geneid | 25929 |
---|---|
ensemblid | ENSG00000082516.9 |
hgncid | 20043 |
symbol | GEMIN5 |
name | gem nuclear organelle associated protein 5 |
refseq_nuc | NM_015465.5 |
refseq_prot | NP_056280.2 |
ensembl_nuc | ENST00000285873.8 |
ensembl_prot | ENSP00000285873.6 |
mane_status | MANE Select |
chr | chr5 |
start | 154887411 |
end | 154938211 |
strand | - |
ver | v1.2 |
region | chr5:154887411-154938211 |
region5000 | chr5:154882411-154943211 |
regionname0 | GEMIN5_chr5_154887411_154938211 |
regionname5000 | GEMIN5_chr5_154882411_154943211 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1508 | 245 | 49 | 50 | 101 | 13 | 31 | 70 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0002 | 0/0 | 1508 | 39 | 9 | 13 | 10 | 3 | 4 | 8 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0003 | 1/0 | 1508 | 33 | 15 | 2 | 14 | 0 | 1 | 10 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0004 | 0/0 | 1508 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0005 | 0/0 | 1508 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0006 | 0/0 | 1508 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0007 | 0/0 | 1508 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0008 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0009 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0010 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0011 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0012 | 0/0 | 1508 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0013 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0014 | 0/0 | 1508 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0015 | 0/0 | 1508 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0016 | 0/0 | 1508 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 4527 | 232 | 40 | 49 | 99 | 13 | 30 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0002 | 0/0 | 4527 | 32 | 6 | 11 | 9 | 3 | 3 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0003 | 1/0 | 4527 | 17 | 3 | 2 | 10 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0004 | 0/0 | 4527 | 9 | 9 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0005 | 0/0 | 4527 | 7 | 7 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0006 | 0/0 | 4527 | 6 | 6 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0007 | 0/0 | 4527 | 4 | 0 | 0 | 4 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0008 | 0/0 | 4527 | 3 | 2 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0009 | 0/0 | 4527 | 3 | 3 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0010 | 0/0 | 4527 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0011 | 0/0 | 4527 | 2 | 0 | 0 | 1 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0012 | 0/0 | 4527 | 2 | 1 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0013 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0014 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0015 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0016 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0017 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0018 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0019 | 0/0 | 4527 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0020 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0021 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0022 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0023 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0024 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0025 | 0/0 | 4527 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0026 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0027 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0028 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0029 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0030 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
c0031 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 878 | 291 | 66 | 53 | 130 | 11 | 29 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
t0002 | 0/0 | 878 | 40 | 17 | 11 | 0 | 5 | 7 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
t0003 | 0/0 | 878 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
t0004 | 0/0 | 878 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
t0005 | 0/0 | 878 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
t0006 | 0/0 | 878 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
t0007 | 0/0 | 878 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
t0008 | 0/0 | 878 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0003 | 0/0 | 5 | 2 | 0 | 0 | 0 | 3 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0004 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0008 | 0/1 | 3 | 0 | 1 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0012 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0016 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 4527 | 232 | 40 | 49 | 99 | 13 | 30 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0001c0004 | 0/0 | 4527 | 9 | 9 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0001c0014 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0001c0025 | 0/0 | 4527 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0001c0029 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0001c0030 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0002c0002 | 0/0 | 4527 | 32 | 6 | 11 | 9 | 3 | 3 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0002c0008 | 0/0 | 4527 | 3 | 2 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0002c0011 | 0/0 | 4527 | 2 | 0 | 0 | 1 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0002c0018 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0002c0021 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0003c0003 | 1/0 | 4527 | 17 | 3 | 2 | 10 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0003c0005 | 0/0 | 4527 | 7 | 7 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0003c0007 | 0/0 | 4527 | 4 | 0 | 0 | 4 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0003c0009 | 0/0 | 4527 | 3 | 3 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0003c0015 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0003c0023 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0004c0006 | 0/0 | 4527 | 6 | 6 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0005c0012 | 0/0 | 4527 | 2 | 1 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0006c0020 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0006c0022 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0007c0010 | 0/0 | 4527 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0008c0031 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0009c0016 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0010c0024 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0011c0028 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0012c0026 | 0/0 | 4527 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0013c0027 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0014c0019 | 0/0 | 4527 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0015c0017 | 0/0 | 4527 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0016c0013 | 0/0 | 4527 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5404 | 193 | 25 | 37 | 99 | 8 | 23 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0001c0001t0002 | 0/0 | 5404 | 36 | 15 | 10 | 0 | 5 | 6 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0001c0001t0003 | 0/0 | 5404 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0001c0001t0006 | 0/0 | 5404 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0001c0004t0001 | 0/0 | 5404 | 8 | 8 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0001c0004t0005 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0001c0014t0001 | 0/0 | 5404 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0001c0025t0001 | 0/0 | 5404 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0001c0029t0002 | 0/0 | 5404 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0001c0030t0001 | 0/0 | 5404 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0002c0002t0001 | 0/0 | 5404 | 32 | 6 | 11 | 9 | 3 | 3 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0002c0008t0001 | 0/0 | 5404 | 3 | 2 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0002c0011t0001 | 0/0 | 5404 | 2 | 0 | 0 | 1 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0002c0018t0001 | 0/0 | 5404 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0002c0021t0001 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0003c0003t0001 | 1/0 | 5404 | 16 | 3 | 2 | 10 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0003c0003t0007 | 0/0 | 5404 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0003c0005t0001 | 0/0 | 5404 | 7 | 7 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0003c0007t0001 | 0/0 | 5404 | 4 | 0 | 0 | 4 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0003c0009t0001 | 0/0 | 5404 | 3 | 3 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0003c0015t0008 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0003c0023t0001 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0004c0006t0001 | 0/0 | 5404 | 6 | 6 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0005c0012t0002 | 0/0 | 5404 | 2 | 1 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0006c0020t0001 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0006c0022t0001 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0007c0010t0001 | 0/0 | 5404 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0008c0031t0001 | 0/0 | 5404 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0009c0016t0001 | 0/0 | 5404 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0010c0024t0001 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0011c0028t0002 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0012c0026t0001 | 0/0 | 5404 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0013c0027t0001 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0014c0019t0001 | 0/0 | 5404 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0015c0017t0004 | 0/0 | 5404 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
a0016c0013t0001 | 0/0 | 5404 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | copy fasta | chr5 | 154882411 | 154943211 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0008 | 0/1 | 3 | 0 | 1 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0016 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0020 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0003 | 0/0 | 5 | 2 | 0 | 0 | 0 | 3 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0001t0006g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0004t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0004t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0004t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0004t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0004t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0004t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0004t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0004t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0004t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0014t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0025t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0029t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0001c0030t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0008t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0008t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0008t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0011t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0011t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0018t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0002c0021t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0003t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0003t0001g0012 | 1/0 | 2 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0003t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0003t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0003t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0003t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0003t0007g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0005t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0005t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0005t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0005t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0005t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0005t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0005t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0007t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0007t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0007t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0007t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0009t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0009t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0009t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0015t0008g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0003c0023t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0004c0006t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0004c0006t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0004c0006t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0004c0006t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0004c0006t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0005c0012t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0005c0012t0002g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0006c0020t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0006c0022t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0007c0010t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0007c0010t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0008c0031t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0009c0016t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0010c0024t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0011c0028t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0012c0026t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0013c0027t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0014c0019t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0015c0017t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
a0016c0013t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0244 | EUR | GBR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0240 | EUR | FIN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | FIN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0283 | EUR | FIN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00558 | hp2 | a0003 | c0007 | t0001 | g0075 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0054 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00621 | hp2 | a0001 | c0014 | t0001 | g0211 | EAS | CHS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0247 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01069 | hp2 | a0012 | c0026 | t0001 | g0105 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01071 | hp1 | a0001 | c0001 | t0003 | g0246 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0061 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0285 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01109 | hp1 | a0002 | c0018 | t0001 | g0046 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01243 | hp1 | a0002 | c0008 | t0001 | g0064 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0055 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0077 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | IBS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0062 | EUR | IBS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | IBS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | IBS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01891 | hp1 | a0003 | c0005 | t0001 | g0079 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01934 | hp1 | a0001 | c0029 | t0002 | g0279 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01952 | hp1 | a0003 | c0003 | t0001 | g0084 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0286 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0073 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01978 | hp1 | a0003 | c0003 | t0001 | g0085 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0076 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0068 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0051 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02055 | hp1 | a0003 | c0005 | t0001 | g0080 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02055 | hp2 | a0002 | c0008 | t0001 | g0066 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02080 | hp1 | a0008 | c0031 | t0001 | g0071 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02080 | hp2 | a0003 | c0007 | t0001 | g0044 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02129 | hp1 | a0003 | c0007 | t0001 | g0045 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02148 | hp1 | a0002 | c0002 | t0001 | g0057 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CDX | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CDX | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0093 