Item | Value |
---|---|
geneid | 9669 |
ensemblid | ENSG00000158417.12 |
hgncid | 30793 |
symbol | EIF5B |
name | eukaryotic translation initiation factor 5B |
refseq_nuc | NM_015904.4 |
refseq_prot | NP_056988.3 |
ensembl_nuc | ENST00000289371.11 |
ensembl_prot | ENSP00000289371.5 |
mane_status | MANE Select |
chr | chr2 |
start | 99337389 |
end | 99401326 |
strand | + |
ver | v1.2 |
region | chr2:99337389-99401326 |
region5000 | chr2:99332389-99406326 |
regionname0 | EIF5B_chr2_99337389_99401326 |
regionname5000 | EIF5B_chr2_99332389_99406326 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1220 | 229 | 64 | 58 | 75 | 9 | 23 | 62 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0002 | 1/1 | 1220 | 110 | 17 | 16 | 63 | 1 | 11 | 46 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0003 | 0/0 | 1220 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0004 | 0/0 | 1220 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0005 | 0/0 | 1220 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 3663 | 108 | 16 | 16 | 63 | 1 | 10 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
c0002 | 0/0 | 3663 | 94 | 12 | 25 | 51 | 2 | 4 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
c0003 | 0/0 | 3663 | 79 | 40 | 7 | 19 | 2 | 11 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
c0004 | 0/0 | 3663 | 44 | 8 | 22 | 3 | 4 | 7 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
c0005 | 0/0 | 3663 | 6 | 0 | 4 | 1 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
c0006 | 0/0 | 3663 | 3 | 2 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
c0007 | 0/0 | 3663 | 2 | 1 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
c0008 | 0/0 | 3663 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
c0009 | 0/0 | 3663 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
c0010 | 0/0 | 3663 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
c0011 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
c0012 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
c0013 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2079 | 95 | 12 | 34 | 34 | 5 | 10 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0002 | 1/1 | 2079 | 84 | 19 | 15 | 38 | 1 | 9 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0003 | 0/0 | 2075 | 47 | 6 | 17 | 22 | 1 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0004 | 0/0 | 2079 | 38 | 16 | 2 | 9 | 3 | 8 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0005 | 0/0 | 2079 | 32 | 1 | 5 | 24 | 0 | 2 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0006 | 0/0 | 2083 | 7 | 7 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0007 | 0/0 | 2075 | 6 | 0 | 0 | 6 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0008 | 0/0 | 2079 | 5 | 0 | 0 | 5 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0009 | 0/0 | 2063 | 5 | 5 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0010 | 0/0 | 2063 | 4 | 4 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0011 | 0/0 | 2079 | 3 | 3 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0012 | 0/0 | 2095 | 2 | 0 | 0 | 0 | 0 | 2 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0013 | 0/0 | 2027 | 2 | 2 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0014 | 0/0 | 2083 | 2 | 2 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0015 | 0/0 | 2079 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0016 | 0/0 | 2075 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0017 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0018 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0019 | 0/0 | 2079 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0020 | 0/0 | 2079 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0021 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0022 | 0/0 | 2083 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0023 | 0/0 | 2079 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
t0024 | 0/0 | 2079 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 0 | 6 | 3 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0002 | 0/0 | 5 | 1 | 2 | 0 | 1 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0239 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 3663 | 94 | 12 | 25 | 51 | 2 | 4 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0003 | 0/0 | 3663 | 79 | 40 | 7 | 19 | 2 | 11 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0004 | 0/0 | 3663 | 44 | 8 | 22 | 3 | 4 | 7 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0005 | 0/0 | 3663 | 6 | 0 | 4 | 1 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0006 | 0/0 | 3663 | 3 | 2 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0009 | 0/0 | 3663 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0011 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0012 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0002c0001 | 1/1 | 3663 | 108 | 16 | 16 | 63 | 1 | 10 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0002c0007 | 0/0 | 3663 | 2 | 1 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0003c0010 | 0/0 | 3663 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0004c0008 | 0/0 | 3663 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0005c0013 | 0/0 | 3663 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 5741 | 36 | 1 | 7 | 24 | 1 | 3 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0002t0003 | 0/0 | 5737 | 46 | 6 | 17 | 21 | 1 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0002t0007 | 0/0 | 5737 | 6 | 0 | 0 | 6 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0002t0010 | 0/0 | 5725 | 4 | 4 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0002t0016 | 0/0 | 5737 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0002t0023 | 0/0 | 5741 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0003t0001 | 0/0 | 5741 | 21 | 10 | 5 | 5 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0003t0002 | 0/0 | 5741 | 2 | 2 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0003t0004 | 0/0 | 5741 | 34 | 13 | 2 | 9 | 2 | 8 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0003t0008 | 0/0 | 5741 | 5 | 0 | 0 | 5 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0003t0009 | 0/0 | 5725 | 5 | 5 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0003t0011 | 0/0 | 5741 | 3 | 3 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0003t0012 | 0/0 | 5757 | 2 | 0 | 0 | 0 | 0 | 2 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0003t0013 | 0/0 | 5689 | 2 | 2 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0003t0014 | 0/0 | 5745 | 2 | 2 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0003t0017 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0003t0021 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0003t0024 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0004t0001 | 0/0 | 5741 | 36 | 1 | 22 | 3 | 4 | 6 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0004t0006 | 0/0 | 5745 | 7 | 7 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0004t0015 | 0/0 | 5741 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0005t0002 | 0/0 | 5741 | 6 | 0 | 4 | 1 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0006t0004 | 0/0 | 5741 | 3 | 2 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0009t0001 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0011t0022 | 0/0 | 5745 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0001c0012t0002 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0002c0001t0002 | 1/1 | 5741 | 75 | 16 | 11 | 37 | 1 | 8 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0002c0001t0005 | 0/0 | 5741 | 30 | 0 | 5 | 24 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0002c0001t0018 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0002c0001t0019 | 0/0 | 5741 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0002c0001t0020 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0002c0007t0005 | 0/0 | 5741 | 2 | 1 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0003c0010t0003 | 0/0 | 5737 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0004c0008t0001 | 0/0 | 5741 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
a0005c0013t0004 | 0/0 | 5741 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | copy fasta | chr2 | 99332389 | 99406326 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0001 | 0/0 | 9 | 0 | 6 | 3 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0007g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0007g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0007g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0007g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0010g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0010g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0010g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0010g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0016g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0002t0023g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0002g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0008g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0008g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0009g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0009g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0009g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0009g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0009g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0011g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0011g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0012g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0012g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0013g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0013g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0014g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0014g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0017g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0021g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0003t0024g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0002 | 0/0 | 5 | 1 | 2 | 0 | 1 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0006g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0006g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0004t0015g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0005t0002g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0005t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0005t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0005t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0005t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0006t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0006t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0006t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0009t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0011t0022g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0001c0012t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0239 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0018g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0019g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0001t0020g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0007t0005g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0002c0007t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0003c0010t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0004c0008t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
a0005c0013t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0004 | t0001 | g0022 | EUR | GBR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00140 | hp2 | a0001 | c0002 | t0003 | g0175 | EUR | GBR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00280 | hp1 | a0001 | c0003 | t0004 | g0054 | EUR | FIN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00280 | hp2 | a0001 | c0004 | t0001 | g0088 | EUR | FIN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00408 | hp1 | a0002 | c0001 | t0002 | g0258 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00408 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00423 | hp1 | a0002 | c0001 | t0002 | g0249 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00438 | hp1 | a0002 | c0001 | t0002 | g0215 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00438 | hp2 | a0002 | c0001 | t0005 | g0234 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00544 | hp1 | a0002 | c0001 | t0005 | g0227 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00544 | hp2 | a0001 | c0004 | t0001 | g0081 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00558 | hp1 | a0002 | c0001 | t0005 | g0199 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00558 | hp2 | a0002 | c0001 | t0002 | g0264 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00609 | hp2 | a0001 | c0003 | t0001 | g0076 | EAS | CHS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00639 | hp1 | a0001 | c0002 | t0003 | g0161 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00639 | hp2 | a0002 | c0001 | t0002 | g0268 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00642 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00642 | hp2 | a0001 | c0003 | t0001 | g0009 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0148 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00733 | hp2 | a0001 | c0004 | t0001 | g0104 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00735 | hp1 | a0001 | c0002 | t0003 | g0173 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00735 | hp2 | a0001 | c0004 | t0001 | g0002 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0012 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00738 | hp2 | a0002 | c0001 | t0002 | g0259 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00741 | hp1 | a0001 | c0004 | t0001 | g0091 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG00741 | hp2 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01070 | hp1 | a0001 | c0004 | t0001 | g0087 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01070 | hp2 | a0001 | c0005 | t0002 | g0021 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01071 | hp1 | a0001 | c0005 | t0002 | g0021 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01071 | hp2 | a0001 | c0004 | t0001 | g0089 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01099 | hp1 | a0002 | c0001 | t0002 | g0251 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01099 | hp2 | a0001 | c0004 | t0001 | g0078 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01106 | hp1 | a0001 | c0004 | t0001 | g0086 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01106 | hp2 | a0001 | c0002 | t0001 | g0157 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01109 | hp1 | a0001 | c0002 | t0003 | g0172 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01109 | hp2 | a0001 | c0004 | t0001 | g0103 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01168 | hp1 | a0001 | c0003 | t0004 | g0036 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01168 | hp2 | a0001 | c0004 | t0001 | g0084 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01175 | hp1 | a0002 | c0001 | t0002 | g0270 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01175 | hp2 | a0001 | c0004 | t0001 | g0098 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01192 | hp1 | a0002 | c0001 | t0005 | g0231 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0155 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01243 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0026 | AMR | PUR | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01255 | hp1 | a0002 | c0001 | t0002 | g0210 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0141 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01256 | hp1 | a0001 | c0004 | t0001 | g0101 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01256 | hp2 | a0002 | c0001 | t0005 | g0275 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01258 | hp1 | a0001 | c0004 | t0001 | g0002 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01258 | hp2 | a0002 | c0001 | t0005 | g0276 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01261 | hp1 | a0001 | c0004 | t0001 | g0095 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01261 | hp2 | a0002 | c0001 | t0002 | g0219 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01346 | hp1 | a0001 | c0002 | t0023 | g0147 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01346 | hp2 | a0002 | c0001 | t0002 | g0269 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01358 | hp1 | a0001 | c0005 | t0002 | g0298 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01358 | hp2 | a0001 | c0003 | t0004 | g0020 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01361 | hp1 | a0001 | c0003 | t0001 | g0071 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01361 | hp2 | a0001 | c0002 | t0003 | g0170 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01433 | hp1 | a0001 | c0002 | t0001 | g0131 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01433 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01496 | hp1 | a0001 | c0002 | t0003 | g0004 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01496 | hp2 | a0001 | c0005 | t0002 | g0296 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01516 | hp1 | a0002 | c0001 | t0002 | g0213 | EUR | IBS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01516 | hp2 | a0001 | c0006 | t0004 | g0044 | EUR | IBS | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01884 | hp1 | a0002 | c0001 | t0002 | g0209 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0121 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01891 | hp1 | a0001 | c0003 | t0014 | g0033 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01891 | hp2 | a0001 | c0003 | t0004 | g0294 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01934 | hp1 | a0001 | c0004 | t0001 | g0097 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01934 | hp2 | a0002 | c0001 | t0002 | g0019 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01943 | hp1 | a0001 | c0004 | t0001 | g0102 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01943 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01952 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01952 | hp2 | a0001 | c0004 | t0001 | g0099 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01975 | hp1 | a0001 | c0002 | t0003 | g0174 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01975 | hp2 | a0002 | c0001 | t0002 | g0245 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01978 | hp1 | a0002 | c0001 | t0002 | g0262 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01978 | hp2 | a0001 | c0004 | t0001 | g0085 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01981 | hp1 | a0001 | c0002 | t0003 | g0171 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01981 | hp2 | a0002 | c0001 | t0005 | g0232 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01993 | hp1 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01993 | hp2 | a0001 | c0004 | t0001 | g0077 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02004 | hp1 | a0001 | c0004 | t0001 | g0005 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02004 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02027 | hp1 | a0001 | c0003 | t0004 | g0056 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02027 | hp2 | a0002 | c0001 | t0005 | g0281 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02040 | hp1 | a0002 | c0001 | t0005 | g0284 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02040 | hp2 | a0001 | c0002 | t0003 | g0162 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02055 | hp1 | a0001 | c0003 | t0001 | g0066 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02055 | hp2 | a0001 | c0011 | t0022 | g0304 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0137 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02080 | hp2 | a0001 | c0002 | t0007 | g0184 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0151 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02083 | hp2 | a0002 | c0001 | t0005 | g0018 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02132 | hp1 | a0002 | c0001 | t0002 | g0272 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02132 | hp2 | a0002 | c0001 | t0005 | g0223 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02135 | hp1 | a0001 | c0003 | t0004 | g0059 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02135 | hp2 | a0002 | c0001 | t0002 | g0289 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02145 | hp1 | a0001 | c0006 | t0004 | g0062 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02145 | hp2 | a0002 | c0001 | t0002 | g0271 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02148 | hp1 | a0001 | c0003 | t0001 | g0111 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02148 | hp2 | a0001 | c0004 | t0001 | g0005 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02165 | hp1 | a0001 | c0009 | t0001 | g0156 | EAS | CDX | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02165 | hp2 | a0002 | c0001 | t0002 | g0212 | EAS | CDX | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02257 | hp1 | a0001 | c0003 | t0013 | g0072 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02257 | hp2 | a0001 | c0003 | t0004 | g0007 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02258 | hp1 | a0001 | c0012 | t0002 | g0278 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02258 | hp2 | a0001 | c0004 | t0001 | g0002 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02273 | hp1 | a0001 | c0002 | t0003 | g0163 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02273 | hp2 | a0002 | c0001 | t0002 | g0019 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02280 | hp1 | a0001 | c0004 | t0006 | g0110 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02280 | hp2 | a0001 | c0003 | t0002 | g0305 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02293 | hp1 | a0001 | c0004 | t0001 | g0005 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02293 | hp2 | a0001 | c0002 | t0003 | g0001 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02300 | hp1 | a0001 | c0004 | t0001 | g0105 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02300 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | PEL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02523 | hp1 | a0002 | c0001 | t0018 | g0193 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02523 | hp2 | a0002 | c0001 | t0002 | g0243 | EAS | KHV | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02572 | hp1 | a0002 | c0001 | t0002 | g0282 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02572 | hp2 | a0001 | c0002 | t0003 | g0128 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02615 | hp1 | a0001 | c0006 | t0004 | g0045 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0069 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02630 | hp1 | a0001 | c0003 | t0004 | g0040 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02630 | hp2 | a0001 | c0002 | t0010 | g0123 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02647 | hp1 | a0001 | c0003 | t0004 | g0291 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02647 | hp2 | a0002 | c0001 | t0002 | g0192 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02683 | hp1 | a0001 | c0004 | t0001 | g0002 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02683 | hp2 | a0001 | c0003 | t0004 | g0047 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02698 | hp1 | a0002 | c0001 | t0002 | g0252 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02698 | hp2 | a0001 | c0004 | t0001 | g0092 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02717 | hp1 | a0001 | c0002 | t0010 | g0122 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02717 | hp2 | a0002 | c0001 | t0002 | g0207 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02723 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02723 | hp2 | a0001 | c0003 | t0004 | g0008 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02735 | hp1 | a0001 | c0004 | t0001 | g0093 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02735 | hp2 | a0002 | c0001 | t0002 | g0211 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02738 | hp1 | a0002 | c0001 | t0002 | g0261 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02738 | hp2 | a0001 | c0002 | t0001 | g0152 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02809 | hp1 | a0001 | c0003 | t0001 | g0119 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02809 | hp2 | a0001 | c0003 | t0011 | g0024 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02818 | hp1 | a0001 | c0003 | t0004 | g0007 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02818 | hp2 | a0001 | c0003 | t0009 | g0029 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02886 | hp1 | a0002 | c0001 | t0002 | g0286 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02886 | hp2 | a0001 | c0003 | t0024 | g0037 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02895 | hp1 | a0001 | c0003 | t0001 | g0112 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02895 | hp2 | a0001 | c0003 | t0011 | g0023 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02896 | hp1 | a0001 | c0003 | t0009 | g0027 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02896 | hp2 | a0001 | c0002 | t0010 | g0125 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02897 | hp1 | a0001 | c0003 | t0009 | g0028 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0113 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02922 | hp1 | a0001 | c0004 | t0006 | g0106 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02922 | hp2 | a0001 | c0003 | t0004 | g0292 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02965 | hp1 | a0002 | c0001 | t0002 | g0283 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02965 | hp2 | a0001 | c0003 | t0002 | g0034 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02976 | hp1 | a0001 | c0003 | t0011 | g0025 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02976 | hp2 | a0002 | c0001 | t0002 | g0235 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03017 | hp1 | a0001 | c0003 | t0004 | g0055 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03017 | hp2 | a0002 | c0001 | t0019 | g0236 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0074 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03041 | hp2 | a0001 | c0002 | t0003 | g0127 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03098 | hp1 | a0005 | c0013 | t0004 | g0295 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03098 | hp2 | a0001 | c0004 | t0006 | g0108 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03130 | hp1 | a0001 | c0003 | t0004 | g0293 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03130 | hp2 | a0001 | c0004 | t0006 | g0010 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03209 | hp1 | a0001 | c0003 | t0001 | g0070 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03209 | hp2 | a0002 | c0001 | t0002 | g0205 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03239 | hp1 | a0001 | c0004 | t0015 | g0096 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03239 | hp2 | a0001 | c0003 | t0004 | g0035 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03453 | hp1 | a0001 | c0003 | t0004 | g0046 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03453 | hp2 | a0001 | c0002 | t0003 | g0126 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03486 | hp1 | a0001 | c0003 | t0013 | g0073 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03486 | hp2 | a0002 | c0001 | t0002 | g0277 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03490 | hp1 | a0001 | c0003 | t0004 | g0051 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03490 | hp2 | a0002 | c0001 | t0005 | g0224 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03491 | hp1 | a0002 | c0001 | t0002 | g0253 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03491 | hp2 | a0001 | c0003 | t0012 | g0063 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03516 | hp1 | a0002 | c0001 | t0002 | g0206 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03516 | hp2 | a0001 | c0003 | t0017 | g0120 | AFR | ESN | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03540 | hp1 | a0002 | c0001 | t0002 | g0208 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03540 | hp2 | a0001 | c0003 | t0004 | g0020 | AFR | GWD | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03579 | hp1 | a0001 | c0002 | t0003 | g0134 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03579 | hp2 | a0001 | c0003 | t0004 | g0049 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03669 | hp1 | a0001 | c0003 | t0004 | g0048 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03669 | hp2 | a0001 | c0003 | t0001 | g0116 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03688 | hp1 | a0001 | c0004 | t0001 | g0090 | SAS | STU | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03688 | hp2 | a0002 | c0001 | t0002 | g0301 | SAS | STU | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03710 | hp1 | a0001 | c0004 | t0001 | g0094 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03710 | hp2 | a0002 | c0001 | t0002 | g0216 | SAS | PJL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0140 | SAS | BEB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03834 | hp2 | a0001 | c0004 | t0001 | g0083 | SAS | BEB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03927 | hp1 | a0002 | c0001 | t0002 | g0287 | SAS | BEB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03927 | hp2 | a0001 | c0005 | t0002 | g0297 | SAS | BEB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG04115 | hp1 | a0002 | c0001 | t0002 | g0237 | SAS | STU | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG04115 | hp2 | a0001 | c0003 | t0004 | g0038 | SAS | STU | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG04184 | hp1 | a0001 | c0003 | t0004 | g0052 | SAS | BEB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG04184 | hp2 | a0001 | c0002 | t0003 | g0182 | SAS | BEB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG04199 | hp1 | a0002 | c0007 | t0005 | g0230 | SAS | STU | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG04199 | hp2 | a0001 | c0003 | t0004 | g0065 | SAS | STU | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18522 | hp1 | a0001 | c0004 | t0006 | g0109 | AFR | YRI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18522 | hp2 | a0001 | c0002 | t0010 | g0124 | AFR | YRI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18612 | hp1 | a0001 | c0002 | t0003 | g0015 | EAS | CHB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18612 | hp2 | a0002 | c0001 | t0002 | g0255 | EAS | CHB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0067 | AFR | YRI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18906 | hp2 | a0001 | c0003 | t0009 | g0030 | AFR | YRI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18939 | hp1 | a0001 | c0003 | t0008 | g0003 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18939 | hp2 | a0002 | c0001 | t0005 | g0233 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18940 | hp1 | a0001 | c0002 | t0003 | g0188 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18940 | hp2 | a0002 | c0001 | t0002 | g0204 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18941 | hp1 | a0001 | c0003 | t0008 | g0003 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18941 | hp2 | a0001 | c0002 | t0007 | g0185 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18942 | hp2 | a0002 | c0001 | t0002 | g0250 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18944 | hp1 | a0002 | c0001 | t0002 | g0248 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18944 | hp2 | a0002 | c0001 | t0005 | g0196 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18945 | hp1 | a0001 | c0003 | t0008 | g0003 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18945 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18947 | hp1 | a0002 | c0001 | t0005 | g0203 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18947 | hp2 | a0001 | c0002 | t0003 | g0165 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18948 | hp1 | a0002 | c0001 | t0005 | g0195 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18948 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18949 | hp1 | a0002 | c0001 | t0002 | g0225 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18949 | hp2 | a0004 | c0008 | t0001 | g0149 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18950 | hp1 | a0003 | c0010 | t0003 | g0159 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18950 | hp2 | a0002 | c0001 | t0005 | g0017 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18951 | hp1 | a0002 | c0001 | t0002 | g0260 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18951 | hp2 | a0001 | c0002 | t0003 | g0015 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18952 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18952 | hp2 | a0002 | c0001 | t0005 | g0017 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18954 | hp1 | a0001 | c0002 | t0003 | g0168 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18954 | hp2 | a0001 | c0003 | t0008 | g0003 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18956 | hp1 | a0002 | c0001 | t0002 | g0263 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18957 | hp1 | a0001 | c0002 | t0003 | g0181 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18957 | hp2 | a0002 | c0001 | t0002 | g0240 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0153 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18960 | hp2 | a0001 | c0003 | t0001 | g0114 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18962 | hp2 | a0002 | c0001 | t0002 | g0246 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18964 | hp1 | a0001 | c0002 | t0003 | g0160 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18964 | hp2 | a0002 | c0001 | t0002 | g0303 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18966 | hp1 | a0001 | c0002 | t0003 | g0164 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18966 | hp2 | a0002 | c0001 | t0002 | g0241 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18968 | hp1 | a0001 | c0002 | t0003 | g0177 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18968 | hp2 | a0001 | c0002 | t0001 | g0130 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18971 | hp1 | a0001 | c0003 | t0004 | g0058 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18971 | hp2 | a0002 | c0001 | t0002 | g0221 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18972 | hp1 | a0002 | c0001 | t0005 | g0220 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18972 | hp2 | a0001 | c0002 | t0003 | g0189 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18978 | hp1 | a0002 | c0001 | t0005 | g0194 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18978 | hp2 | a0001 | c0003 | t0004 | g0043 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18979 | hp1 | a0001 | c0003 | t0004 | g0060 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18979 | hp2 | a0002 | c0001 | t0002 | g0257 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18983 | hp2 | a0002 | c0001 | t0002 | g0288 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18985 | hp1 | a0002 | c0001 | t0002 | g0238 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18985 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18986 | hp1 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18986 | hp2 | a0001 | c0002 | t0007 | g0178 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18987 | hp2 | a0002 | c0001 | t0005 | g0228 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18988 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18988 | hp2 | a0002 | c0001 | t0005 | g0202 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18989 | hp1 | a0001 | c0003 | t0001 | g0118 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18989 | hp2 | a0001 | c0003 | t0004 | g0039 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18990 | hp2 | a0002 | c0001 | t0005 | g0201 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18991 | hp1 | a0002 | c0001 | t0005 | g0279 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18991 | hp2 | a0001 | c0002 | t0003 | g0167 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18992 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18992 | hp2 | a0002 | c0001 | t0002 | g0214 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18993 | hp1 | a0002 | c0001 | t0002 | g0247 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18994 | hp1 | a0002 | c0001 | t0005 | g0222 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18994 | hp2 | a0002 | c0001 | t0002 | g0197 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18995 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18995 | hp2 | a0002 | c0001 | t0002 | g0290 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18998 | hp1 | a0002 | c0001 | t0002 | g0191 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA18998 | hp2 | a0001 | c0003 | t0004 | g0042 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19002 | hp1 | a0001 | c0002 | t0003 | g0180 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19002 | hp2 | a0002 | c0001 | t0005 | g0229 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19005 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19005 | hp2 | a0002 | c0001 | t0005 | g0018 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19006 | hp1 | a0001 | c0004 | t0001 | g0079 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19006 | hp2 | a0001 | c0002 | t0003 | g0166 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19010 | hp1 | a0002 | c0001 | t0002 | g0266 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19010 | hp2 | a0001 | c0002 | t0007 | g0186 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19011 | hp1 | a0001 | c0002 | t0003 | g0016 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19030 | hp1 | a0001 | c0003 | t0004 | g0050 | AFR | LWK | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19030 | hp2 | a0001 | c0002 | t0016 | g0135 | AFR | LWK | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19043 | hp1 | a0001 | c0003 | t0001 | g0068 | AFR | LWK | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19043 | hp2 | a0001 | c0004 | t0006 | g0010 | AFR | LWK | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19058 | hp1 | a0001 | c0003 | t0004 | g0061 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19058 | hp2 | a0002 | c0001 | t0002 | g0267 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19064 | hp1 | a0002 | c0001 | t0002 | g0242 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19064 | hp2 | a0001 | c0002 | t0003 | g0179 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19065 | hp1 | a0001 | c0004 | t0001 | g0080 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19066 | hp1 | a0001 | c0002 | t0003 | g0169 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19066 | hp2 | a0002 | c0001 | t0002 | g0254 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19072 | hp2 | a0002 | c0001 | t0002 | g0280 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19080 | hp1 | a0002 | c0001 | t0002 | g0265 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19081 | hp1 | a0002 | c0001 | t0005 | g0198 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19081 | hp2 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19083 | hp2 | a0002 | c0001 | t0002 | g0285 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19084 | hp1 | a0001 | c0003 | t0001 | g0117 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19084 | hp2 | a0001 | c0005 | t0002 | g0299 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19086 | hp1 | a0001 | c0003 | t0008 | g0082 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19086 | hp2 | a0002 | c0001 | t0002 | g0256 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19088 | hp1 | a0002 | c0001 | t0005 | g0200 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19088 | hp2 | a0001 | c0002 | t0007 | g0187 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19090 | hp1 | a0001 | c0002 | t0007 | g0183 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19090 | hp2 | a0002 | c0001 | t0002 | g0244 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19091 | hp1 | a0001 | c0003 | t0004 | g0041 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19091 | hp2 | a0002 | c0001 | t0020 | g0226 | EAS | JPT | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19240 | hp1 | a0002 | c0001 | t0002 | g0218 | AFR | YRI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA19240 | hp2 | a0001 | c0002 | t0003 | g0133 | AFR | YRI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA20129 | hp1 | a0002 | c0001 | t0002 | g0300 | AFR | ASW | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA20129 | hp2 | a0001 | c0004 | t0006 | g0107 | AFR | ASW | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0012 | EUR | TSI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA20752 | hp2 | a0001 | c0004 | t0001 | g0002 | EUR | TSI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA20805 | hp1 | a0001 | c0004 | t0001 | g0100 | EUR | TSI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA20805 | hp2 | a0001 | c0003 | t0004 | g0057 | EUR | TSI | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA20905 | hp1 | a0001 | c0002 | t0001 | g0176 | SAS | GIH | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
NA20905 | hp2 | a0001 | c0003 | t0012 | g0064 | SAS | GIH | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01123 | hp1 | a0001 | c0003 | t0001 | g0075 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG01123 | hp2 | a0002 | c0001 | t0005 | g0190 | AMR | CLM | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02109 | hp1 | a0002 | c0001 | t0002 | g0217 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02109 | hp2 | a0001 | c0003 | t0014 | g0032 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02486 | hp1 | a0002 | c0007 | t0005 | g0274 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG02486 | hp2 | a0001 | c0003 | t0004 | g0008 | AFR | ACB | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03471 | hp1 | a0001 | c0003 | t0009 | g0031 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG03471 | hp2 | a0001 | c0003 | t0021 | g0302 | AFR | MSL | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG06807 | hp1 | a0002 | c0001 | t0002 | g0273 | AFR | USA | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
HG06807 | hp2 | a0001 | c0002 | t0003 | g0129 | AFR | USA | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
homoSapiens_chm13v2 | hp1 | a0002 | c0001 | t0002 | g0239 | REF | REF | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
homoSapiens_grch38 | hp1 | a0002 | c0001 | t0002 | g0053 | REF | REF | EIF5B_chr2_99332389_99406326 | EIF5B | chr2 | 99332389 | 99406326 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:99369403
|
A | G | 1 | a0005 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1399A>G | p.Met467Val | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/24 | 1565/5741 | 1399/3663 | 467/1220 | chr2 | 99369403 | ||
chr2:99376359
|
A | C | 4 | a0001a0003a0004others(1): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
missense_variant | MODERATE | c.1565A>C | p.Lys522Thr | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/24 | 1731/5741 | 1565/3663 | 522/1220 | chr2 | 99376359 | ||
chr2:99382168
|
G | A | 1 | a0004 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.2071G>A | p.Glu691Lys | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 13/24 | 2237/5741 | 2071/3663 | 691/1220 | chr2 | 99382168 | ||
chr2:99389826
|
A | G | 1 | a0003 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.2380A>G | p.Ile794Val | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 15/24 | 2546/5741 | 2380/3663 | 794/1220 | chr2 | 99389826 | ||
chr2:99389827
|
T | C | 1 | a0003 | 1 | NA18950.hp1 | missense_variant | MODERATE | c.2381T>C | p.Ile794Thr | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 15/24 | 2547/5741 | 2381/3663 | 794/1220 | chr2 | 99389827 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:99360350
|
G | A | 1 | a0001c0005 | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
synonymous_variant | LOW | c.150G>A | p.Lys50Lys | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 2/24 | 316/5741 | 150/3663 | 50/1220 | chr2 | 99360350 | ||
chr2:99361585
|
G | A | 4 | a0001c0002a0001c0009a0003c0010others(1): Show | 97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
synonymous_variant | LOW | c.684G>A | p.Val228Val | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/24 | 850/5741 | 684/3663 | 228/1220 | chr2 | 99361585 | ||
chr2:99364348
|
G | T | 1 | a0001c0005 | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
synonymous_variant | LOW | c.1215G>T | p.Gly405Gly | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/24 | 1381/5741 | 1215/3663 | 405/1220 | chr2 | 99364348 | ||
chr2:99364399
|
T | C | 1 | a0001c0006 | 3 | HG01516.hp2 HG02145.hp1 HG02615.hp1 |
synonymous_variant | LOW | c.1266T>C | p.Thr422Thr | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/24 | 1432/5741 | 1266/3663 | 422/1220 | chr2 | 99364399 | ||
chr2:99379054
|
C | T | 1 | a0001c0004 | 44 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(41): Show |
