geneid | 3685 |
---|---|
ensemblid | ENSG00000138448.13 |
hgncid | 6150 |
symbol | ITGAV |
name | integrin subunit alpha V |
refseq_nuc | NM_002210.5 |
refseq_prot | NP_002201.2 |
ensembl_nuc | ENST00000261023.8 |
ensembl_prot | ENSP00000261023.3 |
mane_status | MANE Select |
chr | chr2 |
start | 186590056 |
end | 186680901 |
strand | + |
ver | v1.2 |
region | chr2:186590056-186680901 |
region5000 | chr2:186585056-186685901 |
regionname0 | ITGAV_chr2_186590056_186680901 |
regionname5000 | ITGAV_chr2_186585056_186685901 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1048 | 275 | 74 | 60 | 88 | 14 | 38 | 56 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0002 | 0/0 | 1048 | 23 | 7 | 6 | 10 | 0 | 0 | 9 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0003 | 1/0 | 1048 | 7 | 6 | 0 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0004 | 0/0 | 1048 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0005 | 0/0 | 1048 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0006 | 0/0 | 1048 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 3147 | 264 | 63 | 60 | 88 | 14 | 38 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
c0002 | 0/0 | 3147 | 22 | 7 | 5 | 10 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
c0003 | 0/0 | 3147 | 7 | 7 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
c0004 | 1/0 | 3147 | 7 | 6 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
c0005 | 0/0 | 3147 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
c0006 | 0/0 | 3147 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
c0007 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
c0008 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
c0009 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
c0010 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 3893 | 134 | 39 | 25 | 45 | 6 | 17 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0002 | 0/0 | 3888 | 71 | 9 | 23 | 23 | 4 | 12 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0003 | 0/0 | 3891 | 53 | 12 | 13 | 16 | 4 | 8 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0004 | 0/0 | 3893 | 15 | 2 | 3 | 10 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0005 | 0/0 | 3895 | 5 | 5 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0006 | 0/0 | 3894 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0007 | 0/0 | 3891 | 3 | 2 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0008 | 0/0 | 3893 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0009 | 0/0 | 3888 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0010 | 0/0 | 3896 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0011 | 0/0 | 3893 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0012 | 0/0 | 3893 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0013 | 0/0 | 3891 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0014 | 0/0 | 3895 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0015 | 0/0 | 3895 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0016 | 0/0 | 3894 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0017 | 0/0 | 3895 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0018 | 0/0 | 3893 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0019 | 0/0 | 3888 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0020 | 0/0 | 3891 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0021 | 0/0 | 3888 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0022 | 0/0 | 3893 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0023 | 0/0 | 3893 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
t0024 | 0/0 | 3895 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0004 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3147 | 264 | 63 | 60 | 88 | 14 | 38 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0003 | 0/0 | 3147 | 7 | 7 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0005 | 0/0 | 3147 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0008 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0002c0002 | 0/0 | 3147 | 22 | 7 | 5 | 10 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0002c0006 | 0/0 | 3147 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0003c0004 | 1/0 | 3147 | 7 | 6 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0004c0009 | 0/0 | 3147 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0005c0010 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0006c0007 | 0/0 | 3147 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 7039 | 119 | 26 | 24 | 45 | 6 | 17 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0002 | 0/0 | 7034 | 65 | 4 | 22 | 23 | 4 | 12 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0003 | 0/0 | 7037 | 50 | 11 | 13 | 14 | 4 | 8 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0005 | 0/0 | 7041 | 5 | 5 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0006 | 0/0 | 7040 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0008 | 0/0 | 7039 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0009 | 0/0 | 7034 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0010 | 0/0 | 7042 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0011 | 0/0 | 7039 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0012 | 0/0 | 7039 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0013 | 0/0 | 7037 | 2 | 0 | 0 | 2 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0014 | 0/0 | 7041 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0015 | 0/0 | 7041 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0016 | 0/0 | 7040 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0017 | 0/0 | 7041 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0018 | 0/0 | 7039 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0019 | 0/0 | 7034 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0021 | 0/0 | 7034 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0023 | 0/0 | 7039 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0001t0024 | 0/0 | 7041 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0003t0001 | 0/0 | 7039 | 5 | 5 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0003t0002 | 0/0 | 7034 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0005t0002 | 0/0 | 7034 | 3 | 3 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0001c0008t0020 | 0/0 | 7037 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0002c0002t0001 | 0/0 | 7039 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0002c0002t0002 | 0/0 | 7034 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0002c0002t0004 | 0/0 | 7039 | 15 | 2 | 3 | 10 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0002c0002t0007 | 0/0 | 7037 | 3 | 2 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0002c0002t0022 | 0/0 | 7039 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0002c0006t0001 | 0/0 | 7039 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0003c0004t0001 | 1/0 | 7039 | 7 | 6 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0004c0009t0003 | 0/0 | 7037 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0005c0010t0003 | 0/0 | 7037 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
a0006c0007t0003 | 0/0 | 7037 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | copy fasta | chr2 | 186585056 | 186685901 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0155 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0005g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0006g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0006g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0008g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0009g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0009g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0010g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0010g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0011g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0011g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0012g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0012g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0013g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0013g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0014g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0015g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0016g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0017g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0018g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0019g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0021g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0023g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0001t0024g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0003t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0003t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0003t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0003t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0005t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0005t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0005t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0001c0008t0020g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0004g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0004g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0007g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0007g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0007g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0002t0022g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0002c0006t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0003c0004t0001g0001 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0003c0004t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0003c0004t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0003c0004t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0003c0004t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0003c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0004c0009t0003g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0005c0010t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
a0006c0007t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0003 | g0239 | EUR | GBR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | GBR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0251 | EUR | FIN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | FIN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | FIN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0040 | EUR | FIN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00408 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00423 | hp2 | a0002 | c0002 | t0004 | g0134 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0166 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0247 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | CHS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01081 | hp1 | a0001 | c0001 | t0015 | g0271 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0148 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01099 | hp1 | a0002 | c0006 | t0001 | g0299 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0284 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0260 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0145 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01192 | hp2 | a0002 | c0002 | t0007 | g0139 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0167 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01516 | hp1 | a0001 | c0001 | t0003 | g0006 | EUR | IBS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0206 | EUR | IBS | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01884 | hp1 | a0001 | c0001 | t0019 | g0029 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0292 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0127 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01952 | hp1 | a0002 | c0002 | t0004 | g0130 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01975 | hp1 | a0002 | c0002 | t0004 | g0129 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02015 | hp1 | a0006 | c0007 | t0003 | g0249 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0253 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02148 | hp1 | a0002 | c0002 | t0004 | g0226 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | CDX | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CDX | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CDX | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CDX | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02257 | hp2 | a0001 | c0005 | t0002 | g0061 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0279 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02572 | hp1 | a0001 | c0003 | t0001 | g0007 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0144 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02615 | hp2 | a0001 | c0005 | t0002 | g0030 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0089 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02630 | hp2 | a0002 | c0002 | t0004 | g0255 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02647 | hp2 | a0002 | c0002 | t0004 | g0156 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0245 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02723 | hp1 | a0003 | c0004 | t0001 | g0080 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0176 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0295 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0177 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02886 | hp1 | a0001 | c0008 | t0020 | g0094 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0293 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0142 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02895 | hp2 | a0001 | c0001 | t0014 | g0158 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02896 | hp2 | a0001 | c0001 | t0023 | g0065 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02897 | hp2 | a0002 | c0002 | t0001 | g0141 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0291 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02970 | hp1 | a0001 | c0001 | t0011 | g0072 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02970 | hp2 | a0001 | c0003 | t0001 | g0007 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02976 | hp1 | a0001 | c0001 | t0016 | g0116 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02976 | hp2 | a0003 | c0004 | t0001 | g0001 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0270 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03098 | hp2 | a0001 | c0003 | t0002 | g0282 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03130 | hp1 | a0001 | c0001 | t0006 | g0277 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03139 | hp1 | a0001 | c0001 | t0012 | g0105 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0276 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03209 | hp1 | a0001 | c0001 | t0011 | g0051 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03209 | hp2 | a0001 | c0001 | t0012 | g0106 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03453 | hp1 | a0001 | c0001 | t0024 | g0109 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03453 | hp2 | a0003 | c0004 | t0001 | g0076 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03486 | hp1 | a0001 | c0001 | t0017 | g0092 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03516 | hp1 | a0003 | c0004 | t0001 | g0075 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0256 | AFR | ESN | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0108 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0280 | AFR | GWD | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03579 | hp1 | a0001 | c0001 | t0008 | g0023 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0242 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0265 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | BEB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0241 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG04204 | hp1 | a0001 | c0001 | t0021 | g0230 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0238 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0113 | SAS | STU | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18522 | hp2 | a0003 | c0004 | t0001 | g0077 | AFR | YRI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | CHB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CHB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | CHB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0296 | AFR | YRI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0278 | AFR | YRI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18948 | hp2 | a0002 | c0002 | t0004 | g0123 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18950 | hp1 | a0001 | c0001 | t0010 | g0162 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18950 | hp2 | a0002 | c0002 | t0004 | g0126 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18951 | hp1 | a0002 | c0002 | t0004 | g0137 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18964 | hp1 | a0002 | c0002 | t0004 | g0128 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18967 | hp1 | a0001 | c0001 | t0013 | g0056 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18972 | hp2 | a0002 | c0002 | t0004 | g0132 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18989 | hp1 | a0002 | c0002 | t0004 | g0124 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18992 | hp1 | a0001 | c0001 | t0010 | g0273 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18993 | hp1 | a0002 | c0002 | t0004 | g0131 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19009 | hp1 | a0001 | c0001 | t0009 | g0070 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19030 | hp1 | a0002 | c0002 | t0022 | g0098 | AFR | LWK | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | LWK | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19080 | hp2 | a0001 | c0001 | t0013 | g0049 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19083 | hp1 | a0005 | c0010 | t0003 | g0064 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19085 | hp1 | a0002 | c0002 | t0004 | g0133 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19088 | hp2 | a0001 | c0001 | t0009 | g0068 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0090 | AFR | YRI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA19240 | hp2 | a0001 | c0005 | t0002 | g0060 | AFR | YRI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0088 | AFR | ASW | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA20129 | hp2 | a0001 | c0003 | t0002 | g0281 | AFR | ASW | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | TSI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0055 | EUR | TSI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0243 | EUR | TSI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | TSI | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | GIH | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | GIH | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0235 | AMR | CLM | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0289 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0234 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02486 | hp2 | a0001 | c0001 | t0008 | g0031 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0290 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG02559 | hp2 | a0003 | c0004 | t0001 | g0135 | AFR | ACB | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03471 | hp1 | a0001 | c0001 | t0018 | g0288 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG03471 | hp2 | a0002 | c0002 | t0007 | g0140 | AFR | MSL | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG06807 | hp1 | a0002 | c0002 | t0007 | g0138 | AFR | USA | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0087 | AFR | USA | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA18955 | hp2 | a0002 | c0002 | t0004 | g0125 | EAS | JPT | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA20300 | hp1 | a0004 | c0009 | t0003 | g0297 | AFR | USA | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA20300 | hp2 | a0001 | c0001 | t0006 | g0149 | AFR | USA | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | LWK | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | LWK | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0155 | REF | REF | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
homoSapiens_grch38 | hp1 | a0003 | c0004 | t0001 | g0001 | REF | REF | ITGAV_chr2_186585056_186685901 | ITGAV | chr2 | 186585056 | 186685901 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:186638460
|
G | A | 1 | a0006 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.898G>A | p.Glu300Lys | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/30 | 1181/7039 | 898/3147 | 300/1048 | chr2 | 186638460 | ||
chr2:186646739
|
A | G | 1 | a0002 | 23 | HG00423.hp2 HG01099.hp1 HG01192.hp2 others(20): Show |
missense_variant | MODERATE | c.1213A>G | p.Ile405Val | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/30 | 1496/7039 | 1213/3147 | 405/1048 | chr2 | 186646739 | ||
chr2:186656364
|
G | T | 1 | a0005 | 1 | NA19083.hp1 | missense_variant | MODERATE | c.1682G>T | p.Gly561Val | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/30 | 1965/7039 | 1682/3147 | 561/1048 | chr2 | 186656364 | ||
chr2:186667690
|
G | A | 5 | a0001a0002a0004others(2): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
missense_variant | MODERATE | c.2347G>A | p.Val783Ile | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/30 | 2630/7039 | 2347/3147 | 783/1048 | chr2 | 186667690 | ||
chr2:186668906
|
C | T | 1 | a0004 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.2578C>T | p.Pro860Ser | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 25/30 | 2861/7039 | 2578/3147 | 860/1048 | chr2 | 186668906 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:186625505
|
G | A | 2 | a0001c0003a0002c0006 | 8 | HG01099.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
synonymous_variant | LOW | c.441G>A | p.Glu147Glu | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/30 | 724/7039 | 441/3147 | 147/1048 | chr2 | 186625505 | ||
chr2:186666727
|
T | C | 1 | a0001c0008 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.2190T>C | p.Ser730Ser | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 22/30 | 2473/7039 | 2190/3147 | 730/1048 | chr2 | 186666727 | ||
chr2:186675918
|
C | T | 1 | a0001c0005 | 3 | HG02257.hp2 HG02615.hp2 NA19240.hp2 |
synonymous_variant | LOW | c.2919C>T | p.Asn973Asn | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/30 | 3202/7039 | 2919/3147 | 973/1048 | chr2 | 186675918 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:186590107
|
G | C | 1 | a0001c0001t0009 | 2 | NA19009.hp1 NA19088.hp2 |
5_prime_UTR_variant | MODIFIER | c.-232G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/30 | 232 | chr2 | 186590107 | |||||
chr2:186590127
|
C | A | 1 | a0001c0001t0014 | 1 | HG02895.hp2 | 5_prime_UTR_variant | MODIFIER | c.-212C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/30 | 212 | chr2 | 186590127 | |||||
chr2:186590127
|
C | G | 1 | a0001c0001t0024 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-212C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/30 | 212 | chr2 | 186590127 | |||||
chr2:186590132
|
C | T | 1 | a0001c0001t0023 | 1 | HG02896.hp2 | 5_prime_UTR_variant | MODIFIER | c.-207C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/30 | 207 | chr2 | 186590132 | |||||
chr2:186590153
|
G | T | 1 | a0002c0002t0022 | 1 | NA19030.hp1 | 5_prime_UTR_variant | MODIFIER | c.-186G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/30 | 186 | chr2 | 186590153 | |||||
chr2:186590288
|
G | A | 2 | a0001c0001t0014a0001c0001t0015 | 2 | HG01081.hp1 HG02895.hp2 |
5_prime_UTR_variant | MODIFIER | c.-51G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/30 | 51 | chr2 | 186590288 | |||||
chr2:186677555
|
A | G | 1 | a0001c0001t0021 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*263A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 263 | chr2 | 186677555 | |||||
chr2:186677629
|
C | T | 1 | a0001c0008t0020 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*337C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 337 | chr2 | 186677629 | |||||
chr2:186677639
|
T | TTTG | 7 | a0001c0001t0005a0001c0001t0010a0001c0001t0014others(4): Show | 14 | HG01081.hp1 HG01192.hp2 HG02622.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*377_*379dupGTT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 380 | INFO_REALIGN_3_PRIME | chr2 | 186677639 | ||||
chr2:186677639
|
T | TTTGTTG | 2 | a0001c0001t0006a0001c0001t0016 | 4 | HG02976.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*374_*379dupGTTGTT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 380 | INFO_REALIGN_3_PRIME | chr2 | 186677639 | ||||
chr2:186677912
|
C | T | 1 | a0001c0001t0006 | 3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*620C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 620 | chr2 | 186677912 | |||||
chr2:186678209
|
TAGTA | T | 10 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(7): Show | 82 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*922_*925delAGTA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 922 | INFO_REALIGN_3_PRIME | chr2 | 186678209 | ||||
chr2:186678341
|
A | C | 1 | a0001c0008t0020 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1049A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 1049 | chr2 | 186678341 | |||||
chr2:186678396
|
A | T | 6 | a0001c0001t0003a0001c0001t0013a0001c0008t0020others(3): Show | 56 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1104A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 1104 | chr2 | 186678396 | |||||
chr2:186678500
|
G | C | 6 | a0001c0001t0003a0001c0001t0013a0001c0008t0020others(3): Show | 56 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1208G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 1208 | chr2 | 186678500 | |||||
chr2:186678575
|
G | A | 1 | a0002c0002t0004 | 15 | HG00423.hp2 HG01952.hp1 HG01975.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1283G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 1283 | chr2 | 186678575 | |||||
chr2:186678647
|
C | T | 10 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(7): Show | 82 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*1355C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 1355 | chr2 | 186678647 | |||||
chr2:186679201
|
C | G | 1 | a0001c0008t0020 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1909C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 1909 | chr2 | 186679201 | |||||
chr2:186679282
|
T | C | 1 | a0001c0001t0011 | 2 | HG02970.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1990T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 1990 | chr2 | 186679282 | |||||
chr2:186679495
|
AT | A | 15 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(12): Show | 91 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*2212delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 2212 | INFO_REALIGN_3_PRIME | chr2 | 186679495 | ||||
chr2:186679495
|
ATT | A | 6 | a0001c0001t0003a0001c0001t0013a0001c0008t0020others(3): Show | 56 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*2211_*2212delTT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 2211 | INFO_REALIGN_3_PRIME | chr2 | 186679495 | ||||