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02257 | hp2 | a0001 | c0004 | t0001 | g0126 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02258 | hp1 | a0001 | c0004 | t0001 | g0127 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02280 | hp2 | a0005 | c0012 | t0002 | g0223 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02300 | hp2 | a0002 | c0002 | t0001 | g0078 | AMR | PEL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02451 | hp2 | a0003 | c0005 | t0001 | g0089 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0242 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02615 | hp1 | a0004 | c0006 | t0001 | g0032 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02630 | hp1 | a0011 | c0028 | t0002 | g0231 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02630 | hp2 | a0001 | c0004 | t0005 | g0039 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02647 | hp2 | a0006 | c0022 | t0001 | g0049 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0284 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02698 | hp2 | a0005 | c0012 | t0002 | g0222 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02723 | hp2 | a0003 | c0005 | t0001 | g0081 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02735 | hp2 | a0014 | c0019 | t0001 | g0072 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0238 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02886 | hp1 | a0002 | c0021 | t0001 | g0094 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02895 | hp1 | a0003 | c0003 | t0001 | g0091 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02965 | hp1 | a0003 | c0005 | t0001 | g0082 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02965 | hp2 | a0001 | c0004 | t0001 | g0121 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02976 | hp1 | a0003 | c0003 | t0001 | g0035 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02976 | hp2 | a0003 | c0003 | t0001 | g0090 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03098 | hp1 | a0004 | c0006 | t0001 | g0275 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03130 | hp1 | a0001 | c0004 | t0001 | g0124 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03139 | hp2 | a0003 | c0009 | t0001 | g0042 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03209 | hp1 | a0001 | c0004 | t0001 | g0128 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0226 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03225 | hp1 | a0004 | c0006 | t0001 | g0278 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03225 | hp2 | a0003 | c0009 | t0001 | g0040 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0287 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03453 | hp2 | a0015 | c0017 | t0004 | g0281 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03486 | hp1 | a0001 | c0004 | t0001 | g0123 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03516 | hp1 | a0001 | c0004 | t0001 | g0125 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03516 | hp2 | a0002 | c0008 | t0001 | g0065 | AFR | ESN | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | STU | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | STU | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03704 | hp2 | a0001 | c0025 | t0001 | g0180 | SAS | PJL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03831 | hp1 | a0002 | c0011 | t0001 | g0048 | SAS | BEB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | BEB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0267 | SAS | BEB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0070 | SAS | STU | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG04199 | hp2 | a0001 | c0001 | t0006 | g0216 | SAS | STU | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | STU | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0227 | SAS | STU | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0047 | SAS | STU | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | STU | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18522 | hp1 | a0003 | c0005 | t0001 | g0086 | AFR | YRI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18522 | hp2 | a0004 | c0006 | t0001 | g0276 | AFR | YRI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18747 | hp1 | a0003 | c0003 | t0001 | g0088 | EAS | CHB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | YRI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18906 | hp2 | a0006 | c0020 | t0001 | g0067 | AFR | YRI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18939 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18940 | hp2 | a0003 | c0007 | t0001 | g0074 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18949 | hp2 | a0003 | c0003 | t0001 | g0013 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18954 | hp2 | a0007 | c0010 | t0001 | g0033 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18956 | hp1 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18959 | hp2 | a0001 | c0030 | t0001 | g0215 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18962 | hp1 | a0003 | c0003 | t0001 | g0083 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18964 | hp2 | a0003 | c0003 | t0001 | g0009 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18982 | hp1 | a0003 | c0003 | t0001 | g0272 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0038 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19000 | hp1 | a0016 | c0013 | t0001 | g0120 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19001 | hp2 | a0007 | c0010 | t0001 | g0034 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19002 | hp2 | a0003 | c0003 | t0001 | g0013 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19006 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19011 | hp1 | a0003 | c0003 | t0001 | g0271 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19030 | hp1 | a0001 | c0004 | t0001 | g0122 | AFR | LWK | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | LWK | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | LWK | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19043 | hp2 | a0010 | c0024 | t0001 | g0225 | AFR | LWK | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19085 | hp2 | a0009 | c0016 | t0001 | g0050 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19087 | hp1 | a0003 | c0003 | t0001 | g0012 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19090 | hp2 | a0002 | c0011 | t0001 | g0059 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19240 | hp1 | a0003 | c0005 | t0001 | g0087 | AFR | YRI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | YRI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ASW | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ASW | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0228 | EUR | TSI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0060 | EUR | TSI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0053 | EUR | TSI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0250 | EUR | TSI | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA20905 | hp1 | a0003 | c0003 | t0007 | g0288 | SAS | GIH | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0010 | SAS | GIH | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0056 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02109 | hp1 | a0003 | c0009 | t0001 | g0041 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0230 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02486 | hp1 | a0013 | c0027 | t0001 | g0248 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02486 | hp2 | a0003 | c0015 | t0008 | g0289 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG02559 | hp2 | a0004 | c0006 | t0001 | g0277 | AFR | ACB | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03471 | hp1 | a0003 | c0023 | t0001 | g0043 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG03471 | hp2 | a0004 | c0006 | t0001 | g0032 | AFR | MSL | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | USA | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | USA | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | USA | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | USA | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | LWK | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0008 | REF | REF | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
homoSapiens_grch38 | hp1 | a0003 | c0003 | t0001 | g0012 | REF | REF | GEMIN5_chr5_154882411_154943211 | GEMIN5 | chr5 | 154882411 | 154943211 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:154889392
|
A | C | 1 | a0015 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.4288T>G | p.Ser1430Ala | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/28 | 4366/5404 | 4288/4527 | 1430/1508 | chr5 | 154889392 | ||
chr5:154891455
|
C | T | 1 | a0015 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.4048G>A | p.Glu1350Lys | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/28 | 4126/5404 | 4048/4527 | 1350/1508 | chr5 | 154891455 | ||
chr5:154891677
|
A | C | 1 | a0006 | 2 | HG02647.hp2 NA18906.hp2 |
missense_variant | MODERATE | c.3826T>G | p.Leu1276Val | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/28 | 3904/5404 | 3826/4527 | 1276/1508 | chr5 | 154891677 | ||
chr5:154896226
|
G | A | 6 | a0002a0006a0008others(3): Show | 45 | HG00597.hp2 HG01081.hp1 HG01109.hp1 others(42): Show |
missense_variant | MODERATE | c.3463C>T | p.Pro1155Ser | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/28 | 3541/5404 | 3463/4527 | 1155/1508 | chr5 | 154896226 | ||
chr5:154896226
|
G | C | 1 | a0012 | 1 | HG01069.hp2 | missense_variant | MODERATE | c.3463C>G | p.Pro1155Ala | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/28 | 3541/5404 | 3463/4527 | 1155/1508 | chr5 | 154896226 | ||
chr5:154896231
|
T | G | 1 | a0011 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.3458A>C | p.Glu1153Ala | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/28 | 3536/5404 | 3458/4527 | 1153/1508 | chr5 | 154896231 | ||
chr5:154896280
|
A | G | 1 | a0014 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.3409T>C | p.Ser1137Pro | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/28 | 3487/5404 | 3409/4527 | 1137/1508 | chr5 | 154896280 | ||
chr5:154898553
|
C | T | 1 | a0010 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.3232G>A | p.Val1078Ile | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/28 | 3310/5404 | 3232/4527 | 1078/1508 | chr5 | 154898553 | ||
chr5:154911849
|
C | T | 9 | a0001a0004a0005others(6): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
missense_variant | MODERATE | c.2045G>A | p.Arg682Gln | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/28 | 2123/5404 | 2045/4527 | 682/1508 | chr5 | 154911849 | ||
chr5:154917961
|
C | T | 1 | a0009 | 1 | NA19085.hp2 | missense_variant | MODERATE | c.1643G>A | p.Gly548Asp | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 12/28 | 1721/5404 | 1643/4527 | 548/1508 | chr5 | 154917961 | ||
chr5:154921417
|
T | G | 1 | a0004 | 6 | HG02559.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
missense_variant | MODERATE | c.1388A>C | p.Gln463Pro | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/28 | 1466/5404 | 1388/4527 | 463/1508 | chr5 | 154921417 | ||
chr5:154927510
|
G | C | 1 | a0005 | 2 | HG02280.hp2 HG02698.hp2 |
missense_variant | MODERATE | c.955C>G | p.Arg319Gly | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/28 | 1033/5404 | 955/4527 | 319/1508 | chr5 | 154927510 | ||
chr5:154931520
|
C | G | 1 | a0016 | 1 | NA19000.hp1 | missense_variant | MODERATE | c.719G>C | p.Cys240Ser | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/28 | 797/5404 | 719/4527 | 240/1508 | chr5 | 154931520 | ||
chr5:154931560
|
T | C | 1 | a0008 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.679A>G | p.Asn227Asp | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/28 | 757/5404 | 679/4527 | 227/1508 | chr5 | 154931560 | ||
chr5:154937111
|
G | A | 1 | a0004 | 6 | HG02559.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
missense_variant | MODERATE | c.241C>T | p.Leu81Phe | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 2/28 | 319/5404 | 241/4527 | 81/1508 | chr5 | 154937111 | ||
chr5:154937976
|
G | T | 1 | a0007 | 2 | NA18954.hp2 NA19001.hp2 |
missense_variant | MODERATE | c.158C>A | p.Pro53Gln | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/28 | 236/5404 | 158/4527 | 53/1508 | chr5 | 154937976 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:154888336
|
C | G | 1 | a0001c0025 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.4401G>C | p.Leu1467Leu | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 28/28 | 4479/5404 | 4401/4527 | 1467/1508 | chr5 | 154888336 | ||
chr5:154889342
|
C | T | 27 | a0001c0001a0001c0004a0001c0014others(24): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
synonymous_variant | LOW | c.4338G>A | p.Ala1446Ala | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/28 | 4416/5404 | 4338/4527 | 1446/1508 | chr5 | 154889342 | ||
chr5:154891327
|
T | C | 1 | a0003c0005 | 7 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(4): Show |
synonymous_variant | LOW | c.4176A>G | p.Gln1392Gln | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/28 | 4254/5404 | 4176/4527 | 1392/1508 | chr5 | 154891327 | ||
chr5:154892388
|
G | A | 27 | a0001c0001a0001c0004a0001c0014others(24): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
splice_region_variant&synonymous_variant | LOW | c.3759C>T | p.Asp1253Asp | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 25/28 | 3837/5404 | 3759/4527 | 1253/1508 | chr5 | 154892388 | ||
chr5:154892457
|
C | A | 1 | a0002c0011 | 2 | HG03831.hp1 NA19090.hp2 |
synonymous_variant | LOW | c.3690G>T | p.Ala1230Ala | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 25/28 | 3768/5404 | 3690/4527 | 1230/1508 | chr5 | 154892457 | ||
chr5:154896122
|
T | C | 1 | a0002c0021 | 1 | HG02886.hp1 | synonymous_variant | LOW | c.3567A>G | p.Pro1189Pro | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/28 | 3645/5404 | 3567/4527 | 1189/1508 | chr5 | 154896122 | ||
chr5:154899193
|
T | C | 1 | a0001c0029 | 1 | HG01934.hp1 | splice_region_variant&synonymous_variant | LOW | c.3132A>G | p.Lys1044Lys | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 22/28 | 3210/5404 | 3132/4527 | 1044/1508 | chr5 | 154899193 | ||
chr5:154899274
|
C | T | 1 | a0002c0018 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.3051G>A | p.Pro1017Pro | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 22/28 | 3129/5404 | 3051/4527 | 1017/1508 | chr5 | 154899274 | ||
chr5:154902567
|
T | C | 1 | a0006c0022 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.2838A>G | p.Thr946Thr | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/28 | 2916/5404 | 2838/4527 | 946/1508 | chr5 | 154902567 | ||
chr5:154902603
|
A | G | 1 | a0002c0008 | 3 | HG01243.hp1 HG02055.hp2 HG03516.hp2 |
synonymous_variant | LOW | c.2802T>C | p.Gly934Gly | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/28 | 2880/5404 | 2802/4527 | 934/1508 | chr5 | 154902603 | ||
chr5:154902675
|
T | C | 12 | a0002c0002a0002c0008a0002c0011others(9): Show | 48 | HG00597.hp2 HG01081.hp1 HG01109.hp1 others(45): Show |
splice_region_variant&synonymous_variant | LOW | c.2730A>G | p.Gly910Gly | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/28 | 2808/5404 | 2730/4527 | 910/1508 | chr5 | 154902675 | ||
chr5:154904511
|
G | A | 1 | a0003c0023 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.2628C>T | p.Ser876Ser | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/28 | 2706/5404 | 2628/4527 | 876/1508 | chr5 | 154904511 | ||
chr5:154911854
|
T | C | 1 | a0001c0030 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.2040A>G | p.Gly680Gly | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/28 | 2118/5404 | 2040/4527 | 680/1508 | chr5 | 154911854 | ||
chr5:154921353
|
G | T | 1 | a0003c0015 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.1452C>A | p.Pro484Pro | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/28 | 1530/5404 | 1452/4527 | 484/1508 | chr5 | 154921353 | ||
chr5:154921380
|
A | C | 12 | a0001c0001a0001c0014a0001c0025others(9): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
synonymous_variant | LOW | c.1425T>G | p.Thr475Thr | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/28 | 1503/5404 | 1425/4527 | 475/1508 | chr5 | 154921380 | ||
chr5:154927412
|
T | C | 13 | a0001c0001a0001c0004a0001c0025others(10): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
synonymous_variant | LOW | c.1053A>G | p.Leu351Leu | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/28 | 1131/5404 | 1053/4527 | 351/1508 | chr5 | 154927412 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:154887481
|
G | A | 1 | a0001c0004t0005 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*729C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 28/28 | 729 | chr5 | 154887481 | |||||
chr5:154887487
|
T | C | 1 | a0001c0001t0003 | 2 | HG01069.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*723A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 28/28 | 723 | chr5 | 154887487 | |||||
chr5:154887540
|
T | A | 1 | a0015c0017t0004 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*670A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 28/28 | 670 | chr5 | 154887540 | |||||