synonymous_variant | LOW | c.1878C>T | p.Thr626Thr | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 11/24 | 2044/5741 | 1878/3663 | 626/1220 | chr2 | 99379054 | ||
chr2:99379341
|
T | C | 11 | a0001c0002a0001c0003a0001c0004others(8): Show | 233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
synonymous_variant | LOW | c.1974T>C | p.Asp658Asp | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/24 | 2140/5741 | 1974/3663 | 658/1220 | chr2 | 99379341 | ||
chr2:99390381
|
C | T | 1 | a0001c0009 | 1 | HG02165.hp1 | synonymous_variant | LOW | c.2566C>T | p.Leu856Leu | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 16/24 | 2732/5741 | 2566/3663 | 856/1220 | chr2 | 99390381 | ||
chr2:99394347
|
A | G | 1 | a0001c0005 | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
synonymous_variant | LOW | c.2961A>G | p.Thr987Thr | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 19/24 | 3127/5741 | 2961/3663 | 987/1220 | chr2 | 99394347 | ||
chr2:99394350
|
G | A | 1 | a0001c0011 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.2964G>A | p.Leu988Leu | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 19/24 | 3130/5741 | 2964/3663 | 988/1220 | chr2 | 99394350 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:99337393
|
C | T | 1 | a0001c0003t0024 | 1 | HG02886.hp2 | 5_prime_UTR_variant | MODIFIER | c.-162C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/24 | 162 | chr2 | 99337393 | |||||
chr2:99337496
|
C | G | 1 | a0001c0011t0022 | 1 | HG02055.hp2 | 5_prime_UTR_variant | MODIFIER | c.-59C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/24 | 59 | chr2 | 99337496 | |||||
chr2:99337496
|
C | T | 1 | a0001c0002t0023 | 1 | HG01346.hp1 | 5_prime_UTR_variant | MODIFIER | c.-59C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/24 | 59 | chr2 | 99337496 | |||||
chr2:99399603
|
G | T | 1 | a0001c0003t0011 | 3 | HG02809.hp2 HG02895.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*189G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 189 | chr2 | 99399603 | |||||
chr2:99400024
|
A | G | 1 | a0001c0003t0021 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*610A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 610 | chr2 | 99400024 | |||||
chr2:99400044
|
T | TAAAG | 2 | a0001c0003t0014a0001c0011t0022 | 3 | HG01891.hp1 HG02055.hp2 HG02109.hp2 |
3_prime_UTR_variant | MODIFIER | c.*634_*637dupGAAA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 638 | INFO_REALIGN_3_PRIME | chr2 | 99400044 | ||||
chr2:99400155
|
T | TATCA | 1 | a0001c0004t0006 | 7 | HG02280.hp1 HG02922.hp1 HG03098.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*742_*745dupATCA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 746 | INFO_REALIGN_3_PRIME | chr2 | 99400155 | ||||
chr2:99400191
|
CAGTAGAG others(45): Show |
C | 1 | a0001c0003t0013 | 2 | HG02257.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*830_*881delAGTAGA others(46): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 830 | INFO_REALIGN_3_PRIME | chr2 | 99400191 | ||||
chr2:99400209
|
ATTAATCT others(9): Show |
A | 1 | a0001c0002t0010 | 4 | HG02630.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*815_*830delATCTTG others(10): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 815 | INFO_REALIGN_3_PRIME | chr2 | 99400209 | ||||
chr2:99400250
|
G | C | 19 | a0001c0002t0001a0001c0002t0003a0001c0002t0007others(16): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*836G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 836 | chr2 | 99400250 | |||||
chr2:99400261
|
A | ATTAATCT others(9): Show |
1 | a0001c0003t0012 | 2 | HG03491.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*866_*881dupAATCTT others(10): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 882 | INFO_REALIGN_3_PRIME | chr2 | 99400261 | ||||
chr2:99400261
|
ATTAATCT others(9): Show |
A | 1 | a0001c0003t0009 | 5 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*866_*881delAATCTT others(10): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 866 | INFO_REALIGN_3_PRIME | chr2 | 99400261 | ||||
chr2:99400386
|
G | A | 6 | a0001c0003t0004a0001c0003t0012a0001c0003t0024others(3): Show | 42 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*972G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 972 | chr2 | 99400386 | |||||
chr2:99400407
|
T | A | 1 | a0001c0004t0015 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*993T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 993 | chr2 | 99400407 | |||||
chr2:99400611
|
A | C | 5 | a0001c0003t0008a0002c0001t0005a0002c0001t0018others(2): Show | 39 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1197A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 1197 | chr2 | 99400611 | |||||
chr2:99400718
|
T | A | 1 | a0002c0001t0019 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1304T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 1304 | chr2 | 99400718 | |||||
chr2:99400812
|
C | T | 1 | a0001c0003t0017 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1398C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 1398 | chr2 | 99400812 | |||||
chr2:99400820
|
G | A | 1 | a0002c0001t0020 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1406G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 1406 | chr2 | 99400820 | |||||
chr2:99401051
|
ATAAT | A | 4 | a0001c0002t0003a0001c0002t0007a0001c0002t0016others(1): Show | 54 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1641_*1644delTTAA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 1641 | INFO_REALIGN_3_PRIME | chr2 | 99401051 | ||||
chr2:99401082
|
G | A | 1 | a0001c0002t0007 | 6 | HG02080.hp2 NA18941.hp2 NA18986.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1668G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 1668 | chr2 | 99401082 | |||||
chr2:99401210
|
T | C | 1 | a0001c0002t0016 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1796T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 24/24 | 1796 | chr2 | 99401210 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:99337721
|
A | G | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.35+132A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99337721 | ||||||
chr2:99337727
|
C | T | 1 | a0001c0011t0022g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.35+138C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99337727 | ||||||
chr2:99337789
|
C | G | 1 | a0002c0001t0002g0303 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.35+200C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99337789 | ||||||
chr2:99337809
|
C | T | 1 | a0001c0003t0021g0302 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.35+220C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99337809 | ||||||
chr2:99337813
|
C | CT | 118 | a0001c0003t0004g0020a0001c0003t0004g0291a0001c0003t0004g0292others(115): Show | 123 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(120): Show |
intron_variant | MODIFIER | c.35+224_35+225insT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99337813 | ||||||
chr2:99337878
|
A | T | 78 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(75): Show | 97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.35+289A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99337878 | ||||||
chr2:99337926
|
C | T | 1 | a0001c0003t0017g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.35+337C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99337926 | ||||||
chr2:99337979
|
A | G | 35 | a0001c0002t0001g0176a0001c0002t0003g0001a0001c0002t0003g0004others(32): Show | 48 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.35+390A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99337979 | ||||||
chr2:99338004
|
T | C | 1 | a0001c0004t0001g0022 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.35+415T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338004 | ||||||
chr2:99338052
|
G | A | 4 | a0001c0003t0001g0026a0001c0003t0011g0023a0001c0003t0011g0024others(1): Show | 4 | HG01243.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+463G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338052 | ||||||
chr2:99338141
|
C | T | 1 | a0002c0001t0002g0301 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.35+552C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338141 | ||||||
chr2:99338145
|
A | G | 62 | a0001c0003t0001g0009a0001c0003t0001g0066a0001c0003t0001g0067others(59): Show | 73 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.35+556A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338145 | ||||||
chr2:99338163
|
C | T | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.35+574C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338163 | ||||||
chr2:99338173
|
GT | G | 263 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(260): Show | 297 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(294): Show |
intron_variant | MODIFIER | c.35+593delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338173 | |||||
chr2:99338272
|
C | A | 112 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(109): Show | 116 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.35+683C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338272 | ||||||
chr2:99338584
|
G | A | 11 | a0001c0003t0001g0009a0001c0003t0001g0066a0001c0003t0001g0067others(8): Show | 12 | HG00642.hp2 HG01123.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.35+995G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338584 | ||||||
chr2:99338604
|
T | C | 2 | a0001c0003t0014g0032a0001c0003t0014g0033 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.35+1015T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338604 | ||||||
chr2:99338652
|
A | G | 1 | a0002c0001t0002g0290 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.35+1063A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338652 | ||||||
chr2:99338922
|
G | GTGTA | 98 | a0001c0012t0002g0278a0002c0001t0002g0019a0002c0001t0002g0191others(95): Show | 101 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.35+1334_35+1335ins others(4): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338922 | |||||
chr2:99338922
|
G | GTGTATA | 5 | a0002c0001t0002g0282a0002c0001t0002g0283a0002c0001t0002g0285others(2): Show | 5 | HG02040.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.35+1334_35+1335ins others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338922 | |||||
chr2:99338922
|
G | GTGTATAT others(1): Show |
3 | a0002c0001t0002g0287a0002c0001t0002g0288a0002c0001t0002g0289 | 3 | HG02135.hp2 HG03927.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.35+1334_35+1335ins others(8): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338922 | |||||
chr2:99338922
|
G | GTGTATAT others(17): Show |
3 | a0001c0005t0002g0296a0001c0005t0002g0297a0001c0005t0002g0298 | 3 | HG01358.hp1 HG01496.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.35+1334_35+1335ins others(24): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338922 | |||||
chr2:99338922
|
G | GTGTATAT others(19): Show |
1 | a0001c0005t0002g0021 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.35+1334_35+1335ins others(26): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338922 | |||||
chr2:99338922
|
G | GTGTATAT others(23): Show |
1 | a0001c0005t0002g0299 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.35+1334_35+1335ins others(30): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338922 | |||||
chr2:99338922
|
GTA | G | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.35+1348_35+1349del others(2): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338922 | |||||
chr2:99338929
|
T | TATATATA others(43): Show |
1 | a0001c0004t0001g0077 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.35+1347_35+1348ins others(50): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338929 | |||||
chr2:99338937
|
T | C | 7 | a0001c0004t0001g0077a0001c0005t0002g0021a0001c0005t0002g0296others(4): Show | 8 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.35+1348T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338937 | ||||||
chr2:99338965
|
AAT | A | 113 | a0001c0003t0001g0076a0001c0005t0002g0021a0001c0005t0002g0296others(110): Show | 117 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.35+1388_35+1389del others(2): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338965 | |||||
chr2:99338971
|
T | C | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.35+1382T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338971 | ||||||
chr2:99338975
|
T | C | 1 | a0001c0002t0001g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.35+1386T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338975 | ||||||
chr2:99338981
|
A | T | 1 | a0002c0001t0005g0281 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.35+1392A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338981 | ||||||
chr2:99338989
|
C | T | 1 | a0002c0001t0005g0281 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.35+1400C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99338989 | ||||||
chr2:99338993
|
A | AATATATA others(21): Show |
1 | a0001c0005t0002g0299 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.35+1417_35+1418ins others(28): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338993 | |||||
chr2:99338993
|
A | AATATATA others(23): Show |
2 | a0001c0005t0002g0296a0001c0005t0002g0297 | 2 | HG01496.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.35+1417_35+1418ins others(30): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338993 | |||||
chr2:99338993
|
A | AATATATA others(29): Show |
2 | a0001c0005t0002g0021a0001c0005t0002g0298 | 3 | HG01070.hp2 HG01071.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.35+1417_35+1418ins others(36): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338993 | |||||
chr2:99338993
|
A | AATATATA others(15): Show |
99 | a0002c0001t0002g0019a0002c0001t0002g0192a0002c0001t0002g0197others(96): Show | 102 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.35+1415_35+1416ins others(22): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338993 | |||||
chr2:99338993
|
A | AATATATA others(17): Show |
4 | a0001c0012t0002g0278a0002c0001t0002g0277a0002c0001t0002g0280others(1): Show | 4 | HG02258.hp1 HG03486.hp2 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.35+1415_35+1416ins others(24): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99338993 | |||||
chr2:99339005
|
C | T | 3 | a0002c0001t0002g0191a0002c0001t0005g0275a0002c0001t0005g0276 | 3 | HG01256.hp2 HG01258.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.35+1416C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339005 | ||||||
chr2:99339006
|
A | ACAAATAT others(14): Show |
1 | a0002c0001t0002g0191 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.35+1417_35+1418ins others(21): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339006 | ||||||
chr2:99339006
|
A | ACAAATAT others(16): Show |
2 | a0002c0001t0005g0275a0002c0001t0005g0276 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.35+1417_35+1418ins others(23): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339006 | ||||||
chr2:99339007
|
T | A | 1 | a0002c0001t0002g0191 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.35+1418T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339007 | ||||||
chr2:99339016
|
T | C | 2 | a0001c0003t0014g0032a0001c0003t0014g0033 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.35+1427T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339016 | ||||||
chr2:99339057
|
A | G | 1 | a0001c0003t0001g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.35+1468A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339057 | ||||||
chr2:99339205
|
G | T | 1 | a0002c0007t0005g0274 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.35+1616G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339205 | ||||||
chr2:99339208
|
A | G | 1 | a0001c0002t0003g0189 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.35+1619A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339208 | ||||||
chr2:99339235
|
A | G | 3 | a0001c0003t0004g0065a0001c0003t0012g0063a0001c0003t0012g0064 | 3 | HG03491.hp2 HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.35+1646A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339235 | ||||||
chr2:99339692
|
T | C | 1 | a0001c0004t0001g0078 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.35+2103T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339692 | ||||||
chr2:99339744
|
T | G | 2 | a0001c0003t0014g0032a0001c0003t0014g0033 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.35+2155T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339744 | ||||||
chr2:99339782
|
C | G | 1 | a0001c0011t0022g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.35+2193C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339782 | ||||||
chr2:99339842
|
G | A | 1 | a0002c0001t0002g0192 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.35+2253G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339842 | ||||||
chr2:99339886
|
T | C | 3 | a0001c0003t0009g0027a0001c0003t0009g0028a0001c0003t0009g0029 | 3 | HG02818.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.35+2297T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99339886 | ||||||
chr2:99339911
|
T | TTTG | 4 | a0001c0002t0010g0122a0001c0002t0010g0123a0001c0002t0010g0124others(1): Show | 4 | HG02630.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+2343_35+2345dup others(3): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99339911 | |||||
chr2:99340175
|
G | A | 13 | a0002c0001t0002g0197a0002c0001t0005g0017a0002c0001t0005g0194others(10): Show | 14 | HG00558.hp1 HG02027.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.35+2586G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340175 | ||||||
chr2:99340323
|
A | T | 12 | a0001c0003t0001g0009a0001c0003t0001g0066a0001c0003t0001g0067others(9): Show | 13 | HG00642.hp2 HG01123.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.35+2734A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340323 | ||||||
chr2:99340373
|
A | G | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.35+2784A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340373 | ||||||
chr2:99340413
|
G | T | 1 | a0001c0003t0017g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.35+2824G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340413 | ||||||
chr2:99340452
|
A | G | 14 | a0001c0002t0003g0016a0001c0002t0003g0177a0001c0002t0003g0179others(11): Show | 15 | HG02080.hp2 HG04184.hp2 NA18940.hp1 others(12): Show |
intron_variant | MODIFIER | c.35+2863A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340452 | ||||||
chr2:99340520
|
G | T | 1 | a0001c0002t0001g0158 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.35+2931G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340520 | ||||||
chr2:99340809
|
A | G | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.35+3220A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340809 | ||||||
chr2:99340833
|
G | T | 1 | a0002c0001t0002g0273 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.35+3244G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340833 | ||||||
chr2:99340840
|
A | G | 112 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(109): Show | 116 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.35+3251A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340840 | ||||||
chr2:99340855
|
C | T | 1 | a0002c0001t0002g0286 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.35+3266C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340855 | ||||||
chr2:99340950
|
G | A | 1 | a0001c0002t0001g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.35+3361G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99340950 | ||||||
chr2:99341112
|
G | T | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.35+3523G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99341112 | ||||||
chr2:99341490
|
G | T | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.35+3901G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99341490 | ||||||
chr2:99341501
|
A | G | 1 | a0001c0002t0001g0176 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.35+3912A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99341501 | ||||||
chr2:99341758
|
A | C | 1 | a0002c0001t0002g0272 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.35+4169A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99341758 | ||||||
chr2:99341763
|
G | T | 266 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(263): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.35+4174G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99341763 | ||||||
chr2:99341814
|
G | A | 1 | a0002c0001t0002g0273 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.35+4225G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99341814 | ||||||
chr2:99342233
|
C | CT | 6 | a0001c0003t0001g0026a0001c0003t0011g0023a0001c0003t0011g0024others(3): Show | 6 | HG01243.hp2 HG02145.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.35+4655dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99342233 | |||||
chr2:99342363
|
G | C | 1 | a0001c0003t0004g0291 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.35+4774G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99342363 | ||||||
chr2:99342560
|
G | A | 3 | a0001c0004t0001g0079a0001c0004t0001g0080a0001c0004t0001g0081 | 3 | HG00544.hp2 NA19006.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.35+4971G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99342560 | ||||||
chr2:99342627
|
CT | C | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.35+5042delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99342627 | |||||
chr2:99342759
|
G | T | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.35+5170G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99342759 | ||||||
chr2:99342785
|
C | T | 1 | a0001c0003t0001g0075 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.35+5196C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99342785 | ||||||
chr2:99342872
|
G | A | 1 | a0002c0001t0002g0204 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.35+5283G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99342872 | ||||||
chr2:99343007
|
C | G | 1 | a0001c0002t0003g0175 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.35+5418C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99343007 | ||||||
chr2:99343202
|
C | T | 3 | a0002c0001t0002g0268a0002c0001t0002g0269a0002c0001t0002g0270 | 3 | HG00639.hp2 HG01175.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.35+5613C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99343202 | ||||||
chr2:99343246
|
