geneid | 25896 |
---|---|
ensemblid | ENSG00000143493.13 |
hgncid | 24484 |
symbol | INTS7 |
name | integrator complex subunit 7 |
refseq_nuc | NM_015434.4 |
refseq_prot | NP_056249.1 |
ensembl_nuc | ENST00000366994.8 |
ensembl_prot | ENSP00000355961.3 |
mane_status | MANE Select |
chr | chr1 |
start | 211940403 |
end | 212035557 |
strand | - |
ver | v1.2 |
region | chr1:211940403-212035557 |
region5000 | chr1:211935403-212040557 |
regionname0 | INTS7_chr1_211940403_212035557 |
regionname5000 | INTS7_chr1_211935403_212040557 |
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 | 962 | 344 | 71 | 62 | 149 | 16 | 44 | 115 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0002 | 0/0 | 962 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0003 | 0/0 | 962 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0004 | 0/0 | 962 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0005 | 0/0 | 962 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0006 | 0/0 | 962 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
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 | 2889 | 328 | 61 | 62 | 144 | 15 | 44 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
c0002 | 0/0 | 2889 | 8 | 8 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
c0003 | 0/0 | 2889 | 3 | 3 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
c0004 | 0/0 | 2889 | 3 | 2 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
c0005 | 0/0 | 2889 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
c0006 | 0/0 | 2889 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
c0007 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
c0008 | 0/0 | 2889 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
c0009 | 0/0 | 2889 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
c0010 | 0/0 | 2889 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
c0011 | 0/0 | 2889 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
c0012 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
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 | 1/0 | 1542 | 99 | 15 | 12 | 60 | 2 | 9 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0002 | 0/0 | 1542 | 93 | 5 | 18 | 48 | 8 | 14 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0003 | 0/1 | 1542 | 71 | 7 | 15 | 33 | 2 | 13 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0004 | 0/0 | 1542 | 36 | 18 | 3 | 7 | 1 | 7 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0005 | 0/0 | 1542 | 15 | 13 | 2 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0006 | 0/0 | 1542 | 7 | 0 | 7 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0007 | 0/0 | 1542 | 4 | 4 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0008 | 0/0 | 1542 | 3 | 1 | 2 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0009 | 0/0 | 1542 | 3 | 2 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0010 | 0/0 | 1540 | 3 | 2 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0011 | 0/0 | 1542 | 3 | 0 | 0 | 3 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0012 | 0/0 | 1542 | 2 | 2 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0013 | 0/0 | 1542 | 2 | 0 | 0 | 0 | 2 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0014 | 0/0 | 1542 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0015 | 0/0 | 1542 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0016 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0017 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0018 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0019 | 0/0 | 1542 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0020 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0021 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0022 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0023 | 0/0 | 1542 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
t0024 | 0/0 | 1542 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0013 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0150 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
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 | 2889 | 328 | 61 | 62 | 144 | 15 | 44 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0002 | 0/0 | 2889 | 8 | 8 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0004 | 0/0 | 2889 | 3 | 2 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0005 | 0/0 | 2889 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0006 | 0/0 | 2889 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0010 | 0/0 | 2889 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0002c0003 | 0/0 | 2889 | 3 | 3 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0002c0007 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0003c0008 | 0/0 | 2889 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0004c0012 | 0/0 | 2889 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0005c0009 | 0/0 | 2889 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0006c0011 | 0/0 | 2889 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4430 | 92 | 14 | 12 | 54 | 2 | 9 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0001t0002 | 0/0 | 4430 | 91 | 5 | 18 | 46 | 8 | 14 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0001t0003 | 0/1 | 4430 | 71 | 7 | 15 | 33 | 2 | 13 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0001t0004 | 0/0 | 4430 | 36 | 18 | 3 | 7 | 1 | 7 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0001t0005 | 0/0 | 4430 | 10 | 8 | 2 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0001t0006 | 0/0 | 4430 | 7 | 0 | 7 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0001t0008 | 0/0 | 4430 | 3 | 1 | 2 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0001t0009 | 0/0 | 4430 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0001t0010 | 0/0 | 4428 | 3 | 2 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0001t0011 | 0/0 | 4430 | 3 | 0 | 0 | 3 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0001t0012 | 0/0 | 4430 | 2 | 2 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0001t0013 | 0/0 | 4430 | 2 | 0 | 0 | 0 | 2 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0001t0014 | 0/0 | 4430 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0001t0015 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0001t0017 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0001t0018 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0001t0019 | 0/0 | 4430 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0001t0020 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0001t0024 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0002t0005 | 0/0 | 4430 | 5 | 5 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0002t0009 | 0/0 | 4430 | 2 | 2 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0002t0016 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0004t0007 | 0/0 | 4430 | 2 | 2 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0004t0023 | 0/0 | 4430 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0005t0001 | 0/0 | 4430 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0006t0001 | 0/0 | 4430 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0001c0010t0002 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0002c0003t0007 | 0/0 | 4430 | 2 | 2 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0002c0003t0021 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0002c0007t0022 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0003c0008t0002 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0004c0012t0001 | 0/0 | 4430 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0005c0009t0001 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
a0006c0011t0001 | 0/0 | 4430 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | copy fasta | chr1 | 211935403 | 212040557 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0150 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0013 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0005g0001 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0005g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0005g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0006g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0006g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0006g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0006g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0006g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0006g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0008g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0008g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0009g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0010g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0010g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0010g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0011g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0011g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0011g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0012g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0012g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0013g0327 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0013g0328 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0014g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0015g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0017g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0018g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0019g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0020g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0001t0024g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0002t0005g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0002t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0002t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0002t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0002t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0002t0016g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0004t0007g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0004t0007g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0004t0023g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0005t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0006t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0006t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0001c0010t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0002c0003t0007g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0002c0003t0007g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0002c0003t0021g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0002c0007t0022g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0003c0008t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0004c0012t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0005c0009t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
a0006c0011t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | GBR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0179 | EUR | GBR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | GBR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0220 | EUR | GBR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0175 | EUR | FIN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00323 | hp2 | a0001 | c0004 | t0023 | g0325 | EUR | FIN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0311 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0290 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | CHS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0257 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00642 | hp1 | a0001 | c0001 | t0009 | g0203 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0283 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0128 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01069 | hp2 | a0001 | c0001 | t0005 | g0019 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01109 | hp2 | a0001 | c0001 | t0010 | g0255 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01167 | hp1 | a0001 | c0001 | t0008 | g0034 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0281 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0120 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0282 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0121 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01175 | hp2 | a0001 | c0001 | t0006 | g0127 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01243 | hp1 | a0001 | c0001 | t0008 | g0033 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0262 | AMR | PUR | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0295 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0184 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01257 | hp2 | a0001 | c0001 | t0006 | g0058 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01258 | hp2 | a0001 | c0001 | t0006 | g0038 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0161 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01496 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | CLM | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | IBS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0119 | EUR | IBS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01516 | hp1 | a0001 | c0001 | t0013 | g0328 | EUR | IBS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0219 | EUR | IBS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | IBS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01517 | hp2 | a0001 | c0001 | t0013 | g0327 | EUR | IBS | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0046 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01952 | hp1 | a0001 | c0001 | t0006 | g0152 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01952 | hp2 | a0001 | c0001 | t0019 | g0308 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0309 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01975 | hp2 | a0001 | c0001 | t0006 | g0005 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0187 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02055 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0043 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02132 | hp2 | a0003 | c0008 | t0002 | g0226 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02135 | hp1 | a0006 | c0011 | t0001 | g0040 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02135 | hp2 | a0001 | c0001 | t0004 | g0126 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02148 | hp2 | a0001 | c0001 | t0006 | g0113 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CDX | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02155 | hp2 | a0001 | c0001 | t0004 | g0122 | EAS | CDX | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02257 | hp1 | a0002 | c0003 | t0007 | g0319 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0314 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0008 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02280 | hp1 | a0001 | c0002 | t0009 | g0030 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0313 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0182 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PEL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0303 | EAS | KHV | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0149 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02572 | hp2 | a0001 | c0001 | t0012 | g0205 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02630 | hp2 | a0001 | c0004 | t0007 | g0324 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0317 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0279 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02723 | hp1 | a0001 | c0001 | t0004 | g0048 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0162 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0263 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0131 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0266 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0212 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02886 | hp1 | a0001 | c0001 | t0010 | g0202 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02895 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02897 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02922 | hp1 | a0001 | c0002 | t0005 | g0003 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02965 | hp1 | a0002 | c0003 | t0021 | g0321 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02965 | hp2 | a0001 | c0001 | t0024 | g0326 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0312 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02970 | hp2 | a0001 | c0001 | t0004 | g0102 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02976 | hp1 | a0002 | c0003 | t0007 | g0320 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0042 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0057 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0132 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03098 | hp2 | a0001 | c0004 | t0007 | g0323 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0045 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0001 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03139 | hp2 | a0001 | c0001 | t0004 | g0101 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03209 | hp2 | a0001 | c0001 | t0010 | g0256 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03225 | hp1 | a0001 | c0002 | t0005 | g0003 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0318 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0247 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03453 | hp2 | a0001 | c0001 | t0017 | g0316 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0261 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0009 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0163 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0009 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0021 | AFR | ESN | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0315 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03579 | hp1 | a0001 | c0001 | t0020 | g0206 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0165 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0274 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0280 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0208 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0060 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0166 | SAS | PJL | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03831 | hp2 | a0001 | c0001 | t0014 | g0273 | SAS | BEB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | BEB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | BEB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0200 | SAS | BEB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0265 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0276 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0243 | SAS | BEB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0269 | SAS | BEB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0238 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0209 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0099 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0197 | SAS | STU | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18522 | hp1 | a0001 | c0002 | t0005 | g0003 | AFR | YRI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18522 | hp2 | a0001 | c0001 | t0004 | g0008 | AFR | YRI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | CHB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | CHB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | CHB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18906 | hp1 | a0001 | c0002 | t0016 | g0027 | AFR | YRI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | YRI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18952 | hp1 | a0001 | c0001 | t0015 | g0181 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18979 | hp1 | a0001 | c0001 | t0011 | g0192 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0107 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18991 | hp1 | a0001 | c0010 | t0002 | g0253 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18991 | hp2 | a0001 | c0006 | t0001 | g0118 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18994 | hp1 | a0001 | c0001 | t0011 | g0186 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA18998 | hp2 | a0001 | c0005 | t0001 | g0073 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19005 | hp1 | a0001 | c0006 | t0001 | g0098 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19012 | hp2 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0130 | AFR | LWK | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19030 | hp2 | a0001 | c0002 | t0005 | g0025 | AFR | LWK | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19043 | hp1 | a0001 | c0001 | t0012 | g0207 | AFR | LWK | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19043 | hp2 | a0001 | c0001 | t0004 | g0103 | AFR | LWK | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19058 | hp1 | a0001 | c0005 | t0001 | g0093 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19065 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19068 | hp2 | a0005 | c0009 | t0001 | g0050 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19081 | hp1 | a0001 | c0001 | t0003 | g0296 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19084 | hp1 | a0001 | c0001 | t0011 | g0185 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19084 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19240 | hp1 | a0001 | c0001 | t0018 | g0022 | AFR | YRI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA19240 | hp2 | a0004 | c0012 | t0001 | g0153 | AFR | YRI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA20129 | hp1 | a0001 | c0002 | t0005 | g0026 | AFR | ASW | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA20129 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | ASW | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0278 | EUR | TSI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0188 | EUR | TSI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0178 | EUR | TSI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0258 | EUR | TSI | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0275 | SAS | GIH | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | GIH | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG02559 | hp2 | a0002 | c0007 | t0022 | g0322 | AFR | ACB | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG06807 | hp1 | a0001 | c0001 | t0008 | g0032 | AFR | USA | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
HG06807 | hp2 | a0001 | c0002 | t0009 | g0031 | AFR | USA | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA20300 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | USA | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | USA | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0013 | REF | REF | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0150 | REF | REF | INTS7_chr1_211935403_212040557 | INTS7 | chr1 | 211935403 | 212040557 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:211942044
|
G | A | 1 | a0006 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.2669C>T | p.Thr890Ile | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 2789/4430 | 2669/2889 | 890/962 | chr1 | 211942044 | ||
chr1:211967939
|
A | G | 1 | a0005 | 1 | NA19068.hp2 | missense_variant | MODERATE | c.2053T>C | p.Tyr685His | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/20 | 2173/4430 | 2053/2889 | 685/962 | chr1 | 211967939 | ||
chr1:211976665
|
T | C | 1 | a0004 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.1525A>G | p.Ser509Gly | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/20 | 1645/4430 | 1525/2889 | 509/962 | chr1 | 211976665 | ||
chr1:211981112
|
C | T | 1 | a0003 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.1211G>A | p.Gly404Asp | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/20 | 1331/4430 | 1211/2889 | 404/962 | chr1 | 211981112 | ||
chr1:211987897
|
C | T | 1 | a0002 | 4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
missense_variant | MODERATE | c.986G>A | p.Ser329Asn | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/20 | 1106/4430 | 986/2889 | 329/962 | chr1 | 211987897 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:211941971
|
A | G | 1 | a0001c0005 | 2 | NA18998.hp2 NA19058.hp1 |
synonymous_variant | LOW | c.2742T>C | p.Asn914Asn | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 2862/4430 | 2742/2889 | 914/962 | chr1 | 211941971 | ||
chr1:211944874
|
G | A | 1 | a0001c0002 | 8 | HG02280.hp1 HG02922.hp1 HG03225.hp1 others(5): Show |
synonymous_variant | LOW | c.2511C>T | p.His837His | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/20 | 2631/4430 | 2511/2889 | 837/962 | chr1 | 211944874 | ||
chr1:211946703
|
G | A | 2 | a0001c0004a0002c0003 | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.2319C>T | p.His773His | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/20 | 2439/4430 | 2319/2889 | 773/962 | chr1 | 211946703 | ||
chr1:211952653
|
A | G | 1 | a0001c0010 | 1 | NA18991.hp1 | synonymous_variant | LOW | c.2232T>C | p.Tyr744Tyr | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/20 | 2352/4430 | 2232/2889 | 744/962 | chr1 | 211952653 | ||
chr1:211981147
|
G | A | 1 | a0001c0006 | 2 | NA18991.hp2 NA19005.hp1 |
synonymous_variant | LOW | c.1176C>T | p.Ser392Ser | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/20 | 1296/4430 | 1176/2889 | 392/962 | chr1 | 211981147 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:211940491
|
T | C | 1 | a0001c0001t0018 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1333A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 1333 | chr1 | 211940491 | |||||
chr1:211940553
|
A | C | 4 | a0001c0001t0005a0001c0001t0018a0001c0002t0005others(1): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1271T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 1271 | chr1 | 211940553 | |||||
chr1:211940628
|
C | T | 1 | a0001c0004t0023 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1196G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 1196 | chr1 | 211940628 | |||||
chr1:211940653
|
G | A | 27 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(24): Show | 246 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*1171C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 1171 | chr1 | 211940653 | |||||
chr1:211940925
|
T | A | 2 | a0001c0001t0012a0001c0001t0020 | 3 | HG02572.hp2 HG03579.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*899A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 899 | chr1 | 211940925 | |||||
chr1:211940925
|
T | C | 1 | a0001c0001t0019 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*899A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 899 | chr1 | 211940925 | |||||
chr1:211940942
|
CTT | C | 1 | a0001c0001t0010 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*880_*881delAA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 880 | chr1 | 211940942 | |||||
chr1:211941081
|
C | T | 1 | a0001c0001t0008 | 3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*743G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 743 | chr1 | 211941081 | |||||
chr1:211941083
|
G | C | 1 | a0001c0001t0006 | 7 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*741C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 741 | chr1 | 211941083 | |||||
chr1:211941150
|
G | A | 1 | a0001c0001t0015 | 1 | NA18952.hp1 | 3_prime_UTR_variant | MODIFIER | c.*674C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 674 | chr1 | 211941150 | |||||
chr1:211941162
|
C | T | 1 | a0001c0001t0017 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*662G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 662 | chr1 | 211941162 | |||||
chr1:211941169
|
A | C | 1 | a0001c0002t0016 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*655T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 655 | chr1 | 211941169 | |||||
chr1:211941320
|
A | G | 5 | a0001c0001t0002a0001c0001t0011a0001c0001t0015others(2): Show | 97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*504T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 504 | chr1 | 211941320 | |||||
chr1:211941321
|
G | A | 5 | a0001c0001t0002a0001c0001t0011a0001c0001t0015others(2): Show | 97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*503C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 503 | chr1 | 211941321 | |||||
chr1:211941324
|
C | G | 5 | a0001c0001t0002a0001c0001t0011a0001c0001t0015others(2): Show | 97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
3_prime_UTR_variant | MODIFIER | c.*500G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 500 | chr1 | 211941324 | |||||
chr1:211941363
|
A | T | 1 | a0001c0001t0012 | 2 | HG02572.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*461T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 461 | chr1 | 211941363 | |||||
chr1:211941393
|
T | A | 2 | a0001c0001t0009a0001c0002t0009 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*431A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 431 | chr1 | 211941393 | |||||
chr1:211941398
|
C | T | 1 | a0001c0001t0014 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*426G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 426 | chr1 | 211941398 | |||||
chr1:211941404
|
C | T | 2 | a0001c0001t0009a0001c0002t0009 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*420G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 420 | chr1 | 211941404 | |||||
chr1:211941444
|
G | A | 1 | a0001c0001t0011 | 3 | NA18979.hp1 NA18994.hp1 NA19084.hp1 |
3_prime_UTR_variant | MODIFIER | c.*380C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 380 | chr1 | 211941444 | |||||
chr1:211941518
|
T | C | 24 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(21): Show | 206 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*306A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 306 | chr1 | 211941518 | |||||
chr1:211941727
|
T | G | 4 | a0001c0004t0007a0001c0004t0023a0002c0003t0007others(1): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*97A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 97 | chr1 | 211941727 | |||||
chr1:211941745
|
C | G | 1 | a0002c0003t0021 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*79G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 20/20 | 79 | chr1 | 211941745 | |||||
chr1:212035474
|
C | A | 5 | a0001c0004t0007a0001c0004t0023a0002c0003t0007others(2): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-37G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/20 | 37 | chr1 | 212035474 | |||||
chr1:212035502
|
C | A | 1 | a0001c0001t0024 | 1 | HG02965.hp2 | 5_prime_UTR_variant | MODIFIER | c.-65G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/20 | 65 | chr1 | 212035502 | |||||
chr1:212035516
|
T | C | 1 | a0001c0001t0013 | 2 | HG01516.hp1 HG01517.hp2 |
