(88): Show | 91 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.586-1048C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105503612 | ||||||
chr7:105503744
|
T | C | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.586-1180A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105503744 | ||||||
chr7:105503761
|
A | T | 33 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(30): Show | 33 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.586-1197T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105503761 | ||||||
chr7:105503830
|
G | A | 33 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(30): Show | 33 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.586-1266C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105503830 | ||||||
chr7:105503892
|
C | T | 33 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(30): Show | 33 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.586-1328G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105503892 | ||||||
chr7:105504070
|
C | CT | 53 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(50): Show | 53 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.586-1507dupA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504070 | ||||||
chr7:105504070
|
C | CTTT | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.586-1509_586-1507d others(5): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504070 | ||||||
chr7:105504070
|
C | CTTTTT | 14 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | NA18945.hp2 NA18950.hp1 NA18955.hp1 others(11): Show |
intron_variant | MODIFIER | c.586-1511_586-1507d others(7): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504070 | ||||||
chr7:105504114
|
G | A | 33 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(30): Show | 33 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.586-1550C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504114 | ||||||
chr7:105504137
|
TCGGCTCA others(92): Show |
T | 33 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(30): Show | 33 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.586-1672_586-1574d others(101): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504137 | ||||||
chr7:105504177
|
C | G | 1 | a0001c0001t0001g0162 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.586-1613G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504177 | ||||||
chr7:105504181
|
C | T | 35 | a0001c0001t0001g0163a0001c0001t0001g0257a0001c0001t0001g0259others(32): Show | 35 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.586-1617G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504181 | ||||||
chr7:105504227
|
G | A | 2 | a0001c0001t0001g0099a0003c0006t0001g0098 | 2 | NA18944.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.586-1663C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504227 | ||||||
chr7:105504230
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0003g0070 | 3 | HG02630.hp2 HG03486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.586-1666G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504230 | ||||||
chr7:105504242
|
C | T | 33 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(30): Show | 33 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.586-1678G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504242 | ||||||
chr7:105504290
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.585+1665G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504290 | ||||||
chr7:105504401
|
GA | G | 56 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(53): Show | 56 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.585+1553delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504401 | ||||||
chr7:105504432
|
C | T | 1 | a0001c0001t0001g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.585+1523G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504432 | ||||||
chr7:105504499
|
A | G | 72 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(69): Show | 72 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.585+1456T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504499 | ||||||
chr7:105504521
|
T | C | 33 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0006others(30): Show | 33 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.585+1434A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504521 | ||||||
chr7:105504537
|
A | T | 75 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(72): Show | 75 | HG00099.hp2 HG00438.hp1 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.585+1418T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504537 | ||||||
chr7:105504544
|
A | G | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | NA19005.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.585+1411T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504544 | ||||||
chr7:105504602
|
T | G | 1 | a0001c0001t0001g0044 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.585+1353A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504602 | ||||||
chr7:105504689
|
T | A | 1 | a0001c0001t0001g0230 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.585+1266A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504689 | ||||||
chr7:105504731
|
C | T | 1 | a0001c0001t0004g0340 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.585+1224G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504731 | ||||||
chr7:105504886
|
T | A | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.585+1069A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504886 | ||||||
chr7:105504912
|
G | A | 1 | a0001c0001t0016g0311 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.585+1043C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504912 | ||||||
chr7:105504933
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.585+1022C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504933 | ||||||
chr7:105504997
|
A | C | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+958T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105504997 | ||||||
chr7:105505000
|
A | G | 4 | a0001c0001t0001g0094a0001c0001t0001g0131a0001c0001t0001g0134others(1): Show | 4 | HG00597.hp1 HG00673.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.585+955T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505000 | ||||||
chr7:105505003
|
A | AT | 6 | a0001c0001t0001g0062a0001c0001t0001g0091a0001c0001t0001g0103others(3): Show | 6 | HG00423.hp1 HG02738.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.585+951dupA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505003 | ||||||
chr7:105505003
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0002g0323 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.585+951_585+952ins others(18): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505003 | ||||||
chr7:105505003
|
A | ATTTTTTT others(12): Show |
4 | a0001c0001t0001g0133a0001c0001t0002g0304a0001c0001t0002g0306others(1): Show | 4 | HG01256.hp1 HG01517.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+951_585+952ins others(19): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505003 | ||||||
chr7:105505003
|
A | ATTTTTTT others(13): Show |
8 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0305others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.585+951_585+952ins others(20): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505003 | ||||||
chr7:105505003
|
A | ATTTTTTT others(14): Show |
5 | a0001c0001t0002g0302a0001c0001t0002g0303a0001c0001t0002g0314others(2): Show | 5 | HG02109.hp1 HG02683.hp2 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.585+951_585+952ins others(21): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505003 | ||||||
chr7:105505003
|
A | ATTTTTTT others(15): Show |
1 | a0001c0001t0002g0316 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.585+951_585+952ins others(22): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505003 | ||||||
chr7:105505021
|
T | G | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+934A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505021 | ||||||
chr7:105505023
|
T | C | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+932A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505023 | ||||||
chr7:105505038
|
C | T | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+917G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505038 | ||||||
chr7:105505061
|
T | C | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+894A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505061 | ||||||
chr7:105505062
|
A | T | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+893T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505062 | ||||||
chr7:105505069
|
C | T | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+886G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505069 | ||||||
chr7:105505070
|
T | G | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+885A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505070 | ||||||
chr7:105505075
|
G | A | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+880C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505075 | ||||||
chr7:105505082
|
C | G | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+873G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505082 | ||||||
chr7:105505086
|
T | C | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+869A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505086 | ||||||
chr7:105505088
|
T | C | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+867A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505088 | ||||||
chr7:105505093
|
T | C | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+862A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505093 | ||||||
chr7:105505094
|
A | G | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+861T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505094 | ||||||
chr7:105505101
|
A | C | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+854T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505101 | ||||||
chr7:105505103
|
A | C | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+852T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505103 | ||||||
chr7:105505104
|
G | C | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+851C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505104 | ||||||
chr7:105505111
|
T | C | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+844A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505111 | ||||||
chr7:105505129
|
T | C | 1 | a0001c0001t0002g0325 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.585+826A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505129 | ||||||
chr7:105505192
|
G | C | 2 | a0001c0001t0005g0285a0001c0004t0001g0294 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.585+763C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505192 | ||||||
chr7:105505214
|
G | T | 14 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(11): Show | 14 | NA18945.hp2 NA18950.hp1 NA18955.hp1 others(11): Show |
intron_variant | MODIFIER | c.585+741C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505214 | ||||||
chr7:105505231
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.585+724C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505231 | ||||||
chr7:105505246
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.585+709C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505246 | ||||||
chr7:105505248
|
C | T | 2 | a0001c0001t0005g0285a0001c0004t0001g0294 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.585+707G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505248 | ||||||