G | A | 4 | a0001c0002t0003g0126a0001c0002t0003g0127a0001c0002t0003g0128others(1): Show | 4 | HG02572.hp2 HG03041.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+5657G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99343246 | ||||||
chr2:99343348
|
T | C | 1 | a0001c0003t0004g0035 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.35+5759T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99343348 | ||||||
chr2:99343382
|
A | C | 112 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(109): Show | 116 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.35+5793A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99343382 | ||||||
chr2:99343490
|
G | T | 266 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(263): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.35+5901G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99343490 | ||||||
chr2:99343540
|
G | A | 78 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(75): Show | 97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.35+5951G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99343540 | ||||||
chr2:99343849
|
A | G | 4 | a0001c0003t0001g0026a0001c0003t0011g0023a0001c0003t0011g0024others(1): Show | 4 | HG01243.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+6260A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99343849 | ||||||
chr2:99343925
|
C | CT | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.35+6347dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99343925 | |||||
chr2:99343957
|
C | T | 1 | a0002c0001t0002g0273 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.35+6368C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99343957 | ||||||
chr2:99344012
|
G | A | 1 | a0002c0001t0002g0277 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.35+6423G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344012 | ||||||
chr2:99344076
|
G | A | 2 | a0001c0003t0008g0003a0001c0003t0008g0082 | 5 | NA18939.hp1 NA18941.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.35+6487G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344076 | ||||||
chr2:99344100
|
T | A | 4 | a0001c0003t0001g0026a0001c0003t0011g0023a0001c0003t0011g0024others(1): Show | 4 | HG01243.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+6511T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344100 | ||||||
chr2:99344123
|
G | A | 4 | a0001c0003t0009g0027a0001c0003t0009g0028a0001c0003t0009g0029others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.35+6534G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344123 | ||||||
chr2:99344142
|
G | A | 2 | a0002c0001t0005g0281a0002c0001t0018g0193 | 2 | HG02027.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.35+6553G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344142 | ||||||
chr2:99344166
|
C | T | 4 | a0002c0001t0002g0264a0002c0001t0002g0265a0002c0001t0002g0266others(1): Show | 4 | HG00558.hp2 NA19010.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+6577C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344166 | ||||||
chr2:99344233
|
A | G | 1 | a0001c0003t0004g0065 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.35+6644A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344233 | ||||||
chr2:99344348
|
G | A | 1 | a0002c0001t0002g0204 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.35+6759G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344348 | ||||||
chr2:99344404
|
T | TTTG | 18 | a0001c0002t0010g0122a0001c0002t0010g0123a0001c0002t0010g0124others(15): Show | 18 | HG01884.hp1 HG02055.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.35+6845_35+6847dup others(3): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99344404 | |||||
chr2:99344404
|
T | TTTGTTG | 31 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0022others(28): Show | 37 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.35+6842_35+6847dup others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99344404 | |||||
chr2:99344442
|
GT | G | 106 | a0001c0012t0002g0278a0002c0001t0002g0019a0002c0001t0002g0192others(103): Show | 109 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.35+6865delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99344442 | |||||
chr2:99344467
|
C | T | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.35+6878C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344467 | ||||||
chr2:99344561
|
G | A | 6 | a0001c0004t0001g0083a0001c0005t0002g0021a0001c0005t0002g0296others(3): Show | 7 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.35+6972G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344561 | ||||||
chr2:99344597
|
C | T | 6 | a0001c0002t0003g0004a0001c0002t0003g0170a0001c0002t0003g0171others(3): Show | 9 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.35+7008C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344597 | ||||||
chr2:99344894
|
C | A | 11 | a0002c0001t0002g0210a0002c0001t0002g0211a0002c0001t0002g0212others(8): Show | 11 | HG00438.hp1 HG00558.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.35+7305C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99344894 | ||||||
chr2:99345043
|
G | C | 266 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(263): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.35+7454G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345043 | ||||||
chr2:99345068
|
A | G | 1 | a0001c0002t0001g0157 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.35+7479A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345068 | ||||||
chr2:99345182
|
G | A | 4 | a0001c0003t0001g0026a0001c0003t0011g0023a0001c0003t0011g0024others(1): Show | 4 | HG01243.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+7593G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345182 | ||||||
chr2:99345307
|
C | T | 1 | a0001c0009t0001g0156 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.35+7718C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345307 | ||||||
chr2:99345422
|
G | A | 1 | a0002c0001t0002g0210 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.35+7833G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345422 | ||||||
chr2:99345438
|
C | G | 1 | a0001c0004t0001g0105 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.35+7849C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345438 | ||||||
chr2:99345445
|
T | C | 4 | a0001c0003t0001g0066a0001c0003t0001g0067a0001c0003t0001g0068others(1): Show | 4 | HG02055.hp1 HG02615.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.35+7856T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345445 | ||||||
chr2:99345611
|
A | AAT | 52 | a0001c0004t0001g0084a0001c0004t0001g0085a0001c0004t0001g0086others(49): Show | 54 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.35+8022_35+8023ins others(2): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345611 | ||||||
chr2:99345611
|
A | AT | 93 | a0001c0002t0001g0130a0001c0002t0003g0170a0001c0002t0003g0177others(90): Show | 101 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.35+8022_35+8023ins others(1): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345611 | ||||||
chr2:99345611
|
A | T | 115 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(112): Show | 139 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.35+8022A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345611 | ||||||
chr2:99345696
|
G | C | 107 | a0001c0012t0002g0278a0002c0001t0002g0019a0002c0001t0002g0191others(104): Show | 110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.35+8107G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345696 | ||||||
chr2:99345780
|
A | G | 1 | a0001c0003t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.35+8191A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345780 | ||||||
chr2:99345787
|
A | T | 3 | a0001c0003t0014g0032a0001c0003t0014g0033a0001c0011t0022g0304 | 3 | HG01891.hp1 HG02055.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.35+8198A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345787 | ||||||
chr2:99345918
|
T | C | 4 | a0001c0003t0009g0027a0001c0003t0009g0028a0001c0003t0009g0029others(1): Show | 4 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.35+8329T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345918 | ||||||
chr2:99345943
|
C | CA | 142 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(139): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.35+8370dupA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99345943 | |||||
chr2:99345943
|
CA | C | 107 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(104): Show | 111 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.35+8370delA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99345943 | |||||
chr2:99345991
|
G | T | 266 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(263): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.35+8402G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99345991 | ||||||
chr2:99346024
|
C | T | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.35+8435C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346024 | ||||||
chr2:99346048
|
A | G | 1 | a0002c0001t0002g0263 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.35+8459A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346048 | ||||||
chr2:99346109
|
T | C | 2 | a0002c0001t0002g0219a0002c0001t0002g0235 | 2 | HG01261.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.35+8520T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346109 | ||||||
chr2:99346119
|
A | C | 3 | a0001c0003t0011g0023a0001c0003t0011g0024a0001c0003t0011g0025 | 3 | HG02809.hp2 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.35+8530A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346119 | ||||||
chr2:99346140
|
T | G | 2 | a0001c0003t0001g0009a0001c0003t0001g0070 | 3 | HG00642.hp2 HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.35+8551T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346140 | ||||||
chr2:99346338
|
T | A | 1 | a0001c0003t0004g0007 | 2 | HG02257.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.35+8749T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346338 | ||||||
chr2:99346407
|
A | G | 1 | a0002c0001t0002g0301 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.35+8818A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346407 | ||||||
chr2:99346589
|
C | CT | 116 | a0001c0003t0004g0059a0001c0003t0004g0060a0001c0003t0004g0061others(113): Show | 126 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.35+9027dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99346589 | |||||
chr2:99346589
|
C | CTT | 21 | a0001c0004t0001g0080a0001c0004t0001g0086a0001c0004t0001g0103others(18): Show | 22 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.35+9026_35+9027dup others(2): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99346589 | |||||
chr2:99346589
|
CT | C | 91 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(88): Show | 114 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.35+9027delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99346589 | |||||
chr2:99346589
|
CTT | C | 6 | a0001c0003t0002g0034a0001c0003t0009g0027a0001c0003t0009g0028others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.35+9026_35+9027del others(2): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99346589 | |||||
chr2:99346589
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0003t0017g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.35+9017_35+9027del others(11): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99346589 | |||||
chr2:99346589
|
CTTTTTTT others(10): Show |
C | 1 | a0002c0001t0002g0273 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.35+9011_35+9027del others(17): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99346589 | |||||
chr2:99346689
|
G | A | 4 | a0001c0003t0001g0026a0001c0003t0011g0023a0001c0003t0011g0024others(1): Show | 4 | HG01243.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.35+9100G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346689 | ||||||
chr2:99346892
|
G | T | 1 | a0002c0001t0002g0277 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.35+9303G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346892 | ||||||
chr2:99346967
|
T | G | 1 | a0002c0001t0002g0239 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.35+9378T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99346967 | ||||||
chr2:99347268
|
A | G | 1 | a0001c0003t0001g0074 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.35+9679A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99347268 | ||||||
chr2:99347505
|
G | GT | 7 | a0001c0002t0003g0188a0001c0005t0002g0021a0001c0005t0002g0296others(4): Show | 8 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.35+9930dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99347505 | |||||
chr2:99347505
|
GT | G | 11 | a0001c0002t0001g0011a0001c0002t0001g0130a0001c0002t0001g0154others(8): Show | 12 | HG02630.hp2 HG02717.hp1 HG02895.hp2 others(9): Show |
intron_variant | MODIFIER | c.35+9930delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99347505 | |||||
chr2:99347577
|
A | G | 2 | a0001c0002t0007g0186a0001c0002t0007g0187 | 2 | NA19010.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.35+9988A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99347577 | ||||||
chr2:99347712
|
T | C | 2 | a0001c0003t0011g0023a0001c0003t0011g0024 | 2 | HG02809.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.35+10123T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99347712 | ||||||
chr2:99347821
|
G | A | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.35+10232G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99347821 | ||||||
chr2:99347953
|
T | TAG | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.35+10368_35+10369d others(4): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99347953 | |||||
chr2:99348076
|
G | A | 1 | a0001c0004t0001g0088 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.35+10487G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99348076 | ||||||
chr2:99348399
|
G | A | 1 | a0001c0002t0001g0131 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.35+10810G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99348399 | ||||||
chr2:99348777
|
A | T | 11 | a0001c0003t0001g0009a0001c0003t0001g0066a0001c0003t0001g0067others(8): Show | 12 | HG00642.hp2 HG01123.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.35+11188A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99348777 | ||||||
chr2:99349001
|
T | G | 107 | a0001c0012t0002g0278a0002c0001t0002g0019a0002c0001t0002g0191others(104): Show | 110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.36-11235T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99349001 | ||||||
chr2:99349017
|
T | C | 2 | a0001c0003t0014g0032a0001c0003t0014g0033 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.36-11219T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99349017 | ||||||
chr2:99349206
|
G | T | 6 | a0001c0003t0002g0034a0001c0003t0009g0027a0001c0003t0009g0028others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.36-11030G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99349206 | ||||||
chr2:99349334
|
T | C | 12 | a0001c0003t0001g0076a0001c0003t0001g0111a0001c0003t0001g0112others(9): Show | 15 | HG00609.hp2 HG02148.hp1 HG02895.hp1 others(12): Show |
intron_variant | MODIFIER | c.36-10902T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99349334 | ||||||
chr2:99349732
|
G | A | 1 | a0003c0010t0003g0159 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.36-10504G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99349732 | ||||||
chr2:99349822
|
G | T | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.36-10414G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99349822 | ||||||
chr2:99349963
|
A | G | 1 | a0001c0004t0001g0102 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.36-10273A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99349963 | ||||||
chr2:99350061
|
G | A | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.36-10175G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99350061 | ||||||
chr2:99350096
|
T | C | 1 | a0001c0003t0004g0293 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.36-10140T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99350096 | ||||||
chr2:99350129
|
T | C | 3 | a0001c0002t0003g0016a0001c0002t0003g0179a0001c0002t0003g0188 | 4 | NA18940.hp1 NA18995.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.36-10107T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99350129 | ||||||
chr2:99350272
|
A | G | 78 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(75): Show | 97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.36-9964A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99350272 | ||||||
chr2:99350368
|
G | A | 1 | a0001c0003t0017g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.36-9868G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99350368 | ||||||
chr2:99350396
|
TC | T | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.36-9834delC | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99350396 | |||||
chr2:99350653
|
A | G | 1 | a0001c0002t0001g0151 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.36-9583A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99350653 | ||||||
chr2:99351050
|
G | A | 2 | a0002c0001t0005g0275a0002c0001t0005g0276 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.36-9186G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351050 | ||||||
chr2:99351068
|
T | C | 266 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(263): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.36-9168T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351068 | ||||||
chr2:99351189
|
A | G | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.36-9047A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351189 | ||||||
chr2:99351250
|
T | C | 1 | a0002c0001t0018g0193 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.36-8986T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351250 | ||||||
chr2:99351264
|
G | C | 1 | a0001c0002t0003g0188 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.36-8972G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351264 | ||||||
chr2:99351265
|
T | A | 1 | a0001c0002t0003g0188 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.36-8971T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351265 | ||||||
chr2:99351271
|
C | A | 1 | a0001c0002t0003g0188 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.36-8965C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351271 | ||||||
chr2:99351273
|
T | G | 1 | a0001c0002t0003g0188 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.36-8963T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351273 | ||||||
chr2:99351274
|
G | T | 1 | a0001c0002t0003g0188 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.36-8962G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351274 | ||||||
chr2:99351284
|
T | C | 78 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(75): Show | 97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.36-8952T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351284 | ||||||
chr2:99351336
|
A | G | 1 | a0001c0003t0004g0058 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.36-8900A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351336 | ||||||
chr2:99351467
|
A | G | 1 | a0002c0001t0002g0259 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.36-8769A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351467 | ||||||
chr2:99351599
|
G | A | 3 | a0001c0004t0001g0079a0001c0004t0001g0080a0001c0004t0001g0081 | 3 | HG00544.hp2 NA19006.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.36-8637G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351599 | ||||||
chr2:99351644
|
C | T | 266 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(263): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.36-8592C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351644 | ||||||
chr2:99351687
|
G | GT | 72 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(69): Show | 91 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.36-8539dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99351687 | |||||
chr2:99351694
|
T | TG | 4 | a0001c0002t0003g0126a0001c0002t0003g0127a0001c0002t0003g0128others(1): Show | 4 | HG02572.hp2 HG03041.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.36-8542_36-8541ins others(1): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351694 | ||||||
chr2:99351792
|
G | T | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.36-8444G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351792 | ||||||
chr2:99351811
|
C | T | 78 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(75): Show | 97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.36-8425C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351811 | ||||||
chr2:99351819
|
T | C | 1 | a0001c0003t0002g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.36-8417T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351819 | ||||||
chr2:99351867
|
T | C | 6 | a0002c0001t0002g0217a0002c0001t0002g0218a0002c0001t0002g0219others(3): Show | 6 | HG01261.hp2 HG02109.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.36-8369T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351867 | ||||||
chr2:99351951
|
C | T | 1 | a0001c0003t0004g0057 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.36-8285C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99351951 | ||||||
chr2:99352048
|
C | A | 1 | a0002c0001t0002g0205 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.36-8188C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99352048 | ||||||
chr2:99352128
|
T | C | 266 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(263): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.36-8108T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99352128 | ||||||
chr2:99352152
|
T | C | 4 | a0001c0003t0001g0066a0001c0003t0001g0067a0001c0003t0001g0068others(1): Show | 4 | HG02055.hp1 HG02615.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.36-8084T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99352152 | ||||||
chr2:99352364
|
T | A | 1 | a0001c0003t0024g0037 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.36-7872T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99352364 | ||||||
chr2:99352525
|
C | CT | 17 | a0001c0002t0001g0150a0001c0002t0003g0128a0001c0002t0003g0168others(14): Show | 18 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(15): Show |
intron_variant | MODIFIER | c.36-7695dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99352525 | |||||
chr2:99352632
|