5_prime_UTR_variant | MODIFIER | c.-79A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/20 | 79 | chr1 | 212035516 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:211942253
|
T | C | 1 | a0002c0007t0022g0322 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2602-142A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942253 | ||||||
chr1:211942263
|
A | G | 3 | a0002c0003t0007g0319a0002c0003t0007g0320a0002c0003t0021g0321 | 3 | HG02257.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2602-152T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942263 | ||||||
chr1:211942310
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0087 | 2 | HG01109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2602-199G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942310 | ||||||
chr1:211942329
|
C | T | 1 | a0001c0001t0002g0177 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2602-218G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942329 | ||||||
chr1:211942384
|
C | A | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2602-273G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942384 | ||||||
chr1:211942393
|
T | C | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2602-282A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942393 | ||||||
chr1:211942597
|
C | T | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2602-486G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942597 | ||||||
chr1:211942615
|
T | C | 6 | a0001c0001t0009g0203a0001c0001t0012g0205a0001c0001t0012g0207others(3): Show | 6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2602-504A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942615 | ||||||
chr1:211942670
|
C | A | 18 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(15): Show | 18 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2602-559G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942670 | ||||||
chr1:211942795
|
A | T | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2602-684T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942795 | ||||||
chr1:211942812
|
C | G | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2602-701G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942812 | ||||||
chr1:211942838
|
A | T | 1 | a0001c0001t0001g0143 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2602-727T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942838 | ||||||
chr1:211942891
|
G | A | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2602-780C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942891 | ||||||
chr1:211942949
|
T | C | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2602-838A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211942949 | ||||||
chr1:211943082
|
A | G | 6 | a0001c0001t0009g0203a0001c0001t0012g0205a0001c0001t0012g0207others(3): Show | 6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2602-971T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943082 | ||||||
chr1:211943218
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2602-1107T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943218 | ||||||
chr1:211943242
|
G | GT | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2602-1132dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943242 | ||||||
chr1:211943259
|
C | G | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2602-1148G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943259 | ||||||
chr1:211943260
|
G | A | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2602-1149C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943260 | ||||||
chr1:211943470
|
C | T | 1 | a0001c0001t0002g0277 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2601+1314G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943470 | ||||||
chr1:211943517
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2601+1267A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943517 | ||||||
chr1:211943627
|
G | A | 1 | a0001c0001t0003g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2601+1157C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943627 | ||||||
chr1:211943723
|
T | A | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2601+1061A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943723 | ||||||
chr1:211943863
|
A | C | 21 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0057others(18): Show | 23 | HG01168.hp1 HG01175.hp1 HG01515.hp2 others(20): Show |
intron_variant | MODIFIER | c.2601+921T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211943863 | ||||||
chr1:211944074
|
T | C | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2601+710A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211944074 | ||||||
chr1:211944208
|
G | A | 1 | a0001c0001t0002g0028 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2601+576C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211944208 | ||||||
chr1:211944276
|
G | A | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2601+508C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211944276 | ||||||
chr1:211944307
|
G | A | 8 | a0001c0001t0012g0205a0001c0001t0012g0207a0001c0004t0007g0323others(5): Show | 8 | HG00323.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2601+477C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211944307 | ||||||
chr1:211944408
|
G | A | 4 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256others(1): Show | 4 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2601+376C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211944408 | ||||||
chr1:211944426
|
T | C | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.2601+358A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211944426 | ||||||
chr1:211944569
|
T | C | 1 | a0001c0001t0003g0165 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2601+215A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211944569 | ||||||
chr1:211944665
|
C | T | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2601+119G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211944665 | ||||||
chr1:211944725
|
C | T | 1 | a0001c0001t0008g0033 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2601+59G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 19/19 | chr1 | 211944725 | ||||||
chr1:211945024
|
A | G | 5 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2416-55T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945024 | ||||||
chr1:211945083
|
C | A | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2416-114G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945083 | ||||||
chr1:211945089
|
C | G | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2416-120G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945089 | ||||||
chr1:211945155
|
A | C | 1 | a0001c0001t0004g0009 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2416-186T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945155 | ||||||
chr1:211945396
|
C | T | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2416-427G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945396 | ||||||
chr1:211945445
|
G | A | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2416-476C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945445 | ||||||
chr1:211945501
|
C | T | 7 | a0001c0001t0002g0012a0001c0004t0007g0323a0001c0004t0007g0324others(4): Show | 8 | HG00323.hp2 HG01515.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.2416-532G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945501 | ||||||
chr1:211945518
|
C | T | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2416-549G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945518 | ||||||
chr1:211945579
|
T | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0139 | 2 | HG01106.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.2416-610A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945579 | ||||||
chr1:211945598
|
C | T | 1 | a0001c0001t0004g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2416-629G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945598 | ||||||
chr1:211945628
|
G | A | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2416-659C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945628 | ||||||
chr1:211945912
|
G | T | 5 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0170others(2): Show | 5 | NA18948.hp1 NA19002.hp1 NA19067.hp2 others(2): Show |
intron_variant | MODIFIER | c.2415+695C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211945912 | ||||||
chr1:211946035
|
G | A | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2415+572C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211946035 | ||||||
chr1:211946173
|
C | T | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2415+434G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211946173 | ||||||
chr1:211946333
|
A | G | 1 | a0001c0004t0023g0325 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2415+274T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211946333 | ||||||
chr1:211946341
|
C | T | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2415+266G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211946341 | ||||||
chr1:211946354
|
A | C | 5 | a0001c0001t0002g0173a0001c0001t0002g0178a0001c0001t0002g0188others(2): Show | 5 | HG01192.hp2 HG01361.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.2415+253T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211946354 | ||||||
chr1:211946462
|
C | T | 44 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0161others(41): Show | 48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2415+145G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 18/19 | chr1 | 211946462 | ||||||
chr1:211946955
|
CCAAG | C | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2317-254_2317-251d others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211946955 | ||||||
chr1:211946983
|
A | G | 5 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2317-278T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211946983 | ||||||
chr1:211947135
|
T | C | 3 | a0001c0001t0003g0167a0001c0001t0003g0295a0001c0001t0003g0296 | 3 | HG01255.hp1 NA19067.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.2317-430A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947135 | ||||||
chr1:211947168
|
G | C | 17 | a0001c0001t0003g0090a0001c0001t0003g0160a0001c0001t0003g0257others(14): Show | 17 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.2317-463C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947168 | ||||||
chr1:211947448
|
T | C | 2 | a0001c0002t0009g0030a0001c0002t0009g0031 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2317-743A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947448 | ||||||
chr1:211947572
|
C | A | 5 | a0001c0001t0004g0045a0001c0001t0004g0046a0001c0001t0004g0047others(2): Show | 5 | HG01884.hp1 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2317-867G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947572 | ||||||
chr1:211947595
|
C | T | 1 | a0002c0003t0021g0321 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2317-890G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947595 | ||||||
chr1:211947624
|
T | C | 2 | a0001c0001t0003g0090a0001c0001t0003g0264 | 2 | HG02083.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2317-919A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947624 | ||||||
chr1:211947626
|
A | G | 2 | a0001c0001t0001g0157a0004c0012t0001g0153 | 2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2317-921T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947626 | ||||||
chr1:211947666
|
C | G | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2317-961G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947666 | ||||||
chr1:211947796
|
A | G | 5 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(2): Show | 5 | HG00738.hp2 HG00741.hp2 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.2317-1091T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947796 | ||||||
chr1:211947799
|
T | C | 1 | a0001c0010t0002g0253 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2317-1094A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947799 | ||||||
chr1:211947948
|
C | T | 4 | a0001c0002t0005g0003a0001c0002t0005g0025a0001c0002t0005g0026others(1): Show | 6 | HG02922.hp1 HG03225.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.2317-1243G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947948 | ||||||
chr1:211947999
|
T | C | 14 | a0001c0001t0001g0105a0001c0001t0003g0013a0001c0001t0003g0014others(11): Show | 22 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.2317-1294A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211947999 | ||||||
chr1:211948068
|
T | C | 88 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(85): Show | 92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.2317-1363A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948068 | ||||||
chr1:211948157
|
T | G | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2317-1452A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948157 | ||||||
chr1:211948162
|
A | AT | 10 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0154others(7): Show | 12 | HG00323.hp2 HG02622.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.2317-1458dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948162 | ||||||
chr1:211948209
|
C | T | 6 | a0001c0001t0009g0203a0001c0001t0012g0205a0001c0001t0012g0207others(3): Show | 6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2317-1504G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948209 | ||||||
chr1:211948461
|
G | A | 1 | a0002c0007t0022g0322 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2317-1756C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948461 | ||||||
chr1:211948478
|
C | T | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2317-1773G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948478 | ||||||
chr1:211948678
|
C | T | 1 | a0001c0001t0001g0010 | 2 | HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.2317-1973G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948678 | ||||||
chr1:211948697
|
G | A | 1 | a0001c0004t0007g0324 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2317-1992C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948697 | ||||||
chr1:211948699
|
T | TTTTTG | 3 | a0002c0003t0007g0319a0002c0003t0007g0320a0002c0003t0021g0321 | 3 | HG02257.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2317-1999_2317-199 others(9): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948699 | ||||||
chr1:211948719
|
G | T | 1 | a0001c0001t0003g0269 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2317-2014C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948719 | ||||||
chr1:211948792
|
C | T | 2 | a0001c0001t0001g0080a0001c0001t0001g0106 | 2 | HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2317-2087G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948792 | ||||||
chr1:211948793
|
G | A | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2317-2088C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948793 | ||||||
chr1:211948803
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.2317-2098C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948803 | ||||||
chr1:211948943
|
G | C | 1 | a0001c0001t0001g0074 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2317-2238C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948943 | ||||||
chr1:211948948
|
A | G | 18 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(15): Show | 18 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2317-2243T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211948948 | ||||||
chr1:211949226
|
T | C | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2317-2521A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211949226 | ||||||
chr1:211949484
|
T | C | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2317-2779A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211949484 | ||||||
chr1:211949529
|
C | T | 1 | a0001c0001t0002g0214 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2317-2824G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211949529 | ||||||
chr1:211949536
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.2317-2831T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211949536 | ||||||
chr1:211949839
|
A | G | 6 | a0001c0001t0009g0203a0001c0001t0012g0205a0001c0001t0012g0207others(3): Show | 6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2316+2730T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211949839 | ||||||
chr1:211949879
|
T | C | 18 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(15): Show | 18 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2316+2690A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211949879 | ||||||
chr1:211949962
|
T | C | 1 | a0001c0001t0014g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2316+2607A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211949962 | ||||||
chr1:211950009
|
A | G | 6 | a0001c0001t0009g0203a0001c0001t0012g0205a0001c0001t0012g0207others(3): Show | 6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2316+2560T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950009 | ||||||
chr1:211950053
|
C | G | 1 | a0001c0001t0002g0271 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2316+2516G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950053 | ||||||
chr1:211950278
|
CTTAT | C | 11 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0051others(8): Show | 12 | HG02132.hp1 NA18945.hp1 NA18963.hp1 others(9): Show |
intron_variant | MODIFIER | c.2316+2287_2316+229 others(8): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950278 | ||||||
chr1:211950421
|
G | A | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2316+2148C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950421 | ||||||
chr1:211950487
|
G | GT | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2316+2081dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950487 | ||||||
chr1:211950598
|
C | T | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2316+1971G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950598 | ||||||
chr1:211950600
|
A | G | 1 | a0002c0007t0022g0322 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2316+1969T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950600 | ||||||
chr1:211950613
|
G | A | 13 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0005g0001others(10): Show | 21 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2316+1956C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950613 | ||||||
chr1:211950697
|
T | C | 2 | a0001c0002t0009g0030a0001c0002t0009g0031 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2316+1872A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950697 | ||||||
chr1:211950777
|
C | A | 1 | a0001c0001t0002g0231 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2316+1792G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950777 | ||||||
chr1:211950782
|
C | T | 1 | a0001c0001t0002g0231 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2316+1787G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950782 | ||||||
chr1:211950943
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2316+1626T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211950943 | ||||||
chr1:211951012
|
C | G | 3 | a0002c0003t0007g0319a0002c0003t0007g0320a0002c0003t0021g0321 | 3 | HG02257.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2316+1557G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951012 | ||||||
chr1:211951170
|
G | C | 1 | a0001c0001t0004g0147 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2316+1399C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951170 | ||||||
chr1:211951201
|
G | A | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2316+1368C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951201 | ||||||
chr1:211951239
|
C | T | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2316+1330G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951239 | ||||||
chr1:211951242
|
C | T | 9 | a0001c0001t0003g0090a0001c0001t0003g0160a0001c0001t0003g0257others(6): Show | 9 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.2316+1327G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951242 | ||||||
chr1:211951257
|
C | T | 1 | a0001c0001t0014g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2316+1312G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951257 | ||||||
chr1:211951316
|
G | GT | 29 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0167others(26): Show | 33 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.2316+1252dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951316 | ||||||
chr1:211951317
|
T | C | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2316+1252A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951317 | ||||||
chr1:211951429
|
G | T | 18 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(15): Show | 18 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.2316+1140C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951429 | ||||||
chr1:211951508
|
A | T | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.2316+1061T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951508 | ||||||
chr1:211951601
|
C | T | 75 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0010others(72): Show | 79 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.2316+968G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951601 | ||||||
chr1:211951714
|
C | T | 5 | a0001c0001t0002g0212a0001c0001t0002g0246a0001c0001t0002g0247others(2): Show | 5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2316+855G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951714 | ||||||
chr1:211951808
|
C | T | 1 | a0001c0001t0002g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2316+761G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951808 | ||||||
chr1:211951812
|
C | T | 5 | a0001c0001t0004g0042a0001c0001t0004g0043a0001c0001t0004g0044others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.2316+757G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951812 | ||||||
chr1:211951813
|
G | A | 5 | a0001c0001t0002g0194a0001c0001t0002g0195a0001c0004t0007g0323others(2): Show | 5 | HG00323.hp2 HG00639.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2316+756C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951813 | ||||||
chr1:211951918
|
G | A | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2316+651C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211951918 | ||||||
chr1:211952064
|
CCAA | C | 4 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256others(1): Show | 4 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2316+502_2316+504d others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211952064 | ||||||
chr1:211952088
|
T | G | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2316+481A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211952088 | ||||||
chr1:211952115
|
T | C | 1 | a0001c0001t0002g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2316+454A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211952115 | ||||||
chr1:211952151
|
C | T | 1 | a0001c0001t0003g0275 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2316+418G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211952151 | ||||||
chr1:211952444
|
C | T | 1 | a0001c0001t0003g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2316+125G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211952444 | ||||||
chr1:211952468
|
C | T | 1 | a0001c0001t0001g0036 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2316+101G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211952468 | ||||||
chr1:211952485
|
G | C | 5 | a0001c0001t0004g0045a0001c0001t0004g0046a0001c0001t0004g0047others(2): Show | 5 | HG01884.hp1 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.2316+84C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 17/19 | chr1 | 211952485 | ||||||
chr1:211952712
|
G | A | 4 | a0001c0001t0004g0100a0001c0001t0004g0107a0001c0001t0004g0134others(1): Show | 4 | NA18990.hp2 NA19012.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.2184-11C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211952712 | ||||||
chr1:211952828
|
G | T | 1 | a0001c0001t0003g0312 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2184-127C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211952828 | ||||||
chr1:211952858
|
T | C | 1 | a0001c0001t0014g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2184-157A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211952858 | ||||||
chr1:211953236
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2184-535C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953236 | ||||||
chr1:211953298
|
T | A | 1 | a0001c0001t0002g0215 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2184-597A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953298 | ||||||
chr1:211953392
|
T | C | 2 | a0001c0001t0008g0032a0001c0001t0008g0033 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2184-691A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953392 | ||||||
chr1:211953404
|
TTTA | T | 3 | a0001c0001t0001g0056a0001c0001t0001g0096a0006c0011t0001g0040 | 3 | HG02129.hp2 HG02135.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.2184-706_2184-704d others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953404 | ||||||
chr1:211953441
|
G | A | 1 | a0002c0007t0022g0322 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2184-740C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953441 | ||||||
chr1:211953447
|
T | C | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2184-746A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953447 | ||||||
chr1:211953524
|
A | G | 3 | a0001c0001t0002g0172a0001c0001t0002g0180a0001c0001t0002g0184 | 3 | HG00642.hp2 HG01257.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.2184-823T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953524 | ||||||
chr1:211953655
|
G | T | 1 | a0001c0001t0008g0034 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2184-954C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953655 | ||||||
chr1:211953669
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2184-968G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953669 | ||||||
chr1:211953863
|
A | G | 5 | a0001c0001t0002g0212a0001c0001t0002g0246a0001c0001t0002g0247others(2): Show | 5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.2184-1162T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953863 | ||||||
chr1:211953974
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2184-1273G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211953974 | ||||||
chr1:211954085
|
T | C | 6 | a0001c0001t0009g0203a0001c0001t0012g0205a0001c0001t0012g0207others(3): Show | 6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184-1384A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954085 | ||||||
chr1:211954092
|
C | T | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184-1391G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954092 | ||||||
chr1:211954111
|
A | T | 93 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(90): Show | 97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.2184-1410T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954111 | ||||||
chr1:211954226
|
C | T | 3 | a0001c0001t0008g0032a0001c0001t0008g0033a0001c0001t0008g0034 | 3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2184-1525G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954226 | ||||||
chr1:211954227
|
G | A | 50 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0028others(47): Show | 52 | HG00140.hp2 HG00597.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.2184-1526C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954227 | ||||||
chr1:211954320
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2184-1619G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954320 | ||||||
chr1:211954416
|
G | C | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184-1715C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954416 | ||||||
chr1:211954431
|
T | C | 1 | a0001c0001t0002g0221 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2184-1730A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954431 | ||||||
chr1:211954466
|
T | C | 2 | a0001c0006t0001g0098a0001c0006t0001g0118 | 2 | NA18991.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.2184-1765A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954466 | ||||||
chr1:211954539
|
G | T | 13 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0005g0001others(10): Show | 21 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2184-1838C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954539 | ||||||
chr1:211954678
|
G | C | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184-1977C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954678 | ||||||
chr1:211954715
|
G | A | 4 | a0001c0001t0001g0051a0001c0001t0001g0076a0001c0001t0001g0110others(1): Show | 4 | HG02559.hp2 NA18993.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.2184-2014C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954715 | ||||||
chr1:211954839
|
C | T | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2184-2138G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211954839 | ||||||
chr1:211955046
|
A | G | 1 | a0001c0001t0003g0162 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2184-2345T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955046 | ||||||
chr1:211955072
|
G | A | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2184-2371C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955072 | ||||||
chr1:211955084
|
A | G | 1 | a0001c0001t0004g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2184-2383T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955084 | ||||||
chr1:211955124
|
G | T | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2184-2423C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955124 | ||||||
chr1:211955320
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2184-2619T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955320 | ||||||
chr1:211955442
|
T | C | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.2184-2741A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955442 | ||||||
chr1:211955486
|
G | A | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2184-2785C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955486 | ||||||
chr1:211955634
|
G | T | 2 | a0001c0001t0003g0090a0001c0001t0003g0264 | 2 | HG02083.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2184-2933C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955634 | ||||||
chr1:211955643
|
G | A | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184-2942C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955643 | ||||||
chr1:211955747
|
A | T | 17 | a0001c0001t0003g0090a0001c0001t0003g0160a0001c0001t0003g0257others(14): Show | 17 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.2184-3046T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211955747 | ||||||
chr1:211956079
|