chr2:186679525
|
A | T | 1 | a0001c0001t0005 | 5 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2233A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 2233 | chr2 | 186679525 | |||||
chr2:186679873
|
A | G | 5 | a0001c0001t0005a0001c0001t0014a0001c0001t0015others(2): Show | 9 | HG01081.hp1 HG02622.hp1 HG02809.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2581A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 2581 | chr2 | 186679873 | |||||
chr2:186680036
|
T | C | 1 | a0001c0008t0020 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2744T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 2744 | chr2 | 186680036 | |||||
chr2:186680037
|
A | G | 2 | a0001c0001t0008a0001c0001t0023 | 4 | HG02486.hp2 HG02896.hp2 HG03540.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2745A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 2745 | chr2 | 186680037 | |||||
chr2:186680263
|
T | C | 1 | a0001c0001t0011 | 2 | HG02970.hp1 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2971T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 2971 | chr2 | 186680263 | |||||
chr2:186680478
|
A | G | 1 | a0001c0001t0013 | 2 | NA18967.hp1 NA19080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3186A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 3186 | chr2 | 186680478 | |||||
chr2:186680518
|
A | T | 1 | a0001c0001t0012 | 2 | HG03139.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3226A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 3226 | chr2 | 186680518 | |||||
chr2:186680589
|
A | C | 5 | a0001c0001t0005a0001c0001t0014a0001c0001t0015others(2): Show | 9 | HG01081.hp1 HG02622.hp1 HG02809.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3297A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 3297 | chr2 | 186680589 | |||||
chr2:186680649
|
C | T | 1 | a0001c0001t0018 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3357C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 3357 | chr2 | 186680649 | |||||
chr2:186680719
|
A | G | 1 | a0001c0001t0019 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3427A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 30/30 | 3427 | chr2 | 186680719 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:186590551
|
C | T | 190 | a0001c0001t0001g0005a0001c0001t0001g0119a0001c0001t0001g0120others(187): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.185+28C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186590551 | ||||||
chr2:186590578
|
A | C | 1 | a0001c0001t0003g0008 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.185+55A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186590578 | ||||||
chr2:186590593
|
A | G | 1 | a0001c0001t0002g0115 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.185+70A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186590593 | ||||||
chr2:186590685
|
G | T | 1 | a0001c0001t0003g0300 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.185+162G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186590685 | ||||||
chr2:186590840
|
C | T | 1 | a0001c0001t0002g0003 | 2 | HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.185+317C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186590840 | ||||||
chr2:186590886
|
A | G | 1 | a0002c0006t0001g0299 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.185+363A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186590886 | ||||||
chr2:186590900
|
T | C | 2 | a0001c0001t0003g0117a0001c0001t0016g0116 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+377T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186590900 | ||||||
chr2:186590952
|
C | T | 4 | a0001c0001t0002g0111a0001c0001t0002g0112a0001c0001t0002g0113others(1): Show | 4 | HG01243.hp1 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.185+429C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186590952 | ||||||
chr2:186590982
|
C | T | 1 | a0001c0001t0002g0110 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.185+459C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186590982 | ||||||
chr2:186591020
|
T | C | 1 | a0001c0001t0003g0118 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.185+497T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186591020 | ||||||
chr2:186591184
|
T | C | 25 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(22): Show | 25 | HG00423.hp2 HG01168.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.185+661T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186591184 | ||||||
chr2:186591394
|
A | G | 165 | a0001c0001t0001g0005a0001c0001t0001g0146a0001c0001t0001g0147others(162): Show | 170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.185+871A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186591394 | ||||||
chr2:186591751
|
GATTAGAT others(1502): Show |
G | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+1230_185+2738d others(2): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186591751 | |||||
chr2:186591947
|
C | G | 1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.185+1424C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186591947 | ||||||
chr2:186592045
|
A | T | 1 | a0001c0001t0008g0108 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.185+1522A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592045 | ||||||
chr2:186592046
|
G | A | 1 | a0001c0001t0003g0144 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.185+1523G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592046 | ||||||
chr2:186592152
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.185+1629T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592152 | ||||||
chr2:186592243
|
A | C | 1 | a0001c0001t0002g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.185+1720A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592243 | ||||||
chr2:186592334
|
G | A | 1 | a0001c0001t0003g0145 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.185+1811G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592334 | ||||||
chr2:186592536
|
T | G | 2 | a0001c0001t0002g0011a0001c0001t0002g0012 | 2 | NA18949.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.185+2013T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592536 | ||||||
chr2:186592574
|
GT | G | 179 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(176): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.185+2063delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186592574 | |||||
chr2:186592581
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.185+2058T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592581 | ||||||
chr2:186592600
|
A | G | 1 | a0001c0001t0002g0003 | 2 | HG02004.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.185+2077A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592600 | ||||||
chr2:186592656
|
A | T | 1 | a0001c0001t0003g0145 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.185+2133A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592656 | ||||||
chr2:186592762
|
G | T | 1 | a0001c0001t0001g0286 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.185+2239G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592762 | ||||||
chr2:186592861
|
A | G | 202 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0095others(199): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.185+2338A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592861 | ||||||
chr2:186592890
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.185+2367C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592890 | ||||||
chr2:186592916
|
C | T | 2 | a0001c0001t0003g0117a0001c0001t0016g0116 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.185+2393C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186592916 | ||||||
chr2:186593265
|
T | G | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2742T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593265 | ||||||
chr2:186593266
|
A | T | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2743A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593266 | ||||||
chr2:186593270
|
T | C | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2747T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593270 | ||||||
chr2:186593273
|
A | G | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2750A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593273 | ||||||
chr2:186593274
|
A | C | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2751A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593274 | ||||||
chr2:186593277
|
A | T | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2754A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593277 | ||||||
chr2:186593284
|
T | C | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2761T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593284 | ||||||
chr2:186593285
|
A | C | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2762A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593285 | ||||||
chr2:186593286
|
G | C | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2763G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593286 | ||||||
chr2:186593290
|
A | T | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2767A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593290 | ||||||
chr2:186593292
|
A | T | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2769A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593292 | ||||||
chr2:186593293
|
G | C | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2770G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593293 | ||||||
chr2:186593295
|
T | C | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2772T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593295 | ||||||
chr2:186593301
|
G | T | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2778G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593301 | ||||||
chr2:186593303
|
G | C | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2780G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593303 | ||||||
chr2:186593315
|
A | G | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2792A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593315 | ||||||
chr2:186593320
|
T | G | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2797T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593320 | ||||||
chr2:186593324
|
T | A | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2801T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593324 | ||||||
chr2:186593326
|
T | C | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2803T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593326 | ||||||
chr2:186593328
|
A | C | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2805A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593328 | ||||||
chr2:186593331
|
G | A | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2808G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593331 | ||||||
chr2:186593332
|
G | T | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2809G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593332 | ||||||
chr2:186593337
|
G | A | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2814G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593337 | ||||||
chr2:186593339
|
C | G | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2816C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593339 | ||||||
chr2:186593351
|
C | A | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2828C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593351 | ||||||
chr2:186593352
|
A | G | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2829A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593352 | ||||||
chr2:186593355
|
ATGTTAAG others(332): Show |
A | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185+2833_185+3171d others(2): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593355 | ||||||
chr2:186593459
|
C | G | 1 | a0001c0001t0003g0284 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.185+2936C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593459 | ||||||
chr2:186593461
|
G | GT | 190 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(187): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.185+2947dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186593461 | |||||
chr2:186593530
|
A | C | 12 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.185+3007A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593530 | ||||||
chr2:186593780
|
G | A | 1 | a0001c0001t0001g0147 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.185+3257G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593780 | ||||||
chr2:186593786
|
G | GT | 191 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(188): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.185+3264dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186593786 | |||||
chr2:186593910
|
A | C | 1 | a0001c0001t0008g0108 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.185+3387A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593910 | ||||||
chr2:186593948
|
A | T | 1 | a0001c0001t0002g0093 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.185+3425A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186593948 | ||||||
chr2:186594005
|
C | T | 1 | a0001c0001t0002g0283 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.185+3482C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594005 | ||||||
chr2:186594350
|
T | A | 1 | a0001c0001t0003g0148 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.185+3827T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594350 | ||||||
chr2:186594388
|
C | A | 1 | a0001c0001t0006g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.185+3865C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594388 | ||||||
chr2:186594477
|
T | A | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.185+3954T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594477 | ||||||
chr2:186594556
|
G | A | 1 | a0001c0001t0003g0289 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.185+4033G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594556 | ||||||
chr2:186594655
|
T | C | 1 | a0001c0001t0002g0150 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.185+4132T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594655 | ||||||
chr2:186594739
|
A | G | 7 | a0001c0003t0001g0007a0001c0003t0001g0278a0001c0003t0001g0279others(4): Show | 8 | HG01099.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.185+4216A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594739 | ||||||
chr2:186594770
|
C | G | 28 | a0001c0001t0001g0013a0001c0001t0001g0119a0001c0001t0001g0120others(25): Show | 28 | HG00423.hp2 HG01168.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.185+4247C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594770 | ||||||
chr2:186594844
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.185+4321G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594844 | ||||||
chr2:186594849
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.185+4326T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594849 | ||||||
chr2:186594920
|
C | T | 1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.185+4397C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186594920 | ||||||
chr2:186595374
|
G | T | 1 | a0001c0001t0002g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.185+4851G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186595374 | ||||||
chr2:186595688
|
TA | T | 195 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(192): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.185+5176delA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186595688 | |||||
chr2:186595796
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.185+5273A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186595796 | ||||||
chr2:186596122
|
A | G | 1 | a0001c0001t0002g0002 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.185+5599A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186596122 | ||||||
chr2:186596372
|
T | G | 5 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0002g0003others(2): Show | 6 | HG01975.hp2 HG02004.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-5649T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186596372 | ||||||
chr2:186596452
|
C | CT | 6 | a0001c0001t0001g0272a0001c0001t0001g0274a0001c0001t0001g0275others(3): Show | 6 | HG00597.hp1 HG00642.hp2 HG01069.hp1 others(3): Show |
intron_variant | MODIFIER | c.186-5554dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186596452 | |||||
chr2:186596815
|
T | C | 2 | a0001c0001t0001g0154a0001c0001t0001g0155 | 2 | NA20905.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.186-5206T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186596815 | ||||||
chr2:186597002
|
T | G | 1 | a0001c0001t0002g0018 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.186-5019T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186597002 | ||||||
chr2:186597151
|
A | G | 1 | a0001c0001t0002g0083 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.186-4870A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186597151 | ||||||
chr2:186597404
|
C | T | 1 | a0001c0001t0015g0271 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.186-4617C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186597404 | ||||||
chr2:186597655
|
C | A | 1 | a0002c0002t0004g0156 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.186-4366C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186597655 | ||||||
chr2:186597854
|
A | G | 212 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(209): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.186-4167A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186597854 | ||||||
chr2:186597875
|
A | G | 1 | a0001c0001t0002g0082 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.186-4146A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186597875 | ||||||
chr2:186598292
|
T | TAC | 5 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(2): Show | 5 | HG01891.hp1 HG02258.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.186-3728_186-3727i others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598292 | |||||
chr2:186598292
|
T | TACACAC | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097 | 3 | HG02257.hp1 HG02258.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.186-3728_186-3727i others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598292 | |||||
chr2:186598294
|
T | C | 10 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(7): Show | 10 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.186-3727T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186598294 | ||||||
chr2:186598294
|
T | TAC | 9 | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0001g0157others(6): Show | 9 | HG00544.hp1 HG02622.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.186-3693_186-3692d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | |||||
chr2:186598294
|
T | TACAC | 10 | a0001c0001t0001g0086a0001c0001t0002g0017a0001c0001t0002g0066others(7): Show | 10 | HG01069.hp1 HG01071.hp2 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.186-3695_186-3692d others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | |||||
chr2:186598294
|
T | TACACAC | 44 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0044others(41): Show | 46 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.186-3697_186-3692d others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | |||||
chr2:186598294
|
T | TACACACA others(1): Show |
14 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0002g0009others(11): Show | 14 | HG01256.hp2 HG01884.hp1 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.186-3699_186-3692d others(10): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | |||||
chr2:186598294
|
T | TACACACA others(3): Show |
6 | a0001c0001t0002g0020a0001c0001t0002g0110a0001c0001t0002g0111others(3): Show | 6 | HG01243.hp1 HG01256.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.186-3701_186-3692d others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | |||||
chr2:186598294
|
T | TACACACA others(5): Show |
2 | a0001c0001t0008g0108a0001c0008t0020g0094 | 2 | HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.186-3703_186-3692d others(14): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | |||||
chr2:186598294
|
T | TACACACA others(7): Show |
1 | a0001c0001t0001g0019 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.186-3705_186-3692d others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | |||||
chr2:186598294
|
TAC | T | 11 | a0001c0001t0001g0013a0001c0001t0001g0119a0001c0001t0001g0121others(8): Show | 11 | HG01168.hp2 HG01192.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.186-3693_186-3692d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | |||||
chr2:186598294
|
TACAC | T | 18 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0002g0159others(15): Show | 18 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.186-3695_186-3692d others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | |||||
chr2:186598294
|
TACACAC | T | 141 | a0001c0001t0001g0005a0001c0001t0001g0146a0001c0001t0001g0147others(138): Show | 146 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.186-3697_186-3692d others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | |||||
chr2:186598294
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0002g0270 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.186-3701_186-3692d others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | |||||
chr2:186598294
|
TACACACA others(5): Show |
T | 1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.186-3703_186-3692d others(14): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598294 | |||||
chr2:186598436
|
A | AT | 196 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0095others(193): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.186-3566dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598436 | |||||
chr2:186598436
|
A | ATT | 8 | a0001c0001t0001g0266a0001c0001t0001g0267a0001c0001t0001g0268others(5): Show | 8 | HG01099.hp2 HG01243.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.186-3567_186-3566d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598436 | |||||
chr2:186598436
|
AT | A | 8 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0002g0021others(5): Show | 8 | HG02622.hp1 HG02723.hp2 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.186-3566delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186598436 | |||||
chr2:186599020
|
A | T | 1 | a0001c0001t0002g0017 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.186-3001A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186599020 | ||||||
chr2:186599197
|
T | C | 1 | a0001c0001t0001g0272 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.186-2824T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186599197 | ||||||
chr2:186599349
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.186-2672C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186599349 | ||||||
chr2:186599385
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.186-2636G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186599385 | ||||||
chr2:186599694
|
G | A | 3 | a0001c0001t0008g0023a0001c0001t0008g0031a0001c0001t0023g0065 | 3 | HG02486.hp2 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.186-2327G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186599694 | ||||||
chr2:186599761
|
T | C | 2 | a0001c0001t0002g0011a0001c0001t0002g0012 | 2 | NA18949.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.186-2260T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186599761 | ||||||
chr2:186600142
|
G | T | 1 | a0003c0004t0001g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.186-1879G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186600142 | ||||||
chr2:186600167
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.186-1854G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186600167 | ||||||
chr2:186600894
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.186-1127G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186600894 | ||||||
chr2:186600959
|
C | CA | 12 | a0001c0001t0001g0010a0001c0001t0001g0099a0001c0001t0001g0100others(9): Show | 12 | HG01168.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.186-1047dupA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186600959 | |||||
chr2:186600997
|
G | T | 296 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(293): Show | 303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.186-1024G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186600997 | ||||||
chr2:186601292
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.186-729C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186601292 | ||||||
chr2:186601301
|
T | A | 292 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(289): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.186-720T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186601301 | ||||||
chr2:186601309
|
A | T | 1 | a0002c0002t0004g0134 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.186-712A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186601309 | ||||||
chr2:186601452
|
T | C | 294 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(291): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.186-569T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186601452 | ||||||
chr2:186601453
|
G | C | 210 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(207): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.186-568G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186601453 | ||||||
chr2:186601461
|
TA | T | 21 | a0001c0001t0001g0010a0001c0001t0001g0073a0001c0001t0001g0074others(18): Show | 21 | HG01168.hp2 HG01891.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.186-548delA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr2 | 186601461 | |||||
chr2:186601894
|
T | C | 1 | a0001c0001t0002g0024 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.186-127T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 1/29 | chr2 | 186601894 | ||||||
chr2:186602194
|
A | AT | 9 | a0001c0001t0001g0013a0001c0001t0001g0119a0001c0001t0001g0136others(6): Show | 9 | HG00642.hp2 HG01106.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.316+53dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186602194 | |||||
chr2:186602257
|
C | A | 1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316+106C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186602257 | ||||||
chr2:186602460
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.316+309G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186602460 | ||||||
chr2:186602728
|
T | C | 2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.316+577T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186602728 | ||||||
chr2:186602876
|
TA | T | 249 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0014others(246): Show | 256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.316+744delA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186602876 | |||||
chr2:186603023
|
A | G | 213 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(210): Show | 219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.316+872A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603023 | ||||||