G | A | 265 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(262): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.36-7604G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99352632 | ||||||
chr2:99352716
|
A | C | 6 | a0001c0003t0004g0020a0001c0003t0004g0291a0001c0003t0004g0292others(3): Show | 7 | HG01358.hp2 HG01891.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.36-7520A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99352716 | ||||||
chr2:99352978
|
A | G | 5 | a0002c0001t0005g0018a0002c0001t0005g0227a0002c0001t0005g0228others(2): Show | 6 | HG00544.hp1 HG02083.hp2 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.36-7258A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99352978 | ||||||
chr2:99353005
|
C | CTTTTT | 8 | a0002c0001t0002g0212a0002c0001t0002g0219a0002c0001t0002g0235others(5): Show | 8 | HG01261.hp2 HG02145.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.36-7208_36-7204dup others(5): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | |||||
chr2:99353005
|
C | CTTTTTT | 16 | a0002c0001t0002g0211a0002c0001t0002g0213a0002c0001t0002g0214others(13): Show | 16 | HG00639.hp2 HG01516.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.36-7209_36-7204dup others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | |||||
chr2:99353005
|
C | CTTTTTTT | 23 | a0002c0001t0002g0019a0002c0001t0002g0204a0002c0001t0002g0205others(20): Show | 24 | HG00423.hp1 HG00438.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.36-7210_36-7204dup others(7): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | |||||
chr2:99353005
|
C | CTTTTTTT others(1): Show |
17 | a0002c0001t0002g0192a0002c0001t0002g0197a0002c0001t0002g0209others(14): Show | 19 | HG01099.hp1 HG01884.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.36-7211_36-7204dup others(8): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | |||||
chr2:99353005
|
C | CTTTTTTT others(2): Show |
21 | a0002c0001t0002g0191a0002c0001t0002g0253a0002c0001t0002g0254others(18): Show | 21 | HG00544.hp1 HG00558.hp1 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.36-7212_36-7204dup others(9): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | |||||
chr2:99353005
|
C | CTTTTTTT others(3): Show |
5 | a0002c0001t0002g0206a0002c0001t0002g0258a0002c0001t0005g0190others(2): Show | 5 | HG00408.hp1 HG00438.hp2 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.36-7213_36-7204dup others(10): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | |||||
chr2:99353005
|
C | CTTTTTTT others(4): Show |
5 | a0002c0001t0002g0207a0002c0001t0002g0225a0002c0001t0005g0232others(2): Show | 5 | HG01256.hp2 HG01258.hp2 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.36-7214_36-7204dup others(11): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | |||||
chr2:99353005
|
C | CTTTTTTT others(6): Show |
1 | a0002c0001t0002g0290 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.36-7216_36-7204dup others(13): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | |||||
chr2:99353005
|
C | T | 1 | a0002c0001t0005g0203 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.36-7231C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99353005 | ||||||
chr2:99353005
|
CT | C | 19 | a0001c0003t0004g0008a0001c0003t0004g0020a0001c0003t0004g0036others(16): Show | 21 | HG01168.hp1 HG01358.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.36-7204delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | |||||
chr2:99353005
|
CTT | C | 9 | a0001c0003t0001g0026a0001c0003t0004g0038a0001c0003t0011g0023others(6): Show | 9 | HG01243.hp2 HG02055.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.36-7205_36-7204del others(2): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | |||||
chr2:99353005
|
CTTT | C | 34 | a0001c0003t0001g0009a0001c0003t0001g0066a0001c0003t0001g0067others(31): Show | 39 | HG00609.hp2 HG00642.hp2 HG01123.hp1 others(36): Show |
intron_variant | MODIFIER | c.36-7206_36-7204del others(3): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | |||||
chr2:99353005
|
CTTTT | C | 27 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0022others(24): Show | 33 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.36-7207_36-7204del others(4): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | |||||
chr2:99353005
|
CTTTTTTT | C | 74 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(71): Show | 93 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.36-7210_36-7204del others(7): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | |||||
chr2:99353005
|
CTTTTTTT others(1): Show |
C | 8 | a0001c0002t0001g0132a0001c0002t0003g0160a0001c0002t0003g0161others(5): Show | 8 | HG00639.hp1 HG02040.hp2 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.36-7211_36-7204del others(8): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | |||||
chr2:99353005
|
CTTTTTTT others(4): Show |
C | 1 | a0002c0001t0002g0241 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.36-7214_36-7204del others(11): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | |||||
chr2:99353005
|
CTTTTTTT others(6): Show |
C | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.36-7216_36-7204del others(13): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99353005 | |||||
chr2:99353009
|
T | C | 1 | a0001c0003t0004g0293 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.36-7227T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99353009 | ||||||
chr2:99353150
|
G | A | 1 | a0001c0003t0012g0064 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.36-7086G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99353150 | ||||||
chr2:99353215
|
A | C | 3 | a0001c0003t0011g0023a0001c0003t0011g0024a0001c0003t0011g0025 | 3 | HG02809.hp2 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.36-7021A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99353215 | ||||||
chr2:99353371
|
A | C | 266 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(263): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.36-6865A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99353371 | ||||||
chr2:99353564
|
T | C | 1 | a0002c0001t0002g0263 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.36-6672T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99353564 | ||||||
chr2:99353653
|
G | A | 6 | a0001c0003t0004g0007a0001c0003t0004g0046a0001c0003t0024g0037others(3): Show | 7 | HG01516.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.36-6583G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99353653 | ||||||
chr2:99353707
|
C | T | 1 | a0002c0001t0002g0289 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.36-6529C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99353707 | ||||||
chr2:99354337
|
G | C | 107 | a0001c0012t0002g0278a0002c0001t0002g0019a0002c0001t0002g0191others(104): Show | 110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.36-5899G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99354337 | ||||||
chr2:99354403
|
A | G | 1 | a0001c0002t0001g0158 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.36-5833A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99354403 | ||||||
chr2:99354685
|
G | C | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.36-5551G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99354685 | ||||||
chr2:99354796
|
CT | C | 41 | a0001c0002t0001g0150a0001c0002t0001g0152a0001c0003t0001g0070others(38): Show | 44 | HG01109.hp2 HG01358.hp2 HG01516.hp2 others(41): Show |
intron_variant | MODIFIER | c.36-5416delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99354796 | |||||
chr2:99354796
|
CTT | C | 100 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(97): Show | 117 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.36-5417_36-5416del others(2): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99354796 | |||||
chr2:99354796
|
CTTT | C | 47 | a0001c0002t0001g0154a0001c0002t0003g0001a0001c0002t0003g0004others(44): Show | 61 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.36-5418_36-5416del others(3): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99354796 | |||||
chr2:99354796
|
CTTTT | C | 109 | a0001c0002t0003g0160a0001c0002t0003g0173a0001c0003t0001g0119others(106): Show | 112 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.36-5419_36-5416del others(4): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99354796 | |||||
chr2:99354826
|
A | G | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.36-5410A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99354826 | ||||||
chr2:99354851
|
G | A | 1 | a0002c0001t0002g0265 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.36-5385G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99354851 | ||||||
chr2:99355138
|
T | A | 1 | a0001c0003t0017g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.36-5098T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355138 | ||||||
chr2:99355271
|
C | A | 1 | a0002c0001t0002g0301 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.36-4965C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355271 | ||||||
chr2:99355391
|
A | G | 2 | a0001c0002t0010g0124a0001c0002t0010g0125 | 2 | HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.36-4845A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355391 | ||||||
chr2:99355413
|
T | C | 1 | a0002c0001t0005g0223 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.36-4823T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355413 | ||||||
chr2:99355492
|
T | TTTTTACA others(18): Show |
4 | a0002c0001t0002g0241a0002c0001t0002g0247a0002c0001t0002g0272others(1): Show | 4 | HG02132.hp1 NA18966.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.36-4744_36-4743ins others(25): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355492 | ||||||
chr2:99355493
|
A | C | 4 | a0002c0001t0002g0241a0002c0001t0002g0247a0002c0001t0002g0272others(1): Show | 4 | HG02132.hp1 NA18966.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.36-4743A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355493 | ||||||
chr2:99355495
|
G | T | 4 | a0002c0001t0002g0241a0002c0001t0002g0247a0002c0001t0002g0272others(1): Show | 4 | HG02132.hp1 NA18966.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.36-4741G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355495 | ||||||
chr2:99355496
|
T | A | 4 | a0002c0001t0002g0241a0002c0001t0002g0247a0002c0001t0002g0272others(1): Show | 4 | HG02132.hp1 NA18966.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.36-4740T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355496 | ||||||
chr2:99355593
|
G | T | 12 | a0001c0003t0001g0009a0001c0003t0001g0066a0001c0003t0001g0067others(9): Show | 13 | HG00642.hp2 HG01123.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.36-4643G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355593 | ||||||
chr2:99355610
|
G | GT | 52 | a0001c0002t0001g0155a0001c0002t0016g0135a0001c0003t0001g0076others(49): Show | 62 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.36-4606dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99355610 | |||||
chr2:99355610
|
GT | G | 162 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(159): Show | 183 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(180): Show |
intron_variant | MODIFIER | c.36-4606delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99355610 | |||||
chr2:99355883
|
G | A | 1 | a0001c0003t0001g0117 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.36-4353G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355883 | ||||||
chr2:99355892
|
C | T | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.36-4344C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355892 | ||||||
chr2:99355907
|
C | A | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.36-4329C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355907 | ||||||
chr2:99355928
|
T | A | 2 | a0001c0002t0001g0136a0001c0002t0001g0158 | 2 | NA18988.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.36-4308T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99355928 | ||||||
chr2:99356149
|
A | G | 1 | a0001c0003t0001g0116 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.36-4087A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99356149 | ||||||
chr2:99356227
|
G | A | 1 | a0001c0011t0022g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.36-4009G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99356227 | ||||||
chr2:99356519
|
G | T | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.36-3717G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99356519 | ||||||
chr2:99356725
|
T | A | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.36-3511T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99356725 | ||||||
chr2:99356836
|
C | G | 9 | a0001c0004t0001g0005a0001c0004t0001g0077a0001c0004t0001g0085others(6): Show | 11 | HG01070.hp1 HG01109.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.36-3400C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99356836 | ||||||
chr2:99356986
|
G | A | 3 | a0002c0001t0002g0240a0002c0001t0002g0242a0002c0001t0002g0263 | 3 | NA18956.hp1 NA18957.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.36-3250G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99356986 | ||||||
chr2:99357284
|
G | T | 2 | a0001c0002t0001g0148a0001c0002t0001g0155 | 2 | HG00733.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.36-2952G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99357284 | ||||||
chr2:99357322
|
G | A | 3 | a0002c0001t0002g0206a0002c0001t0002g0207a0002c0001t0002g0282 | 3 | HG02572.hp1 HG02717.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.36-2914G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99357322 | ||||||
chr2:99357334
|
G | A | 1 | a0001c0002t0001g0137 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.36-2902G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99357334 | ||||||
chr2:99357377
|
G | A | 1 | a0001c0002t0003g0161 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.36-2859G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99357377 | ||||||
chr2:99357492
|
G | A | 1 | a0001c0003t0001g0118 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.36-2744G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99357492 | ||||||
chr2:99357637
|
C | G | 1 | a0001c0004t0001g0087 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.36-2599C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99357637 | ||||||
chr2:99357645
|
T | C | 2 | a0001c0003t0014g0032a0001c0003t0014g0033 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.36-2591T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99357645 | ||||||
chr2:99357702
|
T | C | 3 | a0001c0006t0004g0044a0001c0006t0004g0045a0001c0006t0004g0062 | 3 | HG01516.hp2 HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.36-2534T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99357702 | ||||||
chr2:99357706
|
A | G | 1 | a0001c0012t0002g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.36-2530A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99357706 | ||||||
chr2:99358010
|
G | A | 49 | a0001c0003t0001g0076a0001c0003t0001g0111a0001c0003t0001g0112others(46): Show | 59 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.36-2226G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99358010 | ||||||
chr2:99358144
|
A | G | 1 | a0001c0004t0001g0087 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.36-2092A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99358144 | ||||||
chr2:99358180
|
C | T | 1 | a0001c0002t0001g0146 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.36-2056C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99358180 | ||||||
chr2:99358256
|
G | A | 1 | a0001c0005t0002g0296 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.36-1980G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99358256 | ||||||
chr2:99358450
|
C | T | 2 | a0001c0003t0014g0032a0001c0003t0014g0033 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.36-1786C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99358450 | ||||||
chr2:99358587
|
T | C | 266 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(263): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.36-1649T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99358587 | ||||||
chr2:99359084
|
C | T | 107 | a0001c0012t0002g0278a0002c0001t0002g0019a0002c0001t0002g0191others(104): Show | 110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.36-1152C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99359084 | ||||||
chr2:99359166
|
G | A | 4 | a0002c0001t0005g0196a0002c0001t0005g0199a0002c0001t0005g0200others(1): Show | 4 | HG00558.hp1 NA18944.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.36-1070G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99359166 | ||||||
chr2:99359206
|
C | CA | 112 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(109): Show | 116 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.36-1017dupA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99359206 | |||||
chr2:99359206
|
CA | C | 11 | a0001c0003t0001g0009a0001c0003t0001g0066a0001c0003t0001g0067others(8): Show | 12 | HG00642.hp2 HG01123.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.36-1017delA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr2 | 99359206 | |||||
chr2:99359261
|
C | T | 3 | a0002c0001t0002g0268a0002c0001t0002g0269a0002c0001t0002g0270 | 3 | HG00639.hp2 HG01175.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.36-975C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99359261 | ||||||
chr2:99359262
|
G | A | 37 | a0001c0004t0001g0002a0001c0004t0001g0005a0001c0004t0001g0022others(34): Show | 44 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.36-974G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99359262 | ||||||
chr2:99359407
|
C | A | 36 | a0002c0001t0002g0197a0002c0001t0002g0221a0002c0001t0002g0283others(33): Show | 38 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.36-829C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99359407 | ||||||
chr2:99359747
|
G | C | 3 | a0001c0002t0003g0180a0001c0002t0003g0181a0001c0002t0003g0182 | 3 | HG04184.hp2 NA18957.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.36-489G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99359747 | ||||||
chr2:99359828
|
C | A | 152 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(149): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.36-408C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99359828 | ||||||
chr2:99359879
|
G | A | 10 | a0001c0002t0001g0014a0001c0002t0001g0137a0001c0002t0001g0138others(7): Show | 11 | HG02080.hp1 HG02818.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.36-357G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99359879 | ||||||
chr2:99360101
|
A | G | 266 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(263): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.36-135A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 1/23 | chr2 | 99360101 | ||||||
chr2:99360559
|
A | T | 3 | a0001c0003t0011g0023a0001c0003t0011g0024a0001c0003t0011g0025 | 3 | HG02809.hp2 HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.246+10A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 3/23 | chr2 | 99360559 | ||||||
chr2:99360699
|
TAGGAATG others(3): Show |
T | 107 | a0001c0012t0002g0278a0002c0001t0002g0019a0002c0001t0002g0191others(104): Show | 110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.246+154_246+163del others(10): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr2 | 99360699 | |||||
chr2:99360733
|
G | A | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.246+184G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 3/23 | chr2 | 99360733 | ||||||
chr2:99360758
|
T | A | 266 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(263): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.246+209T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 3/23 | chr2 | 99360758 | ||||||
chr2:99360879
|
C | A | 9 | a0001c0002t0001g0012a0001c0002t0001g0140a0001c0002t0001g0141others(6): Show | 10 | HG00733.hp1 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.247-269C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 3/23 | chr2 | 99360879 | ||||||
chr2:99361014
|
T | C | 1 | a0002c0001t0019g0236 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.247-134T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 3/23 | chr2 | 99361014 | ||||||
chr2:99361032
|
T | C | 1 | a0001c0002t0003g0133 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.247-116T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 3/23 | chr2 | 99361032 | ||||||
chr2:99362073
|
A | AT | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+261dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr2 | 99362073 | |||||
chr2:99362205
|
C | T | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+385C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362205 | ||||||
chr2:99362313
|
A | C | 2 | a0002c0001t0002g0260a0002c0001t0002g0285 | 2 | NA18951.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.919+493A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362313 | ||||||
chr2:99362487
|
T | A | 49 | a0001c0003t0001g0076a0001c0003t0001g0111a0001c0003t0001g0112others(46): Show | 59 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.919+667T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362487 | ||||||
chr2:99362551
|
T | C | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+731T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362551 | ||||||
chr2:99362555
|
C | T | 1 | a0002c0001t0005g0190 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.919+735C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362555 | ||||||
chr2:99362697
|
T | C | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.919+877T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362697 | ||||||
chr2:99362744
|
T | C | 1 | a0001c0002t0010g0124 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.920-901T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362744 | ||||||
chr2:99362822
|
G | A | 1 | a0001c0003t0004g0292 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.920-823G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362822 | ||||||
chr2:99362902
|
G | A | 2 | a0001c0004t0001g0022a0001c0004t0001g0104 | 2 | HG00140.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.920-743G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362902 | ||||||
chr2:99362925
|
A | G | 1 | a0002c0001t0002g0301 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.920-720A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99362925 | ||||||
chr2:99363038
|