chr7:105505680
|
T | A | 35 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0049others(32): Show | 35 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.585+275A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505680 | ||||||
chr7:105505716
|
C | T | 2 | a0001c0001t0005g0285a0001c0004t0001g0294 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.585+239G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505716 | ||||||
chr7:105505743
|
C | G | 19 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(16): Show | 19 | HG01069.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.585+212G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505743 | ||||||
chr7:105505849
|
A | G | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.585+106T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505849 | ||||||
chr7:105505912
|
C | G | 88 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0018others(85): Show | 88 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.585+43G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 4/15 | chr7 | 105505912 | ||||||
chr7:105506146
|
A | AT | 316 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(313): Show | 316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.483+42dupA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 3/15 | chr7 | 105506146 | ||||||
chr7:105506365
|
A | G | 22 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(19): Show | 22 | HG00423.hp2 HG00735.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.399-92T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105506365 | ||||||
chr7:105506420
|
T | G | 11 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(8): Show | 11 | HG01074.hp1 HG01081.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.399-147A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105506420 | ||||||
chr7:105506465
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.399-192A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105506465 | ||||||
chr7:105506493
|
A | G | 22 | a0001c0001t0001g0133a0001c0001t0002g0300a0001c0001t0002g0301others(19): Show | 22 | HG00423.hp2 HG00735.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.399-220T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105506493 | ||||||
chr7:105506569
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.399-296G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105506569 | ||||||
chr7:105506631
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.399-358G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105506631 | ||||||
chr7:105506661
|
G | T | 1 | a0001c0001t0001g0190 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.399-388C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105506661 | ||||||
chr7:105506703
|
G | A | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.399-430C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105506703 | ||||||
chr7:105506797
|
C | T | 3 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | HG02630.hp2 HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.399-524G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105506797 | ||||||
chr7:105506862
|
C | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.399-589G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105506862 | ||||||
chr7:105507140
|
G | A | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.399-867C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105507140 | ||||||
chr7:105507192
|
C | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.399-919G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105507192 | ||||||
chr7:105507198
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.398+917T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105507198 | ||||||
chr7:105507202
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.398+913G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105507202 | ||||||
chr7:105507297
|
T | C | 327 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(324): Show | 327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.398+818A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105507297 | ||||||
chr7:105507298
|
G | A | 2 | a0001c0001t0001g0047a0001c0001t0003g0070 | 2 | HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.398+817C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105507298 | ||||||
chr7:105507374
|
G | C | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.398+741C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105507374 | ||||||
chr7:105507441
|
T | C | 1 | a0001c0001t0001g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.398+674A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105507441 | ||||||
chr7:105507453
|
A | C | 329 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(326): Show | 329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.398+662T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105507453 | ||||||
chr7:105507631
|
T | C | 69 | a0001c0001t0001g0010a0001c0001t0001g0015a0001c0001t0001g0016others(66): Show | 69 | HG00280.hp2 HG00438.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.398+484A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105507631 | ||||||
chr7:105507645
|
T | G | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.398+470A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105507645 | ||||||
chr7:105507918
|
G | A | 5 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(2): Show | 5 | HG02630.hp2 HG03486.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.398+197C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105507918 | ||||||
chr7:105508013
|
G | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.398+102C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 2/15 | chr7 | 105508013 | ||||||
chr7:105508603
|
C | T | 1 | a0001c0001t0001g0162 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-32-59G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508603 | ||||||
chr7:105508640
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(1): Show | 4 | HG00642.hp2 HG00738.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-96C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508640 | ||||||
chr7:105508729
|
A | G | 128 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(125): Show | 128 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.-32-185T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508729 | ||||||
chr7:105508732
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0001g0050 | 2 | HG01074.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-32-188G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508732 | ||||||
chr7:105508796
|
C | T | 10 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(7): Show | 10 | HG01074.hp1 HG01081.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32-252G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508796 | ||||||
chr7:105508813
|
A | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-269T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508813 | ||||||
chr7:105508825
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-32-281A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508825 | ||||||
chr7:105508826
|
A | C | 128 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(125): Show | 128 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.-32-282T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508826 | ||||||
chr7:105508871
|
T | TA | 17 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0044others(14): Show | 17 | HG01884.hp1 HG01891.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-32-328dupT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508871 | ||||||
chr7:105508871
|
T | TAAAAAAA others(4): Show |
5 | a0001c0001t0002g0304a0001c0001t0002g0310a0001c0001t0002g0312others(2): Show | 5 | HG01175.hp2 HG01257.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-338_-32-328dup others(11): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508871 | ||||||
chr7:105508871
|
T | TAAAAAAA others(5): Show |
1 | a0001c0001t0002g0314 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-32-339_-32-328dup others(12): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508871 | ||||||
chr7:105508871
|
T | TAAAAAAA others(6): Show |
4 | a0001c0001t0002g0306a0001c0001t0002g0319a0001c0001t0002g0320others(1): Show | 4 | HG00099.hp2 HG01256.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-340_-32-328dup others(13): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508871 | ||||||
chr7:105508871
|
T | TAAAAAAA others(7): Show |
14 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0303others(11): Show | 14 | HG00423.hp2 HG00735.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.-32-341_-32-328dup others(14): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508871 | ||||||
chr7:105508871
|
T | TAAAAAAA others(8): Show |
4 | a0001c0001t0002g0302a0001c0001t0002g0308a0001c0001t0002g0325others(1): Show | 4 | HG02145.hp1 HG03710.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-32-342_-32-328dup others(15): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508871 | ||||||
chr7:105508871
|
T | TAAAAAAA others(9): Show |
1 | a0001c0001t0002g0309 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-32-343_-32-328dup others(16): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508871 | ||||||
chr7:105508871
|
T | TAAAAAAA others(16): Show |
1 | a0001c0001t0016g0311 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-32-350_-32-328dup others(23): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508871 | ||||||
chr7:105508871
|
TA | T | 36 | a0001c0001t0001g0078a0001c0001t0001g0091a0001c0001t0001g0092others(33): Show | 36 | HG00597.hp1 HG00639.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-32-328delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508871 | ||||||
chr7:105508871
|
TAA | T | 180 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(177): Show | 180 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.-32-329_-32-328del others(2): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508871 | ||||||
chr7:105508871
|
TAAA | T | 16 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0088others(13): Show | 16 | HG00609.hp2 HG01074.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.-32-330_-32-328del others(3): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508871 | ||||||
chr7:105508871
|
TAAAAAAA others(10): Show |
T | 1 | a0001c0001t0001g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-32-344_-32-328del others(17): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508871 | ||||||
chr7:105508907
|
A | T | 1 | a0001c0001t0001g0235 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-32-363T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508907 | ||||||
chr7:105508947
|
G | A | 2 | a0001c0001t0005g0285a0001c0004t0001g0294 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-32-403C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508947 | ||||||
chr7:105508955
|
C | T | 37 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(34): Show | 37 | HG00438.hp1 HG00639.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.-32-411G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508955 | ||||||
chr7:105508957
|
G | A | 37 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(34): Show | 37 | HG00438.hp1 HG00639.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.-32-413C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508957 | ||||||
chr7:105508972
|
G | A | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-428C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105508972 | ||||||