chr2:186603278
|
T | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0002g0003others(2): Show | 6 | HG01975.hp2 HG02004.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.316+1127T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603278 | ||||||
chr2:186603353
|
A | G | 2 | a0001c0001t0003g0117a0001c0001t0016g0116 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.316+1202A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603353 | ||||||
chr2:186603398
|
A | G | 294 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(291): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.316+1247A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603398 | ||||||
chr2:186603496
|
G | A | 10 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0018others(7): Show | 10 | HG00544.hp2 HG00558.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.316+1345G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603496 | ||||||
chr2:186603513
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.316+1362T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603513 | ||||||
chr2:186603603
|
A | G | 1 | a0001c0001t0001g0261 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.316+1452A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603603 | ||||||
chr2:186603668
|
T | G | 1 | a0001c0001t0008g0108 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.316+1517T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603668 | ||||||
chr2:186603830
|
A | T | 8 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+1679A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603830 | ||||||
chr2:186603886
|
A | G | 2 | a0001c0003t0002g0281a0001c0003t0002g0282 | 2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.316+1735A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186603886 | ||||||
chr2:186604171
|
A | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.316+2020A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186604171 | ||||||
chr2:186604323
|
G | A | 1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316+2172G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186604323 | ||||||
chr2:186604499
|
A | T | 12 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.316+2348A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186604499 | ||||||
chr2:186604656
|
G | A | 1 | a0001c0001t0005g0177 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.316+2505G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186604656 | ||||||
chr2:186604704
|
TTTAA | T | 8 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+2558_316+2561d others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186604704 | |||||
chr2:186605092
|
T | A | 1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316+2941T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605092 | ||||||
chr2:186605157
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.316+3006A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605157 | ||||||
chr2:186605458
|
T | C | 294 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(291): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.316+3307T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605458 | ||||||
chr2:186605463
|
T | G | 82 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(79): Show | 84 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.316+3312T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605463 | ||||||
chr2:186605584
|
C | T | 159 | a0001c0001t0001g0005a0001c0001t0001g0146a0001c0001t0001g0147others(156): Show | 164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.316+3433C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605584 | ||||||
chr2:186605617
|
G | C | 82 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0151others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.316+3466G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605617 | ||||||
chr2:186605640
|
C | T | 1 | a0001c0001t0002g0038 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.316+3489C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605640 | ||||||
chr2:186605726
|
G | T | 2 | a0001c0001t0003g0006a0001c0001t0003g0260 | 3 | HG01168.hp1 HG01169.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.316+3575G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605726 | ||||||
chr2:186605740
|
GTA | G | 77 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(74): Show | 78 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.316+3607_316+3608d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605740 | |||||
chr2:186605740
|
GTATA | G | 21 | a0001c0001t0001g0010a0001c0001t0001g0086a0001c0001t0001g0091others(18): Show | 21 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.316+3605_316+3608d others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605740 | |||||
chr2:186605746
|
A | G | 12 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.316+3595A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605746 | ||||||
chr2:186605753
|
T | TATTTATA others(10): Show |
8 | a0001c0001t0001g0172a0001c0001t0001g0231a0001c0001t0001g0232others(5): Show | 8 | HG01496.hp1 HG01884.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+3604_316+3605i others(19): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605753 | |||||
chr2:186605755
|
T | TTTATATG others(43): Show |
174 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(171): Show | 179 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.316+3604_316+3605i others(52): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605755 | ||||||
chr2:186605755
|
T | TTTATATG others(70): Show |
5 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0178others(2): Show | 5 | HG01981.hp2 HG02486.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+3604_316+3605i others(79): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605755 | ||||||
chr2:186605755
|
T | TTTATATG others(97): Show |
1 | a0001c0001t0002g0233 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.316+3604_316+3605i others(106): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605755 | ||||||
chr2:186605755
|
T | TTTATATG others(124): Show |
1 | a0001c0001t0002g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.316+3604_316+3605i others(133): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605755 | ||||||
chr2:186605756
|
A | T | 181 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(178): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.316+3605A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605756 | ||||||
chr2:186605760
|
T | G | 181 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(178): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.316+3609T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605760 | ||||||
chr2:186605760
|
T | TCTTATG | 8 | a0001c0001t0001g0172a0001c0001t0001g0231a0001c0001t0001g0232others(5): Show | 8 | HG01496.hp1 HG01884.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+3609_316+3610i others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186605760 | ||||||
chr2:186605797
|
A | AATAC | 189 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(186): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.316+3649_316+3650i others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | |||||
chr2:186605797
|
A | AATATATT others(47): Show |
8 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+3697_316+3750d others(56): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | |||||
chr2:186605797
|
A | AATATATT others(74): Show |
5 | a0001c0001t0001g0010a0001c0001t0001g0095a0001c0001t0001g0096others(2): Show | 5 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+3670_316+3750d others(83): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | |||||
chr2:186605797
|
A | AATATATT others(101): Show |
7 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0005g0087others(4): Show | 7 | HG02622.hp1 HG02723.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.316+3750_316+3751i others(110): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | |||||
chr2:186605797
|
A | AATATATT others(128): Show |
8 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0002g0059others(5): Show | 8 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.316+3750_316+3751i others(137): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | |||||
chr2:186605797
|
A | AATATATT others(155): Show |
5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0002g0069others(2): Show | 5 | HG01243.hp1 HG02132.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.316+3750_316+3751i others(164): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | |||||
chr2:186605797
|
A | AATATATT others(182): Show |
66 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0027others(63): Show | 67 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(64): Show |
intron_variant | MODIFIER | c.316+3750_316+3751i others(191): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | |||||
chr2:186605797
|
A | AATATATT others(209): Show |
3 | a0001c0001t0002g0002a0001c0001t0009g0070a0001c0008t0020g0094 | 4 | HG01516.hp2 HG01517.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+3750_316+3751i others(218): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | |||||
chr2:186605797
|
A | AATATATT others(236): Show |
2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.316+3750_316+3751i others(245): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | |||||
chr2:186605797
|
A | AATATATT others(70): Show |
1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316+3672_316+3673i others(79): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186605797 | |||||
chr2:186606281
|
G | A | 1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316+4130G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186606281 | ||||||
chr2:186606532
|
C | T | 1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316+4381C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186606532 | ||||||
chr2:186606557
|
C | G | 7 | a0001c0003t0001g0007a0001c0003t0001g0278a0001c0003t0001g0279others(4): Show | 8 | HG01099.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+4406C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186606557 | ||||||
chr2:186606563
|
A | C | 8 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+4412A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186606563 | ||||||
chr2:186606754
|
G | C | 82 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(79): Show | 84 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.316+4603G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186606754 | ||||||
chr2:186606806
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.316+4655G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186606806 | ||||||
chr2:186606818
|
A | G | 1 | a0001c0001t0002g0069 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.316+4667A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186606818 | ||||||
chr2:186606959
|
G | A | 7 | a0001c0003t0001g0007a0001c0003t0001g0278a0001c0003t0001g0279others(4): Show | 8 | HG01099.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.316+4808G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186606959 | ||||||
chr2:186607091
|
T | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0002g0110others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+4940T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186607091 | ||||||
chr2:186607331
|
C | T | 1 | a0001c0001t0002g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.316+5180C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186607331 | ||||||
chr2:186607585
|
A | T | 8 | a0001c0001t0001g0010a0001c0001t0001g0086a0001c0001t0001g0091others(5): Show | 8 | HG02622.hp1 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.316+5434A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186607585 | ||||||
chr2:186607596
|
A | G | 4 | a0001c0001t0003g0234a0001c0001t0003g0256a0001c0001t0014g0158others(1): Show | 4 | HG01081.hp1 HG02486.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.316+5445A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186607596 | ||||||
chr2:186608041
|
A | G | 4 | a0001c0001t0008g0023a0001c0001t0008g0031a0001c0001t0008g0108others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.316+5890A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186608041 | ||||||
chr2:186608257
|
T | C | 28 | a0001c0001t0001g0013a0001c0001t0001g0119a0001c0001t0001g0120others(25): Show | 28 | HG00423.hp2 HG01168.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.316+6106T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186608257 | ||||||
chr2:186608412
|
A | G | 2 | a0001c0001t0002g0270a0001c0001t0021g0230 | 2 | HG03017.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.316+6261A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186608412 | ||||||
chr2:186608580
|
G | A | 1 | a0001c0001t0002g0062 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.316+6429G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186608580 | ||||||
chr2:186608616
|
G | A | 1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316+6465G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186608616 | ||||||
chr2:186608712
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.316+6561C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186608712 | ||||||
chr2:186608905
|
C | T | 12 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.316+6754C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186608905 | ||||||
chr2:186608980
|
A | C | 3 | a0001c0001t0002g0112a0001c0001t0002g0113a0001c0001t0002g0114 | 3 | HG01243.hp1 HG01258.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.316+6829A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186608980 | ||||||
chr2:186609793
|
C | CAT | 192 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(189): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.316+7653_316+7654d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186609793 | |||||
chr2:186609945
|
T | G | 1 | a0001c0001t0002g0042 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.316+7794T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186609945 | ||||||
chr2:186610085
|
C | A | 1 | a0003c0004t0001g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.316+7934C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186610085 | ||||||
chr2:186610132
|
A | G | 1 | a0001c0001t0002g0022 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.316+7981A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186610132 | ||||||
chr2:186610377
|
G | T | 202 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0095others(199): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.316+8226G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186610377 | ||||||
chr2:186610443
|
A | C | 1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.316+8292A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186610443 | ||||||
chr2:186610466
|
C | G | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.316+8315C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186610466 | ||||||
chr2:186610598
|
T | A | 2 | a0001c0001t0003g0117a0001c0001t0016g0116 | 2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.316+8447T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186610598 | ||||||
chr2:186610630
|
C | A | 189 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(186): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.316+8479C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186610630 | ||||||
chr2:186610842
|
C | T | 1 | a0001c0001t0001g0229 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.316+8691C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186610842 | ||||||
chr2:186610929
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.316+8778C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186610929 | ||||||
chr2:186611342
|
C | T | 2 | a0001c0001t0001g0228a0001c0001t0001g0285 | 2 | HG00558.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.316+9191C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186611342 | ||||||
chr2:186611434
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.316+9283C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186611434 | ||||||
chr2:186611664
|
A | C | 1 | a0001c0001t0003g0169 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.316+9513A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186611664 | ||||||
chr2:186611932
|
A | C | 1 | a0001c0001t0012g0106 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.316+9781A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186611932 | ||||||
chr2:186612071
|
A | G | 5 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.316+9920A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186612071 | ||||||
chr2:186612135
|
C | T | 189 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(186): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.316+9984C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186612135 | ||||||
chr2:186612219
|
A | C | 1 | a0001c0001t0001g0227 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.316+10068A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186612219 | ||||||
chr2:186612369
|
A | AT | 103 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0016others(100): Show | 105 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.317-9955dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186612369 | |||||
chr2:186612369
|
AT | A | 6 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0003g0175others(3): Show | 6 | HG01123.hp2 HG01358.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.317-9955delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186612369 | |||||
chr2:186612754
|
A | G | 12 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.317-9585A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186612754 | ||||||
chr2:186612801
|
G | C | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0286 | 3 | HG03130.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.317-9538G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186612801 | ||||||
chr2:186612964
|
A | C | 212 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(209): Show | 217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.317-9375A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186612964 | ||||||
chr2:186613013
|
C | T | 1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.317-9326C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186613013 | ||||||
chr2:186613317
|
G | T | 1 | a0001c0008t0020g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.317-9022G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186613317 | ||||||
chr2:186613474
|
C | T | 1 | a0001c0001t0006g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.317-8865C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186613474 | ||||||
chr2:186613721
|
C | G | 12 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.317-8618C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186613721 | ||||||
chr2:186613773
|
A | G | 191 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(188): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.317-8566A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186613773 | ||||||
chr2:186614188
|
C | T | 1 | a0002c0002t0004g0133 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.317-8151C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186614188 | ||||||
chr2:186614248
|
G | A | 7 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0005g0087others(4): Show | 7 | HG02622.hp1 HG02723.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-8091G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186614248 | ||||||
chr2:186614605
|
T | G | 5 | a0001c0001t0005g0087a0001c0001t0005g0088a0001c0001t0005g0089others(2): Show | 5 | HG02622.hp1 HG03486.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-7734T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186614605 | ||||||
chr2:186614627
|
T | C | 5 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(2): Show | 5 | HG00673.hp2 HG02056.hp1 NA18948.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-7712T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186614627 | ||||||
chr2:186614683
|
C | T | 1 | a0002c0002t0004g0156 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.317-7656C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186614683 | ||||||
chr2:186614738
|
T | G | 1 | a0001c0001t0003g0262 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.317-7601T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186614738 | ||||||
chr2:186614780
|
T | C | 1 | a0001c0001t0003g0238 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.317-7559T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186614780 | ||||||
chr2:186614812
|
A | G | 1 | a0001c0001t0010g0162 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.317-7527A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186614812 | ||||||
chr2:186614921
|
A | G | 33 | a0001c0001t0001g0161a0001c0001t0001g0178a0001c0001t0001g0179others(30): Show | 33 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.317-7418A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186614921 | ||||||
chr2:186615029
|
C | A | 80 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(77): Show | 82 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.317-7310C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615029 | ||||||
chr2:186615084
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.317-7255T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615084 | ||||||
chr2:186615244
|
T | G | 4 | a0001c0001t0003g0234a0001c0001t0003g0256a0001c0001t0014g0158others(1): Show | 4 | HG01081.hp1 HG02486.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-7095T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615244 | ||||||
chr2:186615279
|
T | C | 28 | a0001c0001t0001g0013a0001c0001t0001g0119a0001c0001t0001g0120others(25): Show | 28 | HG00423.hp2 HG01168.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.317-7060T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615279 | ||||||
chr2:186615473
|
G | T | 1 | a0001c0001t0001g0155 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.317-6866G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615473 | ||||||
chr2:186615575
|
T | A | 7 | a0001c0001t0001g0240a0001c0001t0002g0163a0001c0001t0002g0164others(4): Show | 7 | HG00140.hp1 HG00639.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-6764T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615575 | ||||||
chr2:186615679
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.317-6660C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615679 | ||||||
chr2:186615680
|
G | GT | 16 | a0001c0001t0001g0153a0001c0001t0001g0205a0001c0001t0001g0237others(13): Show | 16 | HG01496.hp1 HG01496.hp2 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.317-6649dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186615680 | |||||
chr2:186615825
|
A | G | 5 | a0001c0001t0005g0087a0001c0001t0005g0088a0001c0001t0005g0089others(2): Show | 5 | HG02622.hp1 HG03486.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.317-6514A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615825 | ||||||
chr2:186615936
|
G | A | 294 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(291): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.317-6403G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615936 | ||||||
chr2:186615948
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.317-6391C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186615948 | ||||||
chr2:186616261
|
A | G | 1 | a0001c0001t0002g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.317-6078A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186616261 | ||||||
chr2:186616273
|
AT | A | 238 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(235): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.317-6043delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186616273 | |||||
chr2:186616291
|
T | A | 1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.317-6048T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186616291 | ||||||
chr2:186616404
|
A | G | 294 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(291): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.317-5935A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186616404 | ||||||
chr2:186616432
|
G | A | 12 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.317-5907G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186616432 | ||||||
chr2:186616604
|
G | A | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 4 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-5735G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186616604 | ||||||
chr2:186616643
|
C | T | 7 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0005g0087others(4): Show | 7 | HG02622.hp1 HG02723.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-5696C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186616643 | ||||||
chr2:186617037
|
G | GT | 8 | a0001c0001t0001g0010a0001c0001t0001g0086a0001c0001t0001g0091others(5): Show | 8 | HG02622.hp1 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.317-5291dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186617037 | |||||
chr2:186617037
|
GT | G | 181 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(178): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.317-5291delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186617037 | |||||
chr2:186617108
|
A | G | 82 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0151others(79): Show | 82 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.317-5231A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186617108 | ||||||
chr2:186617278
|
T | C | 1 | a0003c0004t0001g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.317-5061T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186617278 | ||||||
chr2:186617529
|
C | A | 7 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0005g0087others(4): Show | 7 | HG02622.hp1 HG02723.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-4810C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186617529 | ||||||
chr2:186617571
|
C | G | 7 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0005g0087others(4): Show | 7 | HG02622.hp1 HG02723.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-4768C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186617571 | ||||||
chr2:186617575
|
C | CAA | 7 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0005g0087others(4): Show | 7 | HG02622.hp1 HG02723.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-4762_317-4761d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186617575 | |||||
chr2:186617755
|
A | G | 2 | a0001c0001t0001g0298a0001c0001t0003g0296 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.317-4584A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186617755 | ||||||
chr2:186618104
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.317-4235T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186618104 | ||||||
chr2:186618214
|
A | G | 1 | a0001c0001t0001g0219 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.317-4125A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186618214 | ||||||
chr2:186618425
|