chr5:154887577
|
T | A | 1 | a0001c0004t0005 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*633A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 28/28 | 633 | chr5 | 154887577 | |||||
chr5:154887718
|
T | C | 1 | a0001c0001t0006 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*492A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 28/28 | 492 | chr5 | 154887718 | |||||
chr5:154887728
|
A | G | 5 | a0001c0001t0002a0001c0001t0003a0001c0029t0002others(2): Show | 42 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*482T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 28/28 | 482 | chr5 | 154887728 | |||||
chr5:154938191
|
G | C | 1 | a0003c0003t0007 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/28 | 58 | chr5 | 154938191 | |||||
chr5:154938194
|
T | G | 1 | a0003c0015t0008 | 1 | HG02486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-61A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/28 | 61 | chr5 | 154938194 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:154888648
|
C | T | 1 | a0001c0001t0002g0240 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.4360-271G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/27 | chr5 | 154888648 | ||||||
chr5:154888855
|
T | TTTTTG | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(275): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.4359+461_4359+465d others(7): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/27 | chr5 | 154888855 | ||||||
chr5:154888900
|
C | T | 5 | a0004c0006t0001g0032a0004c0006t0001g0275a0004c0006t0001g0276others(2): Show | 6 | HG02559.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.4359+421G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/27 | chr5 | 154888900 | ||||||
chr5:154888919
|
G | A | 8 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0139others(5): Show | 8 | HG00558.hp1 HG00621.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.4359+402C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/27 | chr5 | 154888919 | ||||||
chr5:154888985
|
T | A | 1 | a0001c0001t0001g0177 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.4359+336A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/27 | chr5 | 154888985 | ||||||
chr5:154889066
|
C | T | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4359+255G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/27 | chr5 | 154889066 | ||||||
chr5:154889106
|
G | A | 1 | a0015c0017t0004g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4359+215C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/27 | chr5 | 154889106 | ||||||
chr5:154889143
|
T | A | 45 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(42): Show | 49 | HG00597.hp2 HG01081.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.4359+178A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 27/27 | chr5 | 154889143 | ||||||
chr5:154889505
|
T | C | 1 | a0002c0021t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4263-88A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154889505 | ||||||
chr5:154889545
|
T | C | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4263-128A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154889545 | ||||||
chr5:154889706
|
G | T | 1 | a0001c0001t0001g0260 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.4263-289C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154889706 | ||||||
chr5:154889784
|
T | C | 1 | a0001c0001t0002g0230 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.4263-367A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154889784 | ||||||
chr5:154889809
|
C | T | 1 | a0002c0002t0001g0069 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.4263-392G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154889809 | ||||||
chr5:154890054
|
C | T | 8 | a0001c0004t0001g0121a0001c0004t0001g0122a0001c0004t0001g0123others(5): Show | 8 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.4263-637G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154890054 | ||||||
chr5:154890087
|
T | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.4263-670A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154890087 | ||||||
chr5:154890254
|
T | G | 1 | a0003c0007t0001g0074 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.4263-837A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154890254 | ||||||
chr5:154890269
|
T | A | 1 | a0003c0015t0008g0289 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.4263-852A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154890269 | ||||||
chr5:154890459
|
A | G | 37 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(34): Show | 41 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.4262+782T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154890459 | ||||||
chr5:154890467
|
A | AT | 14 | a0001c0001t0001g0103a0001c0001t0001g0111a0001c0001t0001g0155others(11): Show | 14 | HG00140.hp2 HG02148.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.4262+773dupA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154890467 | ||||||
chr5:154890467
|
AT | A | 11 | a0001c0001t0001g0098a0001c0001t0001g0137a0001c0001t0001g0172others(8): Show | 11 | HG00735.hp2 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.4262+773delA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154890467 | ||||||
chr5:154890614
|
C | T | 2 | a0006c0020t0001g0067a0006c0022t0001g0049 | 2 | HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4262+627G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154890614 | ||||||
chr5:154890936
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(264): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.4262+305T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154890936 | ||||||
chr5:154891004
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.4262+237G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154891004 | ||||||
chr5:154891035
|
C | T | 2 | a0003c0005t0001g0080a0003c0005t0001g0082 | 2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.4262+206G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154891035 | ||||||
chr5:154891051
|
C | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0162a0001c0001t0001g0178 | 6 | HG01106.hp1 HG01123.hp2 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.4262+190G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154891051 | ||||||
chr5:154891055
|
C | CT | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(174): Show | 216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.4262+185dupA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154891055 | ||||||
chr5:154891055
|
C | CTT | 79 | a0001c0001t0001g0024a0001c0001t0001g0096a0001c0001t0001g0100others(76): Show | 85 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.4262+184_4262+185d others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154891055 | ||||||
chr5:154891055
|
C | CTTT | 12 | a0001c0004t0001g0127a0002c0002t0001g0037a0002c0002t0001g0047others(9): Show | 12 | HG01109.hp1 HG01346.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.4262+183_4262+185d others(5): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 26/27 | chr5 | 154891055 | ||||||
chr5:154891786
|
T | C | 1 | a0015c0017t0004g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3761-44A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 25/27 | chr5 | 154891786 | ||||||
chr5:154891831
|
A | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.3761-89T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 25/27 | chr5 | 154891831 | ||||||
chr5:154891977
|
T | C | 37 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(34): Show | 41 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(38): Show |
intron_variant | MODIFIER | c.3761-235A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 25/27 | chr5 | 154891977 | ||||||
chr5:154892035
|
C | G | 7 | a0001c0001t0001g0007a0001c0001t0001g0132a0001c0001t0001g0136others(4): Show | 9 | HG00609.hp1 HG02129.hp2 HG03927.hp1 others(6): Show |
intron_variant | MODIFIER | c.3761-293G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 25/27 | chr5 | 154892035 | ||||||
chr5:154892072
|
A | C | 1 | a0003c0003t0001g0090 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3760+315T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 25/27 | chr5 | 154892072 | ||||||
chr5:154892240
|
C | T | 4 | a0003c0007t0001g0044a0003c0007t0001g0045a0003c0007t0001g0074others(1): Show | 4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3760+147G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 25/27 | chr5 | 154892240 | ||||||
chr5:154892631
|
G | T | 1 | a0001c0001t0001g0145 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.3598-82C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154892631 | ||||||
chr5:154892706
|
A | G | 1 | a0008c0031t0001g0071 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.3598-157T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154892706 | ||||||
chr5:154892776
|
G | A | 2 | a0003c0007t0001g0044a0003c0007t0001g0045 | 2 | HG02080.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.3598-227C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154892776 | ||||||
chr5:154892902
|
G | T | 2 | a0003c0009t0001g0040a0003c0009t0001g0041 | 2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3598-353C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154892902 | ||||||
chr5:154892925
|
C | T | 1 | a0003c0015t0008g0289 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3598-376G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154892925 | ||||||
chr5:154892926
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.3598-377C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154892926 | ||||||
chr5:154892927
|
C | T | 3 | a0001c0001t0001g0132a0001c0004t0005g0039a0015c0017t0004g0281 | 3 | HG02630.hp2 HG03453.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.3598-378G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154892927 | ||||||
chr5:154893037
|
T | C | 52 | a0001c0004t0005g0039a0002c0002t0001g0006a0002c0002t0001g0010others(49): Show | 56 | HG00558.hp2 HG00597.hp2 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.3598-488A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893037 | ||||||
chr5:154893054
|
G | A | 1 | a0002c0021t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3598-505C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893054 | ||||||
chr5:154893097
|
A | AAAAC | 44 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(41): Show | 48 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.3598-552_3598-549d others(6): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893097 | ||||||
chr5:154893105
|
C | A | 2 | a0003c0003t0001g0090a0003c0003t0001g0091 | 2 | HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.3598-556G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893105 | ||||||
chr5:154893224
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3598-675C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893224 | ||||||
chr5:154893249
|
C | T | 8 | a0003c0003t0001g0035a0003c0015t0008g0289a0004c0006t0001g0032others(5): Show | 9 | HG02486.hp2 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.3598-700G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893249 | ||||||
chr5:154893255
|
T | TA | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(161): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.3598-707dupT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893255 | ||||||
chr5:154893255
|
T | TAA | 51 | a0001c0001t0001g0015a0001c0001t0001g0018a0001c0001t0001g0023others(48): Show | 54 | HG00423.hp2 HG00438.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.3598-708_3598-707d others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893255 | ||||||
chr5:154893255
|
TAAAAAAA others(10): Show |
T | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | NA19006.hp1 NA19011.hp2 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.3598-723_3598-707d others(19): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893255 | ||||||
chr5:154893329
|
C | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(59): Show | 76 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.3598-780G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893329 | ||||||
chr5:154893335
|
C | T | 1 | a0002c0002t0001g0061 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3598-786G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893335 | ||||||
chr5:154893343
|
T | C | 3 | a0001c0001t0001g0147a0001c0001t0001g0154a0001c0001t0001g0169 | 3 | HG00423.hp1 NA18968.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.3598-794A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893343 | ||||||
chr5:154893387
|
C | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(143): Show | 175 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.3598-838G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893387 | ||||||
chr5:154893388
|
G | A | 3 | a0001c0001t0002g0227a0001c0001t0002g0236a0001c0001t0002g0237 | 3 | HG01168.hp1 HG01175.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.3598-839C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893388 | ||||||
chr5:154893410
|
C | T | 1 | a0002c0002t0001g0076 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3598-861G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893410 | ||||||
chr5:154893418
|
C | CA | 8 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0261others(5): Show | 8 | HG00438.hp1 HG01109.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.3598-870dupT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893418 | ||||||
chr5:154893517
|
CAT | C | 3 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265 | 3 | HG01070.hp1 HG01934.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.3598-970_3598-969d others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893517 | ||||||
chr5:154893600
|
C | T | 1 | a0002c0021t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3598-1051G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893600 | ||||||
chr5:154893813
|
G | A | 1 | a0015c0017t0004g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3598-1264C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893813 | ||||||
chr5:154893893
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.3598-1344C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893893 | ||||||
chr5:154893903
|
G | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(264): Show | 312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.3598-1354C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154893903 | ||||||
chr5:154894141
|
T | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.3598-1592A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154894141 | ||||||
chr5:154894210
|
G | A | 4 | a0003c0007t0001g0044a0003c0007t0001g0045a0003c0007t0001g0074others(1): Show | 4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3598-1661C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154894210 | ||||||
chr5:154894421
|
G | A | 3 | a0002c0008t0001g0064a0002c0008t0001g0065a0002c0008t0001g0066 | 3 | HG01243.hp1 HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3597+1671C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154894421 | ||||||
chr5:154894519
|
A | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(265): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.3597+1573T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154894519 | ||||||
chr5:154894797
|
C | T | 1 | a0001c0001t0001g0022 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.3597+1295G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154894797 | ||||||
chr5:154894881
|
C | T | 1 | a0015c0017t0004g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3597+1211G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154894881 | ||||||
chr5:154894905
|
T | TA | 12 | a0001c0004t0001g0122a0001c0004t0001g0123a0001c0004t0001g0124others(9): Show | 13 | HG02257.hp2 HG02258.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.3597+1186dupT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154894905 | ||||||
chr5:154894939
|
C | T | 1 | a0002c0018t0001g0046 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3597+1153G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154894939 | ||||||
chr5:154895003
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.3597+1089A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895003 | ||||||
chr5:154895004
|
G | A | 1 | a0002c0021t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3597+1088C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895004 | ||||||
chr5:154895045
|
C | CCTTGTTG others(9): Show |
38 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(35): Show | 42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.3597+1046_3597+104 others(20): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895045 | ||||||
chr5:154895047
|
C | G | 38 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(35): Show | 42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.3597+1045G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895047 | ||||||
chr5:154895048
|