C | CT | 3 | a0002c0003t0007g0319a0002c0003t0007g0320a0002c0003t0021g0321 | 3 | HG02257.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2184-3379dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211956079 | ||||||
chr1:211956129
|
T | G | 99 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(96): Show | 103 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.2184-3428A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211956129 | ||||||
chr1:211956176
|
A | G | 44 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0161others(41): Show | 48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2184-3475T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211956176 | ||||||
chr1:211956228
|
G | A | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2184-3527C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211956228 | ||||||
chr1:211956400
|
T | C | 1 | a0001c0001t0002g0270 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2184-3699A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211956400 | ||||||
chr1:211956808
|
A | G | 93 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(90): Show | 97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.2184-4107T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211956808 | ||||||
chr1:211957028
|
G | A | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2184-4327C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957028 | ||||||
chr1:211957092
|
C | T | 9 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031others(6): Show | 9 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.2184-4391G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957092 | ||||||
chr1:211957266
|
C | T | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2184-4565G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957266 | ||||||
chr1:211957300
|
CT | C | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2184-4600delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957300 | ||||||
chr1:211957335
|
C | T | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184-4634G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957335 | ||||||
chr1:211957477
|
T | C | 12 | a0001c0001t0009g0203a0001c0001t0012g0205a0001c0001t0012g0207others(9): Show | 12 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.2184-4776A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957477 | ||||||
chr1:211957495
|
G | A | 1 | a0001c0004t0023g0325 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2184-4794C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957495 | ||||||
chr1:211957530
|
A | C | 1 | a0001c0001t0003g0285 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2184-4829T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957530 | ||||||
chr1:211957531
|
G | C | 144 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(141): Show | 152 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.2184-4830C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957531 | ||||||
chr1:211957537
|
A | G | 190 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(187): Show | 206 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.2184-4836T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957537 | ||||||
chr1:211957787
|
A | G | 1 | a0001c0001t0004g0044 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2184-5086T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957787 | ||||||
chr1:211957831
|
T | C | 2 | a0001c0001t0005g0019a0001c0001t0005g0020 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2184-5130A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957831 | ||||||
chr1:211957933
|
T | G | 3 | a0002c0003t0007g0319a0002c0003t0007g0320a0002c0003t0021g0321 | 3 | HG02257.hp1 HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2184-5232A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211957933 | ||||||
chr1:211958047
|
C | T | 5 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2184-5346G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958047 | ||||||
chr1:211958070
|
TA | T | 177 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(174): Show | 193 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.2184-5370delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958070 | ||||||
chr1:211958071
|
A | T | 2 | a0002c0003t0007g0319a0002c0003t0007g0320 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2184-5370T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958071 | ||||||
chr1:211958080
|
AAC | A | 7 | a0001c0001t0002g0174a0001c0004t0007g0323a0001c0004t0007g0324others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2184-5381_2184-538 others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958080 | ||||||
chr1:211958082
|
C | A | 4 | a0001c0001t0009g0203a0001c0001t0012g0205a0001c0001t0012g0207others(1): Show | 4 | HG00642.hp1 HG02572.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2184-5381G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958082 | ||||||
chr1:211958083
|
A | C | 1 | a0001c0001t0002g0174 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2184-5382T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958083 | ||||||
chr1:211958237
|
C | T | 190 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(187): Show | 206 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.2184-5536G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958237 | ||||||
chr1:211958324
|
G | A | 3 | a0001c0001t0003g0281a0001c0001t0003g0282a0001c0001t0003g0283 | 3 | HG00738.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2184-5623C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958324 | ||||||
chr1:211958369
|
C | A | 1 | a0001c0001t0004g0009 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2184-5668G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958369 | ||||||
chr1:211958378
|
T | A | 13 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0005g0001others(10): Show | 21 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2184-5677A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958378 | ||||||
chr1:211958430
|
CTTCT | C | 49 | a0001c0001t0002g0212a0001c0001t0002g0246a0001c0001t0002g0247others(46): Show | 53 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.2184-5733_2184-573 others(8): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958430 | ||||||
chr1:211958449
|
T | A | 1 | a0001c0001t0004g0130 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2184-5748A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958449 | ||||||
chr1:211958486
|
C | T | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184-5785G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958486 | ||||||
chr1:211958508
|
TTA | T | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184-5809_2184-580 others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958508 | ||||||
chr1:211958563
|
T | A | 1 | a0001c0001t0003g0165 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2184-5862A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958563 | ||||||
chr1:211958610
|
C | T | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2184-5909G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211958610 | ||||||
chr1:211959661
|
T | C | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2183+6769A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211959661 | ||||||
chr1:211959688
|
TG | T | 5 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2183+6741delC | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211959688 | ||||||
chr1:211959860
|
C | A | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+6570G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211959860 | ||||||
chr1:211959876
|
C | T | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2183+6554G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211959876 | ||||||
chr1:211959943
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2183+6487G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211959943 | ||||||
chr1:211959962
|
TC | T | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2183+6467delG | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211959962 | ||||||
chr1:211960309
|
G | T | 3 | a0001c0001t0012g0205a0001c0001t0012g0207a0001c0001t0020g0206 | 3 | HG02572.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2183+6121C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211960309 | ||||||
chr1:211960333
|
A | C | 4 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.2183+6097T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211960333 | ||||||
chr1:211960417
|
A | T | 1 | a0001c0001t0001g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2183+6013T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211960417 | ||||||
chr1:211960554
|
A | C | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.2183+5876T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211960554 | ||||||
chr1:211960568
|
T | C | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+5862A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211960568 | ||||||
chr1:211960711
|
G | A | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2183+5719C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211960711 | ||||||
chr1:211960770
|
T | A | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2183+5660A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211960770 | ||||||
chr1:211960990
|
A | G | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+5440T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211960990 | ||||||
chr1:211961068
|
C | T | 2 | a0001c0001t0002g0216a0001c0001t0002g0236 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2183+5362G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961068 | ||||||
chr1:211961146
|
A | C | 1 | a0001c0001t0004g0102 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2183+5284T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961146 | ||||||
chr1:211961263
|
C | T | 1 | a0001c0001t0003g0312 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2183+5167G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961263 | ||||||
chr1:211961345
|
A | G | 1 | a0002c0007t0022g0322 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2183+5085T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961345 | ||||||
chr1:211961430
|
C | CT | 7 | a0001c0001t0002g0254a0001c0004t0007g0323a0001c0004t0007g0324others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2183+4999dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961430 | ||||||
chr1:211961523
|
G | A | 4 | a0001c0001t0002g0179a0001c0001t0002g0182a0001c0001t0002g0191others(1): Show | 4 | HG00099.hp2 HG01258.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2183+4907C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961523 | ||||||
chr1:211961560
|
A | C | 13 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0005g0001others(10): Show | 21 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.2183+4870T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961560 | ||||||
chr1:211961591
|
G | A | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2183+4839C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961591 | ||||||
chr1:211961617
|
C | T | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2183+4813G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961617 | ||||||
chr1:211961774
|
C | T | 4 | a0001c0001t0002g0179a0001c0001t0002g0182a0001c0001t0002g0191others(1): Show | 4 | HG00099.hp2 HG01258.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2183+4656G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961774 | ||||||
chr1:211961793
|
G | A | 190 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(187): Show | 206 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.2183+4637C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961793 | ||||||
chr1:211961930
|
A | T | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+4500T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961930 | ||||||
chr1:211961931
|
A | C | 1 | a0001c0001t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2183+4499T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211961931 | ||||||
chr1:211962199
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2183+4231A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962199 | ||||||
chr1:211962260
|
TA | T | 161 | a0001c0001t0001g0056a0001c0001t0001g0070a0001c0001t0001g0141others(158): Show | 175 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.2183+4169delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962260 | ||||||
chr1:211962260
|
TAA | T | 21 | a0001c0001t0002g0174a0001c0001t0002g0196a0001c0001t0002g0208others(18): Show | 23 | HG00642.hp1 HG01069.hp1 HG01069.hp2 others(20): Show |
intron_variant | MODIFIER | c.2183+4168_2183+416 others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962260 | ||||||
chr1:211962376
|
T | G | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+4054A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962376 | ||||||
chr1:211962561
|
A | G | 1 | a0001c0001t0004g0060 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2183+3869T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962561 | ||||||
chr1:211962611
|
A | C | 1 | a0001c0001t0002g0229 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2183+3819T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962611 | ||||||
chr1:211962686
|
C | A | 1 | a0001c0001t0003g0261 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2183+3744G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962686 | ||||||
chr1:211962728
|
T | C | 3 | a0001c0001t0002g0172a0001c0001t0002g0180a0001c0001t0002g0184 | 3 | HG00642.hp2 HG01257.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.2183+3702A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962728 | ||||||
chr1:211962762
|
G | A | 4 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256others(1): Show | 4 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2183+3668C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962762 | ||||||
chr1:211962874
|
G | A | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2183+3556C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962874 | ||||||
chr1:211962898
|
C | A | 1 | a0001c0001t0001g0074 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2183+3532G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962898 | ||||||
chr1:211962899
|
T | A | 1 | a0001c0001t0001g0074 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2183+3531A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962899 | ||||||
chr1:211962900
|
A | G | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2183+3530T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962900 | ||||||
chr1:211962971
|
T | C | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+3459A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211962971 | ||||||
chr1:211963089
|
A | G | 1 | a0001c0001t0002g0174 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2183+3341T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963089 | ||||||
chr1:211963100
|
G | A | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+3330C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963100 | ||||||
chr1:211963438
|
C | T | 3 | a0001c0001t0012g0205a0001c0001t0012g0207a0001c0001t0020g0206 | 3 | HG02572.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2183+2992G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963438 | ||||||
chr1:211963629
|
T | C | 6 | a0001c0001t0009g0203a0001c0001t0012g0205a0001c0001t0012g0207others(3): Show | 6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+2801A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963629 | ||||||
chr1:211963699
|
T | C | 44 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0161others(41): Show | 48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2183+2731A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963699 | ||||||
chr1:211963754
|
A | C | 6 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG02622.hp1 HG02886.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+2676T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963754 | ||||||
chr1:211963774
|
A | G | 2 | a0002c0003t0007g0319a0002c0003t0007g0320 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2183+2656T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963774 | ||||||
chr1:211963790
|
C | A | 1 | a0001c0001t0002g0174 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2183+2640G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963790 | ||||||
chr1:211963791
|
A | C | 1 | a0001c0001t0002g0174 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.2183+2639T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963791 | ||||||
chr1:211963808
|
ACT | A | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+2620_2183+262 others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211963808 | ||||||
chr1:211964063
|
G | A | 6 | a0001c0001t0004g0008a0001c0001t0004g0057a0001c0001t0004g0101others(3): Show | 7 | HG02258.hp1 HG02965.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.2183+2367C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211964063 | ||||||
chr1:211964263
|
C | A | 15 | a0001c0001t0004g0009a0001c0001t0004g0060a0001c0001t0004g0099others(12): Show | 16 | HG01168.hp1 HG01175.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.2183+2167G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211964263 | ||||||
chr1:211964275
|
C | T | 1 | a0001c0001t0004g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2183+2155G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211964275 | ||||||
chr1:211964440
|
C | T | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+1990G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211964440 | ||||||
chr1:211964632
|
A | G | 93 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(90): Show | 97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.2183+1798T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211964632 | ||||||
chr1:211964683
|
C | G | 1 | a0001c0001t0002g0243 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2183+1747G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211964683 | ||||||
chr1:211965185
|
TA | T | 22 | a0001c0001t0001g0078a0001c0001t0003g0090a0001c0001t0003g0160others(19): Show | 22 | HG00323.hp2 HG00408.hp1 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.2183+1244delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965185 | ||||||
chr1:211965214
|
C | T | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2183+1216G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965214 | ||||||
chr1:211965302
|
A | T | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+1128T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965302 | ||||||
chr1:211965312
|
G | A | 1 | a0001c0001t0004g0121 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2183+1118C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965312 | ||||||
chr1:211965314
|
T | TGCAGAGA others(5): Show |
1 | a0001c0001t0004g0120 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2183+1104_2183+111 others(16): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965314 | ||||||
chr1:211965348
|
G | A | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2183+1082C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965348 | ||||||
chr1:211965373
|
G | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | NA19057.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.2183+1057C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965373 | ||||||
chr1:211965434
|
A | T | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2183+996T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965434 | ||||||
chr1:211965499
|
T | C | 1 | a0001c0001t0002g0223 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2183+931A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965499 | ||||||
chr1:211965553
|
C | A | 2 | a0001c0001t0002g0180a0001c0001t0002g0184 | 2 | HG01257.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.2183+877G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965553 | ||||||
chr1:211965577
|
G | T | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+853C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965577 | ||||||
chr1:211965610
|
C | T | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(3): Show | 6 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2183+820G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965610 | ||||||
chr1:211965622
|
AAAG | A | 5 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2183+805_2183+807d others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965622 | ||||||
chr1:211965888
|
G | A | 2 | a0001c0002t0009g0030a0001c0002t0009g0031 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2183+542C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211965888 | ||||||
chr1:211966027
|
T | C | 1 | a0001c0001t0002g0284 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.2183+403A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211966027 | ||||||
chr1:211966259
|
G | A | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.2183+171C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211966259 | ||||||
chr1:211966291
|
C | G | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | NA19057.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.2183+139G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 16/19 | chr1 | 211966291 | ||||||
chr1:211966504
|
T | C | 1 | a0001c0001t0003g0300 | 1 | NA18939.hp1 | splice_region_variant&intron_variant | LOW | c.2115-6A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211966504 | ||||||
chr1:211966529
|
T | C | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2115-31A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211966529 | ||||||
chr1:211966554
|
C | T | 5 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2115-56G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211966554 | ||||||
chr1:211966714
|
C | T | 1 | a0001c0004t0007g0324 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2115-216G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211966714 | ||||||
chr1:211966750
|
T | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2115-252A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211966750 | ||||||
chr1:211966757
|
C | T | 1 | a0001c0001t0014g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2115-259G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211966757 | ||||||
chr1:211966871
|
T | A | 3 | a0001c0001t0002g0244a0001c0005t0001g0073a0001c0005t0001g0093 | 3 | HG01981.hp2 NA18998.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.2115-373A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211966871 | ||||||
chr1:211966996
|
A | T | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2115-498T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211966996 | ||||||
chr1:211967175
|
C | T | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2115-677G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967175 | ||||||
chr1:211967280
|
G | A | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2114+598C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967280 | ||||||
chr1:211967451
|
C | CA | 138 | a0001c0001t0001g0089a0001c0001t0001g0104a0001c0001t0001g0157others(135): Show | 145 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.2114+426dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967451 | ||||||
chr1:211967451
|
C | CAA | 6 | a0001c0001t0002g0016a0001c0001t0002g0174a0001c0001t0002g0232others(3): Show | 7 | HG02027.hp1 NA18944.hp1 NA19003.hp2 others(4): Show |
intron_variant | MODIFIER | c.2114+425_2114+426d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967451 | ||||||
chr1:211967451
|
CA | C | 35 | a0001c0001t0001g0061a0001c0001t0001g0075a0001c0001t0003g0013others(32): Show | 41 | HG00323.hp2 HG01069.hp1 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.2114+426delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967451 | ||||||
chr1:211967499
|
C | G | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2114+379G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967499 | ||||||
chr1:211967543
|
A | T | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2114+335T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967543 | ||||||
chr1:211967616
|
T | C | 1 | a0001c0001t0014g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2114+262A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967616 | ||||||
chr1:211967672
|
C | T | 1 | a0001c0001t0002g0270 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2114+206G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967672 | ||||||
chr1:211967756
|
CTATA | C | 8 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0154others(5): Show | 10 | HG02622.hp1 HG02630.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.2114+118_2114+121d others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 15/19 | chr1 | 211967756 | ||||||
chr1:211968027
|
T | C | 4 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256others(1): Show | 4 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2011-46A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 14/19 | chr1 | 211968027 | ||||||
chr1:211968035
|
C | A | 1 | a0001c0001t0002g0215 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2011-54G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 14/19 | chr1 | 211968035 | ||||||
chr1:211968083
|
C | A | 27 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0167others(24): Show | 31 | HG00423.hp2 HG00733.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.2011-102G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 14/19 | chr1 | 211968083 | ||||||
chr1:211968151
|
A | C | 5 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.2011-170T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 14/19 | chr1 | 211968151 | ||||||
chr1:211968188
|
TTA | T | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2011-209_2011-208d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 14/19 | chr1 | 211968188 | ||||||
chr1:211968330
|
A | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2010+183T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 14/19 | chr1 | 211968330 | ||||||
chr1:211968416
|
A | T | 1 | a0001c0001t0003g0161 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2010+97T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 14/19 | chr1 | 211968416 | ||||||
chr1:211968418
|
T | A | 1 | a0001c0001t0003g0161 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2010+95A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 14/19 | chr1 | 211968418 | ||||||
chr1:211968431
|
T | C | 1 | a0001c0001t0003g0163 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2010+82A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 14/19 | chr1 | 211968431 | ||||||
chr1:211968712
|
GA | G | 156 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(153): Show | 166 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(163): Show |
splice_region_variant&intron_variant | LOW | c.1816-6delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211968712 | ||||||
chr1:211968713
|
A | G | 5 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1816-6T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211968713 | ||||||
chr1:211968793
|
G | C | 4 | a0002c0003t0007g0319a0002c0003t0007g0320a0002c0003t0021g0321others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1816-86C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211968793 | ||||||
chr1:211968897
|
T | C | 1 | a0001c0001t0002g0233 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1816-190A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211968897 | ||||||
chr1:211969199
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1816-492C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969199 | ||||||
chr1:211969234
|
G | A | 4 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256others(1): Show | 4 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1816-527C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969234 | ||||||
chr1:211969282
|
C | CA | 14 | a0001c0001t0002g0212a0001c0001t0002g0233a0001c0001t0002g0241others(11): Show | 14 | HG00323.hp2 HG00597.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1816-576dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969282 | ||||||
chr1:211969293
|
A | C | 7 | a0001c0001t0002g0011a0001c0001t0002g0171a0001c0001t0002g0174others(4): Show | 8 | HG00558.hp2 HG02056.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.1816-586T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969293 | ||||||
chr1:211969298
|
G | A | 173 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(170): Show | 189 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1816-591C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969298 | ||||||
chr1:211969317
|
A | G | 16 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0005g0001others(13): Show | 24 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.1816-610T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969317 | ||||||
chr1:211969390
|
C | T | 2 | a0001c0002t0009g0030a0001c0002t0009g0031 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1816-683G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969390 | ||||||
chr1:211969488
|
T | A | 1 | a0001c0001t0004g0121 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1816-781A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969488 | ||||||
chr1:211969489
|
G | T | 50 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0028others(47): Show | 52 | HG00140.hp2 HG00597.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.1816-782C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969489 | ||||||
chr1:211969551
|
C | CT | 13 | a0001c0001t0001g0063a0001c0001t0001g0077a0001c0001t0001g0094others(10): Show | 13 | HG00597.hp1 HG00741.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1816-845dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969551 | ||||||
chr1:211969551
|
CT | C | 152 | a0001c0001t0001g0061a0001c0001t0001g0135a0001c0001t0001g0136others(149): Show | 162 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1816-845delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969551 | ||||||
chr1:211969551
|
CTT | C | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1816-846_1816-845d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969551 | ||||||
chr1:211969616
|
T | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1816-909A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969616 | ||||||
chr1:211969632
|
T | C | 2 | a0001c0001t0003g0304a0001c0001t0003g0307 | 2 | NA18966.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1816-925A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969632 | ||||||
chr1:211969657
|
A | T | 1 | a0001c0001t0002g0168 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1816-950T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969657 | ||||||
chr1:211969716
|