T | C | 266 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(263): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.920-607T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99363038 | ||||||
chr2:99363199
|
C | G | 3 | a0002c0001t0002g0246a0002c0001t0002g0280a0002c0001t0002g0303 | 3 | NA18962.hp2 NA18964.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.920-446C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99363199 | ||||||
chr2:99363210
|
A | G | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.920-435A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99363210 | ||||||
chr2:99363363
|
T | G | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.920-282T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99363363 | ||||||
chr2:99363489
|
A | G | 2 | a0001c0003t0014g0032a0001c0003t0014g0033 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.920-156A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99363489 | ||||||
chr2:99363625
|
G | T | 1 | a0002c0001t0002g0285 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.920-20G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 4/23 | chr2 | 99363625 | ||||||
chr2:99364759
|
A | G | 3 | a0002c0001t0002g0239a0002c0001t0002g0252a0002c0001t0002g0259 | 3 | HG00738.hp2 HG02698.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1288+338A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99364759 | ||||||
chr2:99364760
|
T | C | 4 | a0002c0001t0002g0243a0002c0001t0002g0244a0002c0001t0002g0248others(1): Show | 4 | HG01978.hp1 HG02523.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288+339T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99364760 | ||||||
chr2:99364879
|
AT | A | 118 | a0001c0002t0001g0013a0001c0002t0001g0150a0001c0002t0001g0154others(115): Show | 122 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.1288+467delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 99364879 | |||||
chr2:99364989
|
T | A | 2 | a0001c0004t0001g0022a0001c0004t0001g0104 | 2 | HG00140.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.1288+568T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99364989 | ||||||
chr2:99365174
|
T | A | 1 | a0001c0004t0001g0091 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1288+753T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365174 | ||||||
chr2:99365207
|
G | T | 107 | a0001c0012t0002g0278a0002c0001t0002g0019a0002c0001t0002g0191others(104): Show | 110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1288+786G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365207 | ||||||
chr2:99365269
|
T | C | 1 | a0001c0003t0001g0117 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1288+848T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365269 | ||||||
chr2:99365399
|
A | G | 266 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(263): Show | 300 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(297): Show |
intron_variant | MODIFIER | c.1288+978A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365399 | ||||||
chr2:99365469
|
G | A | 1 | a0001c0003t0004g0059 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1288+1048G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365469 | ||||||
chr2:99365543
|
T | C | 1 | a0002c0001t0002g0221 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1288+1122T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365543 | ||||||
chr2:99365589
|
C | T | 1 | a0001c0003t0001g0111 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1288+1168C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365589 | ||||||
chr2:99365716
|
T | TCAAAATC others(94): Show |
3 | a0001c0002t0001g0013a0001c0002t0001g0143a0001c0002t0001g0150 | 4 | HG00423.hp2 HG00609.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288+1296_1288+129 others(105): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 99365716 | |||||
chr2:99365719
|
C | T | 3 | a0001c0002t0001g0013a0001c0002t0001g0143a0001c0002t0001g0150 | 4 | HG00423.hp2 HG00609.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288+1298C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365719 | ||||||
chr2:99365720
|
T | G | 3 | a0001c0002t0001g0013a0001c0002t0001g0143a0001c0002t0001g0150 | 4 | HG00423.hp2 HG00609.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288+1299T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365720 | ||||||
chr2:99365721
|
C | T | 3 | a0001c0002t0001g0013a0001c0002t0001g0143a0001c0002t0001g0150 | 4 | HG00423.hp2 HG00609.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.1288+1300C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365721 | ||||||
chr2:99365738
|
G | T | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1288+1317G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365738 | ||||||
chr2:99365848
|
C | A | 1 | a0001c0003t0001g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1288+1427C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365848 | ||||||
chr2:99365883
|
A | G | 1 | a0002c0001t0002g0213 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1288+1462A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365883 | ||||||
chr2:99365964
|
T | C | 1 | a0002c0001t0002g0211 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1288+1543T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99365964 | ||||||
chr2:99366002
|
A | G | 1 | a0001c0003t0002g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1288+1581A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366002 | ||||||
chr2:99366044
|
G | A | 1 | a0001c0002t0003g0129 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1288+1623G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366044 | ||||||
chr2:99366088
|
T | TAC | 78 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(75): Show | 97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1288+1679_1288+168 others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 99366088 | |||||
chr2:99366088
|
TAC | T | 107 | a0001c0012t0002g0278a0002c0001t0002g0019a0002c0001t0002g0191others(104): Show | 110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1288+1679_1288+168 others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 99366088 | |||||
chr2:99366210
|
C | T | 1 | a0001c0003t0021g0302 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1288+1789C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366210 | ||||||
chr2:99366267
|
T | C | 78 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(75): Show | 97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1288+1846T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366267 | ||||||
chr2:99366311
|
A | G | 4 | a0001c0003t0004g0041a0001c0003t0004g0042a0001c0003t0004g0043others(1): Show | 4 | NA18978.hp2 NA18998.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288+1890A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366311 | ||||||
chr2:99366342
|
C | T | 6 | a0001c0003t0002g0034a0001c0003t0009g0027a0001c0003t0009g0028others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1288+1921C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366342 | ||||||
chr2:99366510
|
C | T | 6 | a0001c0003t0002g0034a0001c0003t0009g0027a0001c0003t0009g0028others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1289-1983C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366510 | ||||||
chr2:99366522
|
A | G | 6 | a0001c0003t0002g0034a0001c0003t0009g0027a0001c0003t0009g0028others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1289-1971A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366522 | ||||||
chr2:99366542
|
G | T | 298 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(295): Show | 335 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(332): Show |
intron_variant | MODIFIER | c.1289-1951G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366542 | ||||||
chr2:99366729
|
G | A | 1 | a0001c0002t0001g0143 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1289-1764G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99366729 | ||||||
chr2:99367368
|
C | T | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1289-1125C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99367368 | ||||||
chr2:99367431
|
C | CT | 253 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(250): Show | 286 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.1289-1049dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 99367431 | |||||
chr2:99367431
|
C | CTT | 12 | a0001c0003t0001g0009a0001c0003t0001g0066a0001c0003t0001g0067others(9): Show | 13 | HG00642.hp2 HG01123.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.1289-1050_1289-104 others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr2 | 99367431 | |||||
chr2:99367512
|
C | T | 1 | a0001c0003t0004g0292 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1289-981C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99367512 | ||||||
chr2:99367546
|
C | T | 2 | a0002c0007t0005g0230a0002c0007t0005g0274 | 2 | HG02486.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1289-947C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99367546 | ||||||
chr2:99367577
|
T | C | 1 | a0002c0001t0002g0214 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1289-916T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99367577 | ||||||
chr2:99367715
|
A | G | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1289-778A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99367715 | ||||||
chr2:99367734
|
C | T | 12 | a0001c0003t0001g0009a0001c0003t0001g0066a0001c0003t0001g0067others(9): Show | 13 | HG00642.hp2 HG01123.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.1289-759C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99367734 | ||||||
chr2:99367735
|
G | A | 107 | a0001c0012t0002g0278a0002c0001t0002g0019a0002c0001t0002g0191others(104): Show | 110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1289-758G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99367735 | ||||||
chr2:99367746
|
C | T | 1 | a0001c0002t0003g0175 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1289-747C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99367746 | ||||||
chr2:99367905
|
G | C | 1 | a0001c0004t0001g0100 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1289-588G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99367905 | ||||||
chr2:99368271
|
T | C | 1 | a0001c0002t0001g0136 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1289-222T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99368271 | ||||||
chr2:99368414
|
A | G | 1 | a0002c0001t0019g0236 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1289-79A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99368414 | ||||||
chr2:99368430
|
A | G | 6 | a0001c0003t0002g0034a0001c0003t0009g0027a0001c0003t0009g0028others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1289-63A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 6/23 | chr2 | 99368430 | ||||||
chr2:99368689
|
C | T | 6 | a0001c0003t0002g0034a0001c0003t0009g0027a0001c0003t0009g0028others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1387+98C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 7/23 | chr2 | 99368689 | ||||||
chr2:99368710
|
T | C | 1 | a0002c0001t0005g0199 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1387+119T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 7/23 | chr2 | 99368710 | ||||||
chr2:99368817
|
A | G | 1 | a0001c0005t0002g0296 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1387+226A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 7/23 | chr2 | 99368817 | ||||||
chr2:99369027
|
C | T | 1 | a0001c0003t0001g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1388-365C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 7/23 | chr2 | 99369027 | ||||||
chr2:99369048
|
G | A | 1 | a0002c0001t0002g0256 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1388-344G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 7/23 | chr2 | 99369048 | ||||||
chr2:99369071
|
A | G | 4 | a0001c0003t0001g0026a0001c0003t0011g0023a0001c0003t0011g0024others(1): Show | 4 | HG01243.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1388-321A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 7/23 | chr2 | 99369071 | ||||||
chr2:99369282
|
A | T | 1 | a0001c0003t0004g0055 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1388-110A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 7/23 | chr2 | 99369282 | ||||||
chr2:99369295
|
G | T | 1 | a0001c0002t0001g0146 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1388-97G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 7/23 | chr2 | 99369295 | ||||||
chr2:99369308
|
T | G | 1 | a0001c0003t0001g0067 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1388-84T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 7/23 | chr2 | 99369308 | ||||||
chr2:99369580
|
C | A | 1 | a0001c0002t0001g0150 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1477+99C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99369580 | ||||||
chr2:99369642
|
A | G | 2 | a0002c0001t0002g0219a0002c0001t0002g0235 | 2 | HG01261.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1477+161A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99369642 | ||||||
chr2:99370020
|
A | G | 9 | a0001c0003t0001g0076a0001c0003t0001g0111a0001c0003t0001g0114others(6): Show | 12 | HG00609.hp2 HG02148.hp1 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.1477+539A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99370020 | ||||||
chr2:99370128
|
T | C | 2 | a0001c0002t0001g0013a0001c0002t0001g0150 | 3 | HG00609.hp1 NA18956.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1477+647T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99370128 | ||||||
chr2:99370164
|
A | G | 1 | a0001c0002t0001g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1477+683A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99370164 | ||||||
chr2:99370181
|
T | C | 107 | a0001c0012t0002g0278a0002c0001t0002g0019a0002c0001t0002g0191others(104): Show | 110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.1477+700T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99370181 | ||||||
chr2:99370469
|
T | C | 61 | a0001c0003t0001g0009a0001c0003t0001g0066a0001c0003t0001g0067others(58): Show | 72 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1477+988T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99370469 | ||||||
chr2:99370966
|
A | G | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1478-690A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99370966 | ||||||
chr2:99370980
|
G | T | 1 | a0001c0002t0001g0150 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1478-676G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99370980 | ||||||
chr2:99371215
|
G | A | 1 | a0002c0001t0005g0224 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1478-441G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371215 | ||||||
chr2:99371290
|
A | C | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1478-366A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371290 | ||||||
chr2:99371362
|
T | C | 1 | a0002c0001t0002g0212 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1478-294T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371362 | ||||||
chr2:99371373
|
A | G | 2 | a0001c0004t0001g0022a0001c0004t0001g0104 | 2 | HG00140.hp1 HG00733.hp2 |
intron_variant | MODIFIER | c.1478-283A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371373 | ||||||
chr2:99371413
|
G | A | 1 | a0001c0003t0002g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1478-243G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371413 | ||||||
chr2:99371443
|
A | G | 1 | a0001c0003t0001g0119 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1478-213A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371443 | ||||||
chr2:99371445
|
G | A | 6 | a0002c0001t0002g0197a0002c0001t0005g0194a0002c0001t0005g0195others(3): Show | 6 | NA18947.hp1 NA18948.hp1 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.1478-211G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371445 | ||||||
chr2:99371466
|
C | T | 1 | a0001c0004t0001g0091 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1478-190C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371466 | ||||||
chr2:99371488
|
CA | C | 151 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(148): Show | 181 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.1478-151delA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr2 | 99371488 | |||||
chr2:99371543
|
A | C | 1 | a0002c0001t0005g0227 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1478-113A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371543 | ||||||
chr2:99371559
|
C | T | 1 | a0002c0001t0005g0198 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1478-97C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 8/23 | chr2 | 99371559 | ||||||
chr2:99371990
|
CA | C | 197 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(194): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1552+264delA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr2 | 99371990 | |||||
chr2:99372192
|
C | G | 1 | a0002c0001t0002g0254 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1552+462C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372192 | ||||||
chr2:99372408
|
G | A | 1 | a0001c0011t0022g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1552+678G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372408 | ||||||
chr2:99372482
|
G | T | 1 | a0002c0001t0005g0224 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1552+752G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372482 | ||||||
chr2:99372585
|
G | A | 4 | a0001c0002t0010g0122a0001c0002t0010g0123a0001c0002t0010g0124others(1): Show | 4 | HG02630.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1552+855G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372585 | ||||||
chr2:99372708
|
A | T | 6 | a0001c0002t0003g0004a0001c0002t0003g0170a0001c0002t0003g0171others(3): Show | 9 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1552+978A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372708 | ||||||
chr2:99372774
|
G | T | 1 | a0001c0002t0001g0132 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1552+1044G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372774 | ||||||
chr2:99372875
|
C | T | 197 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(194): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1552+1145C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372875 | ||||||
chr2:99372885
|
T | A | 38 | a0001c0003t0004g0007a0001c0003t0004g0008a0001c0003t0004g0020others(35): Show | 41 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.1552+1155T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372885 | ||||||
chr2:99372899
|
T | G | 1 | a0001c0004t0001g0098 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1552+1169T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372899 | ||||||
chr2:99372996
|
C | A | 2 | a0002c0001t0005g0233a0002c0001t0005g0279 | 2 | NA18939.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1552+1266C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99372996 | ||||||
chr2:99373055
|
T | G | 3 | a0001c0002t0001g0013a0001c0002t0001g0143a0001c0002t0001g0150 | 4 | HG00423.hp2 HG00609.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.1552+1325T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373055 | ||||||
chr2:99373101
|
A | G | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1552+1371A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373101 | ||||||
chr2:99373330
|
C | G | 1 | a0002c0001t0002g0267 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1552+1600C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373330 | ||||||
chr2:99373380
|
G | C | 2 | a0002c0001t0002g0264a0002c0001t0002g0265 | 2 | HG00558.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.1552+1650G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373380 | ||||||
chr2:99373386
|
G | A | 1 | a0001c0002t0003g0134 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1552+1656G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373386 | ||||||
chr2:99373482
|
C | T | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1552+1752C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373482 | ||||||
chr2:99373483
|
G | T | 1 | a0001c0003t0001g0026 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1552+1753G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373483 | ||||||
chr2:99373707
|
T | C | 1 | a0001c0003t0001g0111 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1552+1977T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373707 | ||||||
chr2:99373790
|
A | G | 1 | a0001c0003t0004g0049 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1552+2060A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373790 | ||||||
chr2:99373852
|
G | T | 2 | a0001c0003t0001g0112a0001c0003t0001g0113 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1552+2122G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373852 | ||||||
chr2:99373861
|
C | T | 158 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(155): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1552+2131C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373861 | ||||||
chr2:99373912
|
A | G | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1552+2182A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99373912 | ||||||
chr2:99374063
|
C | T | 6 | a0001c0002t0003g0004a0001c0002t0003g0170a0001c0002t0003g0171others(3): Show | 9 | HG00642.hp1 HG00735.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1553-2284C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99374063 | ||||||
chr2:99374107
|
G | A | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1553-2240G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99374107 | ||||||
chr2:99374268
|
G | A | 1 | a0002c0001t0005g0223 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1553-2079G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99374268 | ||||||
chr2:99374288
|
TA | T | 78 | a0001c0002t0001g0176a0001c0002t0003g0001a0001c0002t0003g0004others(75): Show | 94 | HG00140.hp2 HG00280.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1553-2037delA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr2 | 99374288 | |||||
chr2:99374288
|
TAA | T | 125 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(122): Show | 143 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1553-2038_1553-203 others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | INFO_REALIGN_3_PRIME | chr2 | 99374288 | |||||
chr2:99374719
|
A | G | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1553-1628A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99374719 | ||||||
chr2:99374777
|