C | T | 38 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(35): Show | 42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.3597+1044G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895048 | ||||||
chr5:154895049
|
A | T | 38 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(35): Show | 42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.3597+1043T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895049 | ||||||
chr5:154895098
|
A | C | 1 | a0001c0001t0002g0244 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3597+994T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895098 | ||||||
chr5:154895132
|
T | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(265): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.3597+960A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895132 | ||||||
chr5:154895188
|
G | C | 4 | a0003c0007t0001g0044a0003c0007t0001g0045a0003c0007t0001g0074others(1): Show | 4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3597+904C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895188 | ||||||
chr5:154895335
|
G | GGA | 43 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(40): Show | 47 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(44): Show |
intron_variant | MODIFIER | c.3597+755_3597+756d others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895335 | ||||||
chr5:154895336
|
GAAAA | G | 11 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0099others(8): Show | 15 | HG00140.hp2 HG00642.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.3597+752_3597+755d others(6): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895336 | ||||||
chr5:154895360
|
G | C | 1 | a0001c0001t0001g0173 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3597+732C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895360 | ||||||
chr5:154895521
|
T | G | 4 | a0003c0007t0001g0044a0003c0007t0001g0045a0003c0007t0001g0074others(1): Show | 4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3597+571A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895521 | ||||||
chr5:154895570
|
T | G | 4 | a0003c0007t0001g0044a0003c0007t0001g0045a0003c0007t0001g0074others(1): Show | 4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3597+522A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895570 | ||||||
chr5:154895674
|
TATTAC | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(216): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.3597+413_3597+417d others(7): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895674 | ||||||
chr5:154895757
|
C | T | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3597+335G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895757 | ||||||
chr5:154895762
|
G | A | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3597+330C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895762 | ||||||
chr5:154895785
|
G | A | 13 | a0001c0004t0001g0121a0001c0004t0001g0122a0001c0004t0001g0123others(10): Show | 14 | HG02257.hp2 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.3597+307C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895785 | ||||||
chr5:154895937
|
T | C | 13 | a0001c0004t0001g0121a0001c0004t0001g0122a0001c0004t0001g0123others(10): Show | 14 | HG02257.hp2 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.3597+155A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154895937 | ||||||
chr5:154896019
|
G | A | 4 | a0001c0001t0002g0029a0001c0001t0002g0243a0001c0001t0003g0246others(1): Show | 5 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.3597+73C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 24/27 | chr5 | 154896019 | ||||||
chr5:154896402
|
G | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(144): Show | 176 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.3346-59C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154896402 | ||||||
chr5:154896451
|
C | A | 33 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(30): Show | 37 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.3346-108G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154896451 | ||||||
chr5:154896470
|
T | C | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3346-127A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154896470 | ||||||
chr5:154896501
|
A | G | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(266): Show | 314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.3346-158T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154896501 | ||||||
chr5:154896868
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.3346-525G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154896868 | ||||||
chr5:154897113
|
T | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.3346-770A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897113 | ||||||
chr5:154897177
|
A | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.3346-834T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897177 | ||||||
chr5:154897403
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3345+1037C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897403 | ||||||
chr5:154897440
|
C | G | 3 | a0002c0008t0001g0064a0002c0008t0001g0065a0002c0008t0001g0066 | 3 | HG01243.hp1 HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.3345+1000G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897440 | ||||||
chr5:154897465
|
A | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.3345+975T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897465 | ||||||
chr5:154897724
|
C | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(276): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.3345+716G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897724 | ||||||
chr5:154897745
|
G | GT | 7 | a0001c0001t0001g0149a0001c0001t0001g0253a0004c0006t0001g0032others(4): Show | 8 | HG01981.hp1 HG02559.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.3345+694dupA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897745 | ||||||
chr5:154897902
|
GT | G | 8 | a0001c0004t0001g0121a0001c0004t0001g0122a0001c0004t0001g0123others(5): Show | 8 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.3345+537delA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897902 | ||||||
chr5:154897903
|
T | G | 1 | a0001c0001t0001g0150 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.3345+537A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897903 | ||||||
chr5:154897913
|
T | TG | 4 | a0003c0007t0001g0044a0003c0007t0001g0045a0003c0007t0001g0074others(1): Show | 4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3345+526dupC | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897913 | ||||||
chr5:154897914
|
G | GT | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(135): Show | 169 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.3345+525dupA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897914 | ||||||
chr5:154897914
|
G | GTT | 69 | a0001c0001t0001g0008a0001c0001t0001g0023a0001c0001t0001g0108others(66): Show | 78 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.3345+524_3345+525d others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897914 | ||||||
chr5:154897979
|
A | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(265): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.3345+461T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897979 | ||||||
chr5:154897985
|
C | T | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3345+455G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154897985 | ||||||
chr5:154898076
|
T | G | 3 | a0001c0001t0001g0192a0001c0001t0001g0197a0001c0001t0001g0198 | 3 | HG00609.hp2 HG02056.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.3345+364A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154898076 | ||||||
chr5:154898127
|
C | T | 9 | a0003c0003t0001g0090a0003c0003t0001g0091a0003c0005t0001g0079others(6): Show | 9 | HG01891.hp1 HG02055.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.3345+313G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154898127 | ||||||
chr5:154898386
|
A | G | 3 | a0001c0001t0001g0020a0001c0001t0001g0171a0001c0001t0001g0173 | 4 | HG01167.hp1 HG01169.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.3345+54T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 23/27 | chr5 | 154898386 | ||||||
chr5:154898786
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3135-136A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 22/27 | chr5 | 154898786 | ||||||
chr5:154898934
|
A | G | 2 | a0001c0001t0002g0249a0001c0001t0002g0250 | 2 | HG01099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3134+257T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 22/27 | chr5 | 154898934 | ||||||
chr5:154899328
|
C | T | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(265): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.3015-18G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154899328 | ||||||
chr5:154899572
|
A | C | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3015-262T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154899572 | ||||||
chr5:154899619
|
TA | T | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(258): Show | 305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.3015-310delT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154899619 | ||||||
chr5:154899621
|
A | T | 1 | a0002c0002t0001g0006 | 3 | HG02280.hp1 HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3015-311T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154899621 | ||||||
chr5:154899829
|
T | C | 1 | a0001c0001t0002g0238 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3015-519A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154899829 | ||||||
chr5:154899931
|
T | TA | 9 | a0001c0001t0001g0173a0001c0004t0005g0039a0002c0002t0001g0052others(6): Show | 9 | HG00558.hp2 HG01109.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.3015-622dupT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154899931 | ||||||
chr5:154899983
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.3015-673A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154899983 | ||||||
chr5:154900138
|
A | G | 33 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(30): Show | 37 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.3015-828T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154900138 | ||||||
chr5:154900217
|
T | C | 1 | a0003c0005t0001g0081 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3015-907A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154900217 | ||||||
chr5:154900252
|
A | C | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.3015-942T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154900252 | ||||||
chr5:154900436
|
A | T | 1 | a0001c0001t0001g0207 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3014+903T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154900436 | ||||||
chr5:154900454
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.3014+885C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154900454 | ||||||
chr5:154900839
|
T | G | 1 | a0015c0017t0004g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3014+500A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154900839 | ||||||
chr5:154900844
|
G | T | 4 | a0003c0007t0001g0044a0003c0007t0001g0045a0003c0007t0001g0074others(1): Show | 4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.3014+495C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154900844 | ||||||
chr5:154900885
|
G | GTCCAAAC | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.3014+453_3014+454i others(9): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154900885 | ||||||
chr5:154900949
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3014+390G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154900949 | ||||||
chr5:154901162
|
C | T | 6 | a0001c0004t0001g0121a0001c0004t0001g0122a0001c0004t0001g0123others(3): Show | 6 | HG02257.hp2 HG02965.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.3014+177G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154901162 | ||||||
chr5:154901163
|
A | G | 5 | a0002c0002t0001g0056a0002c0002t0001g0060a0002c0002t0001g0061others(2): Show | 5 | HG01081.hp1 HG01123.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.3014+176T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 21/27 | chr5 | 154901163 | ||||||
chr5:154901508
|
G | A | 2 | a0001c0001t0001g0189a0001c0001t0001g0191 | 2 | HG01884.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2867-22C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901508 | ||||||
chr5:154901656
|
G | A | 273 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(270): Show | 320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.2867-170C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901656 | ||||||
chr5:154901676
|
T | G | 1 | a0001c0001t0001g0030 | 2 | NA18612.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.2867-190A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901676 | ||||||
chr5:154901744
|
A | G | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2867-258T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901744 | ||||||
chr5:154901795
|
T | TTC | 249 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(246): Show | 293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.2867-310_2867-309i others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901795 | ||||||
chr5:154901795
|
T | TTTC | 19 | a0001c0001t0001g0020a0001c0001t0001g0098a0001c0001t0001g0171others(16): Show | 20 | HG00558.hp2 HG00597.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.2867-310_2867-309i others(5): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901795 | ||||||
chr5:154901853
|
G | A | 43 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(40): Show | 47 | HG00597.hp2 HG01081.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.2867-367C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901853 | ||||||
chr5:154901856
|
G | A | 43 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(40): Show | 54 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.2867-370C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901856 | ||||||
chr5:154901894
|
G | A | 1 | a0001c0001t0001g0273 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2867-408C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901894 | ||||||
chr5:154901948
|
A | G | 1 | a0003c0023t0001g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2867-462T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154901948 | ||||||
chr5:154902274
|
A | G | 1 | a0003c0015t0008g0289 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2866+265T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154902274 | ||||||
chr5:154902378
|
G | T | 4 | a0003c0007t0001g0044a0003c0007t0001g0045a0003c0007t0001g0074others(1): Show | 4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2866+161C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154902378 | ||||||
chr5:154902384
|
G | A | 1 | a0001c0025t0001g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2866+155C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 20/27 | chr5 | 154902384 | ||||||
chr5:154902683
|
G | C | 38 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(35): Show | 42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
splice_region_variant&intron_variant | LOW | c.2729-7C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 19/27 | chr5 | 154902683 | ||||||
chr5:154902847
|
C | A | 38 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(35): Show | 42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.2729-171G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 19/27 | chr5 | 154902847 | ||||||
chr5:154902991
|
T | C | 53 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0099others(50): Show | 63 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.2728+89A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 19/27 | chr5 | 154902991 | ||||||
chr5:154903279
|
A | C | 8 | a0001c0004t0001g0121a0001c0004t0001g0122a0001c0004t0001g0123others(5): Show | 8 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2633-104T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903279 | ||||||
chr5:154903515
|
G | C | 11 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0113others(8): Show | 13 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2633-340C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903515 | ||||||
chr5:154903540
|
T | G | 1 | a0002c0021t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2633-365A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903540 | ||||||
chr5:154903636
|
A | G | 3 | a0002c0008t0001g0064a0002c0008t0001g0065a0002c0008t0001g0066 | 3 | HG01243.hp1 HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2633-461T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903636 | ||||||
chr5:154903637
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2633-462A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903637 | ||||||
chr5:154903671
|
T | A | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(265): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.2633-496A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903671 | ||||||
chr5:154903810
|
C | T | 1 | a0003c0009t0001g0042 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2633-635G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903810 | ||||||