chr7:105509024
|
CAAA | C | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-483_-32-481del others(3): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509024 | ||||||
chr7:105509031
|
A | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-487T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509031 | ||||||
chr7:105509050
|
G | C | 1 | a0001c0001t0001g0177 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-32-506C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509050 | ||||||
chr7:105509053
|
A | G | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-509T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509053 | ||||||
chr7:105509184
|
C | CA | 28 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(25): Show | 28 | HG00558.hp2 HG01175.hp2 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.-32-641dupT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAA | 17 | a0001c0001t0002g0301a0001c0001t0002g0302a0001c0001t0002g0305others(14): Show | 17 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(14): Show |
intron_variant | MODIFIER | c.-32-642_-32-641dup others(2): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(3): Show |
6 | a0001c0001t0001g0046a0001c0001t0001g0062a0001c0001t0001g0102others(3): Show | 6 | HG01074.hp1 HG01081.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-32-650_-32-641dup others(10): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(4): Show |
15 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0051others(12): Show | 15 | HG01074.hp2 HG01496.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-32-651_-32-641dup others(11): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(5): Show |
24 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0050others(21): Show | 24 | HG00639.hp1 HG01168.hp1 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.-32-652_-32-641dup others(12): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(6): Show |
19 | a0001c0001t0001g0043a0001c0001t0001g0057a0001c0001t0001g0058others(16): Show | 19 | HG00438.hp1 HG01243.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.-32-653_-32-641dup others(13): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(7): Show |
7 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0263others(4): Show | 7 | HG01891.hp1 HG02165.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-32-654_-32-641dup others(14): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(8): Show |
3 | a0001c0001t0001g0015a0001c0001t0001g0264a0001c0003t0003g0268 | 3 | HG01891.hp2 NA19004.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.-32-655_-32-641dup others(15): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(9): Show |
3 | a0001c0001t0001g0017a0001c0001t0003g0060a0001c0001t0004g0335 | 3 | HG02735.hp1 NA19030.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-32-656_-32-641dup others(16): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0003g0053 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-32-657_-32-641dup others(17): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0003g0066 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-32-658_-32-641dup others(18): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(12): Show |
3 | a0001c0001t0004g0338a0001c0001t0004g0340a0001c0001t0004g0341 | 3 | HG02027.hp2 HG02155.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.-32-659_-32-641dup others(19): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(13): Show |
2 | a0001c0001t0004g0339a0001c0001t0004g0342 | 2 | HG00597.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.-32-660_-32-641dup others(20): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(14): Show |
1 | a0001c0001t0011g0063 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-32-661_-32-641dup others(21): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(16): Show |
2 | a0001c0001t0001g0054a0001c0001t0019g0332 | 2 | HG02055.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-32-663_-32-641dup others(23): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0004g0343 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-32-665_-32-641dup others(25): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(20): Show |
1 | a0001c0001t0005g0055 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-32-667_-32-641dup others(27): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(21): Show |
1 | a0001c0001t0001g0297 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-32-641_-32-640ins others(28): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(25): Show |
2 | a0001c0001t0004g0345a0001c0001t0006g0346 | 2 | HG01070.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.-32-641_-32-640ins others(32): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(27): Show |
1 | a0001c0001t0006g0347 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-32-641_-32-640ins others(34): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
C | CAAAAAAA others(34): Show |
1 | a0001c0001t0004g0334 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-32-641_-32-640ins others(41): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
CAAA | C | 23 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0078others(20): Show | 23 | HG00280.hp1 HG00621.hp1 HG00621.hp2 others(20): Show |
intron_variant | MODIFIER | c.-32-643_-32-641del others(3): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
CAAAA | C | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(158): Show | 161 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.-32-644_-32-641del others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509184
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0061 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-32-653_-32-641del others(13): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509184 | ||||||
chr7:105509260
|
A | G | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-716T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509260 | ||||||
chr7:105509262
|
G | A | 14 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 14 | HG00558.hp2 NA18945.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.-32-718C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509262 | ||||||
chr7:105509284
|
A | G | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-32-740T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509284 | ||||||
chr7:105509296
|
A | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-752T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509296 | ||||||
chr7:105509451
|
C | T | 24 | a0001c0001t0001g0072a0001c0001t0001g0100a0001c0001t0001g0101others(21): Show | 24 | HG00639.hp2 HG01106.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.-32-907G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509451 | ||||||
chr7:105509522
|
G | A | 29 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(26): Show | 29 | HG01074.hp2 HG01243.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-32-978C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509522 | ||||||
chr7:105509599
|
C | T | 128 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(125): Show | 128 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.-32-1055G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509599 | ||||||
chr7:105509674
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-32-1130G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509674 | ||||||
chr7:105509774
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-32-1230A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509774 | ||||||
chr7:105509808
|
C | A | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-1264G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509808 | ||||||
chr7:105509980
|
G | A | 3 | a0001c0001t0006g0344a0001c0001t0006g0346a0001c0001t0006g0347 | 3 | HG01070.hp2 HG01071.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-32-1436C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105509980 | ||||||
chr7:105510022
|
C | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-1478G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510022 | ||||||
chr7:105510295
|
T | C | 128 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(125): Show | 128 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.-32-1751A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510295 | ||||||
chr7:105510412
|
A | C | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1868T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510412 | ||||||
chr7:105510413
|
G | C | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1869C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510413 | ||||||
chr7:105510414
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1870C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510414 | ||||||
chr7:105510419
|
A | C | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1875T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510419 | ||||||
chr7:105510420
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1876A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510420 | ||||||
chr7:105510421
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1877T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510421 | ||||||
chr7:105510423
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1879T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510423 | ||||||
chr7:105510424
|
G | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1880C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510424 | ||||||
chr7:105510427
|
C | G | 1 | a0001c0001t0001g0076 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-32-1883G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510427 | ||||||
chr7:105510427
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1883G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510427 | ||||||
chr7:105510429
|
G | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1885C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510429 | ||||||
chr7:105510430
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1886G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510430 | ||||||
chr7:105510432
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1888T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510432 | ||||||
chr7:105510439
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1895T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510439 | ||||||
chr7:105510442
|
T | G | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1898A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510442 | ||||||
chr7:105510444
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1900G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510444 | ||||||
chr7:105510448
|
A | C | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1904T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510448 | ||||||
chr7:105510451
|
G | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1907C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510451 | ||||||
chr7:105510453
|
G | C | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1909C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510453 | ||||||
chr7:105510457
|
G | C | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1913C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510457 | ||||||
chr7:105510458
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1914G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510458 | ||||||
chr7:105510458
|
C | T | 12 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-32-1914G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510458 | ||||||