T | C | 22 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(19): Show | 22 | HG00323.hp2 HG00642.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1816-1009A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969716 | ||||||
chr1:211969717
|
G | A | 45 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0161others(42): Show | 49 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1816-1010C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969717 | ||||||
chr1:211969722
|
A | AT | 102 | a0001c0001t0001g0096a0001c0001t0002g0011a0001c0001t0002g0012others(99): Show | 106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.1816-1016dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969722 | ||||||
chr1:211969791
|
TCACTG | T | 6 | a0001c0001t0006g0005a0001c0001t0006g0038a0001c0001t0006g0058others(3): Show | 7 | HG01175.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1816-1089_1816-108 others(9): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969791 | ||||||
chr1:211969864
|
G | A | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1816-1157C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969864 | ||||||
chr1:211969906
|
G | T | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1816-1199C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969906 | ||||||
chr1:211969945
|
C | T | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1816-1238G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969945 | ||||||
chr1:211969959
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1816-1252G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211969959 | ||||||
chr1:211970085
|
T | C | 4 | a0002c0003t0007g0319a0002c0003t0007g0320a0002c0003t0021g0321others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1816-1378A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211970085 | ||||||
chr1:211970231
|
C | T | 1 | a0001c0001t0003g0259 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1816-1524G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211970231 | ||||||
chr1:211970255
|
G | C | 1 | a0001c0001t0002g0241 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1816-1548C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211970255 | ||||||
chr1:211970576
|
G | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1816-1869C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211970576 | ||||||
chr1:211970584
|
A | G | 1 | a0001c0001t0003g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1816-1877T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211970584 | ||||||
chr1:211970590
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1816-1883G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211970590 | ||||||
chr1:211970700
|
A | C | 1 | a0001c0001t0003g0265 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1816-1993T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211970700 | ||||||
chr1:211970798
|
C | T | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1816-2091G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211970798 | ||||||
chr1:211970909
|
G | A | 44 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0161others(41): Show | 48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1816-2202C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211970909 | ||||||
chr1:211971013
|
A | T | 4 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(1): Show | 4 | HG02080.hp2 NA18612.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.1816-2306T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971013 | ||||||
chr1:211971199
|
G | GT | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1816-2493dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971199 | ||||||
chr1:211971200
|
T | C | 6 | a0001c0001t0009g0203a0001c0001t0012g0205a0001c0001t0012g0207others(3): Show | 6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1816-2493A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971200 | ||||||
chr1:211971212
|
A | G | 1 | a0001c0001t0003g0296 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1816-2505T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971212 | ||||||
chr1:211971359
|
G | A | 30 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0167others(27): Show | 34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.1816-2652C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971359 | ||||||
chr1:211971463
|
T | C | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1816-2756A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971463 | ||||||
chr1:211971496
|
A | C | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1816-2789T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971496 | ||||||
chr1:211971639
|
G | A | 1 | a0001c0001t0003g0296 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1816-2932C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971639 | ||||||
chr1:211971659
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1816-2952A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971659 | ||||||
chr1:211971678
|
G | T | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1816-2971C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971678 | ||||||
chr1:211971884
|
C | A | 88 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(85): Show | 92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.1816-3177G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971884 | ||||||
chr1:211971910
|
A | G | 1 | a0001c0001t0002g0212 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1816-3203T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971910 | ||||||
chr1:211971915
|
C | CA | 11 | a0001c0001t0001g0053a0001c0001t0001g0087a0001c0001t0001g0092others(8): Show | 11 | HG01884.hp1 HG02723.hp1 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.1816-3209dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971915 | ||||||
chr1:211971915
|
CA | C | 25 | a0001c0001t0001g0071a0001c0001t0001g0141a0001c0001t0002g0245others(22): Show | 25 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.1816-3209delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971915 | ||||||
chr1:211971915
|
CAA | C | 110 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0002g0011others(107): Show | 122 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.1816-3210_1816-320 others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971915 | ||||||
chr1:211971915
|
CAAAAAAA others(7): Show |
C | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1816-3222_1816-320 others(18): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971915 | ||||||
chr1:211971920
|
AAAAAAAA others(10): Show |
A | 2 | a0002c0003t0021g0321a0002c0007t0022g0322 | 2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1815+3229_1816-321 others(21): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971920 | ||||||
chr1:211971932
|
A | G | 2 | a0001c0001t0004g0009a0001c0001t0014g0273 | 3 | HG03490.hp2 HG03492.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1816-3225T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211971932 | ||||||
chr1:211972079
|
C | T | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1815+3087G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211972079 | ||||||
chr1:211972130
|
A | G | 1 | a0001c0001t0003g0303 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1815+3036T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211972130 | ||||||
chr1:211972235
|
C | T | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1815+2931G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211972235 | ||||||
chr1:211972418
|
G | A | 1 | a0001c0001t0003g0267 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1815+2748C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211972418 | ||||||
chr1:211972594
|
T | C | 4 | a0002c0003t0007g0319a0002c0003t0007g0320a0002c0003t0021g0321others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1815+2572A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211972594 | ||||||
chr1:211972722
|
T | C | 5 | a0001c0001t0012g0205a0001c0001t0012g0207a0001c0001t0020g0206others(2): Show | 5 | HG02280.hp1 HG02572.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.1815+2444A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211972722 | ||||||
chr1:211972907
|
C | A | 1 | a0001c0001t0002g0272 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1815+2259G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211972907 | ||||||
chr1:211973076
|
G | C | 1 | a0001c0001t0004g0060 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1815+2090C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973076 | ||||||
chr1:211973224
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1815+1942C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973224 | ||||||
chr1:211973224
|
G | T | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1815+1942C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973224 | ||||||
chr1:211973372
|
A | C | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1815+1794T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973372 | ||||||
chr1:211973409
|
G | T | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1815+1757C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973409 | ||||||
chr1:211973412
|
T | C | 5 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1815+1754A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973412 | ||||||
chr1:211973483
|
T | A | 2 | a0001c0002t0009g0030a0001c0002t0009g0031 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1815+1683A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973483 | ||||||
chr1:211973497
|
A | T | 44 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0161others(41): Show | 48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1815+1669T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973497 | ||||||
chr1:211973541
|
C | G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1815+1625G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973541 | ||||||
chr1:211973766
|
G | A | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1815+1400C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211973766 | ||||||
chr1:211974033
|
C | G | 2 | a0001c0002t0009g0030a0001c0002t0009g0031 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1815+1133G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974033 | ||||||
chr1:211974241
|
A | C | 1 | a0001c0001t0011g0185 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1815+925T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974241 | ||||||
chr1:211974267
|
GAA | G | 27 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0061others(24): Show | 28 | HG00642.hp1 HG02129.hp2 HG02132.hp1 others(25): Show |
intron_variant | MODIFIER | c.1815+897_1815+898d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974267 | ||||||
chr1:211974267
|
GAAAA | G | 33 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0161others(30): Show | 38 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(35): Show |
intron_variant | MODIFIER | c.1815+895_1815+898d others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974267 | ||||||
chr1:211974267
|
GAAAAAA | G | 7 | a0001c0001t0002g0271a0001c0001t0003g0258a0001c0001t0003g0261others(4): Show | 7 | HG02257.hp2 HG03490.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.1815+893_1815+898d others(8): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974267 | ||||||
chr1:211974268
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0002t0009g0030 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1815+888_1815+897d others(12): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974268 | ||||||
chr1:211974268
|
AAAAAAAA others(9): Show |
A | 2 | a0002c0003t0021g0321a0002c0007t0022g0322 | 2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1815+882_1815+897d others(18): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974268 | ||||||
chr1:211974268
|
AAAAAAAA others(11): Show |
A | 5 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(2): Show | 5 | HG00323.hp2 HG02257.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1815+880_1815+897d others(20): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974268 | ||||||
chr1:211974270
|
A | AAT | 8 | a0001c0001t0002g0175a0001c0001t0002g0198a0001c0001t0002g0200others(5): Show | 8 | HG00323.hp1 HG00733.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.1815+895_1815+896i others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | ||||||
chr1:211974270
|
A | AATAT | 8 | a0001c0001t0002g0169a0001c0001t0002g0173a0001c0001t0002g0179others(5): Show | 8 | HG00099.hp2 HG01192.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1815+895_1815+896i others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | ||||||
chr1:211974270
|
A | AATATAT | 12 | a0001c0001t0002g0172a0001c0001t0002g0188a0001c0001t0002g0190others(9): Show | 12 | HG00639.hp1 HG00642.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.1815+895_1815+896i others(8): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | ||||||
chr1:211974270
|
A | AATATATA others(1): Show |
8 | a0001c0001t0002g0168a0001c0001t0002g0170a0001c0001t0002g0171others(5): Show | 8 | HG01258.hp1 HG03139.hp2 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.1815+895_1815+896i others(10): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | ||||||
chr1:211974270
|
A | AATATATA others(3): Show |
10 | a0001c0001t0001g0074a0001c0001t0002g0176a0001c0001t0002g0177others(7): Show | 10 | HG00741.hp1 HG02027.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1815+895_1815+896i others(12): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | ||||||
chr1:211974270
|
A | AATATATA others(5): Show |
7 | a0001c0001t0002g0012a0001c0001t0003g0164a0001c0001t0004g0100others(4): Show | 8 | HG01168.hp1 HG01515.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1815+895_1815+896i others(14): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | ||||||
chr1:211974270
|
A | AATATATA others(7): Show |
1 | a0001c0001t0004g0317 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1815+895_1815+896i others(16): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | ||||||
chr1:211974270
|
A | AATATATA others(9): Show |
4 | a0001c0001t0004g0099a0001c0001t0004g0134a0001c0001t0008g0033others(1): Show | 4 | HG01243.hp1 HG04228.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1815+895_1815+896i others(18): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | ||||||
chr1:211974270
|
A | AATATATA others(11): Show |
2 | a0001c0001t0004g0132a0001c0001t0008g0032 | 2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1815+895_1815+896i others(20): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | ||||||
chr1:211974270
|
A | AATATATA others(19): Show |
1 | a0001c0001t0004g0146 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1815+895_1815+896i others(28): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | ||||||
chr1:211974270
|
A | T | 2 | a0001c0002t0009g0031a0006c0011t0001g0040 | 2 | HG02135.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1815+896T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | ||||||
chr1:211974270
|
AAAAAAAA others(1): Show |
A | 18 | a0001c0001t0003g0018a0001c0001t0003g0090a0001c0001t0003g0160others(15): Show | 18 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1815+888_1815+895d others(10): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | ||||||
chr1:211974270
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0003g0312 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1815+886_1815+895d others(12): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | ||||||
chr1:211974270
|
AAAAAAAA others(5): Show |
A | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1815+884_1815+895d others(14): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | ||||||
chr1:211974270
|
AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0014g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1815+882_1815+895d others(16): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | ||||||
chr1:211974270
|
AAAAAAAA others(11): Show |
A | 4 | a0001c0001t0002g0212a0001c0001t0002g0246a0001c0001t0002g0247others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1815+878_1815+895d others(20): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | ||||||
chr1:211974270
|
AAAAAAAA others(13): Show |
A | 14 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0004g0009others(11): Show | 23 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.1815+876_1815+895d others(22): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | ||||||
chr1:211974270
|
AAAAAAAA others(15): Show |
A | 50 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0028others(47): Show | 52 | HG00140.hp2 HG00597.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.1815+874_1815+895d others(24): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974270 | ||||||
chr1:211974272
|
A | AAT | 14 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0029others(11): Show | 17 | HG01071.hp2 HG02004.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.1815+893_1815+894i others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974272 | ||||||
chr1:211974272
|
A | AATATATA others(5): Show |
1 | a0001c0001t0001g0075 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1815+893_1815+894i others(14): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974272 | ||||||
chr1:211974272
|
A | AATATATA others(7): Show |
1 | a0001c0001t0001g0158 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1815+893_1815+894i others(16): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974272 | ||||||
chr1:211974272
|
A | T | 81 | a0001c0001t0001g0056a0001c0001t0001g0074a0001c0001t0001g0133others(78): Show | 83 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.1815+894T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974272 | ||||||
chr1:211974272
|
AAAAAATA others(3): Show |
A | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | NA19057.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1815+884_1815+893d others(12): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974272 | ||||||
chr1:211974274
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0156 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1815+891_1815+892i others(12): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974274 | ||||||
chr1:211974274
|
A | T | 152 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0010others(149): Show | 159 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1815+892T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974274 | ||||||
chr1:211974276
|
A | AAAATATA others(5): Show |
1 | a0001c0001t0001g0087 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1815+889_1815+890i others(14): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974276 | ||||||
chr1:211974276
|
A | AATATATA others(3): Show |
1 | a0001c0001t0001g0154 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1815+880_1815+889d others(12): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974276 | ||||||
chr1:211974276
|
A | AATATATA others(7): Show |
1 | a0001c0001t0001g0140 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1815+876_1815+889d others(16): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974276 | ||||||
chr1:211974276
|
A | AATATATA others(9): Show |
1 | a0001c0001t0001g0155 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1815+874_1815+889d others(18): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974276 | ||||||
chr1:211974276
|
A | T | 209 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(206): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.1815+890T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974276 | ||||||
chr1:211974308
|
T | A | 20 | a0001c0001t0001g0142a0001c0001t0001g0144a0001c0001t0003g0090others(17): Show | 20 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.1815+858A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974308 | ||||||
chr1:211974308
|
T | TATATATA others(3): Show |
1 | a0001c0001t0004g0125 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1815+857_1815+858i others(12): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974308 | ||||||
chr1:211974308
|
T | TATATATA others(7): Show |
1 | a0001c0001t0004g0126 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1815+857_1815+858i others(16): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974308 | ||||||
chr1:211974308
|
T | TATATATA others(15): Show |
1 | a0001c0001t0004g0122 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1815+857_1815+858i others(24): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974308 | ||||||
chr1:211974309
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0002g0193 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1815+856_1815+857i others(17): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974309 | ||||||
chr1:211974403
|
G | A | 173 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(170): Show | 189 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1815+763C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974403 | ||||||
chr1:211974621
|
A | G | 2 | a0001c0005t0001g0073a0001c0005t0001g0093 | 2 | NA18998.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1815+545T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974621 | ||||||
chr1:211974681
|
A | G | 1 | a0001c0001t0011g0185 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1815+485T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974681 | ||||||
chr1:211974687
|
G | A | 1 | a0001c0001t0005g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1815+479C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974687 | ||||||
chr1:211974764
|
C | T | 10 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1815+402G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974764 | ||||||
chr1:211974925
|
C | T | 1 | a0001c0001t0003g0276 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1815+241G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211974925 | ||||||
chr1:211975004
|
A | G | 1 | a0001c0001t0002g0227 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1815+162T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211975004 | ||||||
chr1:211975070
|
G | T | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1815+96C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 13/19 | chr1 | 211975070 | ||||||
chr1:211975417
|
G | A | 2 | a0001c0001t0003g0268a0001c0001t0003g0269 | 2 | HG00621.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1609-45C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211975417 | ||||||
chr1:211975657
|
C | T | 13 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0005g0001others(10): Show | 21 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.1609-285G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211975657 | ||||||
chr1:211975784
|
C | T | 2 | a0001c0001t0003g0268a0001c0001t0003g0269 | 2 | HG00621.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1609-412G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211975784 | ||||||
chr1:211975838
|
G | A | 1 | a0001c0001t0014g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1609-466C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211975838 | ||||||
chr1:211975957
|
GT | G | 316 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(313): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1609-586delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211975957 | ||||||
chr1:211976044
|
T | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1608+538A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211976044 | ||||||
chr1:211976080
|
G | A | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.1608+502C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211976080 | ||||||
chr1:211976097
|
C | T | 6 | a0001c0001t0009g0203a0001c0001t0012g0205a0001c0001t0012g0207others(3): Show | 6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1608+485G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211976097 | ||||||
chr1:211976098
|
G | A | 4 | a0001c0001t0002g0221a0001c0001t0002g0238a0001c0001t0002g0243others(1): Show | 4 | HG03688.hp2 HG03834.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.1608+484C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211976098 | ||||||
chr1:211976195
|
A | G | 6 | a0001c0001t0009g0203a0001c0001t0012g0205a0001c0001t0012g0207others(3): Show | 6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1608+387T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211976195 | ||||||
chr1:211976262
|
G | A | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1608+320C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211976262 | ||||||
chr1:211976298
|
C | T | 1 | a0001c0001t0004g0146 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1608+284G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211976298 | ||||||
chr1:211976334
|
A | G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1608+248T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211976334 | ||||||
chr1:211976357
|
G | A | 45 | a0001c0001t0002g0284a0001c0001t0003g0002a0001c0001t0003g0017others(42): Show | 49 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.1608+225C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 12/19 | chr1 | 211976357 | ||||||
chr1:211976752
|
C | A | 1 | a0001c0001t0004g0129 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1471-33G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211976752 | ||||||
chr1:211976804
|
A | G | 1 | a0001c0002t0016g0027 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1471-85T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211976804 | ||||||
chr1:211976809
|
G | C | 1 | a0001c0001t0003g0014 | 2 | HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1471-90C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211976809 | ||||||
chr1:211976919
|
G | T | 16 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(13): Show | 16 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1471-200C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211976919 | ||||||
chr1:211977114
|
G | C | 1 | a0001c0001t0002g0204 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1471-395C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977114 | ||||||
chr1:211977387
|
C | T | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1471-668G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977387 | ||||||
chr1:211977388
|
G | A | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1471-669C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977388 | ||||||
chr1:211977422
|
C | T | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1471-703G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977422 | ||||||
chr1:211977612
|
T | C | 6 | a0001c0001t0009g0203a0001c0001t0012g0205a0001c0001t0012g0207others(3): Show | 6 | HG00642.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1470+660A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977612 | ||||||
chr1:211977629
|
T | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1470+643A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977629 | ||||||
chr1:211977760
|
C | T | 17 | a0001c0001t0003g0090a0001c0001t0003g0160a0001c0001t0003g0257others(14): Show | 17 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1470+512G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977760 | ||||||
chr1:211977784
|
A | C | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1470+488T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977784 | ||||||
chr1:211977892
|
TA | T | 5 | a0001c0001t0002g0212a0001c0001t0002g0246a0001c0001t0002g0247others(2): Show | 5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1470+379delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977892 | ||||||
chr1:211977946
|
A | G | 173 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(170): Show | 189 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.1470+326T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211977946 | ||||||
chr1:211978174
|
G | A | 2 | a0001c0006t0001g0098a0001c0006t0001g0118 | 2 | NA18991.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.1470+98C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 11/19 | chr1 | 211978174 | ||||||
chr1:211978557
|
G | C | 2 | a0001c0002t0009g0030a0001c0002t0009g0031 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1231-46C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211978557 | ||||||
chr1:211978572
|
A | G | 2 | a0001c0001t0002g0175a0001c0001t0002g0187 | 2 | HG00323.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1231-61T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211978572 | ||||||
chr1:211978642
|
A | G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1231-131T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211978642 | ||||||
chr1:211978702
|
TAAC | T | 50 | a0001c0001t0002g0015a0001c0001t0002g0016a0001c0001t0002g0028others(47): Show | 52 | HG00140.hp2 HG00597.hp2 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.1231-194_1231-192d others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211978702 | ||||||
chr1:211978831
|
T | C | 228 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(225): Show | 246 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.1231-320A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211978831 | ||||||
chr1:211978833
|
A | C | 1 | a0001c0001t0014g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1231-322T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211978833 | ||||||
chr1:211979335
|
A | G | 3 | a0001c0001t0003g0281a0001c0001t0003g0282a0001c0001t0003g0283 | 3 | HG00738.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1231-824T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211979335 | ||||||
chr1:211979437
|
A | G | 11 | a0001c0001t0003g0161a0001c0001t0003g0162a0001c0001t0003g0163others(8): Show | 11 | HG01433.hp1 HG02698.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1231-926T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211979437 | ||||||
chr1:211979674
|
C | T | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1231-1163G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211979674 | ||||||
chr1:211979683
|
A | G | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1231-1172T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211979683 | ||||||
chr1:211980046
|
C | T | 2 | a0001c0001t0001g0063a0001c0001t0001g0064 | 2 | HG00738.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1230+1047G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980046 | ||||||
chr1:211980282
|
T | C | 1 | a0001c0001t0003g0309 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1230+811A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980282 | ||||||
chr1:211980317
|
G | A | 1 | a0001c0001t0003g0266 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1230+776C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980317 | ||||||
chr1:211980328
|
T | C | 5 | a0001c0001t0002g0212a0001c0001t0002g0246a0001c0001t0002g0247others(2): Show | 5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1230+765A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980328 | ||||||