chr5:154903826
|
A | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0155 | 2 | NA18971.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2633-651T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903826 | ||||||
chr5:154903834
|
A | T | 2 | a0001c0001t0001g0172a0001c0001t0002g0229 | 2 | HG00735.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2633-659T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903834 | ||||||
chr5:154903835
|
T | A | 33 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(30): Show | 37 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.2633-660A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903835 | ||||||
chr5:154903846
|
A | T | 1 | a0001c0001t0002g0234 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2632+661T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154903846 | ||||||
chr5:154904092
|
A | T | 3 | a0003c0009t0001g0040a0003c0009t0001g0041a0003c0009t0001g0042 | 3 | HG02109.hp1 HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2632+415T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154904092 | ||||||
chr5:154904100
|
C | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2632+407G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154904100 | ||||||
chr5:154904104
|
A | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2632+403T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154904104 | ||||||
chr5:154904146
|
AT | A | 4 | a0003c0007t0001g0044a0003c0007t0001g0045a0003c0007t0001g0074others(1): Show | 4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2632+360delA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 18/27 | chr5 | 154904146 | ||||||
chr5:154904756
|
A | G | 4 | a0003c0007t0001g0044a0003c0007t0001g0045a0003c0007t0001g0074others(1): Show | 4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.2510-127T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 17/27 | chr5 | 154904756 | ||||||
chr5:154904822
|
T | C | 1 | a0001c0004t0001g0121 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2510-193A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 17/27 | chr5 | 154904822 | ||||||
chr5:154904964
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2510-335C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 17/27 | chr5 | 154904964 | ||||||
chr5:154905086
|
C | T | 1 | a0014c0019t0001g0072 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2509+277G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 17/27 | chr5 | 154905086 | ||||||
chr5:154905143
|
A | C | 1 | a0001c0001t0001g0264 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2509+220T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 17/27 | chr5 | 154905143 | ||||||
chr5:154905143
|
A | G | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(265): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.2509+220T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 17/27 | chr5 | 154905143 | ||||||
chr5:154905259
|
A | C | 1 | a0003c0023t0001g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2509+104T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 17/27 | chr5 | 154905259 | ||||||
chr5:154905557
|
C | A | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2396-81G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154905557 | ||||||
chr5:154905609
|
A | G | 1 | a0002c0021t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2396-133T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154905609 | ||||||
chr5:154905634
|
G | A | 1 | a0003c0015t0008g0289 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2396-158C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154905634 | ||||||
chr5:154905700
|
G | GT | 58 | a0001c0001t0001g0024a0001c0001t0001g0100a0001c0001t0001g0114others(55): Show | 63 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.2396-225dupA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154905700 | ||||||
chr5:154905700
|
G | GTT | 8 | a0002c0002t0001g0047a0002c0002t0001g0056a0002c0002t0001g0070others(5): Show | 8 | HG01123.hp1 HG01975.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2396-226_2396-225d others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154905700 | ||||||
chr5:154905700
|
G | T | 10 | a0001c0001t0001g0134a0001c0001t0001g0135a0001c0001t0001g0139others(7): Show | 10 | HG00558.hp1 HG00621.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.2396-224C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154905700 | ||||||
chr5:154905760
|
C | T | 1 | a0001c0001t0001g0159 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2396-284G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154905760 | ||||||
chr5:154905959
|
G | A | 18 | a0001c0001t0001g0007a0001c0001t0001g0104a0001c0001t0001g0106others(15): Show | 20 | HG00323.hp2 HG00609.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.2396-483C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154905959 | ||||||
chr5:154906196
|
A | G | 2 | a0001c0001t0001g0031a0001c0001t0001g0267 | 3 | HG03017.hp1 HG03491.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2396-720T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154906196 | ||||||
chr5:154906208
|
C | T | 41 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(38): Show | 47 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.2396-732G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154906208 | ||||||
chr5:154906246
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.2396-770A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154906246 | ||||||
chr5:154906271
|
C | T | 2 | a0003c0005t0001g0087a0003c0005t0001g0089 | 2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2396-795G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154906271 | ||||||
chr5:154906425
|
C | T | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2396-949G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154906425 | ||||||
chr5:154907078
|
C | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2395+513G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907078 | ||||||
chr5:154907194
|
G | C | 1 | a0001c0001t0002g0234 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2395+397C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907194 | ||||||
chr5:154907243
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2395+348G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907243 | ||||||
chr5:154907309
|
A | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2395+282T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907309 | ||||||
chr5:154907330
|
C | T | 17 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0108others(14): Show | 19 | HG00423.hp1 HG02071.hp2 NA18747.hp2 others(16): Show |
intron_variant | MODIFIER | c.2395+261G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907330 | ||||||
chr5:154907424
|
A | G | 1 | a0003c0015t0008g0289 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2395+167T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907424 | ||||||
chr5:154907456
|
T | TGAAAAAA others(1): Show |
13 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0132others(10): Show | 15 | HG00609.hp1 HG02056.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.2395+134_2395+135i others(10): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907456 | ||||||
chr5:154907456
|
T | TGAAAAAA others(2): Show |
251 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(248): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.2395+134_2395+135i others(11): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907456 | ||||||
chr5:154907456
|
T | TGAAAAAA others(3): Show |
4 | a0001c0001t0001g0148a0001c0001t0002g0228a0003c0007t0001g0074others(1): Show | 4 | HG02486.hp2 NA18940.hp1 NA18940.hp2 others(1): Show |
intron_variant | MODIFIER | c.2395+134_2395+135i others(12): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907456 | ||||||
chr5:154907555
|
T | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2395+36A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 16/27 | chr5 | 154907555 | ||||||
chr5:154907835
|
A | G | 1 | a0001c0001t0001g0266 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2168-17T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154907835 | ||||||
chr5:154907880
|
T | C | 1 | a0003c0015t0008g0289 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2168-62A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154907880 | ||||||
chr5:154907900
|
T | C | 1 | a0002c0018t0001g0046 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2168-82A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154907900 | ||||||
chr5:154908038
|
G | C | 1 | a0001c0001t0001g0207 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2168-220C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908038 | ||||||
chr5:154908170
|
TC | T | 5 | a0002c0008t0001g0066a0002c0018t0001g0046a0006c0020t0001g0067others(2): Show | 5 | HG01109.hp1 HG02055.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2168-353delG | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908170 | ||||||
chr5:154908171
|
C | CT | 5 | a0002c0002t0001g0047a0002c0002t0001g0055a0003c0009t0001g0040others(2): Show | 5 | HG01255.hp2 HG02109.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.2168-354_2168-353i others(3): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908171 | ||||||
chr5:154908172
|
C | CT | 40 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0021others(37): Show | 48 | HG00140.hp2 HG00323.hp2 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.2168-355dupA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908172 | ||||||
chr5:154908172
|
C | CTT | 107 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(104): Show | 133 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.2168-356_2168-355d others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908172 | ||||||
chr5:154908172
|
C | CTTT | 29 | a0001c0001t0001g0026a0001c0001t0001g0096a0001c0001t0001g0108others(26): Show | 30 | HG00423.hp1 HG00423.hp2 HG00438.hp2 others(27): Show |
intron_variant | MODIFIER | c.2168-357_2168-355d others(5): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908172 | ||||||
chr5:154908172
|
C | T | 39 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(36): Show | 43 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(40): Show |
intron_variant | MODIFIER | c.2168-354G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908172 | ||||||
chr5:154908212
|
C | T | 2 | a0001c0014t0001g0211a0002c0002t0001g0068 | 2 | HG00621.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.2168-394G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908212 | ||||||
chr5:154908328
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2168-510C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908328 | ||||||
chr5:154908337
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2168-519G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908337 | ||||||
chr5:154908369
|
C | T | 1 | a0014c0019t0001g0072 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2168-551G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908369 | ||||||
chr5:154908418
|
T | A | 1 | a0001c0014t0001g0211 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2168-600A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908418 | ||||||
chr5:154908472
|
C | T | 1 | a0003c0009t0001g0041 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2168-654G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908472 | ||||||
chr5:154908608
|
C | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(276): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.2168-790G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908608 | ||||||
chr5:154908654
|
T | C | 7 | a0001c0001t0001g0020a0001c0001t0001g0098a0001c0001t0001g0171others(4): Show | 8 | HG00735.hp2 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.2168-836A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908654 | ||||||
chr5:154908866
|
G | A | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(265): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.2168-1048C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908866 | ||||||
chr5:154908888
|
G | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0176 | 3 | HG01981.hp2 HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2168-1070C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154908888 | ||||||
chr5:154909019
|
A | G | 8 | a0001c0004t0001g0121a0001c0004t0001g0122a0001c0004t0001g0123others(5): Show | 8 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2168-1201T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909019 | ||||||
chr5:154909055
|
C | T | 5 | a0004c0006t0001g0032a0004c0006t0001g0275a0004c0006t0001g0276others(2): Show | 6 | HG02559.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2168-1237G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909055 | ||||||
chr5:154909107
|
C | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(216): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.2168-1289G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909107 | ||||||
chr5:154909133
|
A | AT | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(136): Show | 166 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.2168-1316dupA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909133 | ||||||
chr5:154909133
|
A | ATT | 63 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.2168-1317_2168-131 others(6): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909133 | ||||||
chr5:154909133
|
A | ATTT | 10 | a0001c0001t0001g0171a0001c0001t0002g0226a0001c0001t0002g0229others(7): Show | 10 | HG00323.hp1 HG01167.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.2168-1318_2168-131 others(7): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909133 | ||||||
chr5:154909533
|
A | G | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(220): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.2168-1715T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909533 | ||||||
chr5:154909553
|
TACC | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(216): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.2168-1738_2168-173 others(7): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909553 | ||||||
chr5:154909620
|
C | T | 11 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0113others(8): Show | 13 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2168-1802G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909620 | ||||||
chr5:154909701
|
G | A | 1 | a0002c0021t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2168-1883C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909701 | ||||||
chr5:154909723
|
A | G | 8 | a0001c0004t0001g0121a0001c0004t0001g0122a0001c0004t0001g0123others(5): Show | 8 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2168-1905T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909723 | ||||||
chr5:154909750
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2168-1932C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909750 | ||||||
chr5:154909800
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2167+1927C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909800 | ||||||
chr5:154909827
|
A | G | 1 | a0015c0017t0004g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2167+1900T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909827 | ||||||
chr5:154909849
|
C | T | 5 | a0004c0006t0001g0032a0004c0006t0001g0275a0004c0006t0001g0276others(2): Show | 6 | HG02559.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2167+1878G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909849 | ||||||
chr5:154909980
|
AG | A | 4 | a0003c0009t0001g0040a0003c0009t0001g0041a0003c0009t0001g0042others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2167+1746delC | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909980 | ||||||
chr5:154909981
|
G | GA | 74 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(71): Show | 86 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.2167+1745dupT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154909981 | ||||||
chr5:154910005
|
A | C | 1 | a0001c0025t0001g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2167+1722T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910005 | ||||||
chr5:154910193
|
T | G | 38 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(35): Show | 42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.2167+1534A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910193 | ||||||
chr5:154910290
|
T | G | 1 | a0001c0029t0002g0279 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2167+1437A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910290 | ||||||
chr5:154910303
|
T | C | 8 | a0001c0004t0001g0121a0001c0004t0001g0122a0001c0004t0001g0123others(5): Show | 8 | HG02257.hp2 HG02258.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2167+1424A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910303 | ||||||
chr5:154910313
|
T | C | 1 | a0001c0001t0001g0014 | 2 | HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.2167+1414A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910313 | ||||||
chr5:154910323
|