chr7:105510459
|
C | G | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1915G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510459 | ||||||
chr7:105510464
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1920T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510464 | ||||||
chr7:105510471
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1927T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510471 | ||||||
chr7:105510482
|
T | A | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1938A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510482 | ||||||
chr7:105510483
|
C | A | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1939G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510483 | ||||||
chr7:105510488
|
G | C | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1944C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510488 | ||||||
chr7:105510489
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1945T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510489 | ||||||
chr7:105510497
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1953T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510497 | ||||||
chr7:105510499
|
G | A | 1 | a0001c0001t0001g0252 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-32-1955C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510499 | ||||||
chr7:105510505
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1961T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510505 | ||||||
chr7:105510508
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1964T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510508 | ||||||
chr7:105510513
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1969T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510513 | ||||||
chr7:105510521
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1977T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510521 | ||||||
chr7:105510531
|
T | G | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1987A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510531 | ||||||
chr7:105510539
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-1995C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510539 | ||||||
chr7:105510545
|
A | G | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-2001T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510545 | ||||||
chr7:105510562
|
T | G | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-2018A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510562 | ||||||
chr7:105510571
|
T | A | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-2027A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510571 | ||||||
chr7:105510577
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-2033C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510577 | ||||||
chr7:105510582
|
A | C | 129 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(126): Show | 129 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.-32-2038T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510582 | ||||||
chr7:105510583
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-2039C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510583 | ||||||
chr7:105510591
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-2047C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510591 | ||||||
chr7:105510609
|
G | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-2065C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510609 | ||||||
chr7:105510618
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-2074T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510618 | ||||||
chr7:105510626
|
A | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-2082T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510626 | ||||||
chr7:105510640
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-2096C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510640 | ||||||
chr7:105510643
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-2099C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510643 | ||||||
chr7:105510659
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-2115C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510659 | ||||||
chr7:105510674
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-2130A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510674 | ||||||
chr7:105510675
|
G | T | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-2131C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510675 | ||||||
chr7:105510694
|
T | C | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-2150A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510694 | ||||||
chr7:105510695
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-32-2151C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510695 | ||||||
chr7:105510825
|
C | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-2281G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510825 | ||||||
chr7:105510838
|
A | C | 1 | a0001c0001t0001g0072 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-32-2294T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510838 | ||||||
chr7:105510900
|
T | C | 330 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(327): Show | 330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.-32-2356A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510900 | ||||||
chr7:105510985
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-32-2441A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105510985 | ||||||
chr7:105511054
|
C | T | 29 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(26): Show | 29 | HG01074.hp2 HG01243.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-32-2510G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511054 | ||||||
chr7:105511135
|
C | CATTCTCC others(679): Show |
28 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(25): Show | 28 | HG00423.hp2 HG00735.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.-32-2592_-32-2591i others(688): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511135 | ||||||
chr7:105511135
|
C | CATTCTCC others(679): Show |
1 | a0001c0001t0002g0319 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-32-2592_-32-2591i others(688): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511135 | ||||||
chr7:105511135
|
C | CATTCTCC others(680): Show |
2 | a0001c0001t0002g0305a0001c0001t0002g0310 | 2 | HG01175.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.-32-2592_-32-2591i others(689): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511135 | ||||||
chr7:105511156
|
C | T | 157 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(154): Show | 157 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.-32-2612G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511156 | ||||||
chr7:105511179
|
G | A | 10 | a0001c0001t0002g0307a0001c0001t0002g0308a0001c0001t0002g0319others(7): Show | 10 | HG00099.hp2 HG01934.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.-32-2635C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511179 | ||||||
chr7:105511323
|
G | A | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-2779C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511323 | ||||||
chr7:105511341
|
G | A | 9 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0034others(6): Show | 9 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-32-2797C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511341 | ||||||
chr7:105511412
|
C | T | 3 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0023 | 3 | NA18945.hp2 NA18959.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.-32-2868G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511412 | ||||||
chr7:105511441
|
TTAA | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-2900_-32-2898d others(5): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511441 | ||||||
chr7:105511442
|
T | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0227 | 2 | HG03688.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-32-2898A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511442 | ||||||
chr7:105511442
|
TA | T | 55 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0031others(52): Show | 55 | HG00438.hp1 HG00639.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.-32-2899delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511442 | ||||||
chr7:105511458
|
A | G | 1 | a0001c0001t0003g0248 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-32-2914T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511458 | ||||||
chr7:105511462
|
G | A | 1 | a0001c0001t0001g0257 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-32-2918C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511462 | ||||||
chr7:105511467
|
G | A | 2 | a0001c0001t0001g0228a0001c0001t0001g0231 | 2 | HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-32-2923C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511467 | ||||||
chr7:105511593
|
T | C | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-3049A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511593 | ||||||
chr7:105511625
|
A | G | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-3081T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511625 | ||||||
chr7:105511678
|
T | C | 1 | a0001c0001t0001g0292 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-32-3134A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511678 | ||||||
chr7:105511703
|
C | T | 19 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0049others(16): Show | 19 | HG01074.hp2 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.-32-3159G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511703 | ||||||
chr7:105511715
|
G | C | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-3171C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511715 | ||||||
chr7:105511726
|
G | A | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-3182C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511726 | ||||||
chr7:105511740
|
A | G | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-3196T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511740 | ||||||
chr7:105511811
|
A | C | 1 | a0001c0001t0001g0258 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-32-3267T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105511811 | ||||||
chr7:105512064
|
G | C | 2 | a0001c0001t0001g0115a0001c0001t0001g0116 | 2 | HG01257.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.-32-3520C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512064 | ||||||
chr7:105512081
|
G | A | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-3537C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512081 | ||||||
chr7:105512093
|
C | G | 37 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(34): Show | 37 | HG00438.hp1 HG00639.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.-32-3549G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512093 | ||||||
chr7:105512098
|
C | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-3554G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512098 | ||||||
chr7:105512131
|
A | G | 128 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(125): Show | 128 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.-32-3587T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512131 | ||||||
chr7:105512144
|
CAA | C | 21 | a0001c0001t0001g0023a0001c0001t0001g0192a0001c0001t0001g0222others(18): Show | 21 | HG00597.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-32-3602_-32-3601d others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512144 | ||||||