A | G | 14 | a0001c0001t0003g0122a0002c0002t0002g0127a0002c0002t0004g0123others(11): Show | 14 | HG00423.hp2 HG01943.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.317-3914A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186618425 | ||||||
chr2:186618505
|
A | G | 1 | a0001c0001t0001g0236 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.317-3834A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186618505 | ||||||
chr2:186618615
|
G | C | 4 | a0001c0001t0003g0234a0001c0001t0003g0256a0001c0001t0014g0158others(1): Show | 4 | HG01081.hp1 HG02486.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-3724G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186618615 | ||||||
chr2:186618687
|
G | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 4 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-3652G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186618687 | ||||||
chr2:186618744
|
GC | G | 189 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(186): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.317-3594delC | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186618744 | ||||||
chr2:186618748
|
C | T | 1 | a0001c0001t0009g0068 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.317-3591C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186618748 | ||||||
chr2:186618925
|
T | A | 7 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0005g0087others(4): Show | 7 | HG02622.hp1 HG02723.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-3414T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186618925 | ||||||
chr2:186619043
|
GTGTGTAT others(9): Show |
G | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 4 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.317-3286_317-3271d others(18): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186619043 | |||||
chr2:186619063
|
G | GTA | 9 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0001g0099others(6): Show | 9 | HG02622.hp1 HG02723.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.317-3264_317-3263d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186619063 | |||||
chr2:186619073
|
A | G | 1 | a0001c0001t0003g0169 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.317-3266A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186619073 | ||||||
chr2:186619111
|
TTA | T | 89 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0151others(86): Show | 89 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.317-3212_317-3211d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186619111 | |||||
chr2:186619291
|
A | G | 27 | a0001c0001t0001g0013a0001c0001t0001g0119a0001c0001t0001g0120others(24): Show | 27 | HG00423.hp2 HG01168.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.317-3048A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186619291 | ||||||
chr2:186619313
|
A | T | 7 | a0001c0001t0001g0240a0001c0001t0002g0163a0001c0001t0002g0164others(4): Show | 7 | HG00140.hp1 HG00639.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.317-3026A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186619313 | ||||||
chr2:186619375
|
T | G | 1 | a0001c0001t0003g0284 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.317-2964T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186619375 | ||||||
chr2:186619566
|
CA | C | 202 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0095others(199): Show | 207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.317-2766delA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186619566 | |||||
chr2:186619575
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.317-2764G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186619575 | ||||||
chr2:186619653
|
A | G | 12 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.317-2686A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186619653 | ||||||
chr2:186619713
|
A | G | 210 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(207): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.317-2626A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186619713 | ||||||
chr2:186619897
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.317-2442C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186619897 | ||||||
chr2:186620075
|
C | A | 1 | a0001c0001t0002g0043 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.317-2264C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186620075 | ||||||
chr2:186620093
|
C | T | 2 | a0001c0001t0003g0234a0001c0001t0003g0256 | 2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.317-2246C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186620093 | ||||||
chr2:186620127
|
G | T | 189 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(186): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.317-2212G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186620127 | ||||||
chr2:186620200
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0003g0006a0001c0001t0003g0260 | 5 | HG01168.hp1 HG01169.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.317-2139C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186620200 | ||||||
chr2:186620547
|
G | A | 1 | a0001c0001t0001g0259 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.317-1792G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186620547 | ||||||
chr2:186620670
|
G | C | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.317-1669G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186620670 | ||||||
chr2:186620673
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.317-1666G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186620673 | ||||||
chr2:186620974
|
G | T | 12 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.317-1365G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186620974 | ||||||
chr2:186621138
|
G | T | 12 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.317-1201G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621138 | ||||||
chr2:186621270
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.317-1069A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621270 | ||||||
chr2:186621404
|
CATT | C | 4 | a0001c0001t0008g0023a0001c0001t0008g0031a0001c0001t0008g0108others(1): Show | 4 | HG02486.hp2 HG02896.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.317-929_317-927del others(3): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | INFO_REALIGN_3_PRIME | chr2 | 186621404 | |||||
chr2:186621430
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.317-909A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621430 | ||||||
chr2:186621490
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.317-849A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621490 | ||||||
chr2:186621500
|
T | A | 2 | a0001c0001t0006g0276a0001c0001t0006g0277 | 2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.317-839T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621500 | ||||||
chr2:186621712
|
A | G | 1 | a0001c0001t0002g0037 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.317-627A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621712 | ||||||
chr2:186621915
|
G | A | 2 | a0001c0001t0002g0026a0001c0001t0002g0115 | 2 | HG01175.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.317-424G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621915 | ||||||
chr2:186621918
|
T | A | 2 | a0001c0001t0006g0276a0001c0001t0006g0277 | 2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.317-421T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621918 | ||||||
chr2:186621928
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.317-411C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621928 | ||||||
chr2:186621988
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.317-351G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621988 | ||||||
chr2:186621996
|
G | T | 1 | a0001c0001t0006g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.317-343G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186621996 | ||||||
chr2:186622180
|
A | C | 10 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0183others(7): Show | 10 | HG00323.hp1 HG00673.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.317-159A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186622180 | ||||||
chr2:186622181
|
G | A | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | HG02056.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.317-158G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186622181 | ||||||
chr2:186622294
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.317-45G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 2/29 | chr2 | 186622294 | ||||||
chr2:186622433
|
G | A | 210 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(207): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
splice_region_variant&intron_variant | LOW | c.408+3G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186622433 | ||||||
chr2:186622542
|
G | T | 82 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(79): Show | 84 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.408+112G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186622542 | ||||||
chr2:186622643
|
T | A | 8 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(5): Show | 8 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.408+213T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186622643 | ||||||
chr2:186622730
|
A | G | 1 | a0001c0001t0001g0232 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.408+300A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186622730 | ||||||
chr2:186623019
|
C | T | 7 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0005g0087others(4): Show | 7 | HG02622.hp1 HG02723.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.408+589C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186623019 | ||||||
chr2:186623049
|
G | C | 2 | a0001c0001t0003g0234a0001c0001t0003g0256 | 2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.408+619G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186623049 | ||||||
chr2:186623301
|
AT | A | 6 | a0001c0001t0002g0002a0001c0001t0002g0039a0001c0001t0002g0040others(3): Show | 7 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(4): Show |
intron_variant | MODIFIER | c.408+876delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 186623301 | |||||
chr2:186623581
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.408+1151C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186623581 | ||||||
chr2:186623592
|
A | G | 1 | a0001c0001t0003g0034 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.408+1162A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186623592 | ||||||
chr2:186623602
|
T | G | 1 | a0001c0001t0002g0114 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.408+1172T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186623602 | ||||||
chr2:186623772
|
A | G | 1 | a0001c0001t0003g0176 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.408+1342A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186623772 | ||||||
chr2:186624267
|
G | A | 1 | a0001c0001t0006g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.409-1206G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186624267 | ||||||
chr2:186624285
|
C | T | 1 | a0002c0002t0004g0156 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.409-1188C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186624285 | ||||||
chr2:186624405
|
GA | G | 4 | a0001c0001t0003g0234a0001c0001t0003g0256a0001c0001t0014g0158others(1): Show | 4 | HG01081.hp1 HG02486.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-1066delA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 186624405 | |||||
chr2:186624621
|
A | G | 2 | a0001c0001t0003g0234a0001c0001t0003g0256 | 2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.409-852A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186624621 | ||||||
chr2:186624701
|
C | T | 1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.409-772C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186624701 | ||||||
chr2:186624902
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.409-571A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186624902 | ||||||
chr2:186624920
|
C | A | 40 | a0001c0001t0001g0045a0001c0001t0002g0002a0001c0001t0002g0011others(37): Show | 41 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.409-553C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186624920 | ||||||
chr2:186624952
|
G | GA | 288 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(285): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.409-511dupA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr2 | 186624952 | |||||
chr2:186625365
|
C | G | 1 | a0001c0001t0015g0271 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.409-108C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 3/29 | chr2 | 186625365 | ||||||
chr2:186625644
|
T | G | 191 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(188): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.523+57T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186625644 | ||||||
chr2:186625651
|
A | ATGTGTGT others(3): Show |
2 | a0001c0001t0003g0295a0001c0001t0005g0177 | 2 | HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.523+65_523+74dupTG others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625651 | |||||
chr2:186625651
|
A | ATGTGTGT others(5): Show |
4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 4 | HG02257.hp1 HG02258.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+74_523+75insTG others(10): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625651 | |||||
chr2:186625662
|
G | GGTGT | 3 | a0001c0001t0001g0010a0001c0001t0001g0086a0001c0001t0001g0091 | 3 | HG02630.hp1 HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.523+89_523+92dupTG others(2): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625662 | |||||
chr2:186625662
|
G | T | 204 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0095others(201): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.523+75G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186625662 | ||||||
chr2:186625669
|
G | GTGTGTA | 3 | a0001c0001t0012g0105a0001c0001t0012g0106a0002c0002t0022g0098 | 3 | HG03139.hp1 HG03209.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.523+87_523+88insAT others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625669 | |||||
chr2:186625669
|
G | GTGTGTGT others(1): Show |
5 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.523+89_523+90insAT others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625669 | |||||
chr2:186625676
|
T | A | 1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.523+89T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186625676 | ||||||
chr2:186625678
|
T | A | 1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.523+91T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186625678 | ||||||
chr2:186625678
|
T | TGTGA | 5 | a0001c0001t0005g0087a0001c0001t0005g0088a0001c0001t0005g0089others(2): Show | 5 | HG02622.hp1 HG03486.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+92_523+93insTG others(2): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625678 | |||||
chr2:186625678
|
T | TGTGTGA | 4 | a0001c0001t0003g0234a0001c0001t0006g0149a0001c0003t0002g0281others(1): Show | 4 | HG02486.hp1 HG03098.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+92_523+93insTG others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625678 | |||||
chr2:186625678
|
T | TGTGTGTG others(1): Show |
79 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(76): Show | 83 | HG00280.hp1 HG00423.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.523+92_523+93insTG others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625678 | |||||
chr2:186625678
|
T | TGTGTGTG others(3): Show |
76 | a0001c0001t0001g0147a0001c0001t0001g0151a0001c0001t0001g0152others(73): Show | 77 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.523+92_523+93insTG others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625678 | |||||
chr2:186625678
|
T | TGTGTGTG others(5): Show |
20 | a0001c0001t0001g0171a0001c0001t0001g0174a0001c0001t0001g0195others(17): Show | 20 | HG00597.hp2 HG00642.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.523+92_523+93insTG others(10): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625678 | |||||
chr2:186625678
|
T | TGTGTGTG others(7): Show |
8 | a0001c0001t0001g0160a0001c0001t0001g0202a0001c0001t0001g0203others(5): Show | 8 | HG00558.hp2 HG02155.hp1 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.523+92_523+93insTG others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625678 | |||||
chr2:186625678
|
T | TGTGTGTG others(9): Show |
1 | a0001c0001t0001g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.523+92_523+93insTG others(14): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625678 | |||||
chr2:186625678
|
T | TGTGTGTG others(11): Show |
1 | a0001c0001t0001g0259 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.523+92_523+93insTG others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625678 | |||||
chr2:186625678
|
TGAGA | T | 69 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0027others(66): Show | 71 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.523+100_523+103del others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | INFO_REALIGN_3_PRIME | chr2 | 186625678 | |||||
chr2:186625712
|
T | G | 1 | a0001c0001t0006g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.523+125T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186625712 | ||||||
chr2:186625813
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.523+226C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186625813 | ||||||
chr2:186625814
|
G | A | 1 | a0002c0002t0004g0156 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.523+227G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186625814 | ||||||
chr2:186625820
|
A | G | 5 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0221others(2): Show | 5 | HG00323.hp1 NA18612.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+233A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186625820 | ||||||
chr2:186626046
|
T | A | 1 | a0002c0002t0022g0098 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.523+459T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186626046 | ||||||
chr2:186626317
|
C | T | 1 | a0001c0001t0001g0268 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.523+730C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186626317 | ||||||
chr2:186626413
|
G | A | 210 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(207): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.523+826G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186626413 | ||||||
chr2:186626442
|
C | A | 1 | a0001c0001t0001g0206 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.523+855C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186626442 | ||||||
chr2:186626595
|
T | G | 1 | a0001c0001t0002g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.523+1008T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186626595 | ||||||
chr2:186626876
|
T | C | 1 | a0001c0001t0012g0106 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.523+1289T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186626876 | ||||||
chr2:186627093
|
A | G | 5 | a0001c0001t0005g0087a0001c0001t0005g0088a0001c0001t0005g0089others(2): Show | 5 | HG02622.hp1 HG03486.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+1506A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627093 | ||||||
chr2:186627159
|
T | C | 2 | a0002c0002t0001g0141a0002c0002t0001g0142 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.523+1572T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627159 | ||||||
chr2:186627173
|
A | T | 1 | a0001c0001t0002g0150 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.523+1586A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627173 | ||||||
chr2:186627199
|
C | T | 5 | a0001c0001t0001g0160a0001c0001t0001g0201a0001c0001t0001g0204others(2): Show | 5 | HG02165.hp1 NA18949.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+1612C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627199 | ||||||
chr2:186627324
|
G | C | 294 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(291): Show | 301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.523+1737G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627324 | ||||||
chr2:186627425
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.523+1838C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627425 | ||||||
chr2:186627733
|
G | A | 210 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(207): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.523+2146G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627733 | ||||||
chr2:186627738
|
G | C | 1 | a0001c0001t0001g0261 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.523+2151G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627738 | ||||||
chr2:186627872
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.523+2285G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627872 | ||||||
chr2:186627923
|
A | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.523+2336A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627923 | ||||||
chr2:186627966
|
A | C | 5 | a0001c0001t0002g0041a0001c0001t0002g0042a0001c0001t0002g0053others(2): Show | 5 | HG00673.hp1 HG02135.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.523+2379A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186627966 | ||||||
chr2:186628015
|
G | A | 161 | a0001c0001t0001g0005a0001c0001t0001g0146a0001c0001t0001g0147others(158): Show | 166 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.523+2428G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186628015 | ||||||
chr2:186628048
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.523+2461T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186628048 | ||||||
chr2:186628096
|
G | C | 4 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0221others(1): Show | 4 | HG00323.hp1 NA18612.hp1 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.523+2509G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186628096 | ||||||
chr2:186628200
|
C | T | 2 | a0001c0001t0002g0050a0001c0001t0002g0057 | 2 | HG02738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.524-2597C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186628200 | ||||||
chr2:186628237
|
A | G | 200 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(197): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.524-2560A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186628237 | ||||||
chr2:186628704
|
G | A | 7 | a0001c0001t0001g0240a0001c0001t0002g0163a0001c0001t0002g0164others(4): Show | 7 | HG00140.hp1 HG00639.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.524-2093G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186628704 | ||||||
chr2:186628843
|
T | C | 12 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.524-1954T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186628843 | ||||||
chr2:186629051
|
A | G | 1 | a0001c0001t0002g0032 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.524-1746A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629051 | ||||||
chr2:186629114
|
A | G | 189 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(186): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.524-1683A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629114 | ||||||
chr2:186629125
|
A | G | 1 | a0001c0001t0003g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.524-1672A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629125 | ||||||
chr2:186629208
|
A | G | 1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.524-1589A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629208 | ||||||
chr2:186629385
|
A | C | 1 | a0001c0001t0002g0024 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.524-1412A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629385 | ||||||
chr2:186629601
|
A | G | 12 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.524-1196A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629601 | ||||||
chr2:186629620
|
T | C | 12 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(9): Show | 12 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.524-1177T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629620 | ||||||
chr2:186629674
|
G | A | 1 | a0001c0001t0003g0148 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.524-1123G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629674 | ||||||
chr2:186629690
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.524-1107G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629690 | ||||||
chr2:186629700
|
G | A | 198 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(195): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.524-1097G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629700 | ||||||
chr2:186629829
|
C | G | 1 | a0001c0001t0001g0203 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.524-968C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629829 | ||||||
chr2:186629851
|
T | A | 1 | a0001c0001t0001g0266 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.524-946T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629851 | ||||||
chr2:186629919
|
A | G | 1 | a0002c0002t0004g0131 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.524-878A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186629919 | ||||||
chr2:186630485
|
G | A | 1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.524-312G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186630485 | ||||||
chr2:186630547
|
A | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.524-250A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186630547 | ||||||
chr2:186630553
|
G | A | 1 | a0002c0002t0004g0156 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.524-244G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186630553 | ||||||
chr2:186630773
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.524-24A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 4/29 | chr2 | 186630773 | ||||||
chr2:186630901
|
AT | A | 5 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(2): Show | 5 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.585+45delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr2 | 186630901 | |||||
chr2:186631422
|
A | G | 8 | a0001c0001t0001g0010a0001c0001t0001g0086a0001c0001t0001g0091others(5): Show | 8 | HG02622.hp1 HG02630.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.585+564A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186631422 | ||||||
chr2:186631633
|
C | T | 1 | a0001c0001t0002g0059 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.585+775C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186631633 | ||||||
chr2:186631649
|
T | G | 4 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0002g0110others(1): Show | 4 | HG01884.hp1 HG02145.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.585+791T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186631649 | ||||||
chr2:186631691
|
T | G | 1 | a0001c0001t0002g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.585+833T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186631691 | ||||||
chr2:186632113
|