chr1:211980480
|
G | C | 5 | a0001c0001t0002g0212a0001c0001t0002g0246a0001c0001t0002g0247others(2): Show | 5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1230+613C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980480 | ||||||
chr1:211980528
|
C | T | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1230+565G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980528 | ||||||
chr1:211980529
|
G | A | 1 | a0001c0001t0001g0041 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1230+564C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980529 | ||||||
chr1:211980720
|
TGA | T | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1230+371_1230+372d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980720 | ||||||
chr1:211980842
|
G | A | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1230+251C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980842 | ||||||
chr1:211980854
|
T | C | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1230+239A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980854 | ||||||
chr1:211980901
|
C | T | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1230+192G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980901 | ||||||
chr1:211980999
|
T | A | 2 | a0001c0001t0003g0281a0001c0001t0003g0282 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1230+94A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211980999 | ||||||
chr1:211981045
|
A | G | 7 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(4): Show | 11 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1230+48T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 10/19 | chr1 | 211981045 | ||||||
chr1:211981346
|
C | T | 3 | a0001c0001t0002g0175a0001c0001t0002g0187a0001c0001t0002g0198 | 3 | HG00323.hp1 HG00733.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1133-156G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211981346 | ||||||
chr1:211981369
|
TAA | T | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1133-181_1133-180d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211981369 | ||||||
chr1:211981536
|
G | A | 3 | a0001c0001t0011g0185a0001c0001t0011g0186a0001c0001t0011g0192 | 3 | NA18979.hp1 NA18994.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1133-346C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211981536 | ||||||
chr1:211981588
|
A | G | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1133-398T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211981588 | ||||||
chr1:211981666
|
T | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1133-476A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211981666 | ||||||
chr1:211981721
|
A | G | 1 | a0001c0002t0009g0030 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1133-531T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211981721 | ||||||
chr1:211981850
|
A | G | 19 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(16): Show | 19 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1133-660T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211981850 | ||||||
chr1:211981945
|
G | A | 17 | a0001c0001t0003g0090a0001c0001t0003g0160a0001c0001t0003g0257others(14): Show | 17 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.1132+731C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211981945 | ||||||
chr1:211982019
|
G | A | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1132+657C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211982019 | ||||||
chr1:211982107
|
T | C | 1 | a0001c0001t0003g0312 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1132+569A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211982107 | ||||||
chr1:211982178
|
G | A | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.1132+498C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211982178 | ||||||
chr1:211982317
|
T | C | 2 | a0001c0001t0001g0049a0005c0009t0001g0050 | 2 | NA18941.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1132+359A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 9/19 | chr1 | 211982317 | ||||||
chr1:211982833
|
T | C | 2 | a0001c0001t0001g0029a0001c0001t0001g0067 | 2 | HG00099.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.998-23A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211982833 | ||||||
chr1:211982913
|
A | G | 2 | a0001c0001t0003g0268a0001c0001t0003g0269 | 2 | HG00621.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.998-103T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211982913 | ||||||
chr1:211982958
|
A | C | 2 | a0002c0003t0007g0319a0002c0003t0007g0320 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.998-148T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211982958 | ||||||
chr1:211982986
|
T | C | 1 | a0001c0001t0002g0271 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.998-176A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211982986 | ||||||
chr1:211983055
|
AT | A | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.998-246delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211983055 | ||||||
chr1:211983374
|
C | A | 4 | a0002c0003t0007g0319a0002c0003t0007g0320a0002c0003t0021g0321others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.998-564G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211983374 | ||||||
chr1:211983712
|
G | A | 2 | a0002c0003t0007g0319a0002c0003t0007g0320 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.998-902C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211983712 | ||||||
chr1:211983855
|
G | GT | 138 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(135): Show | 146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.998-1046dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211983855 | ||||||
chr1:211983860
|
T | G | 1 | a0001c0001t0003g0312 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.998-1050A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211983860 | ||||||
chr1:211983968
|
G | A | 1 | a0001c0001t0002g0272 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.998-1158C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211983968 | ||||||
chr1:211983982
|
A | G | 1 | a0001c0001t0003g0306 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.998-1172T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211983982 | ||||||
chr1:211983999
|
G | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.998-1189C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211983999 | ||||||
chr1:211984016
|
A | G | 14 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0053others(11): Show | 14 | HG00423.hp1 HG00558.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.998-1206T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984016 | ||||||
chr1:211984188
|
A | G | 1 | a0001c0001t0001g0140 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.998-1378T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984188 | ||||||
chr1:211984349
|
A | ACT | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.998-1541_998-1540d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984349 | ||||||
chr1:211984501
|
T | C | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.998-1691A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984501 | ||||||
chr1:211984518
|
T | C | 2 | a0001c0001t0002g0246a0001c0001t0002g0247 | 2 | HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.998-1708A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984518 | ||||||
chr1:211984520
|
C | T | 2 | a0002c0003t0007g0319a0002c0003t0007g0320 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.998-1710G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984520 | ||||||
chr1:211984633
|
T | G | 1 | a0001c0001t0001g0035 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.998-1823A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984633 | ||||||
chr1:211984659
|
A | T | 3 | a0001c0001t0003g0002a0001c0001t0003g0309a0001c0001t0019g0308 | 6 | HG00733.hp1 HG01074.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.998-1849T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984659 | ||||||
chr1:211984712
|
C | A | 1 | a0001c0001t0014g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.998-1902G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984712 | ||||||
chr1:211984812
|
CTTGTT | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.998-2007_998-2003d others(7): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984812 | ||||||
chr1:211984914
|
T | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.998-2104A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211984914 | ||||||
chr1:211985374
|
A | C | 138 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(135): Show | 146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.997+2512T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211985374 | ||||||
chr1:211985569
|
C | A | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.997+2317G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211985569 | ||||||
chr1:211985641
|
G | A | 1 | a0001c0001t0003g0164 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.997+2245C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211985641 | ||||||
chr1:211985676
|
G | C | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.997+2210C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211985676 | ||||||
chr1:211985736
|
T | C | 2 | a0001c0001t0003g0281a0001c0001t0003g0282 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.997+2150A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211985736 | ||||||
chr1:211985744
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.997+2142G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211985744 | ||||||
chr1:211985930
|
C | A | 173 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(170): Show | 189 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.997+1956G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211985930 | ||||||
chr1:211986063
|
T | C | 2 | a0001c0001t0003g0274a0001c0001t0003g0275 | 2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.997+1823A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211986063 | ||||||
chr1:211986485
|
G | C | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.997+1401C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211986485 | ||||||
chr1:211986540
|
T | C | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.997+1346A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211986540 | ||||||
chr1:211986643
|
T | A | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.997+1243A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211986643 | ||||||
chr1:211986755
|
G | T | 3 | a0001c0001t0004g0128a0001c0001t0004g0129a0001c0001t0004g0131 | 3 | HG00741.hp1 HG02738.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.997+1131C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211986755 | ||||||
chr1:211986813
|
T | C | 3 | a0001c0001t0003g0313a0001c0001t0003g0314a0001c0001t0003g0315 | 3 | HG02257.hp2 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.997+1073A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211986813 | ||||||
chr1:211986903
|
C | T | 1 | a0001c0004t0023g0325 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.997+983G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211986903 | ||||||
chr1:211987318
|
C | A | 97 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(94): Show | 101 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.997+568G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211987318 | ||||||
chr1:211987321
|
A | C | 1 | a0001c0001t0003g0312 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.997+565T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211987321 | ||||||
chr1:211987328
|
C | A | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.997+558G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211987328 | ||||||
chr1:211987487
|
T | C | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.997+399A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211987487 | ||||||
chr1:211987685
|
T | C | 1 | a0001c0001t0001g0085 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.997+201A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211987685 | ||||||
chr1:211987788
|
C | T | 1 | a0001c0001t0002g0177 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.997+98G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 8/19 | chr1 | 211987788 | ||||||
chr1:211988130
|
A | T | 1 | a0001c0001t0002g0201 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.880-127T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988130 | ||||||
chr1:211988182
|
G | A | 1 | a0001c0001t0002g0199 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.880-179C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988182 | ||||||
chr1:211988186
|
G | A | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-183C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988186 | ||||||
chr1:211988364
|
A | G | 16 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(13): Show | 16 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.880-361T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988364 | ||||||
chr1:211988398
|
G | C | 1 | a0001c0001t0002g0224 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.880-395C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988398 | ||||||
chr1:211988421
|
C | CA | 15 | a0001c0001t0002g0175a0001c0001t0002g0187a0001c0001t0002g0246others(12): Show | 21 | HG00323.hp1 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.880-419dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988421 | ||||||
chr1:211988429
|
A | AG | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-427_880-426ins others(1): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988429 | ||||||
chr1:211988434
|
A | C | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.880-431T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988434 | ||||||
chr1:211988563
|
T | C | 1 | a0001c0001t0003g0278 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.880-560A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988563 | ||||||
chr1:211988596
|
T | C | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.880-593A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988596 | ||||||
chr1:211988597
|
T | C | 1 | a0001c0001t0002g0196 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.880-594A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988597 | ||||||
chr1:211988657
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.880-654C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988657 | ||||||
chr1:211988681
|
C | T | 1 | a0001c0001t0002g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.880-678G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988681 | ||||||
chr1:211988887
|
T | C | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-884A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211988887 | ||||||
chr1:211989009
|
A | G | 2 | a0001c0002t0009g0030a0001c0002t0009g0031 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-1006T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989009 | ||||||
chr1:211989059
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.880-1056T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989059 | ||||||
chr1:211989163
|
T | C | 5 | a0001c0001t0002g0173a0001c0001t0002g0188a0001c0001t0002g0189others(2): Show | 5 | HG01192.hp2 HG01361.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-1160A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989163 | ||||||
chr1:211989379
|
G | GTT | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.880-1378_880-1377d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989379 | ||||||
chr1:211989481
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.880-1478G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989481 | ||||||
chr1:211989588
|
G | A | 2 | a0001c0002t0009g0030a0001c0002t0009g0031 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-1585C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989588 | ||||||
chr1:211989638
|
A | G | 21 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0057others(18): Show | 23 | HG01168.hp1 HG01175.hp1 HG01515.hp2 others(20): Show |
intron_variant | MODIFIER | c.880-1635T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989638 | ||||||
chr1:211989694
|
C | T | 1 | a0003c0008t0002g0226 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.880-1691G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989694 | ||||||
chr1:211989745
|
C | A | 4 | a0001c0001t0002g0212a0001c0001t0002g0246a0001c0001t0002g0247others(1): Show | 4 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-1742G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989745 | ||||||
chr1:211989821
|
C | CA | 10 | a0001c0001t0001g0059a0001c0001t0001g0096a0001c0001t0002g0212others(7): Show | 10 | HG02129.hp2 HG02572.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.880-1819dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989821 | ||||||
chr1:211989821
|
CA | C | 9 | a0001c0001t0002g0176a0001c0001t0003g0298a0001c0004t0007g0323others(6): Show | 9 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.880-1819delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211989821 | ||||||
chr1:211990064
|
G | A | 16 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0005g0001others(13): Show | 24 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.880-2061C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990064 | ||||||
chr1:211990285
|
TA | T | 82 | a0001c0001t0001g0142a0001c0001t0002g0284a0001c0001t0003g0002others(79): Show | 94 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.880-2283delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990285 | ||||||
chr1:211990285
|
TAA | T | 93 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(90): Show | 97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.880-2284_880-2283d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990285 | ||||||
chr1:211990304
|
G | A | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.880-2301C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990304 | ||||||
chr1:211990330
|
T | C | 1 | a0001c0004t0007g0323 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.880-2327A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990330 | ||||||
chr1:211990341
|
T | C | 1 | a0001c0001t0003g0162 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.880-2338A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990341 | ||||||
chr1:211990522
|
C | T | 2 | a0002c0003t0021g0321a0002c0007t0022g0322 | 2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.880-2519G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990522 | ||||||
chr1:211990549
|
T | C | 1 | a0001c0001t0008g0034 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.880-2546A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990549 | ||||||
chr1:211990708
|
T | C | 1 | a0001c0001t0002g0199 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.880-2705A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990708 | ||||||
chr1:211990757
|
G | C | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-2754C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990757 | ||||||
chr1:211990780
|
T | C | 1 | a0001c0001t0002g0249 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.880-2777A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211990780 | ||||||
chr1:211991086
|
C | T | 4 | a0002c0003t0007g0319a0002c0003t0007g0320a0002c0003t0021g0321others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-3083G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211991086 | ||||||
chr1:211991210
|
T | C | 2 | a0001c0002t0009g0030a0001c0002t0009g0031 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-3207A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211991210 | ||||||
chr1:211991460
|
T | A | 1 | a0001c0001t0002g0271 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.880-3457A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211991460 | ||||||
chr1:211991801
|
C | G | 30 | a0001c0001t0002g0284a0001c0001t0003g0002a0001c0001t0003g0017others(27): Show | 34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.880-3798G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211991801 | ||||||
chr1:211991978
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.880-3975C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211991978 | ||||||
chr1:211992117
|
G | A | 1 | a0001c0001t0003g0276 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.880-4114C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211992117 | ||||||
chr1:211992293
|
G | A | 193 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(190): Show | 209 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.880-4290C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211992293 | ||||||
chr1:211992465
|
A | C | 1 | a0001c0001t0003g0276 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.880-4462T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211992465 | ||||||
chr1:211992491
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.880-4488C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211992491 | ||||||
chr1:211992639
|
T | C | 44 | a0001c0001t0002g0284a0001c0001t0003g0002a0001c0001t0003g0017others(41): Show | 48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.880-4636A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211992639 | ||||||
chr1:211992704
|
A | T | 1 | a0001c0001t0001g0069 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.880-4701T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211992704 | ||||||
chr1:211992714
|
G | A | 1 | a0001c0001t0005g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.880-4711C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211992714 | ||||||
chr1:211992753
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.880-4750C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211992753 | ||||||
chr1:211992781
|
A | G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-4778T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211992781 | ||||||
chr1:211993180
|
C | A | 1 | a0001c0001t0001g0095 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.880-5177G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993180 | ||||||
chr1:211993408
|
G | A | 1 | a0006c0011t0001g0040 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.880-5405C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993408 | ||||||
chr1:211993506
|
T | C | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.880-5503A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993506 | ||||||
chr1:211993508
|
T | C | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.880-5505A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993508 | ||||||
chr1:211993510
|
T | C | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.880-5507A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993510 | ||||||
chr1:211993525
|
C | CA | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.880-5523dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993525 | ||||||
chr1:211993532
|
T | C | 1 | a0001c0001t0002g0234 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.880-5529A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993532 | ||||||
chr1:211993537
|
A | G | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.880-5534T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993537 | ||||||
chr1:211993538
|
G | A | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.880-5535C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993538 | ||||||
chr1:211993540
|
C | T | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.880-5537G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993540 | ||||||
chr1:211993541
|
G | A | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.880-5538C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993541 | ||||||
chr1:211993579
|
C | G | 44 | a0001c0001t0002g0284a0001c0001t0003g0002a0001c0001t0003g0017others(41): Show | 48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.880-5576G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993579 | ||||||
chr1:211993658
|
T | C | 19 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(16): Show | 19 | HG00323.hp2 HG00642.hp1 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.880-5655A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993658 | ||||||
chr1:211993679
|
C | CA | 10 | a0001c0001t0001g0115a0001c0001t0001g0137a0001c0001t0002g0012others(7): Show | 13 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.880-5677dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993679 | ||||||
chr1:211993679
|
C | CAAAA | 6 | a0001c0004t0007g0323a0001c0004t0007g0324a0002c0003t0007g0319others(3): Show | 6 | HG02257.hp1 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-5680_880-5677d others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993679 | ||||||
chr1:211993679
|
CA | C | 7 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0136others(4): Show | 7 | HG03041.hp1 HG03491.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-5677delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993679 | ||||||
chr1:211993833
|
T | C | 1 | a0001c0001t0003g0264 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.880-5830A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993833 | ||||||
chr1:211993834
|
C | T | 10 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-5831G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993834 | ||||||
chr1:211993848
|
G | A | 138 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(135): Show | 146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.880-5845C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211993848 | ||||||
chr1:211994000
|
A | G | 16 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0005g0001others(13): Show | 24 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.880-5997T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994000 | ||||||
chr1:211994152
|
C | G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-6149G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994152 | ||||||
chr1:211994232
|
G | T | 5 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-6229C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994232 | ||||||
chr1:211994423
|
C | CT | 55 | a0001c0001t0002g0208a0001c0001t0002g0210a0001c0001t0002g0211others(52): Show | 56 | HG00323.hp2 HG00423.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.880-6421dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994423 | ||||||
chr1:211994423
|
C | CTT | 4 | a0001c0001t0002g0209a0001c0001t0003g0002a0001c0001t0003g0309others(1): Show | 7 | HG00733.hp1 HG01074.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-6422_880-6421d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994423 | ||||||
chr1:211994423
|
CT | C | 16 | a0001c0001t0001g0065a0001c0001t0002g0239a0001c0001t0003g0013others(13): Show | 24 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.880-6421delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994423 | ||||||
chr1:211994434
|
T | C | 3 | a0001c0001t0004g0128a0001c0001t0004g0129a0001c0001t0004g0131 | 3 | HG00741.hp1 HG02738.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.880-6431A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994434 | ||||||
chr1:211994450
|
T | A | 16 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0005g0001others(13): Show | 24 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.880-6447A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994450 | ||||||
chr1:211994676
|
G | A | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-6673C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994676 | ||||||
chr1:211994686
|
G | A | 1 | a0001c0004t0007g0324 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.880-6683C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994686 | ||||||
chr1:211994764
|
A | T | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-6761T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994764 | ||||||
chr1:211994797
|
A | G | 1 | a0001c0001t0003g0311 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.880-6794T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994797 | ||||||
chr1:211994807
|
C | T | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-6804G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994807 | ||||||
chr1:211994844
|
CAAGAT | C | 3 | a0001c0001t0012g0205a0001c0001t0012g0207a0001c0001t0020g0206 | 3 | HG02572.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.880-6846_880-6842d others(7): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994844 | ||||||
chr1:211994886
|
G | GA | 238 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0086others(235): Show | 258 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.880-6884dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211994886 | ||||||
chr1:211995115
|
ATTTTCAT | A | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-7119_880-7113d others(9): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995115 | ||||||
chr1:211995124
|
C | G | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-7121G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995124 | ||||||
chr1:211995225
|
G | A | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-7222C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995225 | ||||||
chr1:211995331
|
C | T | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-7328G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995331 | ||||||
chr1:211995367
|
A | C | 1 | a0001c0001t0003g0266 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.880-7364T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995367 | ||||||
chr1:211995373
|
TTTTC | T | 4 | a0001c0001t0002g0248a0001c0001t0010g0202a0001c0001t0010g0255others(1): Show | 4 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-7374_880-7371d others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995373 | ||||||
chr1:211995530
|
AT | A | 45 | a0001c0001t0002g0284a0001c0001t0003g0002a0001c0001t0003g0017others(42): Show | 49 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.880-7528delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995530 | ||||||
chr1:211995674
|
C | T | 1 | a0001c0001t0003g0283 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.880-7671G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995674 | ||||||
chr1:211995692
|
A | C | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.880-7689T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995692 | ||||||
chr1:211995828
|
A | G | 17 | a0001c0001t0003g0090a0001c0001t0003g0160a0001c0001t0003g0257others(14): Show | 17 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.880-7825T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211995828 | ||||||
chr1:211996053
|