A | C | 33 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(30): Show | 37 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.2167+1404T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910323 | ||||||
chr5:154910356
|
G | C | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2167+1371C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910356 | ||||||
chr5:154910402
|
C | T | 1 | a0002c0021t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2167+1325G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910402 | ||||||
chr5:154910479
|
G | A | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2167+1248C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910479 | ||||||
chr5:154910531
|
T | C | 1 | a0015c0017t0004g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2167+1196A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910531 | ||||||
chr5:154910624
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2167+1103A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910624 | ||||||
chr5:154910763
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2167+964T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910763 | ||||||
chr5:154910794
|
C | G | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(265): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.2167+933G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910794 | ||||||
chr5:154910878
|
T | G | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2167+849A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910878 | ||||||
chr5:154910912
|
T | G | 4 | a0003c0009t0001g0040a0003c0009t0001g0041a0003c0009t0001g0042others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2167+815A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910912 | ||||||
chr5:154910997
|
C | T | 5 | a0002c0018t0001g0046a0003c0009t0001g0040a0003c0009t0001g0041others(2): Show | 5 | HG01109.hp1 HG02109.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2167+730G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154910997 | ||||||
chr5:154911032
|
T | C | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(216): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.2167+695A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911032 | ||||||
chr5:154911101
|
T | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(265): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.2167+626A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911101 | ||||||
chr5:154911117
|
A | G | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2167+610T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911117 | ||||||
chr5:154911144
|
C | T | 1 | a0002c0021t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2167+583G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911144 | ||||||
chr5:154911191
|
G | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(143): Show | 175 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.2167+536C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911191 | ||||||
chr5:154911232
|
G | A | 1 | a0001c0001t0002g0250 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2167+495C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911232 | ||||||
chr5:154911241
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2167+486G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911241 | ||||||
chr5:154911242
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.2167+485C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911242 | ||||||
chr5:154911375
|
T | C | 1 | a0015c0017t0004g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2167+352A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911375 | ||||||
chr5:154911418
|
T | C | 2 | a0003c0005t0001g0087a0003c0005t0001g0089 | 2 | HG02451.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2167+309A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911418 | ||||||
chr5:154911421
|
G | A | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2167+306C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911421 | ||||||
chr5:154911456
|
C | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2167+271G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911456 | ||||||
chr5:154911460
|
C | T | 1 | a0001c0001t0002g0228 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2167+267G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911460 | ||||||
chr5:154911659
|
A | G | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(265): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.2167+68T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 15/27 | chr5 | 154911659 | ||||||
chr5:154911936
|
G | A | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(216): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.1996-38C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 14/27 | chr5 | 154911936 | ||||||
chr5:154912167
|
C | T | 1 | a0001c0001t0001g0207 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1996-269G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 14/27 | chr5 | 154912167 | ||||||
chr5:154912410
|
C | T | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1995+489G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 14/27 | chr5 | 154912410 | ||||||
chr5:154912490
|
T | G | 1 | a0003c0023t0001g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1995+409A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 14/27 | chr5 | 154912490 | ||||||
chr5:154912530
|
C | T | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1995+369G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 14/27 | chr5 | 154912530 | ||||||
chr5:154912533
|
T | C | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1995+366A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 14/27 | chr5 | 154912533 | ||||||
chr5:154912706
|
CA | C | 50 | a0001c0004t0005g0039a0002c0002t0001g0006a0002c0002t0001g0010others(47): Show | 54 | HG00558.hp2 HG00597.hp2 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.1995+192delT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 14/27 | chr5 | 154912706 | ||||||
chr5:154912727
|
A | G | 1 | a0001c0001t0002g0245 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1995+172T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 14/27 | chr5 | 154912727 | ||||||
chr5:154912812
|
G | C | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1995+87C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 14/27 | chr5 | 154912812 | ||||||
chr5:154913082
|
C | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0168 | 3 | NA18939.hp1 NA18946.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1856-44G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154913082 | ||||||
chr5:154913171
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1856-133T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154913171 | ||||||
chr5:154913190
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1856-152A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154913190 | ||||||
chr5:154913437
|
T | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(276): Show | 324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1856-399A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154913437 | ||||||
chr5:154913627
|
C | G | 1 | a0015c0017t0004g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1856-589G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154913627 | ||||||
chr5:154913682
|
T | C | 1 | a0003c0003t0001g0088 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1856-644A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154913682 | ||||||
chr5:154913873
|
T | C | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1856-835A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154913873 | ||||||
chr5:154914014
|
AATAC | A | 8 | a0001c0001t0001g0023a0001c0001t0001g0187a0001c0001t0001g0188others(5): Show | 9 | HG01884.hp2 HG02572.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.1856-980_1856-977d others(6): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154914014 | ||||||
chr5:154914202
|
G | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0014others(91): Show | 115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.1856-1164C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154914202 | ||||||
chr5:154914303
|
G | A | 1 | a0001c0001t0002g0244 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1856-1265C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154914303 | ||||||
chr5:154914509
|
CT | C | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(210): Show | 252 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1856-1472delA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154914509 | ||||||
chr5:154914509
|
CTT | C | 10 | a0001c0001t0001g0027a0001c0001t0001g0095a0001c0001t0001g0170others(7): Show | 11 | HG00408.hp2 HG01081.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1856-1473_1856-147 others(6): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154914509 | ||||||
chr5:154914598
|
C | A | 1 | a0003c0007t0001g0075 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1856-1560G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154914598 | ||||||
chr5:154914904
|
T | C | 1 | a0001c0001t0002g0251 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1856-1866A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154914904 | ||||||
chr5:154914946
|
G | C | 1 | a0001c0001t0001g0202 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1856-1908C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154914946 | ||||||
chr5:154915103
|
C | T | 1 | a0001c0001t0001g0021 | 2 | HG02970.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1855+1895G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915103 | ||||||
chr5:154915256
|
G | C | 2 | a0001c0001t0001g0217a0001c0001t0006g0216 | 2 | HG04199.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1855+1742C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915256 | ||||||
chr5:154915262
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1855+1736A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915262 | ||||||
chr5:154915493
|
T | C | 1 | a0002c0002t0001g0068 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1855+1505A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915493 | ||||||
chr5:154915687
|
G | A | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1855+1311C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915687 | ||||||
chr5:154915735
|
C | A | 1 | a0002c0021t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1855+1263G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915735 | ||||||
chr5:154915817
|
A | C | 1 | a0002c0002t0001g0053 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1855+1181T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915817 | ||||||
chr5:154915861
|
A | G | 1 | a0001c0001t0001g0022 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1855+1137T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915861 | ||||||
chr5:154915894
|
ATTAT | A | 38 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(35): Show | 42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.1855+1100_1855+110 others(8): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915894 | ||||||
chr5:154915912
|
C | T | 4 | a0003c0007t0001g0044a0003c0007t0001g0045a0003c0007t0001g0074others(1): Show | 4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1855+1086G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154915912 | ||||||
chr5:154916052
|
T | A | 39 | a0001c0001t0002g0245a0002c0002t0001g0006a0002c0002t0001g0010others(36): Show | 43 | HG00597.hp2 HG00741.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.1855+946A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154916052 | ||||||
chr5:154916230
|
T | C | 5 | a0004c0006t0001g0032a0004c0006t0001g0275a0004c0006t0001g0276others(2): Show | 6 | HG02559.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1855+768A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154916230 | ||||||
chr5:154916271
|
G | GA | 12 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0107others(9): Show | 14 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1855+726dupT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154916271 | ||||||
chr5:154916403
|
T | C | 4 | a0001c0004t0001g0121a0001c0004t0001g0124a0001c0004t0001g0125others(1): Show | 4 | HG02257.hp2 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1855+595A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154916403 | ||||||
chr5:154916666
|
T | C | 1 | a0015c0017t0004g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1855+332A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154916666 | ||||||
chr5:154916688
|
A | T | 1 | a0003c0015t0008g0289 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1855+310T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154916688 | ||||||
chr5:154916777
|
G | C | 1 | a0003c0003t0007g0288 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1855+221C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154916777 | ||||||
chr5:154916976
|
G | C | 1 | a0002c0002t0001g0093 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1855+22C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 13/27 | chr5 | 154916976 | ||||||
chr5:154917228
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1674-49T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 12/27 | chr5 | 154917228 | ||||||
chr5:154917235
|
A | C | 58 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(55): Show | 69 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.1674-56T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 12/27 | chr5 | 154917235 | ||||||
chr5:154917562
|
G | A | 2 | a0005c0012t0002g0222a0005c0012t0002g0223 | 2 | HG02280.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.1673+369C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 12/27 | chr5 | 154917562 | ||||||
chr5:154917571
|
T | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1673+360A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 12/27 | chr5 | 154917571 | ||||||
chr5:154917697
|
A | C | 2 | a0001c0001t0001g0258a0001c0001t0001g0259 | 2 | NA18978.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1673+234T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 12/27 | chr5 | 154917697 | ||||||
chr5:154917739
|
G | A | 1 | a0003c0015t0008g0289 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1673+192C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 12/27 | chr5 | 154917739 | ||||||
chr5:154917767
|
C | T | 5 | a0004c0006t0001g0032a0004c0006t0001g0275a0004c0006t0001g0276others(2): Show | 6 | HG02559.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1673+164G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 12/27 | chr5 | 154917767 | ||||||
chr5:154917892
|
C | T | 1 | a0003c0003t0001g0090 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1673+39G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 12/27 | chr5 | 154917892 | ||||||
chr5:154918150
|
G | A | 4 | a0003c0007t0001g0044a0003c0007t0001g0045a0003c0007t0001g0074others(1): Show | 4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1600-146C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154918150 | ||||||
chr5:154918248
|
G | A | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(265): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.1600-244C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154918248 | ||||||
chr5:154918422
|
C | G | 1 | a0003c0015t0008g0289 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1600-418G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154918422 | ||||||
chr5:154918549
|
C | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1600-545G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154918549 | ||||||
chr5:154918607
|
G | T | 1 | a0003c0015t0008g0289 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1600-603C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154918607 | ||||||
chr5:154918666
|
G | C | 2 | a0001c0001t0001g0208a0001c0001t0001g0209 | 2 | HG02622.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1600-662C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154918666 | ||||||
chr5:154918794
|
T | C | 16 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0257others(13): Show | 18 | HG00438.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.1600-790A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154918794 | ||||||
chr5:154918869
|
C | A | 1 | a0001c0001t0001g0203 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1600-865G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154918869 | ||||||
chr5:154919194
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0174 | 2 | HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1599+773C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154919194 | ||||||
chr5:154919197
|
G | T | 4 | a0002c0002t0001g0051a0002c0002t0001g0052a0008c0031t0001g0071others(1): Show | 4 | HG02015.hp1 HG02080.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.1599+770C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154919197 | ||||||
chr5:154919599
|
T | C | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1599+368A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154919599 | ||||||
chr5:154919619
|