C | A | 1 | a0001c0001t0006g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.586-1216C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632113 | ||||||
chr2:186632192
|
G | A | 12 | a0001c0001t0001g0013a0001c0001t0001g0101a0001c0001t0001g0102others(9): Show | 12 | HG01168.hp2 HG01255.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.586-1137G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632192 | ||||||
chr2:186632203
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.586-1126T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632203 | ||||||
chr2:186632355
|
G | T | 1 | a0001c0001t0002g0233 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.586-974G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632355 | ||||||
chr2:186632390
|
G | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0258others(3): Show | 6 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.586-939G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632390 | ||||||
chr2:186632418
|
G | GC | 16 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0086others(13): Show | 16 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.586-911_586-910ins others(1): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632418 | ||||||
chr2:186632419
|
T | G | 16 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0086others(13): Show | 16 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.586-910T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632419 | ||||||
chr2:186632419
|
T | TG | 90 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0045others(87): Show | 90 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.586-910_586-909ins others(1): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632419 | ||||||
chr2:186632427
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.586-902C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632427 | ||||||
chr2:186632649
|
A | G | 1 | a0001c0001t0001g0209 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.586-680A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186632649 | ||||||
chr2:186632981
|
C | CTAGA | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0286 | 3 | HG03130.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.586-329_586-326dup others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr2 | 186632981 | |||||
chr2:186632981
|
CTAGA | C | 86 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0028others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.586-329_586-326del others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr2 | 186632981 | |||||
chr2:186633004
|
C | G | 3 | a0001c0001t0006g0149a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.586-325C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186633004 | ||||||
chr2:186633014
|
T | C | 1 | a0001c0001t0002g0018 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.586-315T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186633014 | ||||||
chr2:186633091
|
C | T | 1 | a0001c0001t0003g0166 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.586-238C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186633091 | ||||||
chr2:186633141
|
C | CA | 12 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0001g0221others(9): Show | 12 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.586-174dupA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | INFO_REALIGN_3_PRIME | chr2 | 186633141 | |||||
chr2:186633226
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.586-103C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186633226 | ||||||
chr2:186633260
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.586-69C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186633260 | ||||||
chr2:186633261
|
A | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0101others(14): Show | 18 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(15): Show |
intron_variant | MODIFIER | c.586-68A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 5/29 | chr2 | 186633261 | ||||||
chr2:186633380
|
T | C | 59 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0011others(56): Show | 60 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(57): Show |
splice_region_variant&intron_variant | LOW | c.631+6T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186633380 | ||||||
chr2:186633527
|
T | C | 60 | a0001c0001t0001g0014a0001c0001t0001g0146a0001c0001t0001g0147others(57): Show | 60 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(57): Show |
intron_variant | MODIFIER | c.631+153T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186633527 | ||||||
chr2:186633631
|
A | T | 1 | a0001c0001t0001g0014 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.631+257A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186633631 | ||||||
chr2:186633765
|
A | T | 130 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0028others(127): Show | 131 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.631+391A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186633765 | ||||||
chr2:186633835
|
A | G | 132 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0028others(129): Show | 133 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.631+461A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186633835 | ||||||
chr2:186633921
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.631+547G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186633921 | ||||||
chr2:186633972
|
G | A | 7 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0005g0087others(4): Show | 7 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.631+598G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186633972 | ||||||
chr2:186634257
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.631+883A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186634257 | ||||||
chr2:186634282
|
CAT | C | 86 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0028others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.631+909_631+910del others(2): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186634282 | ||||||
chr2:186634460
|
G | GA | 244 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(241): Show | 249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.631+1090dupA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | INFO_REALIGN_3_PRIME | chr2 | 186634460 | |||||
chr2:186634985
|
G | A | 5 | a0001c0001t0001g0081a0001c0001t0001g0095a0001c0001t0001g0096others(2): Show | 5 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.632-1097G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186634985 | ||||||
chr2:186635302
|
A | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0101others(13): Show | 17 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.632-780A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186635302 | ||||||
chr2:186635311
|
T | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0286 | 3 | HG03130.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.632-771T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186635311 | ||||||
chr2:186635418
|
C | T | 3 | a0001c0005t0002g0030a0001c0005t0002g0060a0001c0005t0002g0061 | 3 | HG02257.hp2 HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.632-664C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186635418 | ||||||
chr2:186635495
|
C | T | 1 | a0001c0001t0013g0056 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.632-587C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186635495 | ||||||
chr2:186635515
|
T | C | 2 | a0001c0001t0011g0051a0001c0001t0011g0072 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.632-567T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186635515 | ||||||
chr2:186635540
|
C | G | 1 | a0001c0001t0002g0054 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.632-542C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186635540 | ||||||
chr2:186635633
|
T | C | 1 | a0001c0001t0002g0107 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.632-449T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186635633 | ||||||
chr2:186635955
|
A | G | 66 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0071others(63): Show | 69 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.632-127A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 6/29 | chr2 | 186635955 | ||||||
chr2:186636395
|
A | T | 2 | a0001c0001t0006g0276a0001c0001t0006g0277 | 2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.757+188A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 7/29 | chr2 | 186636395 | ||||||
chr2:186636428
|
T | C | 1 | a0001c0001t0001g0016 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.757+221T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 7/29 | chr2 | 186636428 | ||||||
chr2:186636702
|
C | A | 86 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0028others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.758-363C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 7/29 | chr2 | 186636702 | ||||||
chr2:186636720
|
A | C | 229 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(226): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.758-345A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 7/29 | chr2 | 186636720 | ||||||
chr2:186636919
|
A | G | 1 | a0001c0003t0001g0279 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.758-146A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 7/29 | chr2 | 186636919 | ||||||
chr2:186636921
|
A | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0101others(13): Show | 17 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.758-144A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 7/29 | chr2 | 186636921 | ||||||
chr2:186636955
|
G | A | 211 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(208): Show | 215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.758-110G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 7/29 | chr2 | 186636955 | ||||||
chr2:186637015
|
G | A | 14 | a0002c0002t0002g0127a0002c0002t0004g0123a0002c0002t0004g0124others(11): Show | 14 | HG00423.hp2 HG01943.hp1 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.758-50G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 7/29 | chr2 | 186637015 | ||||||
chr2:186637024
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.758-41G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 7/29 | chr2 | 186637024 | ||||||
chr2:186637167
|
CAT | C | 26 | a0001c0001t0001g0294a0001c0003t0001g0007a0001c0003t0001g0278others(23): Show | 27 | HG00423.hp2 HG01099.hp1 HG01943.hp1 others(24): Show |
intron_variant | MODIFIER | c.802+59_802+60delAT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186637167 | ||||||
chr2:186637270
|
C | T | 3 | a0001c0001t0006g0149a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.802+161C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186637270 | ||||||
chr2:186637339
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.802+230G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186637339 | ||||||
chr2:186637481
|
C | CA | 6 | a0001c0001t0002g0057a0001c0001t0002g0083a0001c0001t0002g0111others(3): Show | 6 | HG00558.hp1 HG01243.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+390dupA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 186637481 | |||||
chr2:186637481
|
CA | C | 207 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(204): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.802+390delA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr2 | 186637481 | |||||
chr2:186637501
|
G | A | 2 | a0001c0001t0012g0105a0001c0001t0012g0106 | 2 | HG03139.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.802+392G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186637501 | ||||||
chr2:186637532
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.802+423A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186637532 | ||||||
chr2:186637650
|
T | G | 1 | a0001c0001t0010g0162 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.802+541T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186637650 | ||||||
chr2:186637828
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0208 | 2 | HG02135.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.803-449C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186637828 | ||||||
chr2:186637944
|
A | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0078 | 2 | HG00738.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.803-333A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186637944 | ||||||
chr2:186637947
|
A | G | 1 | a0001c0001t0003g0175 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.803-330A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186637947 | ||||||
chr2:186638119
|
T | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0101others(13): Show | 17 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.803-158T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 8/29 | chr2 | 186638119 | ||||||
chr2:186638476
|
A | C | 1 | a0001c0001t0001g0120 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.903+11A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186638476 | ||||||
chr2:186638499
|
T | C | 149 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(146): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.903+34T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186638499 | ||||||
chr2:186638631
|
C | CGT | 23 | a0001c0001t0001g0074a0001c0001t0001g0101a0001c0001t0001g0102others(20): Show | 24 | HG00423.hp2 HG00558.hp1 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.903+205_903+206dup others(2): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | |||||
chr2:186638631
|
C | CGTGT | 31 | a0001c0001t0001g0136a0001c0001t0001g0236a0001c0001t0002g0012others(28): Show | 31 | HG00544.hp2 HG00673.hp1 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.903+203_903+206dup others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | |||||
chr2:186638631
|
C | CGTGTGT | 26 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(23): Show | 27 | HG00323.hp2 HG00639.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.903+201_903+206dup others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | |||||
chr2:186638631
|
C | CGTGTGTG others(1): Show |
8 | a0001c0001t0001g0016a0001c0001t0001g0120a0001c0001t0002g0003others(5): Show | 9 | HG01934.hp1 HG02004.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.903+199_903+206dup others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | |||||
chr2:186638631
|
C | CGTGTGTG others(3): Show |
1 | a0001c0001t0002g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.903+197_903+206dup others(10): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | |||||
chr2:186638631
|
C | CGTGTGTG others(5): Show |
1 | a0001c0005t0002g0030 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.903+195_903+206dup others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | |||||
chr2:186638631
|
CGT | C | 107 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.903+205_903+206del others(2): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | |||||
chr2:186638631
|
CGTGT | C | 11 | a0001c0001t0001g0045a0001c0001t0001g0151a0001c0001t0001g0153others(8): Show | 11 | HG00639.hp1 HG01081.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.903+203_903+206del others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | |||||
chr2:186638631
|
CGTGTGT | C | 37 | a0001c0001t0001g0185a0001c0001t0003g0004a0001c0001t0003g0006others(34): Show | 40 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.903+201_903+206del others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | |||||
chr2:186638631
|
CGTGTGTG others(1): Show |
C | 4 | a0001c0001t0003g0175a0001c0001t0003g0235a0001c0001t0003g0243others(1): Show | 4 | HG01123.hp2 HG02055.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.903+199_903+206del others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | |||||
chr2:186638631
|
CGTGTGTG others(3): Show |
C | 6 | a0001c0001t0002g0063a0001c0001t0005g0087a0001c0001t0005g0088others(3): Show | 6 | HG01192.hp1 HG02622.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.903+197_903+206del others(10): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638631 | |||||
chr2:186638668
|
GTGTA | G | 5 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0287others(2): Show | 5 | HG02896.hp1 HG02897.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.903+204_903+207del others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186638668 | ||||||
chr2:186638670
|
GTA | G | 3 | a0001c0001t0002g0110a0001c0003t0002g0281a0001c0003t0002g0282 | 3 | HG02145.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.903+206_903+207del others(2): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186638670 | ||||||
chr2:186638672
|
A | G | 23 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0101others(20): Show | 24 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.903+207A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186638672 | ||||||
chr2:186638897
|
C | CT | 27 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0001g0099others(24): Show | 27 | HG00597.hp1 HG01192.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.903+448dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638897 | |||||
chr2:186638897
|
CT | C | 18 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(15): Show | 19 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(16): Show |
intron_variant | MODIFIER | c.903+448delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186638897 | |||||
chr2:186638965
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0208 | 2 | HG02135.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.903+500T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186638965 | ||||||
chr2:186639044
|
A | G | 1 | a0001c0001t0010g0273 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.903+579A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186639044 | ||||||
chr2:186639070
|
T | G | 1 | a0001c0001t0002g0033 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.903+605T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186639070 | ||||||
chr2:186639144
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.903+679A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186639144 | ||||||
chr2:186639204
|
A | G | 1 | a0001c0001t0008g0108 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.903+739A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186639204 | ||||||
chr2:186639478
|
G | T | 5 | a0001c0001t0005g0087a0001c0001t0005g0088a0001c0001t0005g0089others(2): Show | 5 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.903+1013G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186639478 | ||||||
chr2:186639482
|
C | T | 1 | a0002c0002t0022g0098 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.903+1017C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186639482 | ||||||
chr2:186639625
|
C | T | 2 | a0001c0001t0011g0051a0001c0001t0011g0072 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.903+1160C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186639625 | ||||||
chr2:186639721
|
T | C | 7 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0287others(4): Show | 7 | HG01192.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.904-1194T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186639721 | ||||||
chr2:186639809
|
G | A | 1 | a0001c0001t0003g0256 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.904-1106G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186639809 | ||||||
chr2:186640074
|
G | A | 1 | a0001c0001t0003g0289 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.904-841G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186640074 | ||||||
chr2:186640414
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.904-501C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186640414 | ||||||
chr2:186640419
|
G | A | 2 | a0001c0001t0001g0272a0001c0001t0001g0275 | 2 | HG00642.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.904-496G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186640419 | ||||||
chr2:186640440
|
G | A | 52 | a0001c0001t0001g0298a0001c0001t0003g0004a0001c0001t0003g0006others(49): Show | 55 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.904-475G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186640440 | ||||||
chr2:186640619
|
A | G | 7 | a0002c0002t0002g0127a0002c0002t0004g0128a0002c0002t0004g0129others(4): Show | 7 | HG00423.hp2 HG01943.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.904-296A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186640619 | ||||||
chr2:186640670
|
A | G | 1 | a0001c0001t0001g0170 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.904-245A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186640670 | ||||||
chr2:186640759
|
A | G | 144 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0027others(141): Show | 145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.904-156A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | chr2 | 186640759 | ||||||
chr2:186640780
|
AAAGAC | A | 3 | a0001c0001t0013g0049a0001c0001t0013g0056a0005c0010t0003g0064 | 3 | NA18967.hp1 NA19080.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.904-128_904-124del others(5): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr2 | 186640780 | |||||
chr2:186640975
|
T | A | 5 | a0001c0001t0005g0087a0001c0001t0005g0088a0001c0001t0005g0089others(2): Show | 5 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.956+8T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 11/29 | chr2 | 186640975 | ||||||
chr2:186640976
|
A | G | 2 | a0002c0002t0004g0125a0002c0002t0004g0132 | 2 | NA18955.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.956+9A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 11/29 | chr2 | 186640976 | ||||||
chr2:186641170
|
C | T | 11 | a0001c0001t0002g0110a0001c0001t0002g0159a0001c0001t0002g0168others(8): Show | 11 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.956+203C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 11/29 | chr2 | 186641170 | ||||||
chr2:186641631
|
G | A | 1 | a0001c0001t0019g0029 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1159+43G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186641631 | ||||||
chr2:186641675
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1159+87C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186641675 | ||||||
chr2:186641834
|
T | A | 1 | a0001c0001t0003g0244 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1159+246T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186641834 | ||||||
chr2:186641947
|
T | TA | 11 | a0001c0001t0002g0110a0001c0001t0002g0159a0001c0001t0002g0168others(8): Show | 11 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.1159+368dupA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr2 | 186641947 | |||||
chr2:186642022
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1159+434A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642022 | ||||||
chr2:186642059
|
A | G | 77 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0146others(74): Show | 77 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1159+471A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642059 | ||||||
chr2:186642061
|
A | G | 1 | a0001c0001t0023g0065 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1159+473A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642061 | ||||||
chr2:186642110
|
T | C | 1 | a0001c0001t0003g0289 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1159+522T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642110 | ||||||
chr2:186642120
|
C | T | 1 | a0003c0004t0001g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1159+532C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642120 | ||||||
chr2:186642124
|
T | C | 1 | a0001c0001t0002g0110 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1159+536T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642124 | ||||||
chr2:186642150
|
C | A | 1 | a0001c0001t0001g0186 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1159+562C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642150 | ||||||
chr2:186642271
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1159+683G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642271 | ||||||
chr2:186642381
|
CTTG | C | 65 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0071others(62): Show | 68 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1159+798_1159+800d others(5): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr2 | 186642381 | |||||
chr2:186642535
|
CT | C | 193 | a0001c0001t0001g0010a0001c0001t0001g0019a0001c0001t0001g0027others(190): Show | 197 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(194): Show |
intron_variant | MODIFIER | c.1159+964delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr2 | 186642535 | |||||
chr2:186642551
|
T | C | 1 | a0001c0001t0003g0245 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1159+963T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642551 | ||||||
chr2:186642688
|
C | T | 1 | a0001c0001t0005g0090 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1159+1100C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642688 | ||||||
chr2:186642701
|
A | AT | 69 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0071others(66): Show | 72 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1159+1121dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr2 | 186642701 | |||||
chr2:186642732
|
G | T | 2 | a0001c0001t0001g0184a0001c0001t0001g0192 | 2 | HG00408.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1159+1144G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642732 | ||||||
chr2:186642950
|
T | C | 5 | a0001c0001t0001g0146a0001c0001t0001g0222a0001c0001t0001g0223others(2): Show | 5 | NA18942.hp1 NA18960.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1159+1362T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186642950 | ||||||
chr2:186643245
|
C | T | 219 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(216): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1159+1657C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186643245 | ||||||
chr2:186643471
|
C | T | 219 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(216): Show | 224 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1159+1883C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186643471 | ||||||
chr2:186643706
|
T | G | 4 | a0001c0001t0014g0158a0001c0001t0015g0271a0001c0001t0017g0092others(1): Show | 4 | HG01081.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1159+2118T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186643706 | ||||||
chr2:186643770
|
A | G | 2 | a0002c0002t0004g0156a0002c0002t0004g0255 | 2 | HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1159+2182A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186643770 | ||||||
chr2:186644119
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1159+2531T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644119 | ||||||
chr2:186644170
|
CT | C | 4 | a0001c0001t0014g0158a0001c0001t0015g0271a0001c0001t0017g0092others(1): Show | 4 | HG01081.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1160-2515delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644170 | ||||||
chr2:186644270
|