chr7:105512144
|
CAAA | C | 62 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0012others(59): Show | 62 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.-32-3603_-32-3601d others(5): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512144 | ||||||
chr7:105512144
|
CAAAA | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0006others(161): Show | 164 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.-32-3604_-32-3601d others(6): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512144 | ||||||
chr7:105512144
|
CAAAAA | C | 20 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0047others(17): Show | 20 | HG01074.hp1 HG01081.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.-32-3605_-32-3601d others(7): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512144 | ||||||
chr7:105512144
|
CAAAAAA | C | 39 | a0001c0001t0001g0046a0001c0001t0001g0198a0001c0001t0001g0257others(36): Show | 39 | HG00438.hp1 HG00639.hp1 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.-32-3606_-32-3601d others(8): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512144 | ||||||
chr7:105512144
|
CAAAAAAA | C | 20 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0048others(17): Show | 20 | HG01074.hp2 HG01891.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.-32-3607_-32-3601d others(9): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512144 | ||||||
chr7:105512173
|
A | T | 5 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0084others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-32-3629T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512173 | ||||||
chr7:105512253
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-32-3709G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512253 | ||||||
chr7:105512267
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-32-3723A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512267 | ||||||
chr7:105512289
|
A | G | 10 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0200others(7): Show | 10 | HG01074.hp1 HG01081.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-32-3745T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512289 | ||||||
chr7:105512346
|
C | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-3802G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512346 | ||||||
chr7:105512440
|
C | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-3896G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512440 | ||||||
chr7:105512453
|
T | C | 1 | a0001c0001t0002g0327 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-32-3909A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512453 | ||||||
chr7:105512744
|
C | T | 128 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(125): Show | 128 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.-32-4200G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512744 | ||||||
chr7:105512781
|
G | C | 68 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(65): Show | 68 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.-32-4237C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512781 | ||||||
chr7:105512795
|
G | A | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(162): Show | 165 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.-32-4251C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512795 | ||||||
chr7:105512807
|
G | T | 1 | a0001c0001t0001g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-32-4263C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512807 | ||||||
chr7:105512865
|
G | A | 14 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 14 | HG00558.hp2 NA18945.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.-32-4321C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105512865 | ||||||
chr7:105513088
|
T | A | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-4544A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513088 | ||||||
chr7:105513120
|
C | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-4576G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513120 | ||||||
chr7:105513121
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-32-4577C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513121 | ||||||
chr7:105513412
|
C | T | 1 | a0001c0001t0001g0109 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-32-4868G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513412 | ||||||
chr7:105513435
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-32-4891C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513435 | ||||||
chr7:105513449
|
C | G | 2 | a0001c0001t0001g0099a0003c0006t0001g0098 | 2 | NA18944.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.-32-4905G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513449 | ||||||
chr7:105513467
|
T | C | 1 | a0001c0001t0001g0087 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-32-4923A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513467 | ||||||
chr7:105513496
|
T | C | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-4952A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513496 | ||||||
chr7:105513548
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-32-5004C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513548 | ||||||
chr7:105513566
|
T | C | 1 | a0001c0001t0001g0013 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-32-5022A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513566 | ||||||
chr7:105513600
|
G | A | 1 | a0001c0001t0018g0331 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-32-5056C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513600 | ||||||
chr7:105513610
|
GC | G | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-5067delG | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513610 | ||||||
chr7:105513619
|
C | A | 29 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(26): Show | 29 | HG01074.hp2 HG01243.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-32-5075G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513619 | ||||||
chr7:105513647
|
C | T | 5 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0010g0289others(2): Show | 5 | HG01891.hp2 HG02886.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-32-5103G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513647 | ||||||
chr7:105513695
|
G | A | 1 | a0001c0001t0003g0237 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-32-5151C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513695 | ||||||
chr7:105513745
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-32-5201C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513745 | ||||||
chr7:105513779
|
G | A | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-32-5235C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513779 | ||||||
chr7:105513833
|
G | A | 1 | a0001c0002t0001g0196 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-32-5289C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513833 | ||||||
chr7:105513837
|
C | CA | 26 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 26 | HG00558.hp2 HG02074.hp1 HG03490.hp2 others(23): Show |
intron_variant | MODIFIER | c.-32-5294dupT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513837 | ||||||
chr7:105513837
|
CA | C | 22 | a0001c0001t0001g0003a0001c0001t0001g0030a0001c0001t0001g0031others(19): Show | 22 | HG01256.hp2 HG02145.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.-32-5294delT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513837 | ||||||
chr7:105513837
|
CAAA | C | 17 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0049others(14): Show | 17 | HG01074.hp2 HG01884.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.-32-5296_-32-5294d others(5): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513837 | ||||||
chr7:105513837
|
CAAAAAAA others(388): Show |
C | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-5688_-32-5294d others(2): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513837 | ||||||
chr7:105513838
|
AAAAAAAA others(385): Show |
A | 7 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-32-5686_-32-5295d others(2): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105513838 | ||||||
chr7:105514027
|
G | A | 23 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(20): Show | 23 | HG01074.hp2 HG01884.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.-32-5483C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514027 | ||||||
chr7:105514124
|
G | A | 4 | a0001c0001t0001g0054a0001c0001t0003g0053a0001c0001t0005g0055others(1): Show | 4 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-32-5580C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514124 | ||||||
chr7:105514226
|
G | A | 2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-32-5682C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514226 | ||||||
chr7:105514230
|
C | CA | 23 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(20): Show | 23 | HG01074.hp2 HG01884.hp2 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.-32-5687dupT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514230 | ||||||
chr7:105514230
|
C | CAA | 18 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(15): Show | 18 | HG00558.hp2 HG02055.hp2 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.-32-5688_-32-5687d others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514230 | ||||||
chr7:105514245
|
AT | A | 3 | a0001c0001t0001g0272a0001c0005t0001g0040a0001c0005t0001g0041 | 3 | HG01975.hp2 HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-32-5702delA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514245 | ||||||
chr7:105514246
|
T | A | 63 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(60): Show | 63 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.-32-5702A>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514246 | ||||||
chr7:105514299
|
G | T | 52 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(49): Show | 52 | HG00438.hp1 HG00639.hp1 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.-32-5755C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514299 | ||||||
chr7:105514324
|
G | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-5780C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514324 | ||||||
chr7:105514338
|
C | T | 1 | a0001c0001t0008g0154 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-32-5794G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514338 | ||||||
chr7:105514342
|
T | C | 127 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(124): Show | 127 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-32-5798A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514342 | ||||||
chr7:105514414
|
C | T | 40 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(37): Show | 40 | HG00438.hp1 HG00639.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.-32-5870G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514414 | ||||||
chr7:105514432
|
A | G | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-5888T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514432 | ||||||
chr7:105514494
|
C | T | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG01993.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-32-5950G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514494 | ||||||
chr7:105514497
|
AGGAGGCT others(25): Show |
A | 1 | a0001c0001t0003g0237 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-32-5985_-32-5954d others(34): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514497 | ||||||
chr7:105514498
|
G | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0101 | 2 | HG01993.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-32-5954C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514498 | ||||||
chr7:105514536
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-32-5992G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514536 | ||||||
chr7:105514538
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-32-5994T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514538 | ||||||
chr7:105514553
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-32-6009C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514553 | ||||||
chr7:105514560
|
C | T | 30 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(27): Show | 30 | HG01074.hp2 HG01243.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.-32-6016G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514560 | ||||||
chr7:105514590
|
C | T | 1 | a0001c0001t0001g0024 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-32-6046G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514590 | ||||||
chr7:105514607
|
A | AAAAAG | 37 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0257others(34): Show | 37 | HG00438.hp1 HG00639.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.-32-6068_-32-6064d others(7): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514607 | ||||||
chr7:105514669
|
A | T | 2 | a0001c0001t0004g0334a0001c0001t0004g0335 | 2 | HG02735.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-32-6125T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514669 | ||||||
chr7:105514694
|
G | A | 2 | a0001c0001t0001g0261a0001c0001t0001g0282 | 2 | NA18992.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-32-6150C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514694 | ||||||
chr7:105514770
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-32-6226G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514770 | ||||||
chr7:105514772
|
T | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0296a0001c0001t0001g0297 | 3 | HG01255.hp1 HG02148.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.-32-6228A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514772 | ||||||
chr7:105514794
|
TC | T | 30 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(27): Show | 30 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-32-6251delG | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514794 | ||||||
chr7:105514795
|
C | T | 1 | a0001c0001t0002g0304 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-32-6251G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514795 | ||||||
chr7:105514796
|
A | T | 126 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(123): Show | 126 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.-32-6252T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514796 | ||||||
chr7:105514853
|
G | A | 12 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(9): Show | 12 | HG00558.hp2 NA18945.hp2 NA18950.hp1 others(9): Show |
intron_variant | MODIFIER | c.-32-6309C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514853 | ||||||
chr7:105514873
|
G | A | 93 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(90): Show | 93 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.-32-6329C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514873 | ||||||
chr7:105514905
|
C | A | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-6361G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514905 | ||||||
chr7:105514919
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-32-6375G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514919 | ||||||
chr7:105514944
|
G | A | 12 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(9): Show | 12 | HG02145.hp2 HG02451.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.-32-6400C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105514944 | ||||||
chr7:105515024
|
G | C | 96 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(93): Show | 96 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.-32-6480C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515024 | ||||||
chr7:105515040
|
C | G | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-32-6496G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515040 | ||||||
chr7:105515074
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0015g0299 | 2 | NA18998.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-32-6530C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515074 | ||||||
chr7:105515091
|
G | A | 36 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(33): Show | 36 | HG00438.hp1 HG00639.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.-32-6547C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515091 | ||||||
chr7:105515140
|
C | T | 66 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(63): Show | 66 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.-32-6596G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515140 | ||||||
chr7:105515189
|
A | T | 1 | a0001c0001t0001g0106 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-32-6645T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515189 | ||||||
chr7:105515443
|
G | A | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+6609C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515443 | ||||||
chr7:105515483
|
C | T | 32 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(29): Show | 32 | HG00280.hp2 HG00438.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-33+6569G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515483 | ||||||
chr7:105515715
|
A | G | 24 | a0001c0001t0001g0044a0001c0001t0001g0048a0001c0001t0001g0049others(21): Show | 24 | HG01074.hp2 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.-33+6337T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515715 | ||||||
chr7:105515740
|
G | A | 4 | a0001c0001t0001g0054a0001c0001t0003g0053a0001c0001t0005g0055others(1): Show | 4 | HG02055.hp2 HG02572.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+6312C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515740 | ||||||
chr7:105515786
|
TTTTATTT others(6): Show |
T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+6253_-33+6265d others(15): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515786 | ||||||
chr7:105515790
|
A | T | 4 | a0001c0001t0001g0099a0001c0001t0001g0103a0001c0001t0001g0104others(1): Show | 4 | HG02738.hp2 HG03927.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33+6262T>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515790 | ||||||
chr7:105515790
|
AT | A | 18 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0001g0102others(15): Show | 18 | HG00597.hp2 HG00609.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.-33+6261delA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515790 | ||||||
chr7:105515791
|
T | TTTA | 61 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0072others(58): Show | 61 | HG00423.hp1 HG00544.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.-33+6260_-33+6261i others(5): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515791 | ||||||
chr7:105515791
|
T | TTTATTTA | 112 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(109): Show | 112 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.-33+6260_-33+6261i others(9): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515791 | ||||||
chr7:105515791
|
T | TTTATTTA others(4): Show |
54 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(51): Show | 54 | HG00099.hp1 HG00438.hp2 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.-33+6260_-33+6261i others(13): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515791 | ||||||
chr7:105515791
|
T | TTTATTTA others(8): Show |
11 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0028others(8): Show | 11 | HG01261.hp1 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-33+6260_-33+6261i others(17): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515791 | ||||||
chr7:105515791
|
T | TTTATTTA others(12): Show |
1 | a0001c0001t0001g0227 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-33+6260_-33+6261i others(21): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515791 | ||||||
chr7:105515791
|
T | TTTTATTT others(5): Show |
4 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0270others(1): Show | 4 | HG01433.hp1 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33+6249_-33+6260d others(14): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515791 | ||||||
chr7:105515791
|
T | TTTTATTT others(9): Show |
29 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0198others(26): Show | 29 | HG00438.hp1 HG01074.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.-33+6245_-33+6260d others(18): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515791 | ||||||
chr7:105515791
|
T | TTTTATTT others(13): Show |
14 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0224others(11): Show | 14 | HG02040.hp2 HG02165.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.-33+6241_-33+6260d others(22): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515791 | ||||||
chr7:105515791
|
T | TTTTATTT others(17): Show |
5 | a0001c0001t0001g0038a0001c0001t0001g0265a0001c0001t0001g0266others(2): Show | 5 | HG01433.hp2 HG01884.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33+6237_-33+6260d others(26): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515791 | ||||||
chr7:105515791
|
T | TTTTATTT others(21): Show |
3 | a0001c0001t0001g0267a0001c0001t0001g0281a0001c0001t0001g0282 | 3 | HG00639.hp1 NA18992.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-33+6233_-33+6260d others(30): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515791 | ||||||
chr7:105515791
|
T | TTTTTTTT others(9): Show |
2 | a0001c0001t0001g0286a0001c0001t0001g0287 | 2 | HG02886.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-33+6260_-33+6261i others(18): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105515791 | ||||||
chr7:105516195
|
T | C | 1 | a0001c0001t0001g0283 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-33+5857A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516195 | ||||||
chr7:105516241
|
G | A | 14 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 14 | HG00558.hp2 NA18945.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.-33+5811C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516241 | ||||||
chr7:105516298
|
T | C | 2 | a0001c0001t0005g0285a0001c0004t0001g0294 | 2 | HG01884.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-33+5754A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516298 | ||||||
chr7:105516334
|
C | T | 1 | a0001c0004t0001g0081 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-33+5718G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516334 | ||||||
chr7:105516379
|
G | C | 1 | a0001c0001t0001g0026 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-33+5673C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516379 | ||||||
chr7:105516401
|
G | A | 7 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(4): Show | 7 | HG02559.hp2 HG02809.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33+5651C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516401 | ||||||
chr7:105516424
|
C | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+5628G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516424 | ||||||
chr7:105516429
|
A | C | 1 | a0001c0001t0001g0097 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-33+5623T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516429 | ||||||
chr7:105516447
|