GA | G | 4 | a0001c0001t0001g0136a0001c0001t0012g0205a0001c0001t0012g0207others(1): Show | 4 | HG02572.hp2 HG03579.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-8051delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996053 | ||||||
chr1:211996150
|
G | A | 38 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0168others(35): Show | 40 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.880-8147C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996150 | ||||||
chr1:211996243
|
G | A | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.880-8240C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996243 | ||||||
chr1:211996296
|
G | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-8293C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996296 | ||||||
chr1:211996384
|
A | T | 324 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(321): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.880-8381T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996384 | ||||||
chr1:211996471
|
C | A | 1 | a0001c0001t0001g0117 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.880-8468G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996471 | ||||||
chr1:211996705
|
G | T | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.880-8702C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996705 | ||||||
chr1:211996722
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.880-8719A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996722 | ||||||
chr1:211996750
|
C | A | 1 | a0001c0001t0014g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.880-8747G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996750 | ||||||
chr1:211996791
|
C | G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-8788G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996791 | ||||||
chr1:211996815
|
A | C | 1 | a0001c0004t0023g0325 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.880-8812T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996815 | ||||||
chr1:211996925
|
G | A | 3 | a0001c0001t0003g0313a0001c0001t0003g0314a0001c0001t0003g0315 | 3 | HG02257.hp2 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.880-8922C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996925 | ||||||
chr1:211996938
|
C | T | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.880-8935G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996938 | ||||||
chr1:211996968
|
G | A | 2 | a0002c0003t0021g0321a0002c0007t0022g0322 | 2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.880-8965C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211996968 | ||||||
chr1:211997335
|
C | G | 1 | a0001c0001t0001g0136 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.879+9304G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997335 | ||||||
chr1:211997336
|
G | C | 1 | a0001c0001t0001g0136 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.879+9303C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997336 | ||||||
chr1:211997400
|
G | C | 1 | a0001c0001t0001g0139 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.879+9239C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997400 | ||||||
chr1:211997471
|
T | C | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.879+9168A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997471 | ||||||
chr1:211997528
|
G | GA | 115 | a0001c0001t0001g0066a0001c0001t0001g0088a0001c0001t0002g0011others(112): Show | 123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.879+9110dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997528 | ||||||
chr1:211997528
|
G | GAA | 13 | a0001c0001t0002g0028a0001c0001t0002g0169a0001c0001t0002g0190others(10): Show | 13 | HG00423.hp2 HG01361.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.879+9109_879+9110d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997528 | ||||||
chr1:211997528
|
GA | G | 7 | a0001c0001t0001g0039a0001c0001t0001g0091a0001c0001t0001g0136others(4): Show | 7 | HG00140.hp1 HG01109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.879+9110delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997528 | ||||||
chr1:211997528
|
GAAAAAAA others(1): Show |
G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+9103_879+9110d others(10): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997528 | ||||||
chr1:211997550
|
A | G | 15 | a0001c0001t0003g0160a0001c0001t0003g0257a0001c0001t0003g0258others(12): Show | 15 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.879+9089T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997550 | ||||||
chr1:211997551
|
G | A | 138 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(135): Show | 146 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.879+9088C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997551 | ||||||
chr1:211997622
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.879+9017A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997622 | ||||||
chr1:211997694
|
CA | C | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+8944delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997694 | ||||||
chr1:211997696
|
T | G | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+8943A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997696 | ||||||
chr1:211997708
|
A | G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+8931T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997708 | ||||||
chr1:211997725
|
A | C | 1 | a0001c0001t0001g0097 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.879+8914T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997725 | ||||||
chr1:211997793
|
G | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+8846C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997793 | ||||||
chr1:211997878
|
C | CA | 15 | a0001c0001t0001g0089a0001c0001t0002g0190a0001c0001t0002g0235others(12): Show | 15 | HG00544.hp2 HG00597.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.879+8760dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997878 | ||||||
chr1:211997878
|
CA | C | 6 | a0001c0001t0001g0065a0001c0001t0001g0136a0001c0001t0002g0175others(3): Show | 6 | HG00323.hp1 HG02280.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.879+8760delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997878 | ||||||
chr1:211997936
|
T | C | 3 | a0001c0001t0003g0281a0001c0001t0003g0282a0001c0001t0003g0283 | 3 | HG00738.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.879+8703A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211997936 | ||||||
chr1:211998068
|
G | A | 4 | a0002c0003t0007g0319a0002c0003t0007g0320a0002c0003t0021g0321others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+8571C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998068 | ||||||
chr1:211998266
|
C | T | 2 | a0001c0001t0004g0317a0001c0001t0004g0318 | 2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.879+8373G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998266 | ||||||
chr1:211998281
|
G | A | 1 | a0001c0001t0003g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.879+8358C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998281 | ||||||
chr1:211998337
|
A | G | 33 | a0001c0001t0002g0015a0001c0001t0002g0028a0001c0001t0002g0204others(30): Show | 34 | HG00597.hp2 HG01346.hp1 HG01943.hp2 others(31): Show |
intron_variant | MODIFIER | c.879+8302T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998337 | ||||||
chr1:211998366
|
T | C | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.879+8273A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998366 | ||||||
chr1:211998446
|
A | G | 3 | a0001c0001t0008g0032a0001c0001t0008g0033a0001c0001t0008g0034 | 3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.879+8193T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998446 | ||||||
chr1:211998535
|
T | C | 6 | a0001c0001t0003g0017a0001c0001t0003g0289a0001c0001t0003g0298others(3): Show | 7 | NA18939.hp1 NA18950.hp2 NA18998.hp1 others(4): Show |
intron_variant | MODIFIER | c.879+8104A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998535 | ||||||
chr1:211998614
|
T | G | 1 | a0001c0001t0001g0108 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.879+8025A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998614 | ||||||
chr1:211998654
|
CCTATAAA others(39): Show |
C | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+7939_879+7984d others(48): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998654 | ||||||
chr1:211998806
|
CAA | C | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.879+7831_879+7832d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998806 | ||||||
chr1:211998809
|
TAAC | T | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.879+7827_879+7829d others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998809 | ||||||
chr1:211998978
|
T | C | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.879+7661A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211998978 | ||||||
chr1:211999007
|
A | T | 4 | a0001c0001t0002g0222a0001c0001t0002g0223a0001c0001t0002g0224others(1): Show | 4 | HG02080.hp2 NA18612.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+7632T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999007 | ||||||
chr1:211999051
|
C | T | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.879+7588G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999051 | ||||||
chr1:211999421
|
C | T | 1 | a0001c0001t0002g0191 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.879+7218G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999421 | ||||||
chr1:211999471
|
A | G | 1 | a0001c0004t0007g0323 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.879+7168T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999471 | ||||||
chr1:211999475
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.879+7164C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999475 | ||||||
chr1:211999477
|
C | T | 2 | a0001c0001t0004g0047a0001c0001t0004g0048 | 2 | HG02723.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.879+7162G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999477 | ||||||
chr1:211999533
|
T | C | 1 | a0001c0001t0010g0255 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.879+7106A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999533 | ||||||
chr1:211999585
|
A | C | 1 | a0001c0001t0008g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.879+7054T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999585 | ||||||
chr1:211999669
|
C | T | 1 | a0001c0001t0003g0290 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.879+6970G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999669 | ||||||
chr1:211999693
|
G | A | 30 | a0001c0001t0002g0284a0001c0001t0003g0002a0001c0001t0003g0017others(27): Show | 34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.879+6946C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999693 | ||||||
chr1:211999790
|
G | A | 2 | a0001c0004t0007g0323a0001c0004t0007g0324 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.879+6849C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999790 | ||||||
chr1:211999806
|
G | A | 193 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(190): Show | 209 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.879+6833C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999806 | ||||||
chr1:211999825
|
C | T | 1 | a0001c0001t0002g0171 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.879+6814G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999825 | ||||||
chr1:211999877
|
C | G | 16 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(13): Show | 16 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.879+6762G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999877 | ||||||
chr1:211999877
|
C | T | 5 | a0001c0001t0002g0212a0001c0001t0002g0246a0001c0001t0002g0247others(2): Show | 5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+6762G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999877 | ||||||
chr1:211999895
|
TG | T | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+6743delC | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999895 | ||||||
chr1:211999975
|
C | A | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+6664G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999975 | ||||||
chr1:211999975
|
C | G | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.879+6664G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 211999975 | ||||||
chr1:212000030
|
T | G | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+6609A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212000030 | ||||||
chr1:212000202
|
G | A | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+6437C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212000202 | ||||||
chr1:212000255
|
G | A | 2 | a0002c0003t0021g0321a0002c0007t0022g0322 | 2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.879+6384C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212000255 | ||||||
chr1:212000256
|
G | A | 17 | a0001c0001t0003g0090a0001c0001t0003g0160a0001c0001t0003g0257others(14): Show | 17 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.879+6383C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212000256 | ||||||
chr1:212000346
|
C | T | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.879+6293G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212000346 | ||||||
chr1:212000514
|
C | T | 1 | a0001c0001t0003g0257 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.879+6125G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212000514 | ||||||
chr1:212000687
|
C | T | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.879+5952G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212000687 | ||||||
chr1:212000783
|
C | T | 5 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+5856G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212000783 | ||||||
chr1:212000865
|
T | C | 3 | a0001c0001t0003g0281a0001c0001t0003g0282a0001c0001t0003g0283 | 3 | HG00738.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.879+5774A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212000865 | ||||||
chr1:212001004
|
CA | C | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.879+5634delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212001004 | ||||||
chr1:212001064
|
C | CT | 17 | a0001c0001t0004g0009a0001c0001t0004g0060a0001c0001t0004g0099others(14): Show | 18 | HG01168.hp1 HG01175.hp1 HG01175.hp2 others(15): Show |
intron_variant | MODIFIER | c.879+5574dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212001064 | ||||||
chr1:212001064
|
CT | C | 28 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0250others(25): Show | 28 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.879+5574delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212001064 | ||||||
chr1:212001064
|
CTT | C | 158 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(155): Show | 174 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.879+5573_879+5574d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212001064 | ||||||
chr1:212001064
|
CTTT | C | 6 | a0001c0001t0003g0281a0001c0001t0003g0282a0001c0001t0003g0283others(3): Show | 6 | HG00323.hp2 HG00738.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+5572_879+5574d others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212001064 | ||||||
chr1:212001158
|
C | G | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+5481G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212001158 | ||||||
chr1:212001228
|
C | T | 5 | a0001c0001t0002g0212a0001c0001t0002g0246a0001c0001t0002g0247others(2): Show | 5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+5411G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212001228 | ||||||
chr1:212001358
|
C | T | 5 | a0001c0001t0002g0212a0001c0001t0002g0246a0001c0001t0002g0247others(2): Show | 5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+5281G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212001358 | ||||||
chr1:212001400
|
G | A | 2 | a0002c0003t0007g0319a0002c0003t0007g0320 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.879+5239C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212001400 | ||||||
chr1:212002099
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0067 | 2 | HG00099.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.879+4540G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212002099 | ||||||
chr1:212002251
|
T | C | 5 | a0001c0001t0002g0212a0001c0001t0002g0246a0001c0001t0002g0247others(2): Show | 5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.879+4388A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212002251 | ||||||
chr1:212002429
|
A | G | 1 | a0001c0001t0002g0016 | 2 | NA18944.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.879+4210T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212002429 | ||||||
chr1:212002451
|
C | T | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.879+4188G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212002451 | ||||||
chr1:212002473
|
C | G | 1 | a0001c0001t0011g0192 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.879+4166G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212002473 | ||||||
chr1:212002478
|
T | C | 1 | a0001c0001t0004g0047 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.879+4161A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212002478 | ||||||
chr1:212002717
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.879+3922G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212002717 | ||||||
chr1:212002786
|
C | T | 3 | a0001c0001t0003g0313a0001c0001t0003g0314a0001c0001t0003g0315 | 3 | HG02257.hp2 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.879+3853G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212002786 | ||||||
chr1:212002795
|
G | A | 1 | a0001c0001t0006g0152 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.879+3844C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212002795 | ||||||
chr1:212003136
|
C | T | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.879+3503G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003136 | ||||||
chr1:212003155
|
T | C | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.879+3484A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003155 | ||||||
chr1:212003227
|
C | T | 44 | a0001c0001t0002g0284a0001c0001t0003g0002a0001c0001t0003g0017others(41): Show | 48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.879+3412G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003227 | ||||||
chr1:212003305
|
C | CA | 33 | a0001c0001t0001g0056a0001c0001t0001g0091a0001c0001t0001g0092others(30): Show | 33 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(30): Show |
intron_variant | MODIFIER | c.879+3333dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003305 | ||||||
chr1:212003305
|
CA | C | 21 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0154others(18): Show | 21 | HG00741.hp1 HG01109.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.879+3333delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003305 | ||||||
chr1:212003305
|
CAAA | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+3331_879+3333d others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003305 | ||||||
chr1:212003423
|
G | C | 88 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(85): Show | 92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.879+3216C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003423 | ||||||
chr1:212003490
|
CCA | C | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.879+3147_879+3148d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003490 | ||||||
chr1:212003712
|
A | C | 2 | a0001c0002t0009g0030a0001c0002t0009g0031 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.879+2927T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003712 | ||||||
chr1:212003868
|
A | G | 1 | a0001c0001t0002g0220 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.879+2771T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003868 | ||||||
chr1:212003913
|
G | C | 1 | a0001c0001t0020g0206 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.879+2726C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212003913 | ||||||
chr1:212004056
|
C | A | 1 | a0001c0001t0003g0261 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.879+2583G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004056 | ||||||
chr1:212004233
|
T | C | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.879+2406A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004233 | ||||||
chr1:212004362
|
C | A | 2 | a0001c0001t0003g0268a0001c0001t0003g0269 | 2 | HG00621.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.879+2277G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004362 | ||||||
chr1:212004479
|
T | C | 1 | a0001c0001t0002g0191 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.879+2160A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004479 | ||||||
chr1:212004507
|
C | A | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+2132G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004507 | ||||||
chr1:212004520
|
T | G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+2119A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004520 | ||||||
chr1:212004670
|
T | C | 88 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(85): Show | 92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.879+1969A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004670 | ||||||
chr1:212004820
|
C | A | 1 | a0001c0001t0003g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.879+1819G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004820 | ||||||
chr1:212004875
|
C | T | 1 | a0001c0001t0003g0265 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.879+1764G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004875 | ||||||
chr1:212004904
|
C | T | 4 | a0001c0001t0003g0285a0001c0001t0003g0291a0001c0001t0003g0292others(1): Show | 4 | HG00423.hp2 NA18747.hp2 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+1735G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004904 | ||||||
chr1:212004921
|
C | T | 38 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0168others(35): Show | 40 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.879+1718G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004921 | ||||||
chr1:212004965
|
G | C | 1 | a0001c0001t0003g0312 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.879+1674C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004965 | ||||||
chr1:212004970
|
C | T | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.879+1669G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212004970 | ||||||
chr1:212005117
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | HG00738.hp2 HG00741.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.879+1522G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212005117 | ||||||
chr1:212005151
|
T | C | 2 | a0001c0001t0003g0286a0001c0001t0003g0288 | 2 | NA18972.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.879+1488A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212005151 | ||||||
chr1:212005371
|
G | A | 1 | a0001c0001t0011g0192 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.879+1268C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212005371 | ||||||
chr1:212005454
|
T | C | 1 | a0001c0001t0001g0117 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.879+1185A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212005454 | ||||||
chr1:212005479
|
A | G | 3 | a0001c0001t0012g0205a0001c0001t0012g0207a0001c0001t0020g0206 | 3 | HG02572.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.879+1160T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212005479 | ||||||
chr1:212005482
|
C | T | 1 | a0001c0001t0001g0137 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.879+1157G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212005482 | ||||||
chr1:212005623
|
C | G | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.879+1016G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212005623 | ||||||
chr1:212005628
|
T | C | 3 | a0001c0001t0003g0313a0001c0001t0003g0314a0001c0001t0003g0315 | 3 | HG02257.hp2 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.879+1011A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212005628 | ||||||
chr1:212005837
|
C | T | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.879+802G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212005837 | ||||||
chr1:212006059
|
A | G | 1 | a0001c0001t0002g0251 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.879+580T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212006059 | ||||||
chr1:212006398
|
G | A | 10 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.879+241C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 7/19 | chr1 | 212006398 | ||||||
chr1:212006853
|
A | G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.757-92T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 6/19 | chr1 | 212006853 | ||||||
chr1:212006980
|
G | T | 3 | a0001c0001t0003g0290a0001c0001t0003g0310a0001c0001t0003g0311 | 3 | HG00544.hp2 HG00597.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.757-219C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 6/19 | chr1 | 212006980 | ||||||
chr1:212007079
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.756+171C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 6/19 | chr1 | 212007079 | ||||||
chr1:212007114
|
A | G | 1 | a0001c0001t0014g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.756+136T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 6/19 | chr1 | 212007114 | ||||||
chr1:212007231
|
T | C | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.756+19A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 6/19 | chr1 | 212007231 | ||||||
chr1:212007519
|
G | A | 1 | a0001c0001t0003g0160 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.557-70C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212007519 | ||||||
chr1:212007570
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.557-121A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212007570 | ||||||
chr1:212007774
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.557-325G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212007774 | ||||||
chr1:212008127
|
T | C | 1 | a0001c0001t0014g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.557-678A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212008127 | ||||||
chr1:212008148
|
C | T | 1 | a0001c0001t0002g0174 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.557-699G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212008148 | ||||||
chr1:212008149
|
G | A | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.557-700C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212008149 | ||||||
chr1:212008183
|
C | T | 1 | a0001c0001t0003g0312 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.557-734G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212008183 | ||||||
chr1:212008524
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.557-1075C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212008524 | ||||||
chr1:212008643
|
A | C | 93 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(90): Show | 97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.557-1194T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212008643 | ||||||
chr1:212008891
|
G | T | 3 | a0001c0001t0004g0119a0001c0001t0004g0120a0001c0001t0004g0121 | 3 | HG01168.hp1 HG01175.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.557-1442C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212008891 | ||||||
chr1:212009248
|
T | G | 1 | a0001c0001t0002g0242 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.557-1799A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009248 | ||||||
chr1:212009275
|
T | C | 1 | a0001c0001t0004g0122 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.557-1826A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009275 | ||||||
chr1:212009400
|
C | T | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.557-1951G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009400 | ||||||
chr1:212009455
|
T | C | 21 | a0001c0001t0004g0008a0001c0001t0004g0009a0001c0001t0004g0057others(18): Show | 23 | HG01168.hp1 HG01175.hp1 HG01515.hp2 others(20): Show |
intron_variant | MODIFIER | c.556+1920A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009455 | ||||||
chr1:212009515
|
C | G | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.556+1860G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009515 | ||||||
chr1:212009583
|
T | G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.556+1792A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009583 | ||||||
chr1:212009753
|
G | A | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.556+1622C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009753 | ||||||
chr1:212009772
|
T | TC | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.556+1602dupG | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009772 | ||||||
chr1:212009812
|
A | C | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.556+1563T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009812 | ||||||
chr1:212009821
|
T | G | 7 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(4): Show | 7 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.556+1554A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009821 | ||||||
chr1:212009839
|
T | C | 1 | a0001c0001t0003g0257 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.556+1536A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009839 | ||||||
chr1:212009878
|
G | A | 2 | a0001c0002t0009g0030a0001c0002t0009g0031 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.556+1497C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009878 | ||||||
chr1:212009965
|
T | A | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.556+1410A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009965 | ||||||
chr1:212009984
|
C | T | 2 | a0001c0002t0009g0030a0001c0002t0009g0031 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.556+1391G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212009984 | ||||||
chr1:212010155
|
G | A | 173 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(170): Show | 189 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.556+1220C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010155 | ||||||
chr1:212010180
|
A | G | 173 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(170): Show | 189 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.556+1195T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010180 | ||||||
chr1:212010237
|
G | C | 1 | a0001c0001t0002g0244 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.556+1138C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010237 | ||||||
chr1:212010304
|
G | A | 2 | a0001c0002t0009g0030a0001c0002t0009g0031 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.556+1071C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010304 | ||||||
chr1:212010346
|