G | C | 2 | a0001c0001t0003g0246a0001c0001t0003g0247 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1599+348C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154919619 | ||||||
chr5:154919698
|
C | T | 2 | a0001c0004t0001g0127a0001c0004t0001g0128 | 2 | HG02258.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1599+269G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 11/27 | chr5 | 154919698 | ||||||
chr5:154920179
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1463-76A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154920179 | ||||||
chr5:154920190
|
A | G | 4 | a0003c0007t0001g0044a0003c0007t0001g0045a0003c0007t0001g0074others(1): Show | 4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1463-87T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154920190 | ||||||
chr5:154920190
|
A | T | 1 | a0015c0017t0004g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1463-87T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154920190 | ||||||
chr5:154920219
|
A | C | 1 | a0003c0015t0008g0289 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1463-116T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154920219 | ||||||
chr5:154920408
|
T | A | 1 | a0001c0001t0001g0204 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1463-305A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154920408 | ||||||
chr5:154920474
|
T | C | 2 | a0004c0006t0001g0277a0004c0006t0001g0278 | 2 | HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1463-371A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154920474 | ||||||
chr5:154920644
|
C | A | 1 | a0001c0001t0001g0168 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1463-541G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154920644 | ||||||
chr5:154921163
|
C | G | 1 | a0001c0001t0001g0147 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1462+180G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154921163 | ||||||
chr5:154921195
|
T | G | 1 | a0002c0021t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1462+148A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154921195 | ||||||
chr5:154921285
|
G | T | 2 | a0003c0009t0001g0040a0003c0009t0001g0041 | 2 | HG02109.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1462+58C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 10/27 | chr5 | 154921285 | ||||||
chr5:154921565
|
C | T | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1380-140G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154921565 | ||||||
chr5:154921572
|
T | C | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1380-147A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154921572 | ||||||
chr5:154921911
|
G | A | 10 | a0001c0001t0001g0004a0001c0001t0001g0021a0001c0001t0001g0099others(7): Show | 14 | HG00140.hp2 HG00642.hp2 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.1380-486C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154921911 | ||||||
chr5:154921937
|
A | C | 1 | a0001c0001t0001g0146 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1380-512T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154921937 | ||||||
chr5:154921947
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1380-522T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154921947 | ||||||
chr5:154922096
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1380-671T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922096 | ||||||
chr5:154922180
|
G | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1380-755C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922180 | ||||||
chr5:154922220
|
T | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(59): Show | 76 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1380-795A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922220 | ||||||
chr5:154922257
|
T | C | 1 | a0015c0017t0004g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1380-832A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922257 | ||||||
chr5:154922310
|
G | T | 2 | a0003c0003t0001g0084a0003c0003t0001g0085 | 2 | HG01952.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1380-885C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922310 | ||||||
chr5:154922314
|
C | A | 4 | a0003c0007t0001g0044a0003c0007t0001g0045a0003c0007t0001g0074others(1): Show | 4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1380-889G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922314 | ||||||
chr5:154922329
|
G | A | 1 | a0003c0015t0008g0289 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1380-904C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922329 | ||||||
chr5:154922357
|
T | C | 38 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(35): Show | 42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.1380-932A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922357 | ||||||
chr5:154922414
|
G | A | 59 | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0021others(56): Show | 70 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(67): Show |
intron_variant | MODIFIER | c.1380-989C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922414 | ||||||
chr5:154922697
|
G | GT | 49 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(46): Show | 53 | HG00438.hp2 HG00558.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.1380-1273dupA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922697 | ||||||
chr5:154922697
|
G | GTT | 7 | a0002c0011t0001g0048a0002c0018t0001g0046a0003c0009t0001g0040others(4): Show | 7 | HG01109.hp1 HG02109.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1380-1274_1380-127 others(6): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922697 | ||||||
chr5:154922803
|
TCTC | T | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(216): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.1380-1381_1380-137 others(7): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922803 | ||||||
chr5:154922841
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1380-1416G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922841 | ||||||
chr5:154922938
|
C | T | 1 | a0001c0001t0002g0226 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1380-1513G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922938 | ||||||
chr5:154922942
|
C | T | 3 | a0003c0005t0001g0080a0003c0005t0001g0081a0003c0005t0001g0082 | 3 | HG02055.hp1 HG02723.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1380-1517G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922942 | ||||||
chr5:154922943
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | NA18973.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1380-1518C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922943 | ||||||
chr5:154922985
|
C | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.1379+1484G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154922985 | ||||||
chr5:154923217
|
C | T | 6 | a0001c0004t0001g0121a0001c0004t0001g0122a0001c0004t0001g0123others(3): Show | 6 | HG02257.hp2 HG02965.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1379+1252G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154923217 | ||||||
chr5:154923355
|
G | A | 1 | a0002c0002t0001g0069 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1379+1114C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154923355 | ||||||
chr5:154923378
|
C | G | 1 | a0001c0001t0001g0113 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1379+1091G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154923378 | ||||||
chr5:154923609
|
A | T | 38 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(35): Show | 42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.1379+860T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154923609 | ||||||
chr5:154923715
|
C | T | 1 | a0003c0015t0008g0289 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1379+754G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154923715 | ||||||
chr5:154924049
|
G | C | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(265): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.1379+420C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 9/27 | chr5 | 154924049 | ||||||
chr5:154924688
|
A | C | 1 | a0001c0001t0001g0220 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1294-134T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924688 | ||||||
chr5:154924732
|
G | A | 2 | a0003c0003t0001g0090a0003c0003t0001g0091 | 2 | HG02895.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1294-178C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924732 | ||||||
chr5:154924771
|
C | T | 146 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(143): Show | 175 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1294-217G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924771 | ||||||
chr5:154924772
|
G | A | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1294-218C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924772 | ||||||
chr5:154924782
|
G | C | 4 | a0003c0007t0001g0044a0003c0007t0001g0045a0003c0007t0001g0074others(1): Show | 4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1294-228C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924782 | ||||||
chr5:154924846
|
A | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1294-292T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924846 | ||||||
chr5:154924858
|
G | A | 38 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(35): Show | 42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.1294-304C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924858 | ||||||
chr5:154924902
|
A | T | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(265): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.1294-348T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924902 | ||||||
chr5:154924909
|
A | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(220): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.1294-355T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924909 | ||||||
chr5:154924921
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1294-367C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924921 | ||||||
chr5:154924938
|
G | A | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1294-384C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154924938 | ||||||
chr5:154925214
|
C | A | 1 | a0003c0015t0008g0289 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1293+648G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154925214 | ||||||
chr5:154925533
|
G | T | 1 | a0001c0001t0001g0270 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1293+329C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154925533 | ||||||
chr5:154925577
|
T | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1293+285A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154925577 | ||||||
chr5:154925660
|
G | A | 4 | a0003c0009t0001g0040a0003c0009t0001g0041a0003c0009t0001g0042others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1293+202C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154925660 | ||||||
chr5:154925746
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1293+116A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 8/27 | chr5 | 154925746 | ||||||
chr5:154926089
|
G | A | 1 | a0002c0021t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1081-15C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154926089 | ||||||
chr5:154926126
|
G | GA | 5 | a0001c0001t0001g0183a0003c0009t0001g0040a0003c0009t0001g0041others(2): Show | 5 | HG02109.hp1 HG03139.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1081-53dupT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154926126 | ||||||
chr5:154926224
|
A | G | 1 | a0002c0002t0001g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1081-150T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154926224 | ||||||
chr5:154926352
|
G | T | 44 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(41): Show | 48 | HG00597.hp2 HG01081.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1081-278C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154926352 | ||||||
chr5:154926387
|
C | T | 1 | a0002c0018t0001g0046 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1081-313G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154926387 | ||||||
chr5:154926672
|
G | A | 1 | a0001c0025t0001g0180 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1081-598C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154926672 | ||||||
chr5:154926766
|
C | T | 44 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(41): Show | 48 | HG00597.hp2 HG01081.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1080+619G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154926766 | ||||||
chr5:154926784
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1080+601C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154926784 | ||||||
chr5:154926833
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1080+552G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154926833 | ||||||
chr5:154927020
|
C | T | 5 | a0002c0018t0001g0046a0003c0009t0001g0040a0003c0009t0001g0041others(2): Show | 5 | HG01109.hp1 HG02109.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1080+365G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154927020 | ||||||
chr5:154927052
|
G | GA | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(258): Show | 306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1080+332dupT | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154927052 | ||||||
chr5:154927052
|
G | GAA | 7 | a0001c0001t0001g0099a0001c0001t0001g0181a0001c0001t0001g0205others(4): Show | 7 | HG00621.hp1 HG00741.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.1080+331_1080+332d others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154927052 | ||||||
chr5:154927237
|
T | C | 2 | a0007c0010t0001g0033a0007c0010t0001g0034 | 2 | NA18954.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.1080+148A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 7/27 | chr5 | 154927237 | ||||||
chr5:154927819
|
G | A | 2 | a0001c0001t0002g0249a0001c0001t0002g0250 | 2 | HG01099.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.915-269C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 6/27 | chr5 | 154927819 | ||||||
chr5:154927846
|
TTGGGCAT others(2): Show |
T | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0260 | 3 | HG01993.hp1 NA18978.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.915-305_915-297del others(9): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 6/27 | chr5 | 154927846 | ||||||
chr5:154927925
|
A | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(220): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.915-375T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 6/27 | chr5 | 154927925 | ||||||
chr5:154927963
|
C | A | 1 | a0001c0001t0001g0181 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.915-413G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 6/27 | chr5 | 154927963 | ||||||
chr5:154928071
|
G | A | 2 | a0001c0001t0001g0182a0001c0001t0001g0183 | 2 | NA18954.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.914+456C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 6/27 | chr5 | 154928071 | ||||||
chr5:154928223
|
T | C | 1 | a0002c0021t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.914+304A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 6/27 | chr5 | 154928223 | ||||||
chr5:154928234
|
G | A | 43 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0022others(40): Show | 54 | HG00408.hp2 HG00438.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.914+293C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 6/27 | chr5 | 154928234 | ||||||
chr5:154928303
|
T | C | 41 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0208others(38): Show | 47 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.914+224A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 6/27 | chr5 | 154928303 | ||||||
chr5:154928316
|
A | C | 1 | a0001c0001t0001g0257 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.914+211T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 6/27 | chr5 | 154928316 | ||||||
chr5:154928722
|
C | T | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(203): Show | 246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.782-63G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154928722 | ||||||
chr5:154928746
|
C | T | 1 | a0002c0002t0001g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.782-87G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154928746 | ||||||
chr5:154928747
|
G | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(202): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.782-88C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154928747 | ||||||
chr5:154928787
|
C | A | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.782-128G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154928787 | ||||||
chr5:154929141
|
A | G | 3 | a0001c0001t0001g0263a0001c0001t0001g0264a0001c0001t0001g0265 | 3 | HG01070.hp1 HG01934.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.782-482T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154929141 | ||||||
chr5:154929415
|
G | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(221): Show | 265 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.782-756C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154929415 | ||||||
chr5:154929442
|
C | T | 4 | a0003c0007t0001g0044a0003c0007t0001g0045a0003c0007t0001g0074others(1): Show | 4 | HG00558.hp2 HG02080.hp2 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.782-783G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154929442 | ||||||
chr5:154929556
|
C | A | 1 | a0001c0001t0001g0210 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.782-897G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154929556 | ||||||
chr5:154929601
|
C | G | 1 | a0002c0021t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.782-942G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154929601 | ||||||
chr5:154929785
|
A | C | 2 | a0005c0012t0002g0222a0005c0012t0002g0223 | 2 | HG02280.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.782-1126T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154929785 | ||||||
chr5:154929958
|
G | A | 38 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(35): Show | 42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.782-1299C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154929958 | ||||||
chr5:154930006
|
T | C | 1 | a0002c0002t0001g0070 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.782-1347A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154930006 | ||||||
chr5:154930025
|
T | C | 1 | a0001c0014t0001g0211 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.782-1366A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154930025 | ||||||
chr5:154930131
|
T | TCTGCCAT others(11): Show |
1 | a0003c0015t0008g0289 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.781+1309_781+1326d others(20): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154930131 | ||||||
chr5:154930188
|
G | A | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | NA18986.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.781+1270C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154930188 | ||||||
chr5:154930196
|
C | A | 1 | a0015c0017t0004g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.781+1262G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154930196 | ||||||
chr5:154930283
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.781+1175C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154930283 | ||||||
chr5:154930364
|
G | A | 1 | a0001c0030t0001g0215 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.781+1094C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154930364 | ||||||
chr5:154930788
|
G | A | 2 | a0001c0001t0001g0217a0001c0001t0006g0216 | 2 | HG04199.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.781+670C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154930788 | ||||||
chr5:154931446
|
G | A | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.781+12C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 5/27 | chr5 | 154931446 | ||||||
chr5:154931629
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.662-52A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 4/27 | chr5 | 154931629 | ||||||
chr5:154931675
|
T | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(220): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.662-98A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 4/27 | chr5 | 154931675 | ||||||
chr5:154931745
|
T | C | 1 | a0001c0001t0001g0219 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.662-168A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 4/27 | chr5 | 154931745 | ||||||
chr5:154931876
|
G | A | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.661+223C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 4/27 | chr5 | 154931876 | ||||||
chr5:154931906
|
G | A | 1 | a0014c0019t0001g0072 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.661+193C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 4/27 | chr5 | 154931906 | ||||||
chr5:154931948
|
G | C | 1 | a0002c0002t0001g0073 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.661+151C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 4/27 | chr5 | 154931948 | ||||||
chr5:154932016
|
T | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.661+83A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 4/27 | chr5 | 154932016 | ||||||
chr5:154932338
|
C | T | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.510-88G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932338 | ||||||
chr5:154932417
|
T | A | 1 | a0001c0001t0002g0251 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.510-167A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932417 | ||||||
chr5:154932443
|
T | G | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.510-193A>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932443 | ||||||
chr5:154932751
|
A | G | 219 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(216): Show | 260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.510-501T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932751 | ||||||
chr5:154932816
|
T | C | 1 | a0001c0001t0001g0220 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.510-566A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932816 | ||||||
chr5:154932829
|
T | C | 38 | a0002c0002t0001g0006a0002c0002t0001g0010a0002c0002t0001g0011others(35): Show | 42 | HG00597.hp2 HG01081.hp1 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.510-579A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932829 | ||||||
chr5:154932871
|
T | C | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.510-621A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932871 | ||||||
chr5:154932902
|
T | C | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.510-652A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932902 | ||||||
chr5:154932966
|
C | A | 1 | a0001c0001t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.510-716G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932966 | ||||||
chr5:154932986
|
C | T | 3 | a0002c0002t0001g0036a0002c0002t0001g0037a0002c0002t0001g0038 | 3 | NA18951.hp2 NA18998.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.510-736G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932986 | ||||||
chr5:154932991
|
T | C | 8 | a0001c0001t0001g0031a0001c0001t0001g0263a0001c0001t0001g0264others(5): Show | 9 | HG00642.hp1 HG01070.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.510-741A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154932991 | ||||||
chr5:154933163
|
C | T | 5 | a0004c0006t0001g0032a0004c0006t0001g0275a0004c0006t0001g0276others(2): Show | 6 | HG02559.hp2 HG02615.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.510-913G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933163 | ||||||
chr5:154933242
|
C | T | 4 | a0003c0009t0001g0040a0003c0009t0001g0041a0003c0009t0001g0042others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-992G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933242 | ||||||
chr5:154933273
|
T | A | 1 | a0001c0004t0005g0039 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.510-1023A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933273 | ||||||
chr5:154933349
|
G | T | 10 | a0001c0001t0001g0015a0001c0001t0001g0113a0001c0001t0001g0114others(7): Show | 11 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.510-1099C>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933349 | ||||||
chr5:154933404
|
A | G | 5 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | NA19006.hp1 NA19011.hp2 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-1154T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933404 | ||||||
chr5:154933442
|
G | A | 1 | a0003c0007t0001g0075 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.510-1192C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933442 | ||||||
chr5:154933684
|
A | AT | 6 | a0001c0001t0001g0099a0001c0001t0001g0104a0001c0001t0001g0106others(3): Show | 6 | HG00323.hp2 HG00735.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.510-1435dupA | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933684 | ||||||
chr5:154933688
|
T | A | 85 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0028others(82): Show | 96 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.510-1438A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933688 | ||||||
chr5:154933697
|
A | T | 2 | a0001c0001t0001g0270a0003c0003t0001g0035 | 2 | HG00621.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.510-1447T>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933697 | ||||||
chr5:154933722
|
C | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18950.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.510-1472G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933722 | ||||||
chr5:154933769
|
A | G | 269 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(266): Show | 314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.510-1519T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933769 | ||||||
chr5:154933839
|
CCT | C | 44 | a0001c0004t0005g0039a0002c0002t0001g0006a0002c0002t0001g0010others(41): Show | 48 | HG00597.hp2 HG01081.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.510-1591_510-1590d others(4): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933839 | ||||||
chr5:154933864
|
G | C | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 259 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.510-1614C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154933864 | ||||||
chr5:154934106
|
C | A | 1 | a0015c0017t0004g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.509+1735G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934106 | ||||||
chr5:154934164
|
C | A | 2 | a0003c0007t0001g0074a0003c0007t0001g0075 | 2 | HG00558.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.509+1677G>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934164 | ||||||
chr5:154934165
|
G | A | 1 | a0003c0023t0001g0043 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.509+1676C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934165 | ||||||
chr5:154934293
|
C | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(267): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.509+1548G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934293 | ||||||
chr5:154934513
|
T | C | 1 | a0001c0001t0001g0252 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.509+1328A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934513 | ||||||
chr5:154934529
|
C | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0099a0001c0001t0001g0100others(3): Show | 9 | HG00140.hp2 HG00642.hp2 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.509+1312G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934529 | ||||||
chr5:154934604
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.509+1237C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934604 | ||||||
chr5:154934637
|
G | A | 1 | a0002c0021t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.509+1204C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934637 | ||||||
chr5:154934659
|
T | C | 1 | a0015c0017t0004g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.509+1182A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934659 | ||||||
chr5:154934706
|
C | T | 1 | a0015c0017t0004g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.509+1135G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934706 | ||||||
chr5:154934782
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.509+1059A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934782 | ||||||
chr5:154934796
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.509+1045T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154934796 | ||||||
chr5:154935032
|
C | T | 4 | a0003c0009t0001g0040a0003c0009t0001g0041a0003c0009t0001g0042others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+809G>A | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154935032 | ||||||
chr5:154935072
|
T | A | 4 | a0002c0002t0001g0011a0002c0002t0001g0076a0002c0002t0001g0077others(1): Show | 5 | HG01346.hp2 HG01993.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+769A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154935072 | ||||||
chr5:154935306
|
T | C | 4 | a0003c0009t0001g0040a0003c0009t0001g0041a0003c0009t0001g0042others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+535A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154935306 | ||||||
chr5:154935508
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA18950.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.509+333T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154935508 | ||||||
chr5:154935533
|
G | A | 2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.509+308C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154935533 | ||||||
chr5:154935620
|
A | G | 4 | a0003c0009t0001g0040a0003c0009t0001g0041a0003c0009t0001g0042others(1): Show | 4 | HG02109.hp1 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+221T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154935620 | ||||||
chr5:154935791
|
C | G | 2 | a0001c0004t0005g0039a0003c0003t0001g0035 | 2 | HG02630.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.509+50G>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154935791 | ||||||
chr5:154935794
|
G | A | 16 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0257others(13): Show | 18 | HG00438.hp1 HG00642.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.509+47C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 3/27 | chr5 | 154935794 | ||||||
chr5:154936099
|
A | C | 1 | a0001c0001t0001g0014 | 2 | HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.328-77T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 2/27 | chr5 | 154936099 | ||||||
chr5:154936310
|
G | C | 1 | a0001c0001t0001g0270 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.328-288C>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 2/27 | chr5 | 154936310 | ||||||
chr5:154936357
|
CAGTGAGC others(78): Show |
C | 268 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(265): Show | 313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.328-420_328-336del others(85): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 2/27 | chr5 | 154936357 | ||||||
chr5:154936416
|
C | CAAAAAAA | 17 | a0003c0003t0001g0009a0003c0003t0001g0013a0003c0003t0001g0035others(14): Show | 20 | HG01952.hp1 HG01978.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.328-401_328-395dup others(7): Show |
GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 2/27 | chr5 | 154936416 | ||||||
chr5:154936706
|
G | A | 2 | a0001c0001t0001g0273a0001c0001t0001g0274 | 2 | HG02074.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.327+319C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 2/27 | chr5 | 154936706 | ||||||
chr5:154936819
|
A | C | 3 | a0002c0002t0001g0036a0002c0002t0001g0037a0002c0002t0001g0038 | 3 | NA18951.hp2 NA18998.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.327+206T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 2/27 | chr5 | 154936819 | ||||||
chr5:154936951
|
A | G | 1 | a0003c0003t0001g0035 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.327+74T>C | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 2/27 | chr5 | 154936951 | ||||||
chr5:154937003
|
A | C | 1 | a0001c0001t0001g0095 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.327+22T>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 2/27 | chr5 | 154937003 | ||||||
chr5:154937365
|
G | A | 1 | a0001c0029t0002g0279 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.167-180C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/27 | chr5 | 154937365 | ||||||
chr5:154937393
|
T | C | 3 | a0002c0002t0001g0006a0002c0002t0001g0092a0002c0002t0001g0093 | 5 | HG02257.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.167-208A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/27 | chr5 | 154937393 | ||||||
chr5:154937482
|
T | C | 1 | a0002c0021t0001g0094 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.167-297A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/27 | chr5 | 154937482 | ||||||
chr5:154937499
|
T | A | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(218): Show | 264 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.167-314A>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/27 | chr5 | 154937499 | ||||||
chr5:154937520
|
T | C | 1 | a0001c0001t0001g0280 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.167-335A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/27 | chr5 | 154937520 | ||||||
chr5:154937594
|
T | C | 1 | a0015c0017t0004g0281 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.166+374A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/27 | chr5 | 154937594 | ||||||
chr5:154937797
|
T | C | 1 | a0001c0001t0001g0282 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.166+171A>G | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/27 | chr5 | 154937797 | ||||||
chr5:154937884
|
G | A | 5 | a0001c0001t0002g0283a0001c0001t0002g0284a0001c0001t0002g0285others(2): Show | 5 | HG00323.hp1 HG01106.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.166+84C>T | GEMIN5 | ENSG00000082516.9 | transcript | ENST00000285873.8 | protein_coding | 1/27 | chr5 | 154937884 |