A | AT | 30 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(27): Show | 30 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.-33+5604dupA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516447 | ||||||
chr7:105516447
|
AT | A | 9 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0046others(6): Show | 9 | HG02630.hp2 HG02895.hp2 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33+5604delA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516447 | ||||||
chr7:105516501
|
T | C | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+5551A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516501 | ||||||
chr7:105516524
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-33+5528C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516524 | ||||||
chr7:105516600
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0096 | 2 | HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.-33+5452G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516600 | ||||||
chr7:105516717
|
GT | G | 127 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(124): Show | 127 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-33+5334delA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516717 | ||||||
chr7:105516814
|
T | C | 1 | a0001c0001t0001g0065 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-33+5238A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516814 | ||||||
chr7:105516847
|
G | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+5205C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516847 | ||||||
chr7:105516941
|
A | G | 1 | a0001c0004t0001g0093 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-33+5111T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516941 | ||||||
chr7:105516959
|
G | A | 1 | a0001c0001t0002g0328 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-33+5093C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516959 | ||||||
chr7:105516960
|
G | C | 1 | a0001c0001t0003g0237 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-33+5092C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516960 | ||||||
chr7:105516960
|
G | T | 2 | a0001c0001t0001g0075a0001c0001t0001g0076 | 2 | HG01516.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.-33+5092C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105516960 | ||||||
chr7:105517166
|
C | CTTTTTTT others(10): Show |
24 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(21): Show | 24 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.-33+4885_-33+4886i others(19): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105517166 | ||||||
chr7:105517166
|
C | CTTTTTTT others(11): Show |
7 | a0001c0001t0002g0304a0001c0001t0002g0305a0001c0001t0002g0306others(4): Show | 7 | HG01256.hp1 HG01517.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33+4885_-33+4886i others(20): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105517166 | ||||||
chr7:105517181
|
G | T | 36 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(33): Show | 36 | HG00438.hp1 HG00639.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.-33+4871C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105517181 | ||||||
chr7:105517256
|
A | C | 52 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0032others(49): Show | 52 | HG00438.hp1 HG00639.hp1 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.-33+4796T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105517256 | ||||||
chr7:105517309
|
C | T | 30 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(27): Show | 30 | HG01074.hp2 HG01243.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.-33+4743G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105517309 | ||||||
chr7:105517321
|
T | C | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+4731A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105517321 | ||||||
chr7:105517349
|
C | A | 1 | a0001c0001t0001g0039 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-33+4703G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105517349 | ||||||
chr7:105517412
|
C | T | 2 | a0001c0001t0001g0094a0001c0004t0001g0093 | 2 | HG02280.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-33+4640G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105517412 | ||||||
chr7:105517452
|
C | T | 2 | a0001c0001t0009g0068a0001c0001t0009g0069 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-33+4600G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105517452 | ||||||
chr7:105517513
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-33+4539G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105517513 | ||||||
chr7:105517658
|
A | G | 1 | a0001c0001t0001g0092 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-33+4394T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105517658 | ||||||
chr7:105517781
|
T | C | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+4271A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105517781 | ||||||
chr7:105517876
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-33+4176C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105517876 | ||||||
chr7:105517914
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-33+4138G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105517914 | ||||||
chr7:105517968
|
C | T | 1 | a0001c0001t0003g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-33+4084G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105517968 | ||||||
chr7:105518012
|
G | A | 2 | a0001c0005t0001g0040a0001c0005t0001g0041 | 2 | HG02055.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-33+4040C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105518012 | ||||||
chr7:105518020
|
G | C | 127 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(124): Show | 127 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-33+4032C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105518020 | ||||||
chr7:105518079
|
C | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+3973G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105518079 | ||||||
chr7:105518087
|
G | A | 3 | a0001c0001t0001g0241a0001c0001t0003g0240a0001c0001t0014g0239 | 3 | HG02109.hp2 HG02717.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-33+3965C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105518087 | ||||||
chr7:105518127
|
G | A | 1 | a0001c0001t0003g0066 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-33+3925C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105518127 | ||||||
chr7:105518395
|
CTTGT | C | 30 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(27): Show | 30 | HG01074.hp2 HG01243.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.-33+3653_-33+3656d others(6): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105518395 | ||||||
chr7:105518439
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-33+3613C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105518439 | ||||||
chr7:105518469
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | NA18983.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.-33+3583G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105518469 | ||||||
chr7:105518483
|
G | C | 1 | a0001c0001t0001g0243 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-33+3569C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105518483 | ||||||
chr7:105518526
|
C | G | 1 | a0001c0001t0001g0080 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-33+3526G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105518526 | ||||||
chr7:105518548
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-33+3504A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105518548 | ||||||
chr7:105518614
|
A | G | 1 | a0001c0001t0001g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-33+3438T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105518614 | ||||||
chr7:105518627
|
T | C | 1 | a0001c0001t0003g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-33+3425A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105518627 | ||||||
chr7:105518830
|
G | A | 65 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(62): Show | 65 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.-33+3222C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105518830 | ||||||
chr7:105518837
|
C | T | 1 | a0001c0001t0003g0029 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-33+3215G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105518837 | ||||||
chr7:105518880
|
T | C | 8 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0084others(5): Show | 8 | HG02486.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+3172A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105518880 | ||||||
chr7:105519014
|
C | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+3038G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105519014 | ||||||
chr7:105519040
|
T | C | 5 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0010g0289others(2): Show | 5 | HG01891.hp2 HG02886.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33+3012A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105519040 | ||||||
chr7:105519104
|
A | G | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+2948T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105519104 | ||||||
chr7:105519155
|
T | C | 1 | a0001c0001t0001g0290 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-33+2897A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105519155 | ||||||
chr7:105519159
|
C | G | 1 | a0001c0001t0003g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-33+2893G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105519159 | ||||||
chr7:105519213
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-33+2839C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105519213 | ||||||
chr7:105519214
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-33+2838C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105519214 | ||||||
chr7:105519215
|
C | CACAGAGA others(3): Show |
1 | a0001c0001t0001g0244 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-33+2836_-33+2837i others(12): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105519215 | ||||||
chr7:105519237
|
A | AT | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+2814dupA | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105519237 | ||||||
chr7:105519442
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-33+2610C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105519442 | ||||||
chr7:105519508
|
G | A | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+2544C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105519508 | ||||||
chr7:105519534
|
C | A | 1 | a0001c0001t0002g0329 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-33+2518G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105519534 | ||||||
chr7:105519612
|
C | T | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+2440G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105519612 | ||||||
chr7:105519806
|
C | T | 1 | a0001c0001t0002g0303 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-33+2246G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105519806 | ||||||
chr7:105519816
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-33+2236C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105519816 | ||||||
chr7:105519937
|
A | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG02132.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.-33+2115T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105519937 | ||||||
chr7:105519945
|
C | A | 30 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(27): Show | 30 | HG01074.hp2 HG01243.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.-33+2107G>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105519945 | ||||||