A | G | 130 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0028others(127): Show | 131 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1160-2416A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644270 | ||||||
chr2:186644314
|
G | A | 86 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0028others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1160-2372G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644314 | ||||||
chr2:186644335
|
G | T | 1 | a0001c0001t0003g0234 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1160-2351G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644335 | ||||||
chr2:186644393
|
T | G | 1 | a0002c0002t0004g0129 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1160-2293T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644393 | ||||||
chr2:186644395
|
G | A | 1 | a0001c0001t0008g0108 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1160-2291G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644395 | ||||||
chr2:186644560
|
G | A | 8 | a0001c0001t0003g0117a0001c0001t0003g0289a0001c0001t0003g0290others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1160-2126G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644560 | ||||||
chr2:186644820
|
T | TA | 67 | a0001c0001t0001g0044a0001c0001t0001g0071a0001c0001t0001g0073others(64): Show | 70 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(67): Show |
intron_variant | MODIFIER | c.1160-1854dupA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | INFO_REALIGN_3_PRIME | chr2 | 186644820 | |||||
chr2:186644879
|
G | A | 10 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0210others(7): Show | 10 | HG01169.hp1 HG01255.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1160-1807G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644879 | ||||||
chr2:186644937
|
T | C | 226 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(223): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1160-1749T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644937 | ||||||
chr2:186644976
|
G | A | 50 | a0001c0001t0001g0298a0001c0001t0003g0004a0001c0001t0003g0006others(47): Show | 53 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.1160-1710G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186644976 | ||||||
chr2:186645178
|
A | G | 1 | a0001c0001t0002g0283 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1160-1508A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186645178 | ||||||
chr2:186645322
|
T | C | 16 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0101others(13): Show | 17 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.1160-1364T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186645322 | ||||||
chr2:186645336
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1160-1350T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186645336 | ||||||
chr2:186645519
|
A | G | 1 | a0001c0001t0002g0043 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1160-1167A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186645519 | ||||||
chr2:186645524
|
A | C | 1 | a0001c0001t0015g0271 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1160-1162A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186645524 | ||||||
chr2:186645626
|
C | G | 1 | a0001c0001t0002g0048 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1160-1060C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186645626 | ||||||
chr2:186645734
|
G | A | 1 | a0001c0001t0003g0118 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1160-952G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186645734 | ||||||
chr2:186645865
|
G | A | 2 | a0001c0001t0001g0272a0001c0001t0001g0275 | 2 | HG00642.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1160-821G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186645865 | ||||||
chr2:186645943
|
G | A | 1 | a0001c0001t0002g0017 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1160-743G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186645943 | ||||||
chr2:186646026
|
G | A | 5 | a0001c0001t0001g0294a0001c0003t0001g0007a0001c0003t0001g0278others(2): Show | 6 | HG02451.hp2 HG02572.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1160-660G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186646026 | ||||||
chr2:186646139
|
G | T | 1 | a0002c0002t0004g0156 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1160-547G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186646139 | ||||||
chr2:186646150
|
A | G | 2 | a0001c0001t0006g0276a0001c0001t0006g0277 | 2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1160-536A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186646150 | ||||||
chr2:186646199
|
C | A | 1 | a0001c0001t0002g0057 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1160-487C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186646199 | ||||||
chr2:186646203
|
T | C | 1 | a0002c0006t0001g0299 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1160-483T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186646203 | ||||||
chr2:186646345
|
G | A | 52 | a0001c0001t0001g0298a0001c0001t0003g0004a0001c0001t0003g0006others(49): Show | 55 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1160-341G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186646345 | ||||||
chr2:186646461
|
G | A | 1 | a0001c0001t0001g0261 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1160-225G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 12/29 | chr2 | 186646461 | ||||||
chr2:186647080
|
G | A | 3 | a0001c0001t0006g0149a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1351+203G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186647080 | ||||||
chr2:186647238
|
A | AT | 181 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(178): Show | 184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1351+376dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr2 | 186647238 | |||||
chr2:186647628
|
A | T | 4 | a0001c0001t0014g0158a0001c0001t0015g0271a0001c0001t0017g0092others(1): Show | 4 | HG01081.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1351+751A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186647628 | ||||||
chr2:186647672
|
C | A | 4 | a0001c0001t0014g0158a0001c0001t0015g0271a0001c0001t0017g0092others(1): Show | 4 | HG01081.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1351+795C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186647672 | ||||||
chr2:186648003
|
G | A | 4 | a0001c0001t0014g0158a0001c0001t0015g0271a0001c0001t0017g0092others(1): Show | 4 | HG01081.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1351+1126G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648003 | ||||||
chr2:186648248
|
G | A | 1 | a0001c0001t0002g0015 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1351+1371G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648248 | ||||||
chr2:186648375
|
A | C | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1352-1465A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648375 | ||||||
chr2:186648554
|
G | A | 66 | a0001c0001t0001g0016a0001c0001t0002g0002a0001c0001t0002g0003others(63): Show | 68 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1352-1286G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648554 | ||||||
chr2:186648614
|
A | G | 227 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(224): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1352-1226A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648614 | ||||||
chr2:186648666
|
T | C | 1 | a0001c0001t0003g0293 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1352-1174T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648666 | ||||||
chr2:186648746
|
A | G | 2 | a0001c0001t0002g0040a0001c0001t0002g0110 | 2 | HG00323.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.1352-1094A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648746 | ||||||
chr2:186648787
|
C | G | 3 | a0001c0001t0002g0168a0001c0003t0002g0281a0001c0003t0002g0282 | 3 | HG02615.hp1 HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1352-1053C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648787 | ||||||
chr2:186648788
|
C | T | 1 | a0002c0002t0004g0156 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1352-1052C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648788 | ||||||
chr2:186648933
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1352-907T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648933 | ||||||
chr2:186648936
|
A | G | 1 | a0001c0001t0003g0295 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1352-904A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648936 | ||||||
chr2:186648943
|
TACATTTG others(53): Show |
T | 1 | a0001c0001t0003g0246 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1352-875_1352-816d others(62): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr2 | 186648943 | |||||
chr2:186648956
|
A | G | 2 | a0001c0001t0003g0234a0001c0001t0003g0256 | 2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1352-884A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186648956 | ||||||
chr2:186648981
|
TACATTTG others(15): Show |
T | 130 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0086others(127): Show | 135 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.1352-811_1352-790d others(24): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr2 | 186648981 | |||||
chr2:186648981
|
TACATTTG others(37): Show |
T | 130 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0027others(127): Show | 131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.1352-833_1352-790d others(46): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr2 | 186648981 | |||||
chr2:186648994
|
ATATATAT others(13): Show |
A | 2 | a0001c0001t0001g0091a0001c0001t0002g0078 | 2 | HG00738.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1352-837_1352-818d others(22): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr2 | 186648994 | |||||
chr2:186649003
|
C | T | 16 | a0001c0001t0001g0219a0001c0001t0002g0110a0001c0001t0002g0159others(13): Show | 16 | HG01884.hp1 HG01928.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.1352-837C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649003 | ||||||
chr2:186649010
|
GTGTGTA | G | 14 | a0001c0001t0001g0219a0001c0001t0002g0110a0001c0001t0002g0159others(11): Show | 14 | HG01884.hp1 HG01928.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1352-828_1352-823d others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr2 | 186649010 | |||||
chr2:186649016
|
ATATATAT others(13): Show |
A | 16 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0101others(13): Show | 17 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.1352-815_1352-796d others(22): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | INFO_REALIGN_3_PRIME | chr2 | 186649016 | |||||
chr2:186649025
|
C | T | 14 | a0001c0001t0001g0219a0001c0001t0002g0110a0001c0001t0002g0159others(11): Show | 14 | HG01884.hp1 HG01928.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.1352-815C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649025 | ||||||
chr2:186649082
|
TC | T | 7 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0005g0087others(4): Show | 7 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1352-757delC | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649082 | ||||||
chr2:186649083
|
C | T | 221 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(218): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.1352-757C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649083 | ||||||
chr2:186649100
|
A | C | 1 | a0001c0001t0002g0053 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1352-740A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649100 | ||||||
chr2:186649131
|
A | G | 66 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0071others(63): Show | 69 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.1352-709A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649131 | ||||||
chr2:186649393
|
G | T | 1 | a0001c0001t0001g0181 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1352-447G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649393 | ||||||
chr2:186649394
|
A | G | 1 | a0001c0001t0001g0181 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1352-446A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649394 | ||||||
chr2:186649455
|
T | C | 66 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0071others(63): Show | 69 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.1352-385T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649455 | ||||||
chr2:186649703
|
A | G | 15 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0287others(12): Show | 15 | HG01884.hp1 HG02145.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.1352-137A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649703 | ||||||
chr2:186649814
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1352-26A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 13/29 | chr2 | 186649814 | ||||||
chr2:186650094
|
G | T | 1 | a0001c0001t0001g0170 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1397+209G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186650094 | ||||||
chr2:186650227
|
T | A | 1 | a0001c0001t0001g0217 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1397+342T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186650227 | ||||||
chr2:186650270
|
G | A | 1 | a0001c0001t0002g0015 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1397+385G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186650270 | ||||||
chr2:186650361
|
G | A | 2 | a0001c0001t0001g0207a0001c0001t0001g0220 | 2 | HG01361.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1397+476G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186650361 | ||||||
chr2:186650748
|
C | T | 2 | a0001c0001t0011g0051a0001c0001t0011g0072 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1397+863C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186650748 | ||||||
chr2:186650942
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0095 | 2 | HG02055.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1398-1040A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186650942 | ||||||
chr2:186651017
|
A | G | 3 | a0001c0001t0006g0149a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1398-965A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186651017 | ||||||
chr2:186651050
|
A | G | 1 | a0001c0001t0001g0232 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1398-932A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186651050 | ||||||
chr2:186651262
|
T | A | 4 | a0001c0001t0014g0158a0001c0001t0015g0271a0001c0001t0017g0092others(1): Show | 4 | HG01081.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398-720T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186651262 | ||||||
chr2:186651319
|
A | G | 4 | a0001c0001t0014g0158a0001c0001t0015g0271a0001c0001t0017g0092others(1): Show | 4 | HG01081.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398-663A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186651319 | ||||||
chr2:186651644
|
C | A | 1 | a0002c0002t0004g0129 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1398-338C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186651644 | ||||||
chr2:186651649
|
C | A | 3 | a0001c0001t0003g0008a0001c0001t0003g0238a0001c0001t0003g0247 | 4 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.1398-333C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186651649 | ||||||
chr2:186651650
|
G | A | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1398-332G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186651650 | ||||||
chr2:186651719
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1398-263A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186651719 | ||||||
chr2:186651855
|
A | T | 3 | a0001c0001t0006g0149a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1398-127A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 14/29 | chr2 | 186651855 | ||||||
chr2:186652131
|
G | T | 1 | a0001c0001t0003g0300 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1505+42G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186652131 | ||||||
chr2:186652181
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1505+92T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186652181 | ||||||
chr2:186652478
|
C | CCATT | 28 | a0001c0001t0001g0294a0001c0003t0001g0007a0001c0003t0001g0278others(25): Show | 29 | HG00423.hp2 HG01099.hp1 HG01192.hp2 others(26): Show |
intron_variant | MODIFIER | c.1505+390_1505+393d others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 186652478 | |||||
chr2:186652928
|
T | C | 107 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0027others(104): Show | 107 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.1505+839T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186652928 | ||||||
chr2:186652931
|
A | AT | 29 | a0001c0001t0001g0010a0001c0001t0001g0086a0001c0001t0001g0091others(26): Show | 29 | HG01099.hp1 HG01123.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.1505+867dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 186652931 | |||||
chr2:186652931
|
A | ATTT | 9 | a0002c0002t0004g0123a0002c0002t0004g0125a0002c0002t0004g0128others(6): Show | 9 | HG00423.hp2 HG01952.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.1505+865_1505+867d others(5): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 186652931 | |||||
chr2:186652931
|
AT | A | 105 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0027others(102): Show | 105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.1505+867delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 186652931 | |||||
chr2:186652931
|
ATT | A | 42 | a0001c0001t0001g0100a0001c0001t0001g0223a0001c0001t0001g0298others(39): Show | 45 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.1505+866_1505+867d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 186652931 | |||||
chr2:186652961
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1505+872C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186652961 | ||||||
chr2:186652994
|
A | G | 207 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(204): Show | 211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1505+905A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186652994 | ||||||
chr2:186653071
|
G | T | 4 | a0001c0001t0014g0158a0001c0001t0015g0271a0001c0001t0017g0092others(1): Show | 4 | HG01081.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1505+982G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653071 | ||||||
chr2:186653090
|
C | T | 4 | a0001c0001t0014g0158a0001c0001t0015g0271a0001c0001t0017g0092others(1): Show | 4 | HG01081.hp1 HG02895.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1505+1001C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653090 | ||||||
chr2:186653121
|
A | G | 1 | a0001c0001t0001g0206 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1505+1032A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653121 | ||||||
chr2:186653196
|
C | T | 2 | a0001c0001t0003g0234a0001c0001t0003g0256 | 2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1505+1107C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653196 | ||||||
chr2:186653301
|
T | C | 8 | a0001c0001t0002g0159a0001c0001t0002g0168a0001c0001t0008g0023others(5): Show | 8 | HG02486.hp2 HG02615.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1505+1212T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653301 | ||||||
chr2:186653371
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1506-1279A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653371 | ||||||
chr2:186653420
|
C | T | 3 | a0001c0001t0006g0149a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1506-1230C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653420 | ||||||
chr2:186653432
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1506-1218A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653432 | ||||||
chr2:186653533
|
A | G | 52 | a0001c0001t0001g0298a0001c0001t0003g0004a0001c0001t0003g0006others(49): Show | 55 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1506-1117A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653533 | ||||||
chr2:186653562
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1506-1088A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653562 | ||||||
chr2:186653947
|
A | G | 1 | a0001c0001t0001g0229 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1506-703A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653947 | ||||||
chr2:186653988
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1506-662T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186653988 | ||||||
chr2:186654098
|
C | A | 5 | a0001c0001t0001g0146a0001c0001t0001g0222a0001c0001t0001g0223others(2): Show | 5 | NA18942.hp1 NA18960.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.1506-552C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186654098 | ||||||
chr2:186654222
|
A | G | 1 | a0001c0001t0002g0110 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1506-428A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186654222 | ||||||
chr2:186654281
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1506-369C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186654281 | ||||||
chr2:186654332
|
C | CA | 8 | a0001c0001t0001g0157a0001c0001t0001g0205a0001c0001t0001g0240others(5): Show | 8 | HG00544.hp1 HG01361.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1506-301dupA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 186654332 | |||||
chr2:186654332
|
CA | C | 7 | a0001c0001t0001g0216a0001c0001t0001g0222a0001c0001t0001g0267others(4): Show | 7 | HG01081.hp1 HG01255.hp1 HG01934.hp2 others(4): Show |
intron_variant | MODIFIER | c.1506-301delA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | INFO_REALIGN_3_PRIME | chr2 | 186654332 | |||||
chr2:186654545
|
G | T | 1 | a0001c0001t0002g0015 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1506-105G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186654545 | ||||||
chr2:186654611
|
G | T | 44 | a0001c0001t0002g0002a0001c0001t0002g0011a0001c0001t0002g0012others(41): Show | 45 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.1506-39G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 15/29 | chr2 | 186654611 | ||||||
chr2:186654908
|
T | C | 4 | a0001c0001t0001g0146a0001c0001t0001g0222a0001c0001t0001g0223others(1): Show | 4 | NA18942.hp1 NA18960.hp1 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1564+200T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 16/29 | chr2 | 186654908 | ||||||
chr2:186654935
|
C | T | 1 | a0001c0001t0001g0221 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1564+227C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 16/29 | chr2 | 186654935 | ||||||
chr2:186655006
|
A | G | 1 | a0001c0001t0002g0017 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1564+298A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 16/29 | chr2 | 186655006 | ||||||
chr2:186655381
|
G | T | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1564+673G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 16/29 | chr2 | 186655381 | ||||||
chr2:186655565
|
T | G | 1 | a0001c0001t0001g0206 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1565-682T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 16/29 | chr2 | 186655565 | ||||||
chr2:186655602
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1565-645C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 16/29 | chr2 | 186655602 | ||||||
chr2:186655603
|
G | T | 8 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0119others(5): Show | 9 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1565-644G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 16/29 | chr2 | 186655603 | ||||||
chr2:186655639
|
A | G | 3 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103 | 3 | HG01891.hp1 HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1565-608A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 16/29 | chr2 | 186655639 | ||||||
chr2:186656054
|
T | G | 3 | a0001c0001t0001g0217a0001c0001t0001g0218a0001c0001t0001g0221 | 3 | HG00323.hp1 NA18612.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1565-193T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 16/29 | chr2 | 186656054 | ||||||
chr2:186656446
|
T | C | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1719+45T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186656446 | ||||||
chr2:186656533
|
C | A | 66 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0071others(63): Show | 69 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.1719+132C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186656533 | ||||||
chr2:186656572
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0091 | 2 | HG02723.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1719+171C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186656572 | ||||||
chr2:186656694
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1719+293A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186656694 | ||||||
chr2:186656711
|
A | G | 3 | a0002c0002t0007g0138a0002c0002t0007g0139a0002c0002t0007g0140 | 3 | HG01192.hp2 HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1719+310A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186656711 | ||||||
chr2:186656736
|
C | A | 1 | a0001c0001t0001g0179 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1719+335C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186656736 | ||||||
chr2:186656806
|
A | G | 1 | a0001c0001t0002g0053 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1719+405A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186656806 | ||||||
chr2:186656816
|
T | G | 1 | a0001c0001t0002g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1719+415T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186656816 | ||||||
chr2:186656868
|
C | T | 1 | a0001c0001t0001g0259 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1719+467C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186656868 | ||||||
chr2:186656987
|
A | AACAC | 5 | a0001c0001t0005g0087a0001c0001t0005g0088a0001c0001t0005g0089others(2): Show | 5 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1719+620_1719+623d others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186656987 | |||||
chr2:186656987
|
AAC | A | 66 | a0001c0001t0001g0010a0001c0001t0001g0027a0001c0001t0001g0044others(63): Show | 69 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.1719+622_1719+623d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186656987 | |||||
chr2:186656987
|
AACAC | A | 99 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0016others(96): Show | 102 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(99): Show |
intron_variant | MODIFIER | c.1719+620_1719+623d others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186656987 | |||||
chr2:186656987
|
AACACAC | A | 20 | a0001c0001t0019g0029a0001c0003t0001g0007a0001c0003t0001g0280others(17): Show | 21 | HG00423.hp2 HG01099.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.1719+618_1719+623d others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186656987 | |||||
chr2:186656987
|
AACACACA others(3): Show |
A | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1719+614_1719+623d others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186656987 | |||||