A | G | 1 | a0002c0001t0019g0236 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1553-1570A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99374777 | ||||||
chr2:99375018
|
A | G | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1553-1329A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375018 | ||||||
chr2:99375076
|
A | C | 1 | a0001c0003t0017g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1553-1271A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375076 | ||||||
chr2:99375117
|
CTG | C | 38 | a0001c0003t0004g0007a0001c0003t0004g0008a0001c0003t0004g0020others(35): Show | 41 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.1553-1229_1553-122 others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375117 | ||||||
chr2:99375205
|
C | T | 31 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(28): Show | 37 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1553-1142C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375205 | ||||||
chr2:99375415
|
G | A | 1 | a0002c0001t0005g0190 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1553-932G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375415 | ||||||
chr2:99375459
|
C | T | 84 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(81): Show | 103 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1553-888C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375459 | ||||||
chr2:99375469
|
G | A | 1 | a0002c0001t0019g0236 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1553-878G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375469 | ||||||
chr2:99375478
|
A | G | 4 | a0001c0003t0001g0009a0001c0003t0001g0070a0001c0003t0013g0072others(1): Show | 5 | HG00642.hp2 HG02257.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1553-869A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375478 | ||||||
chr2:99375523
|
C | G | 1 | a0001c0004t0001g0103 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1553-824C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375523 | ||||||
chr2:99375724
|
T | C | 197 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(194): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1553-623T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375724 | ||||||
chr2:99375754
|
C | G | 1 | a0001c0002t0003g0129 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1553-593C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99375754 | ||||||
chr2:99376109
|
C | G | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1553-238C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99376109 | ||||||
chr2:99376278
|
A | G | 2 | a0002c0001t0002g0205a0002c0001t0002g0208 | 2 | HG03209.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1553-69A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99376278 | ||||||
chr2:99376321
|
A | G | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1553-26A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 9/23 | chr2 | 99376321 | ||||||
chr2:99376681
|
G | A | 1 | a0001c0003t0004g0050 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1842+45G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99376681 | ||||||
chr2:99376697
|
T | C | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.1842+61T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99376697 | ||||||
chr2:99376713
|
G | A | 36 | a0001c0003t0004g0007a0001c0003t0004g0020a0001c0003t0004g0036others(33): Show | 38 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(35): Show |
intron_variant | MODIFIER | c.1842+77G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99376713 | ||||||
chr2:99376754
|
G | A | 1 | a0001c0012t0002g0278 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1842+118G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99376754 | ||||||
chr2:99376787
|
C | G | 1 | a0001c0002t0001g0150 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1842+151C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99376787 | ||||||
chr2:99377013
|
A | G | 1 | a0001c0002t0001g0153 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1842+377A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99377013 | ||||||
chr2:99377238
|
G | A | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.1842+602G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99377238 | ||||||
chr2:99377427
|
G | A | 1 | a0002c0001t0002g0273 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1842+791G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99377427 | ||||||
chr2:99377564
|
C | T | 1 | a0001c0004t0015g0096 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1842+928C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99377564 | ||||||
chr2:99377570
|
A | G | 1 | a0002c0001t0002g0259 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1842+934A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99377570 | ||||||
chr2:99377694
|
G | C | 4 | a0002c0001t0002g0191a0002c0001t0002g0225a0002c0001t0002g0258others(1): Show | 4 | HG00408.hp1 NA18949.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.1842+1058G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99377694 | ||||||
chr2:99377705
|
A | G | 1 | a0001c0002t0001g0145 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1842+1069A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99377705 | ||||||
chr2:99377736
|
A | G | 4 | a0001c0003t0001g0026a0001c0003t0011g0023a0001c0003t0011g0024others(1): Show | 4 | HG01243.hp2 HG02809.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1842+1100A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99377736 | ||||||
chr2:99377767
|
G | A | 6 | a0001c0004t0006g0010a0001c0004t0006g0106a0001c0004t0006g0107others(3): Show | 7 | HG02280.hp1 HG02922.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1842+1131G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99377767 | ||||||
chr2:99378103
|
T | C | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1843-916T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99378103 | ||||||
chr2:99378450
|
G | A | 1 | a0002c0001t0005g0195 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1843-569G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99378450 | ||||||
chr2:99378497
|
C | G | 158 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(155): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.1843-522C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99378497 | ||||||
chr2:99378503
|
A | G | 1 | a0002c0001t0002g0287 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1843-516A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99378503 | ||||||
chr2:99378873
|
T | G | 1 | a0001c0003t0001g0071 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1843-146T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | chr2 | 99378873 | ||||||
chr2:99378995
|
AT | A | 155 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(152): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1843-9delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 10/23 | INFO_REALIGN_3_PRIME | chr2 | 99378995 | |||||
chr2:99379702
|
A | G | 49 | a0001c0003t0001g0076a0001c0003t0001g0111a0001c0003t0001g0112others(46): Show | 59 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.2061+274A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99379702 | ||||||
chr2:99380207
|
T | A | 78 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(75): Show | 97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.2061+779T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99380207 | ||||||
chr2:99380304
|
A | C | 1 | a0001c0002t0001g0158 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.2061+876A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99380304 | ||||||
chr2:99381029
|
A | G | 1 | a0001c0003t0012g0063 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2062-1130A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99381029 | ||||||
chr2:99381030
|
T | C | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2062-1129T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99381030 | ||||||
chr2:99381116
|
G | C | 1 | a0002c0001t0002g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2062-1043G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99381116 | ||||||
chr2:99381516
|
G | GGT | 22 | a0001c0002t0001g0137a0001c0002t0001g0152a0001c0002t0003g0015others(19): Show | 23 | HG00140.hp2 HG01934.hp1 HG02040.hp2 others(20): Show |
intron_variant | MODIFIER | c.2062-642_2062-641i others(4): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381516 | |||||
chr2:99381516
|
G | GGTGT | 50 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(47): Show | 58 | HG00408.hp2 HG00733.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.2062-642_2062-641i others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381516 | |||||
chr2:99381516
|
G | GGTGTGT | 38 | a0001c0002t0001g0131a0001c0002t0001g0142a0001c0002t0001g0143others(35): Show | 51 | HG00423.hp2 HG00639.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.2062-642_2062-641i others(8): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381516 | |||||
chr2:99381516
|
G | GGTGTGTG others(1): Show |
19 | a0001c0002t0001g0121a0001c0002t0003g0127a0001c0002t0003g0166others(16): Show | 19 | HG01261.hp2 HG01361.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2062-642_2062-641i others(10): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381516 | |||||
chr2:99381516
|
G | GGTGTGTG others(3): Show |
11 | a0001c0003t0001g0026a0001c0003t0004g0041a0001c0003t0004g0043others(8): Show | 11 | HG00280.hp1 HG01243.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.2062-642_2062-641i others(12): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381516 | |||||
chr2:99381516
|
G | GGTGTGTG others(5): Show |
1 | a0001c0003t0017g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2062-642_2062-641i others(14): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381516 | |||||
chr2:99381516
|
G | GTGTGTGT others(4): Show |
1 | a0001c0005t0002g0297 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.2062-643_2062-642i others(13): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99381516 | ||||||
chr2:99381518
|
G | GGT | 43 | a0002c0001t0002g0019a0002c0001t0002g0191a0002c0001t0002g0204others(40): Show | 44 | HG00408.hp1 HG00423.hp1 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.2062-607_2062-606d others(4): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381518 | |||||
chr2:99381518
|
G | GGTGT | 11 | a0001c0012t0002g0278a0002c0001t0002g0206a0002c0001t0002g0215others(8): Show | 11 | HG00438.hp1 HG00438.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.2062-609_2062-606d others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381518 | |||||
chr2:99381518
|
G | GGTGTGT | 9 | a0002c0001t0002g0192a0002c0001t0002g0205a0002c0001t0002g0207others(6): Show | 9 | HG01884.hp1 HG02523.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.2062-611_2062-606d others(8): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381518 | |||||
chr2:99381518
|
G | GGTGTGTG others(1): Show |
23 | a0002c0001t0002g0221a0002c0001t0002g0286a0002c0001t0002g0301others(20): Show | 24 | HG00558.hp1 HG01123.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.2062-613_2062-606d others(10): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381518 | |||||
chr2:99381518
|
G | GGTGTGTG others(3): Show |
5 | a0002c0001t0002g0283a0002c0001t0005g0017a0002c0001t0005g0227others(2): Show | 6 | HG00544.hp1 HG02965.hp1 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.2062-615_2062-606d others(12): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381518 | |||||
chr2:99381518
|
G | GGTGTGTG others(5): Show |
1 | a0002c0001t0005g0220 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2062-617_2062-606d others(14): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381518 | |||||
chr2:99381518
|
G | T | 201 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(198): Show | 235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.2062-641G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99381518 | ||||||
chr2:99381702
|
C | CT | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.2062-454dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381702 | |||||
chr2:99381898
|
C | G | 1 | a0002c0001t0005g0223 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2062-261C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99381898 | ||||||
chr2:99381959
|
A | AT | 7 | a0001c0002t0003g0126a0001c0002t0003g0127a0001c0002t0003g0128others(4): Show | 7 | HG02572.hp2 HG03041.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.2062-193dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr2 | 99381959 | |||||
chr2:99382098
|
C | T | 197 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(194): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2062-61C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 12/23 | chr2 | 99382098 | ||||||
chr2:99382232
|
A | T | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | splice_region_variant&intron_variant | LOW | c.2129+6A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 13/23 | chr2 | 99382232 | ||||||
chr2:99382295
|
G | C | 1 | a0001c0002t0007g0183 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.2129+69G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 13/23 | chr2 | 99382295 | ||||||
chr2:99382329
|
A | G | 1 | a0001c0003t0017g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2129+103A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 13/23 | chr2 | 99382329 | ||||||
chr2:99382414
|
C | T | 1 | a0001c0003t0001g0119 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2129+188C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 13/23 | chr2 | 99382414 | ||||||
chr2:99382634
|
C | A | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2130-146C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 13/23 | chr2 | 99382634 | ||||||
chr2:99382991
|
G | A | 4 | a0001c0003t0001g0066a0001c0003t0001g0067a0001c0003t0001g0068others(1): Show | 4 | HG02055.hp1 HG02615.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2271+70G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99382991 | ||||||
chr2:99383020
|
TTATTGTG others(8): Show |
T | 1 | a0001c0003t0004g0054 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2271+113_2271+127d others(17): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99383020 | |||||
chr2:99383035
|
A | G | 1 | a0001c0004t0006g0109 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2271+114A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99383035 | ||||||
chr2:99383054
|
T | TTG | 3 | a0001c0003t0004g0048a0001c0003t0004g0054a0001c0003t0004g0057 | 3 | HG00280.hp1 HG03669.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.2271+147_2271+148d others(4): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99383054 | |||||
chr2:99383148
|
G | A | 38 | a0001c0003t0004g0007a0001c0003t0004g0008a0001c0003t0004g0020others(35): Show | 41 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.2271+227G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99383148 | ||||||
chr2:99383299
|
C | G | 1 | a0001c0004t0001g0099 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2271+378C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99383299 | ||||||
chr2:99383419
|
T | C | 32 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(29): Show | 38 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.2271+498T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99383419 | ||||||
chr2:99383710
|
A | G | 1 | a0001c0003t0001g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2271+789A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99383710 | ||||||
chr2:99383775
|
A | AG | 39 | a0001c0003t0002g0305a0001c0003t0004g0007a0001c0003t0004g0008others(36): Show | 42 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(39): Show |
intron_variant | MODIFIER | c.2271+855dupG | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99383775 | |||||
chr2:99383836
|
G | T | 1 | a0001c0002t0001g0139 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2271+915G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99383836 | ||||||
chr2:99383863
|
ACT | A | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2271+947_2271+948d others(4): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99383863 | |||||
chr2:99383980
|
C | T | 1 | a0001c0003t0009g0031 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2271+1059C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99383980 | ||||||
chr2:99383984
|
C | T | 1 | a0002c0001t0002g0283 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2271+1063C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99383984 | ||||||
chr2:99384070
|
A | G | 197 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(194): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2271+1149A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384070 | ||||||
chr2:99384114
|
G | T | 1 | a0002c0001t0002g0250 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2271+1193G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384114 | ||||||
chr2:99384154
|
G | A | 2 | a0001c0003t0014g0032a0001c0003t0014g0033 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2271+1233G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384154 | ||||||
chr2:99384191
|
C | T | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2271+1270C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384191 | ||||||
chr2:99384196
|
C | CAAAAAAA others(3): Show |
172 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(169): Show | 205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.2271+1277_2271+128 others(14): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99384196 | |||||
chr2:99384196
|
C | CAAAAAAA others(4): Show |
23 | a0001c0002t0001g0121a0001c0002t0001g0146a0001c0002t0001g0158others(20): Show | 24 | HG00609.hp2 HG00642.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.2271+1276_2271+128 others(15): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99384196 | |||||
chr2:99384196
|
C | CAAAAAAA others(5): Show |
1 | a0001c0003t0017g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2271+1286_2271+128 others(16): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99384196 | |||||
chr2:99384326
|
C | CA | 38 | a0001c0003t0004g0007a0001c0003t0004g0008a0001c0003t0004g0020others(35): Show | 41 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.2271+1406dupA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99384326 | |||||
chr2:99384425
|
G | A | 1 | a0001c0002t0003g0177 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2271+1504G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384425 | ||||||
chr2:99384464
|
C | T | 6 | a0001c0003t0002g0034a0001c0003t0009g0027a0001c0003t0009g0028others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2271+1543C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384464 | ||||||
chr2:99384486
|
A | C | 1 | a0001c0003t0001g0115 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2271+1565A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384486 | ||||||
chr2:99384614
|
G | A | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2271+1693G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384614 | ||||||
chr2:99384646
|
A | G | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2271+1725A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384646 | ||||||
chr2:99384711
|
C | G | 1 | a0002c0001t0002g0261 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2271+1790C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384711 | ||||||
chr2:99384943
|
C | T | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2271+2022C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99384943 | ||||||
chr2:99385140
|
G | A | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2271+2219G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385140 | ||||||
chr2:99385173
|
A | C | 1 | a0002c0001t0005g0224 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2271+2252A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385173 | ||||||
chr2:99385336
|
C | T | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2271+2415C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385336 | ||||||
chr2:99385408
|
T | C | 6 | a0001c0003t0002g0034a0001c0003t0009g0027a0001c0003t0009g0028others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2271+2487T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385408 | ||||||
chr2:99385471
|
C | A | 1 | a0001c0002t0010g0124 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2271+2550C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385471 | ||||||
chr2:99385478
|
G | A | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2271+2557G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385478 | ||||||
chr2:99385531
|
C | T | 197 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(194): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2271+2610C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385531 | ||||||
chr2:99385534
|
G | A | 1 | a0001c0003t0017g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2271+2613G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385534 | ||||||
chr2:99385602
|
G | A | 198 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(195): Show | 232 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.2271+2681G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385602 | ||||||
chr2:99385655
|
A | G | 1 | a0001c0003t0001g0111 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2271+2734A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385655 | ||||||
chr2:99385700
|
A | G | 1 | a0002c0007t0005g0230 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2271+2779A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99385700 | ||||||
chr2:99386027
|
G | A | 197 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(194): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2271+3106G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99386027 | ||||||
chr2:99386143
|
A | G | 3 | a0001c0002t0003g0133a0001c0002t0003g0134a0001c0002t0016g0135 | 3 | HG03579.hp1 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2271+3222A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99386143 | ||||||
chr2:99386312
|
A | G | 1 | a0002c0001t0002g0243 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2271+3391A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99386312 | ||||||
chr2:99386468
|
C | CGT | 36 | a0001c0003t0002g0305a0002c0001t0002g0191a0002c0001t0002g0205others(33): Show | 37 | HG00408.hp1 HG00558.hp1 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.2272-3215_2272-321 others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99386468 | |||||