G | A | 44 | a0001c0001t0002g0284a0001c0001t0003g0002a0001c0001t0003g0017others(41): Show | 48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.556+1029C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010346 | ||||||
chr1:212010420
|
T | C | 1 | a0001c0001t0004g0045 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.556+955A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010420 | ||||||
chr1:212010752
|
T | C | 1 | a0001c0001t0014g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.556+623A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010752 | ||||||
chr1:212010808
|
T | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.556+567A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010808 | ||||||
chr1:212010875
|
C | T | 5 | a0001c0001t0004g0042a0001c0001t0004g0043a0001c0001t0004g0044others(2): Show | 5 | HG02055.hp2 HG02572.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.556+500G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010875 | ||||||
chr1:212010907
|
C | G | 3 | a0001c0001t0012g0205a0001c0001t0012g0207a0001c0001t0020g0206 | 3 | HG02572.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.556+468G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212010907 | ||||||
chr1:212011133
|
G | A | 2 | a0001c0001t0001g0157a0004c0012t0001g0153 | 2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.556+242C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212011133 | ||||||
chr1:212011164
|
CCT | C | 3 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0014g0273 | 5 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.556+209_556+210del others(2): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212011164 | ||||||
chr1:212011236
|
C | T | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.556+139G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 5/19 | chr1 | 212011236 | ||||||
chr1:212011442
|
GAACAGAA | G | 4 | a0002c0003t0007g0319a0002c0003t0007g0320a0002c0003t0021g0321others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-28_510-22delTT others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212011442 | ||||||
chr1:212011467
|
A | T | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.510-46T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212011467 | ||||||
chr1:212011524
|
T | C | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-103A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212011524 | ||||||
chr1:212011715
|
T | G | 1 | a0001c0001t0002g0193 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.510-294A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212011715 | ||||||
chr1:212011869
|
T | C | 3 | a0001c0001t0002g0194a0001c0001t0002g0195a0001c0001t0002g0196 | 3 | HG00639.hp1 HG02622.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.510-448A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212011869 | ||||||
chr1:212012003
|
T | C | 16 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(13): Show | 16 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.510-582A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012003 | ||||||
chr1:212012106
|
G | A | 2 | a0001c0006t0001g0098a0001c0006t0001g0118 | 2 | NA18991.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.510-685C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012106 | ||||||
chr1:212012251
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.510-830A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012251 | ||||||
chr1:212012267
|
G | A | 1 | a0001c0001t0003g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.510-846C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012267 | ||||||
chr1:212012474
|
G | A | 5 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-1053C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012474 | ||||||
chr1:212012679
|
A | G | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.510-1258T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012679 | ||||||
chr1:212012777
|
T | A | 228 | a0001c0001t0001g0053a0001c0001t0001g0133a0001c0001t0002g0011others(225): Show | 246 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.510-1356A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012777 | ||||||
chr1:212012778
|
T | C | 228 | a0001c0001t0001g0053a0001c0001t0001g0133a0001c0001t0002g0011others(225): Show | 246 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(243): Show |
intron_variant | MODIFIER | c.510-1357A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012778 | ||||||
chr1:212012863
|
C | G | 1 | a0001c0001t0001g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510-1442G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012863 | ||||||
chr1:212012884
|
CAAATTTA others(6): Show |
C | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.510-1476_510-1464d others(15): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012884 | ||||||
chr1:212012911
|
A | G | 31 | a0001c0001t0001g0053a0001c0001t0002g0284a0001c0001t0003g0002others(28): Show | 35 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.510-1490T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212012911 | ||||||
chr1:212013076
|
C | T | 1 | a0001c0002t0005g0025 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.510-1655G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013076 | ||||||
chr1:212013113
|
T | A | 1 | a0001c0001t0002g0277 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.510-1692A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013113 | ||||||
chr1:212013139
|
C | T | 45 | a0001c0001t0001g0053a0001c0001t0002g0284a0001c0001t0003g0002others(42): Show | 49 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.510-1718G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013139 | ||||||
chr1:212013168
|
T | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.510-1747A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013168 | ||||||
chr1:212013320
|
T | C | 1 | a0001c0001t0004g0009 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.510-1899A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013320 | ||||||
chr1:212013332
|
T | A | 1 | a0001c0001t0001g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.510-1911A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013332 | ||||||
chr1:212013492
|
T | G | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.510-2071A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013492 | ||||||
chr1:212013782
|
C | T | 88 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(85): Show | 92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.510-2361G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013782 | ||||||
chr1:212013788
|
G | A | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.510-2367C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013788 | ||||||
chr1:212013791
|
C | G | 1 | a0001c0001t0002g0219 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.510-2370G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013791 | ||||||
chr1:212013822
|
C | T | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.510-2401G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013822 | ||||||
chr1:212013864
|
T | C | 2 | a0001c0002t0009g0030a0001c0002t0009g0031 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.510-2443A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013864 | ||||||
chr1:212013880
|
T | C | 1 | a0001c0001t0003g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.510-2459A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013880 | ||||||
chr1:212013986
|
C | A | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.510-2565G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212013986 | ||||||
chr1:212014020
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.510-2599T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014020 | ||||||
chr1:212014167
|
T | TAAGAATA others(317): Show |
1 | a0002c0003t0007g0320 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.509+2718_509+2719i others(326): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014167 | ||||||
chr1:212014167
|
T | TAAGAATA others(318): Show |
1 | a0002c0003t0007g0319 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.509+2718_509+2719i others(327): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014167 | ||||||
chr1:212014167
|
T | TAAGAATA others(329): Show |
1 | a0002c0003t0021g0321 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.509+2718_509+2719i others(338): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014167 | ||||||
chr1:212014167
|
T | TAAGAATA others(330): Show |
1 | a0002c0007t0022g0322 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.509+2718_509+2719i others(339): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014167 | ||||||
chr1:212014251
|
G | A | 3 | a0001c0001t0003g0281a0001c0001t0003g0282a0001c0001t0003g0283 | 3 | HG00738.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.509+2635C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014251 | ||||||
chr1:212014465
|
C | CA | 79 | a0001c0001t0001g0035a0001c0001t0001g0104a0001c0001t0001g0105others(76): Show | 90 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.509+2420dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014465 | ||||||
chr1:212014465
|
C | CAA | 13 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0197others(10): Show | 13 | HG01109.hp2 HG02027.hp1 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.509+2419_509+2420d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014465 | ||||||
chr1:212014597
|
C | T | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.509+2289G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014597 | ||||||
chr1:212014598
|
G | C | 16 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(13): Show | 16 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.509+2288C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014598 | ||||||
chr1:212014671
|
A | G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+2215T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014671 | ||||||
chr1:212014690
|
T | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+2196A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014690 | ||||||
chr1:212014718
|
A | AT | 88 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(85): Show | 92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.509+2167dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014718 | ||||||
chr1:212014915
|
T | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+1971A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014915 | ||||||
chr1:212014954
|
A | AC | 7 | a0001c0001t0001g0061a0001c0001t0001g0110a0001c0001t0003g0269others(4): Show | 7 | HG02055.hp1 HG02523.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+1931dupG | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014954 | ||||||
chr1:212014964
|
G | A | 1 | a0001c0001t0003g0312 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.509+1922C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014964 | ||||||
chr1:212014982
|
T | TA | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+1903dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212014982 | ||||||
chr1:212015018
|
C | A | 1 | a0001c0001t0003g0267 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.509+1868G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015018 | ||||||
chr1:212015031
|
G | A | 2 | a0001c0001t0003g0262a0001c0001t0003g0263 | 2 | HG01243.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.509+1855C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015031 | ||||||
chr1:212015063
|
CGGCAGCC others(35): Show |
C | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+1781_509+1822d others(44): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015063 | ||||||
chr1:212015090
|
G | A | 1 | a0001c0004t0023g0325 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.509+1796C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015090 | ||||||
chr1:212015098
|
C | T | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+1788G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015098 | ||||||
chr1:212015101
|
G | A | 45 | a0001c0001t0001g0053a0001c0001t0002g0284a0001c0001t0003g0002others(42): Show | 49 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.509+1785C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015101 | ||||||
chr1:212015104
|
CG | C | 5 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+1781delC | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015104 | ||||||
chr1:212015105
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.509+1781C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015105 | ||||||
chr1:212015112
|
C | T | 2 | a0002c0003t0021g0321a0002c0007t0022g0322 | 2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.509+1774G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015112 | ||||||
chr1:212015118
|
G | A | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+1768C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015118 | ||||||
chr1:212015150
|
C | A | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+1736G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015150 | ||||||
chr1:212015191
|
A | AC | 20 | a0001c0001t0001g0059a0001c0001t0001g0110a0001c0001t0001g0111others(17): Show | 20 | HG00597.hp1 HG01175.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.509+1694dupG | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015191 | ||||||
chr1:212015195
|
C | G | 1 | a0001c0001t0004g0131 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.509+1691G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015195 | ||||||
chr1:212015268
|
G | A | 2 | a0001c0001t0001g0157a0004c0012t0001g0153 | 2 | HG02622.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.509+1618C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015268 | ||||||
chr1:212015304
|
G | A | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.509+1582C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015304 | ||||||
chr1:212015356
|
G | C | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.509+1530C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015356 | ||||||
chr1:212015511
|
T | C | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+1375A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015511 | ||||||
chr1:212015569
|
A | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+1317T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015569 | ||||||
chr1:212015646
|
T | G | 2 | a0001c0001t0001g0037a0001c0001t0001g0109 | 2 | NA18963.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.509+1240A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015646 | ||||||
chr1:212015710
|
TA | T | 34 | a0001c0001t0001g0052a0001c0001t0001g0110a0001c0001t0001g0111others(31): Show | 34 | HG00408.hp2 HG00423.hp1 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.509+1175delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015710 | ||||||
chr1:212015710
|
TAA | T | 111 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(108): Show | 119 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.509+1174_509+1175d others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015710 | ||||||
chr1:212015710
|
TAAA | T | 24 | a0001c0001t0001g0049a0001c0001t0001g0054a0001c0001t0001g0055others(21): Show | 30 | HG00558.hp1 HG00733.hp2 HG01069.hp2 others(27): Show |
intron_variant | MODIFIER | c.509+1173_509+1175d others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015710 | ||||||
chr1:212015710
|
TAAAA | T | 88 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(85): Show | 94 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.509+1172_509+1175d others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015710 | ||||||
chr1:212015710
|
TAAAAA | T | 14 | a0001c0001t0002g0171a0001c0001t0002g0208a0001c0001t0002g0216others(11): Show | 14 | HG01168.hp2 HG02523.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.509+1171_509+1175d others(7): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015710 | ||||||
chr1:212015710
|
TAAAAAA | T | 36 | a0001c0001t0001g0053a0001c0001t0003g0002a0001c0001t0003g0017others(33): Show | 40 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.509+1170_509+1175d others(8): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015710 | ||||||
chr1:212015710
|
TAAAAAAA others(6): Show |
T | 2 | a0001c0002t0009g0030a0001c0002t0009g0031 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.509+1163_509+1175d others(15): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015710 | ||||||
chr1:212015710
|
TAAAAAAA others(7): Show |
T | 8 | a0001c0001t0009g0203a0001c0004t0007g0323a0001c0004t0007g0324others(5): Show | 8 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.509+1162_509+1175d others(16): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015710 | ||||||
chr1:212015761
|
C | CAAAA | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+1121_509+1124d others(6): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015761 | ||||||
chr1:212015894
|
G | A | 4 | a0002c0003t0007g0319a0002c0003t0007g0320a0002c0003t0021g0321others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+992C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212015894 | ||||||
chr1:212016104
|
A | G | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.509+782T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212016104 | ||||||
chr1:212016139
|
T | C | 5 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+747A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212016139 | ||||||
chr1:212016187
|
A | G | 1 | a0001c0001t0003g0312 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.509+699T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212016187 | ||||||
chr1:212016192
|
T | C | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+694A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212016192 | ||||||
chr1:212016320
|
G | C | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.509+566C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212016320 | ||||||
chr1:212016344
|
G | A | 3 | a0001c0001t0012g0205a0001c0001t0012g0207a0001c0001t0020g0206 | 3 | HG02572.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.509+542C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212016344 | ||||||
chr1:212016370
|
T | C | 1 | a0001c0001t0006g0127 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.509+516A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212016370 | ||||||
chr1:212016774
|
A | C | 175 | a0001c0001t0001g0053a0001c0001t0002g0011a0001c0001t0002g0012others(172): Show | 191 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.509+112T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 4/19 | chr1 | 212016774 | ||||||
chr1:212017033
|
C | G | 1 | a0001c0001t0002g0215 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.372-10G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212017033 | ||||||
chr1:212017052
|
C | T | 1 | a0001c0001t0008g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.372-29G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212017052 | ||||||
chr1:212017200
|
T | C | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.372-177A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212017200 | ||||||
chr1:212017503
|
C | A | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.372-480G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212017503 | ||||||
chr1:212017546
|
C | T | 8 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0154others(5): Show | 10 | HG02622.hp1 HG02630.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.372-523G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212017546 | ||||||
chr1:212017575
|
A | G | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.372-552T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212017575 | ||||||
chr1:212017621
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.372-598T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212017621 | ||||||
chr1:212017675
|
G | T | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.372-652C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212017675 | ||||||
chr1:212017793
|
C | T | 1 | a0001c0001t0002g0214 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.372-770G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212017793 | ||||||
chr1:212018164
|
G | A | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.372-1141C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018164 | ||||||
chr1:212018199
|
T | C | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.372-1176A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018199 | ||||||
chr1:212018204
|
C | G | 5 | a0001c0001t0002g0212a0001c0001t0002g0246a0001c0001t0002g0247others(2): Show | 5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.372-1181G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018204 | ||||||
chr1:212018354
|
T | C | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.372-1331A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018354 | ||||||
chr1:212018503
|
T | TA | 320 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(317): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.372-1481dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018503 | ||||||
chr1:212018649
|
G | A | 207 | a0001c0001t0001g0133a0001c0001t0002g0011a0001c0001t0002g0012others(204): Show | 223 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.371+1473C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018649 | ||||||
chr1:212018660
|
C | T | 2 | a0001c0001t0001g0049a0005c0009t0001g0050 | 2 | NA18941.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.371+1462G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018660 | ||||||
chr1:212018675
|
C | T | 173 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(170): Show | 189 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.371+1447G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018675 | ||||||
chr1:212018695
|
C | T | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.371+1427G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018695 | ||||||
chr1:212018729
|
A | G | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.371+1393T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018729 | ||||||
chr1:212018775
|
T | G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.371+1347A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018775 | ||||||
chr1:212018779
|
A | G | 5 | a0001c0001t0002g0212a0001c0001t0002g0246a0001c0001t0002g0247others(2): Show | 5 | HG02717.hp2 HG02809.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.371+1343T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018779 | ||||||
chr1:212018917
|
T | C | 11 | a0001c0001t0003g0161a0001c0001t0003g0162a0001c0001t0003g0163others(8): Show | 11 | HG01433.hp1 HG02698.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.371+1205A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212018917 | ||||||
chr1:212019020
|
C | T | 5 | a0001c0001t0004g0045a0001c0001t0004g0046a0001c0001t0004g0047others(2): Show | 5 | HG01884.hp1 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.371+1102G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019020 | ||||||
chr1:212019036
|
G | A | 1 | a0001c0001t0002g0199 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.371+1086C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019036 | ||||||
chr1:212019181
|
A | G | 189 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(186): Show | 205 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.371+941T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019181 | ||||||
chr1:212019250
|
C | CAATA | 44 | a0001c0001t0002g0284a0001c0001t0003g0002a0001c0001t0003g0017others(41): Show | 48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.371+868_371+871dup others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019250 | ||||||
chr1:212019262
|
T | A | 123 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(120): Show | 135 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.371+860A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019262 | ||||||
chr1:212019266
|
T | A | 1 | a0001c0001t0002g0272 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.371+856A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019266 | ||||||
chr1:212019421
|
A | G | 10 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.371+701T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019421 | ||||||
chr1:212019483
|
G | A | 2 | a0001c0001t0003g0268a0001c0001t0003g0269 | 2 | HG00621.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.371+639C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019483 | ||||||
chr1:212019632
|
T | G | 3 | a0001c0001t0012g0205a0001c0001t0012g0207a0001c0001t0020g0206 | 3 | HG02572.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.371+490A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019632 | ||||||
chr1:212019640
|
A | G | 1 | a0002c0003t0007g0319 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.371+482T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212019640 | ||||||
chr1:212020011
|
A | T | 2 | a0001c0001t0004g0045a0001c0001t0004g0147 | 2 | HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.371+111T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212020011 | ||||||
chr1:212020041
|
A | G | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | HG02698.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.371+81T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212020041 | ||||||
chr1:212020112
|
C | T | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.371+10G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 3/19 | chr1 | 212020112 | ||||||
chr1:212020817
|
G | A | 3 | a0001c0001t0008g0032a0001c0001t0008g0033a0001c0001t0008g0034 | 3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.224+266C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 2/19 | chr1 | 212020817 | ||||||
chr1:212020848
|
G | A | 16 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0005g0001others(13): Show | 24 | HG01069.hp1 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.224+235C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 2/19 | chr1 | 212020848 | ||||||
chr1:212021003
|
G | A | 1 | a0001c0004t0007g0324 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.224+80C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 2/19 | chr1 | 212021003 | ||||||
chr1:212021219
|
A | G | 1 | a0001c0001t0017g0316 | 1 | HG03453.hp2 | splice_region_variant&intron_variant | LOW | c.95-7T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021219 | ||||||
chr1:212021278
|
T | G | 2 | a0002c0003t0007g0319a0002c0003t0007g0320 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.95-66A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021278 | ||||||
chr1:212021373
|
T | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-161A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021373 | ||||||
chr1:212021387
|
T | C | 30 | a0001c0001t0002g0284a0001c0001t0003g0002a0001c0001t0003g0017others(27): Show | 34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.95-175A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021387 | ||||||
chr1:212021395
|
G | A | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-183C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021395 | ||||||
chr1:212021463
|
T | C | 30 | a0001c0001t0002g0284a0001c0001t0003g0002a0001c0001t0003g0017others(27): Show | 34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.95-251A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021463 | ||||||
chr1:212021620
|
G | C | 1 | a0001c0001t0014g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.95-408C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021620 | ||||||
chr1:212021628
|
T | A | 2 | a0001c0001t0001g0135a0001c0001t0001g0136 | 2 | NA19057.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.95-416A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021628 | ||||||
chr1:212021680
|
T | TA | 26 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0002g0208others(23): Show | 34 | HG00621.hp1 HG00642.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.95-469dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021680 | ||||||
chr1:212021680
|
TA | T | 8 | a0001c0001t0001g0041a0001c0001t0001g0141a0001c0001t0002g0213others(5): Show | 8 | HG00423.hp2 HG01255.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-469delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021680 | ||||||
chr1:212021766
|
T | G | 4 | a0001c0001t0003g0312a0001c0001t0003g0313a0001c0001t0003g0314others(1): Show | 4 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-554A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021766 | ||||||
chr1:212021855
|
A | T | 1 | a0006c0011t0001g0040 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.95-643T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021855 | ||||||
chr1:212021856
|
T | A | 1 | a0001c0001t0001g0139 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.95-644A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021856 | ||||||
chr1:212021889
|
C | G | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.95-677G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021889 | ||||||
chr1:212021948
|
G | A | 3 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031 | 3 | HG00642.hp1 HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.95-736C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212021948 | ||||||
chr1:212022002
|
C | T | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-790G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212022002 | ||||||
chr1:212022522
|
TA | T | 44 | a0001c0001t0002g0284a0001c0001t0003g0002a0001c0001t0003g0017others(41): Show | 48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.95-1311delT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212022522 | ||||||
chr1:212022670
|
A | AATAT | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-1459_95-1458ins others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212022670 | ||||||
chr1:212022829
|
C | T | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-1617G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212022829 | ||||||
chr1:212022869
|
T | C | 88 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(85): Show | 92 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.95-1657A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212022869 | ||||||
chr1:212023224
|
G | C | 5 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-2012C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023224 | ||||||
chr1:212023260
|
T | C | 2 | a0001c0001t0002g0246a0001c0001t0002g0247 | 2 | HG02717.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.95-2048A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023260 | ||||||
chr1:212023535
|
C | T | 1 | a0001c0001t0003g0257 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.95-2323G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023535 | ||||||
chr1:212023588
|