chr2:186656987
|
AACACACA others(7): Show |
A | 3 | a0001c0001t0006g0149a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1719+610_1719+623d others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186656987 | |||||
chr2:186657011
|
CACACACA others(7): Show |
C | 1 | a0001c0001t0001g0174 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1719+612_1719+625d others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186657011 | |||||
chr2:186657015
|
CACACACA others(3): Show |
C | 78 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0081others(75): Show | 78 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.1719+616_1719+625d others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186657015 | |||||
chr2:186657017
|
CACACACA others(1): Show |
C | 6 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0197others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1719+618_1719+625d others(10): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186657017 | |||||
chr2:186657217
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0028 | 2 | HG02451.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1719+816T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186657217 | ||||||
chr2:186657567
|
A | G | 1 | a0001c0001t0016g0116 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1719+1166A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186657567 | ||||||
chr2:186657594
|
T | C | 7 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0005g0087others(4): Show | 7 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1719+1193T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186657594 | ||||||
chr2:186657679
|
G | A | 200 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(197): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.1719+1278G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186657679 | ||||||
chr2:186657885
|
G | C | 64 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0071others(61): Show | 67 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1720-1153G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186657885 | ||||||
chr2:186657953
|
GA | G | 86 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0028others(83): Show | 86 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1720-1075delA | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186657953 | |||||
chr2:186657954
|
A | G | 66 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0071others(63): Show | 69 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.1720-1084A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186657954 | ||||||
chr2:186658023
|
G | T | 59 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0011others(56): Show | 60 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.1720-1015G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186658023 | ||||||
chr2:186658061
|
A | G | 127 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(124): Show | 128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1720-977A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186658061 | ||||||
chr2:186658064
|
G | A | 2 | a0002c0002t0004g0128a0002c0002t0004g0131 | 2 | NA18964.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.1720-974G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186658064 | ||||||
chr2:186658146
|
C | T | 1 | a0001c0001t0003g0289 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1720-892C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186658146 | ||||||
chr2:186658239
|
G | A | 1 | a0001c0001t0019g0029 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1720-799G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186658239 | ||||||
chr2:186658768
|
GTGTT | G | 24 | a0001c0001t0001g0294a0001c0003t0001g0007a0001c0003t0001g0278others(21): Show | 25 | HG00423.hp2 HG01099.hp1 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.1720-267_1720-264d others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | INFO_REALIGN_3_PRIME | chr2 | 186658768 | |||||
chr2:186658807
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1720-231C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186658807 | ||||||
chr2:186658968
|
G | A | 2 | a0001c0001t0011g0051a0001c0001t0011g0072 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1720-70G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 17/29 | chr2 | 186658968 | ||||||
chr2:186659307
|
G | C | 1 | a0001c0001t0002g0036 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1857+132G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186659307 | ||||||
chr2:186659795
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1857+620T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186659795 | ||||||
chr2:186660091
|
T | C | 3 | a0001c0001t0006g0149a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1857+916T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186660091 | ||||||
chr2:186660228
|
C | T | 1 | a0001c0001t0001g0193 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1857+1053C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186660228 | ||||||
chr2:186660299
|
G | A | 7 | a0001c0001t0001g0086a0001c0001t0001g0091a0001c0001t0005g0087others(4): Show | 7 | HG02622.hp1 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1857+1124G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186660299 | ||||||
chr2:186660466
|
C | T | 52 | a0001c0001t0001g0298a0001c0001t0003g0004a0001c0001t0003g0006others(49): Show | 55 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.1857+1291C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186660466 | ||||||
chr2:186660545
|
G | A | 4 | a0002c0002t0001g0141a0002c0002t0001g0142a0002c0002t0022g0098others(1): Show | 4 | HG01099.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1857+1370G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186660545 | ||||||
chr2:186660971
|
G | A | 2 | a0001c0001t0001g0010a0001c0001t0002g0043 | 2 | HG02630.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1857+1796G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186660971 | ||||||
chr2:186661235
|
A | T | 16 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0101others(13): Show | 17 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.1857+2060A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661235 | ||||||
chr2:186661268
|
A | C | 3 | a0001c0001t0006g0149a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1857+2093A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661268 | ||||||
chr2:186661363
|
T | C | 127 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0019others(124): Show | 128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1857+2188T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661363 | ||||||
chr2:186661453
|
A | T | 64 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0071others(61): Show | 67 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.1857+2278A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661453 | ||||||
chr2:186661539
|
G | T | 1 | a0001c0001t0003g0247 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1858-2229G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661539 | ||||||
chr2:186661586
|
T | G | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1858-2182T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661586 | ||||||
chr2:186661598
|
GT | G | 221 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(218): Show | 225 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.1858-2153delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr2 | 186661598 | |||||
chr2:186661603
|
T | TG | 9 | a0001c0001t0001g0298a0001c0001t0003g0117a0001c0001t0003g0289others(6): Show | 9 | HG01891.hp2 HG02109.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1858-2165_1858-216 others(5): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661603 | ||||||
chr2:186661604
|
T | G | 60 | a0001c0001t0001g0010a0001c0001t0001g0027a0001c0001t0001g0044others(57): Show | 63 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.1858-2164T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661604 | ||||||
chr2:186661605
|
T | G | 127 | a0001c0001t0001g0014a0001c0001t0001g0045a0001c0001t0001g0081others(124): Show | 128 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1858-2163T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661605 | ||||||
chr2:186661611
|
T | G | 1 | a0003c0004t0001g0135 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1858-2157T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661611 | ||||||
chr2:186661707
|
C | T | 3 | a0001c0001t0006g0149a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1858-2061C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661707 | ||||||
chr2:186661757
|
C | T | 1 | a0001c0001t0017g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1858-2011C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661757 | ||||||
chr2:186661758
|
G | A | 10 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0210others(7): Show | 10 | HG01169.hp1 HG01255.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1858-2010G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661758 | ||||||
chr2:186661830
|
C | T | 1 | a0001c0001t0003g0243 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1858-1938C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661830 | ||||||
chr2:186661884
|
C | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0227 | 3 | HG02083.hp1 HG02155.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1858-1884C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661884 | ||||||
chr2:186661887
|
A | G | 225 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(222): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1858-1881A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661887 | ||||||
chr2:186661945
|
G | A | 126 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0028others(123): Show | 127 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1858-1823G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661945 | ||||||
chr2:186661963
|
G | A | 2 | a0001c0001t0017g0092a0001c0001t0024g0109 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1858-1805G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186661963 | ||||||
chr2:186662017
|
T | C | 1 | a0001c0001t0002g0053 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1858-1751T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186662017 | ||||||
chr2:186662060
|
T | C | 1 | a0002c0002t0004g0125 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1858-1708T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186662060 | ||||||
chr2:186662205
|
T | C | 1 | a0001c0001t0003g0253 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1858-1563T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186662205 | ||||||
chr2:186662237
|
G | A | 3 | a0001c0001t0001g0207a0001c0001t0011g0051a0001c0001t0011g0072 | 3 | HG02970.hp1 HG03209.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1858-1531G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186662237 | ||||||
chr2:186662305
|
G | A | 1 | a0002c0002t0004g0255 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1858-1463G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186662305 | ||||||
chr2:186663243
|
A | G | 1 | a0002c0002t0004g0134 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1858-525A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186663243 | ||||||
chr2:186663424
|
A | G | 1 | a0001c0001t0001g0044 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1858-344A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186663424 | ||||||
chr2:186663692
|
A | G | 1 | a0001c0001t0006g0277 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1858-76A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 18/29 | chr2 | 186663692 | ||||||
chr2:186663908
|
A | G | 79 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(76): Show | 81 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.1925+73A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 19/29 | chr2 | 186663908 | ||||||
chr2:186663968
|
A | G | 13 | a0001c0001t0001g0027a0001c0001t0001g0044a0001c0001t0001g0071others(10): Show | 13 | HG00140.hp1 HG00738.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1925+133A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 19/29 | chr2 | 186663968 | ||||||
chr2:186664883
|
C | G | 1 | a0001c0001t0003g0292 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2073+242C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 20/29 | chr2 | 186664883 | ||||||
chr2:186664885
|
A | G | 1 | a0001c0008t0020g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2074-241A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 20/29 | chr2 | 186664885 | ||||||
chr2:186664925
|
T | A | 295 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(292): Show | 302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.2074-201T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 20/29 | chr2 | 186664925 | ||||||
chr2:186665096
|
A | AT | 6 | a0001c0001t0001g0207a0001c0001t0001g0220a0001c0001t0002g0021others(3): Show | 6 | HG01361.hp1 HG02132.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.2074-13dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr2 | 186665096 | |||||
chr2:186665096
|
AT | A | 200 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0014others(197): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.2074-13delT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr2 | 186665096 | |||||
chr2:186665096
|
ATT | A | 17 | a0001c0001t0003g0008a0001c0001t0003g0238a0001c0001t0003g0247others(14): Show | 18 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.2074-14_2074-13del others(2): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr2 | 186665096 | |||||
chr2:186665389
|
C | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0101others(11): Show | 15 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.2166+171C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186665389 | ||||||
chr2:186665399
|
T | G | 5 | a0001c0001t0001g0160a0001c0001t0001g0201a0001c0001t0001g0204others(2): Show | 5 | HG02165.hp1 NA18949.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.2166+181T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186665399 | ||||||
chr2:186665505
|
G | T | 2 | a0001c0001t0008g0023a0001c0001t0008g0031 | 2 | HG02486.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2166+287G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186665505 | ||||||
chr2:186665654
|
G | A | 3 | a0001c0001t0008g0023a0001c0001t0008g0031a0001c0001t0023g0065 | 3 | HG02486.hp2 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2166+436G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186665654 | ||||||
chr2:186665691
|
A | G | 1 | a0001c0001t0003g0241 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2166+473A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186665691 | ||||||
chr2:186665694
|
G | A | 1 | a0001c0001t0002g0270 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2166+476G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186665694 | ||||||
chr2:186665793
|
T | C | 79 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(76): Show | 81 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.2166+575T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186665793 | ||||||
chr2:186665972
|
T | C | 1 | a0001c0001t0018g0288 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2167-732T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186665972 | ||||||
chr2:186666308
|
T | C | 1 | a0001c0001t0003g0145 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2167-396T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186666308 | ||||||
chr2:186666364
|
T | C | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2167-340T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186666364 | ||||||
chr2:186666445
|
T | G | 1 | a0001c0001t0002g0168 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2167-259T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186666445 | ||||||
chr2:186666468
|
T | C | 2 | a0001c0001t0002g0020a0001c0001t0002g0078 | 2 | HG00738.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2167-236T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186666468 | ||||||
chr2:186666575
|
C | T | 3 | a0001c0001t0006g0149a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2167-129C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186666575 | ||||||
chr2:186666639
|
A | G | 1 | a0001c0001t0006g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2167-65A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 21/29 | chr2 | 186666639 | ||||||
chr2:186667283
|
G | T | 99 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0019others(96): Show | 99 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.2327+53G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 23/29 | chr2 | 186667283 | ||||||
chr2:186667507
|
G | A | 51 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0008others(48): Show | 54 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.2328-164G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 23/29 | chr2 | 186667507 | ||||||
chr2:186667646
|
T | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0101others(11): Show | 15 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.2328-25T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 23/29 | chr2 | 186667646 | ||||||
chr2:186668041
|
T | G | 1 | a0001c0001t0001g0157 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2433+265T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668041 | ||||||
chr2:186668090
|
G | A | 1 | a0001c0008t0020g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2433+314G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668090 | ||||||
chr2:186668185
|
C | CAT | 3 | a0001c0001t0005g0087a0003c0004t0001g0076a0003c0004t0001g0080 | 3 | HG02723.hp1 HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2433+440_2433+441d others(4): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | |||||
chr2:186668185
|
C | CATATAT | 5 | a0001c0001t0001g0136a0002c0002t0004g0125a0002c0002t0004g0129others(2): Show | 5 | HG01168.hp2 HG01952.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.2433+436_2433+441d others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | |||||
chr2:186668185
|
C | CATATATA others(1): Show |
3 | a0001c0001t0008g0108a0002c0002t0004g0132a0002c0002t0004g0134 | 3 | HG00423.hp2 HG03540.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.2433+434_2433+441d others(10): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | |||||
chr2:186668185
|
C | CATATATA others(3): Show |
3 | a0002c0002t0004g0124a0002c0002t0004g0126a0002c0002t0004g0133 | 3 | NA18950.hp2 NA18989.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2433+432_2433+441d others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | |||||
chr2:186668185
|
C | CATATATA others(5): Show |
1 | a0002c0002t0004g0123 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.2433+430_2433+441d others(14): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | |||||
chr2:186668185
|
C | CATATATA others(7): Show |
1 | a0002c0002t0004g0255 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2433+428_2433+441d others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | |||||
chr2:186668185
|
C | CATATATA others(15): Show |
1 | a0001c0001t0003g0239 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2433+420_2433+441d others(24): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | |||||
chr2:186668185
|
C | CATATATG others(3): Show |
1 | a0001c0001t0002g0025 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2433+415_2433+416i others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | |||||
chr2:186668185
|
CATATAT | C | 4 | a0001c0001t0001g0171a0001c0001t0001g0213a0001c0001t0003g0148others(1): Show | 4 | HG01081.hp2 HG01993.hp2 HG02132.hp2 others(1): Show |
intron_variant | MODIFIER | c.2433+436_2433+441d others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | |||||
chr2:186668185
|
CATATATA others(1): Show |
C | 26 | a0001c0001t0003g0004a0001c0001t0003g0008a0001c0001t0003g0117others(23): Show | 28 | HG00280.hp1 HG00408.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.2433+434_2433+441d others(10): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | |||||
chr2:186668185
|
CATATATA others(3): Show |
C | 3 | a0001c0001t0003g0244a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03130.hp1 HG03139.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2433+432_2433+441d others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | |||||
chr2:186668185
|
CATATATA others(5): Show |
C | 1 | a0001c0001t0001g0240 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2433+430_2433+441d others(14): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | |||||
chr2:186668185
|
CATATATA others(7): Show |
C | 1 | a0001c0001t0001g0228 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2433+428_2433+441d others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668185 | |||||
chr2:186668186
|
A | ATATATGT others(3): Show |
1 | a0001c0001t0019g0029 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2433+415_2433+416i others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668186 | |||||
chr2:186668189
|
T | C | 2 | a0001c0001t0001g0027a0001c0001t0001g0194 | 2 | HG01256.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2433+413T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668189 | ||||||
chr2:186668190
|
A | ATGTATAT others(7): Show |
1 | a0001c0001t0002g0058 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2433+415_2433+416i others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668190 | |||||
chr2:186668192
|
A | G | 76 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(73): Show | 78 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.2433+416A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668192 | ||||||
chr2:186668205
|
TATATATA | T | 6 | a0001c0001t0001g0261a0001c0001t0003g0006a0001c0001t0003g0034others(3): Show | 7 | HG01074.hp2 HG01168.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.2433+430_2433+436d others(9): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668205 | ||||||
chr2:186668205
|
TATATATA others(2): Show |
T | 7 | a0001c0001t0003g0122a0001c0001t0003g0169a0001c0001t0003g0248others(4): Show | 7 | HG01069.hp2 HG03710.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.2433+430_2433+438d others(11): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668205 | ||||||
chr2:186668207
|
TATATATA others(2): Show |
T | 3 | a0001c0001t0003g0243a0001c0001t0003g0291a0006c0007t0003g0249 | 3 | HG02015.hp1 HG02965.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2433+432_2433+440d others(11): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668207 | ||||||
chr2:186668210
|
A | T | 1 | a0001c0001t0001g0151 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2433+434A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668210 | ||||||
chr2:186668210
|
ATATATAT others(3): Show |
A | 1 | a0001c0001t0006g0149 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2433+436_2433+445d others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668210 | |||||
chr2:186668212
|
A | T | 15 | a0001c0001t0001g0016a0001c0001t0001g0151a0001c0001t0001g0171others(12): Show | 16 | HG00280.hp1 HG00558.hp2 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.2433+436A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668212 | ||||||
chr2:186668214
|
A | T | 47 | a0001c0001t0001g0016a0001c0001t0001g0151a0001c0001t0001g0157others(44): Show | 50 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.2433+438A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668214 | ||||||
chr2:186668216
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0219 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(19): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0121 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(21): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0203 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(30): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(17): Show |
1 | a0001c0001t0001g0182 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(26): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(18): Show |
4 | a0001c0001t0001g0179a0001c0001t0001g0191a0001c0001t0001g0210others(1): Show | 4 | HG00423.hp1 HG01169.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(27): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0160 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(28): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0264 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(29): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0170 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(25): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0187a0001c0001t0001g0267 | 2 | HG01934.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(26): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(18): Show |
2 | a0001c0001t0001g0201a0001c0001t0001g0205 | 2 | NA18949.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(27): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(21): Show |
3 | a0001c0001t0001g0194a0001c0001t0001g0223a0001c0001t0001g0266 | 3 | HG01952.hp2 NA18960.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(30): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0196 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(22): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0212a0001c0001t0001g0216 | 2 | HG01255.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(24): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(16): Show |
4 | a0001c0001t0001g0178a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG00280.hp2 HG01358.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(25): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0189a0001c0001t0001g0263 | 2 | HG02015.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(26): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0001g0186 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(27): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0027 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(28): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0259 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(21): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0208a0001c0001t0001g0227 | 2 | HG02083.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(22): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0200 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(23): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(15): Show |
2 | a0001c0001t0001g0184a0001c0001t0001g0192 | 2 | HG00408.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(24): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0222 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(25): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(17): Show |
2 | a0001c0001t0001g0147a0001c0001t0001g0215 | 2 | NA18747.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(26): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0204 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(28): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0091a0001c0001t0001g0161 | 2 | HG02135.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(18): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(10): Show |