chr2:99386468
|
C | CGTGT | 4 | a0001c0012t0002g0278a0002c0001t0002g0261a0002c0001t0005g0194others(1): Show | 4 | HG02258.hp1 HG02738.hp1 NA18978.hp1 others(1): Show |
intron_variant | MODIFIER | c.2272-3217_2272-321 others(8): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99386468 | |||||
chr2:99386468
|
CGTGT | C | 14 | a0001c0003t0004g0036a0001c0003t0004g0038a0001c0003t0004g0041others(11): Show | 15 | HG01070.hp2 HG01071.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.2272-3217_2272-321 others(8): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99386468 | |||||
chr2:99386468
|
CGTGTGT | C | 30 | a0001c0003t0004g0007a0001c0003t0004g0008a0001c0003t0004g0020others(27): Show | 33 | HG00280.hp1 HG01358.hp2 HG01516.hp2 others(30): Show |
intron_variant | MODIFIER | c.2272-3219_2272-321 others(10): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99386468 | |||||
chr2:99386468
|
CGTGTGTG others(1): Show |
C | 11 | a0001c0002t0003g0173a0001c0002t0007g0183a0001c0003t0002g0034others(8): Show | 11 | HG00735.hp1 HG01106.hp1 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.2272-3221_2272-321 others(12): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99386468 | |||||
chr2:99386468
|
CGTGTGTG others(3): Show |
C | 142 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(139): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.2272-3223_2272-321 others(14): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99386468 | |||||
chr2:99386521
|
C | CTG | 3 | a0001c0004t0001g0083a0001c0004t0001g0092a0001c0004t0001g0093 | 3 | HG02698.hp2 HG02735.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.2272-3183_2272-318 others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99386521 | |||||
chr2:99386537
|
T | G | 4 | a0001c0003t0002g0034a0001c0011t0022g0304a0002c0001t0002g0019others(1): Show | 5 | HG01934.hp2 HG01975.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.2272-3181T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99386537 | ||||||
chr2:99386709
|
G | T | 1 | a0001c0003t0017g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2272-3009G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99386709 | ||||||
chr2:99386713
|
G | T | 1 | a0001c0003t0017g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2272-3005G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99386713 | ||||||
chr2:99386715
|
C | CG | 14 | a0001c0002t0001g0121a0001c0002t0001g0139a0001c0002t0001g0141others(11): Show | 14 | HG01175.hp2 HG01255.hp2 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.2272-2996dupG | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99386715 | |||||
chr2:99386741
|
T | C | 1 | a0001c0003t0001g0116 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2272-2977T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99386741 | ||||||
chr2:99387069
|
C | T | 1 | a0002c0001t0005g0195 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.2272-2649C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99387069 | ||||||
chr2:99387427
|
T | C | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2272-2291T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99387427 | ||||||
chr2:99387458
|
A | G | 1 | a0002c0001t0005g0231 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2272-2260A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99387458 | ||||||
chr2:99387538
|
A | G | 1 | a0001c0005t0002g0296 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2272-2180A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99387538 | ||||||
chr2:99387702
|
A | G | 49 | a0001c0003t0001g0076a0001c0003t0001g0111a0001c0003t0001g0112others(46): Show | 59 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.2272-2016A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99387702 | ||||||
chr2:99387713
|
G | A | 38 | a0001c0003t0004g0007a0001c0003t0004g0008a0001c0003t0004g0020others(35): Show | 41 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.2272-2005G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99387713 | ||||||
chr2:99388436
|
G | GT | 159 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(156): Show | 190 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.2272-1275dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99388436 | |||||
chr2:99388436
|
G | GTT | 35 | a0001c0003t0004g0007a0001c0003t0004g0008a0001c0003t0004g0020others(32): Show | 38 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(35): Show |
intron_variant | MODIFIER | c.2272-1276_2272-127 others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99388436 | |||||
chr2:99388611
|
A | G | 1 | a0001c0003t0021g0302 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2272-1107A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99388611 | ||||||
chr2:99388791
|
A | T | 1 | a0002c0001t0005g0190 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2272-927A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99388791 | ||||||
chr2:99388830
|
C | T | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.2272-888C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99388830 | ||||||
chr2:99388855
|
G | A | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2272-863G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99388855 | ||||||
chr2:99389103
|
G | A | 2 | a0001c0003t0014g0032a0001c0003t0014g0033 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.2272-615G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99389103 | ||||||
chr2:99389149
|
T | A | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2272-569T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99389149 | ||||||
chr2:99389370
|
G | A | 4 | a0001c0002t0010g0122a0001c0002t0010g0123a0001c0002t0010g0124others(1): Show | 4 | HG02630.hp2 HG02717.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.2272-348G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99389370 | ||||||
chr2:99389411
|
C | T | 153 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(150): Show | 183 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.2272-307C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | chr2 | 99389411 | ||||||
chr2:99389598
|
G | GAGTA | 197 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(194): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2272-116_2272-113d others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr2 | 99389598 | |||||
chr2:99390119
|
A | G | 1 | a0001c0003t0021g0302 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2404-100A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 15/23 | chr2 | 99390119 | ||||||
chr2:99390157
|
G | T | 197 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(194): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2404-62G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 15/23 | chr2 | 99390157 | ||||||
chr2:99390163
|
C | T | 1 | a0002c0001t0005g0224 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2404-56C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 15/23 | chr2 | 99390163 | ||||||
chr2:99390427
|
G | GT | 158 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(155): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.2586+40dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr2 | 99390427 | |||||
chr2:99390441
|
T | A | 3 | a0001c0003t0004g0036a0001c0012t0002g0278a0002c0001t0002g0269 | 3 | HG01168.hp1 HG01346.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.2586+40T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 16/23 | chr2 | 99390441 | ||||||
chr2:99390441
|
T | TA | 36 | a0001c0003t0002g0305a0001c0003t0004g0007a0001c0003t0004g0008others(33): Show | 39 | HG00280.hp1 HG01358.hp2 HG01516.hp2 others(36): Show |
intron_variant | MODIFIER | c.2586+45dupA | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 16/23 | INFO_REALIGN_3_PRIME | chr2 | 99390441 | |||||
chr2:99390853
|
A | T | 1 | a0001c0003t0001g0071 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2748+148A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99390853 | ||||||
chr2:99390940
|
A | T | 197 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(194): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2748+235A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99390940 | ||||||
chr2:99391095
|
T | C | 1 | a0001c0003t0017g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2748+390T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391095 | ||||||
chr2:99391103
|
C | T | 1 | a0001c0004t0001g0094 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2748+398C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391103 | ||||||
chr2:99391141
|
G | A | 5 | a0001c0002t0003g0015a0001c0002t0003g0162a0001c0002t0003g0165others(2): Show | 6 | HG02040.hp2 NA18612.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.2748+436G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391141 | ||||||
chr2:99391144
|
T | C | 1 | a0002c0001t0005g0224 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2748+439T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391144 | ||||||
chr2:99391353
|
T | C | 1 | a0001c0011t0022g0304 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2748+648T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391353 | ||||||
chr2:99391382
|
G | C | 2 | a0001c0003t0004g0058a0001c0003t0004g0060 | 2 | NA18971.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.2748+677G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391382 | ||||||
chr2:99391389
|
G | A | 2 | a0002c0001t0002g0271a0002c0001t0002g0273 | 2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2748+684G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391389 | ||||||
chr2:99391502
|
C | T | 3 | a0001c0003t0004g0007a0001c0003t0004g0046a0001c0003t0024g0037 | 4 | HG02257.hp2 HG02818.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2748+797C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391502 | ||||||
chr2:99391729
|
C | CT | 22 | a0001c0002t0003g0164a0001c0002t0003g0167a0001c0003t0001g0111others(19): Show | 24 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.2748+1043dupT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 99391729 | |||||
chr2:99391729
|
C | CTT | 12 | a0002c0001t0002g0191a0002c0001t0002g0204a0002c0001t0002g0225others(9): Show | 12 | HG00408.hp1 NA18612.hp2 NA18940.hp2 others(9): Show |
intron_variant | MODIFIER | c.2748+1042_2748+104 others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 99391729 | |||||
chr2:99391729
|
CT | C | 7 | a0001c0002t0001g0144a0001c0002t0003g0126a0001c0002t0003g0128others(4): Show | 7 | HG00140.hp1 HG00408.hp2 HG00733.hp2 others(4): Show |
intron_variant | MODIFIER | c.2748+1043delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr2 | 99391729 | |||||
chr2:99391945
|
C | A | 197 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(194): Show | 231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.2749-1022C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391945 | ||||||
chr2:99391956
|
C | T | 1 | a0001c0003t0001g0117 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2749-1011C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99391956 | ||||||
chr2:99392131
|
G | A | 1 | a0001c0002t0003g0182 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2749-836G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99392131 | ||||||
chr2:99392142
|
C | G | 1 | a0002c0001t0005g0223 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2749-825C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99392142 | ||||||
chr2:99392580
|
G | A | 148 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(145): Show | 178 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.2749-387G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99392580 | ||||||
chr2:99392668
|
A | G | 1 | a0001c0003t0002g0305 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2749-299A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99392668 | ||||||
chr2:99392707
|
G | A | 1 | a0001c0002t0003g0160 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2749-260G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 17/23 | chr2 | 99392707 | ||||||
chr2:99393291
|
T | A | 1 | a0001c0006t0004g0044 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.2880+193T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99393291 | ||||||
chr2:99393337
|
A | G | 1 | a0002c0001t0002g0249 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2880+239A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99393337 | ||||||
chr2:99393403
|
G | A | 1 | a0001c0002t0001g0121 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2880+305G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99393403 | ||||||
chr2:99393460
|
C | T | 1 | a0002c0001t0002g0280 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.2880+362C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99393460 | ||||||
chr2:99393461
|
G | A | 147 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(144): Show | 177 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.2880+363G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99393461 | ||||||
chr2:99393581
|
T | C | 36 | a0002c0001t0002g0221a0002c0001t0002g0283a0002c0001t0002g0286others(33): Show | 38 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.2880+483T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99393581 | ||||||
chr2:99393665
|
A | C | 1 | a0001c0002t0003g0175 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2880+567A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99393665 | ||||||
chr2:99393965
|
A | T | 1 | a0001c0003t0004g0050 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2881-302A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99393965 | ||||||
chr2:99394042
|
A | G | 1 | a0001c0002t0003g0173 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2881-225A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99394042 | ||||||
chr2:99394127
|
C | T | 1 | a0001c0003t0014g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2881-140C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99394127 | ||||||
chr2:99394222
|
A | G | 78 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(75): Show | 97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.2881-45A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99394222 | ||||||
chr2:99394239
|
A | G | 1 | a0002c0001t0002g0287 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2881-28A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 18/23 | chr2 | 99394239 | ||||||
chr2:99395194
|
A | C | 1 | a0001c0002t0001g0140 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.3254+311A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395194 | ||||||
chr2:99395209
|
A | T | 6 | a0001c0003t0002g0034a0001c0003t0009g0027a0001c0003t0009g0028others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3254+326A>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395209 | ||||||
chr2:99395212
|
C | T | 78 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(75): Show | 97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.3254+329C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395212 | ||||||
chr2:99395251
|
C | G | 199 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(196): Show | 233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.3254+368C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395251 | ||||||
chr2:99395643
|
G | A | 3 | a0002c0001t0002g0240a0002c0001t0002g0242a0002c0001t0002g0263 | 3 | NA18956.hp1 NA18957.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.3254+760G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395643 | ||||||
chr2:99395661
|
T | C | 1 | a0001c0003t0004g0294 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3254+778T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395661 | ||||||
chr2:99395737
|
T | A | 78 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(75): Show | 97 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.3254+854T>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395737 | ||||||
chr2:99395779
|
G | A | 1 | a0002c0001t0005g0224 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.3254+896G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395779 | ||||||
chr2:99395845
|
G | A | 1 | a0002c0001t0002g0249 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.3255-915G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395845 | ||||||
chr2:99395991
|
G | A | 1 | a0001c0003t0001g0119 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3255-769G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395991 | ||||||
chr2:99395993
|
T | C | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.3255-767T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99395993 | ||||||
chr2:99396050
|
C | T | 196 | a0001c0002t0001g0006a0001c0002t0001g0011a0001c0002t0001g0012others(193): Show | 230 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.3255-710C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99396050 | ||||||
chr2:99396145
|
A | G | 3 | a0001c0002t0003g0164a0001c0002t0003g0167a0003c0010t0003g0159 | 3 | NA18950.hp1 NA18966.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.3255-615A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99396145 | ||||||
chr2:99396334
|
C | T | 1 | a0001c0002t0003g0179 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.3255-426C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99396334 | ||||||
chr2:99396335
|
G | A | 9 | a0001c0003t0001g0076a0001c0003t0001g0111a0001c0003t0001g0114others(6): Show | 12 | HG00609.hp2 HG02148.hp1 HG03669.hp2 others(9): Show |
intron_variant | MODIFIER | c.3255-425G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99396335 | ||||||
chr2:99396338
|
C | T | 2 | a0001c0003t0014g0032a0001c0003t0014g0033 | 2 | HG01891.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.3255-422C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99396338 | ||||||
chr2:99396366
|
T | G | 2 | a0002c0001t0002g0264a0002c0001t0002g0265 | 2 | HG00558.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.3255-394T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99396366 | ||||||
chr2:99396635
|
T | C | 1 | a0001c0002t0001g0130 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.3255-125T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 21/23 | chr2 | 99396635 | ||||||
chr2:99397112
|
G | C | 1 | a0001c0003t0004g0057 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.3393+214G>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99397112 | ||||||
chr2:99397294
|
CCTTT | C | 3 | a0002c0001t0002g0246a0002c0001t0002g0280a0002c0001t0002g0303 | 3 | NA18962.hp2 NA18964.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.3393+399_3393+402d others(6): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr2 | 99397294 | |||||
chr2:99397449
|
G | A | 8 | a0002c0001t0002g0192a0002c0001t0002g0205a0002c0001t0002g0206others(5): Show | 8 | HG01884.hp1 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3393+551G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99397449 | ||||||
chr2:99397487
|
C | CCA | 38 | a0001c0003t0004g0007a0001c0003t0004g0008a0001c0003t0004g0020others(35): Show | 41 | HG00280.hp1 HG01168.hp1 HG01358.hp2 others(38): Show |
intron_variant | MODIFIER | c.3393+590_3393+591d others(4): Show |
EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr2 | 99397487 | |||||
chr2:99397692
|
A | G | 1 | a0002c0001t0002g0218 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3393+794A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99397692 | ||||||
chr2:99397702
|
G | A | 1 | a0001c0003t0001g0116 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3393+804G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99397702 | ||||||
chr2:99397862
|
A | G | 6 | a0001c0003t0002g0034a0001c0003t0009g0027a0001c0003t0009g0028others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3394-886A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99397862 | ||||||
chr2:99397902
|
A | G | 1 | a0002c0001t0002g0239 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3394-846A>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99397902 | ||||||
chr2:99397931
|
G | T | 60 | a0001c0003t0001g0009a0001c0003t0001g0066a0001c0003t0001g0067others(57): Show | 71 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.3394-817G>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99397931 | ||||||
chr2:99397931
|
GT | G | 50 | a0001c0003t0002g0034a0001c0003t0004g0007a0001c0003t0004g0008others(47): Show | 54 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.3394-804delT | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr2 | 99397931 | |||||
chr2:99397932
|
T | G | 1 | a0001c0003t0017g0120 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3394-816T>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99397932 | ||||||
chr2:99398566
|
T | C | 6 | a0001c0003t0002g0034a0001c0003t0009g0027a0001c0003t0009g0028others(3): Show | 6 | HG02818.hp2 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3394-182T>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99398566 | ||||||
chr2:99398661
|
C | G | 60 | a0001c0003t0001g0009a0001c0003t0001g0066a0001c0003t0001g0067others(57): Show | 71 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.3394-87C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99398661 | ||||||
chr2:99398715
|
C | G | 1 | a0001c0004t0001g0093 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3394-33C>G | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99398715 | ||||||
chr2:99398718
|
C | A | 1 | a0002c0001t0002g0267 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.3394-30C>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 22/23 | chr2 | 99398718 | ||||||
chr2:99398928
|
G | A | 1 | a0001c0004t0001g0105 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3555+19G>A | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 23/23 | chr2 | 99398928 | ||||||
chr2:99399031
|
C | T | 1 | a0002c0001t0005g0220 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.3555+122C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 23/23 | chr2 | 99399031 | ||||||
chr2:99399100
|
C | T | 5 | a0001c0005t0002g0021a0001c0005t0002g0296a0001c0005t0002g0297others(2): Show | 6 | HG01070.hp2 HG01071.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.3555+191C>T | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 23/23 | chr2 | 99399100 | ||||||
chr2:99399176
|
A | C | 2 | a0001c0003t0008g0003a0001c0003t0008g0082 | 5 | NA18939.hp1 NA18941.hp1 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.3556-131A>C | EIF5B | ENSG00000158417.12 | transcript | ENST00000289371.11 | protein_coding | 23/23 | chr2 | 99399176 |