T | A | 4 | a0002c0003t0007g0319a0002c0003t0007g0320a0002c0003t0021g0321others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2376A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023588 | ||||||
chr1:212023627
|
ATAGACTC | A | 4 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0250others(1): Show | 4 | NA18941.hp1 NA18960.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2422_95-2416del others(7): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023627 | ||||||
chr1:212023729
|
A | G | 4 | a0001c0001t0002g0208a0001c0001t0002g0209a0001c0001t0002g0210others(1): Show | 4 | HG03491.hp2 HG03492.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-2517T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023729 | ||||||
chr1:212023842
|
G | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-2630C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023842 | ||||||
chr1:212023852
|
T | A | 4 | a0002c0003t0007g0319a0002c0003t0007g0320a0002c0003t0021g0321others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2640A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023852 | ||||||
chr1:212023876
|
C | CTTTGA | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.95-2665_95-2664ins others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023876 | ||||||
chr1:212023877
|
C | CTTGAG | 7 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031others(4): Show | 7 | HG00642.hp1 HG02257.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-2666_95-2665ins others(5): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023877 | ||||||
chr1:212023877
|
C | G | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.95-2665G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023877 | ||||||
chr1:212023987
|
T | C | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-2775A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212023987 | ||||||
chr1:212024369
|
A | T | 1 | a0001c0001t0008g0032 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.95-3157T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212024369 | ||||||
chr1:212024411
|
C | G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-3199G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212024411 | ||||||
chr1:212024431
|
T | C | 1 | a0001c0004t0023g0325 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.95-3219A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212024431 | ||||||
chr1:212024502
|
A | G | 16 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(13): Show | 16 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.95-3290T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212024502 | ||||||
chr1:212024544
|
C | T | 2 | a0002c0003t0007g0319a0002c0003t0007g0320 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.95-3332G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212024544 | ||||||
chr1:212024772
|
T | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-3560A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212024772 | ||||||
chr1:212024866
|
T | C | 1 | a0001c0001t0002g0200 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.95-3654A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212024866 | ||||||
chr1:212024976
|
G | T | 1 | a0001c0002t0009g0030 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.95-3764C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212024976 | ||||||
chr1:212025031
|
G | T | 1 | a0001c0001t0003g0278 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.95-3819C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025031 | ||||||
chr1:212025055
|
G | A | 3 | a0001c0001t0003g0002a0001c0001t0003g0309a0001c0001t0019g0308 | 6 | HG00733.hp1 HG01074.hp2 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-3843C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025055 | ||||||
chr1:212025086
|
T | A | 4 | a0001c0002t0005g0003a0001c0002t0005g0025a0001c0002t0005g0026others(1): Show | 6 | HG02922.hp1 HG03225.hp1 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-3874A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025086 | ||||||
chr1:212025100
|
T | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-3888A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025100 | ||||||
chr1:212025278
|
A | G | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4066T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025278 | ||||||
chr1:212025294
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.95-4082C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025294 | ||||||
chr1:212025344
|
T | C | 1 | a0001c0001t0002g0252 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.95-4132A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025344 | ||||||
chr1:212025484
|
T | TA | 9 | a0001c0002t0009g0030a0001c0002t0009g0031a0001c0004t0007g0323others(6): Show | 9 | HG00323.hp2 HG02257.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-4273dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025484 | ||||||
chr1:212025501
|
C | G | 1 | a0001c0001t0002g0284 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.95-4289G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025501 | ||||||
chr1:212025515
|
T | G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-4303A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025515 | ||||||
chr1:212025537
|
T | C | 16 | a0001c0001t0003g0160a0001c0001t0003g0257a0001c0001t0003g0258others(13): Show | 16 | HG00408.hp1 HG00621.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.95-4325A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025537 | ||||||
chr1:212025614
|
G | C | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-4402C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025614 | ||||||
chr1:212025659
|
T | C | 1 | a0001c0001t0003g0310 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.95-4447A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025659 | ||||||
chr1:212025690
|
G | GA | 141 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(138): Show | 149 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.95-4479dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025690 | ||||||
chr1:212025705
|
AT | A | 3 | a0001c0001t0010g0202a0001c0001t0010g0255a0001c0001t0010g0256 | 3 | HG01109.hp2 HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.95-4494delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025705 | ||||||
chr1:212025716
|
A | G | 2 | a0001c0001t0003g0013a0001c0001t0003g0014 | 4 | HG01069.hp1 HG01361.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-4504T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025716 | ||||||
chr1:212025740
|
C | T | 5 | a0001c0001t0002g0168a0001c0001t0002g0169a0001c0001t0002g0170others(2): Show | 5 | NA18948.hp1 NA19002.hp1 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-4528G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025740 | ||||||
chr1:212025799
|
T | C | 3 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325 | 3 | HG00323.hp2 HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.95-4587A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025799 | ||||||
chr1:212025855
|
T | TA | 30 | a0001c0001t0002g0284a0001c0001t0003g0002a0001c0001t0003g0017others(27): Show | 34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.95-4644dupT | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025855 | ||||||
chr1:212025882
|
A | G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-4670T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025882 | ||||||
chr1:212025965
|
G | A | 4 | a0002c0003t0007g0319a0002c0003t0007g0320a0002c0003t0021g0321others(1): Show | 4 | HG02257.hp1 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-4753C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025965 | ||||||
chr1:212025966
|
G | C | 1 | a0001c0001t0004g0147 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.95-4754C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212025966 | ||||||
chr1:212026020
|
G | A | 1 | a0001c0010t0002g0253 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.95-4808C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212026020 | ||||||
chr1:212026073
|
C | T | 1 | a0001c0001t0014g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.95-4861G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212026073 | ||||||
chr1:212026269
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.95-5057A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212026269 | ||||||
chr1:212026577
|
A | AAAGG | 173 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(170): Show | 189 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.95-5366_95-5365ins others(4): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212026577 | ||||||
chr1:212026644
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.95-5432T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212026644 | ||||||
chr1:212026703
|
G | A | 1 | a0001c0001t0002g0201 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.95-5491C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212026703 | ||||||
chr1:212027007
|
A | C | 1 | a0001c0001t0002g0204 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.95-5795T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027007 | ||||||
chr1:212027028
|
A | G | 10 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-5816T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027028 | ||||||
chr1:212027086
|
C | A | 1 | a0001c0001t0014g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.95-5874G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027086 | ||||||
chr1:212027130
|
G | A | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-5918C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027130 | ||||||
chr1:212027223
|
G | T | 5 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-6011C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027223 | ||||||
chr1:212027352
|
A | G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-6140T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027352 | ||||||
chr1:212027397
|
C | T | 1 | a0001c0001t0006g0038 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.95-6185G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027397 | ||||||
chr1:212027400
|
T | A | 2 | a0002c0003t0021g0321a0002c0007t0022g0322 | 2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.95-6188A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027400 | ||||||
chr1:212027659
|
G | A | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-6447C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027659 | ||||||
chr1:212027833
|
C | CT | 170 | a0001c0001t0001g0037a0001c0001t0002g0011a0001c0001t0002g0012others(167): Show | 186 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.95-6622dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027833 | ||||||
chr1:212027913
|
G | A | 1 | a0001c0001t0002g0270 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.95-6701C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027913 | ||||||
chr1:212027961
|
G | C | 1 | a0001c0001t0002g0271 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.95-6749C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212027961 | ||||||
chr1:212028073
|
C | T | 2 | a0002c0003t0007g0319a0002c0003t0007g0320 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.95-6861G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028073 | ||||||
chr1:212028135
|
G | T | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-6923C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028135 | ||||||
chr1:212028172
|
T | C | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.95-6960A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028172 | ||||||
chr1:212028269
|
A | G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-7057T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028269 | ||||||
chr1:212028276
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.95-7064C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028276 | ||||||
chr1:212028389
|
A | C | 44 | a0001c0001t0002g0284a0001c0001t0003g0002a0001c0001t0003g0017others(41): Show | 48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.94+6955T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028389 | ||||||
chr1:212028396
|
T | C | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+6948A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028396 | ||||||
chr1:212028450
|
A | G | 10 | a0001c0001t0009g0203a0001c0002t0009g0030a0001c0002t0009g0031others(7): Show | 10 | HG00323.hp2 HG00642.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.94+6894T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028450 | ||||||
chr1:212028541
|
A | T | 1 | a0001c0001t0009g0203 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.94+6803T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028541 | ||||||
chr1:212028774
|
G | A | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+6570C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028774 | ||||||
chr1:212028858
|
A | G | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+6486T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212028858 | ||||||
chr1:212029015
|
G | A | 44 | a0001c0001t0002g0284a0001c0001t0003g0002a0001c0001t0003g0017others(41): Show | 48 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.94+6329C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212029015 | ||||||
chr1:212029118
|
C | T | 1 | a0001c0001t0010g0202 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.94+6226G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212029118 | ||||||
chr1:212029122
|
A | T | 1 | a0001c0001t0001g0036 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.94+6222T>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212029122 | ||||||
chr1:212029144
|
A | C | 2 | a0001c0004t0007g0323a0001c0004t0007g0324 | 2 | HG02630.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.94+6200T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212029144 | ||||||
chr1:212029340
|
C | T | 38 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0168others(35): Show | 40 | HG00099.hp2 HG00323.hp1 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.94+6004G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212029340 | ||||||
chr1:212029631
|
T | A | 1 | a0001c0001t0014g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.94+5713A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212029631 | ||||||
chr1:212029717
|
T | C | 1 | a0001c0001t0004g0149 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.94+5627A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212029717 | ||||||
chr1:212030176
|
C | T | 30 | a0001c0001t0002g0284a0001c0001t0003g0002a0001c0001t0003g0017others(27): Show | 34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.94+5168G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212030176 | ||||||
chr1:212030293
|
G | GT | 51 | a0001c0001t0001g0035a0001c0001t0002g0284a0001c0001t0003g0002others(48): Show | 55 | HG00423.hp2 HG00597.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.94+5050dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212030293 | ||||||
chr1:212030293
|
GT | G | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+5050delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212030293 | ||||||
chr1:212030294
|
T | G | 1 | a0001c0001t0002g0272 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.94+5050A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212030294 | ||||||
chr1:212030552
|
G | C | 1 | a0001c0001t0014g0273 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.94+4792C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212030552 | ||||||
chr1:212030567
|
G | A | 2 | a0001c0001t0003g0274a0001c0001t0003g0275 | 2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.94+4777C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212030567 | ||||||
chr1:212030889
|
C | T | 326 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(323): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.94+4455G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212030889 | ||||||
chr1:212030995
|
AT | A | 3 | a0001c0001t0008g0032a0001c0001t0008g0033a0001c0001t0008g0034 | 3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+4348delA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212030995 | ||||||
chr1:212031101
|
C | T | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+4243G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212031101 | ||||||
chr1:212031450
|
T | C | 1 | a0001c0001t0003g0276 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.94+3894A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212031450 | ||||||
chr1:212031885
|
T | C | 1 | a0001c0001t0002g0277 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.94+3459A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212031885 | ||||||
chr1:212032194
|
T | A | 3 | a0001c0001t0008g0032a0001c0001t0008g0033a0001c0001t0008g0034 | 3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+3150A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032194 | ||||||
chr1:212032195
|
C | A | 3 | a0001c0001t0008g0032a0001c0001t0008g0033a0001c0001t0008g0034 | 3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+3149G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032195 | ||||||
chr1:212032196
|
T | TGGA | 3 | a0001c0001t0008g0032a0001c0001t0008g0033a0001c0001t0008g0034 | 3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+3147_94+3148ins others(3): Show |
INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032196 | ||||||
chr1:212032197
|
C | T | 3 | a0001c0001t0008g0032a0001c0001t0008g0033a0001c0001t0008g0034 | 3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+3147G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032197 | ||||||
chr1:212032199
|
G | T | 3 | a0001c0001t0008g0032a0001c0001t0008g0033a0001c0001t0008g0034 | 3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+3145C>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032199 | ||||||
chr1:212032200
|
C | A | 3 | a0001c0001t0008g0032a0001c0001t0008g0033a0001c0001t0008g0034 | 3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+3144G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032200 | ||||||
chr1:212032201
|
A | C | 3 | a0001c0001t0008g0032a0001c0001t0008g0033a0001c0001t0008g0034 | 3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+3143T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032201 | ||||||
chr1:212032202
|
C | T | 3 | a0001c0001t0008g0032a0001c0001t0008g0033a0001c0001t0008g0034 | 3 | HG01167.hp1 HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.94+3142G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032202 | ||||||
chr1:212032236
|
A | C | 2 | a0001c0002t0009g0030a0001c0002t0009g0031 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.94+3108T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032236 | ||||||
chr1:212032319
|
G | C | 2 | a0002c0003t0021g0321a0002c0007t0022g0322 | 2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.94+3025C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032319 | ||||||
chr1:212032364
|
G | C | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | HG02698.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.94+2980C>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032364 | ||||||
chr1:212032520
|
A | G | 2 | a0002c0003t0021g0321a0002c0007t0022g0322 | 2 | HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.94+2824T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032520 | ||||||
chr1:212032610
|
G | A | 2 | a0002c0003t0007g0319a0002c0003t0007g0320 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.94+2734C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032610 | ||||||
chr1:212032634
|
G | A | 1 | a0001c0001t0001g0010 | 2 | HG02080.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.94+2710C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032634 | ||||||
chr1:212032700
|
C | T | 2 | a0002c0003t0007g0319a0002c0003t0007g0320 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.94+2644G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032700 | ||||||
chr1:212032715
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.94+2629C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032715 | ||||||
chr1:212032746
|
G | A | 1 | a0001c0001t0002g0280 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.94+2598C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032746 | ||||||
chr1:212032759
|
G | A | 5 | a0001c0001t0003g0281a0001c0001t0003g0282a0001c0001t0003g0283others(2): Show | 5 | HG00738.hp1 HG01167.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+2585C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032759 | ||||||
chr1:212032959
|
T | G | 1 | a0001c0001t0006g0152 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.94+2385A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212032959 | ||||||
chr1:212033063
|
G | A | 6 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(3): Show | 6 | HG02622.hp1 HG02886.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+2281C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212033063 | ||||||
chr1:212033078
|
T | C | 1 | a0001c0001t0001g0159 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.94+2266A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212033078 | ||||||
chr1:212033111
|
C | T | 3 | a0001c0001t0005g0019a0001c0001t0005g0020a0001c0001t0005g0021 | 3 | HG01069.hp2 HG01071.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.94+2233G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212033111 | ||||||
chr1:212033463
|
T | G | 2 | a0002c0003t0007g0319a0002c0003t0007g0320 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.94+1881A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212033463 | ||||||
chr1:212033496
|
T | C | 189 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0015others(186): Show | 205 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.94+1848A>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212033496 | ||||||
chr1:212033548
|
T | G | 30 | a0001c0001t0002g0284a0001c0001t0003g0002a0001c0001t0003g0017others(27): Show | 34 | HG00423.hp2 HG00544.hp2 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.94+1796A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212033548 | ||||||
chr1:212033830
|
C | A | 6 | a0001c0001t0003g0018a0001c0001t0003g0312a0001c0001t0003g0313others(3): Show | 6 | HG02257.hp2 HG02280.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+1514G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212033830 | ||||||
chr1:212033922
|
A | C | 2 | a0001c0002t0009g0030a0001c0002t0009g0031 | 2 | HG02280.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.94+1422T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212033922 | ||||||
chr1:212033990
|
G | A | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+1354C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212033990 | ||||||
chr1:212034143
|
C | A | 2 | a0002c0003t0007g0319a0002c0003t0007g0320 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.94+1201G>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034143 | ||||||
chr1:212034173
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1171T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034173 | ||||||
chr1:212034174
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1170T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034174 | ||||||
chr1:212034175
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1169G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034175 | ||||||
chr1:212034177
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1167A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034177 | ||||||
chr1:212034178
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1166T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034178 | ||||||
chr1:212034179
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1165T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034179 | ||||||
chr1:212034180
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1164A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034180 | ||||||
chr1:212034181
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1163A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034181 | ||||||
chr1:212034182
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1162A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034182 | ||||||
chr1:212034183
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1161A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034183 | ||||||
chr1:212034184
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1160G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034184 | ||||||
chr1:212034185
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1159A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034185 | ||||||
chr1:212034186
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1158A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034186 | ||||||
chr1:212034189
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1155A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034189 | ||||||
chr1:212034190
|
T | A | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1154A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034190 | ||||||
chr1:212034192
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1152T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034192 | ||||||
chr1:212034193
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1151A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034193 | ||||||
chr1:212034199
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1145A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034199 | ||||||
chr1:212034201
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1143G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034201 | ||||||
chr1:212034203
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1141G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034203 | ||||||
chr1:212034204
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1140A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034204 | ||||||
chr1:212034205
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1139T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034205 | ||||||
chr1:212034209
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1135T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034209 | ||||||
chr1:212034212
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1132G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034212 | ||||||
chr1:212034213
|
T | A | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1131A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034213 | ||||||
chr1:212034217
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1127T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034217 | ||||||
chr1:212034218
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1126G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034218 | ||||||
chr1:212034219
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1125A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034219 | ||||||
chr1:212034220
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1124G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034220 | ||||||
chr1:212034221
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1123T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034221 | ||||||
chr1:212034222
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1122T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034222 | ||||||
chr1:212034223
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1121G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034223 | ||||||
chr1:212034224
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1120G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034224 | ||||||
chr1:212034226
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1118T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034226 | ||||||
chr1:212034227
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1117T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034227 | ||||||
chr1:212034230
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1114T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034230 | ||||||
chr1:212034232
|
T | A | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1112A>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034232 | ||||||
chr1:212034233
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1111T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034233 | ||||||
chr1:212034234
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1110A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034234 | ||||||
chr1:212034235
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1109G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034235 | ||||||
chr1:212034236
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1108G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034236 | ||||||
chr1:212034237
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1107G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034237 | ||||||
chr1:212034239
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1105A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034239 | ||||||
chr1:212034240
|
T | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1104A>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034240 | ||||||
chr1:212034241
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.94+1103T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034241 | ||||||
chr1:212034279
|
A | G | 1 | a0001c0001t0003g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.94+1065T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034279 | ||||||
chr1:212034725
|
G | A | 2 | a0001c0001t0004g0317a0001c0001t0004g0318 | 2 | HG02698.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.94+619C>T | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034725 | ||||||
chr1:212034793
|
C | CT | 7 | a0001c0004t0007g0323a0001c0004t0007g0324a0001c0004t0023g0325others(4): Show | 7 | HG00323.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.94+550dupA | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034793 | ||||||
chr1:212034882
|
C | T | 1 | a0001c0001t0002g0028 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.94+462G>A | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034882 | ||||||
chr1:212034986
|
C | G | 11 | a0001c0001t0005g0001a0001c0001t0005g0019a0001c0001t0005g0020others(8): Show | 17 | HG01069.hp2 HG01071.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.94+358G>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212034986 | ||||||
chr1:212035051
|
A | G | 2 | a0002c0003t0007g0319a0002c0003t0007g0320 | 2 | HG02257.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.94+293T>C | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212035051 | ||||||
chr1:212035114
|
A | C | 1 | a0001c0001t0003g0018 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.94+230T>G | INTS7 | ENSG00000143493.13 | transcript | ENST00000366994.8 | protein_coding | 1/19 | chr1 | 212035114 |