chr7:105519971
|
A | G | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+2081T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105519971 | ||||||
chr7:105520053
|
A | G | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+1999T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520053 | ||||||
chr7:105520153
|
G | A | 8 | a0001c0001t0001g0080a0001c0001t0001g0083a0001c0001t0001g0084others(5): Show | 8 | HG02486.hp2 HG02622.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33+1899C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520153 | ||||||
chr7:105520181
|
G | C | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+1871C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520181 | ||||||
chr7:105520211
|
G | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-33+1841C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520211 | ||||||
chr7:105520303
|
T | TA | 30 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(27): Show | 30 | HG01074.hp2 HG01243.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.-33+1748dupT | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520303 | ||||||
chr7:105520315
|
C | T | 14 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 14 | HG00558.hp2 NA18945.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.-33+1737G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520315 | ||||||
chr7:105520320
|
G | A | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+1732C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520320 | ||||||
chr7:105520414
|
G | A | 2 | a0001c0001t0001g0247a0001c0001t0003g0248 | 2 | HG01192.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-33+1638C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520414 | ||||||
chr7:105520478
|
T | TGCTGTGC others(224): Show |
27 | a0001c0001t0002g0303a0001c0001t0002g0304a0001c0001t0002g0305others(24): Show | 27 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.-33+1573_-33+1574i others(233): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520478 | ||||||
chr7:105520478
|
T | TGCTGTGC others(225): Show |
1 | a0001c0001t0017g0330 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-33+1573_-33+1574i others(234): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520478 | ||||||
chr7:105520478
|
T | TGCTGTGC others(224): Show |
3 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302 | 3 | HG01069.hp1 HG01071.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-33+1573_-33+1574i others(233): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520478 | ||||||
chr7:105520504
|
G | T | 6 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(3): Show | 6 | HG02615.hp1 HG02630.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33+1548C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520504 | ||||||
chr7:105520519
|
A | AAAAT | 40 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(37): Show | 40 | HG00558.hp2 HG00639.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.-33+1529_-33+1532d others(6): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520519 | ||||||
chr7:105520519
|
A | AAAATAAA others(1): Show |
15 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0257others(12): Show | 15 | HG01433.hp2 HG01496.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.-33+1525_-33+1532d others(10): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520519 | ||||||
chr7:105520519
|
A | AAAATAAA others(5): Show |
1 | a0001c0001t0003g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-33+1521_-33+1532d others(14): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520519 | ||||||
chr7:105520519
|
AAAATAAA others(1): Show |
A | 14 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0001g0077others(11): Show | 14 | HG00741.hp1 HG01261.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.-33+1525_-33+1532d others(10): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520519 | ||||||
chr7:105520519
|
AAAATAAA others(5): Show |
A | 239 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(236): Show | 239 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.-33+1521_-33+1532d others(14): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520519 | ||||||
chr7:105520521
|
A | AATAAATA others(5): Show |
1 | a0001c0001t0001g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-33+1530_-33+1531i others(14): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520521 | ||||||
chr7:105520529
|
A | AATAC | 5 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(2): Show | 5 | HG02615.hp1 HG02630.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33+1522_-33+1523i others(6): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520529 | ||||||
chr7:105520547
|
TAAATAAA others(6): Show |
T | 1 | a0001c0001t0001g0073 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-33+1492_-33+1504d others(15): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520547 | ||||||
chr7:105520559
|
T | TAAATAAA others(5): Show |
1 | a0001c0005t0001g0041 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-33+1492_-33+1493i others(14): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520559 | ||||||
chr7:105520565
|
T | C | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+1487A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520565 | ||||||
chr7:105520615
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-33+1437G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520615 | ||||||
chr7:105520670
|
C | T | 14 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(11): Show | 14 | HG00558.hp2 NA18945.hp2 NA18950.hp1 others(11): Show |
intron_variant | MODIFIER | c.-33+1382G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520670 | ||||||
chr7:105520686
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-33+1366G>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520686 | ||||||
chr7:105520699
|
G | T | 38 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(35): Show | 38 | HG00438.hp1 HG00639.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.-33+1353C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520699 | ||||||
chr7:105520763
|
T | C | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+1289A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520763 | ||||||
chr7:105520769
|
T | G | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+1283A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520769 | ||||||
chr7:105520782
|
A | C | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+1270T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520782 | ||||||
chr7:105520789
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-33+1263C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520789 | ||||||
chr7:105520886
|
T | C | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | NA18944.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-33+1166A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520886 | ||||||
chr7:105520911
|
G | A | 1 | a0001c0001t0003g0070 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-33+1141C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520911 | ||||||
chr7:105520965
|
G | A | 3 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | NA18612.hp2 NA18954.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-33+1087C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105520965 | ||||||
chr7:105521048
|
T | C | 1 | a0001c0001t0001g0254 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-33+1004A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521048 | ||||||
chr7:105521219
|
T | C | 1 | a0001c0001t0001g0255 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-33+833A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521219 | ||||||
chr7:105521236
|
G | C | 1 | a0001c0001t0001g0256 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-33+816C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521236 | ||||||
chr7:105521237
|
GGGGA | G | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+811_-33+814del others(4): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521237 | ||||||
chr7:105521288
|
T | C | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+764A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521288 | ||||||
chr7:105521308
|
T | G | 127 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(124): Show | 127 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(124): Show |
intron_variant | MODIFIER | c.-33+744A>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521308 | ||||||
chr7:105521398
|
ATTTCAGC others(3): Show |
A | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+644_-33+653del others(10): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521398 | ||||||
chr7:105521447
|
A | G | 30 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(27): Show | 30 | HG01074.hp2 HG01243.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.-33+605T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521447 | ||||||
chr7:105521521
|
G | T | 1 | a0001c0001t0001g0042 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-33+531C>A | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521521 | ||||||
chr7:105521522
|
C | G | 1 | a0001c0001t0001g0042 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-33+530G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521522 | ||||||
chr7:105521523
|
A | C | 1 | a0001c0001t0001g0042 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-33+529T>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521523 | ||||||
chr7:105521736
|
G | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(280): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.-33+316C>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521736 | ||||||
chr7:105521802
|
G | A | 38 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(35): Show | 38 | HG00438.hp1 HG00639.hp1 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.-33+250C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521802 | ||||||
chr7:105521820
|
G | GGAGCGGG others(7): Show |
31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+231_-33+232ins others(14): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521820 | ||||||
chr7:105521826
|
G | A | 1 | a0001c0001t0001g0295 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-33+226C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521826 | ||||||
chr7:105521846
|
C | G | 13 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(10): Show | 13 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.-33+206G>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521846 | ||||||
chr7:105521863
|
T | C | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+189A>G | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521863 | ||||||
chr7:105521889
|
A | G | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+163T>C | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521889 | ||||||
chr7:105521907
|
G | A | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG01255.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.-33+145C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521907 | ||||||
chr7:105521919
|
GACC | G | 31 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0002g0302others(28): Show | 31 | HG00099.hp2 HG00423.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-33+130_-33+132del others(3): Show |
PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521919 | ||||||
chr7:105521972
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-33+80C>T | PUS7 | ENSG00000091127.14 | transcript | ENST00000469408.6 | protein_coding | 1/15 | chr7 | 105521972 |