1 | a0002c0002t0002g0127 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(19): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(11): Show |
3 | a0001c0001t0001g0193a0001c0001t0001g0211a0001c0001t0002g0040 | 3 | HG00323.hp2 HG01258.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(20): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0014a0001c0001t0002g0047 | 2 | HG01975.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(21): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(13): Show |
5 | a0001c0001t0001g0019a0001c0001t0001g0071a0001c0001t0001g0185others(2): Show | 5 | HG02155.hp1 HG02451.hp1 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(22): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0044 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(23): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(9): Show |
4 | a0001c0001t0001g0154a0001c0001t0001g0174a0001c0001t0001g0190others(1): Show | 4 | HG01981.hp1 NA18979.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(18): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0275a0001c0001t0002g0084 | 2 | HG00642.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(19): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(11): Show |
5 | a0001c0001t0001g0028a0001c0001t0002g0039a0001c0001t0002g0048others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(20): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(12): Show |
3 | a0001c0001t0001g0183a0001c0001t0001g0268a0001c0001t0002g0107 | 3 | HG01123.hp1 NA18967.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(21): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(13): Show |
5 | a0001c0001t0001g0073a0001c0001t0001g0086a0001c0001t0001g0146others(2): Show | 5 | HG01993.hp1 HG02622.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(22): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0074a0001c0001t0001g0220 | 2 | HG01361.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(23): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0258 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(15): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(7): Show |
4 | a0001c0001t0001g0120a0001c0001t0001g0155a0001c0001t0002g0270others(1): Show | 4 | HG03017.hp1 HG03704.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0172 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(18): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0225a0001c0001t0001g0274 | 2 | HG00597.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(20): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(12): Show |
5 | a0001c0001t0001g0099a0001c0001t0002g0050a0001c0001t0002g0057others(2): Show | 5 | HG01928.hp2 HG02738.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(21): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0100a0001c0001t0001g0152 | 2 | HG02300.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(22): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(14): Show |
2 | a0001c0001t0001g0173a0001c0001t0001g0231 | 2 | HG02056.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(23): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0013 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(4): Show |
2 | a0001c0001t0002g0110a0001c0001t0002g0111 | 2 | HG01256.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(13): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(5): Show |
3 | a0001c0001t0001g0298a0001c0001t0002g0112a0001c0001t0002g0233 | 3 | HG01258.hp2 HG03490.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(14): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0005a0001c0001t0002g0043 | 3 | HG03490.hp2 HG03492.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(15): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0079a0001c0001t0001g0104a0001c0001t0001g0198 | 3 | HG00738.hp2 HG02572.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(17): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0197a0001c0001t0002g0054 | 2 | HG02683.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(18): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0024g0109 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(19): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(11): Show |
1 | a0001c0001t0002g0002 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(20): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0229a0001c0001t0001g0287 | 2 | HG02965.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(21): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(13): Show |
1 | a0001c0001t0001g0224 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(22): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0217 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(23): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(3): Show |
1 | a0001c0003t0002g0281 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(4): Show |
9 | a0001c0001t0001g0101a0001c0001t0001g0143a0001c0001t0002g0022others(6): Show | 9 | HG02132.hp1 HG02258.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(13): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(5): Show |
7 | a0001c0001t0002g0078a0001c0001t0002g0083a0001c0001t0002g0113others(4): Show | 7 | HG00558.hp1 HG00738.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(14): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(6): Show |
3 | a0001c0001t0002g0012a0001c0001t0002g0018a0001c0001t0002g0164 | 3 | HG02602.hp1 NA18949.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(15): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0081 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(17): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0045a0001c0001t0001g0095 | 2 | HG02258.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(18): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0209 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(19): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATAT others(11): Show |
2 | a0001c0001t0001g0218a0001c0001t0018g0288 | 2 | HG00323.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(20): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATTT others(3): Show |
3 | a0001c0001t0001g0102a0001c0001t0001g0103a0002c0002t0022g0098 | 3 | HG01891.hp1 HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATTT others(4): Show |
4 | a0001c0001t0002g0011a0001c0001t0002g0020a0001c0001t0002g0021others(1): Show | 4 | HG03927.hp2 NA18954.hp2 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(13): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATTT others(5): Show |
13 | a0001c0001t0002g0003a0001c0001t0002g0009a0001c0001t0002g0015others(10): Show | 14 | HG00544.hp2 HG01496.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(14): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATTT others(6): Show |
5 | a0001c0001t0002g0026a0001c0001t0002g0035a0001c0001t0002g0115others(2): Show | 5 | HG01106.hp1 HG01175.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(15): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATTT others(7): Show |
4 | a0001c0001t0002g0038a0001c0001t0002g0042a0001c0001t0002g0063others(1): Show | 4 | HG00673.hp1 HG01192.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATTT others(8): Show |
1 | a0001c0001t0001g0096 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(17): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATTT others(9): Show |
2 | a0001c0001t0001g0097a0001c0001t0001g0153 | 2 | HG01496.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(18): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATATTT others(11): Show |
1 | a0001c0001t0001g0221 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(20): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATTTTT others(3): Show |
1 | a0001c0001t0015g0271 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2433+441_2433+442i others(12): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATTTTT others(4): Show |
3 | a0001c0001t0002g0041a0001c0001t0009g0070a0001c0005t0002g0060 | 3 | NA19009.hp1 NA19060.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(13): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATTTTT others(5): Show |
4 | a0001c0001t0002g0053a0001c0001t0002g0163a0001c0005t0002g0030others(1): Show | 4 | HG01358.hp1 HG02135.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2433+441_2433+442i others(14): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATTTTT others(6): Show |
3 | a0001c0001t0002g0036a0002c0002t0007g0138a0002c0002t0007g0140 | 3 | HG02056.hp2 HG03471.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2433+441_2433+442i others(15): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | ATATTTTT others(7): Show |
1 | a0001c0001t0002g0165 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2433+441_2433+442i others(16): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | INFO_REALIGN_3_PRIME | chr2 | 186668216 | |||||
chr2:186668216
|
A | T | 62 | a0001c0001t0001g0016a0001c0001t0001g0151a0001c0001t0001g0157others(59): Show | 65 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.2433+440A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668216 | ||||||
chr2:186668218
|
T | A | 11 | a0001c0001t0008g0108a0002c0002t0004g0123a0002c0002t0004g0124others(8): Show | 11 | HG01952.hp1 HG02148.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.2433+442T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668218 | ||||||
chr2:186668219
|
T | A | 3 | a0001c0001t0008g0023a0001c0001t0008g0031a0001c0001t0023g0065 | 3 | HG02486.hp2 HG02896.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2433+443T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668219 | ||||||
chr2:186668220
|
T | A | 7 | a0001c0001t0008g0108a0002c0002t0004g0123a0002c0002t0004g0124others(4): Show | 7 | HG03540.hp1 NA18948.hp2 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.2433+444T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668220 | ||||||
chr2:186668222
|
T | A | 1 | a0001c0001t0008g0108 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2433+446T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668222 | ||||||
chr2:186668224
|
T | A | 1 | a0001c0001t0008g0108 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2433+448T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668224 | ||||||
chr2:186668225
|
T | A | 1 | a0001c0001t0001g0010 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2433+449T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668225 | ||||||
chr2:186668226
|
T | A | 1 | a0001c0001t0008g0108 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2433+450T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668226 | ||||||
chr2:186668289
|
G | C | 51 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0008others(48): Show | 54 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.2434-473G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668289 | ||||||
chr2:186668361
|
G | T | 1 | a0001c0001t0001g0203 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2434-401G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668361 | ||||||
chr2:186668641
|
C | T | 79 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(76): Show | 81 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.2434-121C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 24/29 | chr2 | 186668641 | ||||||
chr2:186669014
|
T | C | 110 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0016others(107): Show | 110 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.2592+94T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 25/29 | chr2 | 186669014 | ||||||
chr2:186669032
|
T | C | 1 | a0001c0001t0001g0215 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2592+112T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 25/29 | chr2 | 186669032 | ||||||
chr2:186669131
|
A | G | 1 | a0001c0001t0019g0029 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2592+211A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 25/29 | chr2 | 186669131 | ||||||
chr2:186669388
|
A | T | 9 | a0001c0001t0005g0087a0001c0001t0005g0088a0001c0001t0005g0089others(6): Show | 9 | HG01081.hp1 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2593-313A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 25/29 | chr2 | 186669388 | ||||||
chr2:186669456
|
T | G | 79 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0027others(76): Show | 83 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.2593-245T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 25/29 | chr2 | 186669456 | ||||||
chr2:186669498
|
A | T | 1 | a0001c0001t0002g0110 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2593-203A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 25/29 | chr2 | 186669498 | ||||||
chr2:186669859
|
T | C | 1 | a0001c0001t0001g0193 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2706+45T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186669859 | ||||||
chr2:186669984
|
A | G | 1 | a0001c0001t0001g0197 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2706+170A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186669984 | ||||||
chr2:186670051
|
C | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0227 | 3 | HG02083.hp1 HG02155.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.2706+237C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186670051 | ||||||
chr2:186670292
|
T | TTTTG | 79 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(76): Show | 81 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.2706+498_2706+501d others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr2 | 186670292 | |||||
chr2:186670335
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2706+521T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186670335 | ||||||
chr2:186670352
|
G | A | 1 | a0001c0001t0002g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2706+538G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186670352 | ||||||
chr2:186670544
|
G | A | 14 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0101others(11): Show | 15 | HG01168.hp2 HG01255.hp2 HG01517.hp2 others(12): Show |
intron_variant | MODIFIER | c.2706+730G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186670544 | ||||||
chr2:186670607
|
A | G | 1 | a0001c0008t0020g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2706+793A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186670607 | ||||||
chr2:186670616
|
A | T | 3 | a0001c0001t0006g0149a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2706+802A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186670616 | ||||||
chr2:186671088
|
A | C | 4 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0287others(1): Show | 4 | HG02896.hp1 HG02897.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2706+1274A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671088 | ||||||
chr2:186671144
|
G | C | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0286 | 3 | HG03130.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2706+1330G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671144 | ||||||
chr2:186671423
|
T | A | 1 | a0001c0001t0001g0079 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2706+1609T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671423 | ||||||
chr2:186671428
|
C | T | 93 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0016others(90): Show | 93 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.2706+1614C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671428 | ||||||
chr2:186671472
|
C | T | 2 | a0001c0001t0002g0066a0001c0001t0002g0067 | 2 | NA18940.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2706+1658C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671472 | ||||||
chr2:186671582
|
C | T | 1 | a0001c0001t0001g0208 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2706+1768C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671582 | ||||||
chr2:186671640
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2706+1826A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671640 | ||||||
chr2:186671921
|
A | G | 2 | a0001c0001t0011g0051a0001c0001t0011g0072 | 2 | HG02970.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2706+2107A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671921 | ||||||
chr2:186671938
|
A | G | 2 | a0001c0001t0002g0084a0001c0001t0002g0085 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2706+2124A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671938 | ||||||
chr2:186671945
|
C | CT | 105 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0101others(102): Show | 108 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.2706+2147dupT | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr2 | 186671945 | |||||
chr2:186671945
|
C | CTT | 164 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0016others(161): Show | 167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.2706+2146_2706+214 others(6): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr2 | 186671945 | |||||
chr2:186671962
|
C | G | 1 | a0001c0001t0002g0059 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2706+2148C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186671962 | ||||||
chr2:186672045
|
G | A | 4 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 4 | HG01891.hp1 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.2706+2231G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186672045 | ||||||
chr2:186672201
|
C | T | 1 | a0001c0001t0003g0290 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2706+2387C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186672201 | ||||||
chr2:186672695
|
C | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0119a0001c0001t0001g0136 | 3 | HG01168.hp2 HG01255.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.2706+2881C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186672695 | ||||||
chr2:186672806
|
A | G | 2 | a0001c0001t0001g0120a0001c0001t0001g0121 | 2 | HG02698.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.2707-2798A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186672806 | ||||||
chr2:186672977
|
T | A | 3 | a0001c0001t0006g0149a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2707-2627T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186672977 | ||||||
chr2:186673009
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2707-2595T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186673009 | ||||||
chr2:186673120
|
T | C | 77 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(74): Show | 79 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.2707-2484T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186673120 | ||||||
chr2:186673243
|
T | C | 2 | a0001c0001t0017g0092a0001c0001t0024g0109 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2707-2361T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186673243 | ||||||
chr2:186673546
|
GTTTA | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0286 | 3 | HG03130.hp2 HG03195.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2707-2051_2707-204 others(8): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr2 | 186673546 | |||||
chr2:186673619
|
T | A | 9 | a0001c0001t0005g0087a0001c0001t0005g0088a0001c0001t0005g0089others(6): Show | 9 | HG01081.hp1 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2707-1985T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186673619 | ||||||
chr2:186673619
|
T | C | 265 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(262): Show | 271 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.2707-1985T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186673619 | ||||||
chr2:186673756
|
C | T | 1 | a0001c0001t0002g0015 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2707-1848C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186673756 | ||||||
chr2:186673935
|
T | A | 1 | a0001c0001t0003g0167 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2707-1669T>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186673935 | ||||||
chr2:186673937
|
C | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0079 | 2 | HG00738.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2707-1667C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186673937 | ||||||
chr2:186674058
|
C | T | 3 | a0001c0001t0006g0149a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2707-1546C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674058 | ||||||
chr2:186674253
|
G | T | 1 | a0001c0001t0001g0181 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2707-1351G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674253 | ||||||
chr2:186674360
|
G | C | 2 | a0001c0001t0006g0276a0001c0001t0006g0277 | 2 | HG03130.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2707-1244G>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674360 | ||||||
chr2:186674453
|
A | C | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG02145.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2707-1151A>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674453 | ||||||
chr2:186674488
|
C | G | 1 | a0001c0001t0002g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2707-1116C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674488 | ||||||
chr2:186674502
|
A | T | 1 | a0001c0001t0003g0251 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2707-1102A>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674502 | ||||||
chr2:186674590
|
C | A | 1 | a0001c0008t0020g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2707-1014C>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674590 | ||||||
chr2:186674628
|
T | C | 274 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0013others(271): Show | 280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.2707-976T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674628 | ||||||
chr2:186674735
|
C | T | 4 | a0002c0002t0001g0141a0002c0002t0001g0142a0002c0002t0022g0098others(1): Show | 4 | HG01099.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2707-869C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674735 | ||||||
chr2:186674754
|
C | G | 5 | a0001c0001t0005g0087a0001c0001t0005g0088a0001c0001t0005g0089others(2): Show | 5 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.2707-850C>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674754 | ||||||
chr2:186674850
|
C | T | 1 | a0001c0001t0002g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2707-754C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674850 | ||||||
chr2:186674951
|
A | G | 1 | a0002c0002t0007g0139 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2707-653A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674951 | ||||||
chr2:186674994
|
G | A | 52 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0008others(49): Show | 55 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.2707-610G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186674994 | ||||||
chr2:186675133
|
C | T | 1 | a0001c0001t0001g0237 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2707-471C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186675133 | ||||||
chr2:186675353
|
C | T | 1 | a0002c0002t0022g0098 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2707-251C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186675353 | ||||||
chr2:186675429
|
C | T | 1 | a0001c0001t0003g0245 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2707-175C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 26/29 | chr2 | 186675429 | ||||||
chr2:186675742
|
G | A | 1 | a0001c0001t0002g0159 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2820+25G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 27/29 | chr2 | 186675742 | ||||||
chr2:186675757
|
G | A | 1 | a0001c0001t0015g0271 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2820+40G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 27/29 | chr2 | 186675757 | ||||||
chr2:186676005
|
G | A | 141 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(138): Show | 146 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.2928+78G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676005 | ||||||
chr2:186676198
|
G | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG02257.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2928+271G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676198 | ||||||
chr2:186676240
|
G | T | 51 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0008others(48): Show | 54 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.2928+313G>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676240 | ||||||
chr2:186676271
|
G | A | 9 | a0001c0001t0005g0087a0001c0001t0005g0088a0001c0001t0005g0089others(6): Show | 9 | HG01081.hp1 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.2928+344G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676271 | ||||||
chr2:186676385
|
T | C | 5 | a0001c0001t0005g0087a0001c0001t0005g0088a0001c0001t0005g0089others(2): Show | 5 | HG02622.hp1 HG02809.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.2929-428T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676385 | ||||||
chr2:186676403
|
A | G | 3 | a0001c0001t0006g0149a0001c0001t0006g0276a0001c0001t0006g0277 | 3 | HG03130.hp1 HG03139.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2929-410A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676403 | ||||||
chr2:186676408
|
C | T | 2 | a0001c0001t0003g0234a0001c0001t0003g0256 | 2 | HG02486.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2929-405C>T | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676408 | ||||||
chr2:186676480
|
T | G | 1 | a0001c0001t0002g0078 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2929-333T>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676480 | ||||||
chr2:186676529
|
G | A | 1 | a0001c0001t0003g0248 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2929-284G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676529 | ||||||
chr2:186676589
|
A | G | 1 | a0001c0001t0002g0018 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2929-224A>G | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676589 | ||||||
chr2:186676591
|
G | A | 141 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(138): Show | 146 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.2929-222G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676591 | ||||||
chr2:186676650
|
G | A | 77 | a0001c0001t0002g0002a0001c0001t0002g0003a0001c0001t0002g0009others(74): Show | 79 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.2929-163G>A | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 28/29 | chr2 | 186676650 | ||||||
chr2:186676953
|
AAAG | A | 3 | a0001c0001t0001g0196a0001c0001t0001g0231a0001c0001t0001g0232 | 3 | HG02056.hp1 NA18951.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.3051+22_3051+24del others(3): Show |
ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 29/29 | INFO_REALIGN_3_PRIME | chr2 | 186676953 | |||||
chr2:186677083
|
T | C | 51 | a0001c0001t0003g0004a0001c0001t0003g0006a0001c0001t0003g0008others(48): Show | 54 | HG00280.hp1 HG00408.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.3052-114T>C | ITGAV | ENSG00000138448.13 | transcript | ENST00000261023.8 | protein_coding | 29/29 | chr2 | 186